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GMB's Dr Hilary Jones travels 360 miles to bypass NHS lists

GMB's Dr Hilary Jones travels 360 miles to bypass NHS lists

The well-known television GP from Kent made a 180-mile trip from his home in order to undertake a second hip replacement at a hospital in Birmingham.
Now, he is speaking out about his own surgery to show others awaiting treatment that they can also bypass long waiting lists.
To do this, he took advantage of NHS Patient Choice after discovering a hospital that had almost no waiting list.
Patient choice in the NHS provides patients with a legal right to choose where they receive their NHS healthcare services.
GMB star Dr Hilary Jones travels 360 miles to bypass NHS waiting list
Speaking after his procedure at Practice Plus Group's new hospital in Birmingham, Doctor Hilary Jones said: 'It was 180 miles from my home to Birmingham - but as it's a new hospital and it's a private hospital that treats NHS patients, they could get me in very quickly just with a referral from my GP.
'I'd do it again in a heartbeat for faster, quality care and highly recommend it.
"Patient Choice gives people real power - they just need to know it's there."
The GMB and Lorraine star added: "The NHS App is going to be developed further to make this easier, and you can speak to your GP about your choices.
'You can choose to be referred to a private hospital at the outset, or you can switch hospitals like I did if you're facing delays locally.
"It's free for the patient and costs the NHS no more than if that same patient had their op at an NHS hospital.
"For people like me, who are lucky enough to be mobile despite needing an operation, it makes complete sense to find a hospital that can do your operation sooner so you can get on the road to recovery sooner.
'People don't want to be on a waiting list. They want to get on with their lives.
'Every single person who looked after me was amazing and couldn't have done any more. I am delighted with the result so far.'
This comes after a poll of some 1000 adults showed that people awaiting NHS treatment would be willing to travel if it meant they could get what they need sooner.
On average, respondents were happy to travel 60 miles if it meant they'd be seen within three to four weeks, or 49 miles for a six-to-eight-week timeframe.
Around one in 10 said they would even travel over 200 miles if they could get the NHS surgery they need within a month.
Data also found that 55% of Brits had no idea that under NHS Patient Choice, they can choose to travel to a hospital outside of their area.
The research, which was commissioned by Practice Plus Group hospitals, which treat NHS patients as well as those who choose their Wellsoon private healthcare option, revealed that 35% would consider travelling more than 90 minutes if it meant saving £200 or more on the cost of paying for a hip or knee replacement.
Jim Easton, chief executive, said: 'It's fantastic for patients that in the NHS 10-year plan, the government has renewed its commitment to using capacity in the private sector and to creating a new patient choice charter to ensure the NHS is receptive and reactive to patient preferences.
'To achieve the ambitious waiting time targets, we also need more people to know that they can travel outside of their immediate area if they find a hospital that can see them sooner.
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'It is important people realise they have the power to be proactive and get their treatment sooner, get back to work and back on track as soon as possible.
'Dr Hilary found this at our Birmingham hospital, which currently can see people in a few short weeks.
'We're proud to have been able to help him and wish him a speedy and healthy recovery.'
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Eight babies born from pioneering IVF technique to prevent devastating disease
Eight babies born from pioneering IVF technique to prevent devastating disease

