My Nonprofit Reviews

The foundation for children with Microcephaly (FCM) is one of the most under recognized under funded worthy charities in existence. The owners put their own money to fund the majority of the conferences held every other year to families with this terminal disorder. They provide support, education, and many, many more services to these families. Microcephaly is a common disorder that continues to go unrecognized. The owners (Lewis family) stays in contact and knows each and every one of the families they help by name. I learned so much at the conference on how to care for my special needs little guy. It felt wonderful to meet families that were going through the same struggles we were. The FCM provides several scholarships every year to families that cannot afford these educational seminars. They are also fortunate to have great ties with the doctors leading the research on Microcephaly.

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