Quote:
Originally Posted by Kathi49
While I don't have RSD I do have spinal disorders and neuropathic pain. But, wow, I have never run into this with my pain docs. The first group was at a teaching university. And the only reason I left is because they couldn't seem to find the pain generator; otherwise they were okay. The one I see now is affiliated with a local hospital. But with both of them no, no contract, no peeing in cups...none of this! He performs injections when warranted, prescribes meds, conservative therapies; all of it and I have never been questioned on anything for 10 years. I don't know maybe it is the state of Indiana or something. I do know Indiana was one of the first if not the first to have a statewide database. So, maybe that is part of it. I have no idea really and am not doubting your story. Just saying it constantly amazes me what people have to go through. And, oh, yes, I have Medicare, BC/BS and Tricare and have never had a problem at all! And I had access to my records; just had to pay for a couple of them once. And when I ask for copies, they usually just give them to me and/or clear it with the doc. In any case, I love my PM and would follow him to the ends of the earth! And I honestly don't have a problem with the sharing of my medical records. The only problem I can foresee though is that under Obamacare you might be placed in certain "risk pool".
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I problem with many with RSD is the solid confirmation that they in-fact have RSD, for many it may take years, then the other can of worms is how much a doctor really knows about and how to treat RSD. In my wifes case, here in an area just chock full of doctors Washington DC, I've witnessed doctors say they know nothing please go away. And even when we would visit clinics who state they treat RSD, soon will'll find out they don't have a GD clue. The latter makes me the most angry, akin to bate and switch. The switch usually means a lecture and a lap around the pool.