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