ALS-FTD Clinicopathological Overlap

Traveling with ALS: What to Know Before You Go

The ALS Turbocharged Living Scale: A New Way to Measure What Matters

ALS Walk for Life 2026

Finding Your People: Real Stories of Community After an ALS Diagnosis

ALS Awareness Month - Taking Action for ALS

ALS Awareness Month - The Financial Impact

Navigating Tracheostomy Decisions in ALS | My ALS Decision Tool™

ALS Awareness Month - The Diagnostic Journey

ALS Awareness Month - A Day in the Life of an ALS Caregiver

ALS Awareness Month - A Day in the Life of Someone Living with ALS

An Open Discussion on Tracheostomy and Invasive Mechanical Ventilation

Comments by Diana Pisone and Sarvesh Soi

Comments from Laura Freveletti and Erin Reardon Cohn

Dr John M. Coleman III receives the Harvey and Bonny Gaffen Advancements in ALS Award

Brian and Lori Andre receive the Hope Through Caring Award

Honoring John M. Coleman III, MD | Remarks by Cecil Puvathingal

The Strength Around Us

The Gift of Discovery: Tissue Donation and the Future of ALS Research

Hospice Care and ALS: What It Is, When to Consider It, and How It Supports You

Living Fully, Living Well: How Palliative Care Can Help

The Cost of ALS - Where Research Stands and How it Compares to Other Diseases

Better Bowel Days: Managing the Burden of Constipation in People living with ALS

Meet Cecil and Grace: An ALS Story of Courage and Hope

Mission Driven: How the VA is Transforming ALS Care

Development of Designer DNA Drug Therapy for Neurodegenerative Disease

The Importance of Building Cell-Based and Mechanism-Focused Drug Discovery

Remarks from Laura Freveletti CEO Les Turner ALS Foundation

Stress Granules in ALS/FTD

Defective Transport of Large Dense-Core Vesicles Underlies Neurodegeneration in ALS5/SPG11

New Disease Mechanisms and Therapeutic Approaches for C9orf72 ALS/FTD

Insights into RNA Granule and Mitochondria Crosstalk in ALS from Super-Resolution Live Microscopy

Introduction to the 15th Annual Les Turner Symposium on ALS

Functional mobility changes with ALS: What to expect and how to partner with your healthcare team

Remarks by Pope Leo XIV at the Les Turner ALS Foundation's 2025 ALS Walk for Life

ALS Learning Series: Participation in the National ALS Registry

Making Daily Life Easier: Occupational Therapy Solutions for People Living with ALS

Voice Preservation Beyond Recording: Creating and Using My Preserved Voice - Updated 2025

ALS Learning Series: Healey Platform Trial Updates & Les Turner ALS Foundation

Tackling the Delay to ALS Diagnosis: How Can We Do Better?

ALS Learning Series: Breaking Barriers: Building a Health Equity Approach

ALS Awareness Month: “My mom’s diagnosis broke my heart.”

Harvey Gaffen's comments at the 2025 Hope Through Caring Gala

Aaron Lazar: The Impossible Dream

2025 Hope Through Caring Award: Brian Davis and Katy McNeil

2025 Harvey and Bonny Gaffen Advancements in ALS Award: Jean Swidler & Mindy Uhrlaub, End the Legacy

2025 Hope Through Caring Gala: Full Video

Never back down, never give up.

Observational Studies Help in the Quest for Effective ALS Therapies

Family Caregivers: Angels in Agony

Thriving Through the Holidays with ALS

2024 Les Turner Symposium on ALS Poster Session

Introducing the new My ALS Decision Tool - Participating in Clinical Research

Immune System Alteration in ALS- David Gate PhD

Targeting the Ubiquitin-Proteasome System in Neurodegenerative Diseases- Robert G. Kalb, MD

Cell Type-Specific Alterations of Cortical Excitability in a Model of Familial ALS

TDP-43 Pathology in the ALS Motor Cortex

Keynote Presentation: Advances in ALS Clinical Trial Outcome Measures

Remarks from Laura Freveletti CEO Les Turner ALS Foundation

Cryptic Splicing: From Foe to Friend in Tackling Amyotrophic Lateral Sclerosis