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Want to talk with others. Have you found relief from CRPS?
Chronic Pain | Last Active: Jul 10 6:30am | Replies (235)Comment receiving replies
I’ve been told this is what I have 20 months down the line. This was never discussed by my os. It’s ruined my life just wanted to ask as 21% of people get this which I wasn’t aware of if other people in this site were informed. He’s referred me for nerve block at a pain management clinic but I’ve heard there isn’t much success with this and couldn’t bare more pain than I have already. Any input would be appreciated
Replies to "I’ve been told this is what I have 20 months down the line. This was never..."
I had the nerve block because of the insurance game. Have the Sprint stimulator in my leg at this very moment. Cut my pain down immensely. I’m reasonably sure I will need one in the spine. Makes me nervous but push is coming to shove.
Contact Sprint out of Beechwood, Ohio. Talk to them about your situation. I’m amazed at what I have been able to do for the past 45 days.
I have had the nerve blocks. I posted on another post about it and do not care at all to provide more info.
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Hello @everly23. You will notice that I have moved your post into an existing discussion on CRPS so you may connect with members like @livelifes @sprinrosa64 @grannyzoo and @therocket who have all recently shared about their experience with CRPS.
While we wait for others to respond, can you share what you are 20-months "down the line" from and also what you are doing to address your pain at the moment?