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how are you in helping me reach my goal of raising money for my diary and respite care thank you for donating to my Coser that is the date and continue if you wish to here is a picture of the title that we have raised to die alone

February 23, 2023

total black people have been kind enough for the night today love you keep on going you are helping me reach my goal, £1 at a time

total giving page thank you to all those were kind enough to donate to support me. Tease my girls, any other followers that wish to turn also go to my fundraising link on just giving it is in “a view of my previous page I will also put it back on again in the morning so if you want and also find it on my post first thing in the morning tomorrow thank you

thank you to the community for those of you that bon appetit thank you so much pain breathing. Every is still ongoing so feel free to donate if you wish to steal thank you to liberty the chose to do the only evening/afternoon because it means a lot to me and my family means that I will be able to complete my TV and also so so thank you to everybody that I’ve downloaded so far and I appreciate your contributions faces, a screenshot of so that you know what you have helped me week and haven’t, how much of an impact on what you will have on my family/friends participation ❤️to my iPhone

February 23, 2023

⭐️🏁⭐️⭐️🏁

Enjoying some singing fun with my choir this afternoon before going to the library to print off some paperwork. having a lovely lunch in the satellite cafe at trestle ♥️

February 23, 2023

https://vm.tiktok.com/ZMYArSX3C/

🎼❤️

February 23, 2023

Social Care Costs See Thousands Chased For Debt

February 23, 2023

More than 60,000 adults with disabilities and long-term illnesses in England were chased for debts by councils last year after failing to pay for their social care support at home.

Claimants told the BBC they can’t afford the charges amid rising food and rent prices, along with the additional costs of living with disabilities.

Councils took legal action against 330 people in 2021-22.

The Local Government Association said such action was a “last option”.

Councils ask social care recipients to contribute towards the home care they receive in nearly all areas of England, but previous BBC research found charges had risen by thousands of pounds a year for some adults.

Some disabled people have now told the BBC they felt they had little choice but to live without home care, while others said they feared bailiffs being called in over unpaid debts.

Campaign group Disabled People Against Cuts said the charges were discriminatory, leaving disabled people “to live on very, very little money”.

It said financial assessments were too often rushed by stretched local authorities, and they had sometimes not been updated to include recent hikes in energy bills and rent.

In many cases, the campaign group said councils also failed to account for all the additional expenses disabled people face in maintaining their health and wellbeing, such as accessible transport, adapted clothing or special dietary requirements.

Only people who have the highest need for help, and savings or assets of less than £23,250, are eligible for council-subsidised care in England.

Paula Robinson, from Greater Manchester, says she was “shocked and distraught” to receive a letter from her council warning of potential legal action, even while she was appealing against the increased charges that drove her into £3,000 of debt.

She has ME – also known as chronic fatigue syndrome – and an endocrine disorder, and says the stress of the debt led her to question whether “life’s worth living”.

The amount the council charged for her social care package – including visits from carers who prepared meals and helped with bathing – had risen by more than £4,000 a year, from £10 a week to £93 a week.

Paula lives on benefits and says the increased charges “wiped out” her ability to pay for vitamins and physiotherapy that help ease her ME.

Eventually, the council cancelled the £3,000 debt.

But, still facing the higher charges of £93 a week, Paula decided to decline any further social care and now lives without home support.

She said this has led to a deterioration in her physical health.

“I can’t even have family to visit sometimes, because I’m too ill,” she said

Rochdale Borough Council said it uses full financial assessments to ensure payments are fair, and takes a “sensitive, case-by-case approach” to recovering debt.

Data from 79 of 152 local authorities in England – obtained by the BBC through Freedom of Information requests – shows that councils began more than 60,000 debt collection procedures against social care claimants living in the community in 2021-22.

One of those worrying about enforcement action is Julia, who has severe mobility issues and a rare skin condition, and receives 13 hours of support each week at her home in St Leonards-on-Sea.

Julia, who lives on benefits, says she is unable to afford the charges of more than £58 a week, and was taken to court last year by her local authority for a debt of £4,700.

She is now fearful that bailiffs will be used against her.

“I’m always trying to be positive, but the fight is wearing me out and making me more ill,” she said.

East Sussex County Council said the debt recovery process “will only ever begin after extensive discussions and assessments”.

Campaigner Rick Burgess, from Disabled People Against Cuts, is now calling for all councils to update claimants’ assessment to reflect the rising cost of living, and to put in place better support for those struggling with repayments.

Councillor David Fothergill of the Local Government Association, which represents councils in England, told the BBC rising demand and squeezed budgets meant councils had to collect money owed, but that legal action was a last resort.

“What councils should be doing, and I think the vast majority of councils do in the vast majority of cases, is they work with residents to find a solution [for how the debt can be settled].”

The Department of Health and Social Care said regulations ensured local authorities leave claimants with a set amount of money to live off once their social care charges have been paid – known as the “minimum income guarantee”.

The amount changes to meet different people’s circumstances. Single claimants over the state pension age currently have a protected income of £194.70 a week.

Approaches to social care charging differ across Scotland, Wales and Northern Ireland, where expected contributions are lower than in most councils in England.

my love, scrapbook, pages Fortnite, happy scrapbook Wednesday everybody. Hope you enjoyed whatever you did this Wednesday

February 22, 2023













					

phone my Wednesday night scrapbooking

February 22, 2023

can you make them look perfect perfect

February 22, 2023

The pages of the scrapbook with you I have managed to finish this

so proud of and her right hand out just perfect really good camera doesn’t do it justice but I love it. Remember Todo mate if you can afford to do my crowdfunding paid for my support for DNA thank you

My day in the life with Cerebral Palsy using TikTok👩🏾‍🦽

February 22, 2023

https://vm.tiktok.com/ZMYSsREQ1/

Link to my Fundraiser: https://www.justgiving.com/crowdfunding/maya-richards

Please share and view this video to get it on people’s For You pages ❤️ please also donate to appreciate this video if you can afford to. Every little helps ❤️

Energy Firms Told To Pay Out Over Forced Meter Fittings

February 22, 2023

    Energy firms should start compensating customers whose homes were wrongfully fitted with a prepayment meter, without waiting for the results of a major review, the regulator has said.

    Ofgem chief executive Jonathan Brearley said companies must review their own meter installations immediately.

    A six-week pause in forced prepayment fittings lasts until the end of March.

    It came after debt agents for British Gas broke into vulnerable people’s homes to force-fit meters.

    Ofgem is now outlining the terms of its review into the rules, regulations and guidance surrounding prepayment meters.

    The investigation – which will be complete by the end of March – will include submissions from the public. Information about how customers can offer details of their experiences will be announced soon.

    ‘Fix it now’

    Mr Brearley said any systematic problems would lead to fines for suppliers but he said the regulator had been clear to companies about the rules – and rejected the accusation that Ofgem had been too slow on the issue.

    “If companies know they inappropriately installed a prepayment meter, then they should fix it now,” he told BBC Radio 4’s Today programme.

    He said this meant switching the meter back to a regular one, if that was what the customer wanted, and giving compensation.

    Ofgem cannot order companies to do so until its review is complete, but Mr Brearley said companies would know quickly when there were clear issues to settle.

    The regulator will also conduct a targeted investigation into the actions of British Gas, specifically about whether it followed the rules under its licence to support customers in debt before force-fitting prepayment meters.

    Mr Brearley said that “clearly something has gone wrong” at British Gas and that the investigation would be independent and wide-ranging.

    An investigation by The Times newspaper found debt agents working for British Gas expressed excitement at putting prepayment meters into the homes of vulnerable people behind on bills.

    Prepayment meter customers top-up their meter with credit, which then runs down as they use energy at home.

    Charities and campaigners say many have been left unable to afford to put money into their meters owing to soaring energy prices and other cost-of-living pressures.

    However, the trade association for suppliers – Energy UK – has regularly highlighted that suppliers can be left with unpaid debts from customers who do not pay their regular bills.

    Without the option of moving people onto prepayment meters, these mounting debts would have to be recovered from everyone else’s bills.

    “Suppliers have already paused prepayment installations by warrant in order to carry out reviews of their own practices and they will look to put things right if they find cases where prepayment meters have been installed inappropriately,” the trade body said in response to Ofgem’s announcement.

    “The industry has already been talking to Ofgem and the government about how best we can support the most vulnerable customers going forward, including the role a social tariff could potentially play, which needs to be part of the discussion around the use of prepayment meters.”

    There are more than four million UK households on prepayment meters.

    In March last year, 29-year-old Caroline Pugh bought a house in Seaton Carew near Hartlepool.

    During its renovation in August, while Caroline was living elsewhere, her property was broken into and her locks were changed.

    The first she knew about it was when her parents spotted yellow and black tape stuck to her front door.

    “They went in to fit two meters without me knowing. I had to go around and actually sit in my car outside the house and wait for the locksmiths to come and give me my new keys,” she said.

    “It was horrific, I don’t get how people can do something like that. I was shocked.”

    According to Ms Pugh, her provider – Scottish Power – said the meters had been fitted because the previous owner was in debt.

    “There were loads of letters addressed to him. But it’s against the law to open other people’s letters so I returned to the sender and that’s it. I didn’t know anything about the debt,” she said.

    “There’s one [meter] under the stairs, it takes up quite a lot of space, and another above the door as you walk in.

    “I asked them to change the meters back but they said they wouldn’t. To get it done I’d be charged hundreds of pounds. I’m a single mother doing up a house, I don’t have the money for that,” she said.

    A Scottish Power spokesperson said: “We’re sorry for the issues experienced by Ms Pugh. We were only informed in August 2022 – after the prepayment meters had been installed – that she had purchased the property in March, so all bills issued to that point had been sent to the previous owner.

    “As she has smart meters, there’s no need to change her meters in order to change her payment method. We will contact her directly to discuss this and apologise that she wasn’t advised of this at the time.”

    New deals

    Domestic energy bills are set to rise in April, although the government is under pressure to extend support for households.

    Analysts at consultancy firm Cornwall Insight said predictions of falling prices later in the year could lead to “the return of competitive tariffs”, and with it the chance for consumers to “take back some control over their energy bills”.

    But Mr Brearley urged people to take care when deciding whether to sign up to new fixed deals in the summer.

    He said customers should “do your homework” over how prices might change in the future before making a decision.

    my friend Reidi paid for anybody that didn’t get to see it in previous parts as it is still ongoing. Stay tuned to see the next training day for the qualification on Sunday.

