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London Blind Man’s #BedroomTax Victory

September 24, 2013

This is very good news, particularly for me, as I live in London.

When is a bedroom, not a bedroom? Well according to the law, when it is being used for storage.

Why does it matter? Well it matters to anyone hit by the government’s so-called Bedroom Tax.

In the first case of its kind in England, Londoner Surinder Lall’s lawyers argued his spare bedroom was actually being used to store vital equipment to help with his disabilty, arguing his full housing benefit should be reinstated. He won.

Our Political Correspondent Simon Harris reports.

Miley Cyrus Twerks With Dwarf Again And Defends Shows

September 24, 2013

Miley Cyrus has twerked with a dwarf dancer again, readers. The question remains yours to answer- is it okay?

Miley Cyrus has defended recent controversial performances during a show at the iHeartRadio Festival.

 

The 20-year-old sang at the Las Vegas event on Saturday (21 September) night in a revealing fishnet dress.

 

She twerked on stage alongside dwarves and used a banana shaped microphone during the show.

 

The singer then started to cry as she sang her most recent single Wrecking Ball.

 

 

Defending recent shows, Cyrus said she knows “things I’m doing that’s getting me into trouble and it’s just me doing what my heart and soul is telling me what to do.”

 

The former Hannah Montana star also performed on an outdoor stage at the festival during the afternoon.

 

She thanked fans for helping Wrecking Ball top the US Billboard chart, saying: “I couldn’t have done it without all you guys.”

 

The video for the track broke the record for the most Vevo views in 24 hours when it was released earlier this month.

 

Justin Timberlake, Bruno Mars and Drake were among the other performers at the event.

‘Be who you are’

In a recent interview with French radio station NRJ, the singer said: “I’m on such a platform where I can speak to so many people and I think it’s important to send a message to my audience.

 

“Be who you are, do what you do, be who you want to be, live your life and don’t worry about what people have to say about it.”

She added: “I feel like the best way of fighting my haters is just keep letting them do what they do and don’t let them faze you, just keep doing what you do. Success is the best form of revenge.”

 

Britney Spears, who introduced Cyrus on stage on Saturday evening, recently backed Miley’s performances.

 

“She (Miley Cyrus) is on fire right now, she is on fire, she’s just a ball full of energy,” she said.

 

Spears, 31, has worked on a song that will appear on Cyrus’ new album, Bangerz, which is scheduled for release early next month.

Wheelchair User Doug Paulley Wins First Bus Discrimination Case

September 24, 2013

A disabled man has won a legal ruling against a bus company over its wheelchair policy.

 

Doug Paulley from Wetherby, West Yorkshire, took First Bus Group to court after he was told he could not get on a bus because a pushchair user refused to give up the space.

 

A judge at Leeds County Court ruled the “first come first served” policy was unlawful discrimination in breach of the Equality Act 2010.

 

First said it was “disappointed”.

 

Mr Paulley, 35, told BBC Look North: “Somebody with a pushchair in the wheelchair space refused to move when asked by the driver, because their baby was asleep in the pushchair and they didn’t want to wake the baby up.

 

“So I was unable to get on the bus, I was told to get off the bus and wait for the next one.

 

“Having approached them directly in various other ways, this seemed the only way to force them to take the issue seriously and to make adjustments so wheelchair users can reliably take the bus.”

‘Breakthrough’

First’s website states: “Wheelchair users have priority use of the wheelchair space”, but adds that “the driver has no power to compel passengers to move in this way and is reliant upon the goodwill of the passengers concerned” and “if a fellow passenger refuses to move [the wheelchair user] will need to wait for the next bus”.

 

Mr Paulley’s lawyer Chris Fry from Unity Law said his client was awarded £5,500 in compensation and the company had been given six months to change its policy.

 

“This is a breakthrough. There’s no point having an accessible bus if the service itself is inaccessible,” Mr Fry said.

 

In a statement, First Bus Group said it would “take time to consider the findings”.

 

It added: “At First we do recognise how important it is that bus services are accessible to all and our drivers across the country are trained to act in accordance with the law in this area.”

 

Disability campaigner Baroness Tanni Grey-Thompson said: “For millions of disabled people looking to travel to work, the shops or hospital visits public transport is our lifeline.

 

“The decision in Doug’s case will drive the changes that are needed to make public transport accessible for all disabled users.”

Heathrow Airport Recreates Departure Day For Autistic Man

September 23, 2013

What a sweet story.  Heathrow Airport should be thanked profusely for their extreme decency in this case.

Aaran Stewart does not react well to change.

 

The 21-year-old has severe autism and obsessive compulsive disorder, but has to negotiate the hectic bustle of Heathrow airport to attend Boston Higashi High School.

 

To cater for him, staff have attempted to recreate the same conditions every time he flies.

 

Four times a year for five years, Aaran has met the same airport staff, at the same check in desk, visiting the same shops, leaving from the same gate onto a plane on which the exact same seats are reserved.

 

Speaking to Radio 4’s You & Yours at the airport his mother Amanda said Aaran would not be able to fly if any of the details were different.

 

She said: “Without the procedure we wouldn’t be getting on the plane. It has to be carried out absolutely pristinely otherwise we’ll end up with a problem.”

 

The routine includes a visit to shops before heading to the same gate, gate A10. There has been changes however, as one of the outlets on his route has changed hands.

 

Mrs Stewart said: “It was an HMV but now it’s a Dixons, so he retraced his steps inside as if it was HMV.

 

“It’s routine based. If there are any delays he’ll think you’re going to try to change something which will then panic him. When we get to the gate he’ll settle.

 

“Everything’s gone to plan, he’ll wait for the bus, we’ve got the seats we need and we’re off!”

 

Mrs Stewart later explained that on arrival the bus did not display the flight number due to a malfunction on the screen, which led to Aaran growing suspicious about its destination.

 

Fortunately the driver was able to quickly swap buses so he could display BA215 which resulted in Aaran getting on board and making his flight.

 

Mark Hicks, Head of Passenger Support Services at Heathrow said usually up to 2,500 people with disabilities including reduced mobility will use the airport in a day, from people with visual impairment to older people with reduced mobility.

 

Asked about whether the general experience of people with disabilities in airports had worsened, he said people notifying them ahead of their arrival did improve service, but the forecasts for the day could occasionally be outstripped by demand.

 

He added they were striving for a balance which allowed people to retain their ability to travel spontaneously while meeting their needs.

 

Disability Consultant Geoff Adam Spink said of Aaran’s experience: “Hats off to the people who organise it. All too often it’s wheelchairs all round and it doesn’t matter what your disability is, someone will turn up with a wheelchair and can get quite irritated if you don’t sit in it.

 

“Your rights are governed by EU legislation. The EU has updated its guidelines and you have a right to extra assistance at no cost throughout your journey.”

CF Drug Contains Aborted Fetal Cells

September 23, 2013

This whole article has made me feel sick. Personally, I am strongly against all abortion.

When I read that a Cystic Fibrosis drug was on the list of products, I thought I should share the article here, in case anyone wanted to take a different form of medication as a result.

Dyslexic Man Refused Help By Job Centre

September 23, 2013

And yet more Job Centre stupidity…

An unemployed father-of-three was refused support from Job Centre staff, despite being diagnosed with a severe form of dyslexia.

 

Ennis Mustafa, 30, of Hurst Avenue in Chingford, has a condition which impairs his memory, and reading and writing skills.

 

He was diagnosed in 2011 following a request from the Job Centre in Westbury Road, Walthamstow.

 

Since then, he says the centre has done nothing to support him overcome the challenges he faces in finding appropriate work.

 

Mr Mustafa said: “I don’t want a hand out. I just want the help I’m entitled to.”

 

Mr Mustafa recently asked for help to complete an appeal form he had been given after some confusion over an appointment date led to his benefits being stopped for a month.

 

He claims a member of staff insisted dyslexia was not a disability and said workers were not allowed to help clients complete forms.

 

Mr Mustafa complained after receiving advice from the British Dyslexia Association, which informed him that dyslexia is defined as a disability under the Equality Act 2010.

 

 

This means he is entitled to specialist support from job centre staff.

 

But Mr Mustafa claimed he was then told to fill out a complaint form.

 

Mr Mustafa is keen to improve his reading and writing skills and train as a plumber, but needs support to find jobs and approach employers.

 

He said: “It’s a never ending battle for me. I’m trying to do things correctly but the system is letting me down.

 

“I want to work hard and support my kids and make a future for them.”

 

A Department of Work and Pensions spokeswoman said:”Dyslexia is a disability, and we have resources in place to give jobseekers extra support in completing forms and paperwork.

 

“On this occasion, the advice Mr Mustafa was given was incorrect, and we have since apologised.

 

“Action has since been taken to ensure that the person who provided the incorrect advice is aware of latest policy and information about Dyslexia to make them more aware of the condition and its place in the Disability Discrimination Act.”

Especially Stupid Benefit Sanctions

September 23, 2013

I don’t know whether to laugh or cry at these. But they should be shared, just to show the overall stupidity of JCPlus.

A4E Found Guilty Of Racial Discrimination At Tribunal

September 23, 2013

I’ve never liked them, but now I like them even less.

The training company A4e has been found guilty of racial discrimination and been ordered to pay out £50,000 in compensation, the Guardian has learned. Employment tribunal judges found that the company, paid £345m by the Department for Work and Pensions for its back-to-work employment services since 2010, racially discriminated against Rohim Ullah when it unlawfully dismissed him from its Bradford office in 2011.

Two other white managers who were facing almost identical allegations of failing to follow proper procedures – one of whom was also accused of commenting that an Iraqi customer should “fuck off back to his own country” – were not subject to a similar standard of investigation, tribunal judges found.

Ullah, from Yorkshire, who was “very pleased” at winning the two-year battle, said he was picked on by the company because of the colour of his skin.”I believe the reason why they discriminated against me was they had to find a scapegoat [for failures in the office] … and they thought, we’ll get this black person here.”

In their judgment, the tribunal said it could not understand why A4e, which is appealing against the ruling, chose to proceed with allegations of serious misconduct against only Ullah and ignored the similar allegations made against two white members of staff which were “swept under the carpet or treated as minor misconduct [issues]”.

“The other managers were not even questioned regarding these allegations, but every comment that was made against me, they took it [their investigations] to the extreme limit,” Ullah said.

Giving their verdict, the judges said that 40-year-old Ullah was “the subject of unlawful detriment in facing disciplinary proceedings leading to his dismissal and that he was unlawfully dismissed as an act of race discrimination”.

In a statement, A4e said it was proud to have a diverse community of people within its organisation and that it had in place robust policies to protect their rights and to ensure that all staff were treated with dignity and respect.

Disablist Nonsense From IDS

September 23, 2013

I can’t believe this. Does anyone have a link to him saying this?

https://twitter.com/sambarnet/status/382048256378671104

Do Not Support Newly Disabled Claimants Hit By Benefit Cap To Stay In Their Homes Recommends DWP

September 23, 2013

David Barr’s Heartbroken Dad Blames ATOS For His Suicide

September 23, 2013

Another name we can never be allowed to forget.

 

 

 

A HEARTBROKEN dad has blamed benefits axemen for driving his ill son to suicide weeks after being told his money was being stopped.

David Barr, 28, threw himself from the Forth Road Bridge after learning the decision to stop his benefit had been upheld.

An Atos assessor had ruled David was fit to work despite being on anti-psychotic sedatives, sleeping tablets and antidepressants. His condition was recorded on a medical assessment as “anxiety and depression”.

But his dad David snr, 57, said he had a host of problems including sleeplessness, memory loss and paranoia – and believes he may have been a schizophrenic.

David was assessed in May. In June, the Department of Work and Pensions told him he was fit to work – and his employment and support allowance was being withdrawn.

In an appeal letter, David wrote: “I disagree with your decision that I am fit for work. I have serious mental health problems that prevent me from doing everyday tasks which means I cannot work at this moment in time.

“I did try and explain this to the medical examiner.”

He was informed on July 17 of the DWP’s final say – they backed the Atos recommendation.

On the evening of Friday, August 23, he got a bus to the bridge, walked to the middle and jumped. He was recovered from the water but died in hospital that night.

David snr, of Leven, Fife, said: “He needed 15 points to ‘pass’ the test and get his benefits but he only got six. I know the difficulties he had – he should have got 106 points.

“The assessment is ridiculous. They said David was fit for work but, in fact, he was fit for hospital.

“I’m in no doubt this matter was the final straw. I would say they are 90 per cent to blame for him taking his life. He’d just had enough.

“I wish we could have got him checked out, even sectioned if necessary, and placed in a hospital where he could have received proper assessment and care.”

“I just hope something can be done so no one else has to go through this.

“We are devastated by our son’s death. David’s mum is in hospital and hasn’t eaten since David died. She is completely broken by this.”

David jnr worked cleaning buses for three years until 2011. His dad says his son could not cope with the routine of holding down a job.

He said his son was placed on strong medication last year but said his mental health had worsened.

David snr added: “He would claim people were trying to poison him but it was all in his head. He thought the police were following him.”

David’s assessment summary states: “Mr Barr has a mental health problem. He takes triple medication…He reports self harm in the past.

“He reports he attempted an overdose six weeks ago but he would not say what he took. He reports he has had no thoughts of suicide since.

“The evidence overall suggests that he is not at substantial risk.”

David snr is in the process of complaining to the DWP.

The DWP and Atos sent their sympathies to David’s family. A DWP spokeswoman said: “Through a series of independent reviews and by working with medical experts and charities, we have considerably improved the work capability assessment process since 2010.”

An Atos spokeswoman said: “We do everything we can to minimise people’s anxiety during the work capability assessment process and will continue to strive for improvement in this area.”

Scottish Labour welfare spokeswoman Jackie Baillie said: “It’s not the first time vulnerable people with health issues have been incorrectly assessed by Atos and it’s clear that the system needs reformed.”

Details Of Three Successful #BedroomTax Appeals By Disabled People

September 23, 2013

The first tribunal rulings on bedroom tax appeals have emerged – and Inside Housing is now able to reveal the full details.

Four out of five appeals brought with the assistance of Fife Law Centre have been upheld.

The rulings have provoked fierce debate in the sector as to the extent to which tribunals will take room size and intended use into account when assessing councils’ housing benefit awards. The rulings raise questions about the extent to which councils should rely on housing association data when deciding what a bedroom is for the purposes of the under-occupation penalty.

Inside Housing has now obtained all five rulings and has summarised the main points below.

1) APPELLANT: Name withheld upon request by claimant

The basis of the appeal:

Brought by a man living alone in his former family home, which has three rooms originally judged as ‘bedrooms’ including a ‘boxroom’

He is disabled having lost his left leg above the knee four years ago.

He said he needed one of the other bedrooms because his sons come to stay overnight to care for him when he is in discomfort. This was accepted by the council in April – meaning he was only deemed to be underoccupying by one room.

He said he is waiting to hear from his occupational therapist about converting the ‘boxroom’ into a wetroom as his bathroom is too small for him to use.

The claimant’s legal representative argued that the boxroom was too small at 64 square feet to be classified as a bedroom – as space standards in the Housing Act (Scotland) 1987 state a room of between 50 and 70 square feet should only be sufficient for a child under the age of 10. Also, because welfare reform minister Lord Freud has suggested tenants hit by the bedroom tax take in lodgers, the appellant argued that the room should only be classified as a bedroom if it is big enough for a lodger.

