LittleCrow

477d

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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    • Beautiful_Disaster_

      477d

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

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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