ALS Network is a nonprofit organization dedicated to supporting individuals living with amyotrophic lateral sclerosis (ALS) and advancing research toward effective treatments and a cure. The organization provides patient services, community education, advocacy, and funds scientific research focused on ALS.
Biomedical research funding, healthcare access, disability rights, caregiver support programs, and federal and state appropriations for neurodegenerative disease research and treatment
Charitable donations from individuals, corporate sponsorships, fundraising events, and foundation grants
ALS researchers, regional ALS clinics, patient advocacy coalitions, and national ALS advocacy organizations
Non-profit organization
