Our mission:
To discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
Receiving a diagnosis of ALS is challenging and overwhelming. While no two people with ALS will experience the condition the same way, there is a great deal of collective knowledge as well as valuable resources available.
More Resources and Information
Webinars:
Click here for the latest research webinars.
Click here for the latest care services webinars.
We encourage you to seek help from us.
Annie White-Barb, RN
Care Services Manager
(304) 220-0032
[email protected]
Anthony Woodyard
Community Engagement & Development Manager
(304) 207-0015
[email protected]
West Virginia Black Bears to host first Lou Gehrig Day in West Virginia!
Join The ALS Association on June 7th in Morgantown as the Black Bears take on the Williamsport Crosscutters!
This evening of fun will honor West Virginians living with ALS and raise awareness as we work to end this disease.
Tickets can be purchased HERE. A portion of ticket sales will be donated back to the ALS Association.
This event is the product of a collaborative effort between the West Virginia Black Bears, The ALS Association, The SETH Project, and I AM ALS.