Australian women suffering from a rare disease can only rely on the mouth of the stomach to eat – Si-www.40sqw.com

Australian woman suffering from a rare disease of gastroparesis can only rely on the nose intake — Sichuan channel — people.com.cn original title: Australian woman suffering from a rare disease of gastroparesis can only rely on the nose feeding according to the British "Daily Mail" reported on September 26th, recently, New South Wales, Australia’s Walker Chapman? (Charmain Walker-Caunt) – kingtype suffering from a rare disease of gastroparesis, can only rely on a tube through the nose to sustain life for the body conveying nutrition liquid. It is understood that the prevalence of gastroparesis is very small, only 35 of the 1/10000. This disease destroys the Charman digestive nerve from the brain to the stomach, causing her paralyzed from the throat to the intestinal tract of the digestive tract, unable to digest food, eat a piece of bread to vomit for several days. So she can only pass through a catheter about 2 meters across the nose, every day for 24 hours to deliver nutrients to the body. The food was put in front of her, but she was starving, and her weight dropped 20 kilograms in just over 9 days. She may have to cut off her social activities at any time. Although very little expensive treatment effect, but the husband still desperately Charman for her illness, which made her very grateful. Even half a normal life is also a kind of luxury to chapman. Although she is very weak, she is still optimistic about life. She is asking the state to give her help to reduce the economic burden of expensive medical bills. (Zhang Hua, Gao Hongxia dimension: commissioning editor)相关的主题文章: