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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

I have an amazing doctor who has been treating me for my RSD however I feel like we're running out of options and it's not getting any better. My Mom suggested going to the Mayo Clinic to see if they have any ideas. I live in Chicago so the closest clinic is in Minnesota, there will be a lot involved to go travel there, get off work, etc. but am willing to make the trip if it will help. I fell and injured my foot last June, had surgery to repair a ligament, and got RSD from the surgery. I have tried physical therapy, nerve blocks, medications, and I'm still have a lot of problems.

I was hoping if anyone has tried the Mayo Clinic they would be willing to share their experience.

Thank you in advance for your help!

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