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IDS Wants To Scrap The WRAG

November 24, 2013

Yes, readers, you read that right. So, those capable of work should starve until they find some, should they, Sir?

A Letter To My Husband With ASD

November 24, 2013

A letter of expression, realisation, acceptance and thanks, from the wife of a man with ASD.

Interview with a Job Centre Advisor: sanction targets & corruption revealed

November 23, 2013

Slutocrat's avatarSlutocracy

@JobcentreMole is a Job Centre advisor who has taken to Twitter to speak out about the Job Centre’s unfair treatment of people who are claiming benefits. For obvious reasons he is anonymous. I think that what he’s doing is very brave. We did this interview by email. (All emphases are mine).
The Mole says: “I started my career with Jobcentre plus over 15 years ago at such a young age, I have literally done every job at lower (band B) level there is within the Jobcentre. I can assure you my knowledge of Jobcentre Plus is up with the best, I can also assure you I am not alone with my views.” 
Do the management have targets to sanction x number of people, or are your team encouraged to sanction people?

There is 100% no specific target at all, however it is and has been mentioned before that each signer…

View original post 2,691 more words

SOUTH EDINBURGH MSP LAUNCHES NEW PREMISES FOR UNIQUE CHILD CARE SERVICE

November 22, 2013

A press release.

Kezia Dugdale, MSP for Edinburgh South, will today (Friday 22 November) launch the new premises of an after school and holiday club catering for children with and without disabilities.

Kidscene, which is run by the charity Royal Blind, offers a unique child care service with a “reverse integration model,” caring for children with and without disabilities in an integrated setting. Kezia Dugdale MSP is launching Kidscene’s new premises, which have been built at the Royal Blind School’s Canaan Lane campus as part of the school’s current re-development programme.

Richard Hellewell, Chief Executive at Royal Blind said:

“We’re delighted in the interest we have had from parents in Edinburgh and beyond since Kidscene opened in January 2012. Children at Kidscene learn that disability is not a barrier to friendships and play. We are delighted to have Kezia Dugdale MSP along today to launch our new and expanded premises for Kidscene at the Royal Blind School’s Canaan Lane campus.”

To launch the premises Ms Dugdale will cut a cake with Kidscene’s logo on it and unveil a plaque that has been wrapped for the occasion by children attending Kidscene.

Kezia Dugdale MSP said:

“I’m thrilled to be involved in the opening of this new facility, asKidscene offers an excellent environment for children, whether or not they have any disabilities. It is an important part of children’s learning to grow up understanding differences and Kidscene can help them do that.”

Sings of the True Nature of the DWP: Samaritans Cards at the Job Centre

November 22, 2013

So, the JobCentre staff know how serious things are, but like all staff, live in fear of their jobs.

Bournemouth Councillor Susan Phillips Resigns From Role After ‘Too Many Disabled Bays’ Comment

November 22, 2013

Readers, listen to this.

Then read this.

A councillor has resigned from her role as equality and diversity champion after a rant about disabled parking spaces at a shopping centre was recorded.

Susan Phillips said that there should be fewer disabled parking bays as people in wheelchairs ‘aren’t going to walk around’ and use the centre.

Conservative Mrs Phillips was recorded making the controversial remarks to an operator as she paid off a £60 fine for parking in a disabled bay.

She had illegally parked in one of the 144 reserved yellow spaces at the Castlepoint shopping centre in Bournemouth, Dorset.

Although the car park has 2,800 bays in total, the town hall official claimed she spent 45 minutes trying to find a space before parking her Volkswagen Beetle in a disabled bay.

When she returned to her car, Mrs Phillips found a parking ticket on her windscreen.

In the recorded telephone call she had with an operator with Devere Parking Serices, she
said: ‘I actually feel when you have 12 bays all empty for disabled, and I drove around for three quarters of an hour trying to park and couldn’t, I find that people who are disabled basically, they aren’t going to walk around and I think they have far too many disabled parking bays.’

Mrs Phillips stuck to her views and later said: ‘I would say disabled people who drive perhaps don’t frequent the likes of Castlepoint because it’s so far to walk everywhere.

‘There were 10 or 12 disabled spaces free and I was driving around and around but I know that doesn’t make it OK.

 

‘I was against the clock that day. You do the crime and you pay the bill and I should not have parked there.

‘I was very upset about what I’d done, I’ve never parked in a disabled space before.’

Helen Dolphin, a spokeswoman for Disabled Motoring UK, said Mrs Phillips’ comments ‘show how little she knows about the needs of disabled people in her area’.

She said: ‘The fact that they won’t be walking around is probably correct as they will probably be in wheelchairs or mobility scooters.

‘That’s not to say there won’t also be disabled people walking around.

‘It might be that at other times those disabled parking spaces are packed.’

Mrs Phillips has worked as Bournemouth Borough Council’s champion for equality and diversity since May.

She voiced her controversial views despite having undergone training for the role.

To Susan Phillips I say: I’m disabled. I have a Blue Badge and use Blue Badge spaces often. I’m also lucky enough to be able to walk around!

Warning: Job Centres Planning To Get Rid Of Public Phones

November 22, 2013

Spotted here.

Anon
can you post this up so people can be warned
what the hell is the gov up to they are planing to remove all public phones in job centres.
So god knows how the hell people who have no house phone are going to find out why they have not had there money, unless numbers are going to be free phone or you can go in to the jobcentre and ask why, like you could many moons ago

LoveFilm: All We Want For Christmas Is Subtitles

November 21, 2013

From Change.org. Please add your signature. I just did.

Like you I enjoy watching the latest film or must-see TV show. Whether it’s Breaking Bad or the Hunger Games I want to be part of the conversation’s that all of my friends are having. However, as a LoveFilm customer I’m always missing out.

 

Like most of the people with hearing loss I rely on subtitles. There are over 10million of us in the UK yet as one of the biggest on demand and DVD rental companies, LoveFilm just isn’t accessible to us.

 

People with Hearing Loss want to be able to watch what they want, when they want, how they want – just like everyone else. However we can’t do that with LoveFilm Instant’s on-demand service as they don’t offer subtitles on any of their titles.

 

And it’s not just when we’re watching films on our IPad’s, Phones or over the internet. When choosing from LoveFilm’s rental service we can’t even see if the film we are picking has subtitles before it arrives in the post. We’re getting a second class service and this isn’t fair.

 

This Christmas I just want to be able to sit down with my family and enjoy watching a DVD like everyone else. Please help me to get LoveFILM to improve their service for people with hearing loss.

Does Doing Yoga Make You A Hindu?

November 21, 2013

That’s the question this article asks. My personal thoughts on this are that although yoga may have had its roots in Hinduism, it is now a recognised form of physical exercise worldwide.

The reason I’m posting this here is that I know of quite a few physically disabled people who use adapted yoga as a treatment system. Not all of them are Hindu!

What are your thoughts?

Save Disability Studies At University Of Manchester!

November 21, 2013

Students at the University of Manchester have started a petition to bring back disability studies after it was scrapped by the uni. According the the Mancunion student paper, the course will continue at the Manchester Institue of Education, but students are worried it won’t be as in-depth as the degree.

In an open letter to the Greater Manchester Coalition of Disabled People, lecturer Barbara Perry says: “I am extremely concerned over the recent closure of the learning disability studies programme at the University of Manchester. This is a unique and innovative degree programme which includes disabled adults at the core of its work.”

Bedroom Tax Comes Second- In Oxford Dictionaries Word Of The Year Competition

November 21, 2013

I didn’t even know it was in a dictionary!

bedroom tax, noun, informal

(in the UK) a reduction in the amount of housing benefit paid to a claimant if the property they are renting is judged to have more bedrooms than is necessary for the number of the people in the household, according to criteria set down by the government.

The Welfare Reform Act 2012 proposed various changes to the rules governing social security benefits in the UK, including an ‘under-occupancy penalty’ to be imposed on households that were receiving housing benefit and that were judged to have bedrooms surplus to their requirements. Critics and opponents soon began to refer to the new penalty as the ‘bedroom tax’, perhaps as a way of associating it with the term poll tax (a popular name for the unpopular community charge, now replaced by council tax). The first references to the bedroom tax in our corpus appear in 2011 but usage increased dramatically around the time this new provision came into force, in April 2013.

A mainstream institution is listening. This is a funny sort of progress!

DLA The McVey Way

November 21, 2013

A poster that made me smile…

 

Disabled Refugees- And The Silly Reasons They Were Sanctioned

November 20, 2013

Readers, please read the three case studies at the end of this post. Two of them are of sick/disabled people and all three reasons for sanctioning are equally silly.

 

DWP Staff Told To Judge Benefit Claims By Googling Illnesses

November 20, 2013

Readers, I love Google very much, but… really?

Civil servants have been told they can judge whether to pay benefits to ­the sick by ­Googling their illnesses, after proper tests were scrapped.

In a memo leaked yesterday, Department for Work and Pensions staff were instructed to look online when assessing new claims for Disability Living Allowance for under 18s and Attendance Allowance for over 65s.

Shadow Work Secretary Rachel Reeves accused the Tory-led Government of showing “utter contempt” for disabled people.

The Labour MP said: “Out-of-touch ministers need to explain to disabled people how they’ve got to a situation where guidance is being issued telling civil ­servants to look for advice on complex disability cases on the internet.

“It’s just one more sign of the utter incompetence of DWP Ministers and their total contempt for a fair assessment process for disability benefits.

“It beggars belief that staff are instructed to look online for information on complex medical conditions until a full service is resumed.”

The fiasco comes after medical examinations run by hated contractor ATOS were scrapped and the rolling out of the new benefit, Personal Independence Payment — which is replacing DLA — was delayed.

Disabled people whose conditions have worsened are also being assessed by officials surfing the web.

The November 7 DWP staff bulletin stated: “Medical Practitioners will no longer be available as a source of evidence.”

Decision makers are advised to consult the “recognised internet sites such as Cancer Research UK and NHS Choices”.

Other suggestions include phoning the claimant or their carer, discussing the case with colleagues and seeking advice from social services.

But the DWP stressed officials were not just looking conditions up online.

A spokesman said: “Decision makers can also use information from sources including the claim form, care plans, medical reports and carers.”

Launch Of UK Disability History Month 2013

November 20, 2013

Last night in London, disabled people, disability activists, carers and supporters gathered to launch UK Disability History Month 2013. Now in its fourth year, the Month continues to grow, and to be recognised and supported by national mainstream organisations. In fact, this year, it was co-sponsored by the National Union of Teachers.

The Month will, as usual, run from 22 November to 22 December. This year’s theme is Celebrating our Struggle for Independent Living: No Return to Institutions or Isolation. It’s a fitting theme, considering the recent victory in court over the closure of the Independent Living Fund, something which came up a few times through the evening.

As always, it was an educational evening of speeches and video clips, rounded off with a good laugh and a chance to socialise.

The evening began with a video clip from a recent BBC4 documentary, Disowned and Disabled, Breaking Free. This showed what life was like for disabled people who were sent to institutions in the past, and how they broke free.

A representative from the National Union of Teachers spoke about how the Union plans to support the Month, and how they support disabled teachers. I learnt that the Union has a section for disabled teachers, as well as a national seat which is always held by a disabled teacher. I had never thought about disabled teachers in the past. However, having been a disabled pupil in mainstream education and being a passionate supporter of inclusive education, I was very pleased to learn that disabled teachers are accepted and supported by their largest Union.

Then there was a speech by  Jackie Downer, a woman with learning disabilities herself who is now the CEO of her own company. She described the struggles she has faced in her own life, and the progress she has made.

Kirsten Hearn, the Chair of Inclusion London, and Professor Mike Oliver, also spoke about their experiences and the importance of inclusion and independent living.

Professor Jan Walmsley spoke about the history of people with learning disabilities, and the importance of hearing, and learning from, the stories of people who lived in institutions and long stay hospitals. She paid tribute to Mabel Cooper, her personal friend who spent most of her life in a long stay hospital, through a moving video in which Mabel Cooper told her own story.

Richard Rieser, Founder and Co-ordinator of the Month, spoke about other events planned for this year.

The evening was rounded off by comedy from Liz Carr, someone whose work I have followed, admired and enjoyed for a long time.

The month may have started as a way to celebrate our struggles, but if, as I hope it does, it continues to grow, be successful and focus on current issues affecting the lives of disabled people, it might just become a way for us to celebrate our successes and victories as well. There’s a long way to go before disabled people stop facing struggles, but if we continue to fight for our rights, and to celebrate successes and victories, we will never again return to institutions, or to isolation.

The Man Who Can Taste The Tube Map

November 20, 2013

Most London commuters have a love/hate relationship with the Underground depending on their experience of delays. But for one man, travelling on the Tube has a very particular effect.

Since childhood, James Wannerton from Dollis Hill in north London has had a condition called synaesthesia, which links senses normally experienced separately.

It means that when he reads the names of London Underground stations, each one conjures up a particular, strong taste – from sausage and eggs at Tottenham Court Road to putrid meat at Kilburn.

He has now created a new version of the Underground map which he hopes will help people understand the condition.

Synesthesia Linked To Autism Finds Study

November 20, 2013

A condition where people experience a mixing of the senses, such as tasting words, has been linked with autism.

Research suggests synaesthesia is nearly three times as common in adults with autism spectrum disorder than in the general population.

The two conditions may share common features such as unusual wiring of the brain, say UK scientists.

The study helps understanding of how people with autism experience life, says the National Autistic Society.

Synaesthesia is a condition where one sense automatically triggers another. Some people experience tastes when they read or hear words, some perceive numbers as shapes, others see colours when they hear music.

People with synaesthesia might say: “The letter q is dark brown,” or: “The word ‘hello’ tastes like coffee,” for example.

Following anecdotal evidence of links between synaesthesia and Asperger’s syndrome, researchers at the Autism Research Centre at Cambridge University set out to test the idea.

More than 200 study participants – 164 adults diagnosed with high-functioning autism or Asperger’s syndrome, and 97 adults without autism – were asked to fill in questionnaires to measure synaesthesia and autism traits.

The study found one in five adults with autism spectrum conditions – a range of related developmental disorders, including autism and Asperger’s syndrome – had synaesthesia compared with about 7% of people with no signs of the disorders.

Prof Simon Baron-Cohen, who led the research, told BBC News: “Synaesthesia involves a mixing of the senses and it’s a very subjective private experience, so the only way we know it’s happening is if you ask people to report on their experiences.

“And what this new study has done is ask people whether they experience synaesthesia, for example where a sound triggers the experience of colour or a taste triggers the experience of colour, and finding that these unusual experiences are actually much more common in autism than we previously knew.”

The research, to be published in the journal Molecular Autism, suggests that while the two conditions might appear distinct, there could actually be some underlying similarities in brain connectivity.

Hyper-connectivity

Synaesthesia seems to involve unusual connections between brain areas not usually wired together, accounting for the jumbling up of the senses.

One theory about autism is that it involves over-connectivity of neurons, so that a person focuses on small details but finds it difficult to see the big picture.

Future research is needed to explore biological mechanisms behind both conditions, including carrying out detailed brain scans, says the Cambridge University team.

Carol Povey, director of the National Autistic Society’s Centre for Autism, said the study could help improve our understanding of autism.

“People with the condition can find everyday life confusing or even frightening, so research like this, which helps us to understand more about how they experience the world, is valuable,” she said.

“It can help us to develop more appropriate support and to make adjustments according to their needs, which is vital if people with autism are to reach their full potential.

“With the right support at the right time people with autism can live the life they choose.”

Ouch Interview Cerrie Burnell

November 19, 2013

Ouch have caught up with the amazing Cerrie Burnell, on disabilities, diversity on screen and daughters.

Forced to pay the bedroom tax…for a dialysis machine.

November 19, 2013

msjackmonroe's avatarCOOKING ON A BOOTSTRAP

20131118-230856.jpg

http://www.independent.co.uk/news/uk/home-news/welfare-scandal-subject-to-the-bedroom-tax–even-if-the-room-is-used-for-a-kidney-dialysis-machine-8947883.html

For everyone that still doesn’t realise how evil and twisted this is. I don’t care what you call it, ‘bedroom tax’ or ‘spare room subsidy’ or ‘the machinations of a psychopath’, read this article.

And this one: http://www.walesonline.co.uk/news/wales-news/bedroom-tax-sting-kidney-patient-2513203

And this one: http://www.echo-news.co.uk/news/10601794.My___50_a_month_bedroom_tax___for_my_DIY_dialysis_machine/

And this one: http://www.oxfordmail.co.uk/news/10634947.My_bedroom_tax_fight_goes_to_UN/?ref=rc

There are dozens more examples I could link to – this is not an exceptional case.

View original post

Obituary: Authur Verney

November 18, 2013

Campaigner for British Sign Language.

Speechless- Award-Winning Love Story

November 18, 2013

You need to watch this to the end. It’s well worth the watch.

For those who don’t understand Hindi, the conversation between father and son is:

“We had my birthday in the mall and for sister’s birthday we’re going on holiday!”

“Well we can’t take so many friends on a holiday. Next year, promise.”

The Truth About The ‘Welfare Culture’

November 18, 2013

The Conservative Philosophy…

November 18, 2013

Hywel Williams MP To Ask IDS A Question On ILF Today At 2.30pm

November 18, 2013

Spotted on Facebook. Shared so it can be watched by more of us, hopefully.

At 2.30pm on Monday 18 November, the Secretary of State for Work and Pensions Ian Duncan Smith will be asked a question by the Welsh MP Hywel Williams about what the government’s plans are for the future of the Independent Living Fund. It will be screened live on BBC’s Parliament channel. It is impossible to predict what decisions have been made by the government, and what their response to Hywel Williams question will be. Campaigners will respond to any significant developments through Disabled People Against Cuts web site.

Fresh Fears For Kerry McDougall And Family Over Children

November 17, 2013

I’m very sad today to see Kerry McDougall and her family back in the news for all the wrong reasons. I covered their case in detail the first time around and followed it with interest.

A woman deemed too dumb to wed is back in the UK as a married mum… but is facing a fresh investigation.

Desperate Kerry McDougall fears ­social services will try to put her two sons into care and told the Sunday People: “I can’t bear the thought of my boys being taken away.”

Pregnant Kerry fled Scotland for Ireland with Mark McDougall when social services said they could not marry, just two days before their church wedding.

They said Kerry, who has mild learning difficulties, lacked the intelligence to understand the vows.

A few weeks later, in 2009, the couple ran off to Ireland, fearing their baby would be taken off them and fostered.

But Kerry, now 21, and Mark grew homesick and after four years are back in Fife with Ben, three, and Lochlan, two.

Two weeks ago UK social services said they no longer had any concerns but now two social workers say they will look at whether the boys should be put under a protection order.

Lib Dem MP John Hemming said: “It appears the Fife authorites are being vindictive in the way they are dealing with this.”

