5 month old girl 'began turning into stone', there is no cure for the disease
Viral News / 5 month old girl 'began turning into stone', there is no cure for the disease
Viral News - 5 month old girl 'began turning into stone', there is no cure for the disease
A five-month-old child in the UK is struggling with such a rare disease, which is one of the millions. Due to this disease, the innocent child is changing 'stone'. At the time of birth, this baby girl was like other normal children, but after being hit by severe illness named Fibrodysplasia Ossificans Progressiva, the body is becoming stones. Read more in the slide what happens in this disease ...Kapal Alex and Dave living in Hertfordshire in Hertfordshire in Hertfordshire came in that time when he knew that his five-month innocent is struggling with such a disease, which is not treated. Five-month-old girl Lexe Robbins is changing 'stone' due to genetic situation. Due to this condition of the baby, the child's parents are worried.The girl's parents Alex and Dave have warned the parents around the world about potential symptoms. He said that Lexy Robbins was born on January 31. He was like normal children, but one day he found that there is no stir in the thumb of the girl's hand. The fingers of his toe are quite large, which did not look normal from anywhere.It has been reported that muscles and connecting tissue changes in this deadly disease. In this disease, the bones begin to come out of the skeleton, which becomes miserable. Comparison of this situation is often done by changing the body into stonePeople suffering from this fatal disease can be lying on the bed till the age of 20 and the possibility of their life is up to 40 years. Lexsey had X-ray in April. Swelling in his toe was found and his hands and toes were attached to each other.Lexsey's mother Alex said that 'after the X-ray, we were told that he is syndrome and he can not walk. We did not believe because he was physically very strong at that time. He was kicking. We did not believe it, so in May we trace this disease and took it to the expert. 'Alex said that "we had to do a genetic test by the end of May, then X-ray, but the results of the genetic Test took six weeks. His Test was sent to any Lab in America where Fibrodysplasia Ossificans Progressiva was confirmed. 'He told that "he feels like normal children. He sleeps overnight, he smiles and laughs continuously, rarely cry. We want to keep it like this, but due to his serious illness Very restless