The Independent

time18 minutes ago

  • The Independent

Eight babies born from pioneering IVF technique to prevent devastating disease

Eight babies have been born in the UK thanks to a groundbreaking three-person IVF technique to prevent devastating disease, world-first data shows. Four boys and four girls, including one set of identical twins, have been delivered and are all doing well following treatment by a team in Newcastle, who pioneered the technique. One other woman is currently pregnant. The scientific method, known as mitochondrial donation treatment, is designed to prevent children from being born with devastating mitochondrial diseases that are passed down from their mothers. These illnesses can be fatal and often cause devastating damage to organs including the brain, muscle, liver, heart and kidney. Of the eight babies born, three are now aged under six months, two are aged six to 12 months, one is 12 to 18 months old, one is aged 18 to 24 months and one child is aged over two. All the babies are healthy and are meeting their milestones, according to the team from Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle University and Newcastle Fertility Centre. None of the eight babies shows signs of having mitochondrial DNA disease, which tends to affect around one in 5,000 births. The scientists said disease-causing mitochondrial DNA mutations, picked up in three of the children, are either undetectable or present at levels that are very unlikely to cause disease. The main lab method used by the team, known as pronuclear transfer (PNT), involves taking the egg from an affected mother, sperm from her partner and an egg from a donor who is free from disease. The mother of a baby girl born through mitochondrial donation said: 'As parents, all we ever wanted was to give our child a healthy start in life. 'Mitochondrial donation IVF made that possible. After years of uncertainty, this treatment gave us hope – and then it gave us our baby. 'We look at them now, full of life and possibility, and we're overwhelmed with gratitude. Science gave us a chance.' The mother of a baby boy added: 'We are now proud parents to a healthy baby, a true mitochondrial replacement success. This breakthrough has lifted the heavy cloud of fear that once loomed over us. 'Thanks to this incredible advancement and the support we received, our little family is complete. 'The emotional burden of mitochondrial disease has been lifted, and in its place is hope, joy, and deep gratitude.' Professor Sir Doug Turnbull, from Newcastle University and part of the team of researchers, said: 'Mitochondrial disease can have a devastating impact on families. 'Today's news offers fresh hope to many more women at risk of passing on this condition who now have the chance to have children growing up without this terrible disease.' In all the cases, the Newcastle team used the PNT technique after the egg was fertilised. For this, scientists transplanted the nuclear genome (which contains all the genes essential for a person's characteristics, such as hair colour and height) from the egg carrying the mitochondrial DNA mutation into an egg donated by an unaffected woman that had had its nuclear genome removed. Thanks to the procedure, the resulting baby inherits its parents' nuclear DNA, but the mitochondrial DNA is mainly inherited from the donated egg. Scientific progress in this area led Parliament to change the law in 2015 to permit mitochondrial donation treatment. Two years later, the Newcastle clinic became the first and only national centre licensed to perform it, with the first cases approved in 2018. Approval is given on a case-by-case basis by the UK's Human Fertilisation and Embryology Authority (HFEA). The new findings on the eight births, published in the New England Journal of Medicine, show that all the babies are developing normally. Aged 18 months, tests are carried out in areas such as gross motor skills, fine motor skills, cognitive and social development and language skills to check the babies are hitting milestones. The researchers will also check the children when they are aged five. Professor Bobby McFarland, director of the NHS Highly Specialised Service for Rare Mitochondrial Disorders at Newcastle Hospitals NHS Foundation Trust, said he was confident the children would carry on developing normally. He added: 'If we're not picking up subtle signs of problems at five, then we're really very clear that is not going to be a problem.' He added: 'In my work…I see children in intensive care units up and down this country and that's not pleasant. 'It's very difficult for families to deal with these diseases, they are devastating… 'To see babies born at the end of this is just amazing really.' Mary Herbert, professor of reproductive biology at Newcastle University, added: 'PNT happens in the small hours of the morning – those long nights. And it has paid off. 'It's fair to say it's rewarding. In science though, periods of joy are fleeting and brief because you're always thinking what is the next challenge? How do we optimise it further?' She said the slight DNA mutations seen in three of the children are 'way, way below the threshold that would cause disease'. Peter Thompson, chief executive of the HFEA, said: 'Ten years ago, the UK was the first country in the world to licence mitochondrial donation treatment to avoid passing the condition to children. 'For the first time, families with severe inherited mitochondrial illness have the possibility of a healthy child. 'Although it's still early days, it is wonderful news that mitochondrial donation treatment has led to eight babies being born. 'Only people who are at a very high risk of passing a serious mitochondrial disease onto their children are eligible for this treatment in the UK, and every application for mitochondrial donation treatment is individually assessed in accordance with the law.' Dr Andy Greenfield, from the University of Oxford, said: 'It is a triumph of scientific innovation in the IVF clinic – a world-first that shows that the UK is an excellent environment in which to push boundaries in IVF; a tour de force by the embryologists who painstakingly developed and optimised the micromanipulation methods; an example of the value of clinical expertise, developed over decades of working with children and adults suffering from these devastating diseases, being used to support a new intervention and subsequent follow-up, potentially for many years.' Beth Thompson, executive director for policy and partnerships at Wellcome, said: 'This is a remarkable scientific achievement, which has been years in the making. 'The pioneering work behind mitochondrial donation is a powerful example of how discovery research can change lives.' Professor Dagan Wells, from the University of Oxford, said the study showed established methods for avoiding mitochondrial DNA diseases, such as preimplantation genetic testing, perform well and will be suitable for most women at risk of having an affected child. 'A minority of patients are unable to produce any embryos free of mitochondrial disease, and for those women the study provides hope that they may be able to have healthy children in the future,' he added.

Supernanny's Jo Frost speaks out on 'life-threatening' health condition in candid video
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Daily Mirror

timean hour ago

  • Daily Mirror

Supernanny's Jo Frost speaks out on 'life-threatening' health condition in candid video

