Hi there! My name is Alyssa, and I have a disease called spinal muscular atrophy. Here’s the scoop… When I was 5 months old, I was diagnosed with this neuromuscular disease. To put it s…

Hi there! My name is Alyssa, and I have a disease called spinal muscular atrophy. Here’s the scoop… When I was 5 months old, I was diagnosed with this neuromuscular disease. To put it s…

Infant/Toddler t-shirt SMA Spinal Muscular by LittleLihsBoutique

Infant/Toddler t-shirt - SMA - Spinal Muscular Atrophy Awareness

Infant/Toddler t-shirt SMA Spinal Muscular by LittleLihsBoutique

Long-term exercise appears to be beneficial for spinal muscular atrophy (SMA)-like mice, suggesting a potential of active physiotherapy for patient care; according to a study published in the Journal of Physiology.

Long-term exercise appears to be beneficial for spinal muscular atrophy (SMA)-like mice, suggesting a potential of active physiotherapy for patient care; according to a study published in the Journal of Physiology.

Support Spinal Muscular Atrophy Research | Teespring

Support Spinal Muscular Atrophy Research

Support Spinal Muscular Atrophy Research | Teespring

Three Cases of Spinal Muscular Atrophy Associated With Progressive Myoclonic Epilepsy

Three Cases of Spinal Muscular Atrophy Associated With Progressive Myoclonic Epilepsy

Myoclonic Epilepsy,Spinal Muscular Atrophy

Did you know? Spinal Muscular Atrophy (SMA) is a motor neuron disease, affecting the voluntary muscles? Check out this infographic for more SMA facts!

Did you know? Spinal Muscular Atrophy (SMA) is a motor neuron disease, affecting the voluntary muscles? Check out this infographic for more SMA facts!

This video from Muscular Dystrophy UK is all about Hayleigh Barclay. Hayleigh is a 27-year-old woman from South Ayrshire, Scotland, who has spinal muscular atrophy (SMA) type 2. MORE: Teen with mus…

Inspirational Young People With Muscular Dystrophy: Hayleigh Barclay

This video from Muscular Dystrophy UK is all about Hayleigh Barclay. Hayleigh is a 27-year-old woman from South Ayrshire, Scotland, who has spinal muscular atrophy (SMA) type 2. MORE: Teen with mus…

August is Spinal Muscular Atrophy (SMA) Awareness month. SMA is a group of genetic disorders that are characterized by a loss of certain protein that is necessary for the survival of some motor neurons in the spinal cord. The loss of these neurons leads to progressive muscle weakness and muscle atrophy, starting starting with the...  Read more »

August is Spinal Muscular Atrophy (SMA) Awareness month. SMA is a group of genetic disorders that are characterized by a loss of certain protein that is necessary for the survival of some motor neurons in the spinal cord. The loss of these neurons leads to progressive muscle weakness and muscle atrophy, starting starting with the... Read more »

Boy Meets Girl | This is our story, and it could be yours too | A spinal muscular atrophy

Boy Meets Girl | This is our story, and it could be yours too | A spinal muscular atrophy

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