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How should I go about notifying my doctor that I will be needing to switch ASAP? Would it be best just to schedule an appointment to see him to discuss what I should do, or at least seek alternatives to a different pain medication? I have tried fentanyl patches in the past but I had an adverse skin reaction, but I wouldn't oppose trying them again, as I know for sure those have a generic. To be completely honest I'm not sure about what other long acting medications there are that are similar to Oxycontin(and work similar to oxycodone). I'm all ears on success stories with other long acting pain medicines. I'm definitely starting to stress out about the price increase and the implications it might have on me taking pain medications for relief.View Thread
Good luck, Beth, we will all be thinking of you!!!
We hope your recovery time will be short, and not too very painful!!!
Can't wait to get you back on the puter!!!
DennisView Thread
Thanks Lori!
Opioids: Addiction vs. Dependence
http://www.healthcentral.com/chronic-pain/coping-279488-5.htmlView Thread
still dont know how to post a link if someone would like to tell me how i will repoast just google that up there and tell me what ya thinkView Thread

Here is a quick recap of my story. Back in 2005 I had a bad fall that resulted in a severely ruptured disc at L5S1. Following three months of SEVERE pain and all the usual methods to correct it (physical therapy, spinal injections, steroids, pain meds, etc) my surgeon recommended a bilateral discectomy that was performed in December of 2005. This surgery was a huge success and I had almost immediate relief from my pain. Although I would have occasional flare ups over the next several years, I lived relatively pain free until the beginning of 2012 when I managed to re-injure my back after starting a new exercise program (I guess that's what I get for trying to get in shape...ha ha).
Anyway, I went through the normal attempts to calm things down again (spinal injections, physical therapy, medications) with no success until it go to the point that it was simply unbearable so my doctor recommended an anterior fusion which was performed in July of 2012. This surgery did NOT go well and not only did I experience no relief I think things got worse if that is even possible. Following almost 4 months of no noticeable improvement my doctor recommended another back surgery to "tighten things up and prevent movement that was causing me pain", so he performed a posterior fusion in November of 2012. This surgery was slightly more successful and I did experience some relief for a brief period but beginning in about March of this year things started going south once again.
So currently I live in pain 24X7 with no apparent relief in site and I'm not sure how much more I can take. Mornings are the worst and some mornings I quite literally can't get out of bed (however I have to get out of bed because laying down too long also causes pain and has resulted in many a sleepless night). The only thing that seems to help and make life tolerable has been steroids (which I've already received my maximum dose for the month so I can't have any more for a while) and 7.5 Norco's which I take 3 times a day. These do not provide complete relief but they definitely take the edge off and allow me to function as a semi-normal human being.
I think my back doctor has given up on me as yesterday he told me that at this point he would like to refer me to a pain management specialist. I'm not sure exactly what this means but I hope to meet with them in the coming weeks. I've been doing a lot of research on the web and there seems to be mixed responses to what people think of their pain management docs so I thought I would post a message here and ask what to expect? Anything I should do in preparation? What are the odds of them keeping things in check and making life bearable? Basically, any advice, suggestions or comments will be appreciated.
I will say the only saving grace through all of this is that I have an unbelievably supportive wife of 25 years that is my rock and is the only reason I continue to fight through this. I also am fortunate to work for a GREAT company that has been very flexible throughout all of this, allowing me to work from home whenever necessary so I can stay close to an ice pack and recline in a more comfortable position and avoid some of things that make the pain worse such as sitting in one position to long, stairs, etc).
Appreciate any thoughts, comments, smart remarks you may have.
God blessView Thread
I was a cheerleader for three years, and for the first year and a half i would constantly land flat footed and it would send shooting pains through what feels like a tendon right above my ankle bone (its the same feeling from when you jump off a high platform and it hurts your ankles). After we corrected the problem I never had another issue with my ankle hurting, until now.
A month or two ago I woke up in the morning from going out with my friends and went to stand up to learn that my left foot couldn't beat any weight. It felt like a slight stabbing pain, so i wrapped it up and hobbled to the baseball game where i sat down and didn't move it for a few hours, and the pain went away.
Well tonight, i felt the same pain around 10:30 pm but since i was with all of my friends i couldn't sit down and let it rest so i stood on it and walked around on it. The pain consistently got worse but I didn't notice much until about 1:30 am when i had dropped everyone off and i realized i could hardly move my foot without lots of pain. Now it is 3:30 am and I have been laying here for two hours because I cannot put any pressure on my foot without making the pain excruciating. It feels as though someone is taking knives and stabbing that tendon over and over again. I've iced it, elevated it, taken ibuprofen, massaged it, everything i can think of. Does ANYONE have any idea what this could be? I'm making an appointment with my doctor so he will most likely diagnose or figure put something but i would love to have an idea of what I might have and how to get rid of it so I can sleep!,View Thread
I don't know what I can do for pain management either with limitations of meds, if there really is anything.
Thanks.View Thread
I have been having pain in my upper left torso front and back for the last 3 years. I have not had any surgeries or trauma in that region. When I first saw my Dr. we thought maybe I was getting Shingles, even though I had no visible signs of it, but my symptoms seemed to match that of Shingles. Needless to say I have been on several medications- Antidepressants, Pain meds, anti seizure meds and meds for herpes outbreaks. I have had injections, which actually gave me 95% relief and then the Dr. didn't want to do anymore after the trail runs, said they were "too destructive".
I have been to Neurologists, Pain Specialists, Acupuncture, massage therepy, chiroprator, neurosurgeons, meditation group, and the list goes on. I know I'm not alone with my symptons of pain but I feel like I'm always running into dead ends and Dr's that give me false hope. I'm hoping by joining this community that maybe I will find answers or ideas on where to go next. If anyone has options that they have tried, I would love to hear from you!View Thread
Does anyone know which of the 2 meds are best in controlling pain?
Any info would be very helpful for me. I am going thru a change in meds and just do not know what I should do,
Thanks for your input.View Thread
I saw my new pain mgt. dr. today and was prescribed Morphine Sulfate 30mg, TER and Morphine Sulfate 30 mg. Tab and I am absolutely confused as to which one is to be the long lasting one and the one that is to be for breakthrough pain. Does anyone have an answer to my question?
I just don't understand this. Prior to this change in my meds, I was taking methadone 10 mg. ( 2 pills 4 times a day). In other words I was taking 80 mg. of methadone until this change with the new dr.
I have another question too. I was prescribed atenolol 25 mg. for headaches and I have never heard of that being used for headaches only for cardiology purposes.
Could someone help me? I have read the leaflets that came w/ my meds and I still just do not understand.
Thanks.View Thread
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A specific use of vocabulary0% (0)
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I asked straight out for what I think I need67% (2)
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There is no mystery in my case because my doctor takes care of me33% (1)
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I had to resort to more drastic measures such as:0% (0)
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I do have one other huge concern however. I will be going on Medicare in approximately six months and have not been able to find an insurance that will cover the Butrans or the Cymbalta and Lyrica I take.
Is there anyone that knows anything about an insurance that will cover these very pricey medications?
Thanks for your help.View Thread
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