Mark, 30, said: “Kerry and I can hardly sleep. We’re sick with worry.

“We believed all this was behind us. Surely social services only have to look at our boys to see Kerry’s a good mum.

“We’d never have come back here if there was any risk of losing them. We’ve had every ­assessment in Ireland – our sons are happy, healthy kids.”

Mark landed a night warehouseman job on returning to Fife but social services, worried how Kerry would cope with the boys at night, said he couldn’t do it.

Mark had worked full-time in a hotel in Ireland and said despite having relatives on hand to help, social services seems “determined to ruin our lives”.

In January 2010, the couple’s first son Ben was three days old when Irish social services, alerted by the couple’s health records in Scotland, took the boy into care.

Kerry said: “It was the worst day of my life. I was breastfeeding Ben and Mark was begging social services not to take him.”

But after nine months officials ruled Kerry was fit to care for Ben.

The couple wed at Waterford Registrar office, set up home nearby and had Lochlan in November 2011.

But the pair grew increasingly homesick for the UK.

Mark said: “We both have extended families in the UK. We longed for the boys to be brought up with their grans, aunts and uncles.”

Dougie Dunlop, Head of Children and Families and Criminal Justice in Fife said: “As with any family moving back to Fife, we’ll continue to meet Kerry and Mark to discuss their circumstances so they receive the care and support they need.”

Iain Sim Takes #BedroomTax Fight To Cameron In Open Letter

November 17, 2013

Sincere thanks, Sir. Readers, read the letter. Please. It’s heartbreaking.

Iain Sim, Chief Executive has taken the unusual step of writing personally to David Cameron to ask that he intervenes to ‘abolish this most abhorrent of policies – the Bedroom Tax’.

Mr Sim, who has campaigned tirelessly against the Bedroom Tax, was driven to take the fight to the highest level following a recent tribunal ruling, which found in favour of a disabled Coast & Country tenant.

The letter apprises the Prime Minister of the facts of the case, and the hardship and heartache caused to the couple, hard workers who have fallen on hard times due to ill health.

Iain Sim, Chief Executive of Coast & Country, said: “The Bedroom Tax is detestable because it is affecting some of the poorest people in society, who through no fault of their own are living in homes that are classed as too big for them.

“To hear that one couple took on the establishment and won is fantastic news but there are so many more people still affected by this unjust tax.

“I feel so passionately about this issue that I felt that I needed to ensure that the Prime Minister knew just how this policy is affecting real people in their lives. The story of Mr and Mrs A is one of tragedy and certainly not one of ‘scrounging’ from the State.

“I sincerely hope that Mr Cameron feels moved to take some action.”

 A full transcript of the letter is available here and can be used for publication.

Thousands Need Foodbanks Because Of Cuts And Sanctions

November 17, 2013

A Sunday Express investigation has uncovered scores of cases in which people need charity handouts after being denied benefits because of administration errors and punitive sanctions.

As many as 580,000 cuts to benefit payments were made between October 2012 and June 2013, a six per cent rise on the same period a year earlier, before rules were toughened.

Employment Minister Esther McVey said the sanctions, or cuts to benefits are used only against those who were “wilfully rejecting support for no good reason”.

However, our research reveals some sanctions are unfair. We spoke to:

• A blind woman whose benefits were removed because she did not apply for a cleaning job.

• A father with terminal cancer punished after he missed signing on because of a hospital appointment.

• A woman refused benefits because she forgot to “sign on” on the day of her younger brother’s funeral.

• A 33-year-old man with severe dyslexia who had his benefits removed because he could not fill in his claim form correctly.

• A mother of three denied benefits because her husband mistakenly filled in a claim form with the wrong date of birth for one of their children.

• A man whose benefits were removed after he missed two job centre appointments because of the death of his mother following a stroke.

The trust saved our lives. My son would come home from school, open the cupboard and say: ‘When will we have food to eat?’

In other cases people have been hit for using the wrong ink on a claim form and failing to apply for jobs that are too far away for them to reach affordably.

Mother-of-two Suzanne Harkins, 42, a former psychiatric nurse from Paisley, Renfrewshire, was denied benefits after her husband David, 42, failed to complete a course he had been told he did not need to attend.

Mr Harkins, also a psychiatric nurse and former manager of a mental health unit, had been unable to work after suffering a nervous breakdown four years ago.

Mrs Harkins had given up her job to care for her late mother who had Parkinson’s disease and cancer and who died last week.

The family could not afford their mortgage payments and their house was repossessed. They presented themselves as homeless to Renfrewshire Council which offered them a flat to live in days before Mrs Harkins gave birth to her second child.

Soon afterwards the benefits office cut the family’s weekly benefits by £120 after wrongly sending out a duplicate appointment for a course Mr Harkins had already completed.

Last winter the family had to live on £50 a week. Mrs Harkins became so malnourished she could no longer breastfeed.

However, she said she and her family would not have survived without the food bank, which is run by the Trussell Trust: “The trust saved our lives. My son would come home from school, open the cupboard and say: ‘When will we have food to eat?’ ” The benefits office has now admitted its mistake and reimbursed the family.

Geoffrey Reeves, a 55-year-old carpenter and father of two, had worked since he left school at 16 but says he was hit by the recession four years ago when work dried up. Mr Reeves, from Eccles, Greater Manchester, says he has been unable to find another job and has suffered benefit sanctions for failing to make the mandatory 20 job applications a week because there are not enough jobs to apply for.

He said: “I have been working all my life but there just are not the jobs out there. The bills are piling up. I cannot afford to eat. I am suffering from depression because of it all.”

Chris Johnes, UK poverty programme director for Oxfam, said: “We are seeing the impact of arbitrary and harsh sanctions in which people are pushed to the edge of destitution because they are caught up in an unresponsive and callous bureaucracy.

“It is a situation no person should have to be in living in a rich nation like ours.”

Another Betrayal By Paul Maynard MP

November 16, 2013

Readers, for the last couple of days, this brilliant post by Jack Monroe has been flying around cyberspace.

It names and shames the 169 MPs who voted for the bedroom tax- and claimed up to £25K in accommodation expenses themselves.

Until now, I haven’t had time to look at the list in detail. However, when I did, I had a very unpleasant surprise.

I discovered that Paul Maynard, MP with Cerebral Palsy, voted for the Bedroom Tax.

Readers, that in itself would have hurt me more than enough. But then I discovered that Paul Maynard, disabled MP, claimed up to £15K in accommodation expenses himself.

Readers, Paul Maynard MP has never made any secret of the fact that he is not in Parliament to represent disabled people, but his constituents.

Well then readers, please explain to me how he could have voted for a policy that must be significantly contributing to his constituents sharing bath water to save money?

Yet again, I feel betrayed by Paul Maynard MP.

 

Allen Vincent: Man With Asperger’s Arrested For Tweeting

November 16, 2013

Readers, please sign and share this.

Please help sign this to raise awareness for Edlington resident Allen Vincent. He suffers from a list of health problems, including Asperger’s Syndrome. He has been treated terribly by a wide range of people because of his disability, and has no care or support. In his frustration, Allen made his opinions known on twitter, some threatening, but had no intention of hurting anyone. He was arrested and treated terribly by local police. Allen was just being himself, a disabled,vulnerable man who is crying out for someone to help. He now finds himself in police custody. This petition will be sent to his local MP Caroline Flint in an attempt to get the help he deserves.

Very Important!! DWP Bank Details Possible Scam!!

November 16, 2013

Please share everywhere. Spotted on Facebook via reader Amy Wood.

>>>>I’ve just been hearing in a group that someone who is disabled, waiting to hear about a PIP claim….had a call from the DWP…asking for her bank details…NEVER EVER EVER…give your bank details over the phone to these people (it could be a scammer)..get them to send you out a letter about it..REMEMBER you do NOT have to give ANYONE information about yourself over the phone..no matter who it is even the DWP!!!!<<<<

Maida Vale resident in a one bed sheltered housing flat sent £1,200 Bedroom Tax bill by Westminster Council

November 15, 2013

Margo MacDonald MSP’s New Assisted Dying Bill

November 15, 2013

Proposals to give terminally ill people in Scotland the legal right to assisted suicide have been relaunched by the independent MSP Margo MacDonald.

 

Her previous attempt to change the law was defeated in parliament but she said the public now had better awareness of the issue.

 

The Lothians MSP, who has Parkinson’s disease, outlined her Assisted Suicide Bill in Edinburgh.

 

The Scottish government has said it does not support a change in the law.

 

And it is still unclear whether there is majority backing for the measure among MSPs.

 

The bill’s strongest critics have said it could see Scotland becoming a “suicide tourism” destination, along with other countries where the practice is legal, such as Switzerland.

 

There have also been concerns it could fail to safeguard frail, elderly people.

 

Ms MacDonald told the BBC she had learned lessons from her previous attempt to get a bill passed and had brought forward a clearer and more straightforward process.

 

Her bill would allow people whose lives became intolerable through a progressive degenerative condition or terminal illness to seek a doctor’s help in dying.

 

There are also a series of safeguards which aim to prevent abuse of the legislation.

 

The main measures in the bill include:

 

  • Only those who are terminally ill or who are suffering from deteriorating progressive conditions which make life intolerable can seek assisted suicide.
  • An “early warning” aspect, whereby anyone over the age of 16 can inform their GP of their support in principle for assisted suicide.
  • The indication can be noted in the person’s medical records, but must be stated at least seven days before they can formally request help to end their life.
  • Any requests to GPs must be backed up by a second professional opinion, and followed by a 14-day “cooling off” period.
  • The process is then repeated again with a second request, after which one of the doctors concerned supplies a licensed facilitator with a prescription to enable assisted suicide to take place.
  • The facilitator, or “friend at the end”, has no relationship with the patient and is given the task of collecting the prescription and agreeing the process of assisted suicide.
  • If the prescription is not used within 14 days, it must be returned to the chemist.

 

Ms MacDonald said: “I decided as soon as we lost the last one that I had to get a better one and reintroduce it, because so many people think this is the right thing to do for people who have a progressive, degenerative condition who are facing a less than dignified end.

 

“And people who are terminally ill, if they want to go just a bit sooner, they should be able to choose to do so without making anyone subject to prosecution.”

 

In 2010, Ms MacDonald’s End of Life Assistance Bill was defeated by 85 votes to 16, with two abstentions, by MSPs who were allowed a free vote on the legislation, rather than on party lines.

 

But Ms MacDonald said she hoped high-profile cases such as that of Tony Nicklinson in England, who had locked-in syndrome and battled for years for a legal right to end his life, had increased awareness.

 

And she pointed to last year’s report from the Commission on Assisted Dying – set up and funded by campaigners who want to see a change in the law in England and Wales – which said the current system was “inadequate”.

 

Ms MacDonald said she was “pretty certain” support for her bill among MSPs had grown since 2010.

 

Her new bill is launched a day after opponents of assisted dying from across Europe met to speak out against the move.

 

The Euthanasia Prevention Coalition Europe, convened in Brussels, included the Scottish group Care Not Killing, an alliance of 50 groups, including faith-based organisations, which is strongly opposed to Ms MacDonald’s proposals.

 

Assisted suicide – the legal position

It is not illegal to attempt suicide in Scotland, but helping someone take their own life could lead to prosecution.

In England and Wales, the Suicide Act 1961 makes it an offence to encourage or assist a suicide or a suicide attempt, which is almost identical to the situation in Northern Ireland.

The Director of Public Prosecutions has to approve any assisted suicide court action in England, Wales and Northern Ireland.

In 2010, Keir Starmer, then the DPP, issued guidance that made it clear that family or friends who travelled with a loved one to the Swiss suicide group Dignitas would not risk prosecution.

The guidelines were the result of a case brought by Debbie Purdy, a terminally ill woman, who in 2009 won a legal ruling requiring the DPP to set out whether her husband would be committing an offence if he accompanied her to Dignitas to end her life.

Scotland’s prosecution service, the Crown Office, has issued no such guidance.

Assisted suicide is legal in Luxembourg, the Netherlands and Belgium as well as Switzerland.

 

Care Not Killing convener Dr Gordon Macdonald said: “The Scottish Parliament overwhelmingly rejected an attempt by Margo MacDonald to legalise euthanasia and assisted suicide in 2010.

 

“MSPs concluded that vulnerable people would be put at risk from such legislation.

 

“Scotland can learn from the damaging effects of legalising euthanasia and assisted suicide in other parts of Europe and North America.

 

“Europe can learn from Scotland’s example as a country which has rejected the view that some people’s lives are not worth living. We believe that society has a responsibility to protect the most vulnerable.”

 

It is not illegal to attempt suicide in Scotland, but helping someone take their own life could lead to prosecution.

 

The Suicide Act 1961 makes it an offence to encourage or assist a suicide or a suicide attempt in England and Wales, which is almost identical to the law in Northern Ireland.

 

Outside Scotland, the Director of Public Prosecutions (DPP) has to approve any assisted suicide court action in England, Wales and Northern Ireland.

 

In 2010, Keir Starmer, then the DPP, issued guidance that made it clear that family or friends who travelled with a loved one to the Swiss suicide group Dignitas would not risk prosecution.

 

Ms MacDonald is pressing ahead with her fresh bill after getting the necessary 18 signatures from other MSPs to bring it to parliament.

 

She is officially launching the legislation at an event in Edinburgh, along with MSPs representing all the political parties and Silvan Luley, of Dignitas.

 

Assisted suicide is legal in Luxembourg, the Netherlands and Belgium as well as Switzerland.

 

In the House of Lords, the Labour peer and former UK Lord Chancellor, Lord Falconer, has proposed a bill on legalising assisted suicide.

Woman On #ESA First In Scotland To Be Evicted Over #BedroomTax

November 15, 2013

A woman from Glasgow has become the first in Scotland to be evicted due to the Bedroom Tax after falling behind with her rent.

The woman who lives in Pollok was already struggling with rent arrears of several hundred pounds when she was deemed to have an extra bedroom and had her housing benefits cut.

The reduction to her benefit led to her rent arrears increasing by just over three hundred pounds and her landlord, Glasgow Housing Association, instigated eviction proceedings.

Newsnet Scotland understands that lawyers acting on behalf of the woman had lodged papers aimed at preventing the eviction and that it was overturned, but papers did not arrive at GHA offices until after the lady had been evicted.  However, according to a local SNP councillor who tried to persuade the GHA to let the woman back into her house, the organisation claimed not to have received the papers.

Councillor Jim Torrance, who learned of the eviction, went straight to her home, arriving at 2pm he described the woman as “frozen”.  She had been “kicked out” at ten o’clock that morning.

“She was frozen, absolutely stiff outside the house, she was bewildered” he told Newsnet Scotland.

“I went straight to GHA office to try to get her keys back, they had changed the locks on her doors”.

He added: “The last thing we should be doing to these people is throwing them out in the street, six weeks before Christmas.”

The councillor claimed he was initially told the eviction was nothing to do with the Bedroom Tax but on pressing GHA it emerged that a significant amount of her arrears, 32%, was indeed down to housing benefit cuts.

Despite Councillor Torrance pleading on the woman’s behalf, the Housing Association refused to allow her back into her home.  It also emerged that the woman’s medication and clothing had been locked in the house at the time of the eviction and she was forced to wait hours in the cold until the police had returned before she was able to retrieve it.

Newsnet Scotland was also told that three police officers had attended the eviction.  The woman spent the night in a hotel which has no food facilities after GHA refused to let her back into her home pending another court hearing in December.

The woman, Charlene Shearer is a young widow with a teenage son whose husband died seven years ago.

According to Councillor Torrance, she was managing rent arrears prior to the new legislation coming in, but a new system coupled with cuts to her housing benefit led to her arrears climbing back up.  Ms Shearer had been on job seekers allowance but was transferred to employment support, during the change-over her payments didn’t go to GHA properly.

Ms Shearer will now have to wait until December 4th until a new hearing can be held into her case, before she can return to her home.  However Newsnet Scotland understands that GHA has agreed to meet with the woman today where she will be accompanied by someone from Govan Law Centre.

The eviction follows rising tensions over the non-appearance of ten Scottish Labour MPs at a crucial vote aimed at scrapping the Bedroom Tax.  In total forty seven Labour MPs failed to turn up for the vote in the House of Commons which was won by the coalition by only 26 votes.

An anti-Bedroom tax campaign group has announced plans for a peaceful protest outside the offices of one of the Scottish Labour MPs, Anas Sarwar.  The gathering is scheduled to take place Friday at 3pm at 9 Scotland Street, Glasgow.

 

Bob Stewart MP- Caught Sleeping On Job During #BedroomTax Debate

November 15, 2013

Many thanks to Political Scrapbook.

Many people were tired towards the end of Tuesday’s Bedroom Tax debate. However, few of them were actually at work, in the room!

Any employers reluctant to employ disabled people because they think we are more likely to get tired and fall asleep on the job should take note of this!

Over 50,000 disabled people could lose jobs as vital support is cut

November 15, 2013

Attending A PIP Assessment- Simulation

November 15, 2013

This might be useful to you.

Man Detained By Surrey Police Under Mental Health Act Dies

November 14, 2013

A man who was detained under the Mental Health Act has died in hospital after his condition deteriorated at a police station.

The Independent Police Complaints Commission (IPCC) is investigating Surrey police following the death of 33-year-old Terry Smith.

The ambulance service requested police help just after 10pm on Tuesday after being called to an address in Stanwell, Surrey.

Smith was held under the Mental Health Act and taken to Staines police station where he was then arrested on suspicion of a drugs-related offence. His health deteriorated and he was taken from the station by ambulance to St Peter’s hospital in Chertsey, where he died at around 9pm on Wednesday.

IPCC investigators were carrying out house-to-house inquiries on Thursday and distributing leaflets in the Douglas Road area.

After being told about the incident just after 6am on Wednesday, investigators went to Staines police station to assess evidence, including CCTV from the custody suite where Smith was held, and they also took initial accounts from those involved.

IPCC commissioner Jennifer Izekor said: “Our investigation is in its very early stages and our thoughts and condolences are with Terry’s family and friends. What we have established is that Surrey police were called by an ambulance crew to assist them with dealing with a man just after 10pm on the evening of Tuesday 12 November.

“Within 20 minutes of their arrival they detained Mr Smith under section 136 of the Mental Health Act, and he was then taken to Staines police station. Our investigators have seized and viewed CCTV footage from the custody suite where Mr Smith was detained and restrained. At some point Mr Smith became seriously ill. An ambulance was called and took him to St Peter’s hospital.

“I would urge anyone in the Douglas Road area who witnessed any of the events of Tuesday evening to get in touch with us, as it could really help our independent investigation. We have met with Mr Smith’s family to explain our role and how the investigation will progress.”

Smith was described as white and about 5ft 8in and was reported to be acting strangely.

Witnesses can contact the IPCC on 0800 096 9073.

The People So Hungry They End Up In Hospital

November 14, 2013

Food campaigners have warned of a poverty time bomb as the number of malnutrition cases at Greater Manchester hospitals surge.

Nearly 400 men, women, and children across Greater Manchester required hospital care last year care due to a lack of food or poor diet.

The figures has more than doubled in four years, up from just 158 cases in 2008.

Poverty groups believe soaring bills, unemployment, and punishing welfare reforms could be forcing households to slash their food bills – meaning some residents are starving themselves to keep a roof over their heads.

The largest increase was in Bolton, where 70 patients were admitted suffering from malnutrition last year, compared to just 10. And in Trafford, 40 people were seen, up from just nine.

The number of cases in Manchester went up to 66, from 37 in 2008.

The figures also include some people who were diagnosed with eating disorders as a primary diagnosis, although these are understood to make up a minority of the cases.

Other cases could potentially include the possible neglect of children or older people in care.

But campaigners say they are seeing a number of cases of people going hungry and suggested wider social factors could be to blame for the hike.

Joey Ferrigno, manager of Manchester Central Foodbank, told the M.E.N: “One man we saw had not eaten for two days because he wanted to save his money for travel.

“Some people who tell us they haven’t eaten are visibly very worn out. They are emotionally a bit fragile because hunger is such a powerful thing. It can make people ill. It can make people depressed.”

Across England, the figures showed a massive spike in hospital malnutrition cases over the last four years.

Just 3,161 people were treated in English hospitals for malnutrition in 2008. But last year the figure was 5,499.

The figures, from the Health and Social Care Information Centre, were collected by primary care trusts, which were abolished last year as part of a huge NHS shake-up.

Responsibility for public health matters has now fallen to local councils who say they are promoting healthy eating through numerous initiatives, including breakfast clubs and services for young families.

Health officials at Manchester Council say they are beginning to turn the tide through school programmes and healthy eating schemes at nurseries and Sure Start centres.

Malcolm Clark, from the Children’s Food Campaign, said help could also come in the form of a new government pledge to provide free school meals for every children aged five to seven, starting from September 2014.

But he added: “We work with breakfast clubs across the country who tell us there are children coming into school hungry.

“There is definitely also an issue to do with access to quality and nutritious food. Quite a few people have had to cut their food bills. They are buying a lot less, and the food they are buying is much less nutritious.”

#BedroomTax Of £14 Robs OAP Of Last Wish- To Die At Home

November 14, 2013

Readers, we must do something. Can we fundraise? Who do we petition?

A sick pensioner will be robbed of her last wish – to die at home – so the ­Government can claw back £14 a week in Bedroom Tax.

Mary Bennett, 82, has less than a year to live, but must leave her three-bedroom home because she cannot afford to pay the hated charge.

Mrs Bennett is only hit by the tax because her son is her live-in carer, so she cannot claim OAP exemption.

Alan Clark, 47, who gave up his hotel manager job to look after her, blasted: “How dare they take away a dying woman’s wish for the sake of £14 a week. It is a travesty.”

The widow from Runcorn, Cheshire, has a worsening cardiac condition and dementia.

Alan said: “A care home would cost £25,000 a year. She has lived in this house more than 20 years and £10,000 has been spent on ­disability adaptions.”

He has found a smaller rented house in Wales where his sister lives, but fears the upheaval could unsettle his ill mother.

A discretionary grant from Halton Council has covered the shortfall since they fell into arrears, but Alan says they will have to move when it expires in March.

A council spokesman said: ­“Discretionary housing payment cannot exceed March 31 in any given financial year as the council receives annual fund allocation from ­Government.

“Until this grant is known any awards cannot be made into the next financial year.”

A Party Political Broadcast Against The CONservatives

November 14, 2013

By the brilliant Chris Lawton. Watch, share and send viral.

Ronak Patel

November 14, 2013

A mother who has been fighting for justice for nearly three decades after her son was born disabled following errors by hospital staff, says she is still haunted by the whole episode.

 

Ronak Patel, who has severe cerebral palsy, suffered brain damage after Northwick Park Hospital in Harrow, north-west London, failed to spot his mother Smita’s appendicitis during her pregnancy in 1982.

 

That failure resulted in toxins from the burst appendix severely damaging Ronak’s lower brain.

 

Earlier this month, nearly 30 years on, Mrs Patel, a retired civil servant from Pinner, has finally been awarded £7m in compensation to provide for his care.

Long legal battle

“I noticed a few months after he was born he wouldn’t smile like other children – he would only respond when I spoke to him,” she said.

 

“I had difficulty feeding him, so I decided to take him to my local GP who noticed something was wrong.”

 

She and husband Jitendra Patel took legal action when Ronak was aged about four, but seven years later they were told no negligence had been found.

 

The family decided that that was the end of the matter and their son continued to go to a special school, coming home at weekends and school holidays.

 

Ronak, who is unable to use his arms or legs, talk or sit upright unaided, was moved to a care home in 2005.

 

Mrs Patel said: “He is like an overgrown baby, you have to feed him, wash him, even give him a drink and you have to guess when he’s thirsty.”

 

It wasn’t until 2006 that the couple were persuaded to take court action once more.

Husband’s death

After a lengthy court battle the hospital’s insurers agreed an out of court settlement with the family’s solicitor, Sue Jarvis from Blake Lapthorn.

 

North West London Hospital NHS Trust, which looks after Northwick Park Hospital, agreed a figure of £7m to be held in trust for Ronak’s care.

 

But for Mrs Patel the victory was tinged with sadness as her husband had died in 2008.

 

“I lost my husband in 2008 and sometimes I think it was down to worries over Ronak.

 

“I myself have also had health problems and suffered a heart attack.”

 

Ronak is currently being cared for at a private home but the money will help him return home early next year.

 

In a statement, chief executive of North West London Hospital NHS Trust, David McVittie, said: “I am pleased that the court has approved an agreement between the parties that resolves this claim.

 

“This agreement will ensure that Ronak has the assistance he needs throughout his life.”

People Going Blind Because Clinics Lack Capacity Warns RNIB

November 14, 2013

People may be going blind because clinics in England do not have the capacity to treat patients, a charity warns.

The Royal National Institute of Blind People (RNIB) said soaring numbers of patients and new treatments had seen eye care stretched to breaking point.

It said it was “shameful” that people’s eyesight was being damaged by delayed treatment.

It called for NHS England to hold an “urgent inquiry”.

Almost two million people in the UK are completely or partially blind, a figure that is predicted to increase as people live longer.

The charity’s report – Saving money, losing sight – warned of a “looming capacity crisis” in eye clinics across England.

‘Shameful statistics’

A survey of 172 eye clinic staff showed 80% thought their unit was unable to meet current demand and that increased to 94% thinking their department would not be able to cope with further increases.

More than a third of staff said some of their patients were losing sight because treatment was being delayed.

Lesley-Anne Alexander, the RNIB’s chief executive, said: “These statistics are shameful as nobody should lose their sight from a treatable condition simply because their eye clinic is too busy to provide care in a clinically appropriate timescale.

“Hospital managers are ignoring the capacity crisis, often to save money, and are putting patients’ sight at risk and their staff on course for burnout.”

She warned that hospitals may be putting themselves at risk of clinical negligence claims.

‘Meet local needs’

The charity called for NHS England to have an “urgent inquiry” into the quality of care provided.

A spokesperson for NHS England said: “It is important that people have ready access to treatment they need.

“Clearly eye care is a critical matter for patients and can have long-term effects on them, their families and the health service and we would expect clinical commissioning groups to ensure that patients in their area have the ready access to the level of service that they require, but it is important that these are commissioned locally to meet local needs.”

Benefit Victory For Fred Hazle, Father Who Took Son James To Downing Street

November 14, 2013

I know that many of you will be very pleased to read this. As always, your comments are very welcome.

A father has won a victory for his severely disabled son by going to Downing Street to demand the Prime Minister hire his boy if the government thinks he is fit to work.

Fred Hazle, 46, from Grafton Road, Dagenham, was protesting a string of “bullying” letters sent to his 19-year-old son James, who has the mental age of a five-year-old, threatening to stop his £71.95 a week in benefits unless he could “prove” he cannot work.

James needs round-the-clock care and has autism, blindness, epilepsy and severe learning difficulties.

Speaking exclusively to the Post, Fred said he has now secured a promise that the letters will stop, and that James will receive benefits “indefinitely”.

Fred, who works as a bus driver, said: “First they put me on to some call centre. I told them I would go back down there to Downing Street, and about 20 minutes later they got me on to the manager of the Employment and Support Allowance.

“I told them, ‘All you people want to do is fob me off, leave it a year and send more letters. I’m not having it.’”

The manager apologised and said James would receive financial support “for the rest of his life”, and promised to send written confirmation of this to Fred.

“I’m very happy,” he said. “It was never about the money for me.

“No-one with a disability should have to be humiliated in front of people to prove they cannot work.”

Fred hopes to meet with Prime Minister David Cameron and Iain Duncan Smith, the minister for Work and Pensions, to seek an apology and make them change the benefits system to protect disabled people from this treatment.

He added: “I want an apology from Iain Duncan Smith and Mr Cameron, not to me, not to my wife, but to James.”

A spokesman for the Department for Work and Pensions said there had been a “misunderstanding” over the Hazles’ case but confirmed it was resolved and no money would be stopped.

EDM 705

November 14, 2013

Readers, for whatever it’s worth, please get your MP to sign this EDM, on the Bedroom Tax. Thanks.

UNDER-OCCUPANCY PENALTY (No. 2)

That this House believes that the under-occupancy penalty was a mistake and should not have been introduced in the Welfare Reform Act 2012; further believes that it will not achieve the savings projected for it and that as constructed it is likely to have unforeseen consequences that will be unfair to certain groups and individuals; recognises that there is an urgent need to free up social housing to deal with the chronic shortage of social housing in many areas of the country, a legacy of the housing policies of previous Conservative and Labour administrations, including allowing people to buy council houses without replacing the stock, but nevertheless believes that the under-occupancy penalty is flawed and unacceptable in its current form; notes the perverse consequence that in some areas there are more larger properties now lying empty and with inadequate smaller housing; further believes that there should be more automatic exemptions, including for disabled and ill adults who require separate rooms for medical reasons or reasons associated with their disability; further believes that no-one should be subject to the penalty until they have refused a suitable home; further believes that councils should be given more exemptions, including where they can and wish to let houses above the recommended size without penalty to the individual or council; calls on the Department for Work and Pensions to conduct an urgent review of the policy and make changes; and further believes that if the Department refuses to do this, the policy should be scrapped altogether.

Mike Penning Confirms That Travel Costs Will Be Paid For PIP Assessments

November 14, 2013

From Disability Rights UK.

Fiona Mactaggart: To ask the Secretary of State for Work and Pensions whether the costs of assessing transport to personal independence payment assessment centres are borne by Atos under their contractor or paid separately by his Department. [174788]

Mike Penning: Personal independence payment (PIP) assessment providers are required to pay claimants’ travelling expenses in line with guidance issued by the Department. These costs are not passed through to the Department directly.

The Department pays an output fee per assessment and the assessment providers were required to offer output fees which reflected all of their costs when they bid for the contracts at the tender stage.

Fiona Mactaggart: To ask the Secretary of State for Work and Pensions under what circumstances those attending personal independence payment centres have their transport costs paid. [174789]

Mike Penning: Where it is necessary for a claimant to travel to a face-to-face consultation, they are able to claim travel expenses for themselves and a companion or carer, or young children who would otherwise be left unattended.

Payments are made for public transport fares, travel by private motor vehicle and in some circumstances, where prior approval has been given by the assessment provider, taxi fares. Payments relating to other costs related to the journey such as parking, tolls or congestion charges can also be met.

The assessment providers are required to reimburse these expenses within 14 calendar days of the claim.

 

‘Reconsideration’ fiddle for ‘fitness-for-work’ test

November 13, 2013

Mike Sivier's avatarMike Sivier's blog

The number of sick and disabled people wrongly declared “fit for work” after taking the Atos-run work capability assessment for Employment and Support Allowance could be far higher than previously thought, it has been revealed.

It seems the Coalition government has been artificially inflating its figure for the number of people initially awarded the benefit by including the results of informal appeals, known as ‘reconsideration’.

The dodge was uncovered by Labour MP Sheila Gilmore, who sits on the Commons Work and Pensions select committee. She raised concerns about the figures in September.

A reply by Tory Employment Minister Esther McVey has admitted that figures covering the number of people initially awarded the benefit have been artificially boosted by the reconsideration process, in which people who have been found “fit for work” ask DWP civil servants to re-examine their cases.

If the decision remains the same, claimants can lodge a formal appeal…

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HIGH IMPORTANCE! Income Support Still Exists!

November 13, 2013

From Fightback:

HIGH IMPORTANCE this come via Jenny Clarke if you are in the situation where you can claim neither ESA or JSA you can claim Income Support this has been found out via an FOI below:

https://www.whatdotheyknow.com/request/174911/response/428973/attach/3/FOI%204180%20Response.pdf

They certainly kept this quiet in Government as many where under the impression Income Support (IS) had ended.

Captain SKA- Nothing Nothing Nothing

November 13, 2013

A song for IDS.

Traliblazers Surveying High Street Access

November 13, 2013

 

Judge Rules Son, 18, With CP Can’t Live At Home Because Mother Wants To Homeschool Him

November 13, 2013

Readers, I have just read a story that has deeply upset me.

A mother decided, 10 years ago, that she wanted to homeschool her son, who has Cerebral Palsy. However, when he was admitted to hospital as an inpatient two years ago, her local council, Northamptonshire County, informed her that he could not return to the family home. Why? Simply because they felt that she had an ‘alternative stance on education’ which was ‘not in his best interests.’

The mother says the son, known only as ‘T,’ is desperate to come home. However, earlier this year, a judge ruled that T lacked the mental capacity to make decisions related to his welfare or education.

So he was placed in residential care, and enrolled in a school, 100 miles away from his family home. This is a move which, his mother argues, is depriving him of his liberty. She does not feel her son should attend a conventional school because he has now passed compulsory schooling age.

T was not given any say in this decision. His mother argues that he is an adult, and should be treated as such. She wants his views to be respected. She says that her son is desperate to come home, that he is suffering emotionally due to separation from her, as well as physically because he would be cared for better at home, by his family, than in the residential placement.

Most importantly, the mother argues that T has ‘a clear memory’ and ‘intellectual gifts’ which ‘far outweigh his physical abilities.’ She says that he has studied Romeo and Juliet.

However, the court ruled that there was a question over whether the mother would enable T to complete his final year of education.

The mother does not feel it would be in her son’s best interests to attend school. However, the court ruled that the education was good for him, was in his best interests and that he was happy at school. The judge added that T’s time at school is extremely important, educationally and socially.

So, why has this case hit me so hard? Because I have Cerebral Palsy myself, as do many of my friends. I know several people who are severely affected by Cerebral Palsy, but who are highly intelligent and have every ability to express decisions, feelings and opinions.

Due to having close friends who have faced similar situations, of doubts over their intelligence by professionals even though they are highly intelligent, I completely believe the mother when she says that her son has academic abilities and the mental capacity to make his own decisions.

It is not clear whether T can communicate verbally, but if he cannot, I sincerely hope this is not the only reason why the court assumes he lacks mental capacity.

I have to wonder why nothing has been revealed about the mother’s reasons for choosing to homeschool T, in particular. It has been revealed that she has also chosen to homeschool two of her other three children.

However, in T’s particular case there could be any number of reasons for her making the choice. I have known mothers who chose to homeschool their disabled children because conventional schools refused to accept them, as a result of their disabilities.

Others have chosen homeschooling because their children were experiencing bullying, again, most probably a result of their disabilities.

Of course, I know that attending a conventional school is very important for a child’s social development. However, if T was being homeschooled for either of these two reasons, then I cannot see how attending a conventional school could be in his best interests. Surely, after homeschooling him for 10 years, his mother knows his academic abilities and can meet his educational needs?

Surely it is better to lack a busy social life than to experience bullying as a result of disability, a situation that a person cannot help?

I have always been a passionate supporter of appropriate education for every child. However, I have also always strongly believed that parents know their children better than anyone else. T’s mother clearly knows his abilities. She clearly recognizes his intelligence and appreciates it. If she believes that homeschooling is appropriate for her son, then in my personal opinion, her son should be homeschooled. Last I checked, there was nothing illegal about homeschooling in itself.

As for the separation, my heart goes out to them both. Personally, as a disabled ‘child,’ I could not stand to be forced to live 100 miles away from my family. I would hate to be forced into a situation where someone outside my family was meeting my care needs.

It upsets me deeply that this child who shares my disability has been separated from his mother, who he clearly wants to live with and who clearly loves him.

I wish there was something that could be done to change this court ruling, and to reunite this family. Although the judge said success on appeal was not likely, the mother said she would fight on, and personally, I wish her every success with the fight.

 

ESA Form Tip: Side Effects On Meds

November 13, 2013

I found this on Fightback, who found it on ATOS Miracles on Monday.

ATOS Miracles Suzi ATOS Miracles
52 minutes ago
Ive posted this before but another person has fell for the same trick: the ESA form does ask about side effects on meds, but its done very subtly, there is a question that asks if you suffer from alcohol or drug related problem and in small writing just above the answer box it states this also includes meds prescribed by a doctor. It is in this box all side effects of any meds should be written – its a bad way of writing it but it is there xxxxx

#BedroomTax Debate- The Stats

November 13, 2013

Spotted on Facebook.

bedroomtax

 

Bedroom Tax Tories: What they said and why they were wrong

November 13, 2013

Mike Sivier's avatarMike Sivier's blog

“I’m amazed Labour have chosen to spend their allotted day in Parliament arguing for more unfunded spending on housing benefit.” That’s what Matt Hancock, Conservative MP for West Sussex, had to say about the Opposition Day debate on the Bedroom Tax in the House of Commons on November 12.

Hancock is, it seems, author of a book entitled Masters of Nothing, which sums up his understanding of the situation rather well. He clearly has not mastered the fact that the State Under-Occupation Charge will not save money. He has not mastered the fact that emptying dwellings of their current owners will not make them available to new familes as these people are afraid they will themselves be tipped onto the street when their circumstances change – instead the premises will be left empty, at huge cost to social landlords; and he has not mastered the fact that anyone evicted because…

View original post 2,058 more words

#BedroomTax Debate: MPs Named And Shamed

November 13, 2013

With many thanks to the Mirror.

More than 30 Lib Dem MPs voted to uphold the government’s hated Bedroom Tax – despite their own party members having condemned the policy.

Just two MPs, Andrew George and Tim Farron, defied the coalition to vote in support of Labour’s motion to scrap the deductions for social tenants with spare bedrooms with “immediate effect”.

