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An experimental medication may slow the progression of amyotrophic lateral sclerosis, or ALS, researchers reported Wednesday. The research was supported in part by donations from the Ice Bucket ...
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 ...
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.
Under pressure from the ALS community and Congress, FDA officials have recently emphasized the “urgent need” for new ALS treatments and pledged to use maximum “regulatory flexibility” when ...
Wallach was diagnosed with ALS in 2017 at the age of 37 on the same day he and his wife brought home their second daughter from the hospital. [3] Originally visiting the doctor for a persistent cough, Wallach had also mentioned experiencing muscle tremors and weakness in his left hand and was told he probably had a progressive neurodegenerative disease. [2]
In 2011, the institute moved to a new 26,000-square-foot (2,400 m 2) facility, also in Cambridge, allowing for the hiring of more scientists and a bigger lab. [2] Two years later, in 2014, Augie's Quest officially transitioned from MDA to ALS TDI. [12] The same year, ALS TDI received over $3 million through the Ice Bucket Challenge. [1]
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