    February 21, 2023

    call fundraisinghttps://www.justgiving.com/crowdfunding/maya-richards?utm_term=pRB8PDmDD page

    and has a lovely length and 6 feet and whatever they’re going to give up for the length period happy lent everybody has that starts tomorrow

    February 21, 2023

    hi I hope everybody had a good pancake day

    more pictures of the phone I had today at the pancake, place to celebrate Shrove Tuesday

    February 21, 2023

    Peugeot price 20,23

    February 21, 2023

    phone Kai, Riley photo

    February 21, 2023

    Autism: How My Autistic Foster Brother Inspired My Life’s Work

    February 21, 2023

      A woman who passed up going to university to care for her autistic foster brother has described how he inspired her to set up her own behavioural therapy centre.

      Risca Solomon, from Haverfordwest, Pembrokeshire, first met Dan when he was four years old.

      His previous respite placements had broken down due to his challenging behaviour.

      But Ms Solomon, whose parents were foster carers, wanted to help.

      “When I first met Dan I was 18 and on work experience at a special school, and he touched my heart,” Ms Solomon said.

      “I begged my parents, who’d been foster and respite carers since I was 11, to step in.”

      Her parents were reluctant at first due to the level of care Dan would need, something they felt was beyond their level of experience and expertise.

      But they agreed after Ms Solomon promised to be one of his primary care givers.

      “It changed my life,” Ms Solomon said.

      “Instead of going away to study, I enrolled on an Open University course so I could still be around to help out with Dan.

      “I started to look into behaviour analysis, and once I saw the beneficial effects it was having on him I knew I had to spread the word.”

      Behaviour analysis focuses on understanding why people behave the way they do and how behaviours can be changed.

      Ms Solomon said when Dan first came to live with them, his behaviour could be challenging.

      “It was hard not to take it personally; we were providing all this love and care, but it was difficult for us,” she said.

      “But as time went on we learned his trigger actions and showed him there was a simpler way to get what he needed.”

      Part of the therapy involves de-sensitising the trigger points which can provoke challenging behaviour.

      Autistic young people can be hyper-sensitive to noise and light, but by making environments calmer symptoms can be reduced.

      Within a month of living with Ms Solomon and her parents, Dan was able to use sign language to communicate.

      Ms Solomon then helped Dan to learn how to talk.

      “We knew he wanted to talk, he was making some noises, and trying to mimic what we were doing,” Ms Solomon explained.

      “The more I got to know him, the more I realised that it wasn’t a developmental issue, he simply didn’t know how to manipulate his mouth into the shapes required for speech.”

      After studying a masters degree in challenging behaviour at Cardiff University, Ms Solomon tried using Applied Behaviour Analysis (ABA) to teach Dan to speak.

      After finding the right combination of techniques, Dan began to develop speech.

      Documenting Dan’s progress on YouTube, Ms Solomon started getting requests from other families for support.

      At the time, she was preparing to sit a behaviour analyst exam and was then able to create her own therapy company, Skybound.

      Alongside 38 staff members, Ms Solomon now delivers therapy and care to those who need it.

      “We use a system called talk tools, a series of plastic mouthpieces which help to shape the lips and tongue into the position to make the sounds needed for speech”, she said.

      ABA is considered by some people to be a controversial method of treatment, which the National Autism Society has described as polarising.

      But Ms Solomon said it is all about how it is taught.

      “I wouldn’t ask any of our clients to do anything I wouldn’t do myself. I put the pieces into my mouth and show them the shapes they’re creating.

      “We then look for signs of consent for us to help them with the tools.

      “It’s purely based on consent, and for many it’s their favourite part of the therapy; they try to hurry us along to the point at which we get the talk tools out.”

      The National Autism Society’s website acknowledges that some believe ABA has developed considerably and that it can help people to develop vital life skills and stay safe.

      But it points out that some remain fundamentally opposed to ABA.

      Ms Solomon said for the people she works with, “what is a good outcome entirely depends on where we’re starting from.

      “On one end of the scale is a young girl who can use a switch with her head to attract attention, because she loves music, and when she hit the switch she heard a pop song.

      “On the other are lads who are very chatty but whose diets are so severely limited that they were in danger of needing to become tube-fed.

      “We were able to desensitise their food phobia to the extent that they were making their own sandwiches and eating all sorts of things they’d never even tried before.”

      Skybound is now attempting to open a new residential centre to educate clients alongside their families.

      Meanwhile Dan lives two days a week with Risca, her husband and their two young children, and spends the rest of the week with Risca’s parents.

      Holy September at five for a plan to study the level three extended diploma in health and social care just waiting for an interview. Hopefully I will start studying it after the summer. Just waiting to hear about when the interview will be

      February 20, 2023

      Cake flavours, pancake flavours would you create if you could wait for you to die coming out by which direction did why no one with chocolate and vanilla so I would love to know what play with you with create and what hoping you would have on your pancakes please switch this means Easter isn’t that far round the corner, trying to spoil of pills with chocolate on trove Tuesday and then look forward to all our lease rates and Easter bunny chocolate

      February 20, 2023

      happy pancake day to everybody for tomorrow as I will be taking part in a pancake rice so you will see pancake content as well as some rice content tomorrow. I would love to hear what you’re giving up for happy pancake, day thing difference

      February 20, 2023

      Disabled Doctor Felt Shunned By Hospitals In Wales

      February 20, 2023

        Hospitals in Wales “didn’t want to know” about the additional needs of disabled staff, according to a doctor who was looking for work after being paralysed in a car crash.

        “They wanted someone that could easily and quickly fill the post without them having to do anything,” Dr Georgina Budd who qualified as an A&E medic.

        She ended up becoming a GP at a surgery that could accommodate her needs.

        Health boards said they were committed to creating inclusive environments.

        “There shouldn’t be a limit because of my disability,” said Dr Budd, known as Georgie, who spent three years as a clinical fellow in the A&E department at Glangwili Hospital in Carmarthenshire as part of her medical training.

        “I’ve been in situations where I’ve had to deal with a medical emergency and I’m no less effective for being in the wheelchair.”

        But when the time came to find a full-time job, she said she faced barriers.

        “I’ve had colleagues say: ‘You’re going to need to think about your career and how you tailor it to your disability’,” said Georgie.

        “I shouldn’t have to. I should be able to work in the specialty that I want to.”

        Georgie said for one job application, a hospital asked her to do an unpaid “trial shift”.

        “It was all dressed up in language of ‘so we can see how we can help you’,” she said.

        “What really came across was ‘so we can see how many adjustments you would need so we can see if it’s financially viable for us to change things around for you’.”

        She added: “You would think that hospitals are set up for disabled people because they are a big part of our service, but they’re not.”

        Most hospital cupboards are out of a reach for a wheelchair user, she explained, and some buildings were still inaccessible.

        “Life has been built around able-bodied people. It is not built for me and it’s not built for the rest of the disabled community,” she said.

        Working hours is another barrier.

        “It does take me a longer time to get ready and out of the house in the mornings,” she said.

        “Without getting up at a ridiculous hour, I might not be able to be on shift at 08:00 like some doctors.

        “That was a problem at first because ward rounds happen in the morning.

        “We are looking for reasonable adjustments, but it’s very difficult to get those changes made and to get people thinking differently about disability and about a disabled doctor.”

        Originally from Downton in Wiltshire, Georgie started at Cardiff Medical School in 2009.

        On her way to a shift at Glangwili Hospital in 2017, she lost control after a tyre on her car punctured. To avoid oncoming traffic, she swerved into a poll at 50mph (80km/h).

        At the age of 30 she was paralysed from the waist down and she thought her career was over.

        But she fought to complete her doctor training.

        “It is not the end of the world. It’s hard and there are challenges, but I kept telling myself ‘my life isn’t over’,” she said.

        She recalled her first time seeing a patient as a doctor in wheelchair: “She looked at me and… was like, ‘oh, hello, love. Are you one of the patients?’

        “‘No, I’m your doctor today’.”

        Georgie completed her doctor training at Glangwili Hospital in August, but after failing to find a job she changed her specialty and is now a general practice trainee.

        Working as a GP at Tŷ Calon Lân surgery in Mountain Ash, Rhondda Cynon Taf, means more sociable hours and more flexibility.

        Her typical day starts with a carer coming to her home in Merthyr Tydfil at around 08:00.

        “I could probably just about do it myself… but I was slipping because I was so exhausted,” she said.

        “Having [a carer] in just sort of makes the morning run smoother, allowing me to conserve my energy and put it into things that I really want to do.”

        She is co-chairwoman for junior doctors at the British Medical Association in Wales, and is currently doing research with Swansea University on the mental health needs of medical students.

        “GP gives me the opportunity to be more active in medical politics and in research and still see my patients and have a good impact on them,” she said.

        She said it also gives her time to advocate for disabled people, including as chairwoman trustee at Adapt Gateway, a mentoring and support charity for people with disabilities.

        “In an ideal world any child that wanted to grow up to be a doctor and had a disability wouldn’t feel that’s off limits to them,” she said.

        That would require a “perspective change in society” she said.

        “It’s understanding that disability isn’t inability,” she said. “Being in a wheelchair doesn’t limit my ability as a doctor.”

        She said she wants to see full accessibility as the standard in all health buildings so no-one feels left out.

        “I want more disabled kids to know that this kind of opportunity is open to them,” she said.

        “That it doesn’t matter if their legs don’t work. I know a consultant who’s got one arm… he still takes blood and is an effective doctor and why shouldn’t he be?”

        “A lot of what a doctor does is up here,” she added, touching her temple.

        “I’ve put chest drains in, I’ve sutured people… all kinds of crazy stuff.

        “I adapt it for me but I can still do it. It’s just doing it a different way.”

        Georgie spent months in hospital recovering from her accident, an experience she said gives her more empathy for her patients.

        “I think that knowledge is something that can really help the medical community,” she said.

        “Having more doctors that have gone through poor health experiences, chronic illness, disability is important to widening doctors’ understanding of what their patients are going through.”

        She said more understanding of disability was needed in society more generally, recalling upsetting comments she overheard after her friends had to carry her into a non-accessible café.

        “We were sat there and this young woman said really loudly: ‘Why would she even come here, it’s clearly not disabled accessible. Does she not realise that she’s just a nuisance’.”

        Comments like that could be “hard”, Georgie admitted, but said they made her more determined to “normalise” disability.

        “I can spend the next 60 years miserable because I can’t stand up, or I can do something about this,” she said.

        Several health boards in Wales said they follow an all-Wales recruitment process designed to ensure “fair and equal opportunities for all” and that disabled candidates who meet the minimum standard were guaranteed an interview.

        “Only when shortlisting is complete will a candidate’s self-declaration [of a disability] be visible, alerting the appointing manager that reasonable adjustments may be required,” said Lisa Gostling, from Hywel Dda health board.

