Welcome to the spinal muscular atrophy information pages.

Here you can find out more about SMA, how it affects children and adults and what tools and events are out there to help you improve diagnosis and care of the disease.


SMA is a rare and debilitating autosomal recessive neuromuscular disease characterised by motor neuron degeneration and loss of muscle strength.1,2 Age of onset determines the level of motor neuron degeneration.1,2

Visit the page below to learn how the disease works.


Eventually your adult SMA patients may not be able to scroll down this page. SMA is a debilitating neuromuscular disease characterised by motor neuron degeneration and loss of muscle strength.1 The loss of basic motor functions will require appropriate intervention.

The characters shown are real patients and the required consent to use their stories has been obtained from the patients and families.
Photographs are for illustrative purposes only.

At Biogen, we are committed to supporting those with spinal muscular atrophy and their care teams. Our hope for Together in SMA is that by providing educational materials and resources, we can help you tackle the challenges your SMA patients face.

Together in SMA was created in support of that unity, and with the goal of becoming a valued tool for members of the team. Here you’ll find clinical information and care strategies that some people use to help manage the disease.

Biogen is building on our legacy of rare disease research and development to explore potential treatment options. And even then, we’ll still be together in SMA.


1. Lunn MR, Wang CH. Spinal muscular atrophy. Lancet 2008;371(9630):21‌20-21‌33.

2. Darras BT, Royden Jones H Jr, Ryan MM, De Vivo DC, eds. Neuromuscular Disorders of Infancy, Childhood, and Adolescence: A Clinician’s Approach. 2nd ed. London, UK: Elsevier; 2015.

3. Swoboda KJ, et al. Perspectives on clinical Trials in Spinal Muscular Atrophy. J Child Neurol 2007;22(8):957-966.

4. Rothwell E, Anderson RA, Swoboda KJ, Stark L, Botkin JR. Public attitudes regarding a pilot study of newborn screening for spinal muscular atrophy. Am J Med Genet A 2013;161A(4):679-686.