me and Biegus are at the Natural History Museum
Didn’t see the polar bear because I don’t think you posted hopefully you receive thi you this week

Angela me and the line at the natural history museum
With many thanks to Benefits And Work.
Some existing PIP claimants may lose their support group status and be transferred to the universal credit health element, where they may be required to carry out work-related activities, as early as 2026, Benefits and Work can reveal. This directly contradicts the claim by the government that current claimants would not be affected before 2029.
The government announced plans last month to axe the work capability assessment (WCA), which is currently used to decide if claimants should be placed in the limited capability for work-related activity (LCWRA) group for UC or the support group for ESA.
Under the new plans, claimants who get any element of PIP and who claim UC will automatically be eligible for an additional health element with no need to undergo a separate assessment to decide their capability for work.
However, the new system will not automatically recognize any claimant as unable to carry out any work-related activities.
Instead, if you are receiving the UC health element you may be set both voluntary and mandatory work-related requirements by a work coach and you will be subject to sanctions if you don’t meet the mandatory requirements.
When the plans were announced, the government stated that current claimants would not begin being transferred to the new system until 2029 at the earliest.
Only new claimants were said to be affected initially, with the system being rolled out by geographical area between 2026 and 2029.
However, evidence given to the commons work and pensions committee last week by the DWP contradicted this claim.
Conservative MP Nigel Mills asked DWP representatives what the situation would be for existing PIP claimants who had a review assessment between 2026 and 2029:
“You have a long run-in for this. It will be 2029 before you are worried about people who are already in the system. What happens if I get a called for a new PIP assessment every couple of years and I get one of those in 2027? Does that drop me into the new rules or do I stay under the old ones?”
Katie Farrington, Director General for Disability, Health and Pensions at the DWP answered on behalf of the department:
“With the way we will roll this out, we start from 2026 with new claims only, but we will do it in a geographical, staged way. It would depend which area you were in in 2027. Yes, some people might come in under the new rules, and that means they would automatically get your UC health payment and would automatically get the support.”
Given that an increasing proportion of England and Wales, at least, will be moved onto the UC health element beginning in 2026, this would suggest that many thousands of existing PIP claimants who have a review of their award will find themselves being forced onto the UC health element earlier than 2029.
It will essentially be a lottery, with where you live and when you are reviewed deciding whether you are moved over to the new system early or not.
On a more hopeful note, Mel Stride Secretary of State for Work and Pensions, told the committee that legislation would not even be put before the current parliament:
“This is not being rushed—far from it. A lot of people say that it is getting in early, and I am keen to do so, but it requires primary legislation that will go through the House in the next Parliament. As Katie says, it is then 2026 to 2029 for the new claimants before we get on to the stock of the existing claimants at that moment in time in 2029 onwards.”
Assuming that by “next Parliament” Stride means the next elected government rather than the next parliamentary session, then it will be up to whoever wins the election to decide if these changes go ahead.
However, with the rhetoric from the Labour Party often being similar to that of the Conservatives when it comes to benefits, there is no certainty that the plan will be axed even if there is a change in the ruling party after the next election.
It looks like campaigning against the proposals, by “the stock of the existing claimants” needs to start sooner rather than later.
You can read the minutes of the 29 March meeting of the work and pensions committee here.
turn Brandom room
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Picture of me, rolling four years ago, rolling four years ago
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annemari video memory video of the last two years and the phone. I’ve heard please click to watch on the link which I will insert in the title.
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A disabled woman says she does not feel safe in her own home because of the abuse she faces from her stepson.
Sarah – not her real name – who is from Nottinghamshire, said she had faced verbal abuse and threats for six years from the 17-year-old.
She said: “I’m pretty rock bottom. I go to work because work is the only safe place I have.”
PEGS, a social enterprise group which supports parents facing abuse, called for more safeguarding for families.
In a recent survey of 200 service users, PEGS found 75% of parents had had to call the police to de-escalate at least one incident, with a quarter saying they had called police at least five times because of fears over their safety.
They also found 68% of parents did not feel they had received the help they needed after contacting a professional.
‘I’m not safe’
Sarah, who has reported her stepson’s violent, unpredictable outbursts to the police three times, said: “I just live minute-to-minute at the moment.
“I’m not safe if I’m at home.
“He’ll call me a cripple probably at least five to 10 times a day.
“A few months back he said ‘You won’t be here much longer’.
“I said ‘Why do you think that?’ and he said ‘Because I’ll make it happen’.
