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With many thanks to Benefits And Work.
Almost half a million callers to the PIP helpline in the month of April were deliberately disconnected by the DWP before they could even wait in a queue, a freedom of information request by Benefits and Work has revealed. The proportion of calls cut-off before entering the queue is now greater than the proportion who even get to wait for an hour or more before giving up or getting disconnected.
In May, we asked the DWP to tell us the number of calls made to the PIP Enquiry Line on 0800 121 4433 and the number of these which were blocked, for the last three months for which the statistics are available.
The DWP provided us with the following statistics:
February
Calls put in queue 415,552
Calls blocked 34,860
March
Calls put in queue 488,965
Calls blocked 306,865
April
Calls put in queue 388,265
Calls blocked 494,044
The DWP went on to argue that:
“Personal Independence Payment has experienced unprecedented levels of new claims from customers in recent months and as a result we have seen increased call traffic.
“The blocked call figures relate to the enquiry line only and does not impact customers being able to make new claims or raise a dispute.
“We are currently in the process of recruitment [sic] additional resource into telephony so that we can increase the number of calls answered and prevent blocked calls. Although blocked calls relate
to customers unable to join the queue this figure is significantly increased by customers dialling the number multiple times.”
However, whilst claims are at record levels as the DWP says, the number of new claims in the quarter to April 2023 is only up by 20% on the number of new claims in the quarter to April 2022.
This stops well short of being “unprecedented”.
Moreover, whatever the explanation for the increase in calls, it seems that the DWP put 100,000 fewer callers in the queue in April than they did in March. This suggests that the department is dealing with fewer callers as volumes increase, not more.
The worry is that the DWP is now in a downward spiral of increasingly awful customer service.
Forms are not being sent out, letters are not being acknowledged, changes of address or bank details are not being recorded and claimants are being left many months with the horrible uncertainty of not knowing the result of their award review. All this results in a continual increase in the number of desperate callers to the PIP helpline. And amongst them all are the claimants whose health conditions have changed, but who cannot pass on that information or receive the increased award they may be entitled to.
And what these statistics don’t tell us, but we will now attempt to discover, is how many of the callers in the queue ever get answered.
Readers only need to look at some of the many hundreds of comments on our PIP Enquiry Line page to realise the intense distress that this utter failure of service by the DWP is causing to people who simply want to ensure that they meet their responsibilities as claimants.
Plymouth Student’s Plea For More Access At University
A student at the University of Plymouth is calling for more accessibility on campus.
Jude Costello, a wheelchair user, said he was denied access to the campus while the university’s summer ball was being set up earlier this month.
Mr Costello, 20, said it made him feel “alienated” and “not accepted” as a student.
A spokesperson for the University of Plymouth apologised and said an investigation had begun into the issue.
The marine biology student said he also attended a boat party as part of his course, but a ramp was not available for him to access the boat.
He said: “Even aside from the fact it makes getting an education here more difficult, being unable to access classrooms and lectures and things like that, it just makes me feel very alienated.”
‘Exhausting’
Mr Costello, who has chronic pain, fibromyalgia and hypermobility, said he hoped the university could improve accessibility for its students.
He said: “I have to put in so much more work than my able-bodied peers in order to do the things that they do. I don’t get recognised for it, I don’t get that much support for it. It’s exhausting.
“It makes me feel like I’m not accepted as a student here, that I’m a burden to my friends and peers.”
The university spokesperson said: “Everyone at the university wants students to have a great experience here, and we’re keen to work with Jude to further understand how we can best meet his needs and resolve these issues.”
Amelia McLoughlin, the network director for Disabled Students UK, said anecdotally this was an issue across the country.
She said: “It’s sad we continue to hear these same stories across the sector. We would say to be fair on individual institutions as well it’s quite widespread from the information we have.”
She added: “It needs leadership, funding and an acknowledgement that this is happening in the sector.”
https://www.justgiving.com/crowdfunding/maya-richards?utm_term=9nZgZ3QV8 my fundraising page rows that may want to go
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BBC Drama Asks: When Do You Let A Sick Child Die?
How do you decide when to stop treating a sick child, knowing that it will end the child’s life?
For Bafta-winning writer Jack Thorne, that’s the central question in his latest TV show.
