Ryan's Hope for a Cure Charitable Foundation, Inc.
Meet our son, Ryan. He needs your help. We need your prayers.
About the Foundation
About DMD and Links
Fundraising Events & Photos
News & Notes
Contact Us

"Hope sees the invisible, feels the intangible, and achieves the impossible."

- Anonymous
Welcome!

Ryan's Hope Foundation was founded by a Plainville, MA family whose now thirteen-year-old son, Ryan, was diagnosed with Duchenne Muscular Dystrophy (DMD) at age two. The Foundation was formed specifically to speed the rate of scientific research that will lead to a cure for Duchenne Muscular Dystrophy.

Kaitlyn & Delaney's JettRide

Kaitlyn, Ryan, and Delany

Ryan’s sister Kaitlyn (left) and his cousin Delaney are part of the Jett Foundation’s 2014 cross-country JettRide team this summer to raise awareness and funds for the fight against DMD. They joined the ride in Montana and will travel 2,600 miles to the finish line at Point Pleasant Beach, New Jersey. Click here for more information.


Kids Night Out!

Photos from 2014 Kids Night Out

Past Events
Click here for photos from our past events.

Thank you to Panera Bread of Planville, MA a Ryan's Hope Foundation corporate sponsor


Mission Statement
The mission of the Ryan's Hope Foundation is to increase awareness of Duchenne Muscular Dystrophy with the purpose of raising funds for advancing the research that will realize a cure for the disease and ensure that stricken children will have a brighter tomorrow. Click here to find out more.

The Ryan's Hope Foundation is a tax-exempt, non-profit 501(c)(3) organization.
Donations to the Foundation are tax deductible.


6 Maple Terrace
Plainville, MA 02762
508.699.3888
E-mail: info@HopeForRyan.com

© 2004-2014. Ryan's Hope for a Cure Charitable Foundation. All rights reserved.

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