The ALS Association, based in Rockville, MD, is dedicated to supporting individuals and families affected by amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. The organization provides resources, advocacy, and research funding to improve the lives of those living with ALS.
Through a combination of support services and awareness campaigns, The ALS Association strives to raise public understanding of the disease and advance scientific breakthroughs in the quest for a cure. By fostering a community of compassion and empowerment, the organization works to enhance the quality of life for individuals impacted by ALS.
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