        Aneurin Bevan health board said it offered disabled staff access to work assessments, aiming to “create an inclusive environment for our staff and patients”.

        Powys health board said “tailored adjustments will be made, where possible, to roles and/or workplaces through discussion between the manager and the employee”.

        Betsi Cadwaladr heath board said it “welcomes applications from individuals with disabilities and value all staff”.

        A Welsh government spokesperson said it expected “all NHS organisations to comply with the Equality Act 2010, and to follow best practice regarding the recruitment and retention of staff”.

        if you would like to merge of giving page over update, but you can read and donate if you want to it’s not that about emoji retraining which I completed that I feel you might be interested in as my if you like this update on the go for me I will do another one on Sunday when I go so let me know what you think of it. Happy Sunday evening everybody

        February 19, 2023

        staging with my pancake, race, content on Tuesday

        February 19, 2023

        happy Sunday same difference

        please is it open to open this museum PCV exhibition, which I am proudly a part of along with some of my friends who were part of it with me. Hopefully changes attitudes towards people that she’s mobility aids to have a different way of learning.

        February 19, 2023

        Picture of me, giving instructions to the participants of the workshop that we ran at the opening of the exhibition today without trying to be so bossy you laugh out loud, as I am normally quite bossy in my life I really enjoyed this, and this is going to be one of my newest favourite volunteer jobs I think because I learn the skills in a previous workshop for prom to do this piece about now. I am able to share my knowledge with other participants at the community events that we hope

        February 18, 2023

        read my story on the just giving link, and donate if you are willing and able :-) as I appreciate every penny, this is donated to help me reach my goal of succeeding at the very end of the respite parachutes, which I am planning, but the priority being DNA, thank you

        February 18, 2023

        some of you might have already seen me that I am on the link. Only again in Kai umbilical may have missed it the other day.

        my diaper me the link https://www.justgiving.com/crowdfunding/maya-richards?utm_term=EAdJga3G8 please donate if you are willing and able, thanks my

        pictures of me at my volunteering job doing art work demonstrations this afternoon more pictures of what I did today are going to follow tomorrow in tomorrow’s house. Hope you enjoy seeing what I get up to in one my volunteer jobs that are enjoy committing to

        February 18, 2023

        Picture of my example of the art, which I was demonstrating how they could mix colours to make this desired outcome

        February 18, 2023

        could you please close the program which I was demonstrated metres in my brother is here well today how to do the part that we set up for the event

        opening the event with Samantha for 1 1/4 Ward, Wikipedia exhibition who is a picture of me already there exhibition

        February 18, 2023

        I’m going to be a speaker

        volunteer speaker see all about exhibition event

        
        
        
        
        
        					

        Mattresses and pillows that are white call Cameron appropriate for changing weather. Also let me know about this nice tumour and then the other recommendations. Paul company mattresses/beds that are accessible using Zimmer frame and Lesley. Better acceptable, using Zimmer frame or other mobility aids. Thank you and good night from Maya

        February 17, 2023

        and mattresses and pillows. Thank you

        Does anybody know of any good camping beds? Let me know. Thank you Maya

        February 17, 2023

        And took from the course today, so getting to know you in the videos that I wouldn’t otherwise me problem-solving and a challenge and learning how to solve them issues and spending time outside

        February 17, 2023

        what I learnt on my training on the map on the path and Little Streets. We also demonstrated a lot of the rescue/safety equipment and advice what we would need in our path and what was essential and work with optional I enjoy meeting everybody that was there for my DNA safety scales, map, navigation skills, identifying reference points on the Nepal and Learning how to lead other young people along with a minute learning how to take the lead politely, but is 30th of May in a bowl to retrieve it together

        February 17, 2023

        Here is my JustGiving page with an update of how todays training for DofE went, and explaining what your donations will mean for my future ❤️ please read and donate if possible, if not just share and like this link for awareness of the cause!

        February 17, 2023

        https://www.justgiving.com/crowdfunding/maya-richards#cb=f3e51fbdbc72dd4&domain=www.justgiving.com&is_canvas=false&origin=https%3A%2F%2Fwww.justgiving.com%2Ff16857c9b3fe95&relation=opener&frame=f2e4153ebeed402&result=%5B%5D&e2e=%7B%7D

        first day of training for my practical section of DofE, including trying out my new borrowed all-terrain wheelchair kindly donated from my friend who I grew up with in school. How kind of you thank you ❤️

        February 17, 2023

        Ambulance Waits Putting Disabled Children’s Lives At Risk, Doctors Warn

        February 17, 2023

          Thousands of severely disabled children’s lives are at risk because of long waits for ambulances, doctors and other experts have warned.

          Emergency care is a vital part of their everyday lives, the British Academy of Childhood Disability says.

          They often rely on ambulances as part of their healthcare plan, because their condition can become life-threatening in an instant.

          The government says it is taking action to address ambulance delays.

          ‘High-dependency units’

          Almost 100,000 children have life-limiting conditions or need regular ventilator support in the UK.

          Dr Toni Wolff, who chairs the British Academy of Childhood Disability, told BBC News some families with severely disabled children had “what are essentially high-dependency units” of medical equipment at home.

          “As part of their healthcare plan, we would normally say, ‘If the child starts to deteriorate, call for an ambulance and it will be there within 10 or 20 minutes,'” she said.

          “Now, we can’t give that reassurance.”

          Despite their child being classed as a priority, parents have told BBC News they face the difficult decision to wait for an ambulance or take them, often in a life-threatening condition, to hospital themselves – a risk because of the huge amounts of equipment needed to keep them alive,

          Patients with emergencies such as heart attacks and strokes waited 90 minutes on average for an ambulance in December.

          In January, this dropped to 32 minutes – but the target is 18.

          Brain damage

          Twins Emily and Christopher, 12, enjoy rock music, seeing their friends at school and laughing at television programmes such as You’ve Been Framed.

          They also rely on a vast array of machinery, such as ventilators, suction equipment and oxygen tanks, to stay alive.

          Born three and a half months early, they have brain damage and a number of complex conditions.

          Christopher has a tracheotomy and Emily needs constant supervision because of severe choking issues.

          “We can’t leave them longer than it takes to take one breath,” their father, Paul, says from their specially adapted home, in a small village just outside Newcastle.

          “If Christopher’s breathing tube blocks, then he could be dead within minutes.”

          Paul and their mother, Claire, have been medically trained to look after the twins at home but their expertise goes only so far.

          Just before Christmas, Christopher became very poorly with several infections. His breathing tube became congested. They changed it and increased his oxygen but his condition continued to worsen.

          “We couldn’t resolve it at home,” Paul says, “so we had to call for an ambulance. He was struggling to breathe and he was having uncontrollable shaking, where he couldn’t control his limbs.”

          Christopher’s condition was life threatening – it was a category-one emergency, which means an ambulance should aim to arrive within seven minutes – but they were told there could be a three-hour wait.

          “It was terrifying,” Claire says, “Our skillset is only up to a certain level – we aren’t doctors and nurses. At times when we can’t sort it, we need quick access to A&E – that access is what keeps Emily and Christopher alive.”

          After 20 minutes of waiting, and with Christopher continuing to deteriorate, they decided to attempt the journey to the Royal Victoria Infirmary.

          But when they called to cancel the ambulance, the call handler told them they had managed to divert one to their house.

          It took Christopher to the hospital’s accident-and-emergency department, where a resuscitation team was waiting – and after an hour of intense treatment, he survived.

          The North East Ambulance service said it understood delays put patients at risk and had declared two critical incidents because of the “unprecedented pressures” in December.

          But Paul and Claire still carry the trauma of that night.

          “We need emergency care to work – it is vital. Without it, our world would start to shrink,” Paul says.

          “We would need to stay at home, where all our equipment is. We can’t take everything when we are out and about. The children would lose their independence and they’re more at risk of losing their lives.”

          ‘Immediate action’

          Disabled people are far more likely to need emergency care.

          Census figures show 17.7% of people in England have a disability – but the latest Care Quality Commission survey suggests 46% of those who responded after attending A&E were disabled.

          And the Royal College of Emergency Medicine admits the system often fails to meet their needs.

          Its president, Dr Adrian Boyle said: “They are particularly disadvantaged when it comes to emergency care, partly because departments are so full and the hospitals are so full that they’re ending up having to wait a lot longer in areas which are not well designed for them.

          “We’re looking after people in corridors and we’re looking after people in inappropriate clinical areas. And that can’t be good for somebody who comes in with a lot of equipment or has complex needs.”

          An spokesman said the Department of Health and Social Care was taking “immediate action” to reduce the long waits by boosting capacity, with 5,000 more beds and 800 new ambulances, and reforms due to be announced over the next few months would help disabled people “live more independently”.

          fund-raising effort, and the link to donate if you want t https://www.justgiving.com/crowdfunding/maya-richards?utm_term=6pz3rdVJd

          February 16, 2023

          pictures of some of my favourite exhibit that I was part of and was destroyed house tour during this unusual, but oh well honest, educating four members of the community, including the mayor of my local town desert

          February 16, 2023

          courtesy of the event I attended tonight to see some of my are displayed and some we didn’t have a great day. I’ll speak to you again please enjoy the photos of me at the drinks reception. I met some lovely people and had some lovely conversation

          February 16, 2023
          
          
          
          
          

          Photos of me at the drink with

          me enjoying the event with some of the participant, and other staff and coordinators from trestle theatre, and other community group that I am either in or have been involved in for the projects in the past including some of my scrapbook work in exhibition and showcased as an exhibit Pictures of me enjoying the event with some of the participant stuff and coordinators

          February 16, 2023

          let people with cerebral palsy and Gaza reflex/disability is there potential and get involved in the community, who is just like me because they do have a potential just right potential is very different for everybody but we all have potential

          February 16, 2023

          my sincere bully people who have disabilities should have the same patient of themselves Valley able-bodied person

          all about her celebration event, pictures of me, already to celebrate the all about a project with other service users and participants of charities all over Hertfordshire and the surrounding areas celebrating all achievements or goals Andorra campaigning for a more inclusive world for those with disabilities, and

          February 16, 2023

          all about us

          Celebrating people with learning disabilities, and my talent threw up and other forms of media, including recordings et cetera visitors to the museum. How do I listen to I will post a picture of me I will post a picture of me dressed up later this evening for you all for you all to see

          February 16, 2023

          Tycoon little celebration, event and content related to it later this evening and tomorrow

          progress on my next qualification DOB. I am going on training this Friday and then we’ll go for the qualifying and practice expedition in the summer for a little bit of summer camping plus mapreading press compass direction in really excited to go to the next level of the DMV🥰😇

          February 16, 2023

          fundraising efforts and progress that I have made with it. I have made £40 of £1000 go so far managed to save a lot more ♥️♥️❤️

          February 16, 2023

          Accessible Afternoons

          February 16, 2023
          A press release:
          PR Header.jpg

          Accessible Afternoons

          The National Space Centre is extending its opening hours and working with local groups to make the exhibition, planetarium and hands on activities event more accessible to children, families and adults who would appreciate a little bit more space to be themselves.

