A girl who has a strange disease makes anyone who kisses get burnt

Brave Brooke Masson 4-year-old suffered from cystic fibrosis that made her skin so salty that her kissers felt burning.

Rarely, anyone who kissed her felt burning lips

The mother, Emma Robinson, lived in Aberdeen, Scotland, England, told Health: "My child had it when he was more than 2 weeks old. The couple was shocked and hurt when the doctors announced the baby was It was a difficult time, like a nightmare hit the family. "

Poor illness but Brave baby always smile like flowers. In me, a strong desire to live makes many people surprised and moved. During 4 years of treatment in pain, the little angel still endured and seldom cried. So far I've spent 51 weeks in the hospital, taking more than 30 drugs a day to cope with illness. Among them, about 20 pills have the effect of supplementing the function of the pancreas, digesting food. I also get injections every day.

Picture 1 of A girl who has a strange disease makes anyone who kisses get burnt
Baby Brave Brooke Masson.(Photo: Health).

Each Brave morning undergoes 15 minutes of physical therapy. This is a very difficult time, because he is very difficult to breathe. Doctors must give the child a mask to help the airway more airy. Every day, the diet of Brave is always supplemented with a large amount of salt to compensate for the salt being excreted through sweat. Because of the amount of salt on her skin, there are many people who kiss her, they also feel burning.

"When you kiss her, especially on her forehead, her skin instantly burns your lips. Doctors say that Brave's body has 60% salt. Brave is too young to try," she said. New gene therapy test ".

Since the baby was sick, parents had to quit their jobs to take care of their children for 51 consecutive weeks. Sister Emma shared: "She loves to swim but we have no way to bring her to the pool in this cold time. Brave's dream is to become a doctor to treat her own disease. "When he always smiles on his lips, the doctor says he can live up to 19-25 years old, so I always respect every minute of my life."

At the moment, the family takes Brave to travel in hot countries to speed up the process of converting salt in her body faster. Young couples also mobilize people to help save their children from the disease. Currently, the family has received about 5 thousand USD to donate from families, friends and relatives . The young mother said: " Without the help and donations of people, we cannot do it. What for her ".