Lib Dems who voted against the Labour motion (31)

  • Norman Baker (Lewes)
  • Sir Alan Beith (Berwick-upon-Tweed)
  • Tom Brake (Carshalton & Wallington)
  • Jeremy Browne (Taunton Deane)
  • Malcolm Bruce (Gordon)
  • Paul Burstow (Sutton & Cheam)
  • Lorely Burt (Solihull)
  • Sir Menzies Campbell (Fife North East)
  • Alistair Carmichael (Orkney & Shetland)
  • Edward Davey (Kingston & Surbiton)
  • Don Foster (Bath)
  • Stephen Gilbert (St Austell & Newquay)
  • Duncan Hames (Chippenham)
  • Sir Nick Harvey (Devon North)
  • David Heath (Somerton & Frome)
  • John Hemming (Birmingham Yardley)
  • Martin Horwood (Cheltenham)
  • Simon Hughes (Bermondsey & Old Southwark)
  • Mark Hunter (Cheadle)
  • Norman Lamb (Norfolk North)
  • Michael Moore (Berwickshire, Roxburgh & Selkirk)
  • Tessa Munt (Wells)
  • John Pugh (Southport)
  • Dan Rogerson (Cornwall North)
  • Bob Russell (Colchester)
  • Sir Robert Smith (Aberdeenshire West & Kincardine)
  • Andrew Stunell (Hazel Grove)
  • Jo Swinson (Dunbartonshire East)
  • John Thurso (Caithness, Sutherland & Easter Ross)
  • Steve Webb (Thornbury & Yate)
  • Stephen Williams (Bristol West)

Lib Dems who did not vote (21)

  • Danny Alexander (Inverness, Nairn, Badenoch & Strathspey)
  • Gordon Birtwistle (Burnley)
  • Annette Brooke (Dorset Mid & Poole North)
  • Vincent Cable (Twickenham)
  • Nick Clegg (Sheffield Hallam)
  • Michael Crockart (Edinburgh West)
  • Lynne Featherstone (Hornsey & Wood Green)
  • Julian Huppert (Cambridge)
  • Charles Kennedy (Ross, Skye & Lochaber)
  • David Laws (Yeovil)
  • John Leech (Manchester Withington)
  • Stephen Lloyd (Eastbourne)
  • Greg Mulholland (Leeds North West)
  • Alan Reid (Argyll & Bute)
  • Adrian Sanders (Torbay)
  • Ian Swales (Redcar)
  • Sarah Teather (Brent Central)
  • Mike Thornton (Eastleigh)
  • Mark Williams (Ceredigion)
  • Roger Williams (Brecon & Radnorshire)
  • Simon Wright (Norwich South).

Lib Dem MP Jenny Willott (Cardiff Central) was a teller for the Noes.

The only difference in voting pattern between the first and the second vote, which was on the Prime Minister’s amendment, was that Education Minister David Laws did not vote against the Labour motion but did vote in support of the Prime Minister’s amendment.

Tories who voted against Labour’s motion (220)

  • Adams, Nigel, Mr
  • Afriyie, Adam, Mr
  • Aldous, Peter, Mr
  • Arbuthnot, James, Rt Hon
  • Bacon, Richard, Mr
  • Baker, Steve, Mr
  • Barclay, Stephen, Mr
  • Baron, John, Mr
  • Bellingham, Henry, Mr
  • Benyon, Richard, Mr
  • Beresford, Paul, Sir
  • Bingham, Andrew, Mr
  • Binley, Brian, Mr
  • Blackman, Bob, Mr
  • Bone, Peter, Mr
  • Bottomley, Peter, Mr
  • Bradley, Karen, Ms
  • Brady, Graham, Mr
  • Bray, Angie, Ms
  • Three line Aye
  • Bridgen, Andrew, Mr
  • Brine, Steve, Mr
  • Burns, Conor, Mr
  • Burns, Simon, Mr
  • Burt, Alistair, Mr
  • Byles, Dan
  • Cameron, David, Rt Hon
  • Carswell, Douglas, Mr
  • Cash, William
  • Chishti, Rehman, Mr
  • Chope, Christopher, Mr
  • Clappison, James, Mr
  • Clark, Greg, Mr
  • Clarke, Kenneth, Rt Hon
  • Clifton-Brown, Geoffrey, Mr
  • Coffey, Thérèse, Ms
  • Collins, Damian, Mr
  • Colville, Oliver
  • Cox, Geoffrey, Mr
  • Crabb, Stephen, Mr
  • Crouch, Tracey, Ms
  • Davies, David T C, Mr
  • Davies, Glyn, Mr
  • Davies, Philip, Mr
  • Dinenage Caroline, Ms
  • Djangoly, Jonathan, Mr
  • Dorrell, Stephen, Rt Hon
  • Doyle-Price, Jackie, Ms
  • Drax, Richard, Mr
  • Dunne, Philip, Mr
  • Ellis, Michael, Mr
  • Ellison, Jane, Ms
  • Ellwood, Tobias, Mr
  • Elphicke, Charlie, Mr
  • Eustice, George, Mr
  • Evans, Graham, Mr
  • Evans, Jonathan, Mr
  • Evennett, David
  • Fallon, Michael, Mr
  • Field, Mark, Mr
  • Freer, Mike, Mr
  • Fuller, Richard, Mr
  • Garnier, Edward, Mr
  • Garnier, Mark, Mr
  • Gibb, Nick, Mr
  • Gillian, Cheryl, Rt Hon
  • Glen, John, Mr
  • Goodwill, Robert, Mr
  • Gove, Michael, Rt Hon
  • Grant, Helen, Ms
  • Gray, James, Mr
  • Grayling, Chris, Mr
  • Green, Damian, Mr
  • Griffiths, Andrew, Mr
  • Gummer, Ben
  • Gyimah, Sam, Mr
  • Hammond, Stephen, Mr
  • Hancock, Matthew, Mr
  • Hands, Greg, Mr
  • Harper, Mark, Mr
  • Harrington, Richard, Mr
  • Harris, Rebecca, Ms
  • Hart, Simon, Mr
  • Hayes, John, Mr
  • Heald, Oliver, Mr
  • Heaton-Harris, Chris, Mr
  • Hendry, Charles, Mr
  • Herbert, Nick, Mr
  • Hinds, Damian, Mr
  • Hollingbery, George, Mr
  • Hollobone, Philip, Mr
  • Holloway, Adam, Mr
  • Hopkins, Kris, Mr
  • Howarth, Gerald, Mr
  • Howell, John, Mr
  • Hunt, Jeremy, Rt Hon
  • Jackson, Stewart, Mr
  • James, Margot, Ms
  • Javid, Sajid, Mr
  • Jenkin, Bernard, Mr
  • Johnson, Gareth, Mr
  • Jones, Andrew, Mr
  • Jones, David, Mr
  • Jones, Marcus, Mr
  • Kelly, Chris, Mr
  • Knight, Greg, Mr
  • Kwarteng, Kwasi, Mr
  • Lancaster, Mark, Mr
  • Lansley, Andrew, Rt Hon
  • Latham, Pauline, Ms
  • Leadsom, Andrea, Ms
  • Lee, Jessica, Ms
  • Lee, Phillip
  • Lewis, Brandon, Mr
  • Lewis, Julian, Mr
  • Liddell-Grainger, Ian, Mr
  • Lidington, David, Mr
  • Lopresti, Jack, Mr
  • Lord, Jonathan, Mr
  • Luff, Peter, Mr
  • Main, Anne, Ms
  • Maude, Francis, Rt Hon
  • May, Theresa, Rt Hon
  • Maynard, Paul, Mr
  • Mccartney, Jason, Mr
  • Mccartney, Karl, Mr
  • Mcintosh, Anne, Ms
  • Mcpartland, Stephen, Mr
  • Mcvey, Esther, Ms
  • Menzies, Mark, Mr
  • Miller, Maria, Ms
  • Mills, Nigel, Mr
  • Mordaunt, Penny, Ms
  • Morgan, Nicky, Mr
  • Morris, David, Mr
  • Mosley, Stephen, Mr
  • Mowat, David, Mr
  • Mundell, David, Mr
  • Murray, Sheryll, Ms
  • Murrison, Andrew, Mr
  • Neill, Robert, Mr
  • Newmark, Brooks, Mr
  • Newton, Sarah, Ms
  • Nokes, Caroline, Ms
  • Nuttall, David, Mr
  • O’Brien Stephen, Mr
  • Ollernshaw, Eric
  • Opperman, Guy, Mr
  • Ottaway, Richard, Mr
  • Paice, James, Mr
  • Parish, Neil, Mr
  • Patel, Priti, Ms
  • Penning, Mike, Mr
  • Penrose, John, Mr
  • Perry, Claire, Ms
  • Phillips, Stephen, Mr
  • Pickles, Eric, Rt Hon
  • Pincher, Christopher
  • Poulter, Daniel, Mr
  • Prisk, Mark, Mr
  • Pritchard, Mark, Mr
  • Raab, Dominic, Mr
  • Randall, John, Mr
  • Redwood, John, Rt Hon
  • Rees-Mogg, Jacob, Mr
  • Reevell, Simon, Mr
  • Robertson, Hugh, Mr
  • Roberston, Laurence, Mr
  • Rosindell, Andrew, Mr
  • Rudd, Amber, Ms
  • Ruffley, David, Mr
  • Rutley, David, Mr
  • Sandys, Laura, Ms
  • Scott, Lee, Mr
  • Selous, Andrew, Mr
  • Shapps, Grant, Mr
  • Shelbrooke, Alec, Mr
  • Shepherd, Richard, Mr
  • Simpson, Keith, Mr
  • Skidmore, Chris, Mr
  • Smith, Henry, Mr
  • Smith, Julian, Mr
  • Soames, Nicholas, Hon
  • Soubry, Anna, Ms
  • Spelman, Caroline, Rt Hon
  • Stanley, John, Rt Hon Sir
  • Stephenson, Andrew, Mr
  • Stevenson, John, Mr
  • Stewart, Bob, Mr
  • Stewart, Iain, Mr
  • Streeter, Gary, Mr
  • Stride, Mel, Mr
  • Stuart, Graham, Mr
  • Sturdy, Julian, Mr
  • Swayne, Desmond, Mr
  • Syms, Robert, Mr
  • Tapsell, Peter, Mr
  • Timpson, Edward, Mr
  • Tomlinson, Justin, Mr
  • Tredinnick, David, Mr
  • Truss, Elizabeth, Ms
  • Turner, Andrew, Mr
  • Tyrie, Andrew, Mr
  • Uppal, Paul, Mr
  • Vaizey, Edward
  • Vara, Shailesh, Mr
  • Vickers, Martin, Mr
  • Walker, Charles, Mr
  • Wallace, Ben, Mr
  • Wharton, James, Mr
  • Wheeler, Heather, Ms
  • White, Chris, Mr
  • Whittingdale, John, Mr
  • Wiggin, Bill, Mr
  • Williamson, Gavin, Mr
  • Wilson, Rob
  • Wollaston, Sarah, Ms
  • Wright, Jeremy, Mr
  • Yeo, Tim, Mr
  • Young, George, Sir Rt Hon

Tories who did not vote ( 82)

  • AMESS, David, Mr
  • ANDREW, Stuart, Mr
  • BALDRY, Tony, Mr
  • BALDWIN, Harriett, Ms
  • BARKER, Gregory, Mr
  • BEBB, Guto, Mr
  • BERRY, Jake, Mr
  • BLACKWOOD, Nicola, Ms
  • BLUNT, Crispin, Mr
  • BOLES, Nick, Mr
  • BRAZIER, Julian, Mr
  • BROKENSHIRE, James, Mr
  • BRUCE, Fiona, Ms
  • BUCKLAND, Robert, Mr
  • BURLEY, Aidan, Mr
  • BURROWES, David, Mr
  • CAIRNS, Alun, Mr
  • CARMICHAEL, Neil, Mr
  • DAVIS, David, Rt Hon
  • DE BOIS, Nick, Mr
  • DORRIES, Nadine, Mrs
  • DUDDRIDGE, James, Mr
  • DUNCAN SMITH, Iain
  • DUNCAN, Alan, Mr
  • FABRICANT, Michael, Mr
  • FOX, Liam, Rt Hon
  • FRANCOIS, Mark, Mr
  • FREEMAN, George, Mr
  • FULLBROOK, Lorraine, Ms
  • GALE, Roger, Mr
  • GAUKE, David, Mr
  • GOLDSMITH, Zac, Mr
  • GRAHAM, Richard, Mr
  • GREENING, Justine, Ms
  • GRIEVE, Dominic, Rt Hon
  • HAGUE, William, Rt Hon
  • HALFON, Robert, Mr
  • HAMMOND, Philip, Rt Hon
  • HASELHURST, Alan, Rt Hon Sir
  • HENDERSON, Gordon, Mr
  • HOBAN, Mark, Mr
  • HURD, Nick, Mr
  • JOHNSON, Joseph
  • KAWCZYNSKI, Daniel, Mr
  • KIRBY, Simon, Mr
  • LAING, Eleanor, Mrs
  • LEFROY, Jeremy, Mr
  • LEIGH, Edward, Mr
  • LESLIE, Charlotte, Ms
  • LETWIN, Oliver, Rt Hon
  • LILLEY, Peter, Rt Hon
  • LOUGHTON, Tim, Mr
  • LUMLEY, Karen, Ms
  • MACLEOD, Mary, Ms
  • MCLOUGHLIN, Patrick, Rt Hon
  • METCALFE, Stephen, Mr
  • MILTON, Anne, Mrs
  • MITCHELL, Andrew, Rt Hon
  • MORRIS, Anne Marie, Ms
  • MORRIS, James, Mr
  • NORMAN, Jesse, Mr
  • OFFORD, Matthew, Mr
  • OSBORNE, George, Rt Hon
  • PATERSON, Owen, Rt Hon
  • PAWSEY, Mark, Mr
  • RECKLESS, Mark, Mr
  • RIFKIND, Malcolm, Sir
  • ROBATHAN, Andrew, Mr
  • SHARMA, Alok, Mr
  • SIMMONDS, Mark, Mr
  • SMITH, Chloe, Ms
  • SPENCER, Mark, Mr
  • STEWART, Rory, Mr
  • SWIRE, Hugo, Mr
  • VILLIERS, Theresa, Ms
  • WALKER, Robin, Mr
  • WALTER, Robert, Mr
  • WATKINSON, Angela, Ms
  • WEATHERLEY, Mike
  • WHITTAKER, Craig, Mr
  • WILLETTS, David, Mr
  • ZAHAWI, Nadhim, Mr

Tories who abstained

  • PERCY, Andrew, Mr

Ku Bar Girls Wheelchair Access: The Petition

November 13, 2013

Remember this campaign, readers? Well, I’ve been sent a petition related to it. If wheelchair access in public places matters to you, please sign it.

 

Julian Little- Died Battling #BedroomTax Red Tape

November 12, 2013

A KEMSING man has died battling red tape while struggling to recover from a series of heart attacks, strokes and kidney failure.

 

Julian Little, 47, was reeling after he faced the Government’s new bedroom tax even though his spare room had been converted into a dialysis facility by health chiefs.

 

He feared he would have to slash his household bills by 30 per cent to make up the shortfall in his income because the authorities still viewed his bungalow in Norman Close as having two bedrooms.

 

He told the Chronicle that moving to a smaller property would not be an option because the needed room for the medical equipment. He said: “Put simply, if I downsize, I die.”

 

Just days later he passed away.

 

His wife Melissa, 42, said: “He wasn’t well and his death was complicated.” She said she did not know if the stress of the situation had anything to do with it.

 

Mr Little moved into the Kemsing bungalow more than a decade ago after suffering a stroke which put him in a wheelchair. In the following years he had ‘several’ other strokes, three heart attacks, kidney failure and he lost some toes to diabetes.

 

He and Mrs Little had originally lived at the address with their daughter Tabitha but when she got married and moved away, the space was utilised by Guys Hospital for his lifesaving kit.

 

In his last conversation with the Chronicle he said he faced being taxed “for being ill and suffering from a condition I have no control over”.

Labour’s #BedroomTax Motion Fails

November 12, 2013
  • Bedroom Tax:Labour motion calling for the end of housing benefit deductions fails.
    Yes 226 No 252
    I think we just lost… Bedroom Tax won’t be scrapped unless Labour wins next election.

ESA Work Support Group- Disturbing Photo

November 12, 2013

Just spotted on Facebook.

Wanted: Stories For Submission To Dept Of Education

November 12, 2013

 

Lisa Egan On 4Thought TV Tonight, C4 7.55PM

November 12, 2013

 

Disability campaigner Lisa Egan’s film is available to watch now from here, if you can’t watch it on TV tonight.

Lisa Egan

Lisa Egan has lived with a disability since she was born, but since the crisis she’s seen attitudes towards her change. She says she has received some abusive comments online including one which said that she should have been killed at birth to save the taxpayer money. She says austerity has shaken her faith in the goodness of the British people.

Beyonce Sings With Blind Girl

November 12, 2013

 

Blank Agreements At JobCentre Plus- PLEASE READ

November 12, 2013

Spotted here. I think this is very important. Please share everywhere.

The story below was sent to UnemployedNet by a jobseeker who was unhappy with the service she received from her local jobcentre.

She was made to sign a blank jobseeker’s agreement in a session with others who were also made to do the same thing.

The agreement is an important document for unemployed people; it acts as a contract between them and their jobcentre, and any failure to meet its conditions can lead to benefits being taken away.

Other jobseekers will not be surprised that her complaint about this breach of decent practice was met with a flat denial that it took place.

Longer-term readers will remember UnemployedNet’s reports on sanctions targets in the spring; despite official rejections that targets existed an internal Department for Work and Pensions report found that, in some areas, they had been used, meaning a higher likelihood that people would have their benefits removed just to satisfy managers.

As this jobseeker’s story shows, those who do not know what they are signing up to are more likely to break their ‘agreements’, and have their benefits taken away as a result.

The new practice may be a way of setting people up to fail, to find a way of making it easier to remove their benefits.

The UK already has some of the lowest benefits in Europe, and entrenching poverty further by taking them away is a terrible outcome for those who only want to get work.

‘If someone put a blank piece of paper in front of you and asked you to sign it, what would you do?

At the least you’d ask what it is –

It’s an agreement.

But it’s blank – what would I be agreeing to?

Oh, don’t worry about that; we can talk that over later. Just sign.

This is actually what happened when I went to sign on, with a room full of other people, for a new claim, at my local Jobcentre. We were each given a clipboard with the relevant documents on and while one advisor took our passports one by one to be photocopied, another asked us to read over our claim information to check that it was right, then asked us to put our insurance number on our Jobseekers’ agreement and sign it.

