Did you know the lifetime risk of developing ALS is just 1 in 300? There is no known cure for ALS and, once diagnosed, patients typically live only three to five years. These are alarming facts about ALS, but we can help change the course of the disease and ensure that progress is made towards finding life-enhancing treatments and a cure.

The Les Turner ALS Foundation is here to care for those affected by the disease, answer their questions and support them and their loved ones every step of their journey.

I am participating in the 2023 Bank of America Chicago Marathon as part of Team Race for ALS to honor my Uncle Dave. My uncle was diagnosed with ALS in 2022 and is continuing to fight this battle. I am running to fight this battle alongside my Uncle Dave and for those who are deeply affected by this disease. I am running to raise awareness about ALS and ensure that families will continue to receive support/resources that this wonderful foundation provides. I am running in hopes of finding a cure to kick this disease to the curb. Most importantly, I am running for those who can’t. 

I believe in providing the best possible care to people living with ALS and their families in the Chicagoland area and I believe that the funds we raise together will lead to a cure for ALS. This cause is important to me and I’d greatly appreciate your support of my efforts.

Please consider making a donation to help me reach my fundraising goal. Together, we can make an impact and create a world free of ALS.