Guest guest Posted May 14, 2012 Report Share Posted May 14, 2012 Thanks for the questions . My pain management Doc wanted to put me on methadone when I started with him, said the oxy's weren't as effective for my amputee nerve pain. I'd heard horror stories about methadone withdrawal and decided to avoid it as long as I could. I know it's effective, my husband took it when he was dying of cancer. Morphine made him a little too loopy to function so Hospice switched him. Did the job for pain control and kept quality of life high until the end. We knew he'd never withdraw, so it was a perfect choice. So far the oxy's are doing an effective job, although I'll start to build a tolerance. I was on the same thing for about a year and a half after my leg came off and they had to up the dose after a year. I suspect that when my current dose is no longer effective, they'll want to switch me to methadone. I'd been meaning to post the same kind of questions and saved me the trouble. Lou Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2012 Report Share Posted May 14, 2012 Hi Ya Lou Nice to " see " you again! I've missed you. I'm not much on talking on the phone these days. Between the broken leg and mashed foot, and trying to work and do physiotherapy, I'm not the most fun on the phone these days. :-) Withdrawing properly from methadone is not difficult. No more so than from any other narcotic. It's done one day at a time - stepping down a little bit each day. The nice thing about withdrawing from it, is that it is not an extended release drug, so you can cut out a little amount every few days. I split the pill down to 8th's for the first week, then quarters, then halves etc. It has never been a problem. I'm really not happy with being put on an extended release tablet. (Opana ER). It's supposed to work for 12 hours, but I'm finding it starts petering at about 9 hours, so I have to take the break through medication to last until it's properly time for the next Opana dose. It all seems kind of pointless. I ran into the same thing when I took extended release Avinza. It never worked for the length of time it was supposed to work. On another note - are you still taking Lyrica? I keep thinking about your eyesight problems and worrying about you! :-) Hugs from Lyndi aka Lynne Lou Conaway wrote: > Thanks for the questions . My pain management Doc wanted to put > me on methadone when I started with him, said the oxy's weren't as > effective for my amputee nerve pain. I'd heard horror stories about > methadone withdrawal and decided to avoid it as long as I could. I > know it's effective, my husband took it when he was dying of cancer. > Morphine made him a little too loopy to function so Hospice switched > him. Did the job for pain control and kept quality of life high until > the end. We knew he'd never withdraw, so it was a perfect choice. So > far the oxy's are doing an effective job, although I'll start to build > a tolerance. I was on the same thing for about a year and a half after > my leg came off and they had to up the dose after a year. I suspect > that when my current dose is no longer effective, they'll want to > switch me to methadone. I'd been meaning to post the same kind of > questions and saved me the trouble. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2012 Report Share Posted May 15, 2012 Lyndi! You were the one that finally got through to me and got me back to a pain management clinic, and I can't tell you how much that's meant. You and others in this group have been at it a good long time and are still willing to share your knowledge and experience. I don't know why there's such a gap between the information we often get from a primary care we should trust and the experience of knowledgeable patients. Probably has something to do with drug companies with deep pockets and an army of well paid reps. My primary care was an idiot. I suspect he barely scraped by in med school and I know he hasn't bothered to keep up. We have a shortage of primary cares in my town and I took what I could get. As I heard from Lyndi, and then again from every new MD I talked to, blurred vision from Lyrica should have been a red flag. This guy told me it wasn't a problem. Side effects finally took over my life, with blurred vision, loss of balance, and fatigue. When I finally demanded a referral to pain management, my pc shook his finger in my face and told me I was headed down a dangerous path. He did make the referral, then fired me as a patient. My pain management doc is an anesthesiologist with sub-specialties in chronic pain management and also addictions. He's been knowledgeable and compassionate, knew what was causing my pain and ordered an ultrasound to confirm it. He gave me a referral to a new primary care, one with a family practice. Turns out that the surgeon who saved my life, that I respect absolutely, trusts my new pc with his own daughter's care. The clinic that I went to right after I lost my leg had me on time release meds twice a day. This guy gave me the same thing in a slightly smaller dosage 3 times a day and it made all the difference. The stuff just doesn't last for 12 hours! I still need break through meds, but not nearly as many as I needed with twice a day time release. Pain control is good with no side effects. Lyrica is referred to in my house as The Drug From Hell. I'd heard horror stories about methadone withdrawal, that it's stored in bone and takes at least a year for withdrawal symptoms to finally stop. I suspect now that the stories filtering back to me were from people who had more ongoing problems than simple withdrawal. Thanks again and keep the info coming! Lou Quote Link to comment Share on other sites More sharing options...
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