I Am Devin Strong
Check out a list of our events including races, fundraisers, and presentations.
Devin loves making fun and inspirational videos to spread awareness of DMD.
The joy seen in his smile is undeniable. Take a look and see if you can resist smiling back.
We Never Quit (Keep Going) created for Devin 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 duchenne muscular dystrophy.
We advocate, fundraise, share personal experiences, and provide information related to DMD research and resources.
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. Please take time to view the videos, pictures, and articles. If you like what you see, please help us raise more awareness by sharing a link to the website with a friend.
If you'd like to show your support by helping to fund this cause, you can click the following link to make an online donation 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. Thank you!
2017 is Devin's second year serving as MDA's State 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.
There’s more coming
More info coming soon Green Lake, WI
Description coming Green Lake, WI
The Carousel of Possible Dreams August 12, 2017 Devin and I had the great privilege of attending The Carousel of Possible Dreams as guests of CureDuchenne. CureDuchenne was one of the four charities to benefit from this year’s Chicago area event. It’s organized by the Festival of Children Foundation and held at the beautiful Sanfilippo Estate Read more about The Carousel of Possible Dreams[…]
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[…]