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.

April 16, 2013

Garrett's Bear

After Garrett was born we received  a care package in the mail and in that package was a teddy bear.  I didn't give it too much thought about it at the time, but after he died it became one of my most prized possessions.  Even though a teddy bear could never replace a child, it did give something for my empty arms to hold.  I named him my Garrett Bear.

I have always had a desire to do/make something for the families that have lost a child to EB in remembrance of their child.  I have come up with a few things over the years but nothing really stuck until now!

Please take a moment to check out Garrett's Bears!   I hope this will become an on-going successful project!