Guest guest Posted July 21, 2006 Report Share Posted July 21, 2006 I hope your insurance will reemburse you for the visit right? You might be entitled add the amount over what they agree to pay as part of your deductable. I save a few thousand dollars every year in expenses I shouldn't be paying for. Has this happen to anyone else? I get all burned up about how the insurance companies take money for things you didn't get. forgive me but I had to get that out. > > Last night I had to go to Vanderbilt ER for my back pain, it was just > too much. They refused to give me an injection, but insisted on > giving me hydrocodone. My records have a big red flag on them that > says I have a bad reaction to hydrocodone, but they gave it to me > anyway. Where do these people learn medicine? Can they read? > > I broke down today and went to the only pain doc I could find who is > still actually practicing pain management, & he doesn't take > insurance. The visit was $325....ouch. But he told me more than any > of my docs in the past. I had a spinal MRI done in January. The pain > doc I was seeing at the time told me I had a slipped disk (L5), but > never told me I also have a Tarlov cyst on the left of my S2 & a > hemangioma within the S3. > > Basically, a Tarlov cyst is a cyst that grows like a cancer, but is > benign, & also causes excruciating pain. That is the reason my back > BURNS with pain nearly constantly. It fills with spinal fluid, and > continues to grow in size. The only sure way to identify one is by > MRI. The only good news out of that is that it's not in the canal, so > it isn't likely to cause any trouble (except the excruciating pain). > I think it's pretty rotten that my original pain doc, or other > doctors (especially my neurologist), failed to identify this, or even > suspect it. The MRI was done in January, and none of my docs seemed > to know. And I've had this thing at least 10 years, if not longer. > > Hemangiomas are abnormally dense collections of dilated small blood > vessels (capillaries) that may occur in the skin or internal organs. > They grow rapidly, & can eventually impact the adjacent internal > organs. So far, this one isn't causing any specific trouble, but > since it's growing, I may have to have it removed at some future > point. The doc said the location of this one makes the surgery a > dangerous one, & would only be done if it starts causing problems > (other than pain, which I don't know if mine is caused by the Tarlov > cyst alone or both together) or invades an important organ. > > I was very impressed with this new doctor; I just wish he accepted > insurance. The reason he doesn't is because just about every > insurance limits what meds or treatments a doctor can prescribe, even > if they're needed. This way he can give his patients the care & meds > they need, rather than what an insurance company tells him he can or > cannot do. He spent half an hour with me, & was interested in every > aspect of my health, not just the pain. He said his aim was to make > me feel better, & to increase the quality of my life. He did give me > some sad news, though. I was an avid rock climber & figure skater, & > the doc said no way to both activities. He said they'd exacerbate my > conditions & make my pain much worse. He was willing to give me > oxycontin, but after sitting in the waiting room for several hours & > talking to many of his patients who were on oxycontin, I decided > against it. They all said it was just too addictive, & trying to go > off of it is difficult. So, I just told him I wanted MS-Contin, which > I've been on for about 3 1/2 years. I still have the burning pain in > my middle back, but he gave me a prescription for Lidoderm patches, > which I've had before. > > The doctor is from India, & has a beautiful shrine set up in one of > his rooms. His waiting room was packed when I staggered in at 10:30 > this morning, & was still full when I left at 2:45. You really get to > know people when you're packed in like sardines for hours, lol. We > all talked about our different maladies, & even though most faces > were drawn with pain and the heat was terrible (the thermometer in > the shade read 105 at noon) everyone was upbeat. One man in > particular impressed me so very much. He was young (looked to be in > his early 20's), had no arms, & his right ear was gone. Later someone > told me he used to be a lineman for the electric company, & got > jolted with 350000 volts. It literally burned his arms off. Yet, he > was laughing & joking, kind to everyone else there & didn't complain, > though he was in terrible pain. He was so very handsome, and I felt > so badly for such a young man who had such debilitating injuries. > > I even ran into a woman who had been to our home several times a > couple of years ago. We'd lost track of each other & at first didn't > recognize each other. She also has fibro, as well as myofacial pain. > We talked about what had transpired in our lives over the last couple > of years (she loved the story of my being sucked out the door by a > tornado, as did our neighbors in the waiting room). Everyone also > enjoyed the tale of my battle royale with a mouse at 2AM a couple of > weeks ago. They all laughed at the image of me battering around the > bathroom with a broom, while the fluffy rodent raced circles around > me. I eventually slipped on a bath mat and fell into the bath tub, > which really hurt! But, it was good to be able to make other people laugh. > > Well, I'm going to have to go apply one of my Lidoderm patches. I > hate the way they tend to peel off almost immediately, but maybe if I > swab my back down with alcohol, it will stick better. It's after 8:00 > pm & the outside temp is still over 90 deg. F. This heat wave is the > worst one we've had in years, & it's supposed to be hotter tomorrow. > A few days ago a man stepped outside his home & walked a block & > dropped over dead from heat stroke. He was in his early 50's, & in > fairly good health. His core body temperature was 107. The hospitals > are full of people suffering from the heat right now. Our AC runs 24 > hours a day, & it's still nearly 80 in here. > > Ok, time for that lidoderm patch! Welcome to all the newbies, and > I'll try to participate more now that I'm back on my meds & feeling > halfway human again. > > ((((((((((HUGS))))))))) > cyn > > > > > > clmerritt@... > Fibromyalgia-Support-Group co-moderator > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2006 Report Share Posted July 26, 2006 .._,___ What is the difference between MS Contin and Oxycontin? --------------------------------- How low will we go? Check out Yahoo! Messenger’s low PC-to-Phone call rates. Quote Link to comment Share on other sites More sharing options...
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