Back Issues :: Post Fusion Pain Opposite Side
Mar 30, 2014
I'm three weeks out from l5-s1 fusion. For the last week I'm having the same pain I did ore surgery but on the other side. I'm really getting worried. It's different pain than post surgery pain. It's my right butt cheek and right calf pain. It's there all the time. Like a sharp knife in the muscle pain with tingly numbness. If I don't have a disc to herniate, what could this be? I'm done with pain and surgery. I can't take this any more
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I'm 5 months post op from MIS fusion of l4/l5 and in pain.
Had microdiscectomy at the same level november 2013 without any relief. The back pain only got worse. The disc was completely dehydrated and I was offered the fusion 6 months later. Not that much pain after the operation but it has increased a lot. Severe back pain in the lower back and all the way up to the shoulders.
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I am a 40 year old male that has had two back surgeries. First Surgery February 2014 Lumbar Spine Posterior Discectomy Micro-discectomy on L4 & L5. Surgery failed no improvement. My Second surgery March 2015 Anterior lumbar interbody fusion (alif) surgery on L4, L5, & S1 with cage implants and bone grafts harvested from my own hip bone. I experience sciatica on my right leg and most frequent on left leg ;shooting pain down my right/left hip/buttocks, goes down the back of the leg. The last 3 years left foot numbness. My worst pain is in bed getting up is very painful. Before my ALIF surgery I suffered from sciatica foot numbness and pain in mostly my left leg region. After 6 weeks post ALIF surgery or so I started getting pain in my buttock/hip region. This actually started during my physical therapy. At first I was doing water therapy this is when it started. My last day of water therapy I was literally about to go to ER from P.T clinic. From there on it just had gotten worst, no real improvement. I went back for more P.T sessions stretching and other exercises . What Physical Therapist did notice that my hip motion was very limited and not much improved happen during all my sessions about 40 or so. Its being about 10 months after surgery and 4 months of P.T. and pain on hips doesn't go away. I have to be careful going up or down stairs. Getting out of bed or moving around in bed its a battle. I have spoken to my surgeon and he says it will take more time for recovery and possible have to live with this pain as a fact of life. I have also spoke to other doctor s and pretty much same response. Once thing I just found out recently is about Hip Bursitis. I was diagnosed with Arthritis. My surgeon keeps on saying its my Arthritis causing pain but prior to ALIF surgery I never had this buttocks pain , specially getting in and out bed. I was wondering if anyone has had same symptoms after spinal fusion surgery having Hip Pain From Arthritis or Hip Bursitis?
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I have been suffering from nerve pain that ran down my left arm and shoulder and fingers from a bulging disc in the C-5- C-6 so i had been taking oxycodone 10-325 but when we decided to do surgery we cut that down to oxycodone 5/325 since that is what the surgeon would be giving me after surgery so i said okay no problem. I had surgery on 2/26 of this year, But after surgery come to find out he dropped me to a hydrocodone 7.5/325 and can't understand why the 7.5 hydro's weren't working to take away the pain. I had been having a lil bit of pain on the right shoulder before surgery, but nothing like what i had been having in the left so the surgeon side well "let's hope this will fix this side too" well it didn't. In fact it made the right side worse, I now feel like i have a hot knife twisting at the base of my neck whenever i turn my neck to the right or left, which in turn runs down into my shoulder blades and into my right shoulder which makes my shoulder feel like someone it trying to tear my shoulder off at the cuff along with weakness in my right arm which i never had before .. I have also started to notice a tingling in my right pinky finger and ring finger. I have told him over and over about this but all he does is get the X-rays and says the fusion is looking fine. and my primary can't do anything since he told her he would treat my pain for 6 weeks and he is refusing to do anything about the pain what so ever. i am to my wits end and any advice would be welcomed.
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About 2 week's ago I took 2 perc within a night and the next day I got sick, I thought from the pills, but than I was nauseous and have been for the most part ever since. My left side mid to lower back started hurting approx a week ago and it's gotten much worse last night and now I'm having pain in my upper right abdomen as if the pain moved. I'm on muscle relaxers for my back already but it's not affecting/helping my new pain though and the new pain doesn't feel the same. I was just curious if anyone had any idea what it might be, some say kidneys but does that pain or can it move from my back to my abdomen?
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I keep seeing instructions to use a cane on the opposite side from the knee that has been replaced. Just wondering why. I have been using my cane in my right hand for years, and my right knee is the wobbly one. Now it looks like I will have to retrain myself to use the cane in the left hand after my surgery?
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I recently had a CT for another issue, however the CT showed a 6 cm cyst on the left ovary and a 3 cm cyst on the right ovary. I have had a lot of lower back pain, side pain, abdominal pain and constipation. Should I be concerned??
