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Like most chronic patients I've been taking multiple meds for many years. My Dr. has startef requiring a urine and/or blood test to make sure I'm taking my meds. I have been taking 3-5 Norco each day for breaktrhough pain for years. Today, my Dr. said my urine tests have shown Negative for Norco so he will not renew my meds!?! How can this be? A blood test several months ago showed positive, and I've been taking my meds every day, but somehow it's not showing up in the uriine test. So not only does mh Dr. question whether I'm taking mmy meds, his attitude today made me feel like he thinks I'm selling them! This is not true, and I am beside myself wondering what I am going to do.
Has anyone else had this issue? Any suggestions?View Thread
http://www.youtube.com/watch?v=M6dNwFI641E
Thanks for any help or suggestions!!
-JohnView Thread
I take Tramadol for days that otc work, Percocet when pain is severe (like tonight). I also take soma , neurontin .
But I try other options before I do the prescripts , like heat, laying down, epsom salt baths ect..
Sometimes its just damn frustrating.
CloudView Thread
I am a 35 y.o. female & after dealing with lower back & hip pain for about 3 years I may finally have a real diagnosis! In the past, I have been told it was both Spondy and/or Arthritis by different doctors. I have had xrays of my hip and an MRI of my back but never an xray of my spine. It has been very difficult to find a doctor that deals with chroninc back issues! This week I was referred to an ortho who did an xray of my spine and found that my last vertabrae was never formed correctly. He is referring me to a spine surgeon who will most likely set me up with a pain management specialist. He also said he is 95% sure that I won't need surgery. Does anyone know the medical term for this condition? I feel relieved that they found this but still frustrated because I am in so much pain! Sitting at my desk at work for 8 hours a day, (sitting anywhere for an extended period of time), laying down also hurts. I have been experiencing spasms when trying to get up after laying down also. I have been prescribed 2 different anti immflamatories (Naproxen & Meloxicam) but neither has done anything. I have also been through a few months of PT which has also not helped. My Doc gave me Tylenol with codeine which helps a little at night but can't take that during the day. She said they don't like to precscribe narcotics. This is the problem I run in to! Sorry for rambling but I am so frustrated! Any input at all would be appreciated!
KristenView Thread
So I guess my question is how long does it last until I start feeling some relief. This pain is worse than it was before the procedure. The only relief I get is when sitting or laying down. Now I dont think my job would appreciate me doing either of these. My PCP started me on a Medrol Taper to see if that helps (on day 1 now).
This is just awfully painful. Any suggestions, comments, feedback is appreciated!View Thread
Any doctor that I have seen for it has said that it could be a small cyst, but they didn't feel like it would be ok to operate and look, that was when I was 15. And another doctor I went to 6 months ago thought it was only stress and did not prescribe anxiety medication, but instead lower tabs and muscle relaxers, which actually caused more pains and stomach problems. My family doctor at one time did prescribed to me an anxiety medication but, the symptoms were too much for me to handle and I stopped taking the medication.
I have never had a doctor scan me for any problems. I have only gotten blood test taken and nothing ever shows up. I do have a history of depression and anxiety. And I've always assumed that was the cause. My boyfriend and I have looked up possible things and all of them either led to stress or angina, and I want to say angina is a very small possibility.
If anyone has any advice or any way to alleviate the pain, please help. Any advice or resources would be greatly appreciated. I'm really tired of the stabbing chest pains...View Thread
Questions:
Thanks, Charles, BView Thread
thanks
P.S I won't give up:)View Thread
Thanks!
KristenView Thread
I went to the doctor two weeks ago and he sent me to a Rhematologist. She assessed me and did not see any visible swelling or redness in my joints. She did diagnose me with having hyper mobile joints that bend a little funny. She sent me for blood work to check my thyroid, RA factor, ANA and lyme. She also did a full CBC. I was put on Medrol dose pack to help with the pain and it really helped dramatically. For 3 days while taking it I had more energy, didn't need to nap and the pain in my joints felt a lot better.
