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A nurse who needed the toilet 30 times a day was diagnosed with an incurable disease after doctors suspected she had an eating disorder when her weight plummeted. Katie Harpur, 25, a nurse from Belfast, dropped to just five stone while battling the painful symptoms of Crohn’s disease, which left her unable to walk, and she could not eat without throwing up. Diagnosed with Crohn’s in 2014 at the age of 16, she was told it was inevitable that she would eventually need a stoma bag. Fitted with a temporary bag in 2019, Katie had the operation to make her stoma permanent in June 2022 and says it has changed her life. She said: “I used to need to go to the toilet up to 30 times a day and I couldn’t go out and socialise for fear of there not being facilities nearby. “It was incredibly limiting, and I was in a lot of pain to the point where I didn’t even want to go anywhere. “I’d always wanted to travel but it was impossible for me to do so until I got my stoma bag fitted. “Now I’ve booked my first long-haul flight to Tokyo, something I never would have been able to do before the op.” Katie first started experiencing pain and nausea at the age of 14 but said doctors found it difficult to diagnose her. I was in a lot of pain to the point where I didn’t even want to go anywhere Katie Harpur She said: “At first, they suspected that I was bulimic because my weight dropped. “I lost a dangerous amount of weight and weighed just five stone, but I didn’t have an eating disorder, it was just too painful for me to eat and if I did eat, I would vomit. “I remember one doctor told me I was a hypochondriac, but I knew something wasn’t right.” Persevering with medical appointments, Katie said her health deteriorated until she was admitted to hospital. Unable to walk, the then 16-year-old spent two weeks in hospital where she had a colonoscopy. Katie said: “I couldn’t physically walk anywhere, I was so weak, and I ended up in hospital. “The biopsies from the colonoscopy came back and confirmed that I had Crohn’s disease.” Crohn’s disease is a lifelong condition where parts of the digestive system become inflamed. Symptoms include diarrhoea, stomach aches and cramps, blood in your poo, fatigue and weight loss. Growing up, I was so excited to travel but Crohn’s made it impossible. Katie Harpur Katie was put on medication but was told she would eventually need a stoma bag. In June 2019, Katie, then aged 21, underwent a procedure to have a temporary stoma bag fitted. She said: “Going into it, I obviously had body image concerns because I’m still quite young and people tend to have a false idea that stoma bags are dirty. “I knew I would end up with a giant scar too and that made me nervous.” Despite the stoma bag being the solution to Katie’s painful symptoms, she suffered complications which led to her having the procedure reversed. Battling infections and prolapse, her stoma was removed in January 2020. With her symptoms returning, Katie made the decision to have a permanent stoma bag fitted in June 2022. She said: “Because there were so many issues with the first one, I was really nervous, especially as this stoma couldn’t be reversed. “But my condition had gotten so bad and I was in so much pain, that this was really the only option for me at this point.” I hope people can see my experience and know that stoma bags aren’t scary Katie Harpur As Katie approaches 12 months since her stoma operation, she said the procedure has “changed her life”. With no complications or symptoms, she is now able to travel and socialise with friends. “I’ve had no issues at all with it and it’s honestly the best thing I’ve ever done,” she said. “Growing up, I was so excited to travel but Crohn’s made it impossible. I always said I wouldn’t travel far until I had my stoma fitted.” Since her operation, Katie has booked a three-week trip to Tokyo for September this year, something she says she never would have been able to do before. She said: “Not being able to speak Japanese, I would have found it very hard to find a public toilet so wouldn’t have been able to do the trip before. “But now I’m planning to go to Mount Fuji and Super Nintendo World, which I’m really excited for.” Now she is raising awareness for Crohn’s disease on World IBD Day and hopes to break the stigma around stoma bags. “A lot of people think having a stoma bag is the end of the world,” she said. Now I’ve booked my first long-haul flight to Tokyo, something I never would have been able to do before the op. Katie Harpur “I was so young getting mine done and I was nervous about how my body would change but it’s the best thing I’ve ever done, I wish I’d done it sooner. “I hope people can see my experience and know that stoma bags aren’t scary, mine has greatly improved my life and enabled me to start enjoying life again.” Sarah Sleet, chief executive of Crohn’s & Colitis UK, said: “There are more than 500,000 people living with Crohn’s and colitis in the UK. Every day we