In the four-part BBC One series, Best Interests, parents Nicci and Andrew (played by Sharon Horgan and Michael Sheen) confront doctors who say it’s in the best interests of their disabled child Marnie (played by Niamh Moriarty) to turn off her ventilator, allowing her to die.
“I wanted to tell this drama with complexity,” Thorne says, explaining he tried to show the views from all sides of the debate – disabled people to parents and doctors – without “moralising”.
“I hope I managed to steer a path through it,” he adds.
Thorne, known for writing the stage play Harry Potter and the Cursed Child, the TV movie Help and the TV series His Dark Materials, says becoming a father three years ago brought the central question in the series home “hugely”.
“I don’t think I could have written this without being a parent,” he says, describing the “fierce love” that comes with being a father.
But he says he has also come to understand the potential divisions that can arise between parents.
In the series, Marnie’s parents are split on whether to agree with doctors to stop her treatment, setting up a legal battle that sees them take opposing sides.
“Being a parent with someone is a very, very, severe sort of intimacy,” Thorne says. “You’re constantly negotiating.
“That question of who has the child’s best interests, and how you can decide what the child’s best interests are, hopefully that permeates the whole show.”
In England and Wales the concept of parental responsibility is set out in the Children Act 1989, giving parents the responsibility broadly to decide what happens to their child, including the right to consent to medical treatment. But this right is not absolute.
If a public body considers that a parents’ choices are not in the best interests of their child, and an agreement cannot be reached, it can challenge these choices by going to court.
A representative is appointed for the child – separate from their parents and doctors – and a judge makes the final decision, based on the evidence available.
The Department of Health and Social Care has commissioned an independent review of the disagreements that can arise between families and healthcare teams in the care of critically ill children in England. It is due to be completed by October 2023.
Best Interests also touches on the health inequalities in society experienced by disabled people – and what Thorne refers to as the “scars” caused by the pandemic.
He says friends of his were told they wouldn’t get care during the pandemic because they were too ill.
“It’s when we’re in crisis that we show our true selves, and I think our society showed itself to be dangerously ableist.”
Ableism is defined as discrimination that favours non-disabled people above disabled people.
Thorne adds: “I hope it’s clear from the drama that I feel like the treatment of disabled people, particularly through the pandemic, was wrong and inhumane at times.
“But I also don’t want to castigate NHS doctors and nurses who are all working hard or who have their beliefs.”
In Best Interests, Thorne says he was also keen to include scenes of laughter, love and even sex.
“That, in my opinion, is how these things work,” he says. “When you’re going through a tragic experience, it can be funny, it can be silly, it can be all these different things.
“Humanity pokes up in all sorts of weird places.”
Writing is soothing
Speaking at the MacTaggart Lecture at the Edinburgh TV Festival in 2021, Thorne talked about having cholinergic urticaria, a condition that caused him to be allergic to artificial heat and movement, leaving him with welts and in pain.
When he was 20, he spent six months in bed and he says his life was very restricted for 10 years.
In the speech, he was also harshly critical of the TV industry, saying it had “utterly and totally” failed disabled people.
But Thorne says things have “moved on markedly” since he gave the speech.
“I’m very excited that disabled people are starting to move into leadership positions.”
Thorne is also getting used to life after a recent autism diagnosis, something that came about after an appearance on radio programme Desert Island Discs, when a listener wrote to his agent suggesting he might be autistic.
The diagnosis made a lot of sense, he says. “I think it’s been a positive.”
Looking back, Thorne says being autistic helped with his writing career – and he says writing is still the one thing that he finds calming above all else.
“That has been my saving grace really through my life, the ability to be able to write and find comfort in creating situations where I can understand [things] better.
“I just find writing very soothing.”
Watch Best Interests on BBC One and BBC iPlayer from 21:00 BST, Monday 12 June
dying of the afternoon and illustration

https://vm.tiktok.com/ZGJQmYNbp/
click on it to see Margaret to London two years ago. #CommunityAccess #CommunityAccessWithDisability in the community, and travelling with Liverpool called the app and the entrance
https://vm.tiktok.com/ZGJQmkVUE/
TikTok when I visited London two years ago, tycoon today for more videos of when I visited London
Love Island is back for its 10th series.
And while it might have been on screens since 2015, this summer there’s a change for blind and visually impaired fans of the show.
For the first time contestants have provided audio description, describing how they look, their skin tone and outfits.
