Les Turner ALS Foundation

Les Turner ALS Foundation The Les Turner ALS Foundation is the leader in comprehensive ALS care in Chicagoland.

Join us on January 30 for our first ALS Learning Series of the year, featuring Reshma Punjani, MPH, and Janie Gobeli. To...
01/15/2025

Join us on January 30 for our first ALS Learning Series of the year, featuring Reshma Punjani, MPH, and Janie Gobeli. Together, they’ll explore how the National ALS Registry advances research and provides valuable insights into the causes and progression of ALS.

Click the link to sign up today.
https://buff.ly/40kXrwu

Clinical research is essential for understanding ALS and developing new treatments, and those living with ALS are key pa...
01/14/2025

Clinical research is essential for understanding ALS and developing new treatments, and those living with ALS are key partners in this effort. The ALS and Participation in Clinical Research Guide provides the knowledge you need for exploring opportunities to contribute.

Check out our guide also available in Spanish!
https://buff.ly/4aiQell

"When you take action, progress happens," said Chief Outreach and Advocacy Officer, Lauren Webb. "A big thank you to all...
01/10/2025

"When you take action, progress happens," said Chief Outreach and Advocacy Officer, Lauren Webb. "A big thank you to all the advocates who’ve pushed for important changes in home care, air travel, and access to therapy. We’ll keep pushing for the policies that make a real difference for those affected by ALS, bringing hope and better support where it’s needed most."

We're committed to advocating for policies that bring transformative care and treatment to ALS families. Learn how you can support our advocacy efforts.
https://buff.ly/3Pu1HVK

ALS researchers around the United States look for answers to better understand ALS questions. Dr. Eva Feldman, a researc...
01/09/2025

ALS researchers around the United States look for answers to better understand ALS questions. Dr. Eva Feldman, a researcher at the University of Michigan says, “The National ALS Registry is crucial for our research to help identify potential environmental risk factors associated with ALS.”

Learn more about the National ALS Registry and how it supports research at https://buff.ly/3Pqyw5U

01/06/2025

Looking ahead for 2025 we have lots of exciting events and opportunities to engage with our mission.

Our annual Hope Through Caring Gala is coming up this spring as well as the Lew Blond 5K and Lou Gehrig Day baseball games.

Check out our calendar of events and stay tuned to our social channels for more information throughout the year!
https://buff.ly/40bRTVo

Reflecting on 2024: A Year of Hope, Progress, and CommunityWith your support:  ✨ We funded groundbreaking research that ...
12/31/2024

Reflecting on 2024: A Year of Hope, Progress, and Community

With your support:
✨ We funded groundbreaking research that brought us closer to understanding ALS and finding effective treatments.

✨ Our Support Services Team provided thousands of hours of personalized support to ensure that no one faces ALS alone.

✨ Events like the ALS Walk for Life and the Hope Through Caring Gala showcased the power of community, raising critical funds and awareness.

Thank you for standing with us. Together, we are stronger.

Wishing you a joyful and hopeful New Year.

Help us help those who need it most.ALS families need your help now. With your donation today, you can make an immediate...
12/30/2024

Help us help those who need it most.

ALS families need your help now. With your donation today, you can make an immediate, lasting impact in the lives of those facing this relentless disease.

Every gift ensures families receive the urgent care they rely on—right when they need it most.

Donate today.

12/27/2024

Our new My ALS Decision Tool™ is here to help you navigate clinical trials with confidence and clarity.

This tool provides:
Clear information about the risks and benefits of clinical research
Guidance to help you match your treatment goals with the right trials
Expert advice on balancing standard treatments with trial options

Learn more: https://buff.ly/49Gurnr

As the year comes to a close, you have the chance to make a lasting difference for people living with ALS and their fami...
12/26/2024

As the year comes to a close, you have the chance to make a lasting difference for people living with ALS and their families. Give today to double your impact!

Now, thanks to the generosity of the Willow Springs Charitable Trust and an anonymous donor, every dollar donated through December 31st will be matched, up to $25,000. Take advantage of this matching gift opportunity to multiply your impact and extend even more support to ALS families.

helpcureals.org

12/23/2024

Reflecting on 2024! This year, our ALS Learning Series brought you 10 impactful webinars covering everything from the latest in ALS research to caregiving tips and beyond. 💙

We’d love to hear from you: Which webinar was your favorite, and what topics would you like to see in 2025? Drop your thoughts in the comments below!

Visit our website to view recordings of all these amazing webinars and more!
https://buff.ly/3OF213g

In this season of giving, your donation, in any amount, is a lifeline for families navigating the immense challenges of ...
12/20/2024

In this season of giving, your donation, in any amount, is a lifeline for families navigating the immense challenges of ALS. Together, we can drive impactful research, fund essential care, and ensure ALS families feel supported every step of the way.