The appellant also argued that the room was needed to store equipment he needs for his disability, including an exercise bike, walking and ‘mirror’ device. He therefore argued the established use of the room was not as a bedroom.

The ruling:

Tribunal chair Simon Collins QC accepted the first part of the appellant’s argument, that it is ‘relevant to have regard to statutory space standards’. However he rejected the argument that the boxroom was needed to store equipment, saying the equipment could be stored in the second largest bedroom.

Verdict: APPEAL ALLOWED

2) APPELLANT: DAVID NELSON

Basis of the appeal:

The appellant and his wife live in a three bedroom property. One room has been acknowledged as necessary for an overnight carer, as Mr Nelson is disabled. The other room, a ‘boxroom’ was under dispute.

The appellant argued the room, at 66.3 square feet, was too small to be classified as a bedroom with regard to the space standards in the Housing Act (Scotland) 1987.

It was also argued that Mr Nelson’s room is used to store equipment he needs for his disability  and therefore its established use is not as a bedroom.

Thirdly, Mr Nelson argued that he needs to keep the bathroom door open due to his (unspecified) disability. This room faces the boxroom, which meant ‘obliging the appellant to take in a lodger would compromise the appellant’s dignity’.

The ruling:

Mr Collins again accepted the space standards argument, that the boxroom was too small to be used as an adult bedroom.

However, he rejected the other arguments, saying he was ‘not satisfied’ that the disability equipment could not be stored elsewhere in the property. He also rejected the argument about Mr Nelson’s dignity due to the door being left open, saying ‘a bedroom…does not cease to be a bedroom because the appellant is using a nearby bathroom with the door open.’

Verdict: APPEAL ALLOWED

3) APPELLANT: LOUISE MCLEARY

Basis of the appeal:

Ms McLeary is blind, and lives alone in a three bedroom property owned by Kingdom Housing Associaiton.

She was assessed as needing a three bedroom house, and receives a package of support from KHA under contract from Fife Council.

Ms McLeary’s legal representative argued that she was living in exempt accommodation, so her rent is not determined in accordance with the ‘bedroom tax’ rules in the housing benefit regulations.

Instead, Ms McLeary argued that under the Consequential Provisions Regulations 2006, exempt accommodation ‘includes accommodation which is provided by…a housing association…where that body…also provides the claimant with care, support or supervision.’

The council argued that KHA is not obliged to provide the support as it is not in Ms McLeary’s tenancy agreement, so the exempt accommodation rules don’t apply.

The ruling:
Mr Collins rejected the council’s argument, saying there is no requirement that the care provision ‘must be pursuant to a contractual obligation to the claimant.’

Verdict: APPEAL ALLOWED

Police Officers Face Misconduct Probe After Disabled Man’s Death

September 22, 2013

Slightly old, but important.

Six police officers are under investigation for gross misconduct following the death of a disabled man, a watchdog said.

The Independent Police Complaints Commission said four constables, a sergeant and an inspector had been served with notices of gross misconduct.

The investigation was launched after Avon and Somerset Police referred itself to the IPCC after the death of Bijan Ebrahimi on 14 July this year in Bristol.

Mr Ebrahimi was found alight by paramedics in Capgrave Crescent, Brislington after allegedly being seriously assaulted.

Stephen Norley and Lee James, both aged 24 and from Bristol, have been charged with Mr Ebrahimi’s murder and have been remanded in custody.

The IPCC said Mr Ebrahmi had been in contact with officers from Avon and Somerset Police in the days before his death.

He had been arrested on 12 July on suspicion of a breach of the peace and released later the same day.

The IPCC investigation has served notices of gross misconduct to three Pcs who dealt with Mr Ebrahimi between July 11 and 13.

Criminal interviews with these three officers are scheduled to take place over the next few weeks.

The IPCC said the three officers have been suspended by Avon and Somerset Police as a result of information which has come to light during the investigation.

An inspector, sergeant and constable who dealt with Mr Ebrahimi in custody on July 12 have also been served with notices of gross misconduct and they will be interviewed soon.

Rachel Cerfontyne, IPCC deputy chairman, said: “This is a tragic case and my sympathies go to Mr Ebrahimi’s family and friends for their loss.

“Our investigation is into police officers’ and staff decisions and actions in all their dealings with Mr Ebrahimi following his call to police on July 11 until his death on July 14.

“This will also include any previous police contact with him and how those incidents were dealt with, including interactions with other agencies.

“Our investigation is progressing well with some notable actions already completed.

“The police criminal investigation into Mr Ebrahimi’s death will take priority and does constrain what we can say at this stage.

“We will continue to ensure that Mr Ebrahimi’s family are regularly updated with the progress of our investigation.”

Labour To Announce Tomorrow That They Would Create New Offence Disability Hate Crime

September 21, 2013

And sack ATOS! Which of these would be more likely to get them my vote?!

Labour will legislate to introduce a specific criminal charge of disability hate crime amid growing evidence that victims are being let down.

Liam Byrne, the shadow work and pensions secretary, will announce the policy at his party’s conference on Sunday.

He will also reveal that he intends to sack Atos, the controversial company which adjudicates on people’s ability to work, due to its poor record. Two in five assessments are appealed against and 42% of those are successful. The company has also consistently failed to meet targets on average case clearance times since mid-2011, with 35,000 claimants having to wait longer than 13 weeks to receive their decision. “We’ll put Atos out the door”, Byrne will tell Labour’s conference in Brighton.

The Home Office estimates that 65,000 disability hate crimes occur each year. Disability charities say it could be as many as 100,000, which they say is largely driven by “benefit scrounger” rhetoric that Byrne believes is in part stimulated by a system that is not working.

The shadow cabinet minister will tell Labour members that he will challenge the status quo. He is working with the Australian Labor MP Jenny Macklin, who has had success in her home country, to examine how services for the disabled and their funding can be improved.

Byrne will say: “Like most families in this country, I know first-hand that disability can affect anyone. Therefore it affects us all.

“Someone is registered disabled every three minutes. Yet today disabled people are threatened by a vicious combination of hate crime, Atos and the bedroom tax.

“Today we deny disabled people peace of mind, a job, a home and care. We need to change this.” He will add: “We will change the law so hate crime against disabled people is treated like every other hate crime.”

HM Inspectorate of Constabulary, the Crown Prosecution Service (CPS) and the National Probation Service reported this year that victims of disability hate crime were being let down by the criminal justice system, with attacks not being properly recorded.

The three organisations also acknowledged there was no “clear and uncomplicated definition” of what constitutes disability hate crime.

Michael Fuller, the chief inspector of the CPS, said the Law Commission had been asked to consider whether there should be a specific offence of disability hate crime.

Byrne will promise to properly define disability hate crime and ensure that it is recorded on the perpetrator’s criminal record.

He said Labour in power would also review whether the attorney general’s power to review sentences he considers unduly lenient should be extended to offences aggravated by hostility towards the victim based on their disability.

Figures published by the Association of Chief Police Officers show a rapid increase in the number of reported disability hate crimes since records began. In 2009 – the first full calendar year for which the data exists – 1,211 crimes were reported.

This figure rose by 24.8% in 2010, and a further 18.3% the following year. It is unclear whether these rises were caused primarily by an increase in the number of disability hate crimes that are committed or higher rates of reporting.

Ed Miliband To Announce That Labour Will SCRAP #BedroomTax!!!

September 20, 2013

Many, many thanks to Sunny Hundal at Liberal Conspiracy for writing this.

I know we’ll all be thrilled if this promise is kept, readers.

Link Between Swine Flu Jab And Narcolepsy

September 20, 2013

Four families have been told they can apply for government compensation over side-effects of the Pandemrix swine flu vaccine.

Studies have shown the jab increased the risk of narcolepsy tenfold.

Families could be entitled to £120,000 through the Vaccine Damage Payments Scheme if they can prove “severe” disability.

If the bid fails they and other families could still pursue compensation through the courts.

Pandemrix was the most widely used flu vaccine in the UK during the 2009-10 pandemic. Almost six million doses were given, one million to young children.

However, evidence from across Europe has suggested a higher rate of narcolepsy in children after being given the jab.

Approximately one in 55,000 children vaccinated – about 20 in the UK – were thought to have developed narcolepsy.

Disablement test

The sleeping disorder causes people to fall asleep suddenly and unexpectedly. It can be hugely disruptive to daily life.

Compensation had previously been rejected on the ground that a link had not been proved. This has now been reassessed in light of the latest research.

A spokesperson for the Department for Work and Pensions, which runs the Vaccine Damage Payments Scheme, said: “DWP has looked at some vaccine damage payments cases again in light of new information regarding swine flu and narcolepsy provided by the Department for Health.

“We cannot comment on the specifics of individual cases but can confirm that once this new information was taken into account it was decided, on balance of probability, in some cases that causation was proved.”

They will have to pass the department’s “severe disablement” test.

‘Evidence at the time’

The Department of Health said: “Pandemrix was developed specifically for use in a flu pandemic when the number of lives lost and serious cases could have been enormous.

“The decision to recommend that children got this vaccine during the flu pandemic was based on evidence available at the time, along with the advice from the European Medicines Agency, which approved its use.

“We keep all emerging evidence under review and that’s why use of Pandemrix in those less than 20 years old was stopped in the UK in 2011.”

Disabled People Facing Barriers Using Common Gadgets, Finds Scope Report

September 20, 2013

A report from a disability charity says that people with disabilities face barriers when using common gadgets, despite huge technological advances in recent years.

Scope says that there is huge untapped potential for mainstream devices, like smart phones and tablets, to provide support.

Michael Buchanan reports.

A Small But Significant Disability Link In The Niqaab Debate

September 20, 2013

The Niqaab (full face covering used by some Muslim women) has been in the news quite a bit in Britain over the last two weeks after a witness refused to remove it in court. A judge then ruled that while she can wear it in the courtroom, she must remove it on the witness stand.

He was right in my personal opinion, and I’ve said so at my new site.

However, until tonight, I haven’t found a disability link in the story.

Then, tonight on Question Time, the point was raised by Ken Clarke that judges, juries and magistrates can judge whether witnesses are telling the  truth using their facial expression.

David Dimbleby responded with what I like to call a classic reply. He said “So would you not have blind jurors?”

The reply was that blind jurors have their own ways of working out what people are doing.

The point is, putting the religious/cultural point aside, I think that is a very good question.

Of course I personally think blind people should be allowed to serve on juries, with appropriate support. Of course, they can’t help not being able to use facial expressions to see what is being said.

The difference, of course, is that some would say covering your face for religious reasons can be helped. It can, at least, more than a lack of eyesight.

However, there are some women who are forced to wear the niqaab by men, as I’ve said in the post linked above. But, as I’ve also said in the post linked above, I think the niqaab should be removed on the witness stand, where seeing a person’s face is required.

I am not trying to compare the two situations but, since the question of blind jurors was raised, I hope you all agree with me that blind jurors should be allowed. If you don’t please tell us why not.

Home And Away’s Spencer Has Bipolar Disorder

September 19, 2013

Australian viewers of Home And Away will have noticed Spencer Harrington acting a little strange in recent weeks. Tonight, the reason for this was finally revealed. Spencer has had bipolar disorder since the age of 15.

I saw a little bit about bipolar in Neighbours a few years ago when they featured a character called Samantha Fitzgerald. But I have never personally watched a bipolar storyline on a soap from its beginning. I think this is the first bipolar storyline to start on screen, although fans of Eastenders are welcome to tell me that I am wrong!

It will be interesting and educational for me personally to watch the storyline. I am pleased, as always, to see a soap covering disability through a long-term character.

Thank you again, Home And Away.

Guardian Poll: Should Bedroom Tax Be Scrapped?

September 19, 2013

I hope you will all join me in voting a loud and clear YES.

Ed Guiton Obituary

September 19, 2013

For those who remember his Guardian G2 column, Life Goes On.

Liam Byrne MP Appears To Be Listening On #BedroomTax

September 19, 2013

 

 

But can we believe him? Can we get excited?

 

 

What do you think, readers?

RoadBlocks For Justice

September 18, 2013

Spotted on Facebook. Same Difference sends full support to DPAC.

Join us on Saturday 5th October to block roads and stop the Government’s changes to Legal Aid!

Their cuts have already devastated education, healthcare, welfare and housing. Now, the proposed changes to Legal Aid will take away our ability to challenge them and block all but the rich from access to justice. People will not be able to dispute unfair evictions, babies will not have their interests represented in family disputes, and the families of people killed in custody or detention will no longer be able to fight for the truth.

This has nothing to do with saving money, the changes will cost the legal system more than they will save. By removing our ability to challenge it, this Government is undermining the rule of law, so that it can continue to push forward its austerity agenda. It is a historic attack on our rights, and we will not allow it to go unchallenged.

Blocking roads is a proven tool, the Government has not listened to protests or petitioning, and the time for direct action has come.

Join UK Uncut, DPAC, Defend the Right to Protest, Women against Rape, Plane Stupid, Kent Refugee Help and BARAC UK on Saturday 5th October!

See you on the streets!

Results Of The UNISON ‘What Keeps You Awake’ Survey

September 18, 2013

Earlier this year, UNISON conducted a survey asking ‘What Keeps You Awake?”

Now, the results are here.

I’ve been sent some quotes by UNISON, from disabled respondents and carers. They are worrying, aren’t they?

 

“4 years of no pay rise has had its effect on our standard of living. our children have grown up and left home, but we have had to help them financially. We both work and own our home. My husband is disabled but able to work with the assistance of his DLA which we are sure he will lose under ASOS. At our time of life, we should be ok but we are working harder and longer hours to stand still. I fear for the future.”

 

“Being disabled, my worries are around the cuts to the benefit system, access to good healthcare and the thought that the government could strip away my means of survival overnight.”

 

“What keeps me awake is the fact that if my Disability Allowance is cut, I won’t be able to work in my current job as I am required to travel and would not be able to afford transport.”

DWP Reveals The Real Agenda Behind Universal Credit And Welfare Reform

September 18, 2013

johnny void's avatarthe void

greedy-bossFor over two years now Iain Duncan Smith has been pretending that his brutal and bodged welfare reforms have been about encouraging people back to work and making that work pay.

Throughout this period it has often been suggested that a more brutal social security system is really intended to increase competition for jobs and allow employers to force down wages and working conditions for everyone.  Vastly increased benefit conditionality has led to hundreds of thousands of benefit claims being stopped or sanctioned.  With workfare or destitution the only option left for those unable to find a job, exploitative employers have free reign to treat workers like shit, knowing full well if they leave, or are sacked, they will face increasingly desperate poverty.

Few have been cynical enough to suggest that Universal Credit will also make it easier for employers to casualise their existing workforce and make it easier to…

View original post 158 more words

Scotland Could Have Own Paralympic Team In Rio

September 18, 2013

For those of you following issues around Scottish independence, I have just found the disability link.

Any Day Now

September 18, 2013

A gay couple fight to adopt a boy with Downs Syndrome, played by DisAbled actor Isaac Leyva.

This movie covering issues of both sexuality and disability is coming soon to UK cinemas.

Here’s the trailer:

Deaf News: American family sue police after 12 year old Deaf boy was tasered

September 18, 2013

Editor's avatarThe Limping Chicken

A  number of news reports have come out of America in the last 24 hours reporting a horrific story of how a 12 year old Deaf boy was allegedly Tasered by the police. His family are now suing not only the police, but also his school.

