@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: • 15th Annual Les Turner Symposium on ALS • Take Action: ACT for ALS Renewal • ALS Ice Bucket Challenge • Research: Connecting the immune system to ALS to develop new therapies • Gasping for air - The Chicago Reporter • Looking Ahead with Dr. Senda Ajroud-Driss on Tofersen/Qalsody, Illuminate Series • ALS Organizations Urge Congress to Pass the ALS Better Care Act • Young ProfessionALS Group • Volunteer - ALS Walk for Life • Take Action: Illinois State Funding for ALS Care and Research • Cognitive and Language Impairments in ALS & ALS-FTD: Signs & Strategies • Lou Gehrig Day Tickets for Cubs • WGN Radio 720 interview with Laura Freveletti • ALS Awareness Month • Advocacy: Neuromuscular Disease Organizations Urge Withdrawal of Proposed Federal Funding Rule • ALS Learning Series: Tackling the Delay to ALS Diagnosis: How Can We Do Better? • Research: Finding the exact target for potential ALS drug • 2025 Lew Blond Memorial 5K Registration • March of Faces submission • October 2023 Foundation eNews • Leading ALS Organizations Call for Swift Passage of the ACT for ALS Reauthorization Act • Celebration of Life 2023 • 2027 ALS/MND Caregiver Calendar • December 2023 Foundation eNews • Research: Researchers discover cause of neuron excitability in ALS, leading to new potential treatment • Volunteer at the Les Turner ALS Foundation • Join Our Newsletter • November 2023 Foundation eNews • 2026 ALS Walk for Life • Advocacy in Action: $300,000 for ALS Care & Research • January 2024 Foundation eNews • Research: ALS is driven by a domino‑like chain reaction that begins in nerve cells • March 2024 Foundation eNews - Les Turner ALS Foundation • Research: Clinical trials test potential new gene therapies for inherited ALS • More info about Dr. Coleman • External Research | Amyotrophic Lateral Sclerosis (ALS) | CDC • Research: Looking at bridges between neurons for clues to ALS • 2023 ALS Walk For Life Pictures • State of Illinois proclaims ALS Awareness Month in May 2026 • Honoree Spotlight 2023 • Volunteer with us • ALS Better Care Act introduced in U.S. House of Representatives • ALS Support Groups • ABC 7 Interview with Laura Freveletti • Research: Searching for the cause of ALS, researchers look to metabolism within cells • July 2023 Foundation eNews - Les Turner ALS Foundation • ALS organizations advocate for FY27 funding priorities to Congress - Les Turner ALS Foundation • Faces of ALS: Julie Stowell, from the heart • Take Action: ALS Better Care Act • Lou Gehrig Day Photos • Federal Funding Increase for ALS in 2026 • June 2023 Foundation eNews - Les Turner ALS Foundation • Join our Gratitude Group • February 2024 Foundation eNews • Discovering how motor neurons break down in ALS • ALS Better Care Act introduced in Congress • Targeting Key Proteins in the Fight Against ALS • ALS & Participation in Clinical Research • A new clue to ALS and FTD: Faulty protein disrupts brain’s ‘brake’ system - Les Turner ALS Foundation • My ALS Decision Tool: Genetic Testing for Family Members • 2026 Team Race for ALS- Chicago Marathon • Cecil & Grace - Donate from the Heart • Up to the Challenge: The Hernandez Family - Les Turner ALS Foundation • Statement: “The One Big Beautiful Bill” Puts ALS Families at Risk - Les Turner ALS Foundation • 2025 Hope Through Caring Gala • YPG All In For ALS Casino Night • CDC - Amyotrophic Lateral Sclerosis: Login • 2025 Fundamental Rights Survey • Faces of ALS: Celebrating Glenview Tag Days: 25 Years of Community Support & Fundraising - Les Turner ALS Foundation • Share Your EAP Experience • We're in it Together at the ALS Walk for Life! • ALS Research Matters • ALS Clinical Research Learning Institute® | People Living with ALS | NEALS • Submit a Witness Slip • Suburban Mom With ALS Aims to Raise Awareness For Other Younger Patients • "When life gives you lemons, take pictures." • Les Turner ALS Center at Northwestern Medicine • 3 Tips for People with ALS Applying for Social Security Disability Insurance - Les Turner ALS Foundation • 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 • Congress: Oppose Catastrophic Research Cuts • 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