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June 15, 2022
Unique Local Father-Son Duo Emphasizes Love and Acceptance No Matter the Curveballs (Newport Beach Independent)June 6, 2022
Within the Duchenne Community, I’ve Found Camaraderie, Support, and Joy (Muscular Dystrophy News)May 30, 2022
CureDuchenne Conference Underscores Role of Parents as Caregivers (Rare Disease Advisor)May 30, 2022
New-Generation Gene Therapy for DMD Designed to Elicit Minimal Immune Response (Rare Disease Advisor)May 29, 2022
Gene Therapy Shows Promise for DMD, as Trials Continue and Challenges Remain (Rare Disease Advisor)May 28, 2022
CureDuchenne Conference Confirms What I Know, Adds More Insight Into a DMD Life (Rare Disease Advisor)May 28, 2022
Rationale Introduced on Mechanisms of Dystrophin Restoration to Treat DMD (Rare Disease Advisor)May 28, 2022
The Present and Future of Vamorolone for DMD (Rare Disease Advisor)May 10, 2022
A family fights a rare illness together (Spectrum News 1)May 9, 2022
CureDuchenne talks solutions to fill gaps in the CGT space (BioProcess International)May 6, 2022
Rare disease marketing has become a family affair (Medical Marketing and Media)May 3, 2022
Letters to my Younger Self: Hawken Miller (Rare Youth Revolution)April 30, 2022
Newport Beach resident, who started nonprofit after son’s Duchenne diagnosis, won’t stop fighting (The Daily Pilot)April 29, 2022
Organizations Rally to Help Ukrainian Rare Disease Patients (Muscular Dystrophy News)April 21, 2022
Race to Cure Duchenne Muscular Dystrophy (NBC10 Philadelphia)April 14, 2022
CureDuchenne is Filling the Therapeutic Pipeline with Next Generation DMD Treatments (BioSpace)April 1, 2022
Austin parents hosting Champions to CureDuchenne (Good Day Austin (KTBC-TV))February 23, 2022
Why they run: 17-time Austin marathoner raises $250K for sons’ fatal disease (KXAN-TV (NBC Austin))