I asked why we were being asked to sign a blank agreement, and the man said not to worry, we would talk through the agreement with our advisor at the next appointment. No-one else seemed bothered, and I’m not inclined to start a big debate, trying to persuade the other claimants, as well as the advisor, that it’s a wrong thing to do, so I signed it and told myself I would do something about it afterwards.

Why was I concerned? Quite likely, everyone will, at their next interview, agree to conditions, such as ‘I will phone X number of employers/ Apply in writing fro X number of jobs, and there will be no problems.

But what if they don’t agree, and think the demands are unfair? They can’t take away the signature. At best, the advisor would have to tear up the agreement and start again; at worst, the claimant could be in danger of losing benefits. At best, there was no point in having the agreement signed before the details were added; at worst it is surely a legal nonsense to have an agreement signed, then have to debate what the claimant is agreeing to.

My next appointment wasn’t with my actual advisor, but with someone else. My jobseeker agreement never came up, and I can’t remember what the appointment was actually for. (By this time, I had emailed the manager of the North London area with my complaint.)

When I did see my advisor, he still didn’t bring up the matter of my agreement and was happy for me to sign my fortnightly declaration and go. I asked him about the agreement, and he showed it to me on the computer screen. No-one had discussed it with me at any point and the requirements were already filled in. When I looked closely, I was sure it was the same agreement I had had the previous summer. (I didn’t remember having negotiated that one either, except that I had apparently agreed to apply for 12 jobs a week. I am a teacher/supply teacher and I had argued that it takes quite a long time to apply for a teaching job and that 12 a week was unmanageable. She had told me that I should read things before I sign them, but she did reduce the 12 to 3. She then gave me something else to sign and I read it thoroughly, much to her annoyance. After that we got along fine).

My current advisor then told me that it was now ‘illegal’ to stipulate how many times a claimant should e.g. write for a job, and pointless as most people apply online, and he deleted the entries. So now, apparently, I had no agreement. We also got along fine after this, but I thought his manner was a bit odd. I felt sure that my complaint had got back to the people working in the Jobcentre.

I don’t want to get any worker into trouble. The whole thing may have been pretty innocently done, but if so, it was for reasons I cannot fathom.

What reason could anyone give for getting claimants to sign their Jobseekers agreements before they have agreed to the targets? It doesn’t save time, or make things simpler.

I know also that the advisors are given targets from above and are under pressure to fulfill them. I can’t be sure that this wasn’t an attempt to pressure claimants, in turn, to be bound to unreasonable targets for seeking work, and to risk being thrown off the benefits programme.

If, after my email, I had been told that it was a mistake by a Jobcentre employee – that it wouldn’t happen again,- I would have been satisfied. But I asked for such an assurance and was told that it didn’t happen, so I am not reassured at all.

I have responded to this by writing to the Director General assuring him that it did happen, and have always copied in my MP. The DG has six months to respond. I just want to know that unemployed people are not being treated in this way anywhere. As if there aren’t enough things to worry about.

I would love to hear if anyone else has been asked to sign a blank agreement, and what people’s views are. Has there been a change in the rules/ law regarding targets on agreements?’

Oh, Danny Boy- The ATOS Version

November 12, 2013

I grew up listening to Irish music with close family friends. So Danny Boy has always been one of my favourite songs. Yesterday, I discovered that 2013 marks the song’s hundredth year.

While watching a very interesting documentary on the song’s history, I discovered that there have been several original versions recorded.

So, to mark the 100th birthday of a classic, I decided to do to it what I do best- rewrite it with a relevant disability theme. ATOS seemed an obvious fit.

I took Sinead O’Connor’s version- she sings all three verses.

So, here goes, a love song with a disability politics twist.

Oh, Danny Boy, The ATOS Version

Oh Danny Boy, ATOS,

ATOS are calling,

They say you must,

Go for a WCA.

They’ve hearts of stone,

Disabled people are dying,

They say you must,

Go first, and I’ll be next.

But come ye back,

When Labour forms a Government,

Or when our home,

Is empty, dark and cold.

I’ll still be here,

In body or in spirit,

Oh Danny Boy, Oh Danny Boy,

I love you so.

But if you come,

And find ATOS have called me,

And I am dead,

As dead I might well be,

You’ll come and find,

The place where I am lying,

Kneel there and say,

A little prayer for me.

And I will hear,

Though soft you tread above me,

And all my grave,

Will warmer, sweeter be.

 

And you will bend

And tell me that you love me.

And I shall sleep

In peace until you come to me.

But if I live,

And should you die for ATOS,

Let not your dying,

Thoughts be just of me.

But say a prayer,

To God for all our people,

I know He’ll hear,

And help to set us free.

And I will take,

Your sticks and aim at ATOS,

And strike a blow,

Though weak the blow may be.

T’will help the cause,

To which your heart was nearest

Oh Danny Boy, Oh, Danny Boy

I love you so.

PS: If anyone is interested in singing this and putting it on Youtube, I’d be more than happy, please do let me know if your voice is better than mine!

NATIONAL THEATRE ASSISTED PERFORMANCES: NOVEMBER 2013 – JULY 2014

November 12, 2013

A press release:

NATIONAL THEATRE ASSISTED PERFORMANCES:  NOVEMBER 2013 – JULY 2014

Olivier Theatre

 

EMIL AND THE DETECTIVES
by Erich Kästner
adapted by Carl Miller


Growing up is the most exciting adventure of all. Join young Emil as he says goodbye to his mother, leaves his small town and sets off on a journey that will change his life.

CAPTIONED
Monday 30 December at 7pm
Sunday 9 February 2014 at 2pm

AUDIO DESCRIBED
Friday 3 January 2014 at 7pm
Saturday 4 January 2014 at 2pm
Saturday 25 January 2014 at 2pm

TOUCH TOUR
Saturday 4 January 2014 at 12.30pm
Saturday 25 January 2014 at 12.30pm

 

KING LEAR

by William Shakespeare
directed by Sam Mendes


Simon Russell Beale stars as an aged king who
decides to divide his kingdom between

his three daughters, according to which of them is most eloquent in praising him. His favourite, Cordelia, says nothing.

 

CAPTIONED
Sunday 23 March 2014 at 2pm

Tuesday 25 March 2014 at 7pm

 

AUDIO DESCRIBED
Saturday 1 March 2014 at 2pm

Monday 3 March 2014 at 7pm

 

TOUCH TOUR

Saturday 1 March 2014 at 12.30pm

 

Lyttelton Theatre

THE LIGHT PRINCESS
a new musical
music and lyrics by Tori Amos
book and lyrics by Samuel Adamson

The Light Princess brings together iconic singer-songwriter Tori Amos with playwright Samuel Adamson and director Marianne Elliott (Curious Incident) in this spectacular coming-of-age story. A dark fairytale about grief, rebellion and the power of love.

Suitable for 13 years +

CAPTIONED
Sunday 1 December at 2.30pm

Thursday 12 December at 7.30pm


AUDIO DESCRIBED
Saturday 9 November at 2.15pm
Saturday 1 February 2014 at 2.15pm


TOUCH TOUR
Saturday 9 November at 1pm

Saturday 1 February 2014 at 1pm

 

FROM MORNING TO MIDNIGHT
by Georg Kaiser, in a new version by Dennis Kelly

 

Adam Godley leads the cast of From Morning To Midnight by Georg Kaiser, in a new version by Dennis Kelly, directed by Melly Still. Georg Kaiser’s German Expressionist masterpiece explores the tragedy of an ordinary man who steps outside his humdrum life and, over the course of one crazy, alienating day, destroys himself.

 

CAPTIONED 

Tuesday 14 January 2014 at 7.30pm 

 

AUDIO DESCRIBED

Saturday 21 December at 2.15pm

 

TOUCH TOUR

Saturday 21 December at 12.45pm

 

 

 

 

A TASTE OF HONEY

by Shelagh Delaney

 

Bursting with energy and daring, this exhilarating and angry depiction of harsh, working-class life in post-war Salford is shot through with love and humour, and infused with jazz.

 

CAPTIONED

Thursday 3 April 2014 at 7.30pm

 

AUDIO DESCRIBED

Friday 28 March 2014 at 7.30pm

Saturday 29 March 2014 at 2.15pm

 

TOUCH TOUR
Saturday 29 March 2014 at 12.45pm

 

 The Shed


nut
created and directed by debbie tucker green

 

Bein you means not bein me – see, a deficit already – before you even started we running at a loss.

Elayne thinks she’s alright. Nobody else does.

 

debbie tucker green’s plays include truth and reconciliation, random (Royal Court) and generations (Young Vic).

CAPTIONED

Tuesday 26 November at 8pm

 

AUDIO DESCRIBED

Saturday 16 November at 3.30pm

TOUCH TOUR
Saturday 16 November at 2.15pm

 

PROTEST SONG

by Tim Price

Tim Price’s funny and savage monologue explores the reality of the Occupy movement. Rhys Ifans plays Danny.

 

CAPTIONED

Thursday 9 January 2014 at 9pm

 

AUDIO DESCRIBED
Tuesday 7 January 2014 at 9pm

 

TOUCH TOUR
Tuesday 7 January 2014 at 7.45pm

 

THE ELEPHANTOM

by Ross Collins

We have an Elephantom. He turned up on a Tuesday, just after tea-time.

For children and grown-ups of all ages, the story of one little girl and her larger-than-life friend is brought to life with extraordinary puppetry and theatrical ingenuity.

 

CAPTIONED
Saturday 4 January 2014 at 11.30am

 

AUDIO DESCRIBED
Saturday 11 January 2014 at 4.30pm

 

TOUCH TOUR
Saturday 11 January 2014 at 3.15pm

 

RELAXED PERFORMANCE

Saturday 11 January 2014 at 11.30am

 

For anyone who would benefit from a more relaxed performance environment, including people with an autistic spectrum condition, sensory or communication disorders, learning disabilities or families with young children.

 

BLURRED LINES

created by Carrie Cracknell and Nick Payne, written by Nick Payne

 

A blistering journey through the minefield of contemporary gender politics. With songs.

 

CAPTIONED

Tuesday 18 February 2014 at 8pm

 

AUDIO DESCRIBED
Saturday 15 February 2014 at 3pm

 

TOUCH TOUR

Saturday 15 February 2014 at 1.45pm


New London Theatre, Drury Lane

 

WAR HORSE

based on a novel by Michael Morpurgo
adapted by Nick Stafford

 

The National Theatre’s award-winning production continues its record-breaking run at the New London Theatre.

CAPTIONED
Saturday 14 December at 2.30pm
Saturday 7 June 2014 at 2.30pm

AUDIO DESCRIBED
Saturday 23 November at 2.30pm
Saturday 21 June 2013 at 2.30pm

TOUCH TOUR
Saturday 23 November at 12.45pm
Saturday 21 June 2013 at 12.45pm

 

SIGN LANGUAGE INTERPRETED
Saturday 5 July 2014 at 2.30pm

 

Theatre Royal, Haymarket

 

ONE MAN, TWO GUVNORS

by Richard Bean
based on The Servant of Two Masters by Carlo Goldoni

with songs by Grant Olding

 

*****

‘Comic perfection. What are you waiting for? Book now!’

Daily Telegraph

 

CAPTIONED
Saturday 11 January 2014 at 2.30pm

AUDIO DESCRIBED
Saturday 30 November at 2.30pm

TOUCH TOUR
Saturday 30 November at 12.45pm

Apollo Theatre

THE CURIOUS INCIDENT OF THE DOG IN THE NIGHT-TIME

based on the best-selling novel by Mark Haddon
adapted by Simon Stephens

Based on the award-winning novel by Mark Haddon, adapted by Simon Stephens and directed by Marianne Elliott, The Curious Incident of the Dog in the Night-Time is a thrilling new stage play, hailed by The Times as ‘a phenomenal combination of storytelling and spectacle’.

CAPTIONED
Saturday 7 December at 2.30pm
Saturday 26 April 2014 at 2.30pm  

AUDIO DESCRIBED
Saturday 22 March 2014 at 2.30pm

TOUCH TOUR
Saturday 22 March 2014 at 12.45pm

ENDS
11 November 2013
Public Information:

Box Office 020 7452 3000

Information 020 7452 3400 • Fax 020 7452 3030

Email boxoffice@nationaltheatre.org.uk

For more information about facilities and services call 020 7452 3400, visit nationaltheatre.org.uk/access or email access@nationaltheatre.org.uk

For more information contact Susie Newbery, Press Officer, on 020 7542 3061 or snewbery@nationaltheatre.org.uk

Chris Lawton Challenges The Telegraph To Find Him A Job By Friday

November 11, 2013

I can see this going purely viral in Planet Cyberspace!

Helen- Or Tweeting From The Mental Health Ward

November 11, 2013

A reminder of the power of Twitter. I, and many disabled people I know, have been making many of these points about Twitter for years. Facebook too.

With many thanks to Society Guardian for sharing this in their daily bulletin.

In October Helen shared her mental health inpatient experience, as it happened from the ward, and on the most public of platforms – Twitter. I followed her Twitter feed, was intrigued by this stream of instant feedback, and wondered if it might be perceived as a gift or a threat to an NHS Trust.

 

I was lucky enough to have a chat with Helen about her experiences, and this post summarises our conversation:

 

Difficult status coming up…

 

Firstly I wondered what led to Helen choosing to make such a personal experience, which many of us would choose to keep private, so very public:

 

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Helen told me, as a regular use of Twitter it simply seemed ‘quite natural that I would carry on using Twitter’ and that she had actually made retaining her phone a condition of her admission. However, this quickly came under threat when staff attempted to confiscate it. I have previously blogged about inpatient access to smart phones and the law here. It is worth reflecting at this point how smart phones have become an essential day-to-day communication tool for many people – for Helen a text, Facebook update or tweet was infinitely preferable to a conversation on the ward payphone and an invaluable way of keeping in touch with people during a distressing period. 0 

 

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‘It validated me much more than my experiences on the ward’

 

Helen told me that initially she began tweeting her experiences out of both ‘boredom and frustration’ and to elicit the support she felt she needed and was not receiving in person from ward staff. It is telling that Helen felt she received more support from her Twitter community than in person from the ward staff whose role it was to offer just that.

 

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Helen explained to me what this support felt like at the time: ‘it was quite a surreal experience … all these people who we’d never met, reaching out and supporting us – people who’d used services before, people who were carers, people who were professionals and people who never had anything to do with mental health ever, but just were for some reason touched by what I was tweeting and were interested … and there were people who tweeted just to say ‘I’ve been reading all your tweets’ and I just want to say thank you for what you’re doing’ … and there was the chief editor of the Lancet, sent me several tweets -they were so kind, that’s what really stands out to me, they weren’t corporate tweets, they were personal and really kind tweets’.

 

‘I was sat in a beige room, on my own, thinking can I do something positive here?’

 

Helen shared with me how she hoped to challenge mental health stigma by sharing her experiences of acute mental distress. She was particularly struck by her own sense of ‘being the least dangerous person in the world’ contrasted with the (inaccurate) Sun headline which was such a stark contrast to her situation:

 

sun

 

Helen certainly reached a lot of people, as illustrated by the 800 new followers she gained on Twitter during the week, the retweets, and the kind responses she received: ‘do you know I never got a single negative response, not once and I had so many responses, I reckon it was in the hundreds so I don’t know exactly what I achieved, but I must have done something positive’.

 

‘They knew I was an RMN and yet they left me in my room for a whole day and didn’t speak to me’

 

Helen had a poor experience during her inpatient stay; she described how shocked she was that even the fact that she was a nurse herself appeared to make no difference to staff attitudes: ‘the day when I was on my own for the whole day, probably my worst day and I was utterly tormented by voices and thoughts, my husband phoned up in the evening to find out how I’d been that day, and the nursing staff told him that I’d had a settled day.’ Helen took to Twitter to share her outrage at the nursing staff claims:

 

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Humour as a subversive tactic

 

Use of humour can be a subtle means of subversion when we feel there is no other avenue to challenge authority.  Helen’s Twitter exchange with @Sectioned_ is an example of the positive role humour can sometimes play in even the most distressing of circumstances:

 

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‘What I tweeted about was massively boundaried’

 

I wondered if Helen had any regrets about tweeting whilst experiencing psychosis, and what boundaries she put in place to keep herself safe. Helen told me: ‘Even though I was unwell I was discerning … I didn’t put it in such a personal way if that makes sense .. I didn’t give so much detail and I didn’t put the content [of my thoughts] because that felt too personal.’ She also chose how she shared her experiences in a way which other people could relate to: ‘I didn’t go on rants, although I was critical, because I don’t think they’re helpful … I pride myself on being constructive … I think people stop hearing or they get irritated or they start personalising it – so if it is a person accessing services and it’s a professional reading it they might think ‘you’re blaming me for that’ … and the ‘them and us’ starts coming in to play, as someone who uses mental health services and works in them as a nurse I want to avoid that’.

 

Helen told me her partner was worried about the possibility of her being ‘trolled’ with negative comments and she explained that she had planned to simply ignore them if that had happened. In the event it didn’t and Helen had a very positive experience of Twitter conversations.

 

I’m going to storify my tweets and send it to the ward and the chief executive

 

Helen described how her tweets became an instantaneous online journal of her experiences on the ward. They are in effect real time evidence that she plans to storify and then share with the NHS Trust with the intention of giving them feedback and recommending how they can improve their practice:

 

‘I want to motivate, and hopefully give them a way of making positive change, as opposed to just being critical – which wouldn’t be that helpful. And also I’m going to offer to come up and maybe speak to the staff face to face, – what it was like my experience of being nursed on their ward’.

 

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‘I think they [NHS Trusts] are scared to death of social media’

 

I asked Helen to share her thoughts about how NHS Trusts are engaging with social media. Her views were damning of most corporate accounts – both in terms of engagement: ‘you can send a tweet to a Trust Twitter account and you don’t get a response until a week later, which in Twitter time might as well be at least ten years’ and in terms of content: ‘most Trust’s Twitter accounts are basically saying ‘look how good we’ are or ‘here’s the date of my next flu clinic’.

 

Her experience indicates that even NHS Trusts who are well established on Twitter have a lot to learn from experiences such as this.

 

‘With Twitter I’ve found so many allies’

 

I enjoyed Helen’s reflections about the ups and downs of activism, the frustrations she experiences and the way in which her Twitter community sustains her:

 

‘I very much think of the long game now, four years ago I wanted everything to change tomorrow, but now I look at it as if you can even change one or two people a little bit then that’s better than nothing. I love the word radical because I’m a radical, but you have to pace yourself or you get really frustrated and you get angry and you end up pissing people off, and I’ve ended up winding people up, and then you get alienated, so I have learnt not to and to try and take people with me as opposed to burning bridges and leave them behind’.