“When he’s been very angry he’s attacked his father; he’s scarred his father going at him with a piece of metal.”
After Sarah’s most recent call to the police, her stepson was given alternative accommodation but returned after a few weeks.
She said neither he nor the family were given any support.
“We have tried and tried and tried,” she said.
“We’ve been to the GP who has laughed it off as normal teenage behaviour.
“We tried to get him referred to paediatrics.
“He’s been referred to the NHS’s Child and Adolescent Mental Health Services [CAMHS] and was sat on a waiting list for probably two plus years.”
Sarah said she was now being supported by PEGS, which works with parents who are experiencing abuse from their own child.
Michelle John, the founder of PEGS, said: “Parents are quite often told ‘the young person may have A, B or C’.
“That’s not very helpful for them in that situation. What we need to be doing in that situation is going ‘We see you, we hear you and what can we do to safeguard the family as a whole?'”
Becky Sutton, executive director of Local Mental Health Services, Nottinghamshire Healthcare, said: “Child to parent abuse is incredibly serious and can be distressing for everyone involved.
“CAMHS clinicians often work collaboratively with partnership agencies to enhance care packages so that the best outcomes are achieved for young people and their families.
“The average wait for a CAMHS assessment is nine weeks from referral. While any young person is waiting for an assessment or intervention and urgent support is needed, a CAMHS crisis service is available to them 24 hours a day.
“We would encourage any parent with concerns to make contact directly with CAMHS so that we can explore options for further support.”
my fundraising to help me with my best for Coser and to help me have a good summer, including my qualification, which I will have the exams for during the summer time. If you can donate, feel free with not feel free to share it as much as possible, many people in the opportunity to donate as possible. Thank you, Maya to all the members of this community.
fundraising ring for Rosa may want to give to my desk. Please call respite care and Deirdre support made me. Do you have a support as I need this report to pass the qualification. Thank you to those that may donate open next coming weeks days and months if you wish to donate for the do you have a good you will have to donate boy July if you wish to donate to the respite then respite fundraising is all going well it was just easier to 3 the same link link into Rachel
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click on the link to see the video of me playing fairground games this evening. Thank you everybody click and close the TikTok video of me playing playground games with my friends
Strictly Come Dancing winner Rose Ayling-Ellis has backed calls for emergency workers to learn sign language, after staff were unable to tell a deaf widow her husband had died.
Elizabeth Corbett, from Derby, learned about the death of her husband David, 51, via a video call.
Ayling-Ellis, who was the first deaf celebrity to take part in Strictly, backed the campaign on Twitter.
The ambulance service has apologised and said it was working to improve.
Mrs Corbett, 43, who was born deaf, was at work when her children rang her to say her husband had fallen ill.
By the time she got home, paramedics had arrived but they would not let her in the house.
“Not one of them could communicate with me and I couldn’t explain who I was,” she said, of the incident which took place in June 2021.
“I wanted to know what was happening and the police were asking me questions, but they were all wearing facemasks so I couldn’t tell what they were saying.
“Eventually I contacted work and the receptionist spoke to the paramedics who told her that David had died. So I found out over FaceTime that he had gone.”
A post-mortem examination revealed Mr Corbett had suffered a blood clot that caused a fatal heart attack.
Mrs Corbett, a teaching assistant at Royal School for the Deaf Derby, now wants all emergency workers to have some British Sign Language (BSL) skills and the ability to connect to a qualified interpreter instantly.
Ayling-Ellis, writing about the story on Twitter, said paramedics “should have been given the right tools [and] support to be able to communicate with this lady”.
She also responded to comments that suggested the paramedics could have written down their message or asked Mrs Corbett’s children – aged 11 and nine – to tell her that her husband had died.
“Some of the comments are quite upsetting,” the former EastEnders star wrote.
“I just want to break it down as simply as possible. ‘Why can’t the children tell the mother?’ No child should ever do this.
“Imagine going through the most traumatic time of your life.
“You need someone there you can access in the full language. Not writing backwards and forwards.”
She backed calls for paramedics to learn basic BSL and to have emergency interpreters on iPads on call.
“We pay our taxes too; we have every right to receive the same care,” she added.
Mrs Corbett said: “I have been shocked and upset with some of the comments on social media channels, but I have tried not to dwell on them.
“But the fact that Rose has got involved is amazing – she is such an important deaf role model and I’m thrilled she has stood up for me.”
She added she was currently fundraising online in her husband’s memory to buy a specially-adapted minibus for the school – which he also attended.
