Cheltenham Man Sets World Record For Wheelchair Journey
A man has set a new world record by doing the fastest journey from Land’s End to John O’Groats in an electric wheelchair.
Adam Stanton-Wharmby, from Cheltenham, has cerebral palsy and his wheelchair was upgraded by the Mercedes Formula One team to help him complete the route.
He finished the journey in 22 days, six hours and 16 minutes.
“I’m the happiest now than I have ever been,” he said.
Mr Stanton-Wharmby travelled the 874 miles (1,406km) in April, but had been waiting for confirmation from the Guinness World Records team, which he received last week.
“I feel a relief that I’ve got the world record,” he said.
Engineers put lithium batteries into the 38-year-old’s wheelchair and took out 70kg of weight to allow him to travel 60 miles or more on a single charge.
“I said what I wanted to do and I went out and did it, that’s the one thing I’m really pleased about,” he added.
“I said to everyone I wanted to break the world record, and I actually did it.
“I’m the happiest at this point in my life that I’ve ever been.
“To get a world record and to go from Scotland to Cornwall in a wheelchair as a disabled person is amazing.”
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Ukraine War: Sex Lives In Focus For Ukraine’s Injured Veterans
At a modern office in central Kyiv, a 26-year-old Ukrainian veteran is proudly playing a video on his phone that shows him passionately kissing a young woman in a kitchen.
It is an advert for ReSex: a charity that tries to help former soldiers with their sex lives, after suffering physical and mental trauma.
In March last year, invading Russian forces launched a brutal siege of the Ukrainian port city of Mariupol, pounding much of it to ruins. Hlib Stryzhko – then a marine – was one of the city’s defenders.
A Russian blast knocked him from the third floor of a building to the ground. He was then crushed under rubble.
Hlib’s pelvis, jaw and nose was broken, and as well as being badly concussed, he says the heat of the explosion melted his tactical goggles onto his face. He was then captured by Russian forces and taken as a prisoner of war.
The following month, Hlib was released and sent back to Ukrainian territory as part of a prisoner exchange. But he says he received little medical care during his time in captivity.
The BBC first spoke to Hlib just weeks after his release, and later spoke to him during his rehabilitation.
It was while Hlib worked on his recovery that ReSex approached him.
“After my pelvis injury I had problems that took some time to heal. And [the issue of sex] wasn’t talked much about, so I wouldn’t want that to happen to other people like me,” he says.
“That was a motivation to take part in the project.”
Ivona Kostyna is one of the founders of Veteran Hub, the group which runs the ReSex project.
She says they first had the idea for the project back in 2018, after reading about the issue for US soldiers.
After securing funding with the start of Russia’s full-scale invasion, they spoke to Ukrainian soldiers and experts, to ensure they were tailoring their help specifically to the men and women who need it.
They faced some confusion from the public – and veterans – when they first asked for responses to questions online. “People are dying, you’re thinking about sex!” Ivona says.
They also had to confront some of their own preconceptions – like the false assumption that injured veterans would all be struggling with their sex lives.
“There’s sex in the hospital, sex at home, sex before procedures, sex after. There’s a lot of good sex going on,” Ivona says. “We were like, wow, OK, how can we be helpful here?”.
But overall, she says, the response has been overwhelmingly positive.
The charity has printed some 6,000 booklets and sent them out to medical centres, veterans and their families all around Ukraine, and made them available online.
ReSex has also launched a social media campaign with videos, graphics and a helpline. The charity covers everything from masturbation to sex toys and even basic biology.
“We try to cover it all,” Ivona says, adding that there’s also a section of the booklet specifically for young injured veterans who may be virgins.
“So sex after their wound would be their first sex ever, which is quite different from what they might have imagined.”
Kateryna Skorokhod, ReSex’s project manager, says they published separate guides for women and men to ensure respective partners have specific advice tailored to their experiences and their bodies.
She stresses, though, that the focus of the project is more on the emotional side than the physical.
“It’s about how you can accept yourself, how you can love yourself, and how you can build a relationship with yourself and your partner after these injuries – with sex and with intimacy in relationships.”
Relying on veterans answering their questionnaire means there are gaps in their research, she says, adding that they’ve struggled to get any responses from the LGBTQ community.
But they’ve also learnt a great deal about Ukraine’s veterans. Specifically, they realised that traumatic brain injuries are often going undiagnosed and under treated in the country – something she says affects “the libido and the whole sexual performance very much”.
The language used to discuss sex is important too, Ivona says.
“It’s definitely not a dramatic language. It’s definitely not about ‘overcoming obstacles’ – that’s probably good for sport, but it turns out sex is not on the same scale.”
