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.

July 13, 2010

The Butterfly Fund

Just wanted to share the link to an EB Organization that assists families that I recently learned about.  It's called The Butterfly Fund.  Check it out! 

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