 

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‘With Twitter I’ve found so many allies, who have given me hope when I feel there isn’t any, that makes you feel you’re never alone, and you’re all fighting the fight to make things happen and to shift things, … we’re all on a similar journey, different streams, but the flow of the river is the same, if I’ve had a crap day at work and to go on Twitter at the end of the day and see that is brilliant, and it boosts me’.

 

And leaving the ward…

 

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You can find Helen on Twitter @teaandtalking. She is a mental health nurse in Dorset and you can find out about her Tea and Talk mental health awareness raising workshops here. I’d like to say an enormous thank you to Helen for sharing her experiences with me, her inspirational approach to mental health care and to reducing stigma and discrimination.

Mencap’s Chief Executive, Jan Tregelles, On Why She Deserves Her Salary

November 11, 2013

From today’s Guardian. Any thoughts, readers?

I am Mencap’s chief executive and I earn £137,442 a year, which the board of trustees have assessed is the right level for someone who has such a complex, high-risk, job. I know for many of my colleagues, our donors and our beneficiaries that this is a huge amount of money. By writing this article I am simply trying to portray a sense of my responsibilities as chief executive and the complexities of my role.

Learning disability is not just my job. It is a major part of my life and has been for 30 years. Being chief executive of a leading disability charity was never going to be a nine-to-five job, nor would I want it to be. But it is very complex.

Everything I do is about outcomes and making sure people with a learning disability can live the lives they choose. This does not stop at the end of the working day and this is the reality for all charity bosses.

Since taking up my post I have put in place a medium- and a long-term strategy, created a new executive, reshaped our corporate function, built evidence into our campaigns and service modelling, and reduced the cost of running the organisation by £6m.

Mencap delivers 7.9m hours of care and support every year to 10,000 people with a learning disability in England, Wales and Northern Ireland. These are among the most vulnerable people living in our communities, often with severe and complex personal needs.

For them, and for society in general, Mencap is a safety net. We cannot control people’s lives, but we can manage risk – and we manage it well. Every month we have around 40 critical incidents, which can vary from someone not coming back home on time to someone suffering hate crime. It is my duty to every single person that we support to make sure that my teams are equipped to mitigate and manage these risks.

Understandably, sometimes things go wrong, and when they do I meet with the individual and their family to talk things through. Without understanding exactly what people with a learning disability and their families are going through, we simply can’t make things better.

As well as delivering high quality, specialist services we campaign for change and work hard to improve the lives of the 1.4 million people with a learning disability in the UK. We work across health, employment, housing, benefits, the effects of welfare reform, and social care.

It is a priority of mine to invest in our hard-working employees. Every fortnight I spend time with groups of colleagues from different departments to learn about the reality of their work – both the good and the bad. Doing this is essential to my role of understanding and implementing what is needed to get the organisation working well.

For Mencap to make a positive difference to the lives of people with a learning disability, and the 5.8 million family members who support them, I need to network. Last week alone I spent five nights in a row attending internal and external events, meeting with the regulator, the health service, families and Mencap’s Trustees. Without building relationships with these key decision-makers, Mencap would not be able to influence society for the people we support.

90% of the money we spend every year goes directly to support people with a learning disability and we know that people want to know their donations are wisely spent so we work hard to keep our costs down. The majority of our fundraised income, which our generous supporters give us, ensures that we can continue campaigning and providing advice and information for families of people with a learning disability.

It has been an extremely difficult time for the charity sector and unfortunately this looks set to continue. Mencap has been supporting people with a learning disability and their families for 65 years and I am doing everything in my power to ensure that we can continue to meet the changing needs of the people we support long into the future.

Jan Tregelles is the chief executive of Mencap.

ATOS- Ask Two Questions

November 11, 2013

This is from early September. I’ve just found it. I don’t know how useful it is or will be to anyone but I thought I’d put it out there, just in case it might help someone, somewhere, somehow.

This process is not yet complete, but I believe something interesting has just happened for me that may have implications for others here.
So, around 2 months ago, I received a letter from the social, telling me they would be phoning me shortly to talk to me about upcoming changes.
I wrote back to say, I did not have a contact telephone number for them and I was quite happy with my current contract, I did not accept their changes to the terms of our contract, unless they were to give me improved medical care.
3 days after I sent the letter, I received a fat envelope with the ATOS return adress, so I returned it to them.
No contract – Return to sender

several weeks go by, then my Incapacity benefit is not paid to me.
I call last Friday.
Me. “WFT, wheres my dosh”
Them”We received information you have gone away”
Me “Really, where is your evidence of that”
Them “Silence”
Now, I should say here that during 4 phone calls with 6 or 7 different people (sorry no vid/audio), they were DESPERATE to get me to apply for the new benefit.
eg. me. “What am I meant to live on”
them “Well, you will need to fill in this form, so you can apply for an emergency payment” and all kinds of other things to fool me into completing the form.

I wrote to them instead.
With this.
This is NOT a complaint, a query, a request for a statement/agreement and is NOT to be treated as one. By doing so, you will agree to pay £5,000.00 in damages.
Do not refer to me as Mr/Mrs/Ms or any title, which is a legal fiction and is not me. By doing so, you will also agree to pay £5,000.00 in damages.

Thank you for your recent communication.
As stated in my previous letters;
1. I do not accept your new terms & conditions and therefore new offer to contract.
2. I do not wish to change my current contract with you since I am still severely ill and I do not wish to receive you increased payments but a reduction in term.
3. The illness I have is lifelong and incurable.
4. The physical effects of this illness and resultant surgery has left me with quite serious problems, which are being managed by healthcare professionals.
5. Should you wish to offer to me improved medical care I would be interested in considering any offers, however, unless anyone I correspond with has medical qualifications suitable to discuss my case, I do not consent to contracting with anyone else. I certainly do not agree to my details, especially medical details, being passed to ANY 3rd party organisation, if based in the private sector (such as ATOS).
6. It is an offense to attempt to FORCE an individual to contract with a 3rd party, yet I am aware you can try to deceive me (under the commercial maxim let he who will be deceived, be deceived).
7. From your unresponsive correspondence, “Incapacity benefit IS paid for as long as the entitlement conditions are satisfied.” As far as I am aware, I am fulfilling those conditions and have since before I was granted Incapacity Benefit. You should note that word Benefit. This denotes I am the beneficiary of a TRUST. Therefore, you MUST be a trustee, working as a public servant, carrying out your duties FOR MY BENEFIT, not yours or the “governments”.
8. When you discuss the 1998 Social Security act, then claim this is “Lawful”, with all due respect, I suggest you take a look at your terms & conditions of employment. You will find that you are NOT QUALIFIED or EMPLOYED to give LEGAL advice. Once you act outwith the terms of YOUR employment, you make yourself liable for your actions. Go and check this with a true legal professional. The reason I know you are not legally qualified if that you made the mistake of claiming something was “lawful” without actually knowing what lawful means, it is connected with the common law, not statute law. When something is said to be in line with statutes, something is said to be LEGAL, not lawful, the two are NOT the same thing, which demonstrates your non-competence in this matter.
9. If you are claiming I am subject to this particular “act” (1998, social security act), please provide evidence to support your claim. I do not want your opinion this act applies to me, that is not evidence. Just because you have done something a certain way does not make that right in Law.

10. Should you wish me to contract with a 3rd party company, my fee for doing so is £1,000,000 Stirling, to be paid before commencement of contract. A fee of £1,000,000 Stirling is payable should you attempt to force me to complete a questionnaire. That questionnaire, as far as I understand it, is an application (begging) form for a new benefit. Since I do not wish to change the benefit I am in receipt of. This “questionaire” does not form part of the benefit I am currently in receipt of and I have stated, quite clearly, I do not wish to change this benefit, I can only assume you are either trying to deceive me into thinking I have to complete the questionnaire to receive my CURRENT benefit.
11. So my questions to you are quite simple.
a. Is completing the aforementioned “questionaire” a requirement to receive Incapacity Benefit?
b. Is completing the aforementioned “questionaire” a requirement to receive the new “Employment & support allowance”?

Please answer BOTH questions. Failure to do so will result in my assumption that you have attempted to deceive me and I will look to seek retribution to the fullness of the law. (Malfeasance in public office (Scotland) carries a maximum sentence of 14 years Prison I believe. Should you obfuscate, prevaricate or attempt anything other than straight forward yes or no answers, I will have to assume you have something to hide, in which case, I WILL find it.
12. Finally, since you did not address much of what I stated in my previous notices, I do not hold much hope you will be any more responsive this time. Which is why my fee schedule will not have to come into play. Local charities will be delighted.(Yes, even with the benefits agency, I enclosed a schedule of fee’s, for charity of course)

SO, I think I made it clear I wont fall for their bullshit.
SO today, I get a letter from them.

Benefits reply 2.jpg

The interesting parts for me are.
1They failed to answer my quite specific questions, I wonder WHY? They were easy enough.
2. Benefit has been reinstated and yes, a payment was made yesterday!
3. Noting of my not wanting phone calls, but ignoring other legitimate requests.

The concern is the warning “the process will continue”, not with my consent it wont and I will fight you all the way PERSONALLY, so be very careful and remember, I have your name now!

I think the point is, I am fucking buzzing just now. I had hoped for this, but never really expected it.
Now I intend to go on the attack with them personally for failing to answer stuff I have raised.

The other bit I think people may like is that I did something similar with Bedroom tax (I have 2 so called spare rooms according to the system) .

So the thank you is this.
Thanks to the community here for giving me the help and confidence for giving me something to fight back with.
With the bedroom tax, I had tried to use the 1992 social security (analienable benefits) and they must have bottled it because all of a sudden, I get an extention on my “discretionary housing payment”

This is the situation, 6 months ago, I was looking at the prospect of loosing my home as well as being dumped on the dole, unable to work due to illness. It may not be forever, but I should be at least OK until April (the world will probably be over by then and we will all be back in caves)
So thanks guys and to those in doubt, BELIEVE in yourself, get good advice and send letters.
My worse case scenario was loosing house & placed on dole. Now I am back as I was before, except I now can PROVE they are full of shit and the whole thing about ATOS is that it is a con job.
DO NOT FILL IN THAT FORM
ASK THOSE 2 QUESTIONS ABOVE and I would like to wager they wont answer.

BBC Looking For Participants For Famous, Rich And Hungry

November 11, 2013

This sounds interesting and I’ve been asked to share it, so am doing so with pleasure.

BBC are looking for individuals and families to show 4 celebrities what its like on front line of britains food crisis . If you have a story to share get in touch hungry@loveproductions.co.uk or ask to speak to one of the famous rich and hungry team 02070674820
Could campaigners plz share in groups

UN Report On Cuts And Disabled People To Be Presented In Parliament 26 Nov

November 10, 2013

Spotted here. Please share.

Status Update
By Denise Bellamy
Paula Peters

Morning all, the U.N. rapportuer for disabilites is coming to the UK on Monday 25th November, and will be in parliament on November 26th to present the UN report. The UN reporteur will be watching a theatre production of how the cuts have affected disabled people in parliament on Tuesday November 26th from 4-6 pm with MP’s and journalists, at the work shop yesterday, Johnathan Butterworth from Just Fair, is presenting a report on how the cuts are affecting disabled people, most especially the welfare reforms. Johnathan butterworth said, if you want to share your story it can be added as case studies to the report he will be presenting to parliament, but no longer than half a page please, and you can e mail him here at this: jbutterworth@just-fair.co.uk if you want to contribute please send it to him asap please, thanks.

JK Rowling On Lumos, Her New Charity For Disabled Children Worldwide

November 10, 2013

She’s back… to using her fame and fortune for good causes. She’s a special one!

Author JK Rowling has dismissed plans by newspapers to set up their own regulatory body, after editors opposed a cross-party charter to create a new watchdog.

Rowling gave evidence on her experiences with the media to the Leveson Inquiry and insists that “press self-regulation has failed us”.

She spoke to Lizo Mzimba about the press, her charity Lumos, and her Harry Potter spin-off Fantastic Beasts.

What Happened To Daddy

November 10, 2013

On Remembrance Sunday, I thought I would share something relevant, from the Telegraph.

An open letter from a soldier who became disabled in Afghanistan to his young son, explaining why he has ‘robot legs.’

When Daddy was a little boy, just like you, he used to play outside a lot, running around with his friends. His favourite game was playing soldiers.

He used to dress up in his granddad’s old army clothes and have a toy gun, make dens and pretend he was in the Army.

When Daddy left school, all he wanted to do was join the Army, so he went to the recruiting office in town and met a real soldier, who told him all about the Army and what soldiers do.

Daddy was very excited and asked the Army sergeant if he could join. The sergeant said there were some tests he had to pass, so they could be sure he was fit enough to join. Daddy sat at a computer and started the test.

If Daddy had worked harder at school, he would not have had to worry about the test, but he used to mess about in class.

 

Now he realised how important school is. Next, they took his weight on some scales, and his height. Luckily, he passed all the tests and was allowed to join the Army.

After all his training, he was sent to Northern Ireland to join the rest of his regiment. Daddy loved it there, going out in helicopters and out on patrol making sure everyone was safe. Daddy was also sent to Kosovo and to Iraq twice, to keep people safe from the bad men that were in those countries.

In 2009, the Army asked Daddy to go to a dangerous place called Afghanistan, where there were lots of bad men not letting children go to school or the ladies go shopping. They made the people grow drugs in the fields, so the bad men made lots of money.

It was Daddy’s job to go out on patrols with his friends in the Army and look for the bad men, so they could be arrested and taken to the police station.

The bad men did not like the Army being there and used to shoot at the Army and hide bombs under the ground to hurt the soldiers. It was very important for the soldiers to be there, because with them there children could go to school and the mums and dads could enjoy working, growing food and shopping for nice things like we have in our houses.

Daddy had been there for three months and was enjoying keeping the people safe. Then on a very sunny day, Daddy went on a patrol with his Army friends to see if any bad men were about.

He stepped on a bomb hidden under the ground. There was a big bang and lots of dust and dirt went up in the air. Daddy lay on his back, with dust all around him, and because the bang was so loud, he could not hear anything.

Daddy looked down and could not see his legs. His arm was twisted behind his back, so he could not see it. Daddy was not in any pain and it did not hurt.

Some of his Army friends started to put bandages on his legs and arm and phoned for a helicopter to come and take him to hospital, so the nurses could make him better. The next day, Daddy was back in England in hospital and Mummy came to see him.

The doctor told Mummy that in the bomb, both Daddy’s legs had come off and his right arm. Mummy was very upset but loved Daddy so much that she was going to help him get better and get married to him.

Daddy was not angry at the Army, or the people in Afghanistan who he liked helping. He just decided to work hard and get walking again, on new robot legs, and to show other people that with hard work and staying positive you can achieve anything.

To those of us who can no longer see the point in Remembrance Sunday- I personally see this letter as a reminder that the disability community should use the day to think about the many soldiers who became disabled in recent wars.

They gave up so much at the request of our Government. I personally think that we should welcome them into our community with open arms and support them in any way possible to come to terms with disability, and to receive the financial support that they so richly deserve.

Jenny’s DLA was stopped;

November 9, 2013

socialaction2014's avatarSocial Action 2014

Jenny&#039;s DLA was stopped;

A letter a day to number 10. No 557.

Saturday 09 November 2013. Jenny’s DLA was stopped; the reason given was that as she was not expected to survive the required time.

Shares are encouraged and welcomed. If this letter speaks for you and you wish to send your own copy please feel free to copy and paste the text for your own letter.

Website updated, letters and replies plus bonus material featuring Mr Suggs, Eeyore and Ribbit.

Also on the website, download the support compilation three album set from Atona. Not to be missed.

http://www.keithordinaryguy.org.uk/

Dear Mr Cameron,

Chester and Ellesmere Port Foodbank (Wednesday, 6 November 2013): ‘Jenny shared her story with one of our volunteers, and requested that we share it with you (everyone). We are privileged to do so.’

Jenny

Jenny came to the Chester and Ellesmere Port Foodbank last month, having been diagnosed with terminal Cancer…

View original post 300 more words

Romance Novels About Benefit Claimants

November 9, 2013

A message I received recently. Thought these books might make nice Christmas presents for book loving DWP dislikers!

I’ve notice that your ‘samedifference’ webpage includes details of books with disabled characters, so wondered if you would be interested my work. ‘Severe Discomfort’, and its sequel ‘Continual Supervision’, concern a middle-aged disabled couple wrongly accused of benefit fraud, and the team of under-resourced advisers who support them through a nightmare year as they try to establish their innocence.

Despite the serious topic, it’s an upbeat story with plenty of dry humour, a cheerfully racy romance and a devious, hypocritical villain, but it also challenges those insidious myths about benefit claimants and the Social Security system we hear so frequently.

The Amazon link is here: http://www.amazon.co.uk/Sarah-Honeysett/e/B00CGNAZXQ/ref=ntt_athr_dp_pel_pop_1

I’m also serialising a sequel, currently only available in ebook format called ‘Limited Capability’ (I think you’ll see where the titles are drawn from by now!), and putting out episodes free on regular Fridays, since the plan is counter-propaganda rather than profit. Episode One (plus five and nine) will be free this Friday, two, six and ten next etc.

I’d obviously be delighted if you liked what I’ve written and could help promote it in any way.

Best wishes, and good luck with your own writing.

Sarah Honeysett

Father Takes Son With Mental Age 5 To No 10 To Tell PM ‘If He Can Work, You Give Him A Job’

November 9, 2013

  A defiant dad took an emotional stand yesterday over the Government’s “bullying” calls for his severely disabled son to prove he cannot work.

Bus driver Fred Hazle, 49, reached the end of his tether so took his blind lad James, 19, to Downing Street to tell David Cameron: “If my son can work, YOU give him a job.”

The father and son made the journey after receiving a barrage of demanding letters from the Jobcentre – including three in four days – as part of the Government’s “fit to work” scheme.

The letters threaten that James’s £71.95 a week in benefits will be stopped unless there is evidence that he cannot hold down a job.

James needs round-the-clock care and has the mental age of a five-year-old. He has severe learning difficulties, epilepsy and autism.

The demands about losing his benefits have been sent despite James’s doctor already telling officials the teenager can’t work and his condition will never improve.

Fred pleaded yesterday to see the Prime Minister or Work and Pensions Secretary Iain Duncan Smith.

But the battling dad was turned away.

He said: “If they say James can work, they can give him a job. Let’s see them take him on in one of their departments.

“I wanted them to see him and tell me he can work but they wouldn’t. He wasn’t born with a silver spoon in his mouth but it’s not about the money, we can take care of him.

“It’s the fact they are treating him like a second-class citizen because he is disabled.

“He got allowances and benefits when he was a kid but now he’s an adult they come on all threatening even though they’ve got the paperwork.

“It’s disgusting bullying and intimidation on someone who can’t defend himself. I’ve fought the system for my boy for 19 years and I’m not putting up with it any more

At the gates to Downing Street, Fred and James were informed they had to make an appointment and wait three months just to hand a letter in.