It is said that the boy has Attention Deficit Hyperactivity Disorder (ADHD) and was involved in a ‘scuffle’ with a school staff member in which he was allegedly choked and suffered head injuries.

Then, following a later dispute over being able to phone his parents using a videophone, the boy escaped the school to a construction site, where it is alleged that school staff tried to “violently subdue him.”

It is said that when the boy picked up a stick, the staff left the scene. Later, when the police arrived, he was Tasered.

Importantly, it is alleged by the boy’s parents that when the boy…

View original post 31 more words

Petition To Propose A Bill To Abolish #BedroomTax

September 18, 2013

Campaigners are not going to let the Lib Dems stop at a Conference Motion on Bedroom Tax. This Petition has been started, asking them to propose a Bill in Parliament to abolish it.

Please sign. I just did.

Student Carers

September 18, 2013

I think this piece of research is long overdue and very important.

Vest Means Assistance Dogs Can ‘Speak’ To Owners

September 18, 2013

A vest developed by a research team at Georgia Tech is aiming to give trained dogs the ability to “speak” to their owners.

The FIDO project – which stands for Facilitating Interactions for Dogs with Occupations – aims to help service dogs offer more sophisticated communications to aid those who may be visually or otherwise impaired.

The customisable vest is designed to be tugged or bitten by the dog depending on what instruction needs to be given.

In this demo, project leader Melody Jackson, along with professional dog trainer Barbara Currier, show off the technology with the help of service dog Blitz.

Donna Williams’ Survey On BBC Subtitles And Doctor Who

September 17, 2013

Doctor Who fan Donna Williams can’t hear. She has serious issues with the BBC’s subtitles on iPlayer. She wants a message sent to the BBC, so she has created a survey, which she would like shared far and wide.

If you, like Donna Williams, use subtitles and would like to see them improve, please complete the survey and pass it around.

TV Listeners for the Hard of Hearing Never Looked So Stylish or Sounded so Loud

September 17, 2013

A press release:

Geemarc Introduces the New CL7400 Wireless Headset for Television, DVD players, HiFi, Audio/MP3 players and PCs

London, 17 September 2013 – Geemarc Telecom, a leader in the design and manufacture of assistive devices for the Deaf and the Hard of Hearing, today announced a new wireless TV listener headset which puts style firmly on the agenda for anyone with hearing loss. Delivering clear digital sound, the headset can significantly increase the volume, balance and tonality on TVs, DVD players, audio devices and PCs for the wearer, without other people in the room being affected.

“One in six people have impaired hearing with the most dramatic deterioration starting at around 50 years of age, although many people even younger live with hearing loss. But hard of hearing doesn’t mean design and style should be compromised. The new CL7400 is the high-quality, fully featured solution for those that want to look good when wearing a TV listening headset,” says Andrew Grossman, Managing Director, Geemarc Telecom S.A.

Geemarc’s 40 years’ experience in the design and manufacture of assistive listening devices can be seen in essential details such as: the tone adjustment feature, which clarifies difficult to hear high treble or bass voices and sounds; the ability to turn off stereo and channel mono sound through just one earpiece; and the fact that once chosen, settings are intentionally quite hard to change and therefore cannot easily be lost.

Main features and benefits

  • Maximum volume up to 125dBspl (decibel sound pressure level)
  • Stylish, lightweight, wireless over-the-head design
  • Foldable for easy transportation
  • Clear digital sound
  • Balance control for Different Levels of Loss in Different Ears
  • Tone control  for High Low Frequency Hearing Loss(+/-10db)
  • Can be used with or without a hearing aid
  • Operating range of up to 50m allows you to sit in your garden and listen to music or a streamed radio programme. Also works digitally through walls
  • Base plugs directly into your TV, DVD player or audio device
  • Up to 8 hours of in use time. Full battery recharge time is up to 6 hours

Availability and pricing

The Geemarc CL7400 is available from actiononhearingloss.org.uk, Amazon.co.uk and Leading Distributors of Amplified Products. It has an RRP of £129.00 inc. VAT.

Technical specifications

  • Digital 2.4G ISM band AFHSS Transmission
  • Receiving amplification up to 125dBspl
  • Frequency response: 40 – 20,000Hz
  • Operating indoor range of up to 50 meters from the transmitter
  • Charging time of the battery: 6 Hours
  • Continuous usage time: 8 Hours
  • RCA Inputs
  • Built-in rechargeable lithium battery
  • Weight: 260g
  • Braille identification on the headset to the volume key
  • Automatically shuts off after 2 minutes’ loss of signal

Accessories included

  • 1.5m TV Cable with stereo jacks 3.5/RCA
  • 3.5mm Jack to RCA Cord Adaptor
  • UK Power Adaptor

Compatible Accessories
TVs, DVD Players, MP3 Players, Minidisc, Walkmans, iPods

For more information please visit http://www.geemarc.com

Ten Thousand Cuts And Counting

September 17, 2013

Spotted on Facebook:

10kcuts

Scrap Atos – End the Work Capability Assessment.

10 Thousand Cuts and Counting is a ceremony of remembrance and solidarity led by disability activists, Occupy activists and the Dean of St Paul’s Cathedral for those who have had their lives devastated by the austerity programme, including more than 10,000 people who died shortly after undergoing the Atos Work Capability Assessment, the degrading test used by the government to assess the needs of people receiving benefits related to disability and ill health.

Led by disability activists, Occupy activists, David Ison – the Dean of St Paul’s Cathedral, Michael Meacher MP and other representatives.

With all welcome to attend, the event will include Atos testimonies, prayers, silence and meditations, a carpet of white flowers on Parliament Square with poetry, choral music and scenes acted by disabled artists depicting experiences of Atos.

The gathering will demand an immediate end to the Work Capability Assessment, as voted for by the British Medical Association, and a New Deal for sick & disabled people based on their needs, abilities and ambitions as outlined in the WOW petition.

28th September • Parliament Square • London • 12 noon

Disabled people are leading the fight back against the injustices of austerity: we cannot stand idly by while our communities and institutions are devastated by this government.

On Saturday 28th September, the disabled and non-disabled community will gather to remember those who have died and those still suffering as a result of the Government’s austerity assault, which particularly affects disabled people.

The ceremony will remember those who have died and those living who are having their independence and dignity challenged as a result of austerity.

A delegation from the gathering will present to the Prime Minister THE DOWNING STREET DEMAND, in support of the demands set out in the WOW petition (http://wowpetition.com/), which has been signed by 52,000 people and calls for an immediate end to degrading way in which the government assesses the support needs given to valuable people in our community and a New Deal for sick & disabled people based on their needs, abilities and ambitions.

This government is reducing the Welfare State in a way which creates even more economic and social inequality and does not save the country money – this cannot be allowed to continue.

This is what austerity looks like. Come and join us.

Timetable

The People’s Gathering at Parliament – 12pm – Parliament Square

Delivering The Downing Street Demand – 1pm

For more information please see www.10Kcuts.org

Other information

Clothing. Please wear white clothing as a symbol of remembrance. If this is not possible, a white scarf or other small item would be useful. Please also bring a white flower if you would like to lay one in remembrance
Access: Nearest tube: Westminster – step free. Buses: 3, 11, 12, 24, 53, 87, 88, 159, 453. Please get in touch with any specific access enquiries or requests.

Further details regarding accessibility and transport options tbc.

—————————————————-

10 Thousand Cuts and Counting has been called by Occupy London activists and David Ison, the Dean of St Paul’s Cathedral.

Contact email: 10kcutscounting@gmail.com

Also, the organisers are trying to raise £1000 to cover costs. If you would like to help, a link to their Paypal can be found on the event website.

Letter to Raquel Rolnik, UN Special Housing Rapporteur

September 17, 2013

pawprintsofthesoul's avatarpawprintsofthesoul

The information and detail regarding the background to this letter can be found here.

Dear Ms. Rolnik,


United Kingdom:  Coalition Government Welfare ‘Reform’

This is in response to your request for feedback on the above, with particular regard to the Employment Support Allowance and the Work Capability Assessment as I have direct personal experience of both.

May I first express my gratitude to you for enabling this formal communication.  The present inability of the ordinary people of the UK to affect any real understanding within Government concerning the human impact of their present policies is a source of considerable alarm and to finally be invited to share the detail of our experiences is a rare source of hope for me. May I also express my sincere regret at the deeply disrespectful and aggressive behaviour of UK Government representatives towards you personally. I hope you will understand, however, if I…

View original post 1,936 more words

Deaf News: Motion calling for recognition of BSL as an official UK language passed at Liberal Democrat party conference

September 17, 2013

Editor's avatarThe Limping Chicken

Following a debate this morning at the Liberal Democrat party conference, the Liberal Democrats today passed the policy Recognising a Legal Status for British Sign Language, which calls for better access to information and services for Deaf people.

The Liberal Democrats say they are committed to the principle that Deaf people are entitled to identify with their own language and to have this respected, regardless of minority or majority language status.

The key proposals include:

· The recognition of British Sign Language (BSL) as one of the UK’s official languages

· Achieving better awareness of information needs and services for BSL users, particularly in health, education and employment

· The protection of the linguistic integrity of British Sign Language

Commenting, David Buxton, CEO of the British Deaf Association and the Liberal Democrat PPC for Hampstead and Kilburn, said:

“It is very important for this party and other political parties to see…

View original post 282 more words

Stephen Hawking Backs Assisted Suicide By Choice

September 17, 2013

UK cosmologist Prof Stephen Hawking has publicly said he backs the notion of assisted suicide for people with terminal illnesses.

 

In an interview with the BBC he said: “We don’t let animals suffer, so why humans?”

 

Prof Hawking, who has the progressive condition motor neurone disease, has in the past been less candid about the idea, saying “there is always hope”.

 

But he stressed that there must be safeguards to prevent abuse.

 

Prof Hawking himself was once put on a life support machine which his wife was given the option of switching off.

 

When asked if family members of those who wish to die should be able to assist without fear of prosecution, Prof Hawking said yes.

 

But he added: “There must be safeguards that the person concerned genuinely wants to end their life and they are not being pressurised into it or have it done without their knowledge or consent as would have been the case with me.”

 

Hawking, 71, is one of the world’s most famous scientists.

 

Aside from his academic accolades, the Prof learned to adapt to life after being diagnosed with motor neurone disease and given two years to live when he married his first wife, Jane, in 1964.

 

Only 5% of people with the form of MND that he has – a condition called amyotrophic lateral sclerosis (ALS) or Lou Gehrig’s disease – survive for more than a decade after diagnosis.

Citizen Smart’s #BedroomTax Version of Oasis Wonderwall

September 17, 2013

Citizen Smart wrote this for yesterday’s Lib Dem Conference vote- but I think it still applies and will as long as the tax lasts.

 

Oasis never sounded so good!

 

 

 

There IS A House In Britain Full Of Benefit Scroungers

September 17, 2013

I’ve just spotted this on Facebook. I’m sharing it in the hope that you will laugh as much as I did.

bss

Student Commits Suicide After Social Worker Refuses Her Mental Health Support

September 17, 2013

This can never happen again.

A depressed student who was found hanged in her bedroom turned to social workers for help but was dismissed as “a f***ing waste of space” and an “attention seeker”.

Hannah Groves, a 20-year-old undergraduate at Southampton University, desperately sought help from the NHS, warning doctors she wanted to kill herself. For nine days, Hannah repeatedly requested to be admitted into a specialist mental health unit but was ignored.

On October 22 last year, the French student strangled herself.

 

Now, Hannah’s mother Mandy Park is taking legal action against the Southern Health NHS Trust, after a coroner recorded she was not given the help she was entitled to.

SEE ALSO:

 

“It was like she was possessed,” Park said. “But we just couldn’t get the help that she needed and she wanted.The image of finding my daughter will haunt me for ever and I can no longer sleep at night without heavy medication.”

The cruel comments were made by a social worker to a police officer, who had telephoned the mental health team and expressed concerns over Hannah’s welfare. The officer was told: “Yeah, I know her, she is an f***ing waste of space, she’s an attention seeker,” according to the Daily Echo.

During the week before her death, Hannah attended A&E after two suicide attempts in the space of three days and was assessed by the NHS. Despite a trainee doctor flagging up Hannah’s suicidal state of mind, the student was deemed fine to return home.

Following an inquest earlier this month, coroner Keith Wiseman said: “There was at all stages a failure to appreciate the extent of the risk that Hannah was at in the community.

“It is surely self-evident that by the end of the week it was unsafe for both Hannah and her family for her to be at home,” the Sunday Times reported Wiseman saying. “One only has to pause for a moment to visualise Hannah’s mother and teenage brother being forced to leave the house for their own safety in the early hours of the morning and for the police to have to be called, to realise that by then a wholly impossible stage had been reached and that for however modest a period of time Hannah required hospital admission and care.

The trust has admitted liability but denies Hannah should have been hospitalised. “We must always strive to support people in their own homes and be very cautious about admitting people to psychiatric hospitals unless it is absolutely necessary,” a spokesperson for the trust said. “In this case we deeply regret the failure to provide the right level of intensive community support which would have avoided any need for hospital admission.”

Lib Dem Conference Votes Against #BedroomTax

September 16, 2013

Just seen on Facebook:

RESULT – LIB DEM FEDERAL CONFERENCE VOTES OVERWHELMINGLY AGAINST THE BEDROOM TAX AND CALLS FOR IMMEDIATE REVIEW.

Sadly there is no guarantee anyone will listen to the members, but they have made their voices heard, for which they must be thanked.

Are You A Disabled Apprentice?

September 16, 2013

 

 

Serious Bedroom Tax Progress In Nottingham!

September 16, 2013

This is great news. Good to see it’s not only Scotland that’s listening on this.

Leaked ‘Media Advice’ Shows Lib Dems Ordering MPs Not To Refer To Bedroom Tax

September 16, 2013

Please share!

Yorkshire #BedroomTax Families Facing 10 Year Wait For Suitable Homes

September 16, 2013

FAMILIES affected by the so-called “bedroom tax” and other welfare reforms could be forced to wait more than 10 years for a suitable home, a council has warned.

The same Yorkshire authority, which has to slash £48m from its budget over the next two years, is also facing a potential shortfall in rent payments of £2.8m a year as the true impact of austerity and the Government’s welfare reforms is laid bare.

Of those tenants not previously in arrears prior to the introduction of the bedroom tax, or under-occupancy penalty – which sees cuts to housing benefit for tenants deemed to have spare rooms – less than half (45 per cent) in Hull, have paid the 14 to 25 per cent contribution they have lost.

The Labour-led city council – which has now received more than 53,000 calls to a benefits advice hotline set up in April – is also warning of increased homelessness and says that even basic services may be cut or disappear all together.

About 4,500 working age tenants in the city are affected by the bedroom tax, while 3,000 households live in overcrowded council accommodation, and 2,600 are “under-occupying” and require a one-bedroom property.

A report going before councillors next week says: “To move all households impacted to the ‘right size’ of home to match their benefit entitlement is projected to take well in excess of 10 years.”

Deputy council leader Daren Hale said: “Clearly, what the report reflects is the fact that welfare reform, which is very politically motivated, is obviously having disproportionate effects on those areas of greatest need like Hull.

“As well as local authority reductions in funding, the reforms are having a significantly higher impact in places like Hull so you’ve got a double whammy and it’s a case of trying to support people in need as they experience cuts to their benefits.

