National Publications

Vision Magazine 

Spring 2009 

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New Gene Discovery Baseball Knocking out ALS A Healing Journey Cure ALS Campaign Cassandra’s Gift Jane H. Gilbert Appointed Mayo Clinic Honor Roll Advocacy Delivers Roadmap to Cure DynaVox Technology Iraq Troops Fight ALS Charitable Gift Annuities

A Reason for Hope�  

Fall 2007

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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

Spring 2007

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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

Fall 2006

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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

Spring 2006

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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

Fall 2005

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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

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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

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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

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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