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.
Showing posts with label epidermolysis bullosa support. Show all posts
Showing posts with label epidermolysis bullosa support. Show all posts

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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April 14, 2010

On-Line Support

The EB Nurse Web Site


EB Research Partnership

 
The EB Public Lounge on Facebook: a support group for those with EB and their families 
 
The EB Private Lounge on Facebook: a support group for only those with EB and their parents. 


DebRA: Dystropic Epidermolysis Bullosa Research of America: the only national non-profit organization dedicated to both promoting research to find new treatments and a cure for Epidermolysis Bullosa and providing information and support for people with EB and their families.  They also offer their own social media platform called EB Connect.


The EBMRF is a volunteer nonprofit foundation dedicated to the support of medical research of Epidermolysis Bullosa (EB), its causes, the development of successful treatments, and ultimately, its cure.


Befriend EB: making life bearable


Other Useful Links


AdaptHealth: A wonderful wound care product supplier!!

 
The company that makes Mepitel and Mepliex products.


On-line Textbook of Dermatology


International EB Forum

DebRA of the Netherlands