Amyotrophic Lateral Sclerosis subcategories:
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Voice for Joanie is a totally volunteer organization in southwestern Connecticut which provides computers and voice technology for people living with ALS(Lou Gehrig's disease).
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The ALS (Amyotrophic lateral sclerosis) Division of the MDA (Muscular Dystrophy Association) offers the most comprehensive range of services of any voluntary health agency in the nation, and leads the search for a treatment or cure through its aggressive, worldwide research program.
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Augustine (Augie) Nieto, a prominent leader in the nation’s fitness industry for nearly three decades, received a diagnosis of amyotrophic lateral sclerosis (ALS, or Lou Gehrig’s disease) in March 2005. Augie, 48, is approaching his role as co-chairperson of MDA’s ALS division with the same ironclad will and determination that catapulted him to entrepreneurial heights in the fitness world.
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We are the only national organisation in England, Wales and Northern Ireland dedicated to the support of people with MND and those who care for them.
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The Dream Foundation is the first national wish-granting organization for adults over the age of 18. Now in its 10th year, the Dream Foundation has granted thousands of dreams to adults who are emotionally, financially and physically devastated by terminal illness.
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Curt and Shonda Schilling have joined the ALS Association's New England Chapters in the fight against ALS.
Money raised through Curt's Pitch for ALS funds research and patient services for ALS patients in Massachusetts, Connecticut, Rhode Island, New Hampshire, Vermont, and Maine.
Fans are invited to become members of Curt and Shonda’s team by making a one-time gift, or by pledging per strikeout.
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Walk to D'Feet ALS to benefit The ALS Association Massachusetts Chapter is an online and offline grassroots fundraising effort powered by Blue Sky Collaborative.
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The Angel Fund supports research into amyotrophic lateral sclerosis (ALS) at the Day Neuromuscular Research Laboratory at the Massachusetts General Hospital.
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Welcome to the official website of The ALS Association - Jim "Catfish" Hunter Chapter. It is our goal to serve all persons living with and fighting ALS (PALS) in North and South Carolina in every way possible. We work extensively to provide much-needed programs that offer emotional, physical and financial assistance.
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The ALS Association encourages scientific research to find a cure for ALS, heightens awareness of the nature of the disease, stimulates volunteerism and activism, and increases awareness of government leaders to encourage support of research and patient care.