“We are then left with the unpleasant situation of having to collect that money (rent and council tax), because if we don’t it leaves a shortfall in service areas, whether housing repairs, or services getting reduced further.

“It puts us in the position of being the bad guys when really these are Government-enforced.

“We are not under any illusions – this is going to have a drastic effect, not just the bedroom tax and changes to council tax.

“We are also seeing a migrating inwards of families with multiple issues and needs into urban areas because the housing they have to pay towards is cheaper, and there’s a significant influx of families as part of this process. That’s into the city and within the city.”

He added: “Government spending figures show the level of reduction per head of population is four times higher than it is in the East Riding, and the East Riding hasn’t had it good either.

“We’ve got to hope there’s an announcement around things like Siemens (possible investment in manufacturing); we need to see growth in some of these new technology areas.

“The burden of public sector reduction has fallen grossly unfairly on local government. By far and away the largest budget reduction has fallen on the local government family.

“It’s just unsustainable going forward. People will start to see the basic services they rely on either aren’t there or are significantly reduced.”

Measures the council is developing to tackle the housing crisis include shared tenancies and “space saving equipment”, which would see partition walls or screens fitted in bedrooms which children of extreme age gaps are forced to share.

The report says the council will only evict tenants in arrears as a last resort when all other options have been exhausted.

Less than half a per cent of tenancies ended in eviction in 2012/13.

Council leader Stephen Brady said: “I just think the social impact of this is not going to be seen until the next two or three years.

“All councils up and down the country are dealing with this difficult situation. God knows what it’s like in London.

“You always have to try and do your best in the circumstances.”

Billy Connelly Has Early Stages Of Parkinsons

September 16, 2013

And prostrate cancer. Of course I wish him well.

Comedian and actor Billy Connolly has had surgery for prostate cancer and has been diagnosed with Parkinson’s disease.

 

“The operation was a total success, and Billy is fully recovered,” his spokeswoman said.

 

Connolly began working as a welder in the Glasgow shipyards but he gave it up in the late 1960s to become a folk singer before turning to stand-up.

 

He has also starred in films including the Oscar-nominated Mrs Brown.

 

“Billy Connolly recently underwent minor surgery in America after being diagnosed with the very early stages of prostate cancer,” his spokeswoman said.

 

“In addition, Billy has been assessed as having the initial symptoms of Parkinson’s disease, for which he is receiving the appropriate treatment.”

 

 

 

Exercise And MS

September 16, 2013

It’s hardly surprising that Shana Pezaro started comfort eating. After 20 years of unexplained and debilitating symptoms, she had just been diagnosed with multiple sclerosis. Having built up her own stage-school business, she was now losing the ability to walk and was forced to sell up. Then her marriage fell apart.

“My husband had found my illness and disability very difficult to deal with, but we always thought I was going to get better,” says Pezaro. “Then, when I was finally diagnosed with MS in 2007 and we realised I wouldn’t, he just couldn’t handle it. I used to be a dancer, but my body had changed and he told me he just couldn’t find me attractive anymore. Within a year of my diagnosis, we’d split up.”

It was a relief, she says, when he finally left, but the experience nevertheless dealt a blow to her self-esteem, not helped by the fact she had started to put on weight.

“I went from 12st to 15st in the space of three years. The fatigue was so bad that I didn’t have the strength to cook. I was living on microwave meals and snacks. The steroids and other medications made me incredibly hungry. And of course as my legs got worse I was getting less and less exercise – I could barely walk. I was miserable.”

Weight gain is a serious issue for the disabled community. In a study of 30,000 people published this summer by the University of Texas School of Public Health, 42% of adults with a disability were reported as obese, compared with 29% of those without a disability. Gaining weight not only affects a person’s emotional wellbeing, but can also make mobility even harder and symptoms feel worse. Yet fatigue and pain can make sport participation seem daunting. And although things are improving following the success of the Paralympics, access remains a major barrier. Just 18% of people with a disability or long-term limiting illness participate in sport each week, around half the level of the general population, according to a survey by Sport England.

“You don’t have to eat a lot to put on weight if you’re not moving and your body isn’t burning calories,” says Vanessa Daobri, a gym instructor who specialises in working with people with disabilities. “Disabled people often suffer because they don’t know how to exercise. If the disability is a result of an injury or it’s been a slow onset, they may find it hard to accept that they can’t do a sport in the way they used to, so they feel there’s no point.”

Organisations such as Aspire and the English Federation of Disability Sport run inclusive gyms across the country. But not everyone is lucky enough to be near one, and regular gyms are still lagging behind, says Daobri. “Often the staff get the approach wrong – sometimes it’s just laziness, sometimes it’s ignorance. Health and safety is used as a crutch, too.” Another issue, she says, is that disabled people can feel frightened to be seen going to the gym in case their benefits are cut.

Daobri has Ehlers-Danlos syndrome, a disorder affecting collagen. In 2007 she grew from a size 12 to a size 24 in less than a year. She felt “stuck”, until she joined a wheelchair racing group and the coach asked her if she used the gym.

“I just laughed,” she says. ‘I thought gyms were not for me – they were for other people.” She was shown how to use gym equipment in new ways and quickly became “addicted” to exercise. Now, she has made a career out of helping disabled people find ways to get fit.

“Once someone opened the door for me I realised there was a whole world out there,” she says. “Whatever your disability, there’s a version of a sport for you – you just have to be a bit creative.”

After six months of post-divorce counselling, Pezaro decided she wanted to lose weight. “I got a brilliant new carer who got me eating healthily,” she says. “Then I found out there was an MS treatment centre near me that runs lots of different exercise classes.”

She signed up to a class she has come to describe affectionately as “sadistic PE”. “The instructor is ex-military but also a counsellor and herself has MS. So she completely understands us, but she doesn’t let us get away with anything. We adapt everything to our own personal needs. It’s not your average fitness class – it’s not unusual for people to collapse and have a leg spasm in the middle of their situps, or to suddenly fall off their exercise ball, but we just laugh about it.”

At first Pezaro was unable to do most of the exercises, but she persevered and since starting the class three years ago has lost nearly 4st.

“It’s not been easy,” she says. “It took me 30 months to lose 45 pounds. But I didn’t get demoralised. I knew that over the years it would add up. And the more I’ve exercised the better my fatigue is. I still can’t walk, but I now have less weight to lift when I’m using my frame, or getting on and off the toilet, so everything is easier.”

Pezaro’s confidence has been transformed and now she is enjoying dating again. But perhaps most the important gain has been to her sense of control.

“I really worked myself at last night’s class, and today every muscle in my body hurts,” she says. “But I’m so used to living with pain, it’s kind of nice to know that for once, things are hurting for a good reason.”

Up To 10 Years For Benefit Fraud, DPP Says

September 16, 2013

Benefit cheats face increased jail terms of up to ten years under an unprecedented crackdown on those who “flout the system”, Britain’s most senior prosecutor will announce today.

More cases will be pursued and tougher sentences sought by sending suspects straight to Crown Court, Keir Starmer, QC, will say as he sets out new guidelines for the Crown Prosecution Service.

Mr Starmer, the Director of Public Prosecutions, will warn that for the first time the enormous economic cost of benefit fraud will be a major consideration in whether charges are pursued.

Middle-class and “professional” cheats will be targeted as the offence is brought into line with crimes such as money laundering and banking fraud. The CPS will also aim to ensure that those responsible receive similar sentences.

Mr Starmer will say that it is time for a “tough stance” against the perpetrators of benefit and tax credit fraud, which costs Britain almost £2 billion each year. “It is a myth that ‘getting one over on the system’ is a victimless crime. The truth is that we all pay the price. I am determined to see a clampdown on those who flout the system,” he announces in the new guidance.

The move comes after the CPS took over legal work for the Department for Work and Pensions (DWP), which previously had an in-house team. Prosecutors will be told to seek tougher penalties in cases with aggravating factors such as multiple offences, abuse of a position of trust or substantial loss to public funds. Professionally planned frauds, which could include divorcing couples who fail to notify the authorities about their true circumstances, will also be targeted.

Increasing numbers of suspects will be charged under the Fraud Act, which carries a maximum penalty of ten years’ imprisonment. In the past, benefit cheats have usually been pursued under specific social security legislation, which carries a maximum term of seven years.

While benefit fraud of less than £20,000 was previously automatically allocated to the magistrates’ courts, which can only hand out sentences with a maximum of 12 months, the financial threshold will now be abolished. It means that even small cases can be referred to the Crown Court for stronger sentencing if the circumstances are warranted, in an acknowledgement of the widespread and damaging nature of the offence.

Mr Starmer said: “It’s not only taxpayers that suffer. Benefits exist to protect and support the most vulnerable people in our society and, whenever the system is defrauded, it’s also taking money away from those with a genuine need.”

When considering whether to bring a prosecution, lawyers will be to told to weigh up the cost to the public purse of benefit fraud.

Mr Starmer said: “The cost to the nation incurred by benefit fraud should be at the forefront of lawyers’ minds when considering whether a prosecution is in the public interest. The loss of money has a significant impact on communities up and down the country.”

The CPS was given resources to tackle the problem when the DWP legal team was merged into its fraud area about a year ago. The guidelines will be published today to ensure that the tough approach is consistent across England and Wales.

Mr Starmer said: “The guidance for prosecutors is clear that if the evidence demonstrates an element of dishonesty, rather than just knowledge of a fraud, the appropriate charges should be used.

“This will ensure that following conviction, all options are on the table for magistrates and judges, including custodial sentences. Indeed, prosecutors are also instructed not to shy away from using a range a legislation that carries higher sentences where it is merited.”

The move comes amid a general government crackdown on benefit fraud. In August it claimed to have saved hundreds of millions of pounds by introducing better fraud prevention and reducing errors in the tax and benefit system.

Measures included more rigorous monitoring of claims by the DWP and the naming and shaming of fraudsters. The amount of money confiscated from benefit cheats has also risen 50 per cent in the past year.

The What I See Project

September 16, 2013

The What I See Project recognises and aims to amplify the voices of women from around the world. It provides an online platform for a network of women to share their stories and hear each other’s stories in the hope that they will all become more empowered in the process.

The Project is the brainchild of Edwina Dunn, successful entrepreneur and founder of Tesco’s Clubcard. She wanted to celebrate inspiring women from everyday life whose stories would otherwise go unheard. She wanted these women to share their struggles, achievements and inner thoughts, and to express themselves freely through a website that appreciates them for who they really are.

So, she established the What I See Project, which asks women worldwide, from all walks and wheels of life, one very simple, yet very interesting question: “What do you see when you look in the mirror?” The website contains a collection of responses.

A few weeks ago, I was honoured to be contacted by the team at the Project, who asked me to provide my own answer to the question.

I see a very long list of things when I look in the mirror, but I listed some of the most significant and special ones here as my contribution to the Project.

If the Project interests you, you can follow it on Facebook or Twitter, as well as through its website. The team are always on the lookout for interesting women who might like to participate themselves.

All that is left for me to do is to ‘pass the baton’ along to the next woman in line, lifestyle blogger Elizabeth Sellers, whose website is here.

Quest 88 Trike Available On Application From The Nihal Armstrong Trust

September 16, 2013

The Nihal Armstrong Trust have been donated an accessible trike by Quest 88. This is available, on application to the Trust, for a child with Cerebral Palsy.

Their website says:

Quest 88 have kindly donated a new tricycle up to the value of £2000 to our charity, suitable for children 21/2 years to 18 years.

Parents/carers are invited to apply for this trike in the normal way.

Please see our criteria in the apply section.

You will need a letter from an OT or physiotherapist who has seen your child use this trike and recommends it.

The first application that meets all our criteria will be awarded this trike.

 

Ryan Norman

September 15, 2013

How many more of these cases do we bloggers have to cover?

 

A seriously disabled man who has never been able to walk, talk or feed himself has had his benefits stopped and been told he must have a medical to decide if he is fit for work.

Ryan Norman has needed round the clock care since he was a baby but now he has turned 20 his child benefit and tax benefits have automatically stopped.

His mother, Ceneta, his sole carer, claims she is in serious financial difficulties after the benefits dried up on Ryan’s birthday – September 1 – with a wait of several weeks before he is assessed for adult benefits.

 

Ms Norman, of Darlington, County Durham, described her son as a baby trapped in an adult’s body and said she cannot understand why he must prove his disabilities for the adult benefits system when his condition is already well documented.

 

The single mother said she will struggle to provide for Ryan and her two other children, Shane, 15, and Shanice, nine, without money for Ryan’s care.

Ms Norman, 49, said: ‘Everything seems to be such a struggle, the authorities don’t seem to think of him as a person at all.

‘There is no communication between the children’s side and the adult side at all – they blame each other and I am passed from pillar to post. I don’t know what I am going to do.’

Child tax credits are assessed and paid by HM Revenue and Customs (HMRC) and automatically stop when a child reaches 20 if they have been in full-time education.

The adult benefits system is operated by the Department for Work and Pensions (DWP), which introduced a Work Capabilities Assessment last year to determine whether disabled people could be considered fit for work.

 

 

Ryan was born a healthy baby but contracted meningitis at four months old, leaving him severely disabled.

He attended a special school at Education Village, in Haughton, Darlington, but after turning 20 he is now classed as an adult.

Ms Norman, 49, said: ‘Ryan cannot walk or talk, I have to feed him, help him to drink, do everything for him.

‘He will never work or do anything for himself. That did not change overnight when he turned 20.

‘When he was in the hospital with meningitis the doctors did not expect him to pull through. They said he was a little miracle.

‘I look after him, he’s my pride and joy, but I must be saving the Government thousands of pounds by looking after him myself.’

Ms Norman claims she had been given no indication that her payments for Ryan would stop so suddenly and only found out about the need for a medical after calling the benefits office when she noticed her payments had been reduced.

She added: ‘I can understand the need for his benefits to change but it is the gap between the child benefits ending and the adult ones starting. There’s no co-ordination.’

A spokeswoman for Darlington Borough Council said: ‘The changes in benefit referred to are a result of Government policy.

‘DWP are responsible for the assessment for these benefits not the council. However, the council is providing the family with advice regarding completion of the relevant forms and will continue to support the family throughout this matter.’

A HMRC spokeswoman said customers in receipt of child benefit would be written to ahead of the child finishing education.

She added: ‘Once a child who has been in education or training turns 20 payments will stop automatically and with immediate effect.’

A DWP spokesman said: ‘Disabled adults often have different support needs to children, and this is reflected in the different benefits available to people when they reach adulthood.

‘Employment and support allowance is a benefit for adults who are too ill or disabled to work. To apply for it, someone just needs to fill out a form and provide some medical evidence.

‘If we are given all the information we need to enable us to make a decision, there is often no need for a face to face assessment.’

 

The UN Are Listening On Disability Benefit Reforms!!!

September 14, 2013

I love Raquel Rolnik. I just love her.

Please, please share this post everywhere.

Why Aren’t Hearing Loops Working?

September 14, 2013

Hearing loops, systems which helps clarify sound for people who are hard of hearing, often don’t work according to a charity.

Installed into buildings such as shops and theatres they direct sound and speech directly into hearing aids and cochlear implants.

Hearing Link says loops often don’t work or staff have not been trained in how to use them.

Graham Satchell travelled to Eastbourne, which is aiming to be a beacon of excellence for hearing impaired people.

