Peyton's Project came about when our son was diagnosed with Duchenne Muscular Dystrophy (DMD). Our mission is to raise awareness & $ to cure this fatal disease.
Ready for a great day for a great cause? Join us THIS Saturday, 2/29 at College of the Canyons. We have music, prizes, face painting & more. Pre-register here: https://t.co/yl2wu9Ua1h
Peyton’s Project donated this beautiful Bi-Ski to the Disabled Sports Eastern Sierra program at Mammoth Mountain Ski Resort. We were extremely excited to help so many disabled athletes get on the mountain and enjoy the slopes.
🏃♀️ into 2020! When I started this last Oct I couldn’t run 1 mile. Now up to 5 on my way to completing a 1/2 marathon. Our DMD kids don’t give up & either will team Peyton’s Project. I run for that little guy on my 👕 & all our DMD kids so someday SOON they can too! #LAMarathon
Thank you @KING5Seattle for following Peyton today and creating this wonderful piece, raising awareness for rare diseases like Duchenne Muscular Dystrophy. “Life’s too short to be unhappy”. - Peyton. https://t.co/0TcTef3LGF
Today is World Duchenne Awareness Day. The DMD community is constantly fighting battles. We take 2 steps forward and 3 steps back. It's upsetting and depressing but we are strong, we are brave and we will never give up!
Enjoyed our evening eating 🍕, raising awareness for DMD and $ for Avery. He’s an incredible kid and his family has been an inspiration to ours. #averyrocks!
Peyton's Project 2nd Annual Summer Soiree is back! Hosted by @henrydicarlo with performances by the incredible @DJRavidrums. If you attended last year, you know what an amazingly fun event this was while raising money for kids with Duchenne Muscular Dystrophy. See you there!
Today is #rarediseaseday We love this photo because it shows something (and someone) rare might be different but still beautiful, strong, enduring and bring joy to those around them. Today we celebrate our rare kids!
Two years ago today the trial drug we put Peyton on was approved. While we celebrate this monumental victory in the DMD community and all the boys who endured the trial to make Exondys51 accessible, we know this struggle is far from over. We need a cure!
Today is Duchenne World Awareness day. The process of fighting this disease is slow, arduous and daunting BUT our kids are worth the fight. We will persevere. Thank you for supporting Peytons Project and our family. We can’t do this without you. #duchenneworldawarenessday