
There's Good News Tonight: Three men get new hearts and find friendships
There's good news tonight in San Diego, where months long hospital stays helped three men bond while waiting for heart transplants. NBC News' Priscilla Thompson reports on the happy moments when they found out the last of the group was getting a new heart, plus what's next for their friendships, now that they're home.
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BBC News
38 minutes ago
- BBC News
Derbyshire pip claimants relieved but fearful after PM's U-turn
Sharon Arrowsmith, a Labour voter all her life, says she never thought she would have to "fear" the party in she says the government's plans to change who qualifies for certain disability and sickness benefits had left her "terrified". "I can't afford to lose a single penny", she says. "It's unconscionable."But early on Friday, the government confirmed a U-turn on its cuts to disability benefits in a bid to avert rebellion by more than 120 Labour backbenchers - leaving Sharon, from Derbyshire, breathing "a huge sigh of relief". The Universal Credit and Personal Independence Payment Bill was meant to tighten eligibility requirements for personal independence payments (pips), halve the health-related element of universal credit (UC), and increase the UC standard government hoped to save £5bn a year by 2030 with the bill, while slowing the increase in people claiming benefits. It was the changes to who qualifies for pips in particular that caused deep unhappiness amongst pip claimants will continue to receive what they currently get, as will recipients of the health element of universal credit. Planned cuts will only hit future well as changing who will be affected by the cuts, ministers are also expected to fast-track a £1bn support plan originally scheduled for many charities have rejected the Amo Raju, from the Derby-based charity Disability Direct, says the legislation should still be pulled."Welfare reform does need to happen, but it needs to involve disabled people in that decision-making process," he said."Let's pull it, get the right individuals around the table and co-produce the policy in the interests of disabled people." 'There's no fun' Ms Arrowsmith, from Amber Valley, has fibromyalgia, meaning she has difficulty moving about. It causes her chronic fatigue and joint and muscle pain. She struggles to do housework and shopping and often struggles to physically get out of 55-year-old also has other conditions including diabetes type 2, underactive thyroid, and growing cataracts which means she cannot drive and is reliant on autism diagnosis leaves her struggling with impairment of executive function and staying on had to stop working in January due to these conditions, and receives the mobility element of -ip, which is about £400 a month. She also receives universal credit, the vast majority of which is spent on private rent payments and bills. The pip payment used to help her employ someone to help with house tasks, but due to rising costs she says she is now heavily reliant on it to afford food after being left unable to work."I can't afford to lose a single penny. I would no longer be able to buy food or pay rent," she said."I have already cut everything down to the bone. There is no excess. There is no fun."Sharon thought she was likely to lose out because she will not score enough points in certain areas, like being able to wash and dress, which she can mostly manage. The government had been proposing that from November 2026, pip claimants would need to score at least four points from a single pip daily living activity to qualify for the daily living component of pip, as well as scoring a total of at least eight points. Sharon says she is relieved by the climbdown."I'm so proud of [the rebel MPs] for doing that, at the risk of their careers, having the courage to stand up. They are the real Labour people," she she says she worries for new claimants who will be impacted in the future."I am concerned still, I still think they really need to look at this bill and think about the people. Not the money, the people, that's what's important."I feel like I was wrong to vote Labour." Gordon Patten, from Long Eaton, is in his early fifties and is unable to work because of sarcoidosis, a rare condition impacting the lungs that means he must sleep with a machine aid. He also has been diagnosed with depression and type 2 diabetes and has had epilepsy since he was a receives roughly £460 a month through the daily living component of pip, which helps towards expenses such as the electricity bill his breathing aid machine leaves him with, which he says has increased, and hiring a cleaner to help with also receives the standard rate for mobility and is entitled to a mobility vehicle, an element which the government says will not be impacted by the changes. Gordon says he was glad to see the Labour backbenchers who disagree with the policy "standing up" to the prime minister."It is going to be a two-tier situation but we've had this in the past with disability allowance. You're always gonna have that, where people who started on a benefit get more," he he says the Labour Party have "mucked this up completely" for people like him."If you go back to 1945, at the beginning of the welfare state, it was a core [Labour] value"Labour has kind of lost its way with looking after the working person and the vulnerable...I honestly think that being in power has gone to their heads." A Department for Work and Pensions spokesperson said: "Ministers have repeatedly recognised how anxious people are when there is talk of reform which is why we will never compromise on protecting people who need our support."Our reforms will mean the social security system will always be there for those who will never be able to work."

