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Only 65 days remaining until Maywoods!
spinal muscular atrophy
Health, Conditions and Diseases, Neurological Disorders, Muscle Diseases, Spinal Muscular Atrophy
See Also:
- Canadian charity supports research into a cure for SMA.
- 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 personal story of a family with a son Theo, suffering from Spinal Muscular Atrophy. Site also in French.
- A detailed description, news and links with information about Spinal Muscular Atrophy. A personal story of a baby, Ilsa.
- Information on SMA, and the latest updates in research, treatment and funding.
- 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.
- 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 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.
- I am two years old and I have SMA2.
- Information about an annual walk to raise money to find a cure for spinal muscular atrophy. Learn about SMA and read Emily's story.
- Web site promoting public awareness for spinal muscular atrophy.
- 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.
- 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.
- Information page compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
- Overview of SMA, its genetics, clinical presentation and testing. It is written by experts in SMA research and genetic testing.
- This site contains a collection of material pertaining to SMA. I have been searching facts on SMA ever since our son was diagnosed with the disease in 1994.
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