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.

February 3, 2012

EB in the News

 

S. Ind. 8-month-old continues to fight rare skin disease with help from community.  You can read about baby Brody here

January 31, 2012

EB in the News



A very interesting article about the causes of pain 
in those with severe EB.

Scientists Discover Cause Of Severe Pain Experienced By Patients With Epidermolysis Bullosa (EB)