          Accessible Afternoons are on offer for SEN/SEND community, and those with Autisum, ADHD and any Spectrum Disorders looking for a safe space to enjoy a day out on their terms.

          00-NSC-Marketing-Web-AccessibleAfternoon-VisitLeicesterAd-2023.jpg

          Noise is restricted, doors are open, lights are on and the team are on hand to support all visitors in enjoying their experience of the National Space Centre.

          From wide car parking spaces close to the building, an entrance ramp with a gentle incline, accessible and Changing Places toilets, wheelchair loan, sensory backpack loan, Makaton trained staff, large lifts to all floors of the exhibition, to the addition of new activities specifically developed to support sensory learning, and restricted capacity to allow for lots of safe spaces to explore, Accessible Afternoons prove #SpaceForEveryone is the charities true ethos.

          Charlie Isham, Education and Space Communication Manager at the National Space Centre, said; “Working with professionals, we feel empowered to offer something we feel passionately about, a true space for everyone. We have spoken with hundreds of parents for their help and advice, and, although we know every child and adult is different, we have created a safe, fun and educational space that we can continue to develop as we host multiple sessions throughout the year.”

          The next Accessible Afternoon is on 20 March, with a further afternoon planned on 26 June. For more information and to buy tickets please visit the Accessible Afternoons webpage.

          I’m having a meaningful purpose in society as a disabled adult who is 23 years of age. This is my purpose.

          February 15, 2023

          join me as I help open the art exhibition and see how much tai chi when interacting with visitors customers and staff who work at the Museum as well as making sure that it’s how Prezzo Pizza Hut today which do you have it set up yes I am disabled but yeah I can make appointment wit

          I definitely love, super love the fact that I will have an open tuner to eat in this exhibition to share my heart, along with other young people with physical and learning disabilities to the community of St Albans and the community of Hertfordshire, as well as any tourists decide to visit an open museum , I will always be proud of my scrapbook that is part of the expedition and will display it proudly along with the rest of the press okay and the other participants out

          February 15, 2023

          on Saturday or Sunday

          donations, appreciated. Thanks, saying Jay Prince, community, family and society.

          February 15, 2023

          Play the Stone, Cherry Coke whore Prince to find my friend rising effort there and the pages to donate to you. Can you wish to MK 42

          AP Photos for Thursday night

          February 15, 2023

          Thursday night, Salpi

          £45 raised as a result of my fundraising ideas if anybody wants to download movies on the fundraising section of saying different thank you Maya, every donation is very much my friend, Reidi pages when they were perfect, appreciated by me

          February 15, 2023

          fundraising and program

          no considering mobility aid members of the community and pedestrians with walking issues rose with payment or assistance. Dogs consider the members of your community.

          February 15, 2023

          Low power mode, inconsiderately call my ability I use it

          A bundle of cuteness factor naughty one at that

          February 15, 2023

          more pictures of baby boy

          Charlie, watching Grandad, cook dinner and wondering when his is going to be served

          February 15, 2023

          I hope you all enjoyed celebrating and giving to whoever is special to you 🫶🏼🫶🏼❤️❤️♥️ I also hope that you all receive the gift that you wanted and enjoy it snow this Valentine’s Day week. Happy Valentine’s Day to all in the same different community from Maya.

          February 15, 2023

          Valentine’s Day week saying different

          encouraging inclusion by the all about as a festival and showing that people can be included in societal daily living will take pictures of my art on this Friday when I go there on Thursday and Saturday to participate in the project

          February 15, 2023

          all about us our celebration evening tomorrow to celebrate the art of people with learning disabilities in Hertfordshire and the surrounding areas, including my scrapbook set of memories from my child and adult as well as pictures of me when I was a teenager participating in school

          King, Charles spaniel, Charlie ❤️🫶🏼😘

          February 15, 2023

          visiting my grandmas, no chlorine this Thursday night and Wednesday night before going on training on Friday and doing the rest of my all about us projects with Tressel

          Disabled Woman Made 1,000 Calls For Ed Sheeran Tickets

          February 15, 2023
           

          Kat Watkins is a woman who likes to live life to the full.

          She’s visiting South Africa in the spring, then it’s France for the Rugby World Cup, where she hopes to see Wales in the final, having bought a ticket.

          Kat also travels around the UK from her Swansea home to the theatre, museums, spas and concerts.

          But as she is a wheelchair user, Kat can’t get tickets by clicking a website link like most people – watching Ed Sheeran took 1,000 phone calls.

          Because she needs a personal assistant to accompany her, Kat, like other disabled people, generally has to ring up ticket offices.

          This means being restricted to office hours only – trickier if you work full-time – and having to get through phone systems.

          This hasn’t dampened her love of watching concerts, with Kat having seen Take That six times, as well as Westlife and JLS.

          While she praises Cardiff’s Principality Stadium for offering accessible tickets for Ed Sheeran’s mega-concerts without having to provide proof of disability, getting hold of them was another matter.

          “I would ring, get ‘beep, beep, beep’, hang up – and it took 1,000 attempts,” she said.

          “And then when I got through to the wait, it was another 40 minutes. And luckily there were tickets left.”

          Kat did manage to get tickets to Tom Jones and Stereophonics quicker, but was again frustrated she could not simply book online.

          The Principality Stadium said it currently dealt with tickets via the phone to understand customers’ needs, but added it was planning on moving the purchase of accessibility tickets online.

          When Kat visited the O2 arena in London to watch Take That’s Mark Owen, she had to send her personal independence payment award through to prove her entitlement.

          This is a common procedure, but requires people to do it repeatedly for different events.

          Wales has made some progress in trying to ease the process, with the Arts Council of Wales establishing the Hynt scheme which offers people with disabilities a card showing their entitlement to carer tickets.

          They only have to provide proof once when first applying.

          Kat said it has removed a lot of the bureaucracy involved in getting tickets.

          However, even with the card, it doesn’t automatically give people the opportunity to book online at many of the venues.

          An exception is Cardiff’s Wales Millennium Centre – once a person registers the card, all they have to do is sign in online to be offered wheelchair or regular seats with a free companion ticket.
          Tale of two clubs

          At the two biggest football clubs in Wales, Cardiff and Swansea, the contrast is marked.

          Cardiff City’s Disabled Supporters Association (DSA) has been in talks with the club for years about getting an online system in place, but fans needing a carer still have to ring or visit the ticket office.

          In contrast, Swansea City decided in 2016 to develop its own bespoke ticketing system, with users registering their details and eligibility once to gain online ticket access.

          A club spokesman said after they have provided supporting documents to show their accessible needs, they are able to log into their account to get tickets.

          In 2016, Swansea was the first Premier League club to provide the service and shared it with others.

          As an IT specialist, Kieran Jones from Cardiff City DSA finds it frustrating the club had not yet managed to set up a comprehensive online booking system, despite the fact people who need disabled spaces just for themselves can book online.

          “The ticket office moved to a new system and they’re still working with it,” he said.

          “It’s the same system that Wales, the FAW [which uses Cardiff City Stadium for matches], have got so it will eventually allow people to book with a carer, but currently they haven’t got that far.”

          A Cardiff City spokesman said as a Premier League club in 2016, Swansea was in a different income bracket to Cardiff and had more potential to invest in ticketing.

          However, he added “significant steps towards improvement” have been made over the past couple of seasons.

          Alexandra Osborne from Disability Wales describes the ticketing situation at venues as a “big issue, and has been long term”.

          “An awful lot of our members, disabled people from across Wales, are saying that they missed out on another gig, or another concert, ” she said.

          “You’ve always got to spend quite a long time looking it up before the tickets come out to make sure you don’t end up missing out because you’ve called a number that last time is fine but this time is the wrong number.”

          Ms Osborne would like to see online and phone booking options available for disabled people.

          She believes one single UK-wide access card, similar to Hynt but valid for all venues, would make a positive difference.

          “It’s a lot of work to apply for them all and then keep up, to make sure your passes haven’t expired,” she explained.

          “If there was one pass so we could use it in any registered venue, I think it would just help with the awareness and people actually using them because it would be talked about a bit more.”

          pictures of me, enjoying time at Grandma’s and enjoying time at youth group and enjoying lunch, enjoying my 20s with cerebral palsy

          February 14, 2023

          I have taken delivery of my off-road wheelchair for my dear be expectations. Training begins on Friday. Stay tuned for training videos and content with me using my off-road wheelchair that my friend lent me thank you same difference followers will put up a picture on Friday morning of me in my old friend wheelchair for the first time .

          February 14, 2023

          Great news for the Morrison different community

          DWP Uses Secrets And Lies To Unlawfully Snatch Back Money From Claimants

          February 14, 2023

          With many thanks to Benefits And Work.

          The DWP deliberately lied to a claimant about their rights and unlawfully kept legal guidance secret in order to recover an overpayment of over £8,000 which was entirely due to the DWP’s own mistakes.  The High Court has this month prevented the DWP from taking the money back from the mother of two disabled children, but many tens of thousands more claimants may have been hoodwinked in the same way.

          The claimant’s disabled son was on an apprenticeship, but the DWP wrongly considered him to be in full-time education and so incorrectly paid the claimant child elements of universal credit.

          The judge found that the claimant gave all the information that was asked of her and “took all reasonable steps both to clarify her entitlement and to prevent any UC overpayment by actively querying her entitlement on at least four occasions.”

          On each occasion the DWP told her that the award was correct. 

          Nevertheless the DWP eventually realised its error and attempted to recover the overpayment.

          The claimant appealed, but a tribunal agreed that there had been an overpayment, although they also found that the overpayment was solely due to official error and that DWP “repeatedly” miscalculated her entitlement over a prolonged period, in what was a “profound lapse in service”’.

          With the help of an advice centre, the claimant asked the DWP in writing to waive recovery of the overpayment, which the DWP has the power to do. She explained that she had two disabled children with autism and ADHD, that her role as their carer meant that she could not work longer hours and that she was already struggling so badly that she was having to use a foodbank.

          The DWP didn’t even respond to this request.

          The claimant then sent the request again.

          This time the DWP said that as she had already been to a tribunal there was no further route to pursue the matter.