Leader Live
43 minutes ago
- Leader Live
Wrexham: Terry Fox Run returns to raise funds for cancer
The popular non-competitive event will take place on October 6 between 12-3pm at Bellevue Park - and it's completely free to enter. This iconic run takes place all around the world, raising hundreds of millions of pounds for cancer research, in memory of the 22-year-old Canadian athlete who sadly passed away in 1981. Last year, 300 people ran in Wrexham and raised over £13,000. This year, the team want to make it bigger and better than ever. You can register here. Terry lost his right leg to a rare bone cancer, osteogenic sarcoma, and ran using a prosthetic limb. He made headlines across the world in 1980 when he ran 3,339 miles across Canada over 143 days – an average of a marathon a day – to raise money and awareness for cancer research. Terry had to stop his run when the cancer spread to his lungs, and less than a year later, he died. After he had to stop, his words were, 'Even if I don't make it, we need others to continue.' He's now widely considered a Canadian hero and every year since 1981, the Terry Fox Run is held in more than 60 cities around the world and raised more than £500 million for cancer research. Cllr Mark Pritchard, leader of Wrexham Council, said: 'I'm thrilled that the Terry Fox Foundation has brought this event back to Wrexham. "We are the only place in Wales hosting the event and not only will it make for an enjoyable day in one of Wrexham's scenic parks, it will raise money for cancer research in the UK.' MOST READ Professor Chris Bakal is an ambassador for The UK Terry Fox Association. Born in Canada, he is now working as professor of cancer morpho-dynamics at The Institute of Cancer Research in London. He said: 'Following Terry's journey as I grew up in a small town in Canada, he inspired me to become a cancer researcher, and his perseverance and dedication drives our work in the lab. 'Terry also showed me that all of us can do something in the fight against cancer. Every step we make at a Terry Fox Run gets us one little bit closer to beating this disease by supporting cutting-edge cancer research.'


Daily Mail
an hour ago
- Daily Mail
Make Bobby Moore a Knight! Bowel cancer survivors join the masses as campaign to honour England's World Cup-winning captain gains momentum
Bowel cancer survivors have backed calls to honour England football legend Bobby Moore, after using his name to raise tens of millions for charity. The former West Ham and Fulham defender, who captained the Three Lions to the 1966 World Cup victory over West Germany at Wembley, died with cancer in 1993, aged just 51. But the charity fund which bears his name has generated more than £31 million for Cancer Research UK, helping spread awareness, support those with the disease and pay for treatment. Former cancer patients who have been supported by the Bobby Moore Fund today joined the calls from household names across football, sport and entertainment in urging the Government to create a new posthumous knighthood in tribute to the east Londoner's significant contribution to life, both on and off the field. Marcus Hitchens, whose footballer father Gerry Hitchens played alongside a young Bobby for England in the early 1960s, said: 'I remember my father saying what a great person he was, even as a young footballer, my father thought very highly of Bobby, he commanded respect from everyone, including the more seasoned professionals with a lot more years in the game. 'Sadly I think he was let down a bit by the authorities - he wasn't looked after when he left the game, he didn't have the opportunities that some former footballers do when they retire. 'So I think it's the right time to change that now, and give him in death the recognition he sadly failed to get - but completely deserved - during his lifetime.' Mr Hitchens, a sales manager from Carmel, Holywell in north east Wales, said the fund has given him the 'platform' to spread the message about bowel cancer after being diagnosed with it himself as a young man. Mr Hitchens, 66, said: 'Sometimes people are a bit embarrassed about bowel cancer but that is something the fund, in Bobby's name, has been so successful at trying to change over the years. 'It's not for everyone standing up in a room full of people and talking about your poo, but I felt comfortable doing that because I know what difference it makes spreading awareness of bowel cancer, and the Bobby Moore Fund has given me the platform to do that and hopefully reach as many men as possible.' A petition to create a posthumous award for Bobby has now passed 174 signatures, and has been supported by the likes of 1966 hat-trick hero Sir Geoff Hurst, former England captains Bryan Robson and Terry Butcher, and Three Lions regulars including Frank Lampard, Stuart Pearce and Les Ferdinand. Fellow bowel cancer survivor Matt Black said the charity shone a light on an unglamorous disease by using Bobby's name to target men who might not otherwise pay attention to symptoms or get checked out. The 60-year-old property developer from London said: 'The Bobby Moore Fund has given me a platform and a voice. 'Post my operation I was very keen to talk about my situation, how I got through it, what are the signs to look out for, and I became incredibly passionate about that. 'Until 'Bowel Babe' Dame Deborah James came to prominence a few years ago, there was no one really advocating the issues around bowel cancer, about cancer research. 'It wasn't linked to an individual and the Bobby Moore Fund drove that force really hard for last 30 years. 'Middle aged blokes especially don't talk about it, yet Bobby has turned tragedy into something positive, given recognition through sport and through football to the awareness and the issues and the concerns surrounding bowel cancer. 'By linking it with sports, as he has done, it has made his reach beyond what you would normally expect.' He added: 'It is right that he is recognised for this fantastic dedication to saving lives.'