She says it’s important to make sure veterans know they don’t have to have sex unless they want to, and that sex may be difficult or painful at first.
Hlib certainly speaks positively about the project that he’s joined. When asked if he’s had a girlfriend since his injuries, he laughs.
“After I came back from captivity and the hospital, I had a girlfriend, and then another when I was doing the project questionnaire. And now I have a partner,” he says. “I might have missed one.”
But he said he was thankful for every person he had dated in the past year.
“Every partner I had was important to me, in gaining my confidence back. I’m very grateful for that.”
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Maisie Summers-Newton said “all the hard work was worth it” after she won two golds at the Para Swimming World Championships.
The 21-year-old, from Northampton, improved her own European record, claiming SB6 100m breaststroke honours.
She also won a gold in the 200m medley and gained a 400m freestyle silver at the championships earlier this month.
“Being in Manchester was incredible because it meant my family could come and watch,” she said.
She has been a mainstay of the British team since making her debut at the 2018 Europeans in Dublin and is a European, World, Paralympic and Commonwealth champion.
Breaststroke is her main event and she finished in a time of one minute 31.34 seconds to beat her previous best of 01:32.16 set last year, and move closer to the world record of 01:29.87.
Summers-Newton said: “I train eight times a week, two to two-and-a-half hours each session is, getting up at four in the morning and putting all of this effort in.
“When I [swim a personal best] at these major events… that’s where it really shows that it’s paid off and all the hard work was worth it.”
She has combined swimming with teacher training at the University of Northampton and said from March to June she was on a school placement.
Summers-Newton said: “Doing full school hours and also my training hours was quite difficult.
“There were days where I was absolutely exhausted, but I love both and I think it’s really important for me to kind of have my time out of the pool and try not to think about swimming too much, because I think if I was to think about it all the time my head would just kind of explode.”
As well as her university course and placement, she has visited other schools where she was “able to talk to the children all about my sport and swimming and disabilities”.
“I think that’s just creating awareness of it and making it more of a positive thing for children to know about,” she said.
The 21-year-old said she would now take a “well deserved break” before she began to focus on the Paralympic Games in Paris next year.
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Pinterest account and give it a follow if you have not already. I also have beanbags on this Pinterest page that are useful for people with cerebral palsy for repositioning to avoid stiffness and pressure sores as they are ultra soft and ultra comfortable. These used to be my favourite beanbags at school when I used to share a flat with some of my friends #ThingsThatAren’tForDisabledPeoplePacificallyCanBeUsefulThingsLike personal care 24 hour can be facilitated by a regular large bin bags feet for comfortable and 24 hour per stroke, and 12, avoiding curvature of the spine and avoiding pressures were from being in the same position directly to related to disabled people, but disabled people aren’t just their disabilities. They are so much more and sometimes you don’t want something that is looking medical or repositioning because you also want to have a next statically pleasing way of repositioning, especially if you live independently in your own home you don’t want everything about you to be medical and medical equipment, wh
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Mother Struggles To Access Sign Language Classes For Deaf Son
A County Tyrone woman with a deaf baby said she cannot communicate properly with her son due to a difficulty accessing sign language services.
Janine Boyd, 37, whose 10-month old son Mason was born deaf said she constantly worries about his future.
Charities that provide deaf services have said they know it is difficult for families to access services.
There are currently 1,476 deaf children in Northern Ireland, according to a charity.
Ms Boyd’s son is profoundly deaf – he has limited-to-no hearing capability.
Her baby was just a few weeks old when he was diagnosed.
“We were handed booklets and stuff of what to do and told we’d get an appointment for his hearing aids. I didn’t know what to do, I didn’t know anything about being deaf.”
Ms Boyd said charities like the National Deaf Children’s Society (NDCS) gave her some initial support by offering free coaching in basic British Sign Language (BSL).
‘You can’t leave him alone’
But basic classes are not enough.
“I can sign words but I can’t form a sentence so I can’t fully communicate with my son,” she added.
She said Mason, who is already walking, cannot be left alone at any time.
“You can’t even go to the other end of the room without watching him because you can’t shout at him to stop something or if he’s in danger, you just have to sprint to catch him – because he cannot hear anything,” she said.
British Sign Language classes are categorised in six levels from level one (beginner) to level six (advanced) and more advanced classes often have to be paid for.
“Classes for higher levels of sign language are mostly in the evenings. And the classes [for one level] can range in price from £400-£600 per person – so for me and my partner it’s a lot of money,” Ms Boyd explained.
