My Nonprofit Reviews

My son Kevin was diagnosed at the age of 9 with Hypertrophic Cardiomyopathy. We were crushed. How do we deal with this? How do we help HIM deal with it? How do we get others to understand? What about school? Children's Cardiomyopathy Foundation answered those questions and more for us! Not sure how we would have managed such a heart breaking time in our lives without their help!! I spoke with the founder directly. She shared her story and listened to me cry & tell mine. I have NEVER met a more helpful, hands-on organization as CCF! I thank God everyday for them & everything they've done for us! ~Cori Detweiler

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