The ALS Association (ALSA) is the only national not-for-profit voluntary health organization dedicated solely to the fight against ALS, or Amyotrophic Lateral Sclerosis (often called Lou Gehrig's disease). The mission of The ALS Association is to find a cure for and improve living with ALS.

The ALS Society of Canada's home page. Information on coping with ALS, helping those with ALS, research on motor neuron disease, special events and more. Lou Gehrig's disease, lou gehrig and motor neuoron disease.

MND has different names in different countries. Also known as Amyotrophic Lateral Sclerosis (ALS), Lou Gherig s Disease or Maladie de Charcot, MND is a condition which relentlessly destroys the nerves that enable us to control all our movements while leaving the intellect and senses generally unaffected. The UK s MND Association was founded in 1979 to bring together all those people concerned ...

Amyotrophic Lateral Sclerosis, or Lou Gehrig's Disease, is the cause of an eventual parylis.

This website is a service of Ride for Life, Inc., a 501(c)(3) non-profit organization founded by ALS patients, caregivers, and those concerned about people living with ALS.

A Internet portal for the ALS community. Includes the ALS Digest in web format for easy navigation with archives and search engine.

Sharing information, my personal story, tips and words of comfort, to People with Amyotrophic Lateral Sclerosis.

One Life To Give: Michael Zaslow Bravely Fought Lou Gehrig's Disease People Magazine, December 21, 1998 In January 1998, Emmy Award winning actor Michael Zaslow joined friends and colleagues to form ZazAngels, dedicated to raising awareness and funds for ALS research. Amyotrophic Lateral Sclerosis, or Lou Gehrig's Disease, is a neuromuscular disease that robs people of their ability to speak, ...

Amyotrophic Lateral Sclerosis (ALS) (Also known as Lou Gehrig's Disease) Click for Materials En Espa ol and MDAchats Bookmark this page! It's your source for information and news about ALS and will be updated regularly. Quick Definition: Onset Adulthood. Symptoms Generalized weakness and muscle wasting with cramps and muscle twitches common. Progression ALS first affects legs, arms and/or throat ...

To serve as a resource and support for those with ALS Lou Gehrig's Disease or Motor Neurone Disease their families and caregivers.

To serve as a resource and support for those with ALS Lou Gehrig's Disease or Motor Neurone Disease their families and caregivers.

This site primarily explores the possible effect of readily available medications, anti oxidants, liver function and supplements and therapies on the progress of the neurodegenerative illness (ALS) Amyotrophic Lateral Sclerosis or (MND) Motor Neurone Disease. Amyotrophic Lateral Sclerosis, Motor Neurone Disease, Lou Gehrig's Disease and Maladie de Charcote is referred to as ALS/MND throughout.

Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's disease) information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).

The Angel Fund supports research into amyotrophic lateral sclerosis (ALS) at the Day Neuromuscular Research Laboratory at the Massachusetts General Hospital.

Our site has been created for all pals, carers, family of pals and all the friends my wife and I have gained through ALS (Amyotrophic Lateral Sclerosis). My wife Dee, was diagnosed in October 1996 with Limb Onset ALS. On my site you will find a ever growing links page to other ALS Sites and Associated Links, ...

The BUILD project is new, set up to work with people with MND, their carers and families to plan services. The project uses 'action research' to record and report members views and arrive at an action plan for change.

Bert Woodard has lived with ALS - Lou Gehrigs Disease - for over 17 years. Bert has shared his experiences, tips, and inspiration in this downloadable pdf manual to help others with ALS or other life threatening disease ...

Is Heaven the better place Articles and scribbles about day-to day living with ALS - Amyotrofisk Lateral Sclerose.

As someone quite amazed to find herself in her 15th year of ALS and still busily, happily, and contentedly engaged in living, I have reached the point where I find myself saying If I'd known I was going to live this long, I would have taken better care of myself! For that reason, the main focus of this site is on dealing with some of the medical complications we face as a result of ALS. All too ...

Luther Conant was diagnosed as having ALS, Lou Gehrig's Disease, in June, 2000, and Lyme Disease soon thereafter. This is the document of his life from that point on. Also here is as much of his work as humorist, filmmaker, writer, composer, and stand-up philosopher as can be crammed in.

The Curtis R. Vance Foundation is a nonprofit corporation, whose purposes include but are not limited to public education and funding of research for a cure for amyotrophic lateral sclerosis, ALS, commonly known as Lou Gehrig's disease...