Action Deaf Youth, a Belfast-based deaf charity, does offer free BSL classes for all levels but to take full advantage the charity said families should travel to Belfast to attend them.
Ms Boyd said it is a struggle to do that.
“I’m in Dungannon, that’s an hour away [from Belfast]. We have three kids in the house, what do we do with the kids?
“It’s very hard for us to just go down to Belfast for them [classes] and work, get kids in and out of school, and everything else.”
Service cuts
Caroline Doherty is the director of Action Deaf Youth and said recent budget cuts are having an effect on services.
“Part of our services have been severely impacted by the EA (Education Authority) – we are pausing our youth service come September as we can’t afford to run them. As a small charity we are continuously battling with funds and very reliant on donations.”
The National Deaf Children’s Society said access to sign language classes can be a struggle.
“We are aware that finding suitable, funded BSL courses is very difficult for parents as most of them are delivered by FE [Further Education] colleges in the evenings and they can be quite expensive,” it said.
The NDCS receives funding from the Department for Communities (DfC) and funds are also allocated from the EA to support deaf services.
The charity said it can offer basic Family Sign Language courses for ages 0-5 but after that “it can be difficult for parents to access accredited BSL courses”.
“A lack of support could have a catastrophic impact on deaf children’s development,” the charity said.
In a statement, DfC said family sign language learning remained a “key priority for the department”.
“The sign language team is currently planning this year’s funded courses by assessing current learning priorities with its deaf organisation delivery partners and through feedback from parents of deaf children.”

The EA has services to give extra help to autistic children, those needing support with literacy and numeracy, or those with sensory impairment.
That includes children and young people who are deaf and hard of hearing.
It also funds other organisations to deliver some services for deaf children and their parents.
But the authority is facing a budget squeeze, rising need, and limits on recruitment.
The worry is that it will reduce some of the support it can offer.
And that could affect the present and the future for some children and their families who rely on it.

The department added that it currently funds “a range of courses from an introduction to sign language to a degree equivalent British Sign Language level six course”.
A spokesperson for the EA said in a statement that it “recognises the impact that early language development has on deaf children’s progress.
“The EA also understand that finding suitable funded British Sign Language (BSL) courses is very difficult and often courses are only available in the evenings and are not funded.”
“The EA continues to work closely with charities such as the National Deaf Children’s Society to find solutions for the lack of suitable sign language courses for children, young people and parents.”
Ms Boyd said the current system for deaf children and their families was unfair.
“Any other child has access to proper schooling and the ability to speak, why is a deaf child and their family not given the opportunity of learning sign language to be able to communicate effectively to each other?”
Mason is currently waiting to receive a cochlear implant, which provides the sensation of hearing, but does not restore hearing.
“[The implant] is not always going to make someone fully understand the sentence,” said his mother.
“If you were able to sign a full sentence to someone, they can’t get that wrong. A deaf person will fully understand what you’re telling them with sign.”
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fundraising is back on for the next 2 to 3 weeks minimum to get me to a specialist festival for wheelchair users and people that find mobility difficult as well as funding my personal assistant for both the festival and my last qualifying camping exam
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me and my friend being silly three years ago on Wednesday
Double Amputee Boy, 8, Reaches Fell Summit
An eight-year-old boy who had both legs amputated after he was abused as a baby has walked to the summit of a Lake District fell.
Tony Hudgell’s trek up Orrest Head, which overlooks Windermere, has raised more than £19,000 for charity, way beyond his original £500 target.
He was joined by veteran mountaineer Sir Chris Bonington and double amputee former Gurkha Hari Budha Magar.
Tony’s adoptive mother, Paula Hudgell, said seeing him reach the summit was “so incredible”.
“Anybody who knows Tony knows that he is a complete whirlwind,” she said.
“He’s a force to be reckoned with.
“I reckon we could have climbed probably the highest mountain now.
“I think it might have started something.”
Tony, from Kings Hill in Kent, lost both legs after serious injuries were inflicted by his birth parents, who were jailed for 10 years in 2018.
He received Pride of Britain and Points of Light awards for raising more than £1.7m for charity during the pandemic.
His latest challenge supported the Tony Hudgell Foundation, Crohn’s & Colitis UK, the Bendrigg Trust and The Lake District Foundation.
He said his first fundraising walks had left him wanting to climb a mountain.
The family later met Cumbrian guide Steve Watts who made the wish reality.
Mr Watts said they picked Orrest Head because it was the first fell climbed by renowned guidebook author Alfred Wainwright.
However, the author had not prompted the same turnout of wellwishers on the summit as Tony had, he said.