hear about more who are experiencing symptoms and waiting for a diagnosis. “Since the pandemic, the already lengthy waiting times for tests like endoscopies and colonoscopies have soared. “Such delays can be devastating for people, affecting their ability to work, study, socialise and live the lives they want to. “We really need to do more to help young people stay in control of their health, and that means providing them with the tools to get the right diagnosis from their GP as early as possible. My stoma bag has greatly improved my life and enabled me to start enjoying life again Katie Harpur “If you’re experiencing blood in your poo, tummy pain or frequent, urgent diarrhoea, then the symptom checker on our website is a good place to start. “It’s designed to give people the confidence to go to their GP with a letter detailing their symptoms, to help them get the right diagnosis and get back on the road to recovery.” For more information, visit: www.crohnsandcolitis.org.uk. Read More How to check if you have skin cancer: Symptoms and signs to look out for Janey Godley shares heartbreaking cancer update New obesity jab that sparked diabetes row in US could get NHS green light Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

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A former soldier has recounted the terrifying shark attack he suffered during a military exercise which caused him to lose an arm and a leg. Paul de Gelder was a paratrooper who feared for his life during the ordeal, which saw him attacked by a 50-tonne bull shark. The animal tore off two of his limbs during the attack in 2009, and de Gelder spoke about his ordeal during an interview with CBS. The 46-year-old from Melbourne, Australia was taking part in a naval exercise in the Sydney Harbour when it took place. Sign up to our free Indy100 weekly newsletter “I was swimming from point A to point B on the surface on my back and a 10-foot bull shark came up from underneath me,” he said. "It grabbed me by the back of my right leg and my right hand, which was by my side, all in one bite." Describing how he tried to fight back by hitting the shark, de Gelder said: "That's when it started to shake me like a rag doll. As its teeth worked through my flesh and bone like saws, I was overcome by the most intense pain imaginable." He then recalled how he managed to escape the shark’s clutches before having to swim back to his boat surrounded by a pool of blood. "It took me under. The pain and the terror. I thought I was going to die. It removed my hamstring and my hand,” de Gelder added. "I had to swim back to my safety boat with one hand and leg through a pool of my own blood. I didn't think I was going to make it. “I'm very, very lucky and blessed to still be here and breathing today." He returned to work with the armed forces and also became a motivational speaker. However, despite his injuries, he believes that sharks should not be demonised. "I see my role as speaking up for an animal that doesn't have a voice,” he said. "I figure if someone like me who has almost lost their life and two limbs to a shark can understand why they are so important and why they need to be saved, then maybe everyone else should be able to as well." Have your say in our news democracy. Click the upvote icon at the top of the page to help raise this article through the indy100 rankings.

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Lil Wayne has spoken about his issues with memory loss brought on by a number of health problems, saying that he can no longer remember many of his own songs. The rapper, real name Dwayne Michael Carter Jr., has been suffering with epilepsy and recurrent seizures over recent years. The 40-year-old said that early albums such as Tha Carter III, Tha Carter II and Tha Carter IV, hold “no significance” to him now as a result of the memory loss. Speaking in an interview with Rolling Stone, Lil Wayne said: “That’s just my God’s honest truth. You could lie, you could ask me (about) such and such song, I wouldn’t even know what we talking about. Sign up to our free Indy100 weekly newsletter “I don’t even know if that’s when Tha Carter III came out. That’s how much I don’t know,” he added. "And also, I always look at it as the curse part of the gift and the curse. "I believe that [God] blessed me with this amazing mind, but would not give [me] an amazing memory to remember this amazing s**t." The musician is still planning to keep working, and won’t let his memory loss impact his plans for the future. “Even when you say it, I don’t think you actually mean stop working or doing music. You probably just mean you want to retire from everything else but the music,” he said. “When you’re an artist, a real artist like myself, I was born this way. So I don’t think that the real true artists and pioneers, they never retire. They died doing this.” Have your say in our news democracy. Click the upvote icon at the top of the page to help raise this article through the indy100 rankings.