They were told they could be arrested if they caused a nuisance.

They headed for Parliament. In its lobby, which is open to every citizen, Fred asked to speak to Mr Duncan Smith, but was told the minister would not see them as they are not his constituents.

The dad and son were then asked to leave.

Fred feels his lad is being victimised despite the family doing their best to ensure they jumped through the Government’s hoops.

As James neared the end of his education at a blind school in September, Fred and wife Jacqueline put all the paperwork in place for him to receive Employment Support Allowance when he finished.

To prove the teenager’s eligibility, his GP signed him off indefinitely from the fit to work programme.

In early July, the payments began but within a fortnight, letters began arriving on the family’s doormat in Dagenham, East London, saying the funding would be stopped if they did not provide further proof of James’s disability.

A flood of warnings then arrived on August 5, 8 and 9 from the Jobcentre Plus head office in Glasgow.

Despite numerous calls to the Jobcentre hotline explaining the situation, the letters kept coming.

Fred says that after yet another demand, he eventually took James – who was born without optic nerves – to their local Jobcentre to prove his point.

The woman behind the counter burst into tears when she saw James, said Fred.

The dad added: “The GP told the DWP that James’ condition will never get better. It will only get worse.

“The Jobcentre said they want more proof than that so I took him down there.

“The assistant was so shocked she cried. She rang head office to say there was no job he could do – only to be told she wasn’t medically qualified to make an assessment.

“The DWP haven’t sent anyone to see us or told James to go for an assessment anywhere. They’ve had no contact with the boy but they are constantly on at me and his mum. It keeps us up at night with worry.

“All they need to do is sit down with us and meet him. But they hide behind threatening letters instead.

“Then I go to see them and no one will come out. I’m willing to do what needs to be done. I’d get myself arrested just to be noticed but what good will that do my son?

“We don’t have a voice. No one in the Government cares about us little people.”

A DWP spokesman said nothing more could be done without more “evidence”.

The spokesman added: “We’re committed to helping people who are capable of work get off benefits and into paid employment, while giving unconditional support to those who need it.

“A decision on whether someone is well enough to work is taken after a thorough assessment and after consideration of all available supporting medical evidence.

“We’re still waiting for that in Mr Hazle’s case, but have extended the deadline for him to send us his form because of his condition.”

The DWP said the percentage of people with mental health conditions who go into the support group for ESA has more than tripled since 2010.

The numbers receiving ESA is at its highest level ever with 2.4 million claimants.

VICTORY!!! Government Will NOT Appeal ILF Judgement

November 8, 2013

A big thanks to Fightback for keeping so many updated with this very important, brilliant news.

Excellent news in thanks to Paula the government will NOT be appealing the ILF decision meaning a big victory to every disabled person here and a poke in the eye for this government. Well done to the 5 concerned an excellent case of fighting back.. we are winning people the courts are overturning decisions every day. STAY STRONG. Michelle

And a big thanks to all who contacted Mike Penning yesterday on this issue.

WOW Campaigner’s Review Of A PIP Assessment

November 8, 2013

Spotted here. Sharing, with thanks, because I hope it will be useful to some of you.

WOW Campaigner Kenny Blong underwent a PIP Assessment recently, this is his review of what it was like:-

This week I had my assessment for PIP, and as there isn’t really much information available about what exactly goes on in the assessment, I thought i would write up a brief review to help others who are expecting an assessment in the future.
First thing you need to know, is that this assessment is not like the Work Capability Assessment for Employment and Support Allowance. This assessment is not directed around work or work limitations, this is basically to see how your disability affects you on a day-to-day basis, taking into account both your “good days” and your “bad days”.
PIP is made of two parts, the Daily Living  component and the Mobility component. We’ll start with the Mobility component as its the shortest part of the assessment; This part is basically describing what your mobility limitations are, if you have any. This includes walking (not mobilising as it is in ESA assessments). Now the assessor for me, very rarely used the word “pain” when asking her questions, but I advise that you do. Describe how long you can walk, stand etc, before you start to experience pain and emphasise exactly how much pain you often experience doing these activities.
This then brings me on to the Daily Living component, which takes up the bigger portion of the assessment. Your assessor will ask questions on topics such as:
can you cook a meal or do you need help;
can you bathe/shower yourself or do you need help with it;
can you go out on your own or do you need someone to go with you;
can you dress yourself or do you need assistance from someone;
can you take your medication or do you need prompting or help from someone.
When answering these questions, always describe what assistance you need on both your good days and your bad days, whether you are asked to or not. That way, the assessor knows if you do need help, just maybe not all the time (e.g if you have a fluctuating medical condition)
You may be asked about any aids or adaptations you may have and use in your home. You need to describe these in detail and exactly how beneficial these are to you. If you are not asked about them, remember to include them in the above topics.
If you are on strong medication that causes side effects, make sure that these are brought up with your assessor, along with how they can affect you. If you need extra assistance from someone because of these side effects, make sure you explain this to your assessor.

 

All in all, the assessment will go on for about an hour, so there is plenty of time to make sure everything is included, so do not rush! I wish you all luck with your assessments and I hope you all get the assistance that you deserve and are entitled to.

Are You Thinking Of Appealing From WRAG To Support Group?

November 8, 2013

If so, please read this from Fightback.

Word of warning if you are thinking of appealing from WRAG group to Support:
Many JCP advisors are now telling customers that they shouldnt be there and should be in support group. The problem with this is that the courts are very reluctant to put someone into support group without much proof of their illness. There is nothing wrong with asking the decision maker to look again at your claim, but it could firstly trigger another ESA50 and medical, with different results than last time, if you managed to get into the wrag group.
If you decide to take this further to the tribunal, please be aware that the way the court WILL substitute the original DWP decision with their own decision which could see you with less points, and found fit for work if you dont have enough medical evidence to substantiate your claim.

Just remember that, you NEED to show you are not fit for work related activity, so if you only have to attend an interview once a month or less I would seriously think about the implications if you are found fit for work, remember there is now no appeal rate at first, if you dont fit neatly into one of the descriptors for the support group criteria then do your research and use our template letters for the consultants and GP on the forum.

Qualifying for the support group of employment and support allowance (ESA)is not about scoring points. Instead, if the decision maker accepts that any of the following descriptors apply to you, then you will be placed in the support group.

1. Mobilising unaided by another person with or without a walking stick, manual wheelchair or other aid if such aid can reasonably be used.
Cannot either
(i) mobilise more than 50 metres on level ground without stopping in order to avoid significant discomfort or exhaustion
or
(ii) repeatedly mobilise 50 metres within a reasonable timescale because of significant discomfort or exhaustion.

2. Transferring from one seated position to another.
Cannot move between one seated position and another seated position located next to one another without receiving physical assistance from another person.

3. Reaching.
Cannot raise either arm as if to put something in the top pocket of a coat or jacket.

4. Picking up and moving or transferring by the use of the upper body and arms (excluding standing, sitting, bending or kneeling and all other activities specified in this Schedule).
Cannot pick up and move a 0.5 litre carton full of liquid.

5. Manual dexterity.
Cannot either:
(a) press a button, such as a telephone keypad or;
(b) turn the pages of a book
with either hand.

6. Making self understood through speaking, writing, typing, or other means normally used.
Cannot convey a simple message, such as the presence of a hazard.

7. Understanding communication by—
(a) verbal means (such as hearing or lip reading) alone,
(b) non-verbal means (such as reading 16 point print or Braille) alone, or
(c) a combination of (a) and (b),
using any aid that is normally, or could reasonably be, used, unaided by another person.
Cannot understand a simple message due to sensory impairment, such as the location of a fire escape.

8. Absence or loss of control whilst conscious leading to extensive evacuation of the bowel and/or bladder, other than enuresis (bed-wetting), despite the wearing or use of any aids or adaptations which are normally, or could reasonably be, worn or used.
At least once a week experiences
(i) loss of control leading to extensive evacuation of the bowel and/or voiding of the bladder; or
(ii) substantial leakage of the contents of a collecting device;
sufficient to require cleaning and a change in clothing.

9. Learning tasks.
(a) Cannot learn how to complete a simple task, such as setting an alarm clock, due to cognitive impairment or mental disorder.

10. Awareness of everyday hazards (such as boiling water or sharp objects).
(a) Reduced awareness of everyday hazards leads to a significant risk of:
(i) injury to self or others; or
(ii) damage to property or possessions,
such that they require supervision for the majority of the time to maintain safety.

11. Initiating and completing personal action (which means planning, organisation, problem solving, prioritising or switching tasks).
Cannot, due to impaired mental function, reliably initiate or complete at least 2 sequential personal actions.

12. Coping with change.
(a) Cannot cope with any change, due to cognitive impairment or mental disorder, to the extent that day to day life cannot be managed.

13. Coping with social engagement due to cognitive impairment or mental disorder.
Engagement in social contact is always precluded due to difficulty relating to others or significant distress experienced by the individual.

14. Appropriateness of behaviour with other people, due to cognitive impairment or mental disorder.
Has, on a daily basis, uncontrollable episodes of aggressive or disinhibited behaviour that would be unreasonable in any workplace.

15. Conveying food or drink to the mouth.
(a) Cannot convey food or drink to the claimant’s own mouth without receiving physical assistance from someone else;
(b) Cannot convey food or drink to the claimant’s own mouth without repeatedly stopping, experiencing breathlessness or severe discomfort;
(c) Cannot convey food or drink to the claimant’s own mouth without receiving regular prompting given by someone else in the claimant’s physical presence; or
(d) Owing to a severe disorder of mood or behaviour, fails to
convey food or drink to the claimant’s own mouth without receiving —
(i) physical assistance from someone else; or
(ii) regular prompting given by someone else in the claimant’s presence.

16. Chewing or swallowing food or drink.
(a) Cannot chew or swallow food or drink;
(b) Cannot chew or swallow food or drink without repeatedly stopping, experiencing breathlessness or severe discomfort;
(c) Cannot chew or swallow food or drink without repeatedly receiving regular prompting given by someone else in the claimant’s presence; or
(d) Owing to a severe disorder of mood or behaviour, fails to—
(i) chew or swallow food or drink; or
(ii) chew or swallow food or drink without regular prompting given by another person in the physical presence of the claimant

You can be automatically treated as having a limited capability for work-related activity if you are:

suffering from a progressive disease and consequently your death can reasonably be expected within six months.
receiving treatment by way of chemotherapy or radiotherapy (or are likely to receive such treatment within 6 months), or you are recovering from that treatment and Jobcentre Plus is satisfied that you have a limited capability for work-related activity.
suffering from some specific disease or bodily or mental disablement and consequently there would be a substantial risk to the mental or physical health of any person if you were found not to have a limited capability for work-related activity. (regulation 35)
pregnant and there would be a serious risk to the health of you or your child if you did not refrain from work-related activity.
How the work capability assessment is applied
In order to apply the tests for limited capability for work and limited capability for work-related activity a decision maker will first look at the information that you have provided in your initial claim for ESA to see if you pass these tests without the need for further enquiries.

If the decision maker considers that there is not enough information to make a decision you will normally be sent Limited capability for work questionnaire (ESA50) to complete. This form has a number of questions about the activities listed above. Each activity has a section with tick-boxes and space to provide more detailed information about each activity. Michelle

Dear IDS, We Know Your Wife Is Human, But We Are Too

November 8, 2013

ids

When, oh when, will you realise that, Sir, and start treating benefit claimants like people too?

(Graphic going viral on Facebook. I first spotted it in this group.)

Millionaire Landlord Kevin Green Says He May Have To Stop Letting To Benefit Claimants

November 8, 2013

Readers, in between a lot of information about him and about Universal Credit, that little ‘gem’ sticks out.

So, what do you think? Is he discriminating unfairly, or does he have a point?

Are there others who think like this? Have you been refused rented housing because you claim benefits?

ATOS: Use Of CCTV

November 8, 2013

Spotted here. Something useful to know. Please share widely.

Use of ATOS CCTV
ATOSsers should not use the cameras in the Torture chamber (Assessment Centre) to use against you in the ESA WCA.
ATOS would say by the nature of their work (if that’s what …they call it) that they require CCTV for security – they may say it si for the benefit of the claimant ! they are so loving and caring. However I have seen many people suggest that CCTV was used to measure walking and so on. This is illegal !! if this happen to you report them to the Information Commissioner – Illegal use of CCTV – report them make their lives as difficult as they do yours ! YOU have a right to see what they have recorded
If you are concerned that CCTV is being used for harassment, anti social behaviour or other matters dealt with under the criminal law, then these are matters for the police. Images taken for recreation, such as on mobile phones, digital cameras and camcorders, are also exempt from the Act. Law enforcement covert surveillance activities are covered by a separate Act – the Regulation of Investigatory Powers Act (RIPA) 2000 and the Regulation of Investigatory Powers (Scotland) Act (RIPSA) 2000

http://www.ico.org.uk/for_the_public/topic_specific_guides/cctv

Holly Greenhow- Boden Model With CP

November 8, 2013

For Holly Greenhow, seven, everything from speaking to sitting up is a challenge – all because she was born with athetoid cerebral palsy.

But brave Holly, from Cambridgeshire, has refused to let her disability hold her back and has landed a starring role in Boden’s new childrenswear campaign.

Holly, whose condition was caused by a prolonged loss of oxygen at birth, was chosen after attending a casting earlier this year, where she shone in front of the camera.

She spent a day in London modelling clothes from the Boden children’s range and now features in the Meet and Greet mini campaign on their website.

In the Q&A accompanying the campaign, Holly charmingly reveals that the funniest person she knows is her mother and that she would choose to play all day if she ruled the world.

‘Holly has a beautiful smile and modelling is not all about being perfect, so we thought why shouldn’t she be considered,’ said her mother Fiona, 42.

‘There are lots of things she can’t do and will never be able to do because of her disabilities, so it was really nice for her to have this experience.

‘I hope it will help the image of disabled children and also open people’s eyes to the fact there are lots of children out there who aren’t perfect.’

Holly, who has a 10-year-old brother named Oliver, was born with athetoid cerebral palsy, which affects her movement, balance and speech.

She uses a wheelchair to get around and has only recently started to communicate using a special computer system operated by her eyes –  similar to that used by physicist Professor Steven Hawking who suffers from Motor Neurone Disease.

But the seven-year-old has always enjoyed choosing her own clothes, so her mother thought she might like to try modelling.

‘My mum suggested it as Holly loves pretty clothes and particularly likes wearing those designed by Boden,’ explained Fiona, a trade manager for Tesco.

‘Holly has so many things against her and as her mother I just wanted her to be able to do something that any child could or would love to do, given the chance.

‘She went for a casting in April and did the shoot in the summer holidays with lots of other children at a studio in London.

‘Holly really enjoyed it and loved being the centre of attention and we’re really pleased with the finished results.’

Fiona, whose husband Paul, 45, is head of sales for a food manufacturer, hopes that Holly may now have the chance to do some more modelling work, following in the footsteps of other disabled child models such as Seb White who appeared in Marks & Spencer’s 2012 Christmas campaign.

Zena Botha, the studio shoot and model manager for Boden, said the company ‘was delighted that Holly made the cut.’

She added: ‘We are always happy to invite our Mini Boden fans along to model castings and we were delighted that Holly made the cut.

‘Holly was charming and we’re very pleased with the shoot, which is live now on boden.co.uk.’

Matt Jackson, head of campaigns at the disability charity Scope said: ‘There has certainly been a lack of diversity in kids modelling campaigns to date, which means that disabled children are often not represented.

‘The fact that Holly has cerebral palsy and will feature in Boden’s advertising will certainly help to challenge some of the misunderstandings and prejudice that can make life difficult for so many disabled children.

URGENT Contact Penning RE ILF

November 7, 2013

From Where’s The Benefit. I do hope I’m not too late to make a difference.

An urgent update from Liz Carr:

Help save the ILF! Yesterday we won a major victory against the Government when the Court of Appeal ruled that the closure of the Independent Living Fund was unlawful. But the fight is not over – Minster for disabled people, Mike Penning has until tmrw to decide whether or not to appeal this decision. Please, anyone and everyone, email him at mike@penning4hemel.com and tell him why giving disabled people the means to be partners, friends, daughters, sons, employers, employees, friends, cat lovers, sarcastic bastards and all that malarkey is a really rather good idea for everyone?

 

Another Day Stuck In A Vice

November 7, 2013

A song for the DWP.

ART STUDENTS SUPPORT ROYAL BLIND SCHOOL PUPILS IN MOVE TO DIFFERENT CAMPUS

November 7, 2013

A press release:

Students at Edinburgh College of Art are designing an art project to help Royal Blind School pupils remember their historic Craigmillar Park campus after it closes in Summer 2014 and relocates all pupils to its Canaan Lane campus in Morningside.

The four third year art students have taken elements of sound from the Craigmillar Park campus including footsteps, voices and the sound of the lift to create an art installation that will be presented to the pupils on Friday 8 November.  

The idea behind the art project came from one of the four students, whose young son has a visual impairment and other disabilities.

The sounds have been recorded on separate CDs which will be presented to the school in a box that can be handled by the children. The box can be opened to give access to the CDs held onto a concertina of cardboard by raised centre holders. Labels in large type and Braille identify the rooms and people whose voices can be heard on the recordings.  

Art student Penny Kay said:

“As a group who would normally work primarily with the visual senses we are excited by the possibility of producing work that might include elements of sound, touch or movement. Our challenge is to create a piece of art whose primary objective is its appreciation by the children of the school. This piece might also prove of interest to people with full sight in so far as they are given an insight into the perspective of the children through the make up of the sculpture.”

The boxes will be kept in the library at the Canaan Lane campus and will be available for pupils to take them out to listen to the sounds of the Craigmillar campus and remember their experiences there.

Cari Mannion, Depute Head Teacher at the Royal Blind School said:

“Royal Blind School pupils are very keen on art and are looking forward to seeing the project that the students have come up with. This project will help the pupils in their transition to the Canaan Lane campus and will be a lovely memory for them in the future.”

The Royal Blind School is merging its two campuses as the numbers of pupils enrolling have been falling in recent years. Single disability blind children and young people with little or no additional support needs are today mostly catered for in mainstream schools and special units in their home areas.

The changes will see all pupils educated and cared for at the Canaan Lane campus in Autumn 2014. The Royal Blind School’s Craigmillar Park Campus is being sold as part of a move to merge two campuses into one.

The Royal Blind School is also establishing a national education resource centre for visual impairment, which will provide support to visually impaired pupils in maintream schools across Scotland through pupil assessment, advice and training for the education sector.

