The Graham Harden Story

Wednesday, Dec. 19th Premier Movie Event

ESPN Interview at UNC

Graham's Story

A Thank You

Thank you to all of our donors who have lovingly supported Graham and his family as he battles ALS. Your gifts will help offset the $250K+ annual out-of-pocket expenses they face as the disease progresses. Your voices give power to a platform that is influencing ALS advancement nationwide. You are all part of the GForce team!  

Donations are NOT tax deductible.  Checks can be made payable to the Graham Harden II Family Trust and mailed to P.O. Box 1411, Los Altos, CA  94023.


Please Help...

In August of 2016, Graham Harden received the heartbreaking diagnosis of amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. ALS robs its victims of the ability to walk, dress themselves, talk, swallow, and ultimately breathe, all while leaving their minds intact. ALS has no cure and no effective treatment and an average lifespan from diagnosis of 3-5 years. Yet, none of you will be surprised to hear that Graham is doing whatever he can to fight this disease and to prolong the progression to its more debilitating stages. He is one of the toughest competitors we all know and his motto is, "Game on, ALS!"