pain management support group
For all of the chronic pain sufferers out there, whether it be from ... more
See All
Preferences
My Communities
My Discussions
My Email Digests
Thanks!View Thread
My name is Rikku, I'm 20 yrs old and I broke my left shoulder/collar when I was 9. And lately I get spasms there, like really painful, omg, it spreads all the way from my shoulder to my neck type pain. It's not like a regular thing, it just comes and goes on its own and it's been going on for about maybe a yr or two. My last spasm was yesterday. All I did was turn around and it hit me. It hurt, all I could do was hold on to my shoulder and wait for the pain to pass. When it does pass, it's like nothing even happened. My arm is fine, I don't feel like I was just stabbed. So I'm just wondering, is it normal to be having this type of pain after breaking bones?View Thread
II'm sitting here teary eyed over an RFA I have to have a week from tomorrow. I did not fare well with the 8 shots I had in my neck recently, I found them extremely painful. The pain doc told me the pain would be like 100 times worse and I would be sore for about two weeks. I have to admit, I'm terrified, and do not want to do it.
I will be getting Valium and that is it. He informed me I would experience great pain, and be sore for a few weeks.
To make matters worse, I have no tolerance to pain. I've been through approx. 20 sugeries in my life (only one for my neck and spine),and find I have less tolderance with each one.
Is there anyone out there who might be able to offer some words of wisdom to ease this angst I am feeling? Thank you.
PaulaView Thread
Take the Poll
Thanks.
Poll Results
Thanks.
-
It didn't hurt0% (0)
-
It hurt a little0% (0)
-
It hurt a lot0% (0)
Excessive and Chronic Joint Pain- 1.Hands & Fingers: Can not open things I was able to open just a few years ago (example: any type of screw on cap,lids ect.) My hands constantly ache and I have to clench my hands and crack my finger joints to get any sort of relief.I am unable to do regular day to day activities with out expirencing pain-sometimes a dull "ache" and sometimes a sharp pain in my finger & wrist joints. 2. Hips &/Or General Pelvic area: This is the area that gives me the most trouble on a daily basis,and has lasted the longest.I have had hip pain since I was very young, my first memory of it being when I was 7 years old. The pain is mostly centralized in the hip joint.I feel extreme pain ( I deal with a pain level of a 7 or 8 on a daily basis on a "good" day) in no other way to describe it but "inside" the hip joint. There have been incidents where I can walk the night before and wake up the next morning, go to put weight on one leg or another and my hip cannot support my weight and I collapse. Also, there have been multiple incidents where my hip(s) give me no warning what-so-ever and will suddendly "go out" from underneathe me. My hip joints constantly make an audible "pop" noise which others have heard on multiple occasions,and the popping is always acompained by a sharp pain. 3. Knees: My knee joints constantly lock in place and it is very painful to "unlock" the joint.The only way I have found to make the pain stop ( as with my hips when they "lock"as well) is to force the leg back into a straight legged position.It causes a brief,level 10,sharp pain. I cannot sit cross-legged or with one leg bent under me for any amount of time with out my knees "locking"
I also have recently been having very chronic migraines.I have had a headache on a pain scale of a 5 or 6 for almost 6 months now,and it escalates to a migraine occasionally that is joined but a sharp stabbing pain that feels like I am being shocked in my brain.I have also had problems concentrating as well as keeping words in the correct order.I have had many tests,but no doctor seems to know what is wrong with me .I would be greatly appreciative of any help,since this has had a very negative impact on my life.Thank you in advance!View Thread
A potentially confounding factor in this study is that the group of legally-represented patients had a poorer retrn to work rate and that time off from work was also a factor. However, taken into consideration, these confounding factors do not account for the significant standard deviation variation among the fusion group.