For more information please contact:

Davina Shiell, Marketing and Fundraising Manager, Royal Blind

Tel: 0131 229 1456, Mobile: 07713 987797, Email: davina.shiell@royalblind.org

Universal job match

November 7, 2013

blackfoxkitsune's avatarannabellalaws

Now then I’ve been looking around for a solution to a problem many job seekers now or will have. I have to admit it is a chip on my own shoulder as well. The latest in the assault is Universal job match run by Monster.co.uk, in my eyes its a nasty little website that is essentially a Government/DWP sanctioned Trojan Virus that you are FORCED to use daily as a job seeker, it annoys me because I feel that; Why do I have to fight the system to get a few pittance to help me while I’m down on my luck, and WHY do I have to fight a system that is meant to support me in this time for my BASIC human rights?
Well UJM is the latest attack on that my right to privacy, UJM leaves cookies on your comp for up to 10 years with some of the shortest being up…

View original post 701 more words

What The Job Centre Sign Should Really Say…

November 7, 2013

Spotted on Facebook. With thanks to the creator. Your Thursday Treat.

job centre sign

 

Mother Faces Heat Or Eat Choice After Toddler’s DLA Cut

November 7, 2013

I have always hated authorities who think they know children better than their parents do.

The mother of a 20-month-old girl with a serious heart condition says she is being forced to choose between heating her home and eating after one of her financial lifelines was cut.

 

Cat Halliday, of Wood Street, Sheerness, has discovered she is no longer entitled to the £200-a-month disability living allowance (DLA) she was receiving to help towards daughter Tiffany’s care.

 

The youngster has three holes in her heart and suffers from feeding and weight problems, poor circulation and a lowered immune system.

 

She has a likelihood of being autistic and an enlarged heart, pulmonary stenosis and a ventricular ring.

 

Tiffany is also suffering from hypermobility and has throat problems that may require an operation before she has heart surgery next year.

 

Miss Halliday, who cannot work because she cares for her daughter full-time, claims the Department for Work and Pensions has stopped the benefit as it ruled Tiffany did not need more than an hour’s care a day. Miss Halliday insists she does.

 

She mainly uses the money to pay for heating, which needs to be on constantly due to Tiffany’s increased risk of conditions such as pneumonia and hypothermia.

 

The 25-year-old said: “Everything goes towards her care. There are days when I will stay up all night two or three days running to do a drip feed every few minutes or keep an eye on her breathing and massage her joints.

 

“Because she needs to go to the hospital so much, all of my remaining carer’s allowance is spent on travel to and from Medway, Sittingbourne and London.”

 

 

She added: “I’m scared the DLA is going. I’m faced with picking between heating my home and food.

 

“I will go without to make sure Tiff gets what she needs, but it shouldn’t have to be like that.

 

“I feel like her human rights are being taken away – and she’s being punished for being ill.”

 

Miss Halliday plans to ask the Department for Work and Pensions (DWP) to reconsider its decision and she should get an answer within about two months.

 

If she is unsuccessful, she can appeal again – but it could take a year before the case is resolved if she does.

MP Gordon Henderson has taken up her fight and has written to work and pensions secretary Iain Duncan Smith.

 

He said: “I’m very concerned, not just for Miss Halliday, but for any other people in a similar position.

 

“I’ve written to ask him to look into the situation to find a way of either reducing the length of time that appeals take or providing some form of benefit until such time as an appeal is heard.”

 

However, Mr Henderson is also concerned about interim benefits. If an appeal was refused, any money paid would have to be returned.

 

A DWP spokesman said: “Disability living allowance isn’t generally paid on the condition someone has, but because they have specific care and mobility needs.

 

“All young children have care and mobility needs, but parents can claim DLA for children who need a lot more help or supervision than other children of the same age.”

Man Banned From Job Centre For Using Mobile Phone, Police Called

November 7, 2013

This is from late August- but it should have gone much more viral then. I’m sharing it to try to make it go viral now. Thanks to The People Vs The Government, DWP and ATOS Facebook group.


http://m.youtube.com/watch?v=ZJZMdbS-eFo&list=TLOTNQ3_al2KbyuJNykA7JZWU41xHoOK-S&desktop_uri=%2Fwatch%3Fv%3DZJZMdbS-eFo%26list%3DTLOTNQ3_al2KbyuJNykA7JZWU41xHoOK-S

Autism Can Be Detected In Two Month Old Babies Finds Study

November 7, 2013

Autism can be identified in babies as young as two months, early research suggests.

 

US researchers analysed how infants looked at faces from birth to the age of three.

 

They found children later diagnosed with autism had shown diminished eye contact – a hallmark of autism – in the first few months of life.

 

The findings, reported in Nature, raised hope for early interventions to tackle autism, said a UK expert.

 

In the study, researchers led by Emory University School of Medicine in Atlanta used eye-tracking technology to measure the way babies looked at and responded to social clues.

 

They found infants later diagnosed with autism had shown a steady decline in attention to the eyes of other people from the age of two months onwards, when watching videos of natural human interactions.

 

Lead researcher Dr Warren Jones told BBC News: “It tells us for the first time that it’s possible to detect some signs of autism in the first months of life.

 

“These are the earliest signs of autism that we’ve ever observed.”

 

The study followed 59 infants who had a high risk of autism because they had siblings with the disease, and 51 infants at low risk.

 

Dr Jones and colleague Dr Ami Klin followed them to the age of three, when the children were formally assessed for autism.

 

Thirteen of the children were diagnosed with autism spectrum disorders – a range of disorders that includes autism and Asperger’s syndrome – 11 boys and two girls.

 

The researchers then went back to look at the eye-tracking data, and what they found was surprising.

 

“In infants with autism, eye contact is declining already in the first six months of life,” said Dr Jones.

 

But he added this could be seen only with sophisticated technology and would not be visible to parents.

 

“It’s not something that parents would be able to see by themselves at all. If parents have concerns they should talk to their paediatrician.”

 

Dr Deborah Riby, of the department of psychology at Durham University, said the study provided an insight into the timing of atypical social attention in children who might go on to develop autism.

 

 

“These early markers are extremely important for us to identify – the earlier we can diagnose a child who has one of these disorders – such as autism – the earlier we can provide intervention and development,” she said.

 

Caroline Hattersley, head of information, advice and advocacy at the National Autistic Society, said the research was “based on a very small sample and needs to be replicated on a far larger scale before any concrete conclusions can be drawn”.

 

“Autism is a very complex condition,” she said.

 

“No two people with autism are the same, and so a holistic approach to diagnosis is required that takes into account all aspects of an individual’s behaviour. A more comprehensive approach allows all of a person’s support needs to be identified.

 

“It’s vital that everyone with autism can access a diagnosis, as it can be key to unlocking the right support which can enable people with the condition to reach their full potential.”

 

The research is published in the journal Nature.

Hemiplegic Migraines

November 7, 2013

A man from Wales has spoken out about his rare medical condition which causes him to collapse if he smells Chanel No 5 perfume.

Glynn Parry suffers from hemiplegic migraines – a genetic condition which causes one hemisphere of his brain to temporarily shut down leading to paralysis.

The father of three told BBC Radio 5 live’s Drive: “A burning pain occurs in the right side of my brain followed by gradual paralysis… and I have to be rolled into the recovery position.”

“I have two to three attacks a week… It’s a difficult thing to live with and it impacts on every aspect of my life.”

Make Ku Bar Girls Wheelchair Accessible

November 7, 2013

This is a guest post by Geek ‘n’ Proud.

Hi everyone,

I am a student at one of the London Universities. As a wheelchair user, I am very used to having to make enquiries as to whether a venue I haven’t visited before has step free access. I was very disappointed to hear that Candy Bar will be closing in January 2014 due to a 50% increase in rent (for more information, please see: http://mailshots.asweb.co.uk/t/ViewEmail/r/2FD4AA59001241CD2540EF23F30FEDED). This is not only because it is one of only a couple of lesbian bars in London (a fact that I find hard to believe) but also because it is one of the few gay bars that have wheelchair access. This fact puts very large restrictions on people who wish to go to gay bars but require step free access.

In response to the closure of Candy Bar, the Ku Bar plans to radically overhaul its premises to make the entire lower ground floor into “Ku Bar Girls”. I have written to Ku Bar (info@ku-bar.co.uk) asking them to reassure me that if the lower ground floor is not wheelchair accessible they will be putting a lift in as part of the refurbishment. I have not let received a response! I am writing this post to ask others who care about LGBT rights and wheelchair users having access, to write to the Ku Bar as well. To keep up with the campaign please join the FB group https://www.facebook.com/groups/584764861571151/

 

Geek’n’proud

WARNING For Anyone Threatened With Being Sanctioned On ESA

November 6, 2013

From Fightback:

Warning for anyone who is threatened with sanctions on ESA, we have been informed by 2 good sources now that sanction squeezes are being put in place to help JC staff reach sanction targets.

If you have been sanctioned you may be told that by JC staff that you will lose ALL benefits if you dont sign onto JSA whilst you appeal the sanction decision. This allegedly, is a ploy to get the figures down and allow targets being imposed to be reached. Before you sign and commit to saying you are fit for work when you are not because of a disability, remember this will mean you CANNOT just switch back over to esa without a fight, as you are saying in your own words you CAN work full time by signing the JSA claimant commitment. We know this has been the case for a while but we know that JC staff are about to really start applying the pressure as they are being heavily pressurised to do so.
So get advice before you sign on! Michelle

Scrap The Bedroom Tax- Vote In Parliament 12 November!

November 6, 2013

Sue Marsh is requesting that you all email your MP urgently on this very important issue.

Rachel Reeves confirmed yesterday that Labour is calling an Opposition Day debate on scrapping the Bedroom Tax on the afternoon of 12th November. That’s only eight days away, so if we’re going to make any difference to the vote, we need to let our MPs know as soon as possible.

She’s asked you all if you would consider coming to the Commons on the day. She’s booked a wheelchair accessible room in Portcullis House (Boothroyd Room) from 10am-12.30 on the morning of the debate – the idea is to orchestrate a mass lobby from there – and she’ll also be able to come and meet as many of you as possible.

We’ve also been told they’ll try and get tickets for as many people as possible to attend the debate in the afternoon over at the Commons.

For those who can’t attend in person, we’re told there’ll be a mass “virtual lobby” at the same time and the Mirror are supporting the last minute calls to MPs.

If anyone would like to attend either event – or has any questions – contact her parliamentary assistant Keir Cozens – keir.cozens@gmail.com – and hopefully see you there…

You can email your MP from here http://www.theyworkforyou.com/ just by entering your postcode.

A short note, outlining why you think the Bedroom tax is unfair and asking them to either meet you at the parliament lobby, or if you can’t attend, to vote to scrap the tax.

It’s vital we let every MP know on a personal level and particularly to engage in conversation with LibDems. Recently, grassroots members voted overwhelmingly against the Bedroom Tax at this year’s conference http://www.theguardian.com/politics/2013/sep/16/nick-clegg-conference-defeat-bedroom-tax and since, Clegg has ordered an “independent review” (yawn) to tell him what he already knows. http://www.independent.co.uk/news/uk/politics/nick-clegg-orders-independent-study-into-bedroom-tax-8881861.html

We must try to persuade Liberal Democrat MPs to vote with the overwhelming wishes of their own grassroots and members rather than the compromised interests of a few at the top of their party.

There are also now countless examples of Conservatives and Tory councils rejecting the tax that you can send to your Conservative MP to show him that they would be representing constituents by opposing this levy on  principle, not as ordered by the whip. Just because this debate was called by the opposition, plead with them not to allow partisan nonsense to turn such an important issue into a democratic farce. They see the same heartbreaking stories at their surgeries as Labour MPs :

http://speye.wordpress.com/2013/06/13/tory-council-rebels-against-the-bedroom-tax-the-beginning-of-the-end/

Flagship Conservative council of Westminster has just blamed the Council Tax for soaring costs of re-housing tenants. http://londonist.com/2013/08/bedroom-tax-blamed-for-increase-in-westminster-rent-arrears.php

The UN recently reported that the Bedroom Tax may breach the human rights of those subjected to it http://www.theguardian.com/society/2013/sep/11/bedroom-tax-should-be-axed-says-un-investigator

And there have now been legal defeats in both English and Scottish law judging that it discriminates against both disabled adults and children http://disabilitynewsservice.com/2013/09/campaigners-score-bedroom-tax-court-victories/

What more do we need Mr Clegg? Mr Cameron? It discriminates in the eyes of the law, it’s inhumane in the opinion of the UN, it will cost more than it saves and 440,000 of the 660,000 affected have a long term illness or disability..

If you google your county or next biggest town, there are almost certainly local stories with the exact number of constituents set to lose out or facing eviction in your local area.

But even if you just ask your MP to vote to scrap the tax, that’s good enough and you can click below to

EMAIL YOUR MP
We win one little act of faith at a time, one email at a time, one defeat at a time.
I will try to get details of the virtual lobby as soon as possible and post them in a separate post at Same Difference.

Disabled People Win ILF Court Challenge

November 6, 2013

Some very good news, at last!

Five disabled people have succeeded in a legal challenge to the government’s decision to abolish the Independent Living Fund.

 

The £320m ILF currently provides support enabling nearly 19,000 severely disabled people in the UK to live independent lives in the community.

 

The High Court ruled in April that the closure decision was lawful.

 

But the five argued the court had gone wrong in law and there had been a lack of proper consultation over changes.

 

They said that, without ILF funding and support, they would be forced into residential care or lose their ability to participate in work and everyday activities on the same basis as able-bodied people.

‘Powerful’

The scheme’s average payout is £300 a week, and the government has said that councils, which administer most social care, will take over funding this help.

 

Ministers took the decision close the fund on 18 December last year.

 

Court of Appeal judges Lord Justice Elias, Lord Justice Kitchin and Lord Justice McCombe allowed the challenge to the High Court’s earlier ruling, quashing the original decision in favour of the government.

 

Lord Justice McCombe said the evidence upon which the decision had been based did not give “an adequate flavour of the responses received indicating that independent living might well be put seriously in peril for a large number of people”.

 

Welcoming the “powerful” ruling, law firms Deighton Pierce-Glynn and Scott-Moncrieff & Associates, which represented the claimants, said their clients had “feared that the loss of their ILF support would threaten their right to live with dignity, and that they could be forced into residential care or lose their ability to work and participate in everyday activities on an equal footing with other people”.

 

The Court of Appeal decision was described as being “of major importance not just for the claimants, but for all disabled people”.

 

Minister for Disabled People Mike Penning said: “We are very pleased the Court of Appeal upheld how we undertook our consultation on the future of the fund, and they accepted that it had been carried out properly and fairly.

 

“We are disappointed with certain aspects of today’s decision, and we will be examining the judgement very carefully and considering the implications before deciding on the most appropriate way forward, which includes seeking leave to appeal.”

 

The Equality and Human Rights Commission was permitted by the court to intervene in the case and made submissions on the proper application of the Equality Act and UN Convention.

 

The ILF was established in 1988, but the government decided in 2010 that it had become “no longer appropriate or sustainable” to keep running the scheme outside the mainstream social care system. The fund closed to new applicants soon afterwards.

Colchester General Hospital: Cancer Unit Police Probe

November 6, 2013

Comments very welcome.

A hospital cancer unit is being investigated by police after staff said they were being “pressured or bullied” to falsify data relating to patients.

 

“Inaccuracies” were found with waiting time data relating to cancer treatment at Colchester hospital, the Care Quality Commission (CQC) found.

 

Patients’ lives may have been put at risk, the hospitals inspector said.

 

Essex Police said it was looking into whether a “criminal investigation” was needed.

 

Staff told inspectors they were “pressured or bullied” to change data relating to patients and their treatment to make it seem people were being treated in line with national guidelines, the CQC said.

New management

The findings were reported to police “due to the serious failings identified”, it added.

 

Dr Gordon Coutts, chief executive at the Colchester Hospital University NHS Foundation Trust, said: “We are truly sorry that in some cases cancer patients, their carers and families have not always received the high quality of care that they should have expected from our trust.”

 

Professor Sir Mike Richards, chief inspector of hospitals, recommended the trust be put into special measures, which could lead to a new management team being installed or another trust put in charge.

 

 

He said: “It is shocking to think that people’s lives may have been put at risk for the sake of the waiting-time figures.”

Criminal investigation

NHS England said it would lead an incident management team of cancer specialists to ensure the safety of cancer patients at the hospital.

 

There will also be a review looking back as far as 2010 to check whether any other patients had their records changed or “inappropriately recorded”.

 

The CQC said its inspectors visited the trust in August and September after receiving complaints about waiting times for cancer treatment.

 

It said some patients did not get their treatment within the required 62 days and in three cases delays exceeded 100 days.

 

“Six people described problems experienced in their treatment, including delays in receiving care,” the report said.

 

“The provider did not have adequate systems to maintain the safety and welfare of cancer patients.”

 

 

The CQC identified 22 cases where patients experienced delays in their care.

 

Essex Police said it had been contacted by the CQC and was “reviewing information” to “establish whether a criminal investigation is necessary”.

 

In a statement, the CQC said: “We found that the concerns raised by staff in relation to changes made to people’s cancer pathways were not appropriately managed, investigated or responded to by senior staff of the trust.

 

“Staff we spoke to provided examples of bullying and harassment by the management team in respect of changes of the cancer pathways.

 

“We found that managers did not show clear leadership in a way that ensured the safety and welfare of patients by providing a high quality of care.”

 

Royal College of Nursing regional director Karen Webb said: “The CQC report concerning Colchester Hospital does chime with concerns we have voiced on behalf of nurses.

 

“It is right that the hospital is placed in special measures.”

 

About 6,000 people a year receive cancer treatment at the trust.

Obituary: Adam Walker

November 5, 2013

Funny man, football fan, and flirt with Cerebral Palsy. (Oh, and trainer of professionals in communication with disabled children.)

Job Centre Madness, Youtube Style

November 5, 2013

I’ve just watched this, and it’s yet another jobcentre incident that should go viral.

Part Time Workers And Volunteers To Be Hit By Osborne’s Mass Workfare

November 5, 2013

johnny void's avatarthe void

Boycott-workfare-holiday-innDetails of George Osborne’s upcoming – and possibly illegal – mass workfare scheme have emerged and make grim reading for everyone but the companies set to profit from this huge extension of forced labour.

Tender documents unearthed by @refuted reveal the specifications for the six month Community Work Placements scheme which begins in April 2014.  These documents form the basis of a ‘commercial competition’ currently taking place, in which grasping welfare-to-work parasites like A4e and G4S will bid for lucrative government contracts to force long term unemployed people into unpaid work.

Those leaving the Work Programme will either be placed on daily signing at Jobcentres and ‘intensive support’ or face the six month workfare scheme.  This will involve 780 hours of forced unpaid work, over two and a half times the maximum possible community service sentence which can be handed out by the courts.

In some cases this will not…

View original post 489 more words

See Hear Presenter Menmos Costi To Appear In Holby City Next Week

November 5, 2013

Along with his daughter, reports Limping Chicken.