Rachel Tugon's blog

FPWR Reaches $1 Million Mark in Funding PWS Research


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Cicada Power

I don’t know what parts of the country this will resonate with, but where I live, here in the heart of the Bluegrass State, th [ Read more . . . ]

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FPWR Qualifies for the Combined Federal Campaign

After much training, paperwork, email, and many phone calls, we are thrilled to announce that FPWR is now a part of the [ Read more . . . ]

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Working Together to Fund Prader-Willi Syndrome Research!


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The Importance of Advocacy

In a recent message to our membership, Theresa Strong wrote about the alarmingly low level of funding being allotted to the National Institutes of Health.  An official of NIH was quoted as saying [ Read more . . . ]

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One Little Mouse....One Big Dream

Recently, Theresa Strong posted a notice about a new Prader-Willi syndrome research mouse model that came from the work of Uta Francke, a w [ Read more . . . ]

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2008 Fundraisers for FPWR

When you have a chance, take a look at the list of fundraising events that are already scheduled for this year.  www.fpwr.org   [ Read more . . . ]

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2008 FPWR Conference focused on Prader-Willi Syndrome Research & Advocacy


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Message Boards and Hope


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Empowerment

My dear husband, Pete, works for Ford and we have just been through yet another round of contract negotiations.  Eve [ Read more . . . ]

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