Read the entire research here: http://updates.pain-topics.org/2011/03/lumbar-fusion-surgery-for-back-pain.html .View Thread
i'm new to this site but long-time acquainted with chronic pain. my peripheral neuropathy is a by-product of an anti-rejection drug i took for a few years about 11 years ago for a lung transplant. after years of every type of pain control treatment possible, i finally got a NSS implant last november 2010. the trial worked unbelievably well. rejoiced at the possibility of a pain-free walkable life again!
however, after 4 months on the stimulator, several adjustments, and methadone 3 times a day for supplemental relief, i feel as though i'm back to square one. feet swell quickly, stinging/burning is apparent from the moment i wake up and walking is again very painful. my neurosurgeon is aware of my disappointment and advised me to continue as is for at least 6 months more.
needless to say, this is very dis-heartening. have any of you had a similar experience to mine, and what is the outcome. DOES the stimulator's pain relief improve as time passes? (btw, the leads have not shifted out of place), supplemental drugs taken? stimulator explanted? next option? any helpful information would be appreciated.
thank you so much. (someone suggested medical marijuana, but its illegal in this state and i doubt jail would improve my quality of life.)
tofucookieView Thread
KarenView Thread
I've been very ashamed to admit it to anyone. I know that this is ill-advised considering the patch could deliver the medication to quickly, and various other reasons. But I still continue to lay on the hotpack daily. I rarely get a "high" from it so I don't know why I crave the sensation of warmth/burning.
I'm a really messed up dude, I guess, but that is I want to declare annoniminity (sp.). I don't know if other's advice will help me but I need a swift kick in the rear I guess.
Also, I never really have had my pain under control, I just try and go with what the doctor recommends and don't hardly ever ask for an increase in medication.
Please, someone help with this. My legs are awful looking and I don't know if the tissue will ever look normal again. I'm so embarrassed.
Thanks,
anonView Thread
I know it means take one but I can't find it in any translations. Is it a division sign?
Thanks in advance. BTW I wrote this here because the PM group is where I belong with my chronic pain.View Thread
I don't dare try to straighten it the pain is way to sharpView Thread
fasttimeport posted: I am a 36 year old female with three boys. I have fibro and a unknow muscle disorder That causes may muscles to spams so bad I lock up and can not walk . I can see the spames craw up my leg and something jaw spams and locking. I have live with it for 8 years now. It is getting worse and as of the last two year I can feel it spam in my heart now. This last week I was taking to the ER because I could don't stop the spams the meds. This time was bifferent because I lost scence of everything around me and lost focus on anything seveal times. I my getting wores and don't know what to do .I have too much meds and too much pain. I am at the point I would just like to pass on. But I have my boys hold me to life. The ER was mean as always. They always say it is panic attack. But I am clam their is not panic. I just breath hard due to the pain and the spam in may jaws. I am so tied of them treating me as a panic attack. They give me somemuch stop the spams and send me home where after the meds wear off I back in the same shape. I am so tired of people not understanding. And not having a clue does anyone have my problem that can help.View Thread
I'm not sure I'm in the right place or not, but this group was the closest to what I'm going through.
So, I had a surgery back in March 2009 to add inches to my lower left leg to correct a birth defect. I was under the impression that I would initially have the surgery and recover within 6 months tops. I had no idea that 21 months later, I would still be "recovering" from this event.
The first surgery in March went very well. I had an external fixator on my leg for 5 months, wore a cast for a month, then got my walking boot. Everything was supposed to get better and I should have been walking soon.
Unfortunetly a completely unforseen complication occured. During my rehabilitaion and recovery my leg was actually bending the opposite direction! I can't walk on a bent leg! there is no way! It took us (the doctor and myself) to determine that another surgery and more external fixators would have to be installed to correct the curveture in my leg.
June 2010 I had the surgery and shortly after, more complications. The pins supporting my leg had almost all become infected, and there was no real way to treat them. These wounds became larger and more inflamed and I was struggling every day to just make it through until the next. I had to keep the pins on until the bone healed and the pins could be removed, which meant 4 months wearing the fixator. This became more and more difficult for me to cope with since there was no way to treat the growing ulcers around the pins sights.
The end of Oct finally comes and we get to remove the pins!! I was excited to get rid of the damn metal gear and focus on my recovery, the only problem is my ankle still looks crooked to me. The doctor says it is because my muscles have tensed up in that position and need to relax in the straighter position. I can only really do that by standing on it, and that hurts since the muscles are so tense and I have lost ampel amounts of muscle in my lower leg.
I have been taking pain meds the whole time, but now he wants to cut me back, maybe even take me off of them completely and I'm not too confident that completely stopping the meds will be benificial to me. I only take one pill a day. Surprisingly that manages my pain. But if he wants me to continue to "straighten my own limb" I do not want to remove the meds completely.