The Royal National Institute of Blind People praised ITV, calling the move “a remarkable example for the industry”.
“I’m a tall, mixed race woman, I’m 28 years old, half-Swedish, half-Somali,” host Maya Jama says in her audio description.
“I have long brown hair and brown eyes,” she adds, saying that she likes to wear colourful clothes and that she’s smiley and enthusiastic.
Ron Hall, who’s blind in one eye, was the show’s first visually impaired contestant during this year’s winter version.
The 25-year-old thinks ITV are making a positive “first step” when it comes to accessibility.
“It’s quite a nice start that the place that gave me a platform is now following on from me being visually impaired and helping others as well,” he tells BBC Newsbeat.
“Although I’d say it’s quite a big group, people do forget about the blind and visually impaired, because people just live day to day and watch it normally.
“So it’s nice that they’re taking the first step.”
‘You want to know the drama’
Connor Scott-Gardner, who is blind, agrees and thinks it’s good ITV are starting to think of fans like himself.
“I really look forward to the whole season to be honest,” the 29-year-old says.
“In terms of audio description, I think it’s a great step that ITV are taking and providing an element of audio description for blind fans.
“I have checked out the personal audio descriptions and I think it’s interesting – it’s definitely not something I expected.”
But Abi James-Miller, who’s a big Love Island fan, thinks ITV could go further to enhance the experience for blind and visually impaired viewers.
The 24-year-old is visually impaired and often messages other fans on Twitter to find out what’s happening on screen.
While the contestants and host have described themselves, and ITV say a villa tour is set to be uploaded, there’s no audio description available for each episode.
Other reality shows, like Too Hot To Handle and Naked Attraction, offer audio descriptions.
“I feel the descriptions they’ve done don’t go far enough to actually enhance the experience as a watcher,” Abi says.
“I can find out who they are, if they’ve got a tattoo, but you want to know the drama, that’s why I’m watching it.
“I think we need more integrated audio descriptions in Iain Stirling’s presenting and his script.”
ITV says the nature of Love Island “means that there is very little space within the programme to add traditional audio description and no time ahead of transmission to write and record it”.
“This is why we were so keen to create this additional content,” it says.
Abi also says the show should include the audio descriptions on the channel’s streaming service ITVX, instead of YouTube, so they’re easier and less time-consuming for people to access.
ITV told Newsbeat it’s looking to move additional audio descriptions on to ITVX in the future.
Like Abi, Connor thinks there needs to be more audio descriptions of live and pre-recorded shows – Love Island is usually pre-recorded but the final is live – across the industry.
“I don’t think it’s perfect, but I think any push towards accessibility has to be a good thing,” he says.
“And we need to view it as a positive as well as holding various media companies accountable and saying they also need to do more in future.”
A spokesperson for Love Island says ITV is “committed to improving the accessibility of our shows on a continuous basis and we’re always working on new ideas”.
Long time of the day and I hope everybody is enjoying the nice weather. #SummerWeather#Floren#BeautifulWeather
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Good Evening good evening, all member of our community wishing everybody a good evening♥️♥️♥️

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Happy FRIDAY Everyone
Yeah!!! happy Friday to all those who wait for Friday as much as I do. Because for many it is the end of their employment week, volunteer week or College week or any type of education or training or just general student life if you are a student like myself. So hope everybody has a nice weekend and I tell you something I’m definitely thinking yeah it’s Friday
this is your first post of the day to welcome the day in with the positivity pan and a good illustration

A new airplane seat concept that allows wheelchair users to stay in their own chair throughout a flight was revealed this week by a subsidiary of US airline Delta, a move welcomed as a “huge step” by potential customers.
“Unbelievably excited,” is how power wheelchair user and avid traveler Cory Lee described his reaction after a working prototype of the design was demonstrated by Delta Flight Products (DFP) at the Aircraft Interiors Expo (AIX) in Hamburg, Germany, a symposium spotlighting airplane cabin innovations.
DFP’s concept seamlessly converts to and from a traditional airplane seat. The built-in seat folds up to allow a wheelchair to be docked into place. The seat would be installed into pre-existing aircraft seat track systems, so would not involve any structural change to the airplane.
When the seat’s in wheelchair mode, flyers are still able to use the tray table – the center console that houses the tray table rises to the appropriate height when the seat conversion takes place.
