Buttocks / Legs Pain - Sciatic Nerve After Foot Surgery
Feb 20, 2016
Did anybody have problems with nerve pain in their buttocks and/or legs especially the sciatic nerve after ankle/foot surgery? I am almost 5 weeks post op and I'm having pain in my left leg starting in my left butt cheek. I had a lot of work done on my left heel such as lengthening heel cord and cutting heel bone and shifting it. My heel has not been healing well. Doctor has me put clean bandage on everyday and then wrap it with ace bandage. He also put me on antibiotic. My heel does hurt.
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After a L5-S1 in October, I am left with residual left foot and partial leg nerve pain. In addition to numbness, my leg aches. My MRI looks clean, but neurosurgeon referred me to neurologist for possible nerve root injections. He also suspects the it may be radial sympathetic nerve issue. If nothing else, he's willing to take hardware out to see if that helps. I keep falling with my left foot so "numb," so I am frustrated. Is the device that scrambles pain. (can't think of it now) good for nerve pain? (Pain extends to my left lower back.) Has anyone had nerve blocks for nerve pain? I wouldn't have had surgery if I had known my mobility would have been compromised so much.
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Lisa here...Before my S1-L5 fusion, I had some foot pain caused by waiting two weeks to have a laminectomy/discectomy in my L 4 and 5 discs after a herniation (5 years ago). After my fusion - about 7 weeks ago - I have had terrible burning pain, sensations that feel like I am being bitten on a toe or have tape in between my toes. At night the pain is worse. Walking intensifies the pain and weakens my ankle and leg. I can't wear any of my shoes. Does anyone have any experience with this? I've called my neurosurgeon and he wants an x-ray. Suggestions? Comments?
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I had foot surgery 8 weeks ago - quite a major reconstruction that took a few hours.
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when the plaster was removed at 6 weeks I was told that I had nerve damage causing partial foot drop and a lot of numbness and pain. I have just had nerve conduction studies and have started on Gabapentin and physio..
They said either the tourniquet or nerve block has caused it. I can't believe that this can happen, surely they know about these nerves and how to prevent problems.
Has anyone else experienced this and what has the recovery been like. I'm just wondering what my life is going to be like from now on.
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.
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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?!
I had double bunion surgery 7 months ago. With my right foot the pain is making it vert hard for me to get my foot flat onto the ground. I have had xrays and a scan and that show everything seems to have healed ok however due to the pain I am walking on sides of my feet this is causing other issues with alignment etc... So I am off to have a nerve block put into my back to help with this and hopefully get me walking. Sometimes talking to the surgeon is difficult as he does not really know what is going on. Has anyone had a nerve block put into their back for the same sort of reason and if so how was it done and did it help?
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I am a 20 year old female. for the past 8 months i have had pains in my legs shooting down from my buttocks to my knees in both legs but is worse in my left leg but only while I'm sitting down and after i sit for 10 minutes i start to get pins and needles in my left foot and it is starting to happen more frequently and more painfully as time goes by it makes it hard to drive anywhere and painful to be sitting down. I have had a full spinal MRI and my spine is normal.
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i feel like I'm always sick and when i get a cold/flu it never goes away at the moment i have a cough sore throat headaches which i have taken antibiotics for and it went away after 2 weeks of antibiotics but as soon as i stopped taking them it came back even worse. I am constantly yawning and tired.
I had a blood test and my WBC count was low 1.6 but everything else in the test came back normal negative for arthritis. The doctor has said to have another test but he said the low WBC count is most likely just low because of a virus?I have also been loosing hair. It is all making me stressed so the hair loss could be because of that but i don't know are all these symptoms connected? Could the pins and needles and pains be from lupus or another autoimmune disease? i am sick of going to doctors and spending money on MRIs which are useless.
I had ankle surgery to repair my medial malleolus back on May 8. It was fairly routine--just 2 screws. I was in a cast for a week, then was put into a boot but told to treat it like a cast--NO weight bearing for 7 weeks, keep the boot on 24/7 unless in the bathtub. I followed directions religiously.
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I did notice that when I pressed on certain areas of the foot, I would feel a sharp pain. This occurred in the heel (from the bottom), toes (again, from the bottom, primarily the foot pad below the pinky, second, and 4th toes). When I asked the doctor about this, he said (around week 5) that it was just because I hadn't been using the foot.
The problem persisted, and this week, week 7, I was cleared to start partial weight-bearing--walking in the boot while taking approximately 1/2 the weight off my foot via the crutches. I don't have ankle pain to speak of (or at least, not often and only if I overdo it), but I have terrible shooting pains in my heel and toes as I step. It's OK if I take most of the weight on the crutches, but as soon as I go to more than just a little weight on the boot, the pain starts.
This week I also started PT and the therapist told me this is nerve pain--not uncommon after surgery (don't know why the doctor couldn't have told me this, but OK). I couldn't get much of an idea from her how long this will persist or if there is anything I can do about it.
I'm doing my ankle and leg exercises (those are mostly non-weightbearing at this point) and they are going great. The ankle is clearly healing well. But I don't see how I can progress to full weight bearing (supposed to try that next week!) when much more than a little pressure on the foot results in this nerve pain!
Help! Does anyone have experience with this? Is there anything I can do to speed things along? I need to return to my second job (barefoot hoof trimming for horses--how I broke the ankle!) ASAP and I'm fearful this will slow my progress to a crawl! The doctor is useless.
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 will be having PTT surgery(calcaneal osteotomy, lateral lengthening, gastroc recession, tendon transfer) next week and am wondering about your experience with the nerve blocks, in my case a popliteal nerve block. The research from my OS's office shows 13% have residual nerve pain following the block. Most of the posts here show that patients are very happy they had a nerve block for their surgery. Has anyone had residual pain from one?
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6 weeks ago I had foot surgery (modified brostrom procedure to tighten up ligaments near ankle, and a procedure to correct a calcaneonavicular coalition). I have on incision along my ankle, and another incision on my foot. My cast came off 3 weeks after surgery. 5 weeks after surgery, when I was changing my dressing, I saw some some black stitches from the ankle incision on my gauze pad. I called the doctor's office, and the medical assistant said that that was normal. After that, I noticed drainage for a few days when I changed the dressing. I called doctor's office back, because my foot was feeling hot and I was having a burning pain. They put me on an antibiotic (keflex). And I was told to stop walking and go back to non weight bearing. They told me not to clean the incision. I have only been on antibiotic for 3 days, and it is a 10 day course. In the evenings, especially when I am in bed, I wake up because there is so much pain in my foot, it feels like a deep stabbing pain that is sharp, and sometimes burning. Is this normal of a skin infection from an incision? Could it be a bone infection? Or nerve damage? How patient should I be with this doctor and doctor's office?
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I am 7 1/2 weeks post of from Flat Foot Surgery and the outside area of foot from where my incision ends from the double calcaneal osteotomy up to my little toe the soft tissue is halfway numb and very painful. Has anyone else experienced this and