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Why am I in so much lower back pain, left side and my bladder hurts, I've had a vaginal hysterectomy and posterior repair. It can't be a water infection as I'm just finish the a course of antibiotic. Really fed up now. Is anyone else the same?
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For about 1 and a half years I have had constant stomach pain; from a few hours a day to whole days at a time. Some days the pain is bearable but other days I literally cannot move and have to go on my hands and knees to help shift the pain.
The doctors firstly diagnosed me with an acid issue and prescribed Omeprazole. This medication did not help me at all.
I was referred to the Gastroenterologist who done some checks and blood tests and thought it may be a bad case of IBS.
I have taken numerous IBS medication which has also failed to work for me. I am on Tramadol and Co-codamol to help relieve the pain but it only lasts so long.
Often when I get these stomach pains I get cold sweats and a temperature with nausea. The doctors are determined that the issue with IBS with acid issues but I don't have any of the symptoms of IBS besides stomach pain and no certain foods seem to bring the pain on.
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My last back surgery was a T12-L5 fusion to correct scoliosis. I would say it's a failed back surgery because my back is so weak I must use either a cane or walker most of the time. I have constantly had a burning pain in my groin and lower back for which I take oxycodone and use ice to relieve the pain.
Now the question: for more than a year (the surgery was 2 years ago) I have had swelling with fluid around one of the T12 screws. X-rays were done then and again the last of May and both show the screw has backed out somewhat but is still intact. In fact, the more recent x-ray is exactly like the first one, so it seems it isn't moving. My neurosurgeon said he could remove the screw and cut the rod down if I wanted him to. At the time, I said, "No, not yet." That was a couple months ago. However, the edema is getting larger, moving to the right side of my spine and moving lower. It's also getting almost impossible to get a good seating position because of it.
Sorry to be so long about this, but I'm wondering if any of you have had this problem, and if so, what did you do about it? At the moment, I'm facing a total shoulder replacement surgery in 2 weeks, and then possibly eye surgery after that, so I can't do anything soon, it seems. Just trying to see what my options are.
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Would like to ask about anybody's experiences of side effects of Atorvastatin (as oppose to Simvastatin) I think the latter is mostly prescribed because of it's low cost - the one I am on is rather more "up-market" and I particularly requested to change from Simvastatin, and was "lucky" because it is far more expensive and considered the better drug of the two. However, like so many of your experiences on this forum - I can relate to almost all of them. I am breathless to the extent where I have to sit on a kitchen stool to carve a joint or dish up a meal I have leg pains, back pains and every other B***** pain!
I also suffer with anxiety disorder which the side effects of statins do nothing for that!
Please let me know if any other patients have problems with these ghastly drugs - I have stopped mine now and will tell the Doc when I go next week! I have missed about a week's worth of pills, but have not yet noticed any difference! Does anybody know how long it takes for the drug to leave your system?
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8 weeks TKR. In the last week my other knee & ankle has become slightly painful. Op knee, fine just a little discomfort when I get up in the morning, soon goes away.
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I had my surgery a year ago and just within the last few weeks my unoperated hip has been causing me a lot of pain. I've been walking 3 miles 3 times a week and with my limp it becomes painful to the point that I have to stop and sit down before I can continue. My hip is almost bone on bone and it hasn't bothered me too much but since the surgery it has been causing me pain. My doc said to continue walking because it won't deteriorate the hip any faster.
My operated hip is fabulous.
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I am almost 2 years post op from an L5 - S1 spinal fusion. I had three surgeries in 9 months before the fusion. I have never been 100% since. The pain is not as severe or crippling, but there is much that I am unable to do. I cannot stand for more than 20 minutes, cannot walk around for more than 30 minutes and have to alternate sitting with laying down. I take Vicodin 1-2 times each day for the pain. I also have numbness in the left foot from the middle toe to the pinky and around the outside of the foot to the heel. My concern now is that I hear a "clicking" when I get up from sitting or lying down. I live in Minnesota and the winter is brutal! I suffer more with extreme cold and damp weather. Is this something to be concerned with or just another item to learn to accept? Is it possible to have an MRI after a fusion?
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Took Binosto (similar to Fosamax) for a few months beginning this past December. Was feeling well at that time. Since then, began experiencing terrible lower back pain, gas, lower left ab pain and have had a cough for a few weeks. I think that sums it up. Went to my doctor and told her everything. She checked me out. We decided to stop the Binosto thinking it could be causing these symptoms (don't know about the cough, though). She said to give it two weeks to get out of my system. It's been two weeks now and I still feel like crap! Could it take longer than two weeks to feel better? Maybe a month? Two? Do you think it could be the Binosto? I was feeling fine before starting it!
