What Inspires you to Spread ALS Awareness?
May is ALS Awareness Month. It all starts with you. Your passion and commitment to spreading the word brings us closer to a cure. Educating more people about the devastating impacts of ALS helps the Foundation provide more support and research funding to benefit people living with ALS and their loved ones. This May, you can help Freeze ALS and spread awareness by sharing with others why it’s important to you to find a cure!
Stay tuned for updates about ALS Awareness Month 2018.
Together, we can create awareness and Freeze ALS.
ALS Awareness Month Tools & Resources:
See How You Supported ALS Awareness Month 2017:
ALS Awareness Advocate: Be the face of the Foundation and the voice of people living with ALS. We will provide you Awareness Kits containing the necessary tools to engage your friends, family and peers. This role requires little time, minimal effort and no fundraising component, but makes a monumental impact on the ALS community. Click here to learn more and contact email@example.com to request your Awareness Kit today!
Support Tag Days: Lookout for ALS Awareness Advocates in yellow vests with donation jugs! Support communities around the Chicagoland area as they take to the streets to spread awareness about ALS and raise funds for research and patient care. Tag Days now also offers Cyber Drives, the online version that allows you donate without the hassle of pocket change.
*Stay tuned for our 2018 campaign*
How to spread ALS Awareness all year:
- Invite friends and family to attend Foundation events
- Host your own Family & Community outing
- Share, retweet, favorite and like Foundation posts on social media
Did You Know
- Every 90 minutes someone in the U.S is diagnosed with ALS, and every 90 minutes someone with ALS dies. That’s 112 people per week.
- ALS is 100% fatal. There is no known cure for ALS and once diagnosed, patients typically live three to five years.
- The Les Turner ALS Foundation has been Chicagoland’s number one supporter of people living with ALS for over 40 years.
“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 PALS
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