August 23, 2022

Ranchers Raise Money for Rare Disease in True Montana Style (KMHK)

August 16, 2022

Female Carriers of Duchenne Urged to Seek Early Treatment for Heart Problems (Rare Disease Advisor)

August 5, 2022

Arkansans of the Day: the Fawcett family (KTHV-TV (CBS Little Rock))

August 2, 2022

Venture Philanthropy For Duchenne Muscular Dystrophy (Cell & Gene)

July 22, 2022

Patient Advocates Seek to Raise Awareness of DMD Among Spanish Speakers (Rare Disease Advisor)

July 11, 2022

An Inspirational Feat: Crossing Spain’s 500-Mile Camino de Santiago by Wheelchair (Rare Disease Advisor)

July 5, 2022

Unless we do something, we’ll lose all of our sons’: Parents take action on rare disorder (Orlando Sentinel)

June 22, 2022

High Impact Philanthropy: Debra Miller Of CureDuchenne On How To Leave A Lasting Legacy With A Successful & Effective Nonprofit Organization (Authority Magazine)

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)