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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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Senior Member
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Hi everyone,
I met with a new PM doc yesterday. When I told him that my last few SGB had helped with certain of my spreading symptoms, he explained that it was impossible for a SGB to impact any symptoms related to my legs and feet! Talk about embarrassed! He explained that often when patients start to feel better after a block in some areas where they are expected to feel better, they will also start to better in other areas that are in no way impacted by the block (like my feet!). I KNOW that my feet were painful before the last block, I was really scared. I just find it so hard to believe that it was all in my head. And after I walked on them a lot they would go numb - that was NOT in my head, we all know what that numb feeling is with RSD. They were also freezing cold all the time. And my sneakers always felt like they were too tight so I would take them off. My legs used to bother me so I would sit on the end of my chair all the time. After my blocks I swear those symptoms went away for a while, and then I would feel them start to return in 2 or 3 weeks. Other symptoms that would go away that WERE expected to were the really bad red rashes on my chest and neck and face. Plus most of my fingernails would start growing again on my right hand. Has this ever happened to anyone else? My new doc all wrote me a script for methodone (5 mg 3 x a day) for pain. That is a little freaky, but my NP friend told me it should be great for my pain and will have fewer side effects than all the percocet I'm currently taking. Happy Friday!! Sandy |
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"Thanks for this!" says: | Dew58 (05-08-2009) |
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#2 | |||
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Member
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Trust your body and trust what you feel. Don't let anyone tell you what you feel is in your head. It might have nothing to do with the SGB after all, who knows, but that doesn't mean you don't feel what you feel. I don't think the doctor was trying to tell you that it was in your head, just that it wasn't or in his opinion couldn't be from the SGB.
I have no experience with SGBs, so I can't help you with that.
__________________
All the best, Marleen ===================== Work related (car) accident September 21, 1995, consequences: - chondromalacia patellae both knees - RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008 |
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#3 | |||
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Junior Member
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"Thanks for this!" says: | Dew58 (05-08-2009) |
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#4 | |||
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Member
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Pain and feeling pain relief is not in your head, when one is a RSD patient. Keep your chin up, and realize that objectively, your doc is telling you what he knows to be true. RSD is not a black or white disease, or there would be more definitive tests to diagnose and treat this culprit.
Enjoy your pain relief moments, and don't worry about the stuff you can't control. You are not a malingerer, and your doc knows that,too. If he thought you were, you would NOT receive the blocks at all. ![]()
__________________
. A Positive Attitude Will Assist Me Toward An Active Life, Once Again . WC Injury 03/24/07;Two Right Knee Surgeries on 5/22/07 and 01/16/08. Surgeons and Physical Therapists ignored my concerns of burning pain, swelling, and no improvement and getting worse. Diagnosed RSD/CRPS I/Sympathetically Mediated Pain Syndrome/Chronic Pain on 06/2008 by family doc;on 08/2008 and 12/2008 diagnosis confirmed by two WC PM Doctors: Both legs;hips; hands; and spine effected by this culprit. SSDI granted 01/2009. |
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"Thanks for this!" says: | SandyRI (05-08-2009) |
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#5 | ||
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I agree with the others- Trust your feelings- they are real. The only thing cetain about RSD is that the pain in uncertain- No one can say anything definate about it because even the doctors don't really understand what we go thru...
Debbie |
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"Thanks for this!" says: | SandyRI (05-08-2009) |
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#6 | ||
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In Remembrance
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I agree with everyone here. as usual.
The methadone will help. It's a very small dose. I don't know what else you take, but I've been on methadone since 1990 or so, and been from 10-15mg/day, up to a 100, now settled at 50-60 mg/day. With other meds in the cocktail. I wish you the best with you new med. At that dose, side effects shouldn't even be noticeable. The dose I take now, and being less active than I used to be, I need to take Miralax, (Just a little) to well, keep things moving... Feel Better! Pete asb |
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"Thanks for this!" says: | SandyRI (05-09-2009) |
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#7 | ||
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Senior Member
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Thanks guys for your responses! I feel very fortunate to have people that can "relate."
Have a good one. Sandy (from RI - where it is, of course, raining....) |
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#8 | |||
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Member
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I think a very good and sensible reason for the absence of your lower body symptoms after an upper body block is that the SGB helped your upper body vascular system as it is suposed to, thereby reducing the swelling and pressure in the tissues, and consequently relieving some of the pressure and symptoms related to that very same vascular pressure as well in the lower body.. What these doctors just don't get and we can feel, is that the vascular system IS conected throughout our whole body so what they do to one area efects the rest.. This same vascular system seems to be one of the the prime spreading systems for RSD. So it works both ways aparently, and that to makes alot of sence dosn't it after all the sympathetic nerves run along side the veins and main arteries, the vascular system. ![]() ![]() believe in yrself Doc's r guessers They can't feel it ! ![]() S |
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"Thanks for this!" says: | SandyRI (05-10-2009) |
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