Epidermolysis Bullosa. Please watch and pass on.

This video is about Garrett and the disease he was born with, EB. This video is very unique compared to images you might normally see regarding EB. This movie and images gives the public an intimate, true to life view of what living day-to-day is like with a rare debilitating skin disease. Please watch this and share it. Pass it on. Link to it. Blog about it.

The more people become aware of this, the closer we get to finding a cure. If you want to help please visit
http://www.ebkids.org, or befriendeb.com. You can also get more info from visiting: http://dermatology.stanford.edu/research/research.html

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