The ALS Association - DC/MD/VA Chapter

The ALS Association - DC/MD/VA 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 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.