Just a "zebra" trying my best to live life to the fullest with EDS and POTS...and loving the ride.

My Medical ID

Written by Katie. Posted in Ehlers-Danlos Awareness, POTS Awareness

Getting a medical ID bracelet was something I knew I needed, but was not sure where to go to get one.

A lot of people told me to get a USB one that could hold all of my medical information, but when I researched more, I read that many hospitals, doctors offices, etc. refused to use them because of the risk of causing viruses to their computer systems.