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.

March 28, 2013

Rest in Peace my Butterfly Friends

March has been a rough, rough month for the EB community. 

On March 15, a little boy named Harry from England died of complications from Pneumonia.  He was 3 1/2 years old and had bravely fought Junctional Hertliz EB since birth.  Then just two days his little brother Cody died of the SAME thing.  He was 21 months old and he too bravely fought Junctional Hertliz EB since birth.  Their parents were just broken hearted; losing their only two children just days apart.  This is one of the many articles written about them.  Here is another one too.

Then on March 21st, a fellow EBer from Florida, Dona Reynolds, lost her brave battle to RDEB at the young age of 25.  She didn't live too far from me and I tried to make it to her funeral but stuff happens and things don't always go as planned. 

And as if those three weren't enough....I woke yesterday to learned the sad and shocking news that a friend and fellow EB mom died suddenly early Wednesday morning of a heart attack; she was only 37:(  She leaves behind her husband, 4 yr old daughter and 8 month old son who has EB.  Her death has really shook the EB community to its core.  If you are on Facebook you can visit the family's EB page here.  Her funeral is Monday but so far the funeral home doesn't seem to be "on-line". 

I hope we can get through the rest of the month without anymore losses and hopefully April will be a kinder month to the EB Community! 

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