Head teacher of Royal School for the Deaf Derby, Paul Burrows, said: “There are no winners in this story at all – but it should be used as a force for change and to spur on every emergency service to become more deaf aware.
“There is a deep misunderstanding by many around BSL and deaf awareness in general.
“I am so proud of our school and what we are doing to educate our amazing pupils.”
Craig Whyles, divisional director for Derbyshire at East Midlands Ambulance Service, which attended to Mr Corbett, said: “We would like to offer our sincere condolences to the patient’s family and I am deeply sorry for the poor experience they had with our service.
“As an organisation we are currently working with the Nottinghamshire Deaf Society to discuss how we can improve our education to staff around deaf awareness and common emergency communication problems.”
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Monya pretty dress. Call my night out tonight for contact my life and many other things that we get home tonight.
More pizza preparation that I had to do before eating it!
pictures of me two years ago, all dressed up ready to attend virtual (Gateway). #Lockdown #Rosa #Singing #CerebralPalsy

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easter illustration along with
Sunday saying from me to you
Respite crafts and indoor activities :)
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video about the private parts of March 20 04, please click on the link in the title to view it. Thank you to all viewers of my blog and videos.🥰
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TikTok video with a picture and it’s on the iPhone XS describe me within my role of volunteering in the car click on the link to view it
just to bring is the cat in the title so please click if you want to donate blood if you haven’t yet. #Donations #RespiteCare #SupportFullDiary #IWillPutOffTheQualification
Outdoor activities and music fun :)
Please donate to my Justgiving, https://www.justgiving.com/crowdfunding/maya-richards, or GoFundMe, https://www.gofundme.com/f/ashrm-holiday, if you can 🙂







happy Friday, Curve, home and to Reidi saying
Picture of me, ready to go and see a show one year ago

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Lovely pancakes with Mollie
hi, with Mollie and the people in here are really kind and helpful 🙂
how cute is my cat 3 years ago 🐱💜
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Love a science experiment, 2 years ago yesterday
18 holes movie poster, and many more opportunities that I will get involved in June the living event right now I am of me, smoothie tasting pictures and reviews on Thursday time. Remember that my just giving page is open as fundraising continues i’m scored and pleased my audience engagement the link is on this post if you would like to donate thank s to all my viewers

volunteer event took part two of my volunteer TikTok that I did for the club this morning
part two of my volunteer work tick-tock please click here on the link to watch. Part two is that I didn’t fit one video thank you
pictures of me at work in between selling raffle tickets Whitworth my job tonight press the link to watch the TikTok video that I made with many photos and music with them. Ring Phela on
Sweden has “placed on hold” the deportation of a British grandmother with Alzheimer’s, her family have told the BBC.
Kathleen Poole, 74, was told to leave the country after her application to remain post-Brexit was rejected.
Her family have been told that Swedish authorities will continue to plan for the deportation, but have paused any order to carry it out for now.
Mrs Poole’s daughter-in-law said: “I just want an end to this situation”.
The British embassy in Stockholm informed Mrs Poole’s family on Wednesday that Swedish immigration authorities had received a request to stop the deportation at the end of March.
Her removal has been placed on hold until a new decision is made, it said.
“I actually don’t believe it for five minutes, even though they’ve paused it,” Angelica Poole told the BBC, calling for a permanent reversal of the decision.
She said the situation was taking a toll on the family and they fear the deportation order could be revived.
Grandmother-of-four Mrs Poole, who is from Macclesfield, Cheshire, applied for the right to remain in Sweden, where she movedalmosttwo decades ago to be near her only son and his children.
But her application was turned down in September 2022, despite the fact she is bedbound, has spent the last 10 years in a care home, and has no family she is in contact with in the UK.
The case has attracted significant media attention, and campaigners representing EU citizens living in the UK have expressed “grave concern”.
MP Hilary Benn, former Brexit Select Committee chair, has urged the UK foreign secretary, James Cleverly, to intervene.
Her family said Mrs Poole’s application was turned down because she does not have a valid UK passport, which they argue she has not required for some time as she is unable to travel due to her poor health.
They have been offered support to make a new application for a passport by the Foreign Office, Mrs Poole’s family told the BBC, but fear power of attorney arrangements in the UK mean they will be unsuccessful.
“I don’t know where to go from here,” her daughter-in-law said.
“A lot of British people are actually being sent back to the UK, which is not ok but they’re healthy.
“She can not do anything. She’s bedridden. That’s what makes me angry.
“They’re moving a sick person and her health can deteriorate even more by moving her.”
