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I am Steve Martin

living with ALS

Colorado


Awareness doesn't happen simply by putting out information, but by exposing people to personal stories and individual faces.

A disease without faces connected to the disease will never be understood, never have awareness in the general community, and most likely will never receive the support and funding needed to find and have access to effective treatments and medications. To me, I AM ALS is a way to put faces with this disease of ALS, in addition to fighting for change in the political arena and raising money for research. Awareness doesn’t happen simply by putting out information, but by exposing people to personal stories and individual faces. I have a wonderful wife. She’s the best wife in the world. Twenty years of marriage is not enough. I want to live! I have a 15-year-old daughter and a 9-year-old son. They are the best kids in the world. I want to be here for them!


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Join us in Washington DC from May 29th - June 2nd for the 3rd annual ALS Awareness Month flag display and inaugural Community Summit.

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