A Reason for Hope®

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• What Matters Most and Day to Day Heroism
• Dog Tales: Wagging and Working in Loyal Service
• ALS Advocates Deliver Message to Nation’s Capitol
• In Living Color: Glowing Cells Illuminate ALS
• ALS Association is Brand New
• In his Father’s Name
• Living with ALS
  Grass Roots Effort Starts With Single Step
• An Unbreakable Bond

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• A Common Link Gives New Clues for ALS
• The Road Less Traveled
• Gate to Independence – Brain-Computer Interfacing Promises Aid in ALS
• The Walk to D'Feet ALS is Better Than a Hit
• Advocates Prepare to "March and Roll" to Capitol Hill
• The Grandfather of The ALS Association
• A Families Quest to Stop a Killer 
• Living with ALS 
• Your Legacy of Hope

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• The ALS Association Centers Provide Quality Care and Peace of Mind
• Life with ALS Tough Questions Real Answers
• Scientist Obsessed with Unraveling the Mysteries of ALS
• Patient Care Is Top Priority – A Conversation with The ALS Association’s Vice President of Patient Services
• Care Connection: Supports the Entire Family
• Advocacy in Action: Throughout the Year
• Fighting ALS Is a Family Affair
• New Programs to Honor and Show Appreciation
• Living with ALS: Artist Remains at the Easel in Spite of ALS
• The Greatest Gift

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• Repository for ALS:
  Concrete Step Toward Therapy
• ALS Advocates Put Hope into Action
• Weekly Conversations Inspired College Epidemiological Project
• A National ALS Registry Is the Key to Important Questions
• ALS Research Update: A Conversation With ALSA’s Science Director
• 2005 Walk Season Successful Despite U.S. Focus on Hurricane Relief
• The Will Rogers Institute Expands Funding to Include ALS
• A Son’s Commitment to Finding a Cure
• Living with ALS:
  Eric Lowen: It’s more than about what I do. It’s who I am.
• Your Legacy of Hope

• Visionary Scientist Drawn to ALS Research
• ALSA Launches New Program to Accelerate Drug Discovery and Clinical Trials
• Every Family is Touch by ALS, but Some More Than Others
• ALSA - 20 Years of Dedication-A Conversation with ALSA's Board of Trustees Chair
• The Best Way to Find an Angel Is to be One
• A Tower of Strength for People Living with ALS
• Living with ALS-I Am Still the Same Guy Inside
• It's Our Personal Mission to Stamp Out ALS

• Gene Therapy: The Right Time and Place for ALS
• The Schillings Pitch to Strike Out ALS
• A Giant Step to D’Feet ALS
• ALS Advocacy - A conversation with ALSA’s Vice President of Government Relations and Public Affairs
• Physician, Patient, Disease - A Triangle of Irony
• Mary Ann Wilde - Beyond the Loss – Love and Commitment Thrive
• Living With ALS - Meet the over five club
• Laura’s Story: A Family Affair

• Gary Leo A Catalyst for Action
• Growing Up With ALS
• Caregivers Take Care of Yourselves
• Patient Care - Past, Present and Future - A Conversation with ALSA's Vice President of Patient Services
• Biomarkers - Searching for an Accurate ALS Diagnosis
• Dean and Kathleen Rasmussen - Working in Partnership to Find a Cure for ALS
• Living With ALS - The Importance of Being Me

• A Total Approach to Care
• Public Policy Initiatives Light the Way
• New Fellowship Builds a Pathway to Hope
• ALS Research Today: A conversation with ALSA's Science Director
• Larry and Isabelle Barnett: A Portrait of Generosity and Involvement
• Communities Across the Nation Walk to D'Feet ALS®
• Having ALS Doesn't Mean You Stop Living