Les Turner Amyotrophic Lateral Sclerosis Foundation

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The Les Turner ALS Foundation is the leader in comprehensive ALS care in Chicagoland. To provide the most comprehensive care and support to people living with ALS and their families so they can confidently navigate the disease, and advance scientific research for the prevention, treatment and cure of ALS.

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Address: 5550 W. Touhy Avenue Suite 302, SkokieWeb: Sign in to see organisation websiteFacebook: LesTurnerALSEmployees: 22Volunteers: 25Revenue: 2682408ICO: 362916466

The Les Turner ALS Foundation • Care, Community, Cure Comprehensive ALS care and support. Founded in 1977 the Les Turner ALS Foundation is one of the longestserving ALS groups in the country. Our support services team helps people living with ALS receive the best quality of care and access to the most promising therapies and we offer support groups ALS resources and webinars and live events to provide answers and encouragement. Our Les Turner ALS Center at Northwestern Medicine is led by the most wellrespected scientists and clinicians in the field advancing vital research into causes treatments and cures for the disease.

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Paul

What innovative support strategies do you think NGOs like the Les Turner ALS Foundation can implement to better assist families affected by ALS?

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Peter

How can advancements in scientific research be effectively communicated to patients and families to ensure they have access to the most promising therapies?

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Barbara

❤️ So grateful for the incredible work the Les Turner ALS Foundation is doing to support families impacted by ALS! Your commitment to care and research is truly inspiring! #HopeThroughResearch

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Les Turner Amyotrophic Lateral Sclerosis Foundation

Meet Ninfa Queyquep. “My husband Eric passed away in 2012 so it's been some time, but it feels like yesterday. He was diagnosed in 2009.

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Michael

👏 Big shoutout to the Les Turner ALS Foundation for providing such vital resources and support to those living with ALS! Together, we can make a difference in the fight against this disease! 💪 #ALSAwareness

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Les Turner Amyotrophic Lateral Sclerosis Foundation

Join us Monday, Sept 8 for a no-cost, live webinar on participation in the National ALS Registry. Learn how every story contributes to ALS research and helps advance understanding of the disease. Register here: https://buff.

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