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December 22, 2010

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December 22, 2010

Prisms is a great organization for finding information, parent support, fund raisers, & conferences for Smith-Magenis Syndrome (SMS). I've been involved with Prisms since Oct. 2000, shortly after our 4th daughter was diagnosed with SMS. Prisms does a wonderful job at putting newly diagnosed families in touch with 'seasoned' families with kids in similar age groups. Prisms also conducts conferences every 2 yrs & with monies raised in fund raisers all over the country, provide several families with 'scholarships' so that they may attend a conference.

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I've personally experienced the results of this organization in...

I was a recipient of a scholarship for the Conference in Colorado in 2002

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I don't know of anything I, personally, could do to change/improve this organization.

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