DWP May Issue New #BedroomTax Guidelines Following Appeals

September 13, 2013

 

Nick Clegg Confronted By Disabled Woman On #BedroomTax

September 13, 2013

Nick Clegg was left stuck for words after being confronted by a seriously ill lady who is being hit by the Bedroom Tax.

Karen in Basildon phoned in to Call Clegg to complain about the Spare Room Subsidy, which means that she is paying £16 per week extra, despite needing the extra room for her oxygen concentrators.

She has been told she should move the devices to her bedroom, but insists they are so loud, they would stop her and her husband sleeping.

Unfortunately I can’t find the specific clip, only the whole half hour show on Youtube, but this call is about 17 minutes in.

ATOS Tells CP Woman Her Disability Expected To Improve

September 12, 2013

I’ve been hearing about the case of Amy Jones all week. I thank the Huffington Post for the coverage.

I’m extremely scared by her case, as well as shocked. I have lived with CP myself all my life and, in the words of Jack Carroll, “it’s still here!” and it ain’t going anywhere fast.

I’ve seen people with CP get worse over time. I’ve seen people with CP die as a result of complications.

Anyone can tell that Amy Jones does not have a mild case of CP, just by reading the details of her case. It is just unbelievable that someone who called themself a medical professional thought it would improve after actually seeing her,

And as for the reassessment every six months? Don’t even get me started.

Landmark ‘Wet Room’ Ruling Blows Holes In #BedroomTax

September 12, 2013
In a ruling that could open the floodgates for thousands to challenge the under-occupancy legislation, a tribunal found that David Nelson’s spare room was too small to be a bedroom.

And his brother Ian successfully argued that his “spare” room should be turned into a wet room because he struggles to get in and out of the bath.

Around 660,000 social housing tenants across the country have seen their housing benefit reduced by an average of £14 per week because they have an unused bedroom.

The disabled, foster carers and those with children in the armed forces are exempt from the rules.

David, 57, from Glenrothes, Fife, argued that his spare room was too small to be taxed. He said that at just 50 square feet, the room could not be classed as a bedroom but is a box room. Ian, who only has one leg, successfully argued that his “spare” room should be turned into a wet room because he struggles to get into a bath.

At an independent tribunal held in Kirkcaldy, Simon Collins QC ruled that neither brother should have their housing benefits cut as their rooms should be exempt.

Mr Collins, a first tier tribunal judge, ruled that a room under 50 square feet is not a bedroom and a room measuring between 50 and 70 square feet is only suitable for children under 10.

The ruling is expected to spark a deluge of appeals from the 75,000 people in Scotland said to be affected by the benefits cut.

his underlines the already existing concerns that the bedroom tax is in breach of human rights

Deputy First Minister Nicola Sturgeon

David said: “I just don’t know how they could class this as a bedroom.

“You could maybe get a child’s bed in here but even that would be a stretch.

“The council put me in arrears with the bedroom tax but hopefully I won’t have to pay that now.

“A few people along with me – including my brother – won their appeals at the same time. It is great news. I’m delighted and I hope it sets a precedent for other people in the same situation.”

Deputy First Minister Nicola Sturgeon said after the ruling: “This underlines the already existing concerns that the bedroom tax is in breach of human rights.”

But a spokeswoman for the Department for Work and Pensions said that the Scottish Government had been given money by Westminster to ensure that vulnerable people are not badly affected by the legislation.

She said: “It’s simply not affordable to pay housing benefit for people to have spare rooms, and our reforms in the social sector mean families receive help for the number of bedrooms they need.

“These are exactly the same rules as in the private sector.

“Scotland has been given £10million this year to help vulnerable people.

“We are monitoring this spending carefully.”

Sex And Cancer

September 12, 2013

Does this apply to other conditions/ disabilities as well? Similarities? Differences?

Cafe Bans Eczema Man From Inside

September 12, 2013

What are your thoughts on this, readers? It seems to me like unfair treatment because of a disability which can’t be helped. Surely the regulars know him and his situation. Anyone else should ask him or ask the owners or staff.

A Carnoustie cafe has told an eczema sufferer he has to sit outside because his constant scratching is putting customers off their food.

Finlay Munro said the owners of Franco’s told him not to come back because of a skin problem which makes him scratch himself without realising.

He has suffered from atopic eczema since he was two.

He said: “I’m not happy about it. This is just a skin condition I have — it’s not contagious.

“I handed over my loyalty card, but the woman didn’t sign it. She said she knew I had a disability. I said are you saying you don’t want me back?

“She said yes.”

Mr Munro added: “I can see it from the point of view of the customers. If you’re sitting next to somebody who’s involuntarily scratching, it’s quite worrying.

“But if they’d asked me I would have explained it to them.”

Mr Munro, 60, said he had been told by his doctor that “a disability goes with” his condition.

Janet Franco owns the cafe and said customers had been refusing to pay.

She said: “He’s been in the cafe quite a few times and it never really bothered us until we started to get complaints from the customers.

“He was scratching so much there were dead skin particles floating around the shop.

“We did actually feel sorry for him, but we couldn’t charge the customers for their meals.”

Ms Franco said she called the Citizens Advice Bureau for advice before she explained her view to Mr Munro.

She said: “We told him he could come and get takeaway, or come and sit outside and read his book and eat. But he couldn’t be in the cafe if he was going to be scratching like that.

“It has happened before, but this time we had eight complaints within an hour.

“He wasn’t asked not to come back, he was just told he can’t sit and do that in the cafe.”

Asked what Mr Munro would do in colder weather, Ms Franco said: “In that case our doors won’t be open and there won’t be a through wind, so he can sit at one of the corner tables.”

Mr Munro denied he had been offered the two options, and said his daughter had emailed Franco’s to “clarify these alternatives”.

Ms Franco said: “If he and his daughter want to speak to us we will explain the situation again.

“We lost in excess of £120 the other day and we’re only a small business — we can’t afford that kind of loss.”

Hayley Milne

September 12, 2013

A Paralympic swimming star of the future. Watch this space!

Food Banks: ‘I Didn’t Ask To Be Ill’

September 12, 2013

“I get really, really upset sometimes,” says Andrew Burton-Fullick, sitting in the front room of his small terraced house in Grantham. “I don’t sleep well now. Day-to-day life is a struggle. My partner works his socks off for us and he’s had time off with stress. It’s hand-to-mouth all the time. And I’ve done nothing wrong.”

Until January 2011, Burton-Fullick, 56, had been working as a care assistant in a nursing home, which he had done for 23 years. The year before, he had had a heart attack, and when he later developed heart complications his doctor told him he’d have to give up work. On top of this, he has been living with diabetes since he was a toddler and it is seriously affecting his health – his sight is deteriorating, he is suffering hearing loss (he wears hearing aids in both ears) and has nerve damage in his hands and legs. He also has arthritis, which makes walking difficult, and will soon be going into hospital for surgery on his bladder. A large plastic tub full of drugs is on the table next to him.

He was given benefits that came to nearly £400 a month – less than he had been earning, but just about enough, combined with his partner’s salary as a hospital porter, to live on. Then, as part of a reassessment by Atos, he was told he was no longer eligible for the new incapacity benefit, his benefits would be stopped immediately and that, despite his numerous health problems, he was fit for work and should go and find a job. He appealed, but lost. He isn’t even eligible for jobseeker’s allowance.

And there are no jobs for him. When he turned down a position because it was only 16 hours a week and almost all of his salary would have gone on commuting costs, he says the staff at the Jobcentre called him “lazy”. “Well, how come I worked for 23 years in the care trade and only had to stop through illness? I didn’t ask to be ill. I didn’t ask for this to happen,” he says. “I know people who run businesses and they’ve told me they wouldn’t touch me with a bargepole. There are well people out there looking for jobs, so people like me aren’t going to get a look-in.”

The couple survive on one low salary. There are no luxuries or treats. Holidays are never considered; the one day out they’ve had all year was a trip to Nottingham for the recent Gay Pride festival and that had to be carefully budgeted for. Burton-Fullick needs new glasses, but can’t afford them; their immersion heater broke 18 months ago but they don’t have the money to get it fixed. They can usually afford to eat (though Burton-Fullick will sometimes skip meals), but when the money runs out before payday, the food bank steps in.

Burton-Fullick first used it at the beginning of last year. Their house got flooded and the unexpected expense left them without any money. He was referred by the Citizens’ Advice Bureau, which issued a food bank voucher. “We were so thankful, and we still are,” he says. “It means a lot. It means we’re not struggling.” He used it a couple of times last year, and has done the same a couple of times so far this year (it’s not meant to be used regularly).

At 1pm the Grantham food bank opens, and we slowly walk the few streets from his house. Burton-Fullick uses a shopping trolley to steady himself (he would like a mobility scooter but can’t afford one). The food bank is on the ground floor of a Victorian terraced building, with posters in the bay window. One reads: “Restoring dignity, reviving hope, building community.” Inside, several volunteers are packing supermarket carrier bags with food, while other volunteers sit at tables with food bank users, or “clients” as they’re called.

Brian Hanbury, the food bank’s coordinator, sits down with Burton-Fullick and asks him how he has been. “You’re about the 3,000th client,” Hanbury says. “We’ve had 33 tonnes of food come through this little building within the last two years. I’m only telling you this because I know when people find themselves in a hard place, they think they’re on their own. We’re estimating there are close to 6,000 people in this area who are just a few steps away from not being able to put food on their plate.”

The food bank asks clients to write their stories in a book – they range from young people leaving abusive homes and ending up in a hostel, to people who had to have time off work for illness, to those affected by the new bedroom tax. Hanbury estimates around 40% of his clients come in because of Jobcentre sanctions against them stopping their benefits. Hanbury leaves us sitting at a table and when I look over to Burton-Fullick, he looks as if he’s going to cry. After a while, he says: “I get so angry.”

Back at home, he unpacks the bags. “They say there’s three days’ food here but I can make it last a lot longer than that. They are very generous.” He has also been given a bag of toiletries, including loo roll, toothbrushes and shower gel (the food bank started providing this after a young mother said how horrible it made her feel to have to wash her children using supermarket value brand washingup liquid).

The food donation includes tinned vegetables, pasta sauces, packets of spaghetti, a bag of porridge, chocolate biscuits and stir-fry sauce. He runs through a list of meals he can make: “I’ve got some mince in the freezer so I’ll do a cottage pie, curries I can do, I can convert this,” he says, holding up a packet of pasta sauce, “into a risotto.”

He seems so cheerful unveiling each item – we laugh at the incongruousness of a large jar of bratwurst – and you momentarily forget what an outrage it is that thousands of people are having to rely on food banks such as Grantham’s in order not to go hungry. “Sometimes,” he says, “I sit here and get so angry. I would love to get Mr Cameron to live at the end of the month on what we have to live on. I’m not asking for thousands of pounds, I’m not asking for people to feel sorry for me. I just want a fair deal.”

Disability And Comedy

September 12, 2013

An article by a disabled comedian, Ted Shiress.

Miley Cyrus Twerking On German TV With Dwarves

September 12, 2013

I’ve just heard about this after watching The Last Leg tonight.

Had Miley Cyrus tried to learn Sign Language or Braille, had she come on stage in a wheelchair or using a white stick, I would have said she was making her disabled audiences feel wanted and cool and included.

Had she danced with a blind person or a wheelchair user as part of her routine, I would probably have said the same thing.

However, my only question in this case is- because of the short stature of people with dwarfism, they have the appearance of children. I can’t decide whether slapping them, as you would slap a child, reinforces that image.

In this case, I do think Miley Cyrus was having a bit of fun. Had she left out the slaps, I would have thanked her for being inclusive.

So readers, I’ll open this up for your discussion. #isitok for Miley Cyrus to dance with a backing band of dwarves?

Andrea Begley Has Written A Book!

September 11, 2013

Spotted on her Facebook page:

My book, ‘I Didn’t See That Coming’, is out on October 24th and will also be available in braille, large print and an audio book in conjunction with the RNIB

I’d love to read it!

Video Of UN Investigator Raquel Rolnik Calling For Axing Of Bedroom Tax

September 11, 2013

I’ve just found this- thanks to the Youtube user who published it.

No One Should Have A Gun License- Especially Not Blind People

September 11, 2013

A few years ago, I lost a close family member to a gun that was used for no reason.

I came away from that very painful experience with a very strong hatred of guns. I feel very strongly against gun licenses. I feel very strongly that America’s gun laws should be changed. I feel very strongly that no one, in America or anywhere, should be legally allowed to own a gun.

Until now, I’ve never had any reason to write this here.

Today, however, I have learnt that some US states allow blind people to hold gun licenses and legally own guns. Readers, I feel very strongly that if there should be any minimum requirement for owning a gun, it should be full eyesight.

Some disability rights campaigners may disagree with my view. Some disability rights campaigners may say that blind people have a right to do, to own, anything they wish.

Readers, in most cases, I would fully agree that blind people, that all disabled people, have every right to do, and to own, anything they wish.

However, there is something else that I have always felt very strongly about. That is, that in doing anything they wish to do, all disabled people should know their own limits. I have always felt very strongly that disabled people should never try to use equal rights or disability rights as an excuse to do something that puts themselves, or anyone else, in serious danger.

When I heard that blind people are allowed to hold gun licenses in some states, my mind instantly filled with ‘what if’s.’ Very dangerous ‘what if’s.’

The Guardian mentions a case of a blind man whose guns were confiscated after he accidentally shot himself in the leg. Last year, this man won a legal battle to keep and shoot guns.

I sincerely hope that he did not do himself any serious harm in that particular incident. However, it could have been so much worse.

What if a blind person using a gun accidentally shot another person dead? What if they accidentally shot themselves dead? I, for one, think that would be really tragic.

My personal opinion is that America’s second amendment law needs to change for everyone. However, if that can’t happen, then at the very least, the states that allow blind people to own and carry guns really need to change that law.

I  strongly disagree with Ian Macrae, editor of Disability Now, who feels it should not be society’s job to say that blind or disabled people should be excluded from doing something because it is too dangerous.

Guns are not cars- guns cannot be adapted to meet the needs of disabled people.

I feel very strongly that there are some times when disabled people must accept that there are things they can’t do because, quite simply, it would be too dangerous. As sad as some may feel about this, for blind people, gun ownership is one of those things.

If blind people find it too difficult to understand and accept that they cannot do certain things because of extremely high levels of danger to themselves or others, then in matters of life or death such as gun ownership, I feel  very strongly that society should step in and stop them through a law of exclusion.

The consequences of not having such a law could potentially be far too serious to even think about. There would be no return from death, so it is not a chance that should be taken.

LD Care Providers Have Learned Lessons From Winterbourne View

September 11, 2013

Three years ago next month, whistleblower Terry Bryan set in train a sequence of events that was to send a devastating shockwave through the adult care sector and culminated last week in the sale of what remained of the company he was working for.

That company was Castlebeck and the shockwave has become known as Winterbourne View, the name of its hospital facility for people with learning disabilities and autism near Bristol, where Bryan was a charge nurse and where he had witnessed what he described in an email to management as the “confrontational and aggressive” approach of named staff towards vulnerable patients.

The whole nation was to see such behaviour, and worse, on TV seven months later, after Bryan – his complaints having prompted no action by the company or regulatory bodies – approached BBC’s Panorama team. An undercover reporter went into Winterbourne to film covertly and the resulting programme led to the prosecution and conviction of 11 staff, six of whom were jailed; the closure of the unit; the collapse of Castlebeck into administration; and, most significantly, a government decision to stop using similar hospitals in England and to find, by next June, new forms of care for 1,300 people languishing in them. The hospitals had sprung up since the rundown of long-stay learning disability institutions, and claimed to offer short-term assessment and treatment of people with challenging behaviour. In reality, care commissioners were using them routinely to “park” such people, often for years at a time. All too often, there was little assessment going on and still less treatment.

