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← Return to Miserable nerve pain
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Autoimmune Diseases | Last Active: Feb 21 6:36am | Replies (39)
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Thank you for the great idea! My old neurologist wanted to do Botox on my migraines(in 2021). I told her I had bell palsy 2x (years ago/long time) and didn’t feel comfortable with Botox. I’m not sure. But if it were the only treatment that is “safe” enough for me I would try it. I’d need it in both feet/legs (back?) so thank you so much. When I see pain mgmt dr at the end of the month I’ll ask her about Botox. 🙂
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I posted this earlier but I don't see it. I will try it again...
I'm so glad you're interested. I should mention I had side effects but I'm not the norm so I need to get the doctors feedback before doing Botox again. My side effects were congestion which triggered vertigo and balance issues but this happens when I'm congested and I have a lot of allergies/sensitivities. I had a few others but I still think it's worth trying. Let me know how it goes and please use my reply button so I don't miss your response. I wish you all the best.