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Bramford Pub Offers Free Sign Language Classes To Local Residents
A village pub is offering free British Sign Language (BSL) classes for the local community.
The Bramford Cock in Bramford, Suffolk, holds two classes at the pub every other Monday.
Landlady Teresa Brinkley had the idea after speaking with hearing-impaired customer, David.
She said: “I’ve wanted to do it for a little while… We sort of railroaded him into helping teach us some of the basics.”
David, who lives in the village, has been hearing impaired since birth and wears two hearing aids.
“[Teresa] approached me to see if I knew anything about sign language, which I did, and she asked if I’d run a basic sign language course,” he said.
Twelve people turned up for the first session about six weeks ago, and David taught them how to finger spell the alphabet and say simple phrases, such as ‘good morning’.
To David’s surprise, the group swiftly mastered their first lesson.
“They picked this up within the week, so I had to quickly jump to lesson three,” he said.
Ms Brinkley said she practises with the village residents, adding: “When someone asks for a drink, I literally sign it all out and then try to teach them before I actually pour it.”
The landlady has since welcomed more class attendees: “It’s just for an hour, it’s a relaxed environment… then we just sit there and chat, and practise is all.”
David said: “If they’d had sign language when I was at school growing up, it would’ve made my life a lot easier.”
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Designers Make Bespoke Fashion For Conjoined Twins
A dad who struggles to dress his conjoined twin daughters has welcomed calls to make mainstream fashion more accessible.
Seven-year-olds Marieme and Ndeye share many things, but not the same sense of style.
So staff and students at the University of South Wales’ fashion department are creating bespoke designs just for them.
Now the team of designers are helping them express their individuality and feel more comfortable in their clothes.
“When I first heard about the girls I thought what an amazing project to be involved in,” said Susan James, a technical instructor in fashion at the university, which offers modules in adaptive fashion.
“To give them something they can’t normally get – to be able to go into a store and that excitement and everything that brings with it.”
The girls are joined at the pelvis, sharing one pair of legs. Ndeye has a left arm and Marieme a right, and they share use of a middle arm. Their father Ibrahima struggles to dress them.
“It is giving me grey hairs every day,” he joked. “You have to buy two identical tops to join them together.
“They have two legs, so they can have regular trousers, but their hips are very wide so you have to take it to the alteration shop.”
Although the girls are conjoined, they have different taste in clothes.
Ndeye likes pink. Marieme likes red. Ndeye would like a unicorn motif. Marieme is obsessed with cats.
The girls are thriving, but still face many challenges and are dependent on each other to live. Ndeye’s system works hard to help support Marieme, which makes her hotter and sweat more than her sister.
Now the fashion department has joined a t-shirt for Ndeye with a sweatshirt for Marieme, and adapted a winter coat with less thermal padding for Ndeye and more for Marieme.
The girls’ bodies and needs are unique. But there are calls for more wearable fashion for all disabled people.
‘It gave me dignity’
BBC reporter Matthew Bassett, who was paralysed 12 years ago after he dived into the sea at Broadhaven in Pembrokeshire and hit his head, shared some of the lesser known challenges of being in a wheelchair.
“When I was first in a wheelchair I was buying jeans off the shelf making the most of it,” he said.
“But they didn’t quite fit, they were quite low on the back, and if they weren’t low on the back they were high on the legs, so I was always showing my ankles.
“I ended up having to ask friends or family to always pull up these jeans. It’s not what you want to ask everyone to do is it? A grown man asking someone to pull up your trousers every couple of hours.
“But I had to do it because if they go to low they give you pressure sores, they give you marks.
‘When I got a pair of jeans that covered up my back it just felt so great, it gave me dignity, independence.”
But Matthew has to buy these online, and they cost £80 a pair.
“I would love to see bigger chains jumping on board and that will bring the price down of styles, and everyone will win then,” he said.
‘They weren’t comfortable or practical’
Philippa Gouldson, 20, is a second year fashion design student at the University of South Wales.
