Recently, Little Alfi Jones from Wales has become famous throughout the world: despite his young age (he was only two years old), he became the “owner” of an unusually rare illness. Until this moment, she did not even have a name. The child was originally born with many serious health problems, among which deafness, partial blindness, a hole in the heart. In addition, the boy cannot walk. The new disease is called “restructuring of an unbalanced chromosome”. After the studies, doctors concluded that a rare disease affects the 11th and 15th chromosomes.
According to preliminary estimates, due to the congenital dislocation of the thigh, the boy will never be able to walk, perhaps he will even need plastic surgery in Moscow prices for Medusl and other operes. Even such tragic events in the life of 37-year-old Maria Jones, the mother of a little British, did not force her to desperate, although she has six more children. A woman still calls her youngest son a “ray of sunlight”.
Alfie’s mother admitted that despite all the hardships that happened to the boy, he can be called truly happy, since everyone who meets him in the way immediately fall in love with this little man. Today his parents, looking at him, see only a son in him, and not a sick person. Alfi became a kind of adhesive, which holds the whole family together, which had before had some problems.
42-year-old Kent Jones, Father Alfi, shared his information that he did not know how long their son will live, since doctors have never encountered a similar disease. Therefore, parents do not know what can be expected from the future.
To date, one of the priority areas for the boy’s parents is to raise 30 thousand dollars to purchase everything necessary for organizing a special sensory room, including devices vital for the child.