Rick Salanitri, DFP president, told CNN Travel at AIX that the goal is to make the conversion seamless.
Though still only a prototype, the design is already generating significant buzz among wheelchair users who could be among potential customers. It’s hoped that the concept could enter commercial use within 18 months if it passes testing and is adopted by airlines.
“For decades, people with disabilities have been fighting for more accessible air travel, and this feels like a huge step (or a giant roll) toward real inclusivity,” Lee told CNN Travel via email.
Lee’s visited 43 countries and counting, documenting his adventures on his blog. He loves exploring the world, but said at present air travel is “tremendously difficult” for him.
As airlines can’t typically accommodate powered chairs, Lee usually has to use a non-electric, airport-owned one, which he can’t control himself. This, he said, leads to a “scary” loss of independence.
This discomfort continues when he boards a plane and must be lifted by staff into an aisle wheelchair, and then again onto an airplane seat.
“During those transfers, I’ve nearly been dropped on several occasions,” said Lee.
Once on board, Lee spends the whole journey concerned that his personal wheelchair may be damaged during flight (“It has been damaged so badly that I couldn’t even drive it out of the airport on two different occasions,” he explained.)
Lee’s experiences are not unique. Air travel is infamously inaccessible, with disability activists vocal about the dehumanizing and dangerous air experience for wheelchair users.
New design
To produce this new seat design, DFP partnered with UK-based consortium Air4All. Air4All comprises aviation design company PriestmanGoode, advocacy group Flying Disabled, aerospace company SWS Certification and wheelchair design company Sunrise Medical.
Flying Disabled’s Christopher Wood kickstarted the consortium a few years ago. His two adult children are wheelchair users who love to travel, and Wood’s seen firsthand the issues they encounter on airplanes.
“I did research to try and create a solution,” Wood tells CNN Travel at AIX. First, he looked into working with nonprofits. Eventually he concluded he needed to go directly to an aviation company. He approached Priestman Goode and Air4All was formed.
“I found like minded people,” said Wood.
Somewhere along the line, DFP – described by Salanitri as “a product development company inside of the airline” – and Priestman Goode started talking about the concept.
“We thought the idea had some merit,” said Salanitri. DFP bookmarked the idea, and then revisited it when they were approached by Delta Air Lines customer service team to see if they could develop “some sort of carrier that they could put customer wheelchairs in.”
That was an “aha” moment, said Salanitri.
‘Well, we came across this other idea here,’” he recalled saying.
That was around 18 months ago, and the product’s been in development ever since.
DFP said it brought in a disability focus group to weigh in every step of the way. One of the key pieces of feedback, said product innovation manager Tyler Anderson-Lennert, was the height of the center console, which now elevates when the seat is in wheelchair mode.
“This has been done with some serious backing from the community to give their feedback,” added Flying Disabled’s Wood, who said it was important that this wasn’t an airline “lecturing to the community,” but rather a collaborative, instructive process.
Real world implication
At AIX, the DFP team has spent the past few days demonstrating their seat to aviation industry insiders. Wood said the reaction has been “genuine enthusiasm.”
What’s perhaps most striking at first look is that the seat maintains the same aesthetic whether it’s in its traditional airplane seat mode, or in its wheelchair conversion. The team wanted to make it “stylish” and they’ve succeeded.
The conversion process, as demonstrated to CNN Travel by DFP engineers, is also incredibly swift and smooth, taking around 90 seconds.
The team is now working on the next steps to make the concept a reality.
“We’re going through the testing and development and certification for the chair that is going to make that chair viable to go on an aircraft – we’re projecting within 18 months,” said Anderson-Lennert.
Salanitiri said DFP has also started informal discussions with the US Federal Aviation Administration, as well as the UK Civil Aviation Authority.
Although DFP is a subsidiary of Delta, Salanitiri said he cannot confirm whether or not Delta will be the first airline to implement the seat design.
The ultimate goal, added Wood, is getting the seat on every airline.
The team hopes implementing the concept would be straightforward for airlines to install, though they currently don’t know what costs could look like.
“Here’s the perfect world,” said Salanitri. “I pick up the front row of all domestic airplane seats and I drop these in, no other changes, I’d have to integrate a little bit of IFE [in-flight entertainment] into it, there’ll be some regulatory certification that goes into it, but it’s a very low time, low cost modification in the perfect world.”
