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Member
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Join Date: Mar 2013
Location: Arizona
Posts: 453
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Member
Join Date: Mar 2013
Location: Arizona
Posts: 453
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I absolutely agree with everything Rrae says. I just finished with my trial SCS and it was an agonizing decision just to do that. She is SO RIGHT - Do not let ANYbody make the decision for you, especially the SCS Rep. Weigh out all of the information you can find.
Prior to SCS trial I had received a total of 12 nerve blocks (Stellate ganglion blocks as my CRPS is in my hand and arm.) I had those approx. 2 weeks apart. They gave me very good results, but going in to have my neck punctured got old too and I guess scar tissue can start to develop. Still, if the pain gets really bad again I may go back to those. They are far less invasive than SCS. My back hurt pretty bad and is still very sore from the trial.
For me, for now, I'M NOT READY TO DECIDE on the permanent SCS implant. I will also look into more information on Calmare therapy as it is less invasive as well.
I still intend to post the details of my experience for anyone it may help. If you have questions please ask. This is a great place for support, help and information. There is a lot of wisdom here.
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