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Fox News
24-06-2025
- Health
- Fox News
Teen with unnamed condition can't eat any food, baffling doctors worldwide
A teenager who is unable to eat any food at all has a condition so rare that doctors said they haven't found anyone else with the same ailment. Finley Ranson, age 14, was born with an extreme response to all food, with his body reacting as if it was a virus and causing him to bleed internally. "I've got a rare condition where I can't have fat into my stomach," the boy told news agency SWNS. "It is impacting my life, as I've not been able to eat any food or drink other than water." (See the video at the top of this article.) The boy's digestive system cannot tolerate lipids, which are fatty compounds or oils that are found in foods. When Ranson, who is from England, was 4 years old, he was taken to a London hospital, "where a central line fed nutrients and minerals into his heart," his mother said. "It was a game-changer. He was happy, bouncing and starting to put on weight." Finley now regularly receives the lipid infusions via a tube, which enters his chest and goes to the central vein in his heart. He receives carbohydrates, proteins, vitamins and minerals three times a day into his stomach via a different tube. He started undergoing the six-hour process every week when he was 4 years old. For the past five years, it has been twice a week. "We have to bypass the gastrointestinal tract completely," Dr. Manas Datta, a pediatrician who has treated Finley since birth, told the BBC. Doctors tried introducing separate ingredients from the tube into the boy's stomach, but "as soon as they put the lipid in, we took 10 steps back," the boy's mother, Rhys Ranson, told SWNS. Ranson's condition is so rare that it doesn't even have a name, although he has dubbed it "Finley-itis." His condition has baffled medical professionals, who believe he may be one of the only people whose body reacts to lipids in this way. "That's the unfortunate thing that we bump up against in medicine with rare diseases that confound doctors," Dr. Neeta Ogden, an allergist and immunologist in Edison, New Jersey, who is not involved in Ranson's care, told Fox News Digital. For more Lifestyle articles, visit Dr. Stephen Tilles, an allergy and immunology specialist in Seattle, told Fox News Digital that Ranson's condition is not the sort of thing typically associated with a food allergy. "Obviously, it's an adverse reaction to the lipid component of food, but that's not on the list of things that allergists will encounter in their practices," said Tilles, who is also unaffiliated with Ranson's care. Doctors originally believed Ranson might be allergic to breast milk, but after being fed hypoallergenic milk through a tube, he still failed to thrive, his mother reported. "His stools were all blood and mucus, and he wouldn't put on weight" when he was a baby, Rhys Ranson told SWNS. "We have to bypass the gastrointestinal tract completely." She is now being trained to perform the lipid infusions at home, which she hopes will improve her son's quality of life. "We're unsure what the future looks like," she said. "We hope there's a day that comes [when] he can have a normal diet … but if not, as long as Finley's happy and healthy and thriving the way he is, we're happy to continue what life is like for us at the moment."
Yahoo
07-05-2025
- Health
- Yahoo
Teen unable to eat due to rare digestive condition
Like most teenagers his age, Finley is given a cake every year to celebrate his birthday, but he can never eat it - or any other food. If he did, he would bleed internally. The 14-year-old's digestive system cannot tolerate lipids - fatty compounds or oils which are found in foods - so he has them injected directly into his heart. The treatment is a six-hour process which he has undergone every week since he was four years old, and over the past year it has increased to twice a week as he has grown. Finley's case is so rare that doctors have considered presenting it to a medical journal, as they believe he may be one of the only people whose body reacts to lipids in this way. Dr Manas Datta, a consultant paediatrician at Broomfield Hospital in Chelmsford, Essex, who has treated Finley since he was born, said it was "horrific" seeing how Finley's body responded to food. "Even when he was on breast milk, he was reacting," Dr Datta told the BBC. "We had never seen this type of case before - I remember many days where Finley came to the hospital so unwell." Finley has undergone more than 20 operations and visits the hospital regularly for treatment [Family photo] Finley, from Battlesbridge, Essex, underwent more than 20 operations at Great Ormond Street Hospital in London as doctors tried to understand his condition. His mum, Rhys, 37, felt her son had been a "guinea pig" due to "trials and errors", and it had been "a lightbulb moment" when doctors finally worked out how to treat her son. "It's heartbreaking at times - people don't see what Finley goes through day-to-day," she said. "They see the happy, chirpy young man, but psychologically he goes through a lot." Rhys said she does not try to hide the sociable aspect of food from her son. "He's always helped cook, we always go out to restaurants, he's always had a birthday cake," she told the BBC. "He might not be able to eat it, but he's had the same normality in that respect as everybody else." Finley, who is also autistic, said the look and smell of food does not make him hungry or feel like he is missing out. "Having my feed is all I know, so I just see other people eating and it doesn't bother me," he added. Rhys said there is no name for her son's condition so he calls it "Finley-itis" [Steve Hubbard/BBC] Finley receives a lipid infusion via a portacath, or tube, which enters his chest and links directly to the central vein in his heart. "We have to bypass the gastro-intestinal tract completely," Dr Datta said. "Not only the fat, but he even cannot tolerate the normal carbohydrates and proteins as well," he added. Finley receives carbohydrates and proteins - along with vitamins, minerals and electrolytes - three times a day into his stomach via a different tube. "I can't remember when I had [the infusion] first because it's just my life now - I can't really escape it," Finley said. "There isn't a name for what Finley has" said Rhys, adding her son called his condition "Finley-itis". "There's no-one else that we know that has the lipid element infused directly." "We are actually thinking about reporting this case to some sort of journal because it's such a rare condition," Dr Datta said. The hope is that Finley will be able to eventually do infusion treatments at home, instead of travelling to Broomfield Hospital twice a week. "There might be a time that he is able to tolerate fat," Rhys said, "but if not, we just carry on with what our 'normal' is and go from there." Dr Manas Datta has treated Finley since he was a baby and said the 14-year-old was "a very determined chap" [Steve Hubbard/BBC] Finley has plans to abseil down a tower block at Southend Hospital on 16 May to raise money for the Mid and South Essex Hospitals Charity. "The building is 154ft (47m) - it's a bit high, but I feel like I'll be all right," Finley said. "The hospital and all the [staff] have given me care through my life, and I just wanted to give back and raise money for them to help other people." Finley's mum - who completed the same abseil on Finley's behalf a couple of years ago as he was too young - said her son was "remarkable". "He's the most lovable little boy who wants to help other people because of what he's gone through - I'm so proud of him." Follow Essex news on BBC Sounds, Facebook, Instagram and X. More on this story Related internet links
