recently diagnosed with ra have been on a regiment of painreleivers for chronic clusterheadaches (percocet and vicodin) now prescribed mtx and enbrel for moderate ra and i find myself increasing dosage of opiate to cope with pain do rheumys typically prescribe opiates and or muscle relaxers?





I've had the same problem. I had broken my pelvis in eight locations, i had a rod placement in my back, my knee was reconnected with optical fiber as well as my elbow, mynerves and ligaments were torn all through-out my right side from my hip, down & i had other internal issues as well. 6 mths in the hospital and the whole time they had me on the morphine pump, time released and quick release. When I finally got out of the hospital, the had me on percocet and the quick and time released morphine. I winged myelf off of it because of the side-effects was experiencing. I'd rather be in pain than having cold and hot sweats, headaches, terrible and insane dreams that seemed like reality when i awoke, and other minor things that just didn't suit me. It took me about ten minutes to realize when i woke up that my dreams were dreams. I went to the Dr and told him I was done with it and I had winged myself off of it and he was disappointed. We talked for an hour and he decided I'll still need the medication, And he prescribed the same amount to me again. It took one day for me to rebel against it and not begin taking the medication again. I know there are alternative, but I'm not sure what to suggest. Morphine isn't for me and i'm not sure how to convince my Dr to try something else. What should I suggest and how should I approach the conversation in a way my Dr would understand.? Please respond soon. I'm calling today and setting up my appointment and explaining why my medications are not for me. This problem has been going on since mid 2008, So it isn't my first rodeo. Also, He demands I take Amitriptyline HCL 75 mg and I refuse. I took it while i was in the hospital, but i didn't know how to feel. now that i'm fully aware of my nervous system, that drug is the most awful thing they've ever created. there is no way anybody could function on something that extreme. He don't believe it effects me in the way i describe, but I will not touch it anymore. I've been getting them for 2 years, and since i've been an outpatient for about a year, i've been prescribed this medicine every since and i've taken it 3 times. The next day my muscles are dead, i have no energy, i'm drained and tired, i have a headache, and i feel wothless and i just want to sit and/or sleep. I don't know how to feel and it drives me insane. Please help.