British woman Eloise Christine, 25, has to be fed through a tube after botched surgeries that left her unable to eat normally. Reported Metro.
At age 18, Eloise began to feel nauseous after every meal. The girl went to the hospital, but the doctors did not notice her rare disease and diagnosed an eating disorder. For several years, the girl continued to suffer from nausea, and after many hospitalizations, Christine’s mother forced the doctors to conduct additional examinations.
New tests revealed that Christine has malrotation, a rare birth defect in the development of the intestines, in which the intestines are unable to return to their normal position in the abdominal cavity. “Everything I eat makes me nauseous. “My intestines and stomach are twisted, so the food reaches a certain place, and then it can’t go any further, and I feel nauseous,” the girl explains.
Eloise was fitted with a gastrostomy tube through which she could eat and receive nutrients. He later underwent three surgeries to correct the malrotation, but all of them were unsuccessful. As a result, the girl has to eat through a tube.
Kristin has become insecure that she can’t go to a cafe with her friends. The girl admits that sometimes she does not control herself and eats her favorite dish, although she suffers from nausea attacks afterwards.
In order to overcome the difficult moral and psychological situation, Kristin started blogging on the social network. “Communicating with people with similar problems makes it much easier to overcome it. After all, these are people who know exactly how you feel,” he says. The girl wants to inform the users and give hope of recovery to the lucky ones.