Her family said they have been left confused by the update and renewed their pleas for the situation to be resolved permanently.
On Tuesday, Sweden’s Minister of Migration, Maria Malmer Stenergard, said in a statement: “Decisions related to residence applications are applied directly by the Swedish state agencies and courts in line with the EU-UK Withdrawal Agreement.
“As laid down in the constitution, the Swedish government is not permitted to interfere in or comment on individual decisions taken by these independent state bodies.
“With regard to the case in question, I have been informed that the Swedish Migration Agency is in contact with the family concerning additional information.”
volunteer😆🙃 employment
working on the raffle on tonight
accessible through well, Dad, Maranda disability access is slowly improving in a big city 😁😋😆
phone activities 😅🥰😃
my friend version with my want to join night, but I haven’t managed to private jet call my David expedition support and my please click on the link in the title if you want to donate but haven’t yet arrived yet ceiling paint will come up. When can you donate thank you mate to all the members of this community 😍🤣respite
New Terminal Illness Rules For PIP, DLA And AA
With many thanks to Benefits And Work.
New terminal illness rules for personal independence payment (PIP), disability living allowance (DLA) and attendance allowance (AA) came into force on Monday, meaning that the six month rule has now been replaced by a twelve month rule, in line with universal credit.
The law now says that a person with a progressive disease is considered to be terminally ill when their death as a consequence of that disease can reasonably be expected within 12 months, as opposed to 6 months.
Form DS1500 has now been replaced with form SR1.
There’s more details on the .gov website on the Get benefits if you’re nearing the end of life page.
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A sweet shop worker who sold bags of treats to raise funds for the Down’s Syndrome Association said he had received “awesome” support.
Billy, who has Down’s, told colleagues at The Shop, Kettering, Northamptonshire, he wanted make more people aware of the condition.
So he created “Billy’s Pouch” and filled it with his favourite sweets.
The 28-year-old raised nearly £400 by selling about 400 bags, both in the shop and through online sales.
The Shop offers work experience to young people with additional needs, while boosting their skills.
Billy, who has worked there for about six months, pitched the idea during a daily staff meeting.
He said it was “my special idea” to raise awareness for World Down’s Syndrome Day on 21 March.
Claire Scott, who owns the business with her partner Geoff Littlewood, said Billy’s initiative had received “amazing” support.
The Shop was set up by a special school in Kettering and the couple took it over when it was threatened with closure – just three months before the Covid-19 pandemic.
Luckily, Mr Littlewood was able to use his IT skills to move sales online, which brought in a new customer base and kept the business running while the shop was shut.
Ms Scott said it had been “scary” moving from education to retail, but it meant everything to see their team thrive.
“It’s boosting their confidence and their communication, literacy, numeracy, IT and social skills. To see a job from start to the finish, seeing customers come in and buying the products that they’ve made is amazing,” she said.
“They’re working as part of a team, being able to solve problems.”
For Lula, who has worked at The Shop for seven years, the skills gained means she has been recruited for a weekend job at a cafe.
call me on quarantine right now tomorrow #FavourableCalledWhenYouHavePainCreamCreamer #Purpose #SpecialRead Janine is a
A deaf woman is calling for ambulance crews to learn basic sign language after paramedics were unable to tell her that her husband had died.
Elizabeth Corbett was at work when she received a distressed video call from her children to say her husband David, 51, had fallen ill.
By the time she got home, paramedics had arrived but could not explain to Mrs Corbett what had happened.
East Midlands Ambulance Service (EMAS) said it was deeply sorry.
Mrs Corbett, 43, from Chellaston in Derby, eventually learned of her husband’s death via a video call to her employer.
She said: “David had been mowing the grass and had sat down for a cool drink with the children when he suddenly stopped talking.
“At first the kids thought he was joking – because he was a big joker – but then they started to panic when they couldn’t wake him up.
“They contacted me and I told them to ring for an ambulance, while a colleague drove me home.
“The children were amazing, they performed CPR until the paramedics arrived.
“But when I got there the kids were stood on the lawn crying and the emergency services wouldn’t let me in the house.
“Not one of them could communicate with me and I couldn’t explain who I was.
“I wanted to know what was happening and the police were asking me questions, but they were all wearing facemasks so I couldn’t tell what they were saying.
“Eventually I contacted work and the receptionist spoke to the paramedics who told her that David had died. So I found out over FaceTime that he had gone.”
Mrs Corbett, who was born without hearing, is now calling for all emergency workers to have sign language training and a fully charged iPad so that they can connect to a qualified interpreter instantly.
