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Links: Spinal Muscular Atrophy (SMA) - International - Medical Condition

Andrew's Buddies

Welcome ...to fightsma.com, the website for Andrew's Buddies. This is a national organization committed to accelerating a cure for spinal muscular atrophy (SMA), the number-one inherited killer of children under two. On this site, you will find up-to-date reports from the research front. And you will find ways that you can become involved in this fight yourself.

Canada - Families of Spinal Muscular Atrophy

Welcome to the web site of Families of Spinal Muscular Atrophy - a comprehensive, on-line information and resource center. We invite you to explore our pages and reach out to our 'extended family.'

Families of Spinal Muscular Atrophy

Welcome to the web site of Families of Spinal Muscular Atrophy - a comprehensive, on-line information and resource center. We invite you to explore our pages and reach out to our 'extended family.'
Families of SMA was founded in 1984 for the purpose of raising funds to promote research into the causes and cure of the Spinal Muscular Atrophies, and to support families affected by SMA. Since then, this all-volunteer, non-profit organization has raised more than $8 million for research into SMA.

Jenny's World

Hi, I'm Jenny Luscombe and I have Spinal Muscular Atrophy. Living with this disorder is a challenge and anyone that knows of the condition will know first hand. I have been married to John since 1968, we have a daughter Lisa, married to Gareth and they have given us 2 Grandsons, Heath, Liam and a Granddaughter Brittany.

MDA Clinics/Services

MDA's 230 hospital-affiliated clinics offer quality medical care available from doctors, nurses and therapists experienced in dealing with neuromuscular diseases. These clinics also serve

Our SMA Angles

Some are here with us and some are waiting for us in heaven. Some are "naughty" and some are "nice". Some are babies and some are kids...
But no matter what, they are ALL our angels!

Relying on Joy

If you are interested in finding out about Spinal Muscular Atrophy, I thought I would provide some informative links.

SMA.net

The purpose of SMA.net is to provide a source of information for research, prevention and treatment of Spinal Muscular Atrophy (SMA).

USA - Families of Spinal Muscular Atrophy

Families of SMA was founded in 1984 for the purpose of raising funds to promote research into the causes and cure of the Spinal Muscular Atrophies, and to support families affected by SMA. Since then, this all-volunteer, non-profit organization has raised more than $8 million for research into SMA.

Wyatt's Web Site

The goals of the Foundation are numerous. Educating the public about SMA Type I is a major goal. This site, which we dedicate to Wyatt, parents & family & friends, and to the medical practitioners that touched Wyatt's life, is one of the Foundation's ways of educating the public about the terrible toll SMA Type I takes.
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