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September 9, 2011 Letter From Jeff Wuchich
Dear AHC Families, Friends, & Supporters, What exciting times for the AHC Foundation & the efforts to find a CURE, while raising awareness & improving the quality of life for AHC sufferers...
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October 2011 Letter from Jeff Wuchich
Dear Friends, Exciting times continue here at the AHC Foundation. We’ve expanded both our regular Board & our Medical Advisory Board, so the additional ideas (and people to implement them) mean...
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Rare Disease Blog Hop
There are less than 30 days to World Rare Disease Day on February 29. The RARE project is the host today of a Rare Disease Blog Hop. Over 40 bloggers are uniting to blog today to raise awareness about...
View Article30 Days Until Rare Disease Day- Campaign “Soft Launch” Tomorrow
Rare Disease Day in 30 Days. Starting tomorrow, we’ll be soft launching a a campaign that will have its “official launch” on Rare Disease Day. Our campaign site should go live then www.ahc2012.org I’ll...
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Birthday Wish…
My birthday wish continues to be that we find a cure for AHC so that Matthew and every AHC child and adult may be able to live life to the fullest! Meanwhile the work continues towards achieving...
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“C-ing” the Future
At the AHCF Family Meeting in San Francisco, I wrapped up the festivities with a presentation on a vision for our future direction. I began with a personal dream, embodied in the picture to the...
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The Missing “C”
President’s Message- 11/8/12 The Missing “C” Dear AHC Families, Friends, & Supporters, Happy November! It is amazing how quickly time flies. It seems like just yesterday we gathered in San...
View ArticleLynn Egan assumes role of Interim President
Dear AHC Families, The AHCF Board of Directors is pleased to announce that Lynn Egan, our current Vice President, will act as interim President, assuming the responsibilities of President of the...
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