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I have had ongoing pain for the past 2 months, worse when breathing in on the right side of my chest. My doctor has diagnosed pleurisy and said it should resolve on its own. I have now developed a very sore collarbone on the opposite (left) side. Could these two symptoms be related? I have health anxiety and am convinced I have terminal breast cancer....silly I know!
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My L4-L5 synovial cyst that I had removed two months ago has recurred again - this was the 2nd removal, so I've now grown 3 synovial cysts from the same dysfunctional facet joint.
One surgeon has recommended removing the bad facet joint which is causing the cysts and doing a microscopic fusion just at that level on that one side. I have no instability and no back pain issues elsewhere, so this is sounding like my best option, and not a very extensive surgery. I was wondering if anyone has had a fusion with a facet joint removal and how it worked out.
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Having dealt with lower back pain for 20 something years and having had all the therapies the doctors could throw at me (traction, aqua therapy - read hot tub- inversion table, multiple PT sessions, electrical stimulation, po narcotics, epidural steroidal injections and more). It has now come to the point that surgery is the next option.
My spinal surgeon wants to fuse L2 to the sacrum due to multi-level disc bulging and herniation at the end of April 2014.
Then people have steered me in the direction of what Laser Spine Institute can do and I actually have approval from insurance to have treatment there and the process of getting treated there is also underway parallel to the above mentioned surgery.
So my dilemma is what to do. LSI offers what seems to be a minimally invasive, faster recovery option, but with newer technology that is not necessarily proved to give long lasting results.
On the other hand a full lumbar traditional fusion statistically gives relief to 30%, 30% get worse and 30% stay the same as for pain relief and with a 3-6months recover. And once you get fused like that, you paint yourself way into a corner if it is not an improvement for you.
The traditional surgeon does not have much good to say about LSI, but I am thinking of course he is not going to recommend that since he does the traditional approach.
Doing the LSI treatment does not exclude a traditional fusion later, however we have great insurance now, with great short term disability coverage and now is the ideal time to do a traditional fusion and be able to have the months of recovery without worries.
Reading about LSI people have varied opinions, many people say they have had great results and others say they are a quackery out to get people's money. Our insurance have said they would cover treatment though.
Don't know what to do.
Does anyone have experience with someone getting lumbar spine treatment at LSI and what was the experience.
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I had an l4/l5 fusion 11 weeks ago. During the day I'm doing really well. Starting my phased return to work and going on my exercise bike. Have little discomfort during the day other than if I reach incorrectly or sit for too long etc.
I am really struggling at night. As soon as I get into bed in any position I am in immense pain. I struggle to sleep and wake up constantly through the night. My physio has changed all my exercises to ensure nine involve laying down so at least now I only have to worry about night times.
Has anyone else had this problem?? Anyone got any advice?? Am taking ibuprofen during the day and codydramol at night but doesn't seen to help.
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I have been out of work since oct 5th 2015 i had sinus surgrey done then had high blood pressure coming out of surgery kept up with the family doctor they refused to put me on bp medicine they sent me for an ultrasound to check the kidneys and they found out i have gallstones and then a week later i was in the ER with horrible stabbing pain in my back and right side loss of appetite and nausea and when i would eat i would take a couple of bites and then i would feel full right away they did another ultrasound and then they found out that i had a kidney stone i passed that kidney stone but still are having the stabbing sharp dull pain in my back and right side, loss of appetite, nausea, when hungry i take a couple of bites and then i feel full and sick, and i started getting chest pains and the pains hurt worse when i breathe and also am constipated. They just did a CT SCAN but haven't heard anything yet on it. Could it be my gallbladder or could it be something else?
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I had back surgery in March 2013 that left me with mechanical instability, acquired spondylolisthesis and lots of pain.
I have 2 ortho spine surgeons telling me that I need a bi-level spinal fusion surgery to repair the damage, but after the botched first surgery, the thought of another surgery scares me to death. Plus, since surgery is what spine surgeons do, the recommendation seems obvious.
I also started seeing a new pain management doctor (we moved to a new state) and he is suggesting that I consider a spinal cord stimulator trial, with surgical implantation if we find that it helps the pain.
So...I'm left confused. I see the positives and negatives of each, but I'm just not sure if one makes more sense over the other. I think that my spondylolisthesis will worsen over time and could pose a threat of nerve damage, while the spinal cord stimulator is designed to mask pain and does nothing to address the instability.
I'd love to know if anyone else has faced a similar decision...or has thoughts, ideas, comments, suggestions for considering one over the other.
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