          The claimant wrote yet again, saying:

          “What do you mean there is ‘nothing you can do for me?’ Your own guidance says I can ask for a waiver of my overpayment (see paras 5.83-5.85 of your own benefit overpayment recovery guide) and this route was recommended to me by Mrs S Wiggins, the complaints handler who dealt with my UC complaint. All of this was carefully outlined in my waiver letter and the supporting documents I sent with it. As I have asked you to waive my overpayment, as a public body, you have an obligation to consider, and make a decision on it. Neither me nor my caseworker have received such a decision, why is that?”

          Astonishingly, the DWP relied with an outright lie:

          “Neither myself or anyone working for Universal Credit can reconsider your overpayment as you have exhausted all appeal routes with us. The legislation you have quoted does not apply directly to the processes that we have here.”

          The claimant, with the help of the Public Law  Project, launched a judicial review of this decision in the High Court.

          One of the findings the judge made was that: “Fortunately, the claimant had the assistance of Public Law Project (‘PLP’), and so she did not accept this manifestly unlawful statement of the position.”

          In lay person’s speak, ‘manifestly unlawful statement of the position’ could reasonably be translated as ‘barefaced lie’.

          One of the grounds on which the claimant appealed was that the DWP had kept secret its detailed policy on when an overpayment should be waived.

          The judge held that the failure of the DWP to publish the Decision Makers Guide to Waiver was unlawful because a claimant would not be able to fully understand the DWP’s policy on waiving overpayments.

          The DWP agreed to publish the Decision Makers Guide to Waiver as part of its Benefits Overpayment Recovery Guide, see the link at the end of this article.

          The judge also found that the claimant had reasonably relied on the DWP’s repeated reassurances that she was entitled to the payments to her detriment by spending money she would later be asked to repay.  If she had known the true position she would have acted differently, possibly by finding a different course for her son or seeking to claim benefits for her son in his own right.

          Accordingly, the judge found that the DWP’s refusal to waive the overpayment was unlawful and breached the claimant’s legitimate expectations and so the DWP could no longer recover the £8,000 it had wrongly paid.

          In the course of her deliberations, the judge also looked at statistics on overpayments and recovery by the DWP.

          She found that from 1 April to 2021 31 March 2021 337,000 UC claimants were asked to repay overpayments whose cause was error by the DWP.  The total value of those overpayments was £228 million.

          Amazingly, the DWP claims that just 47 claimants asked for their overpayments to be waived in the whole of 2020 and just 7 of those requests were granted.

          As the judge commented:   “If the claimant’s experience of twice having her request for waiver rebuffed without consideration is not unique to her, the number of requests in fact made may exceed the number recorded . . .”

          In fact, many thousands may have requested a waiver and been ignored, whilst many thousands more may have had no idea that they even had the right to ask.  Undoubtedly, the test for waiving an overpayment is a hard one to pass, but the DWP have a legal duty to allow claimants to have their request properly considered.

          Instead, the department continues to push struggling claimants even deeper into poverty, with only a very rare court case like this one shining a light on their dishonest and unlawful tactics

          You can download the full decision from this link.

          You can read the chapter on discretion and waiver in the DWP’s Benefit overpayment recovery guide here.

           

          Playing a clave at choir today :)

          February 14, 2023

          Staffordshire Disabled Gymnast Looks To Retain Schools Title

          February 13, 2023

            A disabled gymnast is hoping to qualify for a chance to retain her national school championship title.

            Hannah Louise, 18, who has hypermobile joints caused by Ehlers-Danlos syndrome, took up disability acrobatic gymnastics four years ago.

            She is competing in a regional qualifier in Fenton Manor on Saturday, and says the sport provides her with an escape.

            “It’s just a way of getting everything out,” said the Uttoxeter resident.

            Health challenges forced her to stop practising artistic gymnastics a decade ago.

            “I struggled with joint pain since I was two years old, so I couldn’t do everything that my friends were doing,” she said.

            “I was nine, nearly 10 when I got my diagnosis. It was hard because I’ve always been involved in sport.”

            Having Ehlers-Danlos means her joints dislocate very easily, she suffers with chronic pain and fatigue, and uses a wheelchair because she cannot walk long distances.

            Persuading mum

            She was inspired to join Stafford’s Style 90 Gymnastics club four years ago after seeing her older brother compete.

            “It took me about a year of persuading my mum to let me do it because she was a bit cautious,” she said. “That was so amazing – to be able to find myself again.”

            She partners with able-bodied gymnasts to deliver routines, wearing supports and a neck-brace to protect her joints.

            “I’ll be sat in my wheelchair and they’ll do a handstand on my knees, me holding them so they don’t fall, obviously, or standing on my knees in my wheelchair,” she said.

            Her coach, Lily Gibbons, said she was “unbelievably proud” of the athlete’s achievements.

            “She has so many things she has to overcome,” she said. “Over the last 12 months she’s really suffered with her health. But whenever she’s here she always works hard.

            “She amazes us sometimes with the things she’s able to do.”

            The gymnast believes those with disabilities should have the opportunity to compete at international level, like able-bodied peers.

            “The representation for disabled athletes isn’t there,” she said. “The sport I do, disability acrobatic gymnastics, you can only go to national level.

            “I’m currently British champion, but that’s the highest I can get.”

            She also hopes to qualify to compete again at the British national NDP finals in May, and says the support of mum Andrea makes everything possible.

            “My mum is my biggest advocate and I’m so grateful for her,” she said.

            Uno and preparing salad for Wacky Wheels Youth Groups lunch

            February 13, 2023

            Here is a picture of the salad I helped to prepare. We also made pizza, and my support worker showed me how to make a vegan pizza as she is vegan.

            Music with Wacky Wheels with our own instruments and then playing them for our own wacky wheels music video – which I filmed!

            February 12, 2023

            Puzzle fun plus maze game fun! 😁

            February 11, 2023

            #Brandom #Paula #Disabled #WheelchairUser

            February 10, 2023

            people need to think about where they put up when parking on pedestrian road before exiting the vehicle, especially work men or electricians et cetera who has banned the other day. I was out a diet

            February 10, 2023

            videos of discos and me having fun in 2021, 20,22 and 2020 till now in 2023

            Hollyoaks Newcomer Annabelle Davis Discusses Importance Of Representation With New Soap Role

            February 10, 2023

            Hollyoaks star Annabelle Davis has discussed the importance of having diversity and representation on-screen.

            The actress, who recently made her soap debut as newcomer Lacey Lloyd, opened up about the topic on Loose Women today (February 8), sharing: “I think it’s really important that on TV, you are shown all of this diversity and we can all learn from it really, raising all the awareness.”

            Describing her auditioning process, Annabelle said she first heard of the role through her work on Tracey Beaker spin-off The Dumping Ground, adding that she enjoyed being able to take on a character that wasn’t originally written as a little person.

            “It was lovely actually, Lucy Allan, who I worked with on The Dumping Ground, approached me just saying ‘I’ve got a role, it’s not written for a little person but I’d love you to take a look and see if you would like to play her,'” she said.

            “It’s lovely to be given a role that isn’t made for a little person because that doesn’t really define who you are but on the other hand, it is nice to explore things, some perspective from a little person and actually give viewers that.”

            The actress also comes from a strong acting background, being the daughter of legendary Star Wars and Harry Potter actor Warwick Davis.

            Describing life growing up with a famous dad, Annabelle recalled how she’d visit him at work.

            “It was surreal. My mum was amazing, she would pick us up from school and take us down to Dad on set, we’d sit in his trailer and wait for him to finish, then go back to the hotel,” she shared.

            Following Annabelle’s Hollyoaks debut, Warwick gave his support for his daughter’s latest role, saying that he would be tuning in to watch her.

            “Shout out to my daughter, @AnnabelleLDavis who debuts in the British Soap @Hollyoaks tonight. Never seen the show but will be watching tonight!” he tweeted.

            Jared O’Mara: Former MP Jailed Over £52,000 Fraud To Pay Drug Debt

            February 10, 2023

              An ex-MP who tried to claim £52,000 of taxpayers’ money to help fund a cocaine habit has been jailed for four years.

              Jared O’Mara sent fake invoices to the Independent Parliamentary Standards Authority (IPSA), the body which regulates MPs’ business costs and pay.

              He was thousands of pounds in debt to a drug dealer, his trial heard.

              O’Mara, who quit the Labour party about a year after being elected as Sheffield Hallam MP, was convicted of six counts of fraud.

              Gareth Arnold, who submitted invoices to IPSA on behalf of O’Mara, was given a 15-month jail term suspended for two years.

              The court heard fake invoices worth £24,000 were rejected by IPSA and a false £28,000 contract of employment submitted by O’Mara meant the total value of the fraud was £52,000.

              O’Mara was elected to Parliament for Labour in June 2017, unseating former deputy Prime Minister Nick Clegg.

              He quit the party the following year and became an independent after he was suspended by the party over comments he had posted online before becoming an MP.

              The 41-year-old stood down in 2019, the same year the fraud offences took place.

              Through his barrister, O’Mara apologised to the 70,000 voters in the South Yorkshire constituency for failing to resign in October 2017, the month he was suspended by Labour.

              However, Judge Tom Bayliss KC called the apology “entirely disingenuous” and said the fraud was “cynical, deliberate and dishonest”.

              “You must have realised early on that you were wholly unsuited to the role, but you carried on regardless, you brazened it out; drawing a salary, but doing little or no parliamentary work,” he told O’Mara.

              “You are not here because of that and I do not aggravate your position because of it. It is irrelevant to these proceedings. That is a matter between you and those who elected you.

              “You are here because you abused your position to commit fraud and you have shown not the slightest degree of remorse in respect of that.”

              McDonald’s postcode

              The court previously heard O’Mara made claims totalling £19,400 to IPSA for services he said had been provided by a “fictitious” organisation called Confident About Autism South Yorkshire.

              Prosecutors said the former politician had used the postcode of a McDonald’s restaurant in the city as the company’s business address and the firm’s name had no online search engine results.

              He was also found guilty of trying to claim £4,650 for services he said his 30-year-old “chief of staff” Arnold, of School Lane, Dronfield, Derbyshire, had provided to him.

              He also submitted a false contract of employment for a friend, pretending he worked as a constituency support officer on a salary of £28,000.

              All the invoices were rejected by IPSA due to a lack of detail about the work carried out, the jury was told.

              The jury heard O’Mara, who has autism and cerebral palsy, was experiencing mental health issues at the time of the offences, but the judge concluded he was “able to exercise appropriate judgement and make rational choices”.

