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New Diagnosis of Prader-Willi syndrome?

FPWR was founded by parents of children with Prader-Willi syndrome (PWS). We know what you are experiencing! Please know that much progress in research is being made to help children with PWS.

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Rachel's Corner

FPWR Reaches $1 Million Mark in Funding PWS Research
Cicada Power
One Little Mouse....One Big Dream
2008 FPWR Conference focused on Prader-Willi Syndrome Research & Advocacy
Working Together to Fund Prader-Willi Syndrome Research!
Prader-Willi Families Photo Gallery Launched!
FPWR Qualifies for the Combined Federal Campaign
The Importance of Advocacy
2008 Fundraisers for FPWR
Message Boards and Hope

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