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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Informal Poll on SCS

View Poll Results: SCS?
Did you have a SCS put in? 11 73.33%
Did you have a SCS put in?
11 73.33%
If you were given relief from the SCS how long? 8 53.33%
If you were given relief from the SCS how long?
8 53.33%
Did you still have to take pain meds? 10 66.67%
Did you still have to take pain meds?
10 66.67%
Any complications after having one put in? 8 53.33%
Any complications after having one put in?
8 53.33%
Did the trial work better after the implant? 3 20.00%
Did the trial work better after the implant?
3 20.00%
Has it affected your mobility in anyway? 5 33.33%
Has it affected your mobility in anyway?
5 33.33%
If you were oftered one, why didn't you have one put in? 4 26.67%
If you were oftered one, why didn't you have one put in?
4 26.67%
Multiple Choice Poll. Voters: 15. You may not vote on this poll

 
 
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Old 05-27-2007, 04:58 AM #19
cjay cjay is offline
Junior Member
  
Join Date: Jan 2007
Location: MN
Posts: 21
15 yr Member
cjay cjay is offline
Junior Member
 
Join Date: Jan 2007
Location: MN
Posts: 21
15 yr Member
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Jose, is totally right in everything that she states in her post. I had my SCS implanted in 1999. My Pain Dr, who did my trial and implantation of the SCS, does a good majority of the training of Drs as to the procedure of implanting an SCS. He does this for Metronics. In fact in the video that they gave me prior to having mine done (so I could see what it was all about), my Dr is in that video.

Jose, it sure sounds like you and I had a quite similar experience with our SCS. Thank You for sharing this with us all.

cjay
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