              Prosecutor James Bourne-Arton told the sentencing hearing the fraud was not a victimless crime as it “undermines public trust and confidence” in MPs.

              Judge Bayliss, sentencing O’Mara, of Walker Close, Sheffield, told him the fraud was designed to get him out of “significant financial difficulties”.

              He continued: “Those difficulties were caused by a hedonistic and self indulgent lifestyle, fuelled by the consumption of large amounts of vodka and cocaine.”

              Art about challenges I have faced for the All About Us exhibition!

              February 10, 2023

              This will be held in the Old Town Hall, St. Albans Hertfordshire, to showcase people with learning disabilities and challenges they face in their lives, to hopefully create a more inclusive society, community, and world 🥰

              my choir and my friend boy in joyed this very much and would definitely do it again if I was 02

              February 9, 2023

              drumming last week

              The pages I managed to complete last night include this Backpage.

              February 9, 2023

              See the front page in an upcoming post in a few days time. Me and my support worker has been working on it together tonight and all I have to do is get a photo of me on Friday night when I went to the concert printed off and I will put that underneath the writing and that page will be complete. What do you think of the page so far? 🎨🖌️🖍️

              Deaf Nottingham Artist Holds British Sign Language-Themed Exhibition

              February 9, 2023

                A deaf artist is holding an exhibition of work highlighting the role British Sign Language (BSL) has played in her life.

                Zoe Milner, 21, from Nottingham was born profoundly deaf and BSL was her first language.

                The exhibition – named I Talk With My Hands – will showcase art informed by her experiences.

                It is due to take place at the Window Gallery at charity City Arts in Hockley from 9 February until 29 March.

                Pride

                Ms Milner said: “I feel deaf representation is important and this exhibition gives me an opportunity to raise awareness.

                “It is important people understand our perspective. I’d like people to learn what deaf culture looks like.”

                She said she hoped to inspire the deaf community and other disabled people to express pride in their identity.

                Suzannah Bedford, director at City Arts, said: “We are incredibly proud to be able to share Zoe’s work with the people of Nottingham.

                “The exhibition is presented in our Window Gallery, which gives local people and passers-by access to high-quality art in the street, without the need to set foot inside a gallery.”

                Visually Impaired Warwickshire Man Completes Step Challenge

                February 8, 2023

                  A visually impaired fundraiser has completed a year-long five-million-step challenge.

                  Martyn Parker, from Warwick, raised almost £2,000 for Warwickshire Vision Support.

                  His final steps were taken at Warwickshire Racecourse during the weekend’s Park Run, and were met with applause from runners.

                  “It’s been brilliant,” said Mr Parker. “It really has.”

                  To complete the five million steps, Mr Parker worked out he would need to walk more than 13,000 each day.

                  When he started the challenge in 2022, Mr Parker had recently lost his guide dog and had suffered with the side-effects of Covid-19.

                  “I had two lots of Covid in six weeks,” he said, “which took me from being able to do four laps of this without too much difficulty to staggering around a lap.”

                  Now though, he has a new guide dog, called Harper, and completing his charity work means so far 2023 “couldn’t have been better”.

                  He was cheered over the line when he completed his challenge at Warwickshire Racecourse and thanked his friends at Park Run who he said were “fantastic”.

                  “Nothing’s been too much trouble,” he said.

                  “There’s been a couple of times when I’ve turned up without a sighted person to guide me and they’ve found someone to do it for me.”

                  Mr Parker has worked with Warwickshire Vision Support for years and wanted to raise money to support its work.

                  “There’s something in the region of 23,000 [people] across the county who have some sight loss who we could help, but in order to help them we need to raise the funds,” he said.

                  “Any little can help, £10 for instance could pay for telephone befriending calls for somebody to ring somebody who might be lonely and isolated because of the sight loss.”

                  Picture of me with an adventurous hairstyle just experimenting because I was bored and wanted a nice hairstyle for my enrollment at college 2-years ago.

                  February 8, 2023

                  Ed Davey Says We Need To Give Carers A Pay Rise

                  February 7, 2023

                  This being one of Same Difference’s favourite campaigns, we couldn’t agree more.

                  Barista Scheme For Deaf People Comes To London

                  February 7, 2023

                  Four baristas who are deaf are to start new jobs in London as part of a South African-based scheme to create work opportunities for deaf people.

                  They will be based at four WeWork office locations in Holborn and Covent Garden and will use an iPad to show customers how to order through sign language.

                  One of the baristas, Prisilla Kwakye, 21, from Croydon, said she was “really excited”, having previously faced difficulties finding a job.

                  The four baristas start next week.

                  The scheme is the brainchild of Gary Hopkins, 58, from Cape Town, South Africa.

                  Seven years ago he founded a social enterprise called I Love Coffee, which trains deaf people to become baristas, and has since helped more than 100 individuals.

                  He said the scheme gives its participants “the confidence to reach their goals and explore other job opportunities”, including computer science and project management courses.

                  ‘Build my confidence’

                  Ms Kwakye, who starts on 6 February, said becoming a barista would open new doors for her.

                  “I can build my confidence up, upskill myself and maybe in the future set up my own business. So the opportunities are endless,” she said.

                  Before being helped by I Love Coffee, Ms Kwakye said she experienced “a lot of rejections” and that having to contact companies through an interpreter “creates barriers”.

                  “Companies like this are really important as they create job opportunities for the deaf community that we wouldn’t normally have.”

                  She added she was looking forward to making new friends “and have conversations with customers about signing”.

                  It’s hoped more baristas will be trained as the scheme expands. But Mr Hopkins said he hopes for a world without I Love Coffee “because then it means we’ve actually created that bridge between the hearing and the deaf”.

                  “We have seen our baristas grow beyond where they started and that is always a joy for us.”

                  Mathieu Proust, chief operating officer for international at WeWork, said he was looking forward to seeing I Love Coffee’s “positive work for the deaf community ripple across the capital”.

                  Picture of me waiting to be interviewed by somebody for the learning disability care awards.

                  February 7, 2023

                  Autism: Employers Ignorant About Disability – Autistic Man

                  February 6, 2023

                    “A lot of employers are really ignorant.”

                    Autistic man Nath Trevett, from Rhondda Cynon Taf, said employers often misinterpreted autism traits and need training to support people at work.

                    While 53.6% of all disabled people are in work, that figure is only 21.7% for autistic people, according to the Office for National Statistics.

                    The National Autistic Society called it a “waste of talent” while the Welsh government vowed to improve job access.

                    Autism means people may act differently to the way the others do.

                    The Equality Act 2010 made it harder for employers to unfairly screen out disabled people and ensured there was a duty to make reasonable adjustments for people at a substantial disadvantage because of their disability.

                    But Nath, a part-time Welsh translator, said there were still barriers and did not realise until he was made redundant how difficult it was for people like him to find work.

                    He said: “I really find it stressful actually making applications and looking for work. A lot of employers are really ignorant and that has an effect.

                    “They don’t know anything about autism and so they won’t appreciate that people on the spectrum think and talk in a different way and I just think that’s ignorant and discriminating.”

                    Nath said he was “fortunate” to be employed by an understanding organisation but thinks others are not as lucky.

                    “One symptom is that people with autism have a tendency to go into detail and I just hate it when an employer jumps to the conclusion that is a bit too much and think that they’re in inappropriate for the role when they’re actually trying to do is win their trust,” he said.

                    “There needs to be a lot more education and training and understanding and acceptance otherwise people on the spectrum will only go on suffering and feel discriminated and be rejected and it’s just not good for anyone’s mental health.”

                    He said employers needed to realise that “not all autistic people suffer in the same way as each other” so they can adapt accordingly.

                    Andrew Edwards struggled for seven years to get a job before eventually getting employed at Your Space Marches, an autism charity based in Wrexham.

                    He worked at a football broadcasting channel in the early 2000s and said, at that time, few people had experience with autistic people.

                    “People with autism need step by step guidance that is clear. They can bring a lot of skills to the job in that they will be very dedicated and enthusiastic but it is more keeping the job is the issue”.

                    How an autism diagnosis changed my life.

                    He said he would struggle to work a traditional 40-hour week and some autistic people may struggle to work but employers should be encouraged to be flexible.

                    “It would drain me too much emotionally and physically and my mental health would suffer to work full time,” he said.

                    Because of this, Andrew is also on benefits to help subsidise his income and said being able to work flexibly gave him and his family “freedom” and “a sense of purpose” after his mother died.

                    Karen Davies works with an employability service at Pembrokeshire council as part of initiative to help get more autistic people in work.

                    The workshop in Haverfordwest is preparing its trainees for manufacturing jobs and has received a grant from the Department for Work and Pensions.

                    In 2018, they employed 15 disabled people which has now risen to 70 and includes a number of autistic people.

                    Ms Davies said: “We have three cafes, a shop, a sawmill, and admin and social media, all of which support people with a wide range of disabilities within the workplace.”

                    She said the group wanted to showcase the skills of people with disabilities and encourage workplaces to make changes.

                    “Our focus will be educating employers in the processes we have developed in-house so that other employers can take people with autism and support them in their workplace.”

                    The National Autistic Society said it was very concerned about the employment gap.

                    External affairs manager Chris Haines said autistic people “deserve the same opportunity as everybody else to succeed in work and reach their potential”.

                    “The employment gap remains far too wide and we’re really concerned that autistic people have some of the lowest rates of employment of any group. We think is a huge waste of talent.”

                    While it is not possible for every autistic person to be in work, he said small changes employers could make, such as quiet spaces, using clear and precise language and staff training, could make a “big difference”.

                    He wants the Welsh government’s young person’s guarantee of training and work to be accessible to autistic people, coupled with a national campaign “to improve understanding” of autism among employers.

                    A Welsh government spokeswoman said: “Our network of disabled people’s employment champions are playing a vital role in helping to create a culture shift in attitudes to help autistic people in the workplace.”

                    She added that there were a number of pilot schemes in place to improve the experience of autistic people.

                    Pictures of me at Macmillan coffee morning 1-year ago

                    February 6, 2023

                    Me posting with some paintings at an art gallery/ exhibition. Approximately 2 years ago.

                    February 5, 2023

                    Picture of me having a big, big ice cream just because I could.

                    February 4, 2023

                    MrBeast: Why Has YouTuber Faced Criticism For Blind Surgery Video?

                    February 3, 2023

                    The world’s most popular YouTuber has responded to criticism following a video of him funding multiple life-changing operations.

                    In the post, MrBeast reveals that he paid for sight-restoring cataract surgery for a thousand people.

                    But the clip, which has over 71 million views, has divided opinion with some calling it “charity porn”.

