My name is farid I come from Algeria I suffer from a genetic disease
rare neuromuscular "muscular dystrophy" that affects some of people. It is manifested by muscle weakness ,,,
Neuromuscular diseases are very diverse, among the most common myopathies include deuchenne, becker,
My myopathy was declared 17 years ago when I was 10 years old.
1999-2000.
The diagnosis of my disease was established 1 year later, following a problem of diagnosis, the neurologist doctor had initially thought of a fatigue problems!!!
they did me a biopsy at the right shoulder ,nothing else,,
I am definitely sitting in a wheelchair at 21 years old.
So far it mainly affected the legs and some back muscles but for some months I'm also moving less well my arms.
I went back to university in 2010 I did higher studies in computer science.
this year august 2017 I graduated I am a computer engineer :)
bye :)
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