After a running accident when she was 14, she spent five months in a wheelchair, and still has physiotherapy now. Her experience is now helping to inform her designs.
“Becoming a wheelchair user, all my lovely clothes in my wardrobe I wanted to wear, they just weren’t comfortable or practical,” she said.
“I really struggled getting them on. My mum had to help me.
“That’s one thing I’ve really focused on, making someone feel good in their clothes, but giving some dignity back as well, I think that’s such an important thing.”
High street chains are beginning to take notice. Last month, Primark became the latest to announce plans to offer more affordable accessible underwear range in its shops.
But adaptive clothing is still generally harder to find and more expensive than items on the high street.
“Something like this does tend to be more expensive. But the more we do of it, the more we can bring the price down,” said Susan back at the University of South Wales.
“It would be great if a label or a brand would take it on, make it more mainstream.”
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Pinterest update for Wednesday night
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Somerset Boy Receives Life-Changing Spider-Man Bionic Arm
A nine-year-old boy, who was born with one hand, is one of the first children to receive a Spider-Man bionic arm.
Kaden Taylor from Burnham-on-Sea received his 3D-printed Hero Arm as a surprise after mentioning to his family that he would like to wear one.
Despite being offered prosthetics before, he never agreed to one, until he saw the design by Open Bionics.
“I can cut with a knife and fork now and play tennis. And I can pick up more things,” Kaden told BBC Radio Somerset.
Kaden’s mum, Colette Taylor, added: “Kaden has never worn any prosthetics, we’ve always offered him options and he always refused.
“When I showed him the Hero Arm, he shouted: ‘Yes please!’
“It’s already made a difference,” Ms Taylor added.
“The first thing he wanted to do was go on a walk and hold my hand with it, which is so lovely.
“It’s just such a life-changing thing for him to have.”
Kaden’s family was able to buy the arm due to the community fundraising for him.
Within two months, they raised over £13,000.
“It blew up, it was crazy,” Ms Taylor said.
“We had people who I’ve never spoken to before come out and message me.”
Kaden added: “Thank you, you’re all amazing.”
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Pain Hyperacusis: ‘Hearing My Children’s Laughter Is Like Torture’
For the last 18 months Karen Cook has been living with an ever-worsening and rare health condition in which everyday sounds cause her crippling and debilitating pain.
“Something as beautiful as my children’s laughter, hearing their voices – is like torture for me,” she told BBC North West.
The 49-year-old has pain hyperacusis, a condition which means she is often forced to shut herself away from her husband and young sons.
“Sound is everywhere – it’s like air, you can’t escape it,” said Karen, from Southport, Merseyside.
Noises like the wind rustling leaves in trees, or traffic driving past her house can cause Karen immense pain.
Warning: Some readers may find parts of this article distressing
The condition is so severe that, on Christmas Day, she had to sit in another room and watch while her boys, aged seven and 11, excitedly unwrapped their presents.
Karen has not been able to find any cure or even treatment to ease the pain caused by hyperacusis, which is accompanied by the far more common and widely known tinnitus.
She said the hyperacusis developed relatively suddenly in 2022 and had gradually become worse.
While it can be brought on by sound trauma, research suggests some people may be predisposed to suffering from it.

What is hyperacusis and how does it differ from tinnitus?
There are different types of hyperacusis that vary in severity.
The NHS website says “you may have hyperacusis if some everyday sounds seem much louder than they should. It can sometimes be painful.
“You may be affected by sounds like jingling coins; a barking dog; a car engine; someone chewing; a vacuum cleaner.”
Tinnitus is the name for hearing noises that do not come from an outside source.

Karen now wears ear plugs and ear defenders even when she’s at home alone, and her only way to communicate is through whispers or written notes.
“My house is a prison,” she said. “Sound keeps me prisoner.”
Describing the pain, Karen said: “It’s like somebody poured burning lava into my ears and my head burns, pain all over my head, especially behind my eyes.
“It’s like a migraine kind of pain – it’s like you want to split your head open to relieve the pressure.”
