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.
Showing posts with label Jackson Gabriel Foundation; EB in the news and on TV; Tripp the drummer boy. Show all posts
Showing posts with label Jackson Gabriel Foundation; EB in the news and on TV; Tripp the drummer boy. Show all posts

August 5, 2011

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

 

 



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