In terms of ticket fare, Salanitri said the wheelchair version of the seat will likely be within “the price point of a standard domestic first class seat.”
Key step
Flying Disabled’s Wood said he’s thrilled his team’s found a potential way to improve what he calls the biggest barrier to accessible air travel, but he acknowledges that there are other unresolved issues and more to be done.
Wheelchair traveler Lee agrees, pinpointing aircraft restrooms as the next problem that should be addressed.
“Currently, they are so small that it’s impossible for a caregiver and I to go in for me to use the restroom,” he said. “Currently, I have to severely limit my food and liquid intake in the days leading up to a flight, so that I won’t need to use a restroom onboard the plane.”
“Until air travel is inclusive for everyone, including wheelchair users, it isn’t inclusive at all.”
Cory Lee, travel blogger and power wheelchair user
Still, Lee said he’s thrilled that “an airline has finally acknowledged that there needs to be a wheelchair spot on planes, and is trying to make it happen.” He adds that he’s “immensely looking forward” to a time when he can stay in his own wheelchair on a flight.”
“On a daily basis, I receive messages from other wheelchair users saying that they want to travel, but they’re terrified that their wheelchair will get damaged, so they choose to just do road trips,” Lee said. “In 2023, they shouldn’t be saying that. Until air travel is inclusive for everyone, including wheelchair users, it isn’t inclusive at all.
😀 how do you say Woodlarks selfie of me?
The Mother Bringing Autism Out Of The Dark In Iraq
Iraqi mother Shaimaa Alhashimi was tired of a lack of understanding towards her two autistic children by a society which preferred to look the other way. So she decided to do something about it by posting videos of her home life – gaining supporters, and critics, along the way.
“Why are you proud of them? They are crazy. And despite their condition, you are making money off your children.”
It is an unpleasant comment, typical of the kind posted on Shaimaa Alhashimi’s Instagram page by people seeking to shame her.
The trolls are responding to videos uploaded by the mother of two autistic and blind children, who is shattering social taboos by sharing insights into their home life in Baghdad.
“I didn’t want other parents to suffer like me and I wanted to offer a glimmer of hope to every mother and father,” she says.
Shaimaa radiates calm and now has 144,000 followers but it’s been a long road.
“Seventeen years ago, we did not know much about autism, and our understanding was that the child would sit in a corner, is not very social, and speaks very little,” the mother-of-three says.
Social stigma
Aya, 17, and Mohammed, 11, are on the autism spectrum. They are also blind due to the incomplete development of the brain’s outer layer which affected their optic nerve.
Shaimaa says Aya was four years old when she started showing signs of autism – such as spinning herself around and starting to walk on her tiptoes. There are no official figures for how many children have autism in Iraq and it’s often difficult to get a diagnosis.
Shatha Ali Khadum, a psychologist and director of the Babylon Centre for Autism, Speech and Learning Difficulties in Baghdad, estimates about 20,000 children in Iraq are autistic.
But this is probably an undercount as there’s a sense of shame associated with having a disability in Iraq and parents would not want their children “labelled” as such.
“There is currently no government support specifically for this group, and there are no government centres or shelters dedicated to them,” says Ms Khadum.
When Aya was 11, she experienced an incident in one of those centres, which made Shaimaa decide to take matters into her own hands and home school her.
One day, when Shaimaa was late to pick her daughter up, the girl was left in the guard’s room on her own. Shaimaa believes there was an attempt to harass her.
When she was checking Aya’s body for any signs of harassment or struggle, she says discomfort was visible on her face and Aya even pushed her mother’s hand away.
“Even to this day, when we try to hug Aya, she leaves a small distance, and if we pull her closer to us, she pulls away.”
Shaimaa says no specialist school would accept her children, because they were both blind and autistic.
She also ruled out sending them to a private school, though she can afford it, because other parents who had tried to enrol their autistic children said they were not welcomed in class.
“I don’t want to make myself or my children go through this situation,” says Shaimaa. “When you send an autistic child to school and they feel happy, then lose that feeling, do you know what that does to them?”
This led Shaimaa and her husband to invest their time, effort, and money in developing their children.
Shaimaa got in contact with specialists in the UK, Sweden, and the US, and also brought in a Braille teacher for Mohammed.
Despite his young age, Mohammed has a big role in family life, especially when it comes to his sister Aya.
