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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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 05-24-2007, 10:19 AM #1
Curious Curious is offline
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Poll Informal Poll on SCS

Here is a link from Roz about the SCS:
http://www.rsdfoundation.org/en/en_c...uidelines.html

you can chose more than one answer.
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Old 05-24-2007, 10:41 AM #2
buckwheat
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Hi Everyone,

Come out, come out where ever you are. We are all bonded by this hell. Their is strength in more.

I checked the last question.

My first consultant (Doc) could not have put one in fast enough. I did not have one because after consulting with at least 2 other opinions, I was told I was not a good candidate for one. Please respond. Hugs, Roz

P. S.- This is my mistake, on the fifth question down it should say:
Did the trial work better than the real implant?

Last edited by buckwheat; 05-24-2007 at 11:05 AM.
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Old 05-24-2007, 11:36 AM #3
cjay cjay is offline
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Default Scs

Question # 2: I had some relief from implanted SCS for approx 1 yr

Question # 5: The trial worked much better than the implanted SCS

I had it implanted in 1999 and they shut it off 1 year later. In that years time I ended up having 4 revisions done on it.
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Old 05-24-2007, 01:26 PM #4
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Hi Their,
Over 60 views and only 2 replys, that's pretty sad.

I already know I am not a candidate for the SCS.

Please reply. Roz
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Old 05-24-2007, 01:33 PM #5
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I haven't had one put in yet, but as my doc said that if I've had my rsd for over 2 years that there would be no nerve blocks, just gonna go with a scs. I'm waiting to see how the answers come out.
Mary
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Old 05-24-2007, 01:38 PM #6
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Thanks Mary,

This is exactly why it is vital for those with experience to reply. Hugs, Roz
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Old 05-24-2007, 01:39 PM #7
Curious Curious is offline
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roz..the views can be the same people checking over and over...to see if others have voted.

and you can vote...and not post a reply, for those who haven't voted yet.
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Old 05-24-2007, 03:59 PM #8
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Default Poll Answers

Q1. Did you have a SCS put in?

A. Yes

Q2. If you were given relief from the SCS how long?

A. Very good for about 18 months, then the RSD "migrated" to another area, and the SCS does not cover it anymore.

Q3. Did you still have to take pain meds?

A. Yes, but fewer than before. Now that is has moved, I am taking more than before.

Q4. Any complications after having one put in?

A. Main complicatin is more of an inconvienience than a complication. The scars from the surgery are very painful. (Same thing happened after foot surgery - still hurts after 7 years.) The spot selected for the SCS generator was not large enough and it is puching against the skin from the inside, extremely unconfortable. And the installer did not drive the wore anchors far enough into the verebra, making a shart point from the inside. Nothing health-threatening, though.

Q5. Did the trial work better after the implant?

A. No, about the same.

Q6. Has it affected your mobility in anyway?

A. No

Mike
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Old 05-24-2007, 04:13 PM #9
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Hi Mike,

Thanks so much for sharing your wisdom and experience. Wishing you a day full of love and joy. Hugs, Roz
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Old 05-24-2007, 10:06 PM #10
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I just re-read my earlier post. WOW! What a lot of tyos. My hands are a little off today. Hope it was still somewhat legible.

Mike
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