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Welcome to AWOL Zebra: EDS from A to Z 

AWOL - A Way of Life

A Message from CHristie Hanchey
Hi there!

My name is CHristie Lynn Hanchey. I started this group because I need interactions with people that may be suffering with the same issues as I am. I felt like the black sheep in my local support group. I felt lost in other groups because my posts would get lost. I need answers and conversation is how I process things.

 
I have specific questions and know in my heart there are others who are suffering and not being heard. So, I thought, let me present my issues and hopefully others will feel encouraged to join me.
 
I have hEDS. Sticky fascia. I have been working on a program that I have tailored to my problems because I followed what others said was the right way and got worse.

How could these specific exercises bring me down? When I mentioned fascia to my health care provider, my concerns went unheeded. I am tired of not being heard by the support system I was assured would be there for me and being dismissed by the professionals I trusted.

I want to share my journey. Hopefully, others will see that we don't have a one-size-fits-all disease with a cookie cutter fix all. I hope you will join me as I try to have fun, enlighten, and put a positive spin on this debilitating invisible illness.

Work on your fascia before it stops working for you.
-CHristie ❤️☮️😊

See photos of before and after below. I worked on my facial fascia, my stomach, my feet and my back. Join today and have access to all of the videos where I show you how I got these results by working on my fascia! 
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Get to know CHristie

I was a disc jockey. Until hEDS took away my ability to walk and talk. I got it back through Fascial Remodeling. I am an avid podcaster and voice for those living with hEDS.

Horizon

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