We’re excited to welcome you to the official blog of SMA DMD Support Network — a space dedicated to sharing knowledge, hope, and support for families affected by Spinal Muscular Atrophy (SMA) and Duchenne Muscular Dystrophy (DMD).
Our mission is simple: to make life easier and more hopeful for children living with these rare neuromuscular diseases. Through this blog, we’ll be sharing helpful tips, treatment updates, personal stories, and expert advice.
Whether you’re a parent, caregiver, medical professional, or someone simply looking to understand more, we’re here to walk this journey with you. Together, we can build a stronger, more informed community.
Stay tuned for more updates — and thank you for being part of our network.
With care,
The SMA DMD Support Team
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