People are never prepared for a diagnosis if ALS. Patients and their families face change, challenges, and choices. Our organization strives to educate patients and their families about the disease and help them cope.
We encourage all patients, family members, and caregivers to use the Resource Guide, Living With ALS Manuals, and Patient Bill of Rights as tools to improve quality of live.
Talk to us!
Patient Services Program and Referral Service
Michelle Hammond-Susten
Director of Patient Services
Phone: (404) 636-9909
Toll Free: (888) 636-9940
Email: michelle@alsaga.org