“Talk about endeavour, willpower. For an eight-year-old? Follow that,” Mr Watt said.
“How many more is he going to inspire?
“It’s not just about the money, it’s the legacy.
“It’s opening the world to other children and other adults like Tony and Hari.”
Mrs Hudgell said it had been “so emotional” when Tony was joined as a surprise by Mr Budha Magar, who became the first double above-the-knee amputee to climb Everest in May.
“Hari is a superhero – the same as Tony – and it just shows that, being differently abled, what you can achieve,” she said.
“You can achieve anything if you just put your mind to it.”
Mr Budha Magar lost his legs when he stepped on an improvised explosive device in Afghanistan in 2010.
Surprising Tony near the summit of Orrest Head, he left the eight-year-old speechless.
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Hull Disabled Mum’s Anger At Being Removed From Council
A disabled new mother has complained she is being “pole-axed” from her council seat.
Labour’s Sarah Harper-Riches has served as Hull’s Bricknell ward councillor since May 2022, but has been recalled because she has not attended a formal council meeting since January.
Liberal Democrat-controlled Hull City Council said it had acted in accordance with local government rules.
Ms Harper-Riches said she had been left “absolutely devastated” and “baffled”.
The Local Government Act 1972 allows for recall of a councillor if they have not attended formal meetings for longer than six months, unless they request an extension in advance.
Due to a recent flare-up of her chronic fatigue syndrome, coupled with motherhood, Ms Harper-Riches said she did not submit a request.
However, she insisted she had been active in her ward, attending community events and gathering casework.
Ms Harper-Riches said: “I am absolutely devastated. It feels like I have been pole-axed from the council. I am baffled.
“Had I been notified by the council then of course I would have attended a meeting. But there was nothing.”
Ms Harper-Riches said she was focussed on breast-feeding her daughter and managing her health condition.
“I am a politician but I am a person first and foremost,” she said. “I understand my role as a councillor involves attending meetings but my return to work has to be carefully managed and appropriate.”
‘Archaic’
Hull’s Labour group said Ms Harper-Riches had fallen foul of “archaic” legislation and claimed it was aware of other councils that alerted elected members in advance of disqualification.
Councillor Hester Bridges, deputy leader of the Labour group on Hull City Council, said she was “bitterly disappointed” at the decision to recall Ms Harper-Riches, who she described as “a hard-working councillor”.
Hull City Council said Ms Harper-Riches had not attended a meeting since 19 January.
It added: “As a consequence, the seat she occupied became vacant by virtue of Section 85 of the Local Government Act 1972.”
The authority said Ms Harper-Riches was informed the six-month period had passed prior to the vacancy being made public.
An election will be held to fill the councillor vacancy subject to a request from two electors, the council added.
A Local Government Association spokesman told the BBC it believed the current legislation was “out of date”.
Changes, which would allow councils to hold some statutory meetings remotely, are expected to be voted on in the House of Commons later in the year.
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A dancer says modifying dolls for poorly children so they look like them “takes away that fear factor”.
Tonia Payne-Cheney from Eckington, Worcestershire, has Ehlers-Danlos syndrome and uses a feeding tube.
She and her friend began modifying teddies first but, because they couldn’t be wiped down in hospital, the 26-year-old started adding feeding tubes to dolls.
“It takes away that fear factor when [children] see it,” she said.
While Barbie brought out a range of inclusive dolls in August last year, Ms Payne-Cheney says she has been modifying dolls for years.
“I can give the dolls to the child…and they can see that they have the same as their doll,” she said.
Her syndrome, an inherited condition, affects the connective tissues supporting her bones.
Ms Payne-Cheney, a dancer and choreographer for Ballet Cymru, said she also goes into schools to help children understand about feeding tubes and uses the dolls as a way to do so.
“They get to hold it and touch it and play with it where they wouldn’t be able to before,” she said.
Ms Payne-Cheney said the children responded “great”.
“Now if a child goes into that school who has a tube they can be confident that everyone will know what it is and know not to touch it,” she said.
Ms Payne-Cheney said she also had other genetic conditions which left her completely bed-bound and had to undergo a “massive brain and spinal operation”.
“I got back to being well…but then I got really poorly again and was in Spain in a coma for five months and now I’ve been left with a breathing tube that I have to have all the time [as well]”.
“But we just have to get on with it, you know I carry on doing my trapeze and dancing and horse-riding,” she said.
























































































