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My mom, Stephanie, was diagnosed in February 2020 and she passed away in December 2021. We walk in honor of her. 

If you have ALS, you are always wondering what is going to happen next?

You lose the use of your right hand..  what next?
You lose the ability to eat and need a feeding port and pump... what next?
Then you start losing the ability to speak, so you get a machine that talks for you... what next?
You lose the ability to walk..  what next?
You eventually lose control of all body functions ... you cannot even open your mouth to take medication.

We appreciate your support!

Join us for the walk on Saturday, September 14, 2024

Check in begins at 9:00am, Walk kicks off at 10:30am

Soldier Field in Chicago

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

ALS is scary. Really scary. Its rapid progression can mean tomorrow is often worse than today. As a result, people living with ALS are overwhelmed and unsure of what questions to ask and what to do next. But that’s where the Les Turner ALS Foundation comes in. The 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.

We are proud to be members of the Les Turner ALS Foundation family. Join us as we work to support people living with ALS and those who love them every step of the way! Please join our team on event day or consider making a donation to help us reach our fundraising goal. Together, we can make an impact in the fight against ALS.

To learn more about ALS or the Les Turner ALS Foundation, please visit lesturnerals.org.