There are many resources available to help ALS patients and their caregivers, including:
ALSA is a national not-for-profit organization providing help to those facing the disease through research, patient and community services, public education, and advocacy.
Access for patients and caregivers is available through the ALS Association.
List of all past and current clinical trials including studies related to ALS.
This group includes neurologist-published reviews of alternative and off-label treatments for ALS.
This online community is committed to making a difference for patients and their health.