I also went to see an orthopedic surgeon who took X-rays of my hip and knee. He did not see any visible issues and thought the Rhematologist would of found something out instead. Well I met with the Rhematologist yesterday and she told me all my blood work was completely negative and nothing was wrong. I told her the pain had come back full force since being off of the Medrol and she said I was OK and didn't have Lupus, RA or thyroid issues and that my main problem was Fibromyaligia. She didn't give me any meds to help and told me I needed to see a Psychiatrist for possible depression. I am not depressed, I am in pain all the time and can barely take care of myself and my son. At this point I am going back to see my regular doctor and find out what is going on with me. I am not having pain in my muscles so I have no clue how it could be Fibromylagia. Has anyone had similar issues like this? It's slowly taking over my life and the pain is so unbearable.
Also, I am on Norvasc for Hypertension. I also take Xanax and Celexa for anxiety I had years ago that is now controlled.View Thread
Alternately, if you have tips or advice on what makes a good support group, I'd be glad to know.
Thanks,
MarshaView Thread
Well I've been around here for a little while now and I would really appreciate some Wisdomm of how to reduce Muscel spasam that is very sereve!
I tripped last week on thd Dog and fell onto the bathroom counter and really wacked out my whole back and spasam much worse!
$ days latter I tripped and almost fellover the Landury cart!Thank God some stopped me but I tweeked everythinh else out and I can hardlley move my neck,stff back Etc!
Help!!!77graceView Thread
other sample medication my doctor gives me to try but pain never seems to go away it all got worse after I had surgery by them trying to fix one problem lead to more problems I'm just turned 42 and feel so depressed I lost my job can't motivate sometimes wish I don't wake up.
Does other ever feel this way.View Thread
I have been having one of my really bad Pain days,you know ,the kind where it feels like I just can't hang in there and wish I could just sleep through ll this pain and forget it all!
But then I rremember all the times that when I feel really bad and hurt so much that if I call someone else who I know is also suffering I start to feel better, and Viola.I do!!!Sure I still hurt but not as bad at all and I belelive that my attitude can make me or Break me!
Can you relate???
Thanks,77graceView Thread
Anyway ,I'm in a bad spot!!I get really bad headaches and hav for over 30 yrs.Thnkfully they are not as bad as before where I had them for 4 days ,threw up etc,
But ,they always start in my neck where I have tumors growing on the nerves on my spine!!!I use imitrex along with zanaflex and then have other pain meds for neck and back!But I'm in a cycle now because I'm having rebound headaches and I don't know how to get through them without something!!!
In the old days befor Imitrex and I was Sober I just tuffed it out but now it seems impossible!
Any idea's would be helpfull!
Thanks77graceView Thread
I am new to the boards, but I desperately need some advice. A few years ago, doctors discovered that I have a major issue with one of my discs. There's a bulge, a tear, and there is no fluid left in it. We've tried everything, and doctors have finally said that without a fusion, I will not improve. Doctors didn't want to do it initially, because of my age. I'm 35. They said when I'm 50, I can have it. They've changed their minds.
The problem is that I do not have just the one disc out. The disc above and below it are having issues, too. One has a tear, and the other is bulging. My fear of this surgery is that after a year or two, I'll need the other discs fused. It's another reason why doctors have said they don't want to do it until I'm older. I'm at a crossroads.
I need to decide if I will have the worst disc fused. I would like to hear the experience of someone who had multiple disc problems, but only had the worst disc fused. If you had it fused, did you have to subsequently have other discs fused? Was the fusion successful? Did you have to have the other discs fused? If so, how long after the first fusion did you have the others? How much limitation to your life is there? Also, if you had a failed fusion, can you share your experience with me?
My fear is that the fusion will fail and I will end up in worse shape than I am now. I do understand that is a possibility regardless. I just so happen to be that person...if the doctors say something has an 89% success rate, I'm the 11% that fails.
Initially, the surgeon ignored my other 2 discs. I also have a compressed nerve. He was rude to me, and kind of a jerk, to be honest. He thought I made up the nerve pain. He thought I was overreacting and being overdramatic, that my pain and limitations were in my head. After I allowed him to run further tests, he realized his mistake. He saw the compressed nerve, and told me during a follow up that it was really bad. He also saw the additional damage to my discs. I only let him run them, because whether it was him or another doctor, I needed them done. When I ask him what the risks are, his answer was "Well, it's better than what you have now."
