Web site promoting public awareness for spinal muscular atrophy.

A place for people to find support for Spinal Muscular Atrophy (SMA) / Werdnig-Hoffman.

International support group and resource center for this disease, includes current research.

I am two years old and I have SMA2.

A detailed description, news and links with information about Spinal Muscular Atrophy. A personal story of a baby, Ilsa.

Overview of SMA, its genetics, clinical presentation and testing. It is written by experts in SMA research and genetic testing.

Provides detailed medical/genetic information for a variety of neuromuscular disorders. Primarily intended for medical professionals and is very technical.

Canadian Chapter of Andrew's Buddies, fighting Spinal Muscular Atrophy SMA.

A personal story of a family with a son Theo, suffering from Spinal Muscular Atrophy. Site also in French.

Canadian charity supports research into a cure for SMA.

Elizabeth has Spinal Muscular Atrophy Type 1. She is in a clinical study at Stanford for SMA type. She has beat the odds. Read about her journey through life.

Information about an annual walk to raise money to find a cure for spinal muscular atrophy. Learn about SMA and read Emily's story.

Information page compiled by the National Institute of Neurological Disorders and Stroke (NINDS).

Large on-line source of information and inspiration regarding children with SMA. See their faces, read their stories, remember those who have passed and fight with those who are fighting.

Information on SMA, and the latest updates in research, treatment and funding.

Dedicated to fighting spinal muscular atrophy by helping fund research for treatment and a cure, and providing support to families affected by SMA Type I.

A tax-exempt, not-for-profit organization dedicated to providing information and support to family, friends, individuals and caregivers on all aspects regarding the genetic disease SMA.