HeyJaredAWOL Zebra : Fascia and living with hEDS
I have hEDS. If I don’t talk with someone I think I’ll go crazy! The answer? I share my daily life as a sort of medication. AWOL Zebra aims to educate, share and have fun. Learn how to fight this invisible illness with me, CHristie Lynn Hanchey. Restoring my body back to health.
- Indexed episodes, last 90 days
- 14
- Latest publication
- Sep 3, 2026
- Audience
- Checking…
- Earliest in this view
- Jul 9, 2026
Latest episodes
New day. New place. New me??? (opens the original)
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There is no handbook for this illness. But I am determined to share as much and give you as best of a guideline as possible to make the most of what you’ve been given.
Movin’ in and movin’ out… (opens the original)
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Took my one and only to college and now trying to see the direction my life is going.
Pandiculate with me… (opens the original)
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Just because it feels like it’s over doesn’t mean it is. Every movement can be therapy.
The Sound of a Bucket List: Meet Ella Coonen… (opens the original)
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The Sound Of A Bucket List. Meet Ella Coonen. The subject of a documentary directed by David Kaye. I was honored to get the opportunity to meet this incredible young woman. See how she is managing her life after receiving one of several diagnoses last year. EDS being one of them. A rare genetic variation that will cause her to lose her hearing entirely.
Skatetown, USA… (opens the original)
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Every minute I have to work on my body. If I had to do my hair like I did in the 80s today, I would never be out in public.
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