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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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#1 | ||
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AND I AM PAIN FREE. Whenever an area tries to overpower the pulsating effect, I can change programs and send a stronger pulse to the area to stop the pain. In the last two days, I have become more mentally euphoric and physically euphoric. I cannot bend my back more than 5 degrees any way for this entire week (or take a shower - good thing you only know me online huh?) but I can squat again - I can very easily squat down low and keep my back straight to pick things up or to sit down/stand up.
The only pain I have is in the back where they put in the trial leads. The surgery went well. They even gave me a picture of my spine with the leads in and the cord to my stimulator. I plan on scanning it to my computer and putting it here for you all to see.
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. . CHRISTINE . . I AM NOT A DRUG SEEKER, I AM A PAIN RELIEF SEEKER. |
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#2 | |||
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![]() This is Awesome News... I am so Happy for You... My doc keeps suggesting a SCS to me and when I hear news like this it helps me to make my decision towards the trial... Many Hugs ![]() ![]() ![]() ![]() Dawn
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Live Well, Love Much, Laugh Often . |
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#3 | ||
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I am glad for you. I have a spinal cord stimulator in and have had it in for about 7 months. It helps a lot, but it does not take away all the pain. To tell you the truth I don't know what I would do without it. It is a help.
Tracy |
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#4 | ||
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I can feel my pain trying to creep in, I then change the program to something different. I just feel so nice right now and am glad I took the chance. Should it only control half in the future, that is half more than I had before.
Thanks.
__________________
. . CHRISTINE . . I AM NOT A DRUG SEEKER, I AM A PAIN RELIEF SEEKER. |
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#5 | ||
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The only drawback I have with my spinal cord stim is that I am so afraid to turn it up to much higher because I start to get a really bad burning sensation in my fingers. So I leave it set as is and just pray that the pain subsides. I went from having it set at .80 to 1.10-1.20 in about 7 months. The other thing is that it was originally set for most pain in my hand and part of my arm. The pain has now gone up into my shoulder and started in my right hand so in time he might have to go in and redo things to try and cover for at least up to my shoulder in my left hand. I am just avoiding that possibility if I can at all help it. It does help take away most of my pain though except in my shoulder. Thank God for that or like I said I don't know how I would be able to live with all this pain.
Tracy |
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#6 | |||
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Hi Tracy annd Christine ~ what brand Stimulator do you guys have? My PM Doc showed me a new stimulator by Boston Scientific, which is REALLY SMALL, and it is "rechargeable", so I am curious if this is what you have.
When the permanent leads get placed in the neck (after the Trial) for RSD of the hands/arms, ar you able to move your neck and back normally, or do you have to be "cautious" with certain movements/activites so that the leads do not "migrate" or become displaced? Also, how PAINFUL was the permanent implant and the recuperation period from the surgery? I'm "willing" to try the Trial, but to tell ya the truth--is sounds so Scarey ![]() Thanks!
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Brokenwings . |
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#7 | ||||
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Quote:
Due to Kaiser docs being extremely busy (and my PM is a great doc-so I think people are asking for him more), The trial last 7-10 days. On Monday I will be going into the doctors office, where he will remove the temporary leads and I will have to go back to where I was before the trial for approx 1-2 months. Then he will implant the permanent. Quote:
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Hugs, I am going on forever.
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. . CHRISTINE . . I AM NOT A DRUG SEEKER, I AM A PAIN RELIEF SEEKER. |
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