Hi, it’s me, I am a baker and fondant artist. I also have hyper-mobile Ehlers Danlos Syndrome. Sounds like a small thing to have, until you learn its a connective tissue disease. Then you realize that is what we are all made of!! So mine is broken, forever. I’m not the only one, you may also have it. But no one really ever talks about it because it’s incurable. However, each and every health issue you have individually, well, there’s a pill for that, or a physical therapist, a pain management specialist, another specialist. You will become a doctor/nurse, of yourself, because most of the doctors will never mention it and the others have never heard about it. This is my life with hyper-mobile Ehlers-Danlos Syndrome. Let’s just see what happens next.

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