ALS Association

The ALS Association is a global nonprofit organization dedicated to fighting amyotrophic lateral sclerosis. It drives scientific research for treatments and a cure, while providing comprehensive care and resources to individuals living with ALS. Their strategy integrates research funding, patient and caregiver support, and advocacy to influence public policy and accelerate therapeutic advancements.

Founded in 1985, The ALS Association emerged from the urgent need for a unified national effort against ALS. It was established as the first nationwide organization solely committed to addressing the disease through care, research, and advocacy. This foundational insight focused on consolidating resources and voices to combat ALS's devastating impact.

The primary beneficiaries are individuals diagnosed with ALS, their families, and caregivers, who receive vital support, education, and services. The organization’s vision is a world free of ALS. They actively pursue this by accelerating new therapies, improving quality of life, and striving to make ALS a livable disease until a cure is found.