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.

August 5, 2011

RIP: Lexus M. Johnson

Lexi Johnson lost her battle to EB on July 5th, 2011.  
She was 15.  

 You can read a wonderful article written about her here

EB in the News

Skate park dream comes true for man with rare skin disease

Community Spurs To Action For Toddler With Rare Skin Condition


Jackson Gabriel Foundation Awards a $50,000 Grant In Support of Dr. Jakub Tolar's Research To Treat And Cure Epidermolysis Bullosa


Butterfly children offered glimmer of hope