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sturkik

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CURE JM FOUNDATION
July 18, 2012

Our son was diagnosed with JDM in August 2010. It is a very rare and incurable disease. The first few months were a blur as we went from the hospital to drs appointments for treatment. Once we settled into our new routine, I Googled JDM and found the Cure JM site. It has been a god-send. It is filled with information on the disease, personal stories, information on fundraising and a forum where you can post questions to parents who also have children with the disease. Because it is so rare, families are spread across the world. This website makes you feel not so alone in the world.

More feedback

How would you describe the help you got from this organization?

Life-changing

How likely are you to recommend this organization to a friend?

Definitely

How do you feel you were treated by this organization?

Very Well

When was your last experience with this nonprofit?

2011

MY ROLE:
Client Served