Our son, David, has a devastating condition that affects 1 in 6,000 children called Spinal Muscular Atrophy (SMA). David is unable to sit up by himself or crawl, and we have been advised that sadly he will never walk. At present there is no cure.
However, the scientific community and pharmaceutical companies across the world are making significant advancements. They know the specific gene affected, and are running clinical trials.
The SMA Trust is dedicated to finding a cure for SMA. So please dig deep and donate now.
Thank you.
Jonathan & Patricia Dee
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