Nerve Pain :: Failed Fusion And Broken Hardwar
Jul 10, 2014
I am 10 months post op spinal fusion and hardware revision from a "failed fusion and broken hardware". My fusion and hardware extend from T10-L5. Immediately after surgery i had numbness and tingling in my right thigh and right side of my lower back. Over the past couple months the numbness and tingling has spread completely across my entire mid/lower back. I have constant pain down the back of my left thigh down to my ankle.
Sometimes it gets pretty severe to the point where it is hard to walk and all i can do is cry and try and massage my leg. Also things have gotten to the point where it feels like there is something crawling on my back and its so numb so I cant relieve the itch by scratching because I cant feel it. It is really starting to drive me crazy at times!
Also, I felt that I started to slowly get better. Better movement, more activities, etc.
And I now feel I am going backwards. Is it possible to regress? I am starting to feel very discouraged and all my pain management dr does is keep increasing my meds for nerve pain. How do I get him to listen to me or find the cause of the nerve damage?
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I'm a 38 year old with ankle and foot problems all my life. I was born with flat feet and I was always spraining my ankles. I acquired PTTD/Flat Foot on my left about a year ago and finally was diagnosed by an orthopedic foot and ankle expert. He recommended surgery and after a second opinion I decided I might as well get this taken care of so that I can go back to a normal life of walking through the streets of Europe.
I had my surgery about 2.5 weeks ago and I wanted to lend advice to those about to take on this crazy surgery. Firstly, the morning of surgery when the anesthesiologist was performing the nerve block it hurt like hell and made me even more panicked about the surgery. The relaxing medication they gave me did nothing to settle my nerves. I woke up from surgery a few hours later and I could feel all sorts of shocking pains coming from my foot. I asked if I should be feeling all the pain and they said that the nerve block failed. The anesthesiologist was busy for another hour and so I writhed in pain (crying hysterically) for the hour and vomited multiple times due to the extra anesthetic they gave me due to the failed nerve block.
Once the new anesthesiologist came she figured out that my nerve split into two and the other guy had not seen this split. After she was finished it was completely numb and I was worn out. I was sent home. Over the next day I vomited profusely, found out that I cannot breath when I take Oxycontin, I lost balance and fell on my foot and I was taking anything I could get my hands on for constipation. I finally found the foul tasting milk of magnesia and I can now go to the bathroom every few days.
My pain was managed by a morphine twice a day while in the splint, but now that I am in the cast my heel is killing me especially at night and the dr gave me hydrocodone which didn't touch the pain last night. Is it normal to have more pain at this point?
When will I be fairly pain free and when will I be able to leave the house? I live in Santa Barbara and i have an ocean view so I should not be complaining but i am feeling pretty horrid and ready to get out. When I think about leaving I worry about falling again and having my throbbing leg down.
Am I alone in all of this? Many experiences I have been reading say that after 5 days everything was hunky dory.
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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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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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Ok. So i have broken my fifth metatarsal and have been put into a non weight bearing air cast for two weeks.
Due to the break, the doctor has given me a blood thinner Innohep 4500 UI to take everyday to prevent a blood clot.
My problem is: For the past 3 days my calf (same leg as broken foot) has felt like it's been cramping. Elevating it relieves the pain a little but i am required to attend my courses at University - meaning i'm on crutches all day. Sitting/standing makes the pain increase. The pain has gone from mild to severe; i can almost cry from the pain coming from my calf.
It is extremely painful when trying to stretch any of the muscles in my right leg now, Should I be concerned about a potential clot? (I do not show any of the typical signs i.e. the swelling/heat/redness) Or is this muscle related? I have trawled through the net for similar cases but cannot find anything!
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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 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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Does anyone that has back problems have sharp nerve pain in their groin private area? I have had back problems for years and sometimes would get a sharp pain up my vagina. After a bad muscle strain in my back and using the elliptical machine I've had twitching and burning all over but also in my private area. Like around my **** it will twitch or vibrate, and then I will get the sharp shooting pain up my vagina and around my butt. I notice it more if I bend over that's why I thought it might be my back. I remember when the stabbing pain started I thought it was a female problem and my OBGYN said everything looked normal with my cervix and my paps have always been normal so she didn't know. She seems clueless.
