My Nonprofit Reviews
Review for Cure JM Foundation, Encinitas, CA, USA
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.
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