The ALS Association is the only national not-for-profit health agency dedicated solely to the fight against ALS through research, patient and community services, public education, and advocacy. The Association's affiliate network includes chapters in communities throughout the nation.
My dad was diagnosed with ALS in 2016 at the age of 61, and died in 2018. It devastated our family. ALS is a cruel, unrelenting disease that, little by little, strips everything away from a person. There is no cure. It is a death sentence.
My dad and my step-mom were served well by the ALS Association. I want to pay it forward and help other families living with ALS. Your support will help do this, plus fund desperately needed research. There is promising research happening and help cannot come soon enough to those who don't have much time. So THANK YOU!
If you want to learn more, visit The ALS Association.