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.

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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.

Speech software, ALS, stroke, SGD, aphasia, speech disorders, augmentative communication, AAC, communication devices, assistive technology ...

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 ...

This website is sponsored by the World Federation of Neurology to link researchers and clinicians worldwide with the goal of finding effective treatment and a cure for ALS.

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

The Les Turner Amyotrophic Lateral Sclerosis Foundation is the nation's largest, independent ALS organization devoted to raising money for research, patient services and educational materials and to maintaining quality of life for every person with ALS.

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.

Project A.L.S. 511 Avenue of the Americas PMB #341 NYC 10011 tel: 800-603-0270 fax: 212-337-9915 email: projectals@aol.com Copyright Project A.L.S. 2001 ...

The ALS March of Faces is a patient/caregiver governed and operated non-profit organization, dedicated to heightening public awareness of ALS, and advocating on issues that concern and/or benefit PALS (People with ALS).

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, ...

Hosted by: Culet Communications Last update: June 26, 2002 ...

The University of Miami ALS Clinical and Research Center provides the highest level of care and multi-dimensional support for patients with Amyotrophic Lateral Sclerosis (ALS) and supports the families from the time of diagnosis to the end stages of the disease, while conducting advanced research into the cause and cure of ALS.

LEF Site Search -Please Select- Protocols Health Conditions Products LE Magazine Medical Abstracts What's Hot FDA Information The Total LEF Site Research Funded Research Track Record Health Concerns Innovative Doctors Innovative Clinics Medical Advisory Scientific Advisory Free Product Directory Click for a FREE copy of our Product Directory LEF Membership What is LEF Become a Member Renew ...

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 ...

Information and news for those with ALS or Lou Gehrig's Disease - news, research, treatments, chapter events, advocacy, support groups, more.

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

Voice for Joanie is a totally volunteer organization in southewestern Connecticut which provides computers and voice technology for people living with ALS(Lou Gehrig's disease) ...

The ALS Massachusetts Chapter is a multi-faceted grass-roots organization that carries out ALSA's mission and strategic goals at the community level. The chapter - with supporting services from the National Office - actively pursues The Association's goals. Primarily, ALS MA Chapter exist to serve people with ALS, 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.

Home | Facts | Services | Objectives | Newsletter | Other Services | Membership | Donations | Diary | Contact | Mission Statement - To improve quality of life for people living with MND. Home Facts Services Objectives Newsletter Other Services Membership Donations Diary Contact MNDA Carer's Sheets ***** PDF Files for download: Monthly Newsletter Membership Form Donation Form Download Top of Page ...

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, ...

Local chapter of The ALS Association, serving DC, MD, VA. Patient services, support groups, equipment loans, clinic contacts and information about ALS (Lou Gehrig's disease). Phone: 202-331-1448.

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.

Learn more about Amyotrophic Lateral Sclerosis, ALS Research, Medical Research, New Medical Discoveries, Neuromuscular Diseases, Lou Gehrig's Disease and more here at New Hope Discoveries.

Information about the Neuromuscular and ALS Center of New Jersey, ALS, and Neuromuscular Diseases. Also links to other ALS sites and current and archived articles from ALS News of New Jersey.

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 ...

The ALS Family Charitable Foundation Homepage. Home of the Cliff Walk ...

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.

Tell me when this page is updated John's Town Bible Study BHS Class of 1983 Poetry Family Photo Album About Me ALS experts PALS Pages ALS Street Addresses Mini Biography about ALS Mini Biography Page Two Mini Biography Page Three Mini Biography Page Four Mini Biography Page Five Mini Biography Page Six Michelle Scott July 26th Amy Sweigard August 14th The LORD is good, a strong hold in the day ...

We are a non-profit Organization for Lou Gehrig's Disease located in Kentucky.

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...

Welcome, Guest - Webring Home - Help/Support - Sign In PALS (People with Amyotrophic Lateral Sclerosis) Home Health & Wellness Health Care About this Ring PALS (People with Amyotrophic Lateral Sclerosis)is a Webring designed for PALS and each Site contains information regarding this illness. ALS is also know as MND (Motor Neurone Disease) and Lou Gehrig's Disease. Ring Poll Vote/View ...

Als patients control drooling with effective medicine.