“If Aya gets anxious, Mohammed calms her down, and if she gets upset, he goes to comfort her,” says Shaimaa.
Hurtful encounters
When Shaimaa and her family go out in public, they get a lot of stares.
She recalls an incident in a children’s playground where Mohammed was trying to climb up the slide, but not using the stairs. Some parents were worried that their children would try to do the same and hurt themselves.
“As a mother, I wish there was a law to hold such people accountable, especially since these situations have affected my mental health,” says Shaimaa. “I would go home, not wanting to go out with my children again.”
As a result, Shaimaa got Aya and Mohammed badges which read “I have autism, be patient with me”.
Shaimaa gets emotional when she tells me how another mother approached Mohammed one day to read his badge.
The mother then went back to her three children and told them to help Mohammed if he needed it. It’s a sign of how society is changing.
Shaimaa created her Instagram page in 2020 after Covid shut all government centres. At the start, she received comments such as “Why does this girl speak so slowly?”.
Shaimaa tried to ignore them but then she noticed her followers replying and explaining that Aya has autism spectrum disorder.
Another positive step to a more inclusive world.
One of the hidden sides of autism is the physical and mental pressures parents face.
Mohammed needed two years to learn the piano and Shaimaa repeats words to Aya several times a day to develop her ability to communicate.
“Before, I had an immense fear of what was to come, my children’s condition, what will happen to them if I am not around?” she says.
“These thoughts haunt every mother every day. But now, it does not. Instead, I have hope and motivation. Aya relies on herself 70% of the time and Mohammed 90%.”
Shaimaa’s top tip to parents is patience.
“When you scold them or they sense you are annoyed, it’s over. It may be difficult to make progress now but who knows in a year or two.”
no problem, paying of this Wednesday morning

A woman who used virtual reality to understand her child’s visual impairment says seeing the world through her daughter’s eyes is “mind blowing”.
Caroline Henderson’s daughter Aibhilin, seven, was diagnosed with ocular albinism and nystagmus at 11 weeks old.
When Caroline and her husband Carl used a VR headset developed in Belfast, they found it “overwhelming”.
It showed them just how frustrating her visual impairment was for Aibhilin.
“It was very overwhelming and it made us realise just how frustrating and how her world is very different to the way her dad and I see the world,” says Caroline.
“It made perfect sense why the playground and classroom can be really frustrating and she doesn’t read non-verbal social cues.”
The software was developed in Belfast by Sara McCracken, whose twins were born at 29 weeks and registered blind at just six months.
Peter and Connie have oculocutaneous albinism and nystagmus, which means their eyes move involuntarily from side to side and they have reduced vision.
Ms McCracken wanted the wider world to understand how people with visual impairments, like her twins, see every day.
The system recreates more than 30 eye conditions in a variety of settings such as a school classroom, a busy street, bus or play park.
The team involved include experts from the Royal Victoria Hospital in Belfast and Ulster University.
“We’ve developed software that can be manipulated to create lots of different eye conditions,” says Ms McCracken.
“It’s a very effective way of giving people who don’t have clinical information or knowledge a really immersive impression of visual impairment.
“It’s very effective for parents to be able to understand and change the way they advocate for their child but also for schools to understand the impact it has on children in the classroom or playground and, beyond that, for adults who have a visual impairment too.”
For Caroline, the Empatheyes software has made her more understanding of Aibhilin’s behaviour.
She says children with visual impairments often get very tired by the end of the week, their vision has deteriorated, and the way they are parented or taught needs to be adapted.
“I think sometimes the children with visual impairment, you’re seeing the tip of the iceberg and not understanding what’s underneath and driving that behaviour,” she explains.
“Thursdays and Fridays are Aibhilin’s most challenging days at school.
“But now, understanding her nystagmus and the way that she sees the world, and she’s tired because she’s held it together all week.
“I think without doing the VR technology we wouldn’t understand the difference between the Aibhilin we have on a Monday and the Aibhilin we have on a Friday.”
Empatheyes works as a social enterprise. Its team is based at the Innovation Factory in west Belfast.
Its software is being used in schools, healthcare settings and offices across the UK and Ireland.
Next month it will be shown to an international audience at the Vision 2023 conference in Denver.
“The United States is a massive market and they don’t have anything like it there,” says Ms McCracken.
