Donald Trump is now seeking to have his federal criminal trial delayed until after the 2024 election. In a court filing late on Monday, Mr Trump’s lawyers asked the judge for a lengthy delay to his classified documents case, saying that due to the extraordinary nature of the case it would not be possible to try it before the election. Mr Trump has been charged with 37 federal counts over his handling of classified documents after leaving the White House. The filing was submitted just hours before a Georgia grand jury was slated to meet on Tuesday as part of the investigation into the efforts of the former president and his allies to overturn his 2020 election loss in the state. Fulton County District Attorney Fani Willis has been investigating Mr Trump after he called Georgia Secretary of State Brad Raffensperger in early 2021 and urged him to “find 11,780 votes” to flip the state in his favour. As his legal troubles heat up, Mr Trump is lashing out at Iowa Republican Governor Kim Reynolds for staying neutral in the 2024 race. Other GOP presidential candidates including Ron DeSantis jumped to defend her from Mr Trump’s attacks. Read More Trump strains relations with Iowa Republicans with no-show at charity event Trump says ‘damaged’ DeSantis is ‘desperately trying to get out’ of 2024 race Trump’s encounter with Guy Fieri at UFC fight sparks mixed reactions Trump lawyer Alina Habba leaves his defence team in New York fraud case

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A young woman whose health “deteriorated rapidly” after being diagnosed with long Covid and suffering a liver bleed is now in a wheelchair, feeds herself through a tube in her chest and has been unable to urinate in three years. Abigail Snowball, 29, was told she suffered from a rare condition known as Fowler’s Syndrome a few months after she was diagnosed with long Covid in July 2020 and her bladder stopped working. The social worker, from Northumberland, says she was “never sick” and enjoyed long runs before testing positive for coronavirus in early 2020 and feeling a sharp pain under her ribs which scans showed was a bleed on her liver. Abigail had not fully recovered from the virus and since the diagnosis, her health has gone from bad to worse, to the point where she has not been able to urinate in three years. She now depends on her husband Mark, 34, to carry her to the bathroom so she can empty her bladder, which can take up to four hours, and has not been able to enjoy a mouthful of food for nearly a year. “I had never really been ill before,” Abigail told PA Real Life. “As a child, I was always really lucky and never poorly. I look back at pictures from before Covid and I don’t even recognise myself.” Abigail had completed a 20-mile race, the Run Northumberland BIG 20, just a week before testing positive for Covid and having to quarantine away from Mark, who works in maintenance for Nissan. “It was very much at the start of the pandemic, back at the time when there weren’t any vaccines or much testing,” she said. “It was just tiredness like I’ve never felt before in my entire life. I remember having a cup of tea and struggling to lift the mug up.” Like many other people’s experience of catching Covid, Abigail’s health improved over the next 10 days. “I did get better, but I never fully recovered,” she said. But a couple of months later, while visiting her parents, Jane and Ray Cresswell, in Cornwall on holiday, she suddenly began feeling a sharp pain under her ribs. “It was a really strange location to have pain,” she added. She visited the GP a week later and was admitted to Northumbria Specialist Emergency Care Hospital (NSECH) in July 2020, where scans revealed Abigail had suffered a bleed on her liver. “That’s when they diagnosed me with long Covid,” she said. “There was no other explanation, because they tested for blood disorders and carried out a scan. “They asked me if I had a fall or accident, but there was literally nothing.” Abigail was recovering from her liver bleed in hospital late one evening when a nurse asked when the last time she urinated was. “I actually thought, ‘god, it wasn’t since this morning’,” she said. “From that point, my bladder never regained any function. That was really the start of my health declining quickly.” Doctors hoped her bladder block was simply a result of the liver “trauma” and that she would be on the mend soon. But, sadly, this was not the case. A few months later, Abigail was diagnosed with a rare condition called Fowler’s Syndrome, which causes women to have problems passing urine. Abigail’s condition has deteriorated over the past few weeks and she is now losing weight rapidly. “I am now sleeping on the sofa downstairs and my husband Mark is having to carry me to the toilet and back again,” she said. “We can spend up to four hours at a time trying to drain my bladder, and the pain is just unbearable. “I went from running 20 miles to using a wheelchair. You don’t realise how inaccessible the world is until you are in that position.” Since the diagnosis, Abigail has spent more than 350 days in hospital and undergone 12 surgeries, including one in October 2021 to try and reconstruct her bladder. To make matters worse, she developed intestinal failure last year, which means she can no longer eat food. “I haven’t eaten anything in a year now,” she said. Instead, she is fed through TPN (total parenteral nutrition), a tube in her chest which delivers nutrients directly into the blood stream. Abigail and Mark, who married earlier this year in May, both received close to six months of training on how to perform the feeding procedure given there is a high risk of infection. “We had never even heard of that – being fed through a line into your heart,” she said. Abigail has been told by doctors that her liver bleed was “extremely likely” to have been caused by Covid. While Covid is known to harm the lungs, it has also been found to affect other organs, including the heart, liver and kidneys, but wider research is needed to better understand its long-term effects. Liver problems are common among patients with Covid-19, according to a study carried out by researchers at Oxford University and published in the peer-reviewed journal Hepatology Communications. Abigail, whose condition is considered “severe”, is hoping to receive specialist treatment in London, known as bladder Botox, which involves injecting Botox into the bladder every three to nine months, but there is no guarantee this will work. “Because of how severe and complex my case is, we’ve exhausted all our options here and the doctors are saying that I need to see the specialists in London,” she said. “Removing my bladder completely remains on the cards, but it’s incredibly high risk because of my intestinal problems. “There is no cure for Fowler’s, so it’s about managing it in the best way possible.” The combination of health conditions has left Abigail unable to perform everyday tasks. “It’s funny because the things I want to be able to do are so normal,” she said. “Just being able to wake up, take the dog for a walk and go to work. “Things that in the past, I completely took for granted.” To help cover the costs, Abigail’s friend Emma Holt has set up a GoFundMe which has received thousands of pounds in donations. “We never imagined in our wildest dreams that we would raise the amount of money that we have already,” she said. “It’s the one thing that really keeps us going, when things are really difficult. “Knowing that we have so many people behind us and supporting us is amazing.” Fowler’s Syndrome is most often caused by infection or following surgery or trauma, but a link to long Covid has yet to be established and more research is needed. Dani Coombe, CEO, Fowler’s Syndrome UK said: “It’s too early to say if long Covid is a trigger for Fowler’s syndrome; we haven’t seen an increase in Fowler’s and retention post-Covid yet, and there is no indicator that urinary retention gets worse. “Our research into what patients believe triggered their urinary retention shows that infection is the most common trigger at 57 per cent, followed by surgery in 32 per cent of patients and trauma at 19 per cent. “It would be noteworthy to see in coming years if there is an increase in women with Fowler’s because of the trauma of Covid-19.” Read More Fake meat is dying, but that shouldn’t mean the end of veganism What I gained (and lost) from walking 10,000 steps a day for five months Woman behind ‘not real’ plane tirade identified as marketing executive with $2m home Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

