Congratulations to everyone running with Team Race for ALS in the 2024 Bank of America Chicago Marathon this weekend! Click the link to learn more about our runners https://buff.ly/4eDaSxP.. If you're in the area, join us at the race on Sunday at Charity Mile (Adams and Loomis). Just look for our blue Les Turner tent and help us cheer our participants on!
Les Turner ALS Foundation
Non-profit Organizations
Skokie, IL 1,742 followers
We provide care for those affected by ALS, support their loved ones, and provide hope through research and advocacy.
About us
Founded in 1977, the Les Turner ALS Foundation is the leader in comprehensive ALS care in Chicagoland. Although we're one of the largest independent ALS groups in the country, we treat each person like family and we're committed to supporting them every step of the way. Our individualized approach ensures each person living with the disease receives the best quality of care, and our local community of support provides their loved ones with answers and encouragement. Our Les Turner ALS Center at Northwestern Medicine is led by the most well-respected and successful clinicians and researchers in the field, advancing vital care and research in pursuit of life-enhancing treatments and a cure. About ALS: Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease or motor neuron disease (MND), is a progressive disease that causes muscle weakness, difficulty speaking and swallowing and generally, complete paralysis. In most cases, while the body continues to deteriorate, the mind remains unaffected. The disease does not discriminate, striking any age, gender and race. In the US, someone is diagnosed every 90 minutes, and approximately 35,000 people are living with ALS at any given time. There is no known cure for ALS and once diagnosed, patients typically live only three to five years.
- Website
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http://www.lesturnerals.org
External link for Les Turner ALS Foundation
- Industry
- Non-profit Organizations
- Company size
- 11-50 employees
- Headquarters
- Skokie, IL
- Type
- Nonprofit
- Founded
- 1977
- Specialties
- ALS, Amyotrophic Lateral Sclerosis, and Lou Gehrig's disease
Locations
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Primary
5550 W. Touhy Avenue
Suite 302
Skokie, IL 60077, US
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259 E. Erie St.
Lavin Family Pavilion, Floor 19
Chicago, IL 60611, US
Employees at Les Turner ALS Foundation
Updates
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Join us on Nov 4th in person or online for the Les Turner Symposium on ALS where Pietro Fratta will dive deep into groundbreaking research on ALS and TDP-43, a key protein involved in the disease's progression. Learn how his lab is uncovering the molecular mechanisms behind TDP-43 mislocalization and exploring more effective therapies. Register today! https://buff.ly/4dHBQDk
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Join us this October for the ALS Learning Series, featuring Dr. Tavee as she shares insights on complementary & alternative therapies. Learn how nutrition, exercise, and mind-body practices can make a difference. A Q&A will follow the presentation. https://buff.ly/3zUEwQ5
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Whether you're seeking advice, a listening ear, or just a break, our Young Adult Support Group is here for you. This group is open to anyone ages 18-30 who has been affected by ALS. Click the link to learn more and join us every 3rd Tuesday of the month starting on October 15. #ALS #SupportGroup #Community Register today. https://buff.ly/4eCfEeu
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Have you lost a parent, family member, or loved one to ALS? You're not alone. Our new monthly bereavement group for young adults aged 18-30 is here to provide support, understanding, and healing. Click the link to learn more. https://buff.ly/3XZb6cZ
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The National ALS Registry is committed to helping advance research. Since 2010, the ALS Registry has funded over 20 research grants in the U.S. and internationally. To learn more, visit https://buff.ly/3TnjtfL
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Living with ALS can feel overwhelming, but you don’t have to navigate it alone. We’re excited to introduce another session of our newly diagnosed support group, created specifically to provide a safe space for those living with ALS to connect, share, and support one another. Sign up today to join a community that understands the journey. https://buff.ly/3XVPoWZ #ALSsupport #StrongerTogether #ALSCommunity
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The 23rd annual ALS Walk for Life was an incredible success, and we couldn’t have done it without you! This year, over 2,000 walkers and 164 teams came together to raise crucial funds for ALS care, advocacy, and research – all while showing off their spirit and enthusiasm. Click the link to check out the photos on Flickr. https://buff.ly/3XUSwCJ Have photos that you want to share with us? Send them to [email protected]
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Are you between the ages of 18-30 and looking to connect with other people who are affected by ALS? You’re not alone. Join this community of young adults who understand the unique challenges you face. Connect, share experiences, and find the support you need. Click for more info.https://buff.ly/4eCyZfL