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.

October 28, 2013

EB Awareness Week 2013- day 4

Today I will be sharing some pictures that show the reality of having EB and being a toddler :-)


These are Joey's feet.  All the wounds you see are self inflicted from him just itching his feet:( 


Even with oral and topical medication to help reduce the itching sometimes there is nothing we can do.  And if you have ever tried to reason with a 2 year old you know how hard that is:-)



WARNING graphic pictures below
















 
 
 
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