Veteran Canadian journalist and author Peter C. Newman, who held a mirror up to Canada, has died. He was 94. Newman died in hospital in Belleville, Ontario, Thursday morning from complications related to a stroke he had last year and which caused him to develop Parkinson’s disease, his wife Alvy Newman said by phone. In his decades-long career, Newman served as editor-in-chief of the Toronto Star and Maclean’s magazine covering both Canadian politics and business. “It’s such a loss. It’s like a library burned down if you lose someone with that knowledge,” Alvy Newman said. “He revolutionized journalism, business, politics, history.” Often recognized by his trademark sailor’s cap, Newman also wrote two dozen books and earned the informal title of Canada’s “most cussed and discussed commentator,” said HarperCollins, one of his publishers, in an author's note. Political columnist Paul Wells, who for years was a senior writer at Maclean’s, said Newman built the publication into what it was at its peak, “an urgent, weekly news magazine with a global ambit. But more than that, Wells said, Newman created a template for Canadian political authors. "The Canadian Establishment’ books persuaded everyone — his colleagues, the book-buying public — that Canadian stories could be as important, as interesting, as riveting as stories from anywhere else,” he said. “And he sold truckloads of those books. My God.” That series of three books — the first of which was published in 1975, the last in 1998 — chronicled Canada’s recent history through the stories of its unelected power players. Newman also told his own story in his 2004 autobiography, “Here Be Dragons: Telling Tales of People, Passion and Power.” He was born in Vienna in 1929 and came to Canada in 1940 as a Jewish refugee. In his biography, Newman describes being shot at by Nazis as he waited on the beach at Biarritz, France, for the ship that would take him to freedom. “Nothing compares with being a refugee; you are robbed of context and you flail about, searching for self-definition,” he wrote. “When I ultimately arrived in Canada, what I wanted was to gain a voice. To be heard. That longing has never left me.” That, he said, is why he became a writer. The Writers’ Trust of Canada said Newman’s 1963 book “Renegade in Power: The Diefenbaker Years” about former Prime Minister John Diefenbaker had “revolutionized Canadian political reporting with its controversial ‘insiders-tell-all’ approach.” Newman was appointed to the Order of Canada in 1978 and promoted to the rank of companion in 1990, recognized as a “chronicler of our past and interpreter of our present.” Newman won some of Canada’s most illustrious literary awards, along with seven honorary doctorates, according to his HarperCollins profile. Read More Ukraine war’s heaviest fight rages in east - follow live Charity boss speaks out over ‘traumatic’ encounter with royal aide Chicago to move migrants from police stations to tent camps before winter under mayor's plan Teens killed in car by deputy in upstate New York were 15 and 17, police say Texas AG Ken Paxton's impeachment trial defense includes claims of a Republican plot to remove him

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