Your generosity—big or small—creates real change. A gift of $25 provides 10 blood sampling kits essential for advancing ALS research. $100 delivers 2 hours of vital respite care for an ALS family, and $1,000 provides a specialized shower chair or Hoyer lift, providing critical support not covered by insurance.

buff.ly/3uZebxB

Did you know that the Centers for Medicare and Medicaid Service has directed Medicare Advantage plans to cover QALSODY® ...
12/19/2024

Did you know that the Centers for Medicare and Medicaid Service has directed Medicare Advantage plans to cover QALSODY® (tofersen) for treatment of SOD1-ALS? We’re proud to have helped make this groundbreaking treatment possible, and people living with SOD1-ALS must be able to access it without delay. Learn more:

As 2024 comes to a close, we invite you to join us for our last ALS Learning Series of the year, featuring Dr. Suzana K....
12/18/2024

As 2024 comes to a close, we invite you to join us for our last ALS Learning Series of the year, featuring Dr. Suzana K.E. Makowski, medical director of Compassionate Care ALS. She’ll be talking about discovering gratitude and hope as we embrace a new season and year.

Secure your spot now.
https://buff.ly/4g58QHi

Having dedicated his career to protecting others, Bryan now faces a new, personal battle. "There’s not a minute of the d...
12/17/2024

Having dedicated his career to protecting others, Bryan now faces a new, personal battle. "There’s not a minute of the day where I’m not thinking about it,” he says.

Still a man devoted to helping others, Bryan and his family have dedicated their own time to fundraising for the Les Turner ALS Foundation.

By supporting families like Bryan’s, you help fuel the care and breakthroughs that bring hope in the face of ALS. Let’s ensure every family receives the support they need—and move one step closer to a cure. Donate now. buff.ly/3uZebxB

Last week some of our staff had the opportunity to attend the International Alliance of ALS/MND Association's Meeting an...
12/16/2024

Last week some of our staff had the opportunity to attend the International Alliance of ALS/MND Association's Meeting and Allied Health Professionals Forum. This was a great opportunity to share resources and knowledge with the community!

Today, Bryan and his wife, Jackie, are experiencing firsthand the challenges that ALS brings – and the importance of com...
12/13/2024

Today, Bryan and his wife, Jackie, are experiencing firsthand the challenges that ALS brings – and the importance of community support in facing this devastating disease.

Determined to raise awareness and help others, they’ve been actively fundraising for the Les Turner ALS Foundation.

Through their network of fellow firefighters, family members, friends, and colleagues, Bryan and Jackie have shared their journey, hoping to inspire others to join in the fight against ALS. This holiday season, you can stand beside them by making a gift to the Foundation.

buff.ly/3uZebxB

12/12/2024

Introducing the newest My ALS Decision Tool™—empowering you with the knowledge to make informed decisions about participating in clinical research.

This tool helps:
Understand the risks and benefits of clinical trials
Align personal treatment goals with trial options
Navigate the informed consent process with confidence
Balance standard treatments and research participation

Access our new tool
https://buff.ly/3D9El4L

We are still accepting runners for Team Race for ALS to participate in the 2025 Bank of America Chicago Marathon!   We h...
12/11/2024

We are still accepting runners for Team Race for ALS to participate in the 2025 Bank of America Chicago Marathon! We have limited spots still available – come on and join the fun!

Join our team for the 2025 Bank of America Chicago Marathon and receive these benefits:

* Guaranteed entry into the 2025 Bank of America Chicago Marathon on Sunday, October 12, 2025 (you will be required to purchase your entry but if you fundraise $3000 or more, we will refund your entry fee)
* Official Team Race for ALS technical running t-shirt/singlet
* Customized donation page and assistance with fundraising to insure you reach your goals
* Eligibility for free training with a training program in your area
* Pre-race pasta dinner with the team the weekend of the Marathon
* Fundraising incentives
* And much, much more!!

Reach out to Kim at [email protected] for more information on how to be a part of the team!

Address

5550 Touhy Avenue, Ste 302
Skokie, IL
60077

Opening Hours

Monday 8:30am - 4:30pm
Tuesday 8:30am - 4:30pm
Wednesday 8:30am - 4:30pm
Thursday 8:30am - 4:30pm
Friday 8:30am - 4:30pm

Telephone

+18476793311

Alerts

Be the first to know and let us send you an email when Les Turner ALS Foundation posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organization

Send a message to Les Turner ALS Foundation:

Videos

Share

Category

Les Turner ALS Foundation

To people living with ALS and those who love them, we are experts leading the fight against ALS. Unlike national ALS organizations, we provide individualized care, local community support and hope through scientific research, so you feel comforted, confident and loved every step of the way.