Hope and help for people with ALS.

Since 1977, the Les Turner ALS Foundation has been Chicagoland's leader in patient services, research, and education for Amyotrophic Lateral Sclerosis (ALS) and other motor neuron diseases (MND).

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March of Faces Banner

The Foundation is currently accepting submission forms for the ALS March of Faces Banner. We currently have 15 banners and will be creating another one to display at our upcoming events. These banners are pictorial displays of brave individuals, both past and present, stricken with ALS. To add a photo of your loved to the new banner, please complete and submit the form no later than Friday, August 28. 

Contact Mariah, at mmontenegro@lesturnerals.org with any questions.

Walk for Hope. Walk for Help. Walk for Life


Save the Date

The 5th Annual Les Turner Symposium on ALS and NeuroRepair will take place on Monday, November 16 at the Prentice Women’s Hospital. Join us as we celebrate research, patient care and education. The Symposium will feature keynote speaker, Kevin Eggan, PhD Professor of Stem Cell and Regenerative Biology at Harvard University along with Les Turner ALS Researchers and Clinicians.

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