was born July 25, 2000. When I was 14 months old, the doctors told
my mommy and daddy that they thought I had this disease called
Spinal Muscular Atrophy (SMA). At 15 months old, that diagnosis
This horrible disease makes my muscles very weak, which is why I
can't get myself in a sitting position on my own, like other kids my
age. I see other kids walking and running, but my legs are too weak
to ever let me be able to do that. I would crawl after them, but my
muscles just won't hold me up. I am sure things could be much worse,
cause as you can see by my picture, I can still control the muscles
that let me smile.
Please help them find a treatment and a cure for my disease! My
life, along with many other SMA angels, depends on it!
Lots of Love,
Supported by SMA