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 26, 2010

Personal Pages of others with EB

A handsome little angel named Jameson

Daylon: His journey towards a cure

Keric: the 4th EB patient to receive the bone marrow transplant

Hannah: The 5th EB patient to receive the bone marrow transplant

Jonah and his journey living with EB

Evan: A happy little guy with Junctional EB

Little Lady Leah: An Angel in Heaven

Cristina's Story : "Through the eyes of a patient"

Everlasting Butterfly : In memory of an Angel named Ava 

In memory of Xantha Maree Marshall

Fallyn: the 6th EB patient to receive the bone marrow transplant

Samantha: the 7th EB patient to receive the bone marrow transplant

Rafi: the 8th EB patient to receive the bone marrow transplant

McKenzie:the 9th EB patient to receive the bone marrow transplant

Bruce and EB : "An Adult living with RDEB"
The story of an angel named Janna 

Oxlee's Place

Jonathon's Story

Jamie Gibson: An Ethereal Suite

Jessica and EB : A girl from the mid-west living with RDEB

Beautiful Daisy: A spunky little girl with Junctional EB

John-Hudson and EB : The stroy of a little boy in NYC living with RDEB

Grace : An Angel in Heaven

An EB Angel named Jennifer


**if you'd like your page added on her, please let me know and i'd be happy to include it!**    
    
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