Jo Frost, who shot to fame on the hit show Supernanny in the early 2000s, has opened up about a health condition she suffers with in a candid video Supernanny legend Jo Frost has bravely opened up about the "life-threatening" medical condition she battles in a heartfelt new video. ‌ The telly favourite shot to stardom in the early noughties with her hit show Supernanny, where she'd step into chaotic households to help struggling parents tackle their children's challenging behaviour. ‌ These days, Jo operates as a parenting guru, offering her expertise through online private sessions whilst sharing educational content across her social media platforms. ‌ In her most recent post, she courageously discussed her health struggles after receiving an anaphylaxis diagnosis, defiantly declaring she refuses to let the condition "define" her whilst expressing her determination to spread awareness. According to the NHS, anaphylaxis is described as a "life-threatening allergic reaction that happens very quickly" and can be sparked by food, medication or insect stings, reports the Express. When someone displays symptoms of anaphylactic shock, immediate medical intervention is crucial, as without treatment it can lead to cardiac or respiratory arrest. ‌ Opening her video, the 55 year old revealed: "I've survived more anaphylactic shocks than I'm prepared to go into detail about right now. I have anaphylaxis, a life-threatening medical condition to certain foods that will compromise my body so horrifically to the point of hospitalisation." She continued, addressing her followers: "Absolute millions of my community around the world, children and adults, live cautiously and anxiously navigating this journey with not nearly enough compassion, education, and empathy from those who do not." ‌ Jo expressed that she is "unapologetic" about her condition, comparing it to "shoving a loaded gun in her face". "I did not ask for it, and it does not define who I am and the impact that I make in the world daily. But it does impact how I live my life daily, like the precautions I take, the energy I have to use to discern with hypervigilance," she explained. Taking aim at those who disregard her condition in public settings, Jo also stressed the significance of checking food labels for safety. ‌ The television personality stated: "By the way, I speak on behalf of those who also have coeliac disease, too, because we are not all faddy eaters,' she asserted. Coeliac disease is an autoimmune disorder where ingestion of gluten leads to damage in the small intestine. "I'm not looking to be treated special; I'm looking to be treated with the same dignity and attentiveness as you just showed others." In closing, Jo urged her audience to "get curious" and "learn more" about her condition, while also asking them to refrain from leaving "passive aggressive comments" on her social media post. Jo's followers rallied around her on social media, with one expressing: "Thank you Jo. Been living with this my whole life and see how it has gotten so much worse for children now. Education is so important as well as looking at our food supply and what is in it. We need to look at the root cause and source as well." Another supporter chimed in: "Thank you for using your voice... many could benefit from empathy and understanding!! Wishing you healthy days, Jo!!"

Equalities boss in trans doctor row 'Googled' policies of other health boards, tribunal told
Equalities boss in trans doctor row 'Googled' policies of other health boards, tribunal told

Daily Mail​

timean hour ago

  • Daily Mail​

Equalities boss in trans doctor row 'Googled' policies of other health boards, tribunal told

An NHS equalities boss Googled the trans policies of other health boards as they did not have their own, a tribunal was told yesterday. Nurse Sandie Peggie was suspended from Victoria Hospital in Kirkcaldy after she complained about having to share a changing room with trans medic Dr Beth Upton. The 51-year-old nurse has since sued the health board and medic, and the landmark employment tribunal she brought against them returned yesterday. Isla Bumba, NHS Fife's equality and human rights lead officer, told the tribunal she had researched the policies of other health boards as there was no policy in place regarding trans employees in 2023. And she revealed she had been using a search engine to investigate the trans patient policies of other health boards after being tasked with writing one. As the tribunal returned for what is expected to be another eleven days, she said she would 'hazard a guess at being female' but that she has not had a chromosome test. 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The inquiry was told Ms Bumba looked at policies from other health boards, with NHS Highland's policy saying that 'staff must be treated in accordance with their self-declared gender regardless of whether under medical supervision or have a gender recognition certificate'. As well as not having a policy for staff, they did not have a policy for patients. And Ms Bumba said: 'I had been tasked with writing a trans policy for patients, because we also did not have one at that time, and so part of my scoping I was contacting or leaning on the other equality leads. 'Having discussions with them, trying to get copies if I could, or be referenced to their existing policies if they had one and doing my own research on what other policies were - so I would have been Googling them, I could have came across English policies online, but I reached out directly to some of my Scottish colleagues for their policies.' Ms Bumba has been at the health board for just over three years, and she told the tribunal her job was to make sure NHS Fife was adhering to the Equality Act among other duties. The witness disputed the definition of biological sex when questioned by Mrs Peggie's lawyer Naomi Cunningham. She told the barrister: 'I think you've simplified what could be deemed biological sex, but in actual fact it's far more complex. 'I don't know anything about Beth's body, I didn't at the time I don't now, I don't need to know. But it wouldn't be something that I would ever have the information of exactly what she is made of biologically. 'Nor do I know what my own body is made of biologically. 'I hazard a guess that I would be female, but no one knows what their chromosomes are or their hormonal composition unless you've had that test and I at least have not and I'm not sure Beth has.' On her email signature she was listed as an 'LGBT ally', the tribunal heard, and Ms Cunningham challenged her on it. The lawyer, who highlighted other things she does not list including being a 'disability ally', said: 'Doesn't singling out LGBT ally on your email signature give the impression that the board's human rights and equality lead thinks that the protected characteristics of sexual orientation and gender reassignment are the most important ones and they come first?' But Ms Bumba, who studied at Aberdeen University, said: 'I don't think having that on my email signature suggests that its my top priority no. A priority, but not necessarily the top priority. 'Being an LGBT ally does not mean that I'm not an ally to other protected characteristics.' Following her involvement in the incident in early January 2024, Ms Bumba said she did not have any more involvement until July. The inquiry heard of a Daily Mail article which told of the incident involving Mrs Peggie and Dr Upton, 30. Ms Bumba, who said she was not aware of the identity of the nurse and doctor concerned at this point, said she told a follow up meeting: 'I did remind the group that the nurse involved was entitled to her personal beliefs and that gender critical beliefs were protected under the Equality Act specifically, however, that being said, the NHS expects its employees to conduct themselves in a certain way that aligns with our values and ethics.' The tribunal continues.

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