I have children and a job. I'm unable to keep up with my life. I'm a slave to my pills, and I hate it more than anything. If the fusion will give me my life back, then I will be on the table tomorrow. Before I make this decision, I need more information.View Thread
Thank you so much in advance for any help anyone can provide!View Thread
I was a tennis player who played up to 10hrs/week. I was a cyclist who rode 25-30 miles at a time/2-3 days a week. I'm competitive, but love to do it for the fun. I haven't missed my sports, soccer included, as bad as I have the past couple of weeks. I'm HATING spending most of my days lying on the couch. Watching Animal Planet, Sci-Fi, most recently (probably why I'm so bummed): the Olympics. I used to be an ameteur skateboarder. I flew down stairs and rode as fast as I could down hills. The rush I got from all these sports I loved was incomparable to anything I've ever experienced; much like the feeling displayed on athelete's faces as they push themselves to the limit while millions watch.
I would trade anything, especially the handful of med's, to get back to that place. I don't accept that I'll never return there. I just can't. I also can't accept that 20+ doctors cannot figure out why I have chronic pain in my leg, on my sit bone, SI joint, buttock, down the leg. Recently it has caused a pinching pain in my low back. That "insignificant disc bulge at L-5,S1 is not that bad", according to the docs. "Arthritis in (my) SI joint is common and no cause for concern"...
Well doc, IT F-kin' hurts! I was riding my bike one day, slipped off the pedal and crashed on the seat from a standing position...not a big deal, so I rode another 25 miles. It happened twice. I kept riding and playing Tennis. I had a 9-5 deal where I was expected to sit before a computer all day. I hated sitting. Dealt with some awful burning pain down the leg, in my crotch, for about 2 months until my boss forced me to go to urgent care...that was the death of me. I NEVER imagined I would still be in this much pain years later.
Sometimes I feel like my docs are my opponent. My family no longer cheers me on. My team consist of a 4 yr old and a wonderful spouse of whom shouldn't be asked to take on such a burden. Sometimes I wish I could suffer in silence. I'll take pain over imposition any day. These boys are the light of my life. Well, what's left of it.
I'm no longer planning competitions, play dates nor family vacations. I'm a slave to the medication but still can't function on an acceptable level. If I state this, I "must be seeking a fix", or "must be in need of more drugs"...
Well, f-U medical community. Gimme back my bike. Gimme my tennis racket and some balls. Gimme a chance to play on the floor with my son. I want to clean my house!! I want to go to work. I want to go to the beach.
If only I could be as determined as those athelete's competing in the Olympics. That's what I want. Not another doc appointment. Not another pill.
If only my family (extended) could understand what it's like to be so stuck. None of them have ever felt this way, yet they are convinced it's in my head. So weeks, months, a year goes by and my son grows older; yet hardly any phone calls, only guilt-coated comments they breathe my way as if I wasn't suffering enough. No wonder my dad "checked out" after 26 yrs of chronic pain/Fibro/CFS.
I would never cause such devestation to my family, but the lack of support is enough to drive anyone mad.
So I ask, why me?? Why not my sister, or brother? I wouldn't wish this on anyone, but I cannot accept that this is a life sentence. I refuse to. Yes it sucks. Maybe I've become a stronger person for it all....but Christ!! Lessons learned! Let me move on!
I wonder if anyone else feels like the dark cloud hovering over the hopes, dreams and aspirations that every healthy individual within their family circles? They always forecast a dark day where I am concerned so avoidance, like an umbrella, protects them from me. GEESH!! All I did was push myself as hard as I could. I am an athelete. I have to get back in the game! HELP!View Thread
I cannot take being hurt anymore. My cousin just died and I just can't take anything at all... It doesn't matter... I just couldn't be mean to anyone....View Thread
Makes no difference, but I ythank God for the "good" people like Bren_Bren & Anon...
I'm sorry, but how could anyone who is suffering say such things. I hope you all get better...View Thread
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