Garrett's House is dedicated to the support, advice, and education of a genetic skin condition called Epidermolysis Bullosa or EB for short. Currently there is no cure or effective treatment for EB. Please take a moment to learn about EB, and how you can support others who struggle with EB everyday. Garrett's House also honors the memory of those who lost their brave fight against EB. Please check out the Garden of Angel to learn more about the precious butterfly angels.

March 2, 2012

EB Fundraiser

What: Praying for Ava Rose benefit

When: Monday, March 19, 7 to 11 p.m.

Where: Kilcoyne's, 129 S. Main Ave., West Scranton, PA

Details: All proceeds benefit the family of Ava Rose Navarro and Epidermolysis Medical Research Foundation. Call 969-4331 or visit the Praying for Ava Rose Facebook page for more information.
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March 1, 2012

Rachael Anilyse




Check out this site I stumbled upon tonight.  I didn't know her personally but remember her mom from the EB groups many years ago.
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