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.

January 20, 2013

This Little Light

A good friend of mine has a blog called, This Little Light.  Today she chose to write about my family.  You can find the post here: A Gift to the EB Community

1 comment:

  1. Thank you Sara for allowing me to share a bit about you and your family and thank you for all that you do!