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The Ryan's Quest Team is comprised of serious athletes to first timers out to support the cause who compete
in road races and triathlons. No matter each members personal endeavour, we all share one common goal on race day-to Fight Duchenne Muscular Dystrophy.
Ryan’s Quest is a 501 (c)(3) tax exempt public charity. Our mission is to raise awareness and funding for Duchenne muscular dystrophy with the purpose of allocating funds for research that has the greatest potential of finding a cure or treatment for this disease. It is our HOPE to find a cure for Duchenne muscular dystrophy to save our son Ryan’s life and the lives of all boys affected by this disease.
This disease is the number one lethal genetic disorder of children worldwide. It is a progressive muscle disorder that causes the loss of muscle function and independence. Boys affected by Duchenne, lose the ability to walk between the ages of 8 and 12, require respiratory support by their late teens and survive only into their twenties. One-third of all cases of Duchenne are the result of a spontaneous genetic mutation…which means this could happen to anyone. There is a 100% fatality rate.
Every day, two boy's die of Duchenne...it doesn't have to be that way in the future. Every dollar today, means a chance for boys with Duchenne tomorrow
If you would like to join our TEAM and help make a difference in the lives of children fighting this disease please email us at
trin4ryan@ryansquest.org
.
Learn more about
Ryan's Quest.
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