In 2010, Winterbourne had a turnover of £3.7m, charging average fees of £3,500 a week. Astonishingly, according to adult safeguarding expert Margaret Flynn who undertook a local serious-case review into Panorama’s revelations, no commissioner who sent patients there ever visited. While few will shed tears over the demise of Castlebeck, you have to feel that other agencies should be carrying some of the can.

To their credit, groups representing 80% of providers of care and supported housing for learning-disabled people recognise that Winterbourne has lessons for them. They have come together in the Driving Up Quality Alliance, which today launches a quality code and a self-assessment tool, designed to improve standards of care and support and ensure a focus on the individual.

The code, endorsed by the Department of Health, has been piloted by eight organisations. They found the experience not altogether comfortable. As the alliance says: “We found out that too many people are sent away from their communities for too long and … that the professionals responsible for organising, paying for and checking that people are doing well were not doing their jobs very well”.

If only other agencies with a stake in the Winterbourne affair had taken a cue for such introspection: the police, called 29 times to incidents at the unit in three years; the local A&E unit, which must have dealt with a stream of Winterbourne patients with injuries including broken bones; and the unit’s retained GP, who declined, on legal advice because of patient confidentiality issues, to share any patient information with Flynn’s review. All these, and others, had cause to reflect on their practice and why no alarm was raised.

In one of a clutch of articles on Winterbourne in the latest issue of the Journal of Adult Protection, Flynn and Vic Citarella, who co-led the review, acknowledge its limitations and the partial evidence they had to work with. They say: “It is not known why this hospital was spared the attentions of a public inquiry.” Generally speaking, we call for public inquiries far too easily, but in the case of Winterbourne, it would certainly have concentrated more minds.

Railway Worker Suspended For Helping Wheelchair User Reinstated

September 11, 2013

A railway worker suspended after going on to a train track to help a disabled woman who had fallen off the platform edge has been reinstated.

The customer service assistant at Southend Central station in Essex was one of a number of people who went to the elderly woman’s aid on 28 August.

The Rail Maritime and Transport union (RMT) said the c2c employee would now return to work.

RMT general secretary Bob Crow said it was a “victory for common sense”.

The worker had faced a disciplinary hearing after suggestions he had not followed correct health and safety procedures.

The woman suffered a fractured hip in the fall.

Worker a ‘hero’

A c2c spokesman said: “A c2c employee has returned to full duties following our investigation into the incident at Southend Central station.

“While the employee helped members of the public to remove the passenger from the track, he accepted his immediate duty was to ensure all trains were stopped.

“This is to protect the safety of all involved, including those who were already on the track aiding the passenger.”

Mr Crow added: “Our member is a hero who should never have been facing the sack for saving a disabled woman from a life-threatening situation.

“Our member has thanked the union, his work colleagues and the public for all of their support.

“This incident has shown once again how important station staff are to passenger safety and security.”

UN Investigator Will Call For Axing Of #BedroomTax

September 11, 2013

VICTORY!!!

ATOS Assessor Told Depressed Gay Man To Seek Cure

September 11, 2013

I feel that this case should go viral. I just can’t believe it. He only got a warning! If you ask me he should have been struck off.

Universal Credit – Mystery man leaks “Security concerns” to Radio 4

September 10, 2013

Brian Wernham's avatarbrianwernham

An interview with a ‘former insider’ who had worked at a senior level on the Universal Credit security team at DWP. I do not know for sure who it is…

banksy-99

“Concerns about IT security … officials lost their nerve, not the ministers … the Civil Service not up to the job…”

Here is the whole interview conducted by BBC reporter Jon Manel with the ‘mystery man’ voiced over by an actor:

View original post

Ouch Talk Show: Sex Special

September 10, 2013

I don’t usually post the details of the Ouch! Talk Show here, but this one is a special on a subject about which I have a strong personal opinion.

How does a young man lose his virginity when his arms and legs don’t work? What’s it like to be both gay and disabled? And is falling in love with your care worker ever a good thing?

Disabled panellists Asta Philpot, Daryl Beeton and Kirsty Liddiard talk sex and relationships with presenters Rob Crossan and Kate Monaghan.

Warning: This programme contains adult themes and some may find it an uncomfortable listen.

But the tone is friendly and informal. Parents of disabled teenagers might appreciate listening to this with their child as a helpful discussion-opener.

A high quality version is on Audioboo

Here are some useful links so you can find out more about the people and subjects on talk show 100.

  • Asta Philpot, 32, is from Leeds. He can’t use his arms or legs due to arthrogryposis and campaigns for access to sex for people in a similar boat via his personal website. In the 2007 BBC documentary, One Night Only, Asta took two disabled men to a specialist brothel in Spain where he had lost his virginity a year earlier (see Is it OK for disabled people to go to brothels? from the Magazine).
  • Kirsty Liddiard spoke to 25 disable people about their sex lives for her PhD. She continues to specialise in this field at Rierson University in Toronto, teaching on the disability studies course and she’s on the board of directors at the Rose Centre for young adults with disabilities which, amongst other things, helps its clients with matters relating to sex.
  • Daryl Beeton runs Kazzum, a theatre company for young people. He is gay and has a mobility impairment. You may remember him as a contestant on BBC Two’s Beyond Boundaries programme.
  • Regard is an organisation which supports people in the UK who are gay and disabled.
  • Fringe disability organisation Outsiders are concerned with “sexual freedom” and expression. They run an annual Sex Maniacs Ball – which isn’t quite what the name suggests it might be.

Subscribe to the podcast feed to get the latest shows

Download the transcript

Judge Orders Separation Of Autistic Son And Abusive Mother

September 10, 2013

Any thoughts, readers?

A vulnerable young man must be forcibly separated from his abusive mother and made to live in a council-run care home against his will, a judge has ordered. Judge Martin Cardinal gave permission for local authorities to deprive the man, known as WMA, of his liberty, allowing them to stop him from leaving the home if they thought he might run away.

WMA, 25, who is autistic and suffers from development disorders, has rarely been allowed outside by his mother. He lacks all social skills, as well as the ability to look after himself. However, the court heard that he wanted to stay at home despite his mother “dominating” his life and verbally and mentally abusing him. “WMA needs a relationship with his mother but at times contact might not be in his best interests,” the judge wrote.

His mother, identified as MA, struggles to care for either herself or her son, the court heard. She kept their house in such squalid condition that the pair had to be moved to a new property by the local council. The judge called photographs of the house revolting. MA denied accusations that she had threatened to kill both herself and her son if they were separated.

The court heard that WMA, whose disorder doctors likened to Asperger’s, led an isolated and insular life with his mother. She was arrested for neglecting him in 2011 but no charges were brought. The court heard that MA, who is in poor health, routinely refused help for her son and held him back. Care workers worried that there was often a lack of food in the house.

However, during a short stay in a care home WMA appeared to enjoy social contact, the judge heard, and began to learn skills such as how to make toast.

In his decision, at Birmingham crown court on 23 July but only recently published, the judge wrote: “Whatever she may say about being a good mother to WMA, and I am sure she intends to be one, [MA] is, in practice, a poor one; for she has done little to forward his learning, social and self-care skills.”

Accepting the proposals of council care workers, the judge ordered that the pair be allowed only “telephone contact for the first two weeks and unsupervised contact twice weekly for a maximum of two hours”.

He added that contact should “involve a member of staff being able to supervise it, though not actually be in the room”. After a month, he said that contact between WMA and his mother should be “simply monitored rather than supervised”, but he warned that “contact need not be de-stabilising or undermining”.

The decision was handed down in the court of protection, which handles the affairs of people adjudged not to have mental capacity to do so themselves.

It came to light after news that the number of requests to deprive vulnerable people of their liberty for their own safety has hit a record high. According to Health and Social Care Information figures released in late August, there were nearly 12,000 deprivation of liberty safeguards requests made in England in 2012-13, a rise of 66% since 2010.

Attitudes To Benefits Softening, Finds Survey

September 10, 2013

Readers, do you think this is true?

Blind People Hit By Social Care Crisis, Finds Study

September 10, 2013

The number of blind people getting help from councils has dropped by over 40% in England in six years, data shows.

The analysis by the Royal National Institute of Blind People – based on official figures – found just under 32,000 got support last year – down from nearly 56,000 in 2005-6.

It warned that if current trends continued, no-one would be getting support from councils within a decade.

The charity said the situation was “wholly unacceptable”.

People with sight problems may need help with activities such as cooking and shopping.

Those who are newly diagnosed may also be entitled to rehabilitation support, which can include help learning to use aids, like canes.

‘Toughest time’

The data included people of all ages and once again illustrates the problems councils are encountering in providing means-tested social care.

Much of the attention on the issue has been associated with the struggle elderly people are facing in getting support.

But the RNIB said its research showed others were affected too.

Chief executive Lesley-Anne Alexander said: “Not only does sight loss have a massive emotional impact, but it also means having to re-learn almost every aspect of your life.

“Being left alone to cope with sight loss is wholly unacceptable. No matter how tight the budgets of government are, this is essential support which must be provided. The government needs to act now.”

A spokesman for the Local Government Association said: “Councils would love to be able to provide the same level of support they did in 2005 but a 43% cut to local government funding means that simply is not possible.

“Councils are having to take incredibly difficult decisions on how they prioritise their budgets and unfortunately a tightening of eligibility criteria has been unavoidable across all care services, including those for the visually impaired.

“Councils continue to provide on-going support to the people who would have the toughest time coping without help.”

Care and Support Minister Norman Lamb said: “We recognise the pressures on local councils to deliver these services and that is why we have allocated them with additional funding for adult social care over the next two years, which will provide an extra £100m in 2013/14, and £200m in 2014/15. This is on top of the £3.8bn pooled health and social care budget we have set up to help make sure everyone gets properly joined up health and care services from whoever is best placed to deliver it – whether that’s the NHS or the local authority.”

Bradford Council To Probe The WCA

September 9, 2013

I can’t tell you what a big piece of progress this is. A council is listening. A council. I really never thought I’d see this day.

 

A full-scale investigation into controversial Government disability assessments is to be started by Bradford Council – the first local authority believed to be doing so.

 

The Council has branded the tests “unfair” and could hold public hearings as it investigates their effects on vulnerable people in the district.

 

Anyone who wants to claim disability benefits now has to undergo a test called the Work Capability Assessment (WCA) to see if they are able to work.

 

But the testing scheme, contracted out to healthcare firm Atos, has come under fire from disability rights groups. And in July, the Council branded the process “unfair, inaccurate, and bad value for money”.

 

A motion passed by the full Council said the tests were “causing fear and distress” among vulnerable disabled people, that they discriminated against those who had fluctuating conditions and that the appeals process was too lengthy.

 

Now, a committee will investigate the local effects of the programme during a two-month inquiry. The Council’s Health and Social Care Overview and Scrutiny Committee is expected to start its investigation later this month. It would publish its findings in the New Year. The committee hopes to speak to disabled people and their carers, including those who have appealed against the result of their asessments.

 

 

They will also be gathering the views of organisations working with disabled people, such as Disability Advice Bradford and Mind, as well as the Department of Work and Pensions and Atos itself. The committee will discuss the methods it will use to gather evidence when it next meets on Thursday, but it could involve questioning people at specially-convened public hearings.

 

The announcement was welcomed by Coun Mohammad Shabbir, whose Respect group had originally raised the concerns.

 

Coun Shabbir is the manager of mental health charity Sharing Voices, and said his colleagues were frequently speaking to vulnerable people who were scared of the testing process.

 

He said: “I think this needs to be a robust investigation, meeting as many vulnerable people in that situation, and the organisations that represent them, as possible.” In July, the Government announced it would bring in other contractors to run the assessments, as well as Atos, in a bid to tackle waiting times.

 

A DWP spokesman said: “Through a series of independent reviews and by working with medical experts and charities, we have considerably improved the WCA process since 2010.

 

“The percentage of people entitled to Employment and Support Allowance is now at its highest level with more than half of people completing a WCA eligible for the benefit, but everyone has the right to appeal a decisioni.”

Tourettes Action says ‘ʞɔnɟ the firewall’ in a bid to combat prejudice

September 9, 2013

fuck the firewall

 

-LIDA unveils stealth email campaign as Tourettes Action steps-up effort to fight stigma –

 

 

 

NEWS (London 5th September, 2013) Direct and Digital agency, LIDA, has created a guerrilla email marketing campaign for Tourettes Action, aimed at highlighting the barriers which exclude people with Tourette Syndrome from society.The campaign emails are being sent out this week encouraging people to share and spread the creative virally. Although littered with swear words, the email is cleverly designed to trick firewalls that normally filter them out. By literally breaking through the digital barriers, the campaign raises awareness of the problems that people with Tourette Syndrome face in everyday life, and how they are effectively ‘filtered out’ by society.

 

 

 

The campaign plays on public perceptions of Tourette Syndrome.  In fact, chronic swearing affects only one in 10 sufferers, but is the only thing that people know about the condition, so the campaign is using it as a hook to engage readers to raise awareness of the wider issues surrounding Tourette Syndrome.

 

 

 

Tourettes Action chief executive Suzanne Dobson said: “People with Tourette Syndrome are routinely excluded and misunderstood by society – including from schools and, later, the workplace because of stigma associated with the condition. When we went out into the community to ask people what they knew about Tourette Syndrome, people said things like: “They are really frightening and aggressive” and “They are really violent people who can’t control their bodies.” In reality, many people with Tourette Syndrome can and do make a positive contribution to society, and are unfairly stigmatised. We hope this campaign will challenge assumptions and prejudice.”

 

 

LIDA Executive Creative Director Nicky Bullard said: “ ‘ʞɔnɟ the firewall’ is an original, disruptive and highly engaging campaign, which has great viral potential. It’s a brilliantly simple, cost-effective way to raise awareness about Tourette Syndrome through cleverly crafted copy, and help Tourettes Action fight the societal firewall that sufferers face.”

LCD Drops Sponsorship Of Simon Stevens For Labour Party Conference Over Offensive Tweets

September 9, 2013

 

 

I’m not going to pretend to agree with Simon Stevens’ views on anything. I’ve had a bit of a run-in with him myself when he called me disablist because of my views on I’m Spazticus.

I now realise that is nothing compared to the run-ins he has had with others.

I wish he could see that he is entitled to do, and to think, what he likes- but so  is everyone else. Personal criticism is never necessary.

Dr Stephen Duckworth: Use Work As Therapy

September 9, 2013

 

The paralysed man in charge of assessing benefit claimants has said the UK expects too little of disabled people.

Dr Stephen Duckworth, who broke his neck during a rugby accident 33 years ago, said society is letting down the disabled by not demanding a contribution from them.

The 53-year-old now leads the team that  will assess those who apply for the personal  independence payments, which will replace the disability living allowance.

 

Dr Duckworth said: ‘We need to move to a culture where employers recognise employment is therapeutic as opposed to illness-creating.

‘It is far better to go back to work to get better than to wait to get better to get back to work. Use work as a therapeutic intervention.’

 

Dr Duckworth – who trained himself to breathe by using his diaphragm rather than his chest muscles – believes more than 20 per cent of  Britain’s five million disabled have wrongly become dependent on benefits.

