Awareness Month

What is ALS Awareness Month?

ALS Awareness Month, recognized globally each May, is an opportunity to share information with your community about Amyotrophic Lateral Sclerosis (ALS), a fatal neurodegenerative disease, and the unmatched work of the Les Turner ALS Foundation. We invite you, your passion and commitment to a cure, to join us as we spread the message of hope and help for people living with ALS. Above all, ALS Awareness Month is a way for community members to rally around people living with ALS and their families and spread awareness.

Together, we will spread the message of hope and help.

ALS Awareness Month Tools & Resources: 

Below you’ll find digital resources to help let your community know it’s ALS Awareness Month.

Les Turner ALS Foundation Word Cloud

ALS Awareness Month Coloring Book

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Donate to Awareness Month

Did You Know?

  • The lifetime risk of developing ALS is just 1 in 300.
  • 90-95% of ALS cases are sporadic, meaning there is no family history of the disease.

“Although I cannot conduct research in the labs at Northwestern Medicine or provide care at the Lois Insolia ALS Clinic, what I CAN do, just like we ALL CAN, is spread awareness about ALS.”
— Cindy, daughter of person living with ALS

How to spread ALS Awareness all year:

  • Invite friends and family to attend Foundation events
  • Host your own fundraiser with Fundraise Your Way
  • Engage with us on social media! Share, comment, like, retweet and favorite Foundation posts on social media



Care. Community. Cure.

We provide individualized care, local community support and hope through
scientific research.