She is also hoping to raise £60,000 for Royal School for the Deaf Derby, which her husband – who was also deaf – had attended and where she works as a teaching assistant.
She said once the paramedics had realised she was deaf, they had removed their facemasks.
“But for a deaf person in such a stressful situation it was very difficult to lipread, despite their efforts,” she said.
A post mortem revealed Mr Corbett had had a blood clot which caused a fatal heart attack.
The dad-of-two, who had worked at Toyota for almost 30 years, died on 15 June.
Craig Whyles, divisional director for Derbyshire at EMAS said: “We would like to offer our sincere condolences to the patient’s family and I am deeply sorry for the poor experience they had with our service.
“We would like to speak to the patient’s family about their experience and urge them to get in touch with us at their earliest convenience.
“As an organisation we are currently working with the Nottinghamshire Deaf Society to discuss how we can improve our education to staff around deaf awareness and common emergency communication problems.”
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we had lots of fun and really enjoyed ourselves. The average an adult with cerebral palsy. You have been friends for about the last 10 to 15 years for some of the members and me being a member of last 10 years. Thank you wacky wheels
Heart Hairstyle ♥️
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It could seem like an unusual journey from winning Paralympic gold in Rio to becoming a children’s author.
However, Ellie Robinson makes it sound like the most natural career path in the world.
She retired from swimming after the Tokyo Paralympics in 2021 and is now juggling her studies with writing.
Her first book – The Gold Medal Mysteries – is out on 13 April but she is giving a sneak preview in southern Scotland on Saturday.
Ellie, from Northampton, was diagnosed with Perthes disease in her right hip in 2012 – a condition affecting the hip joint in children.
She went on to enjoy huge success in swimming, winning her Paralympic gold in the S6 butterfly, aged just 15, in 2016.
After that chapter ended, Ellie was aware many sports people had difficulties moving on but said she had found it fairly straightforward.
“I think there’s this kind of narrative that there’s a bit of an identity crisis or they struggle to transition into that next area,” she said.
“It’s been such an integral part of one’s identity that you almost kind of grieve the loss of this huge piece of your life.
“I was quite fortunate, it was in lockdown when nothing was really happening – training had kind of ground to a halt.”
She started doing a history degree and did a lot of writing as well.
“I was able to find what my next step was while I was still an athlete,” she explained.
“I don’t know – I can’t say I hacked it – but I feel like my transition was incredibly smooth because I knew what that next step was, and I naturally kind of fell into it.”
It helped when a literary agent saw an interview where she spoke about her love of writing and followed up on it.
In some ways, Ellie was glad to leave parts of her old life behind.
“I hated training – I couldn’t say it when I was an athlete – because it wouldn’t sound great,” she said.
“But now I have finished sport I can proudly say – I hated training and I loved competing.”
That doesn’t mean she has left the world of sport behind – her first book combines her love of history and sport in a mystery story.
“The majority of the life lessons that I’ve learned or the personal development that I’ve made, it’s been made through swimming,” she admitted.
“So there are a lot of life lessons in the book that the characters learn, there’s a lot of progression that they go through themselves.
“I want to say about 90% of it is what I’ve learned in my own life and what I’ve learned through swimming.”
It also helped with planning her work where her “inner swimmer” has come out.
“I think I have to be incredibly disciplined, so what I do is I map everything out,” she said.
“Swimming was quite regimented, particularly on race days, on competition days, we’d have to do like full timelines, which were so precise they were to the minute.
“It think that the disciplined, regimented aspect of swimming has definitely played a part in balancing the studies with the book at the same time.”
Now she is coming to Moat Brae in Dumfries – the place credited with helping inspire JM Barrie to write Peter Pan – for the Big DoG Festival of Children’s Literature.
Not a bookworm
She hopes her book can capture the imagination of readers like her younger self.
“I wasn’t necessarily an avid reader but once I found a book that I liked I would finish it really quickly,” she said.
“I wasn’t a bookworm – the librarian at my secondary school would definitely vouch for that.”
However, Ellie said that a love of sport did not mean you could not also enjoy reading.
“It is not actually an accurate reflection of children and society nowadays – you can be both into sport and into books as well,” she said.
So perhaps the worlds of the Paralympics and literature need not be so far apart after all.












































































