Quest Blog Advertisement RECENTLY ON THE BLOG... More Quest Blog Posts Advocacy Access to Neuromuscular Disease Care for Black People and People of Color By Myrna Traylor | February 1, 2023 Lifestyle Inclusion, Expression, and Advocacy in the Art World By Rebecca Hume | January 31, 2023 Health Simply Stated: Updates in Oculopharyngeal Muscular Dystrophy (OPMD) By Sujatha Gurunathan | January 26, 2023 Health To Tilt or Not to Tilt: The Benefits of Tilt in Space Wheelchairs By Joanna Buoniconti (Updated Version) | January 24, 2023 News MDA Welcomes its 2023 National Ambassadors By Mindy Henderson | January 23, 2023 Advocacy MDA’s 2023 Advocacy Plan By Mark Fisher | January 20, 2023 Advertisement Get Involved The Value of Volunteerism By Rebecca Hume | January 19, 2023 Health Navigating the Long Journey to a Rare Disease Diagnosis By Shaila Wunderlich | January 18, 2023 News 2023 MDA Clinical & Scientific Conference Keynote Speaker – FDA’s Peter Marks, M.D., Ph.D. By Mindy Henderson | January 17, 2023 Independence Introducing MDA Connect By Chelsey Wheeler | January 11, 2023 Get Involved 2023: Year of the Volunteer By Donald S. Wood, Ph.D., President and CEO, Muscular Dystrophy Association | December 30, 2022 View All