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To lead the fight to cure and treat ALS through
global, cutting-edge research, and to empower
people with Lou Gehrig's Disease and their
families to live fuller lives by providing them
with compassionate care and support.
The ALS Association seeks to promote awareness and understanding of ALS and the work of The ALS Association by providing up-to-date information and education materials to the ALS community - people with ALS their families, caregivers, researchers and members in the health care fields.
- Erika Lizee
- (818) 880-9007
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