October 19, 2022

Rebels With a Cause (Modern Luxury Riviera)

October 14, 2022

Rare Disease Clinical Trials: Strategies Learned from Duchenne Muscular Dystrophy (Applied Clinical Trials)

October 6, 2022

New Mexico Single Mom’s Big Challenge: Raising Identical Twin Boys With Duchenne (Rare Disease Advisor)

October 5, 2022

CureDuchenne Hosts Annual ‘Napa in Newport’ to Help Find a Cure for Duchenne Muscular Dystrophy (Newport Beach Independent)

September 24, 2022

Parents of son diagnosed with Duchenne muscular dystrophy are hopeful cure will be found soon (ABC7 (Los Angeles))

September 15, 2022

Calves To Cure helps Worden boy battle rare disease (KTVQ-TV (CBS Billings, MT))

September 13, 2022

Austin women’s event raises money for cure to fatal muscular disease (KXAN-TV (NBC Austin))

September 9, 2022

Billings Family Hosts Cattle Sale For Their Son (YourBigSky- KSVI/KHMT)

September 8, 2022

The Millers and Ryan Getzlaf on NBC4 (NBC4)

September 7, 2022

World Duchenne Awareness Day (Good Day LA - KTTV (Fox11))

September 5, 2022

CureDuchenne Ventures Takes Investment to Next Level (Orange County Business Journal)

September 1, 2022

‘Calves to Cure’ Auction Aims to Rustle Up Funds for CureDuchenne (Muscular Dystrophy News)

September 1, 2022

This Longhorn Has Been Running for a Cure for Duchenne Muscular Dystrophy for Nearly 20 Years (Alcalde)

August 25, 2022

A Montana Family’s Battle: We Can Only Do So Much for Grant (Montana Talks)

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)