He said ‘at least a million, probably north of a million’ of those ‘deemed to be disabled… have got there through system failure and the way society is organised’.

The father of four – who receives DLA himself and will be assessed for the new benefit – said that minor injuries had become ‘a very common avenue towards multiple benefit receipt’.

 

In an interview, he details a claimant’s possible path after an accident ‘that could have happened at work as a result of lifting a box of photocopy paper’.

He says: ‘It gave you a bit of a limp; you get a no-win, no-fee solicitor, a claims farmer, coming up to you.’

As a result, he continues: ‘You get, say, £6,000 in damages from your employers, that builds your impairment, you’re off work for six months, then drop from full pay to half pay, then statutory sick pay.’

After which, Dr Duckworth says ‘you’re feeling the financial pinch’, and he envisages the claimant realising he can get an enhanced income from employment support allowance, and going on to claim it.

The scenario, he says, is: ‘Do my work capability assessment, get signed off on to the employment and support allowance at £106, so have a bit to pay the loan sharks back, [but] I am depressed and my partner has left me… my life is falling apart.’

Dr Duckworth, who served on the board of the Olympic Delivery Authority for London 2012, was suicidal after being paralysed as a medical student, but he refused his parents’ offer to look after him.

He said: ‘When I broke my neck, my mum and dad said, “Don’t worry, Stephen, we will build you a granny annexe”, and I screamed until I was blue in the face.

‘If they had built me one I would still be living there, they’d have wrapped me  in cotton wool and I’d never have got  back to London.’

Police: Stop Using Cells For Mentally Unwell

September 9, 2013

Police stations “should stop being used” as places to detain mentally ill people, according to one of Britain’s most senior police officers.

 

Ch Supt Irene Curtis says A&E would be a “better place” when mental health units are unable to take them.

 

Care minister Norman Lamb has described the standard of some crisis care as a “national scandal.”

 

The Association of Chief Police Officers says dealing with mentally ill people takes up a fifth of police time.

 

Police can detain people where no crime has been committed but they suspect the person is mentally unwell. The temporary police power is called a section 136.

 

During 2011-12, 9,000 people were detained in police custody under section 136.

 

Police say that is just a fraction of the number of mentally unwell people they have to deal with. About a fifth of all police time is now spent dealing with the mentally unwell, according to the Association of Chief Police Officers.

 

Irene Curtis, President of the Police Superintendents’ Association of England and Wales, said mentally ill people should instead be taken to hospital when mental health services were unable to take them.

 

“I think as long as there is an option to have a police station cell as a back-up then they will always be used and I think until you get to the stage where you actually say no, enough is enough, then police station cells should stop being used per se.

 

“If there are no spaces at the mental health unit, then my belief is that an accident or emergency unit at a local hospital must be a better place than a police station.”

 

Care minister Norman Lamb said a closer working relationship between the police and mental health services was needed.

 

“It shouldn’t be about police just saying we’re just going to take them, march them into an A&E department and abdicate our responsibility. That’s not the right way.

 

“It should be police together with mental health, reaching a conclusion about what is in that patient’s best interests.”

 

He also said: “Some of the care that is received by people in a moment of crisis in mental health is frankly unacceptable. It’s a national scandal.”

 

Freedom of Information requests by BBC Panorama to 52 mental health trusts in England suggest that the number of adult acute beds available in mental health units fell by 17% between 2008 and 2013.

 

However, one trust Panorama spoke to said that bed numbers were not the best indicator of the quality of care provided, and the majority of people with even acute mental illnesses could be treated at home.

 

This figure is based on data from 27 trusts and excludes trusts which have merged, taken on additional services or provided incomplete data.

 

Panorama: ‘Locked up for being ill?’ will be broadcast on BBC One on Monday 9 September at 20:30 BST and then available in the UK on the BBC iPlayer.

London Surgeons Helping Children Of Agent Orange

September 9, 2013

The Vietnam War ended nearly 40 years ago, but the casualties continue as birth defects plague the country.

There are claims that thousands of children continue to be born with horrific facial deformities due to the 20 million gallons of Agent Orange chemical sprayed by the United States.

The Vietnamese call the disfigured youngsters ‘the children of Agent Orange’.

Da Nang in central Vietnam is thought to have the highest level of congenital deformity in the world.

Inside Out’s Mark Jordan joins a team of top London plastic surgeons on their unpaid mission to help these deformed children to ‘Face the World’.

Inside Out is broadcast on Monday, 9 September at 19:30 BST on BBC One London and nationwide on the iPlayer for seven days thereafter.

Blue Badge And Concessionary Travel Regulations For England

September 9, 2013

This PDF gives the guidelines for how eligibility for Blue Badges and concessionary bus travel will be decided under PIP.

I can’t see anything too scary or unexpected. I’m just sharing it in the hope some of you will find it useful.

Double Amputee James Simpson Completes Race

September 9, 2013

A soldier who lost both legs in an explosion has become the first British double amputee to complete a gruelling obstacle course.

 

Lance Bombardier James Simpson lost his limbs after he stepped on an explosive device in Afghanistan in 2009.

 

The 27-year-old, from Rawdon in Leeds, spent months training for the Spartan Race, which took place in Ripon.

 

The event is a four mile (7km) open country run with 25 surprise obstacles including leaping over flaming logs.

 

He also had to scale 30ft (9m) high cargo nets, crawl under barbed wire and wade through muddy ditches.

‘An inspiration’

L/Bdr Simpson has been described as an inspiration by the organisers of the event, which is a shorter version of the Spartan Beast, a 12 mile-long course dubbed the “obstacle race from hell”.

 

He completed the course in just over four hours, wearing what he calls “stubbies” – small pads that fit to the bottom of his thighs.

 

He was given a standing ovation from fellow racers and spectators as he crossed the finishing line.

 

L/Bdr Simpson said afterwards: “It’s been brilliant. I knew it was going to be really tough, I was under no illusions. I had to dig, I really did.

 

“I’m really happy.”

 

L/Bdr Simpson, who is leaving the Army to become a student, has so far raised more than £2,500 for the SSAFA military charity through donations made on his Just Giving web page.

 

Race director Richard Lee said: “James is an inspiration to everybody.

 

“One of our core values is overcoming adversity and accepting challenges.

 

“What James has achieved today represents everything we believe in. We are proud of him.”

‘Freak Show’ Heading For West End

September 8, 2013

I’m not at all happy to read this. A man with EDS and a man with dwarfism in a ‘freak show?’ Erm, 1813 called, people! It wants its attitudes to disability back.

If someone mentions freak shows, you might think of Victorian-era circus attractions, widely regarded as dehumanising and politically incorrect.

 

What you may not realise is the sideshow genre, popular in the 19th Century, is enjoying a revival.

 

Dr Haze’s Freak Show recently finished a run at the Great Dorset Steam Fair and its Circus of Horrors performers are now heading for London’s West End.

 

So who are the stars in this troupe of unusual and remarkable humans?

 

Dr John Haze, who comes from a circus background, said: “Some of our performers are what we call ‘born freaks’ but many are turning something negative into something very positive. Others are born completely normal and turn themselves into freaks.

 

“People are entertained by people who look unusual. Anything that can shock us for a moment – whether it’s their appearance or something they do – as long as it doesn’t hurt anyone, then it’s great.”

 

However the performers are highly skilled individuals and their acts should not be replicated in any way.

 

Gary Stretch

 

 

Gary Stretch has an extreme case of Ehlers-Danlos syndrome, which affects collagen in the body, causing stretchy skin.

 

His act includes pulling his chest skin over his face, making his features disappear, in a move called the Wise Monkey – hear no evil, see no evil, speak no evil.

 

Dr Haze said: “When he discovered the condition as a child, he would charge other kids 50p to have a pull on his skin,” he said.

 

But the condition also meant he had to give up football and later, his job on a building site.

 

“Any bang and he would bruise really easily,” Dr Haze explained.

 

When asked whether it was right for Gary to cash-in on his condition, Dr Haze said: “What is he supposed to do? Live at home and never go out?

 

“He has found a way to use his condition to have a very good life.

 

“He is not well enough to do tours any more but he is still very much part of our group and does still do gigs with us.”

 

Captain Dan

 

 

Captain Dan the Demon Dwarf’s “magic” act includes eating live light bulbs and opening beer bottles with his eye socket.

 

Much of his routine, however, is adult-themed and in 2007 he hit the headlines after accidentally supergluing his penis to a vacuum cleaner during a performance.

 

The mishap occurred after he mended an attachment needed for his act but failed to leave enough time for the glue to dry.

 

Dan, who has been with the circus for a decade, lives on a narrow boat in Nottinghamshire with his dog.

 

If you think he looks familiar, you may have seen him in one of his many movies – he was an Ewok in Star Wars: Return of the Jedi, appeared in Labyrinth with David Bowie and shared a kiss with Miss Piggy in Muppets Treasure Island.

 

When asked whether his character was an alter ego, Dr Haze said: “No, I think Captain Dan and Dan Blackner are the same person.”

 

Wolf Boy

 

Mexican-born Jesus “Chuy” Aceves, the human wolf boy, has hypertrichosis, which means his whole face is covered in thick, dark hair.

 

His original high-wire walking act was adapted for the Circus of Horrors where he walks on a ladder of swords.

 

He was the subject of a 2005 BBC documentary – It’s Not Easy Being a Wolf Boy – when he shaved for the first time in the hope of getting a regular job closer to his family.

 

Dr Haze said: “There hadn’t been a wolf boy in England for years so it was a big coup to bring him over.

 

“He is working away from home but, the good thing is, we tour for a short period so he is not away from his family for long.

 

“He lives in a poor part of Mexico and was doing carpentry and construction for a low wage.

 

“People probably take the mickey out of him more in that environment than in the Circus of Horrors – that’s the big difference. When he goes on stage he is a superstar – at home he’s not a superstar.

 

“He has tried to shave it off but his skin underneath is blue. He tried it out but didn’t really like it. He said ‘this is how God has made me’.”

 

Earlier this year, Circus of Horrors was forced to advertise Jesus’s job to UK applicants to comply with employment laws but no British people qualified and he was able to keep his job.

 

About 50 people in the world have the condition and half are in Jesus’s family.

 

Hannibal Helmurto

 


 

Sword swallower Hannibal Helmurto spent two weeks in intensive care after rupturing his oesophagus swallowing a neon light “sword”.

 

Other aspects of his act include squirting liquid from his facial piercings and lifting a large plank of wood suspended from a hook through his nose.

 

He is one of just a handful of sword swallowers in the world.

 

When Dr Haze first met Hannibal, he had just quit his office job to work in a piercing parlour.

 

“He wore a normal suit and had no tattoos,” Dr Haze recalled.

 

“Ten years later he turned up at the Hackney Empire and he had completely changed his body.”

 

Apart from being covered in tattoos and piercings, he had a forked tongue and two “floating” ribs – deliberately broken to enable him to perform tricks.

The 2020 Paralympic Games…

September 7, 2013

Are awarded to the city of…. Tokyo!

IPC_logo_(2004).svgolympic-logo

 

japan flag

 

Open thread for your reactions.

Cannabis Picnic Protest Planned In Berkshire

September 7, 2013

Hundreds of campaigners plan to risk prosecution by smoking cannabis in one of Berkshire’s biggest open spaces in a bid to get the drug laws changed.

A group calling for the drug to be legalised has organised a protest picnic at Kings Meadow in Reading next month.

One of the organisers, Clark French from the Berkshire Cannabis Community group, has the neurological condition multiple sclerosis and uses the drug to ease his symptoms.

But Mr French said the event is open to anyone – not just those who want the drug legalised for medicinal purposes.

Georgie Ready- Teen With CP Kicked Off Beauty Course Because She Can’t Hold Nail Polish

September 6, 2013

Madness.

 

Heartless college bosses booted a teenage girl who suffers from cerebral palsy off a beauty therapy course — because she struggles to hold a pot of NAIL VARNISH. Pretty Georgie Ready, 18, was left distraught after her local college told her she could not study the BTEC course because she did ‘not meet the criteria’. Bizarrely she had been accepted onto the course but when she attended an open day at Tresham College in Corby, Northants., staff changed their mind. Shockingly, she was told by a member of staff that letting her onto the course would be “like letting a visually impaired person perform heart surgery.” The row comes after Britain’s triple gold medal-winning Paralympian Sophie Christiansen, who also has cerebral palsy, said there was still a major problem with discrimination against disabled people in this country.

Tobii Working On A TV That Runs On Eye-Gaze Technology

September 6, 2013

I’ve been hearing of the firm Tobii for years. They originally developed their products to help disabled people control computers, and see themselves as leaders in AAC and assistive technology devices and solutions.

However, now, according to the BBC, they are working on putting their technology to all kinds of commercial products which could be used and enjoyed by everyone.

In particular, Gaze TV, which was recently unveiled at a trade show in Berlin.

As someone who always welcomes new ways to make everything accessible to disabled people, I find this a very exciting idea.

It would be very useful for people with limited mobility, who struggle to walk a few steps to pick up a remote control to change the channel on today’s TVs.

However, it would be even more useful for the group of disabled people at which Tobii technology was originally aimed. Wheelchair users, particularly those without hand movements, for who eye movements and blinking are their only form of communication, and in this case, independence.

Imagine being a disabled person unable to use a remote control independently. Today, you have two choices. You either watch what everyone else is watching, even if that means being bored out of your mind, or you wait for someone to be in the room to change the channel for you.

But what if you are alone in a room, the programme you were watching with interest has finished, and you can’t communicate this to anyone? Today, you have no way of changing the channel, or even turning the TV off.

The finished Gaze TV seems like it would solve the problem of boredom. It would also allow disabled people to watch TV, not just independently based on choice and taste, but also independently  in the more literal sense- sitting in a room by themselves. This would allow carers some time to themselves, knowing that the person they care for is enjoying themselves safely.

Those of us lucky enough to physically be able to use a remote control have been channel surfing and changing volumes at will for years. It’s about time people with severe physical disabilities were given this simple pleasure. I send sincere thanks to Tobii and Haier, the people behind the hardware, for thinking up this idea.

I look forward to being able to watch TV with my severely disabled friends one day- and being able to watch them control the channel and the volume in the blink of an eye!

 

 

The UK’s First Centre For Adults With Autism

September 6, 2013

A pioneering centre for adults with autism has been officially opened by the Countess of Wessex.

The £1.5m Chitra Sethia Autism Centre, at the Fulbourn Hospital site near Cambridge, is the first of its kind in the UK.

The countess, who is Patron of the National Autistic Society, said Cambridgeshire was blazing a trail and she hoped the centre would be replicated across the country.

Centre director Professor Simon Baron-Cohen said it would be supporting adults who had been overlooked in their childhood.

Thoughts On Educating Yorkshire: Episode 1

September 6, 2013

I really enjoyed watching the first episode of Educating Yorkshire. It reminded me strongly of my schooldays. Ryan reminded me strongly of myself when I first started secondary school, although I had that personality for different reasons- because I thought that if I didn’t do my work and wasn’t polite to the teachers, they would remove me from mainstream education. Also, detention would have meant missing physio, and physio was very important- so I avoided detention at any cost.

I have a few more general disability-related thoughts to share on the programme because of Bailey, the girl with a facial disfigurement.

