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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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Junior Member
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Hi everyone, I was just wondering if anyone else was having trouble with getting their doctor's to listen to them? ![]() When I go to see him---I can't be in pain, even though its over 50 some miles & thats one way. If I am in pain then he has it in my notes that I'm to be put on the schedule for surgery for the spinal cord stimulator---I don't get a say in it at all. The research that I've done says that a stimulator doesn't work, there are even doctors that won't advise their patients to have it. He told me that the success rate was alot higher than I've read about, not that it surprises me any at all--not after all that I've gone through with them over the years. I know that this might sound stupid but why is it that all that matters to the doctors is MONEY?? I thought that they took an oath to "help" their patients---or is that just when it suits them?? The ones that have heard of this disease know that there is no "cure" for this & that we are the ones that have to deal with this pain on a daily basis not them so what does it hurt them to give us something that will control the pain?? I just want the pain that I'm in 24/7 to be better controlled than it is---why do they make it sound like I'm asking them to give me a million dollars? Was just curious if anyone else was going through the same stuff that I am & how many of you there are. Hope that I'm not the only one having these kind of problems with the doctor. Thanks & hope to hear from anyone else having these kind of problems & what you did to actually get help. Thanks. Janet |
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"Thanks for this!" says: | AintSoBad (09-25-2009), bassman (09-28-2009), cindi1965 (09-26-2009), dreambeliever128 (09-26-2009), fmichael (09-27-2009), Hockey (09-28-2009), hope4thebest (09-25-2009), loretta (09-26-2009), rtmcmahon631 (10-04-2009) |
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