Spinal Muscular Atrophy (SMA): New Treatments Offer Hope
Insurance reverses decision, will pay for toddler's $2 million drug
SMA Gene Therapy Zolgensma 'Saved All of Our Lives': A Family's Story
Two New Treatments for Spinal Muscular Atrophy Offer Hope
Young SMA patient's ongoing campaign aims to raise S$375,000 for
Spinal Muscular Atrophy Treatment: Claire's Story
A $2.1 million gene therapy raised a family's hopes for a daughter
Insight: What happens when a $2 million gene therapy is not enough
Giving a family hope for the future
Hope for Kaeli, Kaeli Price, Patient Stories
Spinal Muscular Atrophy » Powell Center for Rare Disease Research
Petition · Help save Spinal Muscular Atrophy (SMA) patients! Ionis
B.C. teen with rare disease wins fight to receive costly drug from