Firstly, she was portrayed as a girl who wears a lot of makeup. After her facial disfigurement was revealed, I was very pleased to see that Mr Mitchell and the other teachers were so understanding about her makeup. It’s a classic example of that old saying- the teacher knows things about all students that all students don’t know about each other. So if the teacher is nicer to a student than you expect there is a reason why.

However, on the show’s website, Bailey is described as ‘a leading light of the cool crowd.’ The thought of a child who looks ‘different’ being considered ‘cool’ in a mainstream school makes me very happy. I was a child who was ‘different’ and there were very few children in my year less cool than me. So I am glad to see Bailey has popularity, and is recognised for more than her different appearance.

Bailey said that she has to wear foundation. However, she didn’t reveal whether the foundation she wears is the special medical sort used by people with birthmarks and similar facial disfigurements. Maybe it is that sort- I would like to see that revealed though. It is available, and I hope she has heard of it.

I would like to see them showing the stories of some other students with physical disabilities or learning difficulties. I will continue to watch the programme with interest, but a part of me- the campaigner for inclusion where possible- will be disappointed if there are no other disabled students shown as lead stories in the series.

On another note- is that isolation system a Yorkshire thing or have people heard of it in other parts of the UK? Cause I haven’t heard of it before- not that I’m complaining!

Edinburgh Council To Stop Counting Boxrooms As Bedrooms To Fight #BedroomTax

September 6, 2013

Progress! Progress! Share! Share! Share!

Box rooms will no longer be classed as bedrooms under a new plan aimed at helping out tenants hit by the controversial bedroom tax.

A new policy set to be approved by the city council will see any space measuring less than 50sq ft that has no ventilation and lets in no “natural light” redesignated so that it is not considered a bedroom for letting purposes.

The move is designed to partially relieve the financial pressure on Edinburgh residents caused by the bedroom tax.

Under the controversial welfare reforms brought in by the government at Westminster, social tenants deemed to have more bedrooms than they need have had their housing benefit reduced since April.

A review of 257 pre-1919 ­tenements across the Capital that have two or more bedrooms will also be carried out to determine which properties have box rooms that do not meet the new guidelines.

Tenants would then not be charged extra rent for having the additional box room.

The proposal, which it is estimated will cost the council £172,000 a year, will go before the health, wellbeing and housing committee on Tuesday.

City housing vice-convener Councillor Cammy Day said: “We are trying to help people affected by the bedroom tax.

“We have come under massive pressure with the bedroom tax, so this is one way of trying to help those who are feeling the effects of it. This policy is financially hurting the people of Edinburgh and is costing the council millions of pounds. It is the Tory-Lib Dems fault. We urge them to rethink the policy.”

North Ayrshire is the only other council in Scotland that has a minimum size for rooms to be classed as bedrooms. The policy will allow council tenants to apply for a review of their property size.

The number of council tenants facing rent arrears soared from 969 to 2561 in just eight weeks after the bedroom tax came into force on April 1.

Edinburgh Tenants Federation vice-convener Maureen Jarvis said of the box room policy: “I think this is a good idea as it will help tenants cope with the bedroom tax, but the number of properties affected will be minimal.”

Cllr Steve Burgess, housing spokesman for the Greens, said the council’s move on reclassifying box rooms was welcome, but added: “What I was hoping was we might be able to identify a means of redesignating all property that would allow relief from the bedroom tax.

“I’m concerned as to whether we’ve explored all avenues in that respect and I’m going to seek reassurances we have done that. It seems to me there may be more we can do.”

The local authority has investigated redesignating all properties to have two public rooms rather than one in a bid to dodge the bedroom tax.

However, a report said the move would cost £672 a year for each of the 15,000 affected homes, meaning rental income would be slashed by 20 per cent and would hurt the city’s long-term housing plans.

Conservative Group leader Cllr Cameron Rose said: “While it’s desirable to improve the minimum standard of bedroom accommodation in the long term, this proposal seems to funnel £172,000 worth of taxpayers’ money to reduce rents, but doesn’t appear to help those who are already occupying such a bedroom.”

UN to probe human rights impact of controversial charge

A SENIOR United Nations official will visit Scotland to investigate the impact of the controversial bedroom tax on human rights.

Raquel Rolnik – the UN’s special rapporteur on housing – will carry out a two-week tour of cities across Britain, meeting tenants affected by the policy. She will also discuss the tax, which has hit the pockets of low-income households, with officials, campaigners and academics.

SNP MSP Christina McKelvie welcomed the visit, saying: “It is encouraging that Westminster’s bedroom tax, which is an utterly inhumane and unjustifiable policy, is being examined by the United Nations in relation to a reported breach of The Universal Declaration of Human Rights.

“It penalises disabled and economically deprived people for where they live when smaller alternatives are simply not available.”

Details Of Andrea Begley’s Debut Album

September 5, 2013

I’ll be buying this.

The Voice winner Andrea Begley has announced details of her debut album.

 

Titled The Message, the album contains cover versions of Andrea’s favourite songs including Bruce Springteen’s Dancing in the Dark as well as original tracks.

 

A reworking of Jake Bugg’s Lightning Bolt also appears on the album.

 

Begley, 27, from Northern Ireland beat finalists Leah McFall, Mike Ward and Matt Henry to win the BBC singing contest in June.

 

 

Since winning the competition Andrea has focussed on completing her debut record as well as working on a book about her experiences on The Voice.

 

The singer’s coach from the show, Danny O’Donoghue, joined her in the recording studio to give his support and produce the album’s title track, The Message, which is a track written by Begley.

 

Andrea says: “Danny has been a fantastic source of support to me both throughout the show and beyond it.

 

“He has always believed in me and in my songs and it was a total honour and privilege for him to produce one of my own songs for the album.

 

“I couldn’t stop smiling while I stood in the studio with him working on the track. I count myself a very lucky person.”

 

Andrea says The Message: “Offers the listener a first taste of the direction I intend to go as an artist beyond this point.”

 

The Message will be released on 21 October.

 

Andrea has also announced her first headline shows following the release of her debut album.

 

She’ll be performing at the Ulster Hall in Belfast on 3 November, and the Union Chapel in Islington on 4 November.

 

The track listing for The Message is as follows:

 

1. Ho Hey

 

2. Dancing In The Dark

 

3. Secret Smile

 

4. Breakfast At Tiffany’s

 

5. The Message

 

6. Lightning Bolt

 

7. Angel

 

8. Latch

 

9. Autumn

 

10. Take On Me

 

11. Falling Slowly

 

12. Love Will Tear Us Apart

Railway Worker Suspended- For Helping Disabled Woman

September 5, 2013

He should have been promoted, not suspended!

A railway worker has been suspended after going on to train tracks in Essex to help a disabled woman who had fallen off the platform edge.

The member of platform staff at Southend Central station was one of a number of people who went to the elderly woman’s aid on 28 August.

The tracks were clear by the time the next train arrived at the station.

A spokesman for train company c2c said its employee had been suspended while an investigation took place.

“Start Quote

What did they expect him to do – just stand by and watch?”

Bob Crow RMT

He said: “We have strict rules regarding the safety procedure for the quickest way of stopping trains in an emergency.

“An employee has been suspended while our investigation into this incident continues.”

‘Absolutely diabolical’

Bob Crow, general secretary of the National Union of Rail, Maritime and Transport Workers, said the decision to suspend the worker was “diabolical”.

“What did they expect him to do – just stand by and watch?” he said.

“All this person did was what anyone with any common sense would have done.

“He is one of our members and we will be supporting him. This is absolutely diabolical.”

The nearest train was about a quarter of a mile away when the people were on the tracks. The driver did not have to apply emergency brakes.

An East of England Ambulance spokeswoman said paramedics were called at about 18:15 BST to treat a disabled woman, aged in her early 70s, who had fallen off the platform.

She added the woman, a wheelchair user, was taken to hospital for checks and was not critically injured.

DWP Telling JCP’s Not To Refer To Foodbanks

September 5, 2013

More DWP madness. Seems it’s the day for it.

Referred to a psychologist – for wanting to record Jobcentre interviews

September 5, 2013

SKWAWKBOX's avatarSKWAWKBOX

dwpp

My series of posts about the fake psychometric ‘test’ and the DWP/Cabinet Office’s attempts to deny it, became big news earlier this year. Among the facts that the DWP denied, then admitted, then denied again and admitted again, were:

  • they were threatening jobseekers with benefit sanction if they refused to participate
  • that no qualified psychologists were involved in the decision to threaten potentially-vulnerable into becoming guinea-pigs
  • that no training was given to Jobcentre Plus (JCP) advisers in how to select people for the test beyond telling them to do it
  • that the experiment had been subjected to none of the usual validations or safeguards

and more. The whole thing stank of the contemptuous, reckless attitude of the DWP and the Cabinet Office’s ‘Nudge Unit’ toward unemployed people.

It turns out that the psychological abuse of jobseekers – and the abuse of psychology by the government – are by…

View original post 422 more words

IDS Urgent Question On Universal Credit

September 5, 2013

Boris Must Apologise For Last Leg Holocaust Comments

September 5, 2013

Proud to see The Last Leg covered by the mainstream media. What a shame about the reason for the coverage.

Coronation Street To Explore Right To Die Through Hayley Cropper’s Cancer Storyline

September 5, 2013

Spoiler alert: This story contains plot details

Coronation Street is to explore the issue of the ‘right to die’ when terminally ill Hayley Cropper decides she wants to take control of her death.

Hayley, the first transgender character in a British soap, has been diagnosed with inoperable pancreatic cancer.

The show has revealed that as her health deteriorates she will decide she wants to take her own life.

Both sides of the ‘right to die’ debate will be shown as her husband Roy is vehemently against her decision.

Coronation Street Producer Stuart Blackburn said: “This is a very sensitive issue and we will be exploring the effects of her decision on husband Roy who has a huge emotional and moral dilemma over her choice to die this way.”

Blackburn said Hayley becomes very concerned about losing control as the disease progresses.

“The palliative care Hayley receives is superb but she is scared that the pain relief can cause confusion and a loss of clarity.

“She is concerned she could regress to being Harold, she’s already had one such nightmare. She wants to die in peace with clarity of thought, she wants to die as Hayley – the identity she has spent her whole life fighting for,” he added.

It was announced in January that Julie Hesmondhalgh, who has played Hayley for 15 years, is leaving the soap at the end of the year.

She said filming the cancer storyline scenes were “hard to do” and admitted they were “going to be pretty hard to watch”.

“I feel the storyline really honours their relationship and their love story – it’s fitting and it’s proper and it’s what people are living with every single day and I think it’s important to tell those stories,” she said.

Universal Credit Is Poor Value, Says National Audit Office

September 5, 2013

Serious progress! And it’s all over the BBC too!

The government’s flagship welfare reform has been badly managed, is “overambitious” and poor value for money, the spending watchdog has said.

 

The National Audit Office said risks were taken with the universal credit to hit targets, IT systems had “limited functionality” and an unfamiliar project management approach was used.

 

A national rollout of the new benefit has been delayed following IT glitches.

 

Work and Pensions Secretary Iain Duncan Smith said these had now been fixed.

 

Mr Duncan Smith told the BBC: “This will be delivered within budget and within the timescale.”

 

He said the pilot scheme, which has begun with 1,000 people in the Manchester area, “is demonstrating that the IT we put forward for this actually works”.

 

Under the government’s plans, six key means-tested benefits – jobseeker’s allowance, employment support allowance, housing benefit, working tax credit, income support and child tax credit – are to be combined into a single payment which ministers say will ensure that claimants are always better off in work and also reduce fraud.

 

The transformation, championed by Mr Duncan Smith, requires the merging of complex computer systems in benefits offices, HM Revenue and Customs and local councils – which the government insists can be done.

 

All new claimants were supposed to receive the universal credit from next month as part of a phased implementation plan but this has been delayed following a number of pilots earlier this year.

‘Poor governance’

Instead, new claimants at six “hub job centres” in England, Wales and Scotland will receive the new benefit from October.

 

The watchdog’s report identified “early setbacks”, and says: “At this early stage of the Universal Credit programme the department has not achieved value for money.

 

“The department has delayed rolling out Universal Credit to claimants, has had weak control of the programme, and has been unable to assess the value of the systems it spent over £300 million to develop.

 

“These problems represent a significant setback to Universal Credit and raise wider concerns about the department’s ability to deal with weak programme management, over-optimistic timescales, and a lack of openness about progress.”

 

The report said there was still potential for universal credit to bring about “considerable benefits” if the department put “realistic plans and strong discipline in place”.

 

The setbacks the watchdog identified include:

 

  • Officials were “unable to explain” the reasoning behind the timescales or their feasibility
  • There were no “adequate measures” of progress
  • Computer systems lack the function to identify potentially fraudulent claims, relying instead on manual checks
  • £34m investment in IT systems has been written off
  • The Department for Work and Pensions (DWP) lacked IT expertise and senior leadership
  • Delays to the rollout will reduce the expected benefits of reform

 

Expenditure on IT systems has accounted for more than 70% of the £425m spent to date but the report suggested officials do not yet know whether the infrastructure in place will support a national rollout.

 

ORIGINAL TIMETABLE

  • From October 2013 to April 2014 about half a million new claimants were due to receive universal credit instead of jobseeker’s allowance, employment support allowance, income support, housing benefit, working tax credit and child tax credit.
  • At the same time, another half a million existing claimants and their families were due to be transferred to the new credit when their family circumstances change significantly, for instance if they get a job or have another child.
  • From April 2014 a further 3.5 million claimants and their families were due to move to universal credit.
  • And from the end of 2015 to the end of 2017 a further three million people are due to be moved over, focusing on housing benefit claimants

 

While steps were taken at the end of 2012 to get to grips with some of the problems, the watchdog said the “underlying issues” had not been addressed and there was no “detailed view” about how the system was supposed to work.

 

Amyas Morse, the head of the National Audit Office, said the “relatively high risk trajectory” was met by “weak management, ineffective control and poor governance”.

‘Missteps’

The project suffered a tragic setback earlier this year when Philip Langsdale, the DWP’s chief information officer, died four months after taking over responsibility for it.

 

The man drafted in over the summer to take over the running of universal credit has admitted there have been “missteps”.

 

“It’s clear to me there were examples of poor project management in the past, a lack of transparency where the focus was too much on what was going well and not enough on what wasn’t and with suppliers not managed as they should have been,” Howard Shiplee told the Daily Telegraph – while claiming things had been “put right”.

 

“I’m not in the business of making excuses, and I think it’s always important to acknowledge in any project where things may have gone wrong in order to ensure we learn as we go forward,” the former London 2012 executive added.

 

Labour accused ministers of trying to cover up a “Titanic-sized IT disaster” while trade unions said the watchdog’s report was a “damning indictment” of the state of the project.

 

“Mr Duncan Smith swore blind this benefit shake-up was fine,” said Labour’s welfare spokesman Liam Byrne. “Now we learn he has completely lost control of his department at a potential cost of hundreds of millions of pounds.

 

“The Conservatives welfare revolution has now finally collapsed. It is now mission-critical that David Cameron and Iain Duncan Smith swallow their pride and agree to the cross-party talks we proposed in the summer. We cannot risk another day.”

‘Medical Cannabis’ Campaigner Jenny Kush Killed By Drunk Driver

September 5, 2013

I thought this might interest those of you interested in the legalisation of cannabis for medical use. I don’t know how big this issue is in the UK, but it seems Jenny Kush was well known in America.