“There’s a lot of excitement already from professionals over there to see this VR system that we created right here in Northern Ireland.”
https://vm.tiktok.com/ZGJxwGTfs/video of the day click on the video of remind me of the day and Tuesday Salpi
good frame of the night

Phone of the evening

https://vm.tiktok.com/ZGJxwrof9/more footage of the concert retirement to wait for #LiveMusic #ILoveThatHasText
you certainly don’t throw you Tuesday morning
A woman living with a terminal cancer diagnosis was told she would have to wait 12 weeks to receive a blue badge to park in accessible spaces.
Sarah Jackson, from Whitchurch in Shropshire, struggles to walk and said the delay affected her independence.
“If I can’t park in a disabled spot I’m having to get to my appointments two-three hours early to get a space near to where I need to be,” she said.
Shropshire Council said it was training staff to speed up the process.
After the BBC contacted the local authority about Mrs Jackson’s case, it confirmed her blue badge had been ordered.
Mrs Jackson, 51, was first diagnosed with breast cancer five years ago, but last year was told the disease had spread.
After applying for personal independence payments, she said she was told she would automatically qualify for disabled parking.
Government figures show the average wait is 17 days for a blue badge, however when her case was passed to her local council, Mrs Jackson was told she would need to wait for 12 weeks.
‘Like tempting fate’
“It seems ridiculous,” she said, adding that not being able to park in accessible spaces was making getting to her hospital appointments “really difficult”.
“It makes something that’s not a great experience anyway 10 times worse.”
It is possible to fast-track applications for people with a terminal diagnosis, but life-expectancy needs to be a year or less.
“I’m very much hoping I don’t have less than a year” said Mrs Jackson. “It feels very much like tempting fate.”
Shropshire Council said it understood the impact on people waiting for their applications to be processed.
“We have a responsibility to ensure our assessment is fair and robust for each applicant, which does take time,” a spokesperson said.
“Nevertheless, we want to make the application process as efficient as possible and we are investing new staff in the Blue Badge Team who are currently being trained to undertake the assessments and to develop how we can streamline the application process.”
call positivity 👩🏾🦽💕
you’re flying of the day for Monday morning
With many thanks to Benefits And Work.
A media hate campaign against support group claimants has begun, as the government moves to abolish the work capability assessment (WCA) and allow unqualified jobcentre work coaches to decide whether claimants are capable of work. Sick and disabled claimants are even being blamed for the rise in immigration into the UK.
The lead article in the Telegraph of 24 May revealed “Millions on benefits do not have to seek work”.
The sub-headline added “Taxpayers face bankrolling payments indefinitely for 3.7 million given exemption from having to find a job.”
The article highlighted the number of people claiming ESA and UC because of conditions such as anxiety and depression, back pain, wrist and hand disorders and carpal tunnel syndrome.
It went on to say that “Britain’s growing worklessness crisis comes as official figures on Thursday are expected to show net migration has soared to record levels of between 700,000 and 1 million.”
Iain Duncan Smith was cited as saying that the UK needs to concentrate less on bringing in workers from abroad and more on getting British people on sickness benefits back into the labour market.
He said “Companies should now be ending their addiction to cheap labour. They should be focusing on improving productivity by a greater increase in technology, and by training and getting back into work these people on sickness benefits.
“There is no reason why many of these people on these benefits should not be in work. We’ve got a real problem”
Elsewhere in the paper IDS was quoted as saying:
“Sadly, by being exempt from welfare rules designed to help people into work, they are bound to suffer further – for being in work is acknowledged as a strong health treatment, particularly for those with depression or anxiety.”
Meanwhile, the Jeremy Vine on 5 show last week put out a tweet seen by millions of people which said
“Is it time to crack down on jobless benefits?
“Nearly four million people in the UK are being supported by the state without ever having to look for a job.
“That’s because they’ve been deemed too sick to work.
“Is it wrong for taxpayers to fund them indefinitely?”
After arousing considerable outrage the tweet was deleted, but a programme on the subject went ahead all the same.
Clearly the DWP are expecting considerable resistance to their project to abolish the WCA. That they are determined to go ahead with it is clear from the announcement that the combined PIP and WCA assessment contracts have now been awarded. Attacking support group claimants in the media as workshy and responsible for record levels of immigration is one way of convincing the public that the DWP are on the right track.































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