November 9, 2012
CFRI has been an integral part of my life and that of my family since I was diagnosed with Cystic Fibrosis at 22 months old. Their dedication to collecting and proliferating knowledge on CF as well as funding the research that is vital to an eventual cure is essential to helping those with CF function in their daily lives and live with hope that one day CF will be a distant memory. Their executive director, Carroll Jenkins, is possibly the kindest and most compassionate woman I've ever met, going out of her way to make personal connections with individuals with CF and their families and help them in every way possible. I just can't speak highly enough of this organization.
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MY ROLE:Client Served