@lesturnerals

lesturnerals has been a member of Linktree for 4 years and joined in November 2021. The social media accounts linked to from lesturnerals are: Instagram. Besides social media accounts, lesturnerals has populated their site with Support ACT for ALS Renewal, Join Our Newsletter, 15th Annual Les Turner Symposium on ALS, 2026 ALS Walk for Life, Take Action: Illinois State Funding for ALS Care and Research, The ALS Turbocharged Living Scale: A New Way to Measure What Matters, Lou Gehrig Day Tickets for Cubs, Advocacy in Action: $300,000 for ALS Care & Research, ALS Awareness Month, My ALS Decision Tool: Tracheostomy and Invasive Mechanical Ventilation (IMV), ALS Learning Series: Tackling the Delay to ALS Diagnosis: How Can We Do Better?, Honoring Dr. John Coleman’s Impact on the ALS Community, 2025 Lew Blond Memorial 5K Registration, Research: ALS is driven by a domino‑like chain reaction that begins in nerve cells, October 2023 Foundation eNews, Research: Clinical trials test potential new gene therapies for inherited ALS, Celebration of Life 2023, Take Action: Illinois State Funding for ALS Care and Research, December 2023 Foundation eNews, Research: Looking at bridges between neurons for clues to ALS, Volunteer at the Les Turner ALS Foundation, State of Illinois proclaims ALS Awareness Month in May 2026, November 2023 Foundation eNews, Volunteer with us, ALS Support Groups, January 2024 Foundation eNews, Research: Searching for the cause of ALS, researchers look to metabolism within cells, March 2024 Foundation eNews - Les Turner ALS Foundation, ALS organizations advocate for FY27 funding priorities to Congress - Les Turner ALS Foundation, More info about Dr. Coleman, Take Action: ALS Better Care Act, External Research | Amyotrophic Lateral Sclerosis (ALS) | CDC, Federal Funding Increase for ALS in 2026, 2023 ALS Walk For Life Pictures, Join our Gratitude Group, Honoree Spotlight 2023, Discovering how motor neurons break down in ALS, ALS Better Care Act introduced in U.S. House of Representatives, Targeting Key Proteins in the Fight Against ALS, ABC 7 Interview with Laura Freveletti, A new clue to ALS and FTD: Faulty protein disrupts brain’s ‘brake’ system - Les Turner ALS Foundation, July 2023 Foundation eNews - Les Turner ALS Foundation, 2026 Team Race for ALS- Chicago Marathon, Faces of ALS: Julie Stowell, from the heart, Cecil & Grace - Donate from the Heart, Lou Gehrig Day Photos, Statement: “The One Big Beautiful Bill” Puts ALS Families at Risk - Les Turner ALS Foundation, June 2023 Foundation eNews - Les Turner ALS Foundation, YPG All In For ALS Casino Night, February 2024 Foundation eNews, 2025 Fundamental Rights Survey, ALS Better Care Act introduced in Congress, Share Your EAP Experience, ALS & Participation in Clinical Research, ALS Research Matters, My ALS Decision Tool: Genetic Testing for Family Members, Submit a Witness Slip, Lou Gehrig Day Photos, "When life gives you lemons, take pictures.", Up to the Challenge: The Hernandez Family - Les Turner ALS Foundation, 3 Tips for People with ALS Applying for Social Security Disability Insurance - Les Turner ALS Foundation, 2025 Hope Through Caring Gala, CDC - Amyotrophic Lateral Sclerosis: Login, Faces of ALS: Celebrating Glenview Tag Days: 25 Years of Community Support & Fundraising - Les Turner ALS Foundation, We're in it Together at the ALS Walk for Life!, ALS Clinical Research Learning Institute® | People Living with ALS | NEALS, Suburban Mom With ALS Aims to Raise Awareness For Other Younger Patients, Congress: Oppose Catastrophic Research Cuts, Les Turner ALS Center at Northwestern Medicine, ALS Clinical Research Learning Institute®, Call for Comments: Proposed Decision on Medicare & Seat Elevation Systems, Communication Passport, ALS clinical trials and studies, FDA Approves tofersen (Qalsody) for Treatment of SOD1-ALS - Les Turner ALS Foundation, Note from the CEO, Faces of ALS: Jessica Morris, Regimen F Drug Science and MOA Public Webinar., Ina Turner Jones, Les Turner ALS Foundation Names Laura Freveletti as New Chief Executive Officer, Calming the destructive cells of ALS, Visit Our YouTube Channel!, Lois Insolia Clinic at the Les Turner Center at Northwestern Medicine, Watch For Love & Life: No Ordinary Campaign | Prime Video, Muscular Dystrophy Association Celebrates Historic Advancements in Accessible Air Travel as Congress Passes FAA Reauthorization | Muscular Dystrophy Association, How a Mayer Brown Partner Balances Work With Full-Time Caregiving | The American Lawyer, 2024 ALS Clinical Research Learning Institute Application, Empowering Change and Elevating Voices: 2024 #RAREis Global Advocate Grant, Weekend Break: A marathon that’s making waves for ALS research at a La Grange pool, 2024 ALS Walk for Life, YPG March Madness Brackets, Innovating Rare Disease Treatment: Integrating Digital Tools from Day One, 14th Annual Les Turner Symposium on ALS, All in for ALS Casino Night, 2024 Les Turner Symposium on ALS Photos, Free ALS support groups, Faces of ALS, What is ALS?, Join the National ALS Registry, Les Turner ALS Foundation History, Mission & Vision.