I don't know what to do anymore. I can't work due to my condition, I haven't been able to do anything "fun" in almost 2 years, the meds are giving me mood swings, flu like symptoms from reducing my doseage and I feel utterly trapped.
Sorry this post was so long, I just wanted to explain the situation and possibly get some feedback.
Thanks for listening
PixiView Thread
Corporate whistleblowers and congressional critics contend such arrangements—which are common in orthopedic surgery—amount to kickbacks to stoke sales of medical devices. They argue that the overuse of surgical hardware ranging from heart stents to artificial hips is a big factor behind the soaring costs of Medicare, the government medical-insurance system for the elderly and disabled.
Conservative spine surgeons argue that a spinal fusion is appropriate only for a small number of conditions, such as spinal instability, spinal fracture or a severe curvature of the spine known as scoliosis, and that financial incentives have caused the procedure to become overused. The most hotly debated use of spinal fusion surgery centers on patients who merely suffer from aging disks, a condition known as degenerative disk disease.
Fusion by the Numbers View Interactive
See hospitals' case counts and total Medicare reimbursements for spine fusion, 2004-2008.One health insurer, the nonprofit Blue Cross and Blue Shield of North Carolina, announced in September that it would stop paying for spine fusions performed on such patients beginning on Jan. 1. The insurer said that the procedures are "considered not medically necessary."
Some recent studies have suggested poor outcomes for spinal fusion. A study published in the Journal of the American Medical Association, or JAMA, in April found that Medicare patients with a condition called spinal stenosis who had more than two vertebrae fused, a procedure known as a complex fusion, were nearly three times more likely to have life-threatening complications than patients who had a less invasive procedure known as a decompression.
Another study of workers' compensation cases published this year in the online edition of the journal Spine showed that patients who had a spinal fusion were much less likely to return to work within two years after their surgery than a group of patients with similar conditions who didn't have surgery, and that 27% of them had to be re-operated on. Their rate of permanent disability was more than five times as high as the patients whose spines weren't fused, and their daily intake of powerful narcotic painkillers increased by 41% after surgery.
Read the entire Wall Street Journal article here: http://online.wsj.com/article_email/SB10001424052748703395204576024023361023138-lMyQjAxMTAwMDIwMTEyNDEyWj.html .View Thread
Everything is just such a horrible, horrible mess. Please pray for me and my husband Tim.View Thread
See Related Pain Management Communities
Women's Health Newsletter
Find out what women really need.
Spotlight: Member Stories
Helpful Tips
- Smoking Pot Decreases Neuropathic Pain
- Transplanted Stem Cells Prevent Disc Degeration
- Naloxone ?Reboots? Opioid Pain-Relief System
Related News
Related Drug Reviews
- Drug Name User Reviews
Report Problems to the
Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Other Member Communities
- Dieting Club: 10 - 25 Lbs Member Community Share Your Tips and Support!
- Caregiving Member Community The Support and Understanding You Need!
- Parenting Friends Talking Member Community Get Support from Members Like You!
-
More Related Communities
The opinions expressed in WebMD User-generated content areas like communities, reviews, ratings, or blogs are solely those of the User, who may or may not have medical or scientific training. These opinions do not represent the opinions of WebMD. User-generated content areas are not reviewed by a WebMD physician or any member of the WebMD editorial staff for accuracy, balance, objectivity, or any other reason except for compliance with our Terms and Conditions. Some of these opinions may contain information about treatments or uses of drug products that have not been approved by the U.S. Food and Drug Administration. WebMD does not endorse any specific product, service, or treatment.
Do not consider WebMD User-generated content as medical advice. Never delay or disregard seeking professional medical advice from your doctor or other qualified healthcare provider because of something you have read on WebMD. You should always speak with your doctor before you start, stop, or change any prescribed part of your care plan or treatment. WebMD understands that reading individual, real-life experiences can be a helpful resource, but it is never a substitute for professional medical advice, diagnosis, or treatment from a qualified health care provider. If you think you may have a medical emergency, call your doctor or dial 911 immediately.
Health Solutions From Our Sponsors
©2005-2013 WebMD, LLC. All rights reserved.
WebMD does not provide medical advice, diagnosis or treatment. See additional information.