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My 50 year old husband has been a Type 1 diabetic since he was 21. It was a late presenting of juvenile diabetes or so they said then. He has always done well managing his diabetes, wearing a pump for the past 15 or so years. In the past week or so, he has begun to have severe pain/tingling in his feet/ankles - mainly at night when he is trying to go to sleep. He usually has to get up and walk several times before he can finally sleep - he is only getting about four hours of sleep per night. He has an appointment with his dr - but not until the week after New Years.
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i can't cope anymore with the pain! All my nerves hurt neck scapula biceps pain all the way down arm forearm aching hand aching does anyone else have the forearm hand aching pain.
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I have had diabetes for several years now. I have nerve pain in my feet that is usually not too bad and comes and goes. Lately, my left ankle feels like there is a hair being dragged across causing a tickling feeling. Tonight, my right ankle has this sharp stabbing pain in it that has almost caused me to fall while walking. I have medicine for the nerve pain but don't like the side effects so I quit taking it. Could the stuff going on with my ankles be due to diabetes?
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I had DeNovo surgery on my ankle 4 months ago - lesion was 11 x 13. Surgery went well. I was NWB for 6 weeks, then in boot for 4-6 more weeks with PWB. Started PT at 10 weeks and was out of boot at 12 weeks. No problem with recovery or PT until that point. After I was fully weight bearing I had much more pain. On sides and bottom of foot as well as at surgery site. Still have lots of pain and sensitivity if I walk barefoot. PT was successful as far as ROM and strengthening but he doesn't want to push me any further because of pain.
OS says too early to say it did or didn't work, but I think it didn't and he won't do MRI until 6 months. He'll give me pain meds, but I don't like them and don't react well to them. The foot pain is bad! Could it be nerve pain?
I knew this was a long recovery, but I wasn't prepared for this! I ran for 30 years, which could have contributed to this problem, but now I'm wondering if I will ever walk pain-free again?!
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I fractured my 5th metatarsal and sprained my ankle about 5 weeks ago and was given a cam boot walker. I can finally sort of walk on it if i don't put much pressure on the broken part. But man oh man my calf just aches and throbs as if i just ran a marathon, and all i did was some chores around the house. i wonder if i should be walking on it or is the pain in the calf a sign i shouldn't? or is it just cause the muscle atrophied? when does the pain subside?
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I met an accident around 2.5 years ago and broke my left arm humerus. So I had a surgery and "they" fixed it using a humerus plate. After that, I took ample rest and finally my left arm is all good, not 100% but still up to acceptable level ( I do half my job using left hand and the remaining with right, as in throwing ball with left and writing using right hand). A couple of months ago, I started exercising so as to lose some weight, and it finally led me to join a gym. At first it was hard to get in routine with all these gym workouts, but in no time, I got used to it. Now comes the main issue. Since last month, while gymming, my left humerus has started to cause me pain. It occurs only when I am working out using my arms. It never happened before. This worries me now. Apart from work out, I never feel any pain there. Also, the pain is not something that can make me cry, but something, that makes me stop from whatever I am doing. I am uploading a copy of my X-ray as well.
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Just a little background over the past 5 weeks.
I fell over and broke my left humerus 5 weeks ago yesterday. Initial visit to A&E which resulted in X-rays and put in a collar and cuff for the first 4 days.
I then visited Orthopedics and more X-rays taken and put into a Brace.
I was in the brace until week 4, when it was replaced by a plaster U slab as the brace was causing my arm and hand to be considerably swollen. My U slab had to be changed twice due to it moving constantly in this time and in my opinion not isolating the break.
I had an appointment yesterday at Orthopedics where it was replaced yet again, and told my next appointment is on the 18th of December.
My concerns,
Various different stories told as to healing times.
I am 5 weeks since the break, when will they decide if it needs operating.
