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 13, 2012

March 2, 2012

EB Fundraiser

What: Praying for Ava Rose benefit

When: Monday, March 19, 7 to 11 p.m.

Where: Kilcoyne's, 129 S. Main Ave., West Scranton, PA

Details: All proceeds benefit the family of Ava Rose Navarro and Epidermolysis Medical Research Foundation. Call 969-4331 or visit the Praying for Ava Rose Facebook page for more information.

March 1, 2012

Rachael Anilyse




Check out this site I stumbled upon tonight.  I didn't know her personally but remember her mom from the EB groups many years ago.

February 21, 2012

EB Info for Hospital

This can be printed out on colored paper and hung above your child's bed or on the door to remind the medical staff to enter with care.


STOP!!! 

PLEASE READ BEFORE TOUCHING ME!!


I have Epidermolysis Bullosa.  It is a connective tissue disorder that causes fragile skin, internally and externally.


Here are the ways you can SAFELY care for me


  1.  If you have not worked with an EB patient before, please ask my parents how to care for me,


  1. I CAN NOT have ANY tape, even paper or hypoallergenic tape used on my skin.  Mepitac tape is the ONLY safe tape that can be used on my skin.


  1.  A Blood Pressure Cuff MUST be used over clothing or bandages, otherwise, the pressure will rip my skin


  1.  When taking blood, the tourniquets MUST be placed over clothing or bandages because the pressure will rip my skin.  Blood draws may be difficult and can only be taken by an EXPERIENCED NICU nurse or while using IV radiology to find the best vein and avoid multiple sticks.   Do not rub the skin with alcohol wipes.  Gently dab the skin with an alcohol pad.  


  1. DO NOT slide me during bed transfers.  Lift me by rolling me from side to side into your arms or let my parents show you how to move me.


  1. For diaper changes, it usually takes two people.  DO NOT grab my feet or ankles.  Instead, one person should lift me with one arm under the back of my knees, and the other should change the diaper.  DO NOT rub the skin with wipes.  Use warm water to clean the area and gently pat dry. 


  1. Coat exam gloves and any tubing that comes into contact with the skin, externally and internally with a non-petroleum-based lubricant.  


  1.  Temperatures CAN NOT be taken rectally or in the ear.  Under the arm is the safest method, using a non-petroleum-based lubricant.  Infrared Thermometers can also be used, but are not always accurate in EB patients due to temperature regulation issues. 


  1. PLEASE USE common sense and ask questions if you are unsure about my care.  



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February 3, 2012

EB in the News

 

S. Ind. 8-month-old continues to fight rare skin disease with help from community.  You can read about baby Brody here