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LittleCrow

Updated 1y ago

Looking for Advice on SI Joint Fusion Surgery

Hi, all. I'm new here, and am hoping to find some folks with similar experiences to befriend and get tips and information from 🥰 I have been diagnosed with SI joint dysfunction (due to my Ehlers-Danlos), and I've been through so many shots that they stopped working. My doc (who is amazing), said I'm at the point of an SI fusion now, and to call the office to schedule it if and when I feel ready. I'm not new to large surgeries, but I have not had a fusion before. I'm almost practically bed ridden, since I can't walk due to the pain. Has anyone had an SI fusion? My doc does the minimally invasive procedure, so I'm just looking for folks who have had it done to give me some insight. Thanks ❤️

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ChronicPainWarrior_

2y

Following . But not sure on EDS , Think I have it & steroid injections didn’t help made me worse and flared up my siatica 😣

The content in this post is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

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