During these uncertain times, how can we help?
See below to access our COVID-19 Resource Hub, and to explore our growing directory of both COVID-19-specific and virtual volunteering opportunities.
Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support. The DC/MD/VA Chapter is based in Rockville, MD with an office in Richmond, VA.
The ALS Association - DC/MD/VA Chapter is a 501(c)(3) non-profit organization dedicated to serving the needs of people living with ALS (Amyotrophic Lateral Sclerosis a.k.a. Lou Gehrig’s Disease) and their families in Washington, D.C., Maryland and Virginia. The ALS Association National Office and the ALS Association - DC/MD/VA Chapter operate under a shared mission: to support people living with ALS and to leave no stone unturned in the search for a cure. The ALS Association - DC/MD/VA Chapter is currently serving almost 700 people living with ALS and their families. These services include assistive technology devices, social worker visits, medical equipment loan closet, transportation grants, and many other services. All of the Chapter’s services are provided free of charge to the families.
The ALS Association - DC/MD/VA Chapter accepts donations. Donate Now.