
Porter Family
Our son, Grant, was almost 6 years old when he was diagnosed in January of 2017 with Duchenne Muscular Dystrophy. Our daughter Wrenna, and Grant’s best friend, was 4. To […]
Our son, Grant, was almost 6 years old when he was diagnosed in January of 2017 with Duchenne Muscular Dystrophy. Our daughter Wrenna, and Grant’s best friend, was 4. To […]
Where to start? Darren is adopted. He came to us at 2 months old. I immediately requested any and all evaluations available because mom had been using meth while pregnant […]
Our youngest son, Henry, was diagnosed with Duchenne in August 2011 – shortly before his 3rd birthday. It was a fluke test that shocked even the doctors as it was […]
In 2013, our oldest son, Joshua, was diagnosed with Duchenne muscular dystrophy. He was 5 years old at the time and we were devastated with the diagnosis. After doing some […]
Our son was diagnosed April 1, 2019. We have spent the past 2 years doing research, completing a clinical trial and being an advocate for our son and Duchenne Muscular […]
We are the Edwards Family in North Dakota. Our 11 year old son Grant has Duchenne. Diagnosed at age 4. Grant’s younger brother Christian age 8 is unaffected. I carry […]
We have two sons and a daughter and no family history of Duchenne. In April of 2018, we took our kids to the pediatrician for a well check. We mentioned […]
This presentation by Lauren Morgenroth, CGC and Ana Christensen, MPH at TRiNDS is part of the “A Holistic View of Clinical Trials” webinar and covers the following topics: the clinical […]
What is the role of exercise in patients with Duchenne Muscular Dystrophy? Special guest, Dr. Aaron S. Zelikovich, MD Original Webinar date: February 23, 2021Please submit your questions or comments […]