When asked what impact the condition has had on her life, fighting back tears, she said it had been “devastating”.
“I miss being a mum, I miss the clatter of the noise when they come in from school.
“I miss just life, I sat and watched them through the window opening their Christmas presents, because it was too loud for me to be in the room and they’d come up to the window and show me.
“It’s completely erased me.”
Karen said she was missing out on so many parts of life that most people take for granted.
“I miss listening to music, watching TV or a film with sound, chatting to my friends on the phone,” she explained.
“I miss wearing nice clothes and make-up, going for a night out with my husband Nick.”
Karen said she used to be “very active” and loved going on camping and skiing holidays.
“I was always on the go,” she said. “My life literally stopped so abruptly.”
Nick said he was losing his “best friend” of more than 20 years.
“Life was an adventure,” he said. “We’d have no plans, we’d just go out for the day and wherever we ended up it was fantastic. Travelling of any description – we bought a caravan in Covid – as well as hiking, football matches, any excuse to get out and about.”
He added “everything” they had known as a family had changed.
Karen used to work as an airline crew member for 25 years, a career which she said “wasn’t just a job it was part of my identity and independence”.
It was also where she met Nick.
So much of their life has changed beyond recognition.
“It is literally Groundhog Day,” said Karen. “Every day is the same.
“Honestly if I didn’t have children I’d have given up.
“But we’re going to try and fight and find someone – anyone – who might be able to help.”
Ken Devore has lived with the condition for 30 years and said some people can improve over time.
Mr Devore, who is a board member of the US charity Hyperacusis Research., added: “There really is no treatment.
“For me, time, quiet environments and just avoiding loud noise is the key to managing it and not making it worse.”
For some patients, the NHS advises reintroducing sounds like white noise, which can help build up tolerance levels.
That has not worked for Karen, however.
She has also tried various medications and holistic therapies, but nothing has helped.
Nonetheless Karen said she was “determined” to find treatment for the sake of her boys, who tell people about their mum’s “poorly ears”.
“One day there might be a cure for this and I’ve promised myself I will try everything and anything.”
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nativity zone for you all for this Monday evening as I know the weekend feel wrong at the start of it
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Mental Health Inpatients Were Ordered To Attend Work Coach Interviews
With many thanks to Benefits And Work.
Three inpatients at a mental health clinic in Dorset were told that they had to attend jobcentre interviews, in a disturbing incident which highlights the dangers of giving inadequately trained work coaches any discretion whatsoever. It also underlines the foolhardiness of the Tory plans to abolish the work capability assessment (WCA) and allow work coaches to decide who is capable of work.
According to the Guardian, the three claimants were all inpatients at Forton Clinic near Dorchester and were in receipt of universal credit. At least one of the patients appears to have been sectioned.
All three claimants were told that they had to attend interviews with work coaches or risk having their benefit sanctioned This is in breach of DWP guidance which does not require inpatients to attend interviews and allows work coaches to waive the requirement for any sort of claimant commitment whilst a claimant is an inpatient in a hospital.
Fortunately, Citizens Advice have an outreach worker base at the clinic and they were able to persuade to DWP to remove the requirement for two of the patients to attend. However, the third interview did go ahead in order to prevent the UC claim being delayed.
Management at the Jobcentre in question have refused to guarantee that other inpatients at the clinic will not be asked to attend interviews in the future.
Under Conservative plans, the WCA is to be abolished for new claims in 2026/27. Instead, claimants who get PIP will be entitled to an additional health element in their UC. But decisions about whether a claimant is capable of work and what work-related activities, if any, they should undertake will be entirely left up to poorly trained work coaches.
Whilst these plans may never be put in place if there is a change of government later this year, incidents such as this demonstrate how disastrous it would be if they are not shelved.
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Millie, update of the Pinterest page 4 only beautiful sunny morning
Tractor with rabbit figurine from Peppa Pig
Rowing boat with Peppa Pig figurine is for Kerrigan
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w LOL, good night/good evening so how are you all?
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Early evening, saying how old
Painting of the afternoon
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