Christie Cox was always bendy and sometimes witty. It wasn't until she was properly diagnosed with Ehlers Danlos Syndrome at 48 years old that she understood her quirkiness. Following decades of unrecognizable and untreatable health issues, since learning of her condition she has gone from being disbelieved to determined. Mrs. Cox now devotes her focus, energy, and passion to supporting others facing a similar fate. She graciously thanks the EDS community for their ongoing support. They voted for the book title, cover and contributed art and insights. To learn more about how she supports the EDS Zebra community, visit www.journey2joyous.com