I am taking serious pain relief which is barely touching it, and causing sickness.
Its seems like i am being a nuisance asking questions or going back to the hospital, am i being paranoid.
I have managed to take pictures of the X-rays every time they have been taken and week 5 looks the same as day 1.
I know Orthopedic Surgeons undergo the same training. I have a problem that my Surgeon is a lower limb specialist. I have asked to see the Surgeon who specialises in my the area of my break, but only to be told that they are all the same.
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I broke my pinky toe and was walking more on my heel. Now the inner edge of my heel hurts a lot with either walking on it or just even pressing on it! Is it more of a bruise (& treat accordingly) or is it plantar fasciitis?
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I have broken my tib and fib -(think it's called a bimalleolar fracture?) I did it on a pair of high heels at Xmas party, stupid or what? I climbed up one step and it was gone over, my future for next however many months mapped out for me I a nano second! I have the usual metal plate and screws like many of you folk in here. I had my cast off on Monday and went to a physio today who advised me to not use the airboot and "try " to use just the crutches in the house and airboot outside. I a m confused as the consultant at the hospital said keep boot on for two weeks then ditch it AND the crutches. I am really confused, I want to push myself but don't want to do any damage. I am so down, fed up and FRUSTRATED? I have been given exercises from the physio man which he said to do every couple of hours and push through the pain as he said it needs to get moving ASAP. My ankle is so swollen, STIFF and painful. I just don't know what advice is the best? I am 49 WAS fit doing spinning, gym, swimming and lots of classes.
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I have recently been diagnosed with EBV. I didn't present with the "normal" symptoms. I first experienced joint pain, then muscle pain, followed by extreme fatigue and muscle weakness. That lasted for about a month, then I developed sharp electric pains in my nerves and associated muscle weakness and numbness that comes and goes in my arms and legs. The nerve sensations have lasted for about 2 months. I seem to be healing
As I haven't experienced as many sharp electric pains, just numbness and tingling. I have been to a neurologist and have had an MRI of the head and neck which came back normal. Has anyone ever experienced anything of this sort of nature? I've been experiencing symptoms from EBV for 3 months now.
It's also important to note I was tested for Lyme and other blood work was done. Everything was normal except the ebv (which showed I had either contracted ebv in the last 6 months or it was.
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I've been having issue with my arm for 6 months now, tingling, numbness, burning in my forearm, hand and up to my shoulder. I also have a stiff neck. It all started with pain in my hand,thumb and wrist while using the mouse (I am a computer IT analyst) and slowly started to affect the whole arm, shoulder and neck.
I have had an ultrasound to check for tendonitis, Nerve studies to check for Carpal tunnel and cubital tunnel and they didn't find anything. I had an MRI of my neck and it's normal apart from some cysts adjacent the nerve roots.
One doctor wants me to see an orthopedic surgeon to have them checked and another thinks they are asymptomatic and aren't the cause of my problem.
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3 weeks I broke my humerus in 3 spots and had surgery to have a plate and screws installed after that I was sent home with a one week prescription to pain meds and I ran out last week so this past week has been hell, lots of pain. I see the surgeon in 2 days any chance he'll prescribe me more meds for the pain or do I gotta live like this for who knows how long?
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I have been dealing with pain in my feet for several years which has gotten progressively worse. The past 6 months or so have been so bad that 3 months ago my doctor prescribed Gabapentin which helped significantly for a brief few weeks, but I am at the highest levels now and there is a new pain in my right ankle that will just not go away. I am weaning off of the Gabapentin so that I can try Lyrica. I am being scheduled for a nerve conduction test to try and determine what is wrong exactly. I am not diabetic. I believe it is from too many years of standing/walking on concrete (I'm a caterer/chef) without proper foot support. My doctor seems to support this opinion, she does not seem to have any answers. Just had blood work done, I am in excellent health otherwise! Am so worried that I'll be unable to continue working. Pain is relentless. Cannot live on pain pills, just do not want to go down that road! Anyone out there have experience with this sort of problem? How about Lyrica?
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