Check out a list of our events including races, fundraisers, and appearances.
These are a number of different videos that Devin has been a part of over the years.
We’ve been blessed with the opportunity to participate in many amazing experiences. We’d like to share some of these moments with you.
We Never Quit (Keep Going) is the official Devin Strong Theme Song created by Chad Nissen of Grimelab.
What is Devin Strong?
Devin Strong is a nonprofit company registered in the State of Wisconsin. We created it to share Devin's story with the world and by doing that, work toward a cure for muscle disease.
We advocate, fundraise, share personal experiences, and provide information related to all types of muscle disease.
Devin is a remarkable young man and our hope is that you develop an interest in his story and are compelled to join us on this journey toward a world free of duchenne muscular dystrophy, ALS, SMA, and other related muscle disease. Please take time to view the videos, pictures, and articles we share. Feel free to share them with a friend.
If you feel you'd like to support this cause with a donation, you can click the following link to make one online directly to the Muscular Dystrophy Association. We'd love to hear from you with any thoughts or questions you may have. Please feel free to contact us using the form below.
2016 is Devin's first year serving as the State Goodwill Ambassador for Wisconsin.
Team Momentum is a huge part of our lives. Devin serves as an honored hero and athlete.
The Summer of 2016 was a very exciting time as Devin was featured in an MDA national campaign. #liveunlimited
Celebrate Devin Argall Day on January 14th. It was made official in a ceremony with the Mayor of Manitowoc.
The Manitowoc Company
Investors Comm. Bank
We offer a lot of options for businesses to support our cause and provide great promotion in return. Check out our sponsorship levels for the 2017 Season.
This is a selection of some of the videos we’ve made or have been included in.
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[…]
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[…]
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[…]
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[…]
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[…]
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[…]
if I CAN if it’s unacceptable, I can confront it. if it’s unbearable, I can endure it. if it’s unbeatable, I can defeat it. if it’s never been done, I can be the one. Christ strengthens me. I wrote this in the hospital today. I was thinking about everything we’ve been through with DMD, Read more about If I Can[…]
“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[…]
We put together a video to share the 26 most impactful moments in our life, related to muscular dystrophy, over the past year. This is something we plan to do every year about a week before the Chicago Marathon. We hope you enjoy the video. It’s been a wild ride!