SMA Awareness Month on the ends. And I want to once again talk about little boy Artyom, he has SMA type 1, and he with his parents lives near me. He always needs a specially adapted for his life. He as all children with SMA waits and hopes that in soon time will created drug from SMA and it will receive all the children and people with SMA. We all believe in it.

My name is Monika Lemeshonok, I am painter from Belarus. From born I have rare disease of the spinal cord - Spinal Muscular Atrophy Type 2. From this disease, I can’t walk and move, I'm in a wheelchair. But I love life and around the world. I express my love for life through painting artwork, I have art exhibitions throughout Europe and many art lovers appreciate my works.
Showing posts with label drug from SMA. Show all posts
Showing posts with label drug from SMA. Show all posts
Tuesday, August 30, 2016
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