                    The 24-year-old, real name Jimmy Donaldson, tweeted in response to suggestions that the video was made purely for financial gain, saying the “average MrBeast video lost $1,500,000 last year”.

                    MrBeast, who has 131 million subscribers and recently became the world’s most popular YouTuber, initially said he did not expect so many people to view the video.

                    As more people watched the video, there were questions and concerns over the cost and inaccessibility of eye surgery in some parts of the world.

                    Some people also suggested rich influencers should not be used to try and fix wider problems in society and healthcare.

                    But not everyone agrees, with some praising for him raising awareness.

                    Andrew Hodgson, president of the National Federation of the Blind of the UK, told BBC Newsbeat: “Anything that puts a spotlight on such treatable eye conditions like cataracts and provides funding for people to undergo surgery to restore their sight should be welcomed.

                    “Why would anybody criticise this work and raising awareness of it through film and social media channels?”

                    A spokeswoman for Sightsavers, an international charity, added they were “encouraged to see the subject of the global eye health burden being raised to a large public audience”.

                    “Eye health is often a forgotten topic when it comes to global health conversations, but eye health equals opportunity, allowing children to learn and adults to earn,” they added.
                    Presentational white space

                    One Twitter user notes “the fact it took charity for these people to get help highlights the problem”.

                    But another user said “paying for 1000 blind people to have eye surgery is a nice thing to do, but using that act of generosity into content turns it into a tacky and tasteless act of charity porn”.

                    Dr Jeff Levinson, the surgeon who worked on behalf of the social media star, says in the video “half of all the blindness in the world is people who need a 10 minute surgery”.

                    MrBeast is known for videos featuring huge cash giveaways and prizes, as well as charity work.

                    In 2021, he launched a separate philanthropy-themed YouTube channel, which itself has more than 10 million subscribers, and he has a licensed charity that functions as a food bank to feed communities across the US.

                    More than two million people are living with sight loss in the UK, of which 340,000 are registered as blind or partially sighted, according to the NHS.

                    In the instance that an individual’s quality of life is impacted by their declining sight, the NHS provides assessment and surgery if and whenever necessary.

                    The Royal College of Optometrists reported that in the UK just under 44,000 cataract procedures were carried out in one month alone in 2021.

                    Despite the mixed response, MrBeast’s impact on those who received surgery is visible in the emotional reaction of those he helped.

                    “I didn’t think I was ever going to see again,” said one patient who had previously been a cashier, but had been forced to stop working when his sight loss became so advanced.

                    Pictures of me drinking pre drinks at Butlins before I went out to the club. I went to Butlins on holiday one year ago and really enjoyed it. Here’s a picture of me saying cheers to my friend and having us clink our glasses together.

                    February 3, 2023

                    
                    
                    
                    
                    
                    					

                    project at the museum to All About Us project to raise awareness for disability differences and hopefully equality I hope to see his teachers over I have contributed one of my lovely script which I have completed hopefully it helps people see that everybody can be included in art and in life as art can be a favourite past times tables and people who are not and like it helps people understand that we are different in some way but can have similar interests passions etc

                    February 2, 2023

                    👩🏽‍🦽🥰 evening time difference what do you think I should take camping with me? Anything useful as disabled individuals that you think I might find useful as a wheelchair user talk keeping warm excetera let me know in comments as I am willing to take any suggestions for staying warm cosy and not to stick thank you for any of you or suggestions that I would🥰

                    February 2, 2023

                    training in just a few weeks time 4D movie night hamper and other outdoor pursuit including orienteering has all part of my DAB qualification it is the countdown it’s going to countdown

                    February 2, 2023

                    the one-pound appeal for my fundraiser please everybody donate at least £1 or even 25p to my just giving page hope you say you do Florence firmly and can unity 🥰🤣💵

                    February 2, 2023

                    donate donate to allow me to continue achieving my goal and 16

                    ☺️🙂 find my just giving in my recent post from last week don’t know as much or as little as you want every pound counts thank you saying different community🙂🤩

                    February 2, 2023

                    British Gas Admits Agents Break Into Struggling Customers’ Home

                    February 2, 2023

                    The boss of British Gas owner Centrica has said he is horrified that debt collectors have broken into vulnerable customers’ homes to fit energy meters.

                    The Times found debt agents working for British Gas expressed excitement at putting meters in the homes of people who had fallen behind on energy bills.

                    “This happened when people were acting on behalf of British Gas. There is nothing that can be said to excuse it,” Chris O’Shea told the BBC.

                    The firm has suspended installations.

                    The move follows an undercover investigation by the Times, whose reporter went with agents working for Arvato Financial Solutions’ – a company used by British Gas to pursue debts – to the home of a single father with three children.

                    After establishing the property was unoccupied, the reporter observed the agents work with a locksmith to force their way in and install a prepayment meter.

                    It reported that the locksmith said: “This is the exciting bit. I love this bit.”

                    Mr O’Shea told BBC Radio 4’s Today programme: “The contractor that we’ve employed, Arvato, has let us down but I am accountable for this.

                    “This happened when people were acting on behalf of British Gas. There is nothing that can be said to excuse it.”

                    Agents also fitted a prepayment meter by force at the home of a young mother with an infant baby, the newspaper said.

                    Others who experienced similar treatment, according to materials seen by The Times, include a mother whose daughter is disabled and a woman described as having mobility problems.

                    Centrica said the suspension – where it applied to the court for a warrant to install a pre-payment meter – would last “until at least after winter” and that protecting vulnerable people was its priority.

                    Business Secretary Grant Shapps said he was “horrified” by the findings.

                    “Switching customers – and particularly those who are vulnerable – to prepayment meters should only ever be a last resort and every other possible alternative should be exhausted,” he said.

                    “These findings suggest British Gas are doing anything but this.”

                    Energy firms are required to have exhausted all other options before installing a prepayment meter, and should not do so for those “in the most vulnerable situations”.

                    It comes amid the rising cost of living and as household bills soar in part due to mounting energy costs.

                    line

                    Why is this allowed and what can you do?

                    • Regulator Ofgem rules state that energy suppliers must have effective checks and balances in place when switching the mode of a smart meter
                    • The regulator advises customers with concerns to speak to their supplier. Under Ofgem rules they must offer payment plans you can afford and you can ask for emergency credit if you use a prepay meter and can’t top up
                    • Breathing Space, sometimes called the Debt Respite Scheme, is a free government scheme that could give you up to 60 days’ space from creditors to set up a debt solution. Step Change debt charity can help you to apply
                    • Citizens Advice offers this guide: Stop your energy supplier moving you to prepayment

                    line

                    Mr Shapps said the energy minister would hold a meeting with British Gas “in the coming days”, adding: “He will be demanding answers to ensure this systemic failure is addressed.”

                    A spokesperson for energy regulator Ofgem said: “It is unacceptable for any supplier to impose forced installations on vulnerable customers struggling to pay their bills before all other options have been exhausted and without carrying out thorough checks to ensure it is safe and practicable to do so.”

                    People using prepayment meters pay for their gas and electricity by topping up their meter, either through accounts or by adding credit to a card in a convenience store or Post Office.

                    This is a more expensive method of paying than by direct debit, but is sometimes the only option for people who have struggled to pay and are in debt to an energy supplier.

                    Many rented properties also have prepayment meters.

                    Problems can arise when residents no longer have any credit left on the meter and have no money to top it up – leaving them unable to cook or heat their homes.

                    Last month, the Citizens Advice charity called for a ban on energy companies “forcing” customers onto prepayment meters because they are struggling to pay bills.

                    In response to The Times, Gillian Cooper, head of energy policy at Citizens Advice, said: “It’s truly shocking to see the extent of bad practices amongst some energy suppliers.

                    “Our frontline advisers know only too well the desperate situations so many struggling customers have found themselves in. Time and time again we have called for a ban on forced prepayment meter installations until new protections for customers are brought in.

                    “Ofgem and the government need to act now – serious reforms must be made before these suppliers can be trusted again.”

                    BBC News has contacted Arvato Financial Solutions for comment.

                    Down’s Syndrome Discrimination: Bangor Nursery Apologies To Pupil

                    February 2, 2023

                    The mother of a girl with Down’s syndrome who was discriminated against by her former nursery school has said its apology will never be enough.

                    Michelle and Alan Cummins, whose daughter Amelie attended Trinity Nursery School in Bangor, County Down, brought a case against the school.

                    It came after they were told Amelie, who is now five, would have to start 15 minutes later than other children.

                    The school settled the case and apologised to the Cummins family.

                    Trinity Nursery School accepted it treated Amelie less favourably due to her special educational needs and acknowledged it failed to make reasonable adjustments for her.

                    However, Mrs Cummins said its apology “isn’t enough and it will never be enough”.

                    “Two years is a long time to have to put us through this torment,” she told BBC News NI.

                    “It’s not something that we’ll get over lightly.

                    “We had to drive it forward, because it’s not acceptable, and if we’d have done nothing about it we’d have been as bad as them.”

                    Amelie has a statement of special educational needs, which provided for her to attend mainstream nursery school with 22.5 hours of classroom support each week.

                    She joined Trinity Nursery School in September 2020, but her family was told she had to start school 15 minutes later every day than all the other children in her class, even though she had a dedicated classroom assistant.

                    Amelie’s parents alleged the school also wanted Amelie to finish 15 minutes earlier but they refused to accept that.

                    Amelie’s parents removed her from the nursery school three months later.

                    Worst experiences

                    “We refused – how much education must my daughter lose out on? It just wasn’t acceptable and we raised it, so the environment became quite hostile,” Mrs Cummins said.

                    “Starting nursery is supposed to be positive… it was far from it.”

                    The family subsequently lodged a discrimination case against Trinity Nursing School with the support of the Equality Commission.

                    Mr and Mrs Cummins said the case was one of the worst experiences the family has ever gone through, with the two-year settlement process being “quite stressful”.

                    “We knew in our hearts that it was the right thing to do and that we should stick with it because we don’t want this to happen to any other child,” Mr Cummins said.

                    “Our daughter has been discriminated against – so there was not a celebration of that occurrence, we wish it had never happened – however we do feel vindicated that we were right to seek the Equality Commission’s help and to take the case,” he added.

                    The family now hope others will take strength from their actions and pursue their own cases.

                    Mary Kitson, senior legal officer for the Equality Commission for Northern Ireland, said it is unacceptable that any pupil be treated less favourably because of their disability.

                    “All children must be provided with opportunities to flourish at school, regardless of whether or not they have a disability,” she said.

                    “We welcome, as part of the settlement terms, Trinity Nursery School’s agreement to work with the commission in respect of its duties under the Disability Discrimination legislation and good practice in education.”

