florida-imaging-dmd-study-MRI

Imaging DMD Study

University of Florida April 23-25, 2017 Devin enrolled in the Imaging DMD study which has been designed to compare the muscles of boys with duchenne to muscles of boys without DMD over a period of 5 years. They observe and document the amount of muscle damage shown in the images from the MRI along with data from Read more about Imaging DMD Study[…]

Devin and Reagan Create Art

MDA WI and Upper MI Office Milwaukee, WI March 10, 2017 Devin and Reagan joined forces with Mat Hintz of Hintz Studios to create a beautiful piece of art featuring a Harley-Davidson motorcycle. The artwork will be auctioned off at the Muscular Dystrophy Association’s annual Black-N-Blue Ball held in Milwaukee, WI. The Black-n-Blue Ball is Read more about Devin and Reagan Create Art[…]

cure duchenne Celeste Graham and Devin argall

CureDuchenne Cares

Family Workshop Milwaukee, WI April 22, 2017 We were honored to be the host family for the CureDuchenne Cares family workshop held in Milwaukee, WI. Our family had a wonderful time and learned a lot of very valuable information. The CureDuchenne team is absolutely outstanding! Please attend a workshop if you have the opportunity. They need Read more about CureDuchenne Cares[…]

National Association of Letter Carriers (NALC)

Thank You For Your Support

Dear Friends, I am writing to share some wonderful news. My son Devin is walking, running, and can even ride a bike all by himself. That may not seem all that amazing on its own, but Devin’s circumstances are quite unique. Devin lives with Duchenne Muscular Dystrophy (DMD), a terminal muscle disease. It’s a disease Read more about Thank You For Your Support[…]

Debra Miller President and CEO of CureDuchenne

Debra Miller Interview

This is the first of a new series of interviews we’ll be sharing to help bring our readers closer to others involved in the Duchenne community. I was honored to have the opportunity to ask Debra Miller a few questions about her experience as the President and CEO of CureDuchenne. She was very generous with her time Read more about Debra Miller Interview[…]

Imaging DMD study logo

A Chance Meeting Left Me in Shock

I don’t always do a great job at recognizing all the amazing things that happen in life, especially day-to-day as they occur. Today however, something happened that left me in complete shock. Devin and I were at the University of Florida for the Imaging DMD study. Devin was in a room going through a series Read more about A Chance Meeting Left Me in Shock[…]

Bring Me to the Payers – The Fight for Access to Exondys51

“The Day” On September 19, 2016, the US Food and Drug Administration (FDA) approved the first ever treatment for Duchenne Muscular Dystrophy. Eteplirsen, otherwise known by its brand name Exondys51, was developed by Sarepta Therapeutics. Exondys51 is a novel medicine that uses a technique called exon skipping which allows an error in mutated RNA to Read more about Bring Me to the Payers – The Fight for Access to Exondys51[…]