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The ALS Association is an American nonprofit organization that funds global amyotrophic lateral sclerosis (ALS) research, provides care services and programs to people affected by ALS through its nationwide network of clinical care centers, and works with ALS advocates around the country for state and federal policies that serve people living with amyotrophic lateral sclerosis (ALS), also ...
Lee Wilson discovered she has a "100%" chance of developing ALS, after losing her father and grandmother to the disease ... For premium support please call: 800-290-4726 more ways to reach us ...
In 1983, the Foundation started patient support groups. [7] The groups are now offered online at no cost. [8] In 1992, Les Turner ALS became a founding member of the International Alliance of ALS/MND Associations. [7] In 2002, the Foundation's main event, the ALS Walk for Life was started. [7] [9]
PatientsLikeMe launched its first online community for ALS patients in 2006. [7] From there, the company began adding other communities for other life-changing conditions, including multiple sclerosis (MS), Parkinson's disease, fibromyalgia, HIV, chronic fatigue syndrome, mood disorders, epilepsy, [8] organ transplantation, progressive supranuclear palsy, multiple system atrophy, and Devic's ...
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I was diagnosed with familial ALS, or genetic ALS, in 2022. Also known as Lou Gehrig's disease, amyotrophic lateral sclerosis runs in my family.
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