                    A spokesperson for Trinity Nursing School said: “Whilst we cannot comment on individual pupils, as a school we will take on board all learning from the case and are firmly committed to the principle of equality of opportunity for all disabled pupils.

                    “We will also work with the Equality Commission in ensuring that all of our policies, practices and procedures conform in all respects with national equality legislation in relation to Disability Discrimination in education, as well as best practice.”

                     
                     
                     
                     

                     

                    Me in a place called the waffle House 2 years ago because I love waffles and sweet things

                    February 2, 2023

                    If You Can’t Get Through To The DWP On The Phone, Is This The Solution?

                    February 1, 2023

                    With many thanks to Benefits And Work.

                     

                    Many Benefits and Work readers know only too well the misery of spending day after day trying to get through to the DWP on the phone without success. 

                    There’s more than enough evidence of this in the hundreds of comments below our articles on the subject:

                    Which DWP number are you struggling to get through on?

                    0800 121 4433 PIP Enquiry Line

                    Earlier this month, one of our members contacted us in despair at her inability to communicate with the DWP . 

                    Jane, (not her real name) a full-time carer had moved house and had tried for three solid months to phone the PIP enquiry line in order to inform them of their change of address.  As she put it, this was something DWP letters told them they must not fail to do ‘on pain of imprisonment’.

                    Jane made numerous attempts to get through on different days and at different times but without success.  She kept a record of all these attempts. She then sent a registered letter but received no response.

                    Jane was very concerned not only that she might be accused of failing to declare a change of circumstances, but also that any DWP mail sent to her old address would not be forwarded and their claim might be stopped.

                    We suggested to Jane that she contact her MP, pointing out just how unfair and distressing such treatment is and would they please contact the DWP themselves as Jane was unable to.

                    We are quite certain that MPs have their own hotline for the DWP and we know that contacts from MPs are generally treated seriously by the department.

                    Jane’s MP’s constituency office responded the same day, issuing her with a case number.

                    A week later, we got an email from Jane saying:

                    “I’m in shock ! The DWP complaints team have just got back to me and it’s all sorted now. I can’t tell you what a relief that is. I know there’s millions of people struggling with the system at the moment so I really appreciate this, and thank you for the suggestion. Good luck with your work, it’s so necessary.”

                    It really shouldn’t be so difficult to contact the DWP, especially when you there is a legal requirement for you to do so.

                    So, we’re suggesting that members consider following Jane’s example.  Keep records of your attempts to contact the DWP and, after you’ve made reasonable attempts to do so, ask your MP’s office to do it for you.

                    We know that most constituency offices are very busy places and that they deal with a  vast range of problems on behalf of people who are often close to despair.

                    But we think that the growing impossibility of contacting the DWP not only causes enormous stress and fear, but almost certainly leads to some people losing their benefits and possibly being threatened with legal action.

                    It’s not an issue that is the subject of campaigns by national charities and the DWP can no doubt produce highly dubious statistics showing how quickly most calls are answered.

                    So, it really is time that MPs were made aware of how big a problem this has become and that they need to do something about it.

                    So, if you can’t get through to the DWP, instead of it just being your problem, share it with your MP.

                    You can find out who your MP is here.

                    You can then either contact them via the form on the website or Google them to find their constituency office.

                    We know not all MPs offices will be helpful, so we’d really like to hear from you if you try, or have tried in the past, to get support from your MP in relation to benefits.

                    Let us know in the comments below.

                    My first day at mainstream college but this was 2 years ago I was transitioning from mainstream college but in special needs courses to mainstream courses with support assistance in there to help me because of my disability people said I would never be in mainstream classes look at me 2 years on done at least two mainstream courses including this year’s one which will be course number three that I have just completed and awaiting the certificate. I definitely probed them wrong here didn’t I.

                    February 1, 2023

                    Rose Ayling Ellis Shocked By Stage Show Rant

                    February 1, 2023

                    DWP Implicated After Claimant’s Body Left Undiscovered For Three Years

                    January 31, 2023

                    The DWP failed to make any checks before they cut off payments to a 38 year old claimant who subsequently died and was left undiscovered in her flat for more than three years, a pre-inquest hearing has been told.

                    Laura Winham had schizophrenia and had been sectioned under the Mental Health Act in the past.  Her family were no longer able to have contact with her because, as a result of her condition, she believed that they were trying to harm her.

                    Because of this, Laura was entirely dependent on her social housing provider and other welfare services to ensure her safety.

                    In 2014, Laura’s housing association contacted local mental health services to say that she had “untreated mental health issues” and was very thin and isolated.  No action was taken.

                    In 2016, the DWP contacted Laura to say that she was being transferred from DLA to PIP and that she had to apply for PIP or her DLA would stop.

                    Laura failed to respond and, after several written reminders, her DLA was stopped.  In spite of Laura having a severe mental illness and very clearly being a vulnerable person, no attempt was made by the DWP to check on her wellbeing or her ability to take part in the transfer process before her money was cut off.

                    Lauras gas was subsequently disconnected for failure to pay the bill.

                    Police visited the flat over a minor issue in 2017 and reported to social services that she was neglecting herself, had little food, no working phone and no contact with local care agencies.

                    Social services subsequently tried to phone Laura, even though they had been told there was no working phone, and then simply sent her a list of local food banks.

                    In May 2021, Laura’s body was discovered after her family visited to tell her of the death of her father and looked through the letterbox.  The police found her mummified and skeletal body when they forced entry.  There were unopened bills from creditors and markings on the calendar which stopped in November 2017. 

                    One of the last ones read “I need help”.

                    Laura’s family say that all the services that were involved in Laura’s case let her down:

                    “Everybody who was in contact with Laura and had a duty to her at some stage simply wiped their hands of her and forgot her. She was abandoned and left to die.”

                    They say they are sharing their story “because we do not want any other families to suffer in this way.”

                    The DWP were far from the only agency that let Laura down.  But they are an extremely large, well-resourced agency with no excuse for cutting off a vulnerable claimant’s money simply because they were unable to manage a transfer process aimed at reducing the benefits bill.

                    The cut in income almost certainly contributed to Laura’s isolation through the loss of her phone and increased her difficulties with self-care because she could not pay for basic necessities such as gas.

                    No doubt the DWP will claim that systems have now been put in place to ensure that such a tragedy could never occur again.  Claimants who depend on he DWP will know that nothing could be further from the truth.

                    Laura’s inquest is being held today.

                    You can read the full story in the Guardian.

                    A Christmas wreath with a difference that I made in virtual learning for leisure service

                    January 31, 2023

                    Influencer ‘Vulnerable’ On Instagram Over Disability Fetishism

                    January 30, 2023

                      An entrepreneur and fashion influencer says she has been left feeling “vulnerable and unprotected” after facing daily sexual harassment.

                      Sandie Roberts uses social media to run her company Roll with Style – a fashion guide for wheelchair users.

                      She has 39,000 followers on Instagram and said her problem comes from people with a fetish for disabled women.

                      Mrs Roberts wants Meta – the company that owns Facebook and Instagram – to do more to protect people.

                      Speaking to BBC Radio Gloucestershire, the 52-year-old, from Cirencester, said she has been dealing with sexual harassment online for around 18 months and when she first encountered it, she found it difficult to deal with it.

                      “I felt terrified they would find me in real life. It made me feel completely objectified,” she said.

                      “It took a lot for me to get past that and continue to post content.

                      “It has made me feel very unsafe, every time I go to work I put myself in a vulnerable position. It makes me feel physically sick.”

                      Although Mrs Roberts says that she will sometimes posts pictures of herself in revealing clothing, she does not believe that should make it ok to be objectified or make it her fault.

                      “I have posted lingerie photos, so people might say ‘you are asking for it’. I do not agree with that at all,” she said.

                      Because Mrs Roberts, who has been in a wheelchair since 2019, uses her social media to advertise products, she cannot turn her account to private.

                      But if she removes the followers who harass her, the algorithm will assume her content is unpopular and show it to less people.

                      “If you were in an office, they could be fired for sexual harassment. If you were in a shop, you could get security to deal with them,” Mrs Roberts said.

                      “On social media, you have to leave your shop open all the time and anyone can wander in, they can sexually harass you all they like and you can do absolutely nothing about it.”

                      Presentational grey line

                      Meta has provided the following advice on features that can help people encountering similar problems:

                      • Limits – this can be particularly useful for public figures. It lets you hide direct messages and comments from two groups of people – those who do not follow you, and people who only followed you recently
                      • DM [direct messages] controls – this allows people to turn off DMs completely or choose who can DM them, such as choosing to only receive DMs from people you follow 
                      • Comment controls – allows you to turn off comments from specific people or turn them off completely, on a post by post basis
                      • Hidden Words – allows you to filter DMs and comments that contain abusive terms so you never have to see them
                      • Blocking – this prevents people from interacting with you. They can not find your account, or see or interact with your content

                      Presentational grey line

                      At its worst, Mrs Roberts said she had people flooding her account with messages at around 1,000 per hour.

                      “I tried deleting them – it took two of us working flat out to do it and we removed over 64,000 of them from my account,” she said.

                      “But this killed my account flat. I am damned whatever I do. It is exhausting.”

                      A solution Mrs Roberts suggested is making it an option to sift through people who want to follow her, which is currently only an option for private accounts.

                      But online safety expert, Hera Hussain, said it is platforms such as those run by Meta that should be doing more to keep Mrs Roberts – and those like her – safe.

                      “The solution is not for Sandie to leave the platform,” Ms Hussain said.

                      “The solution is not for her to spend hours sifting through harassment messages.”

                      Ms Hussain added that one of the issues is that platforms are secretive about how their algorithms are run, which makes it difficult for people to predict how their actions will affect their accounts.

                      “This is a very traumatic experience for someone running a business,” she said.

                      Mrs Roberts said: “I work so hard on my account. I’m targeted with my content, my captions are search engine optimised, my hashtags carefully selected.

                      “I work with well known brands and I love my job.

                      “Where are we supposed to turn when we are being attacked by these vile people in a place of our business?

                      “I’ve reported many accounts for porn only to be told Instagram are too busy to even look into it.”

                      In a statement, Meta said: “We do not allow gender-based hate speech, threats of sexual violence and exploitation or unwanted harassment on our apps.

                      “We will remove this content when we become aware of it.

                      “We really encourage everyone to use our safety features, which we have developed in direct consultation with safety experts and our community.”

                      How I celebrated Christmas while we were in lockdown but allowed to visit our bubbles.

                      January 30, 2023

                      Picture of me at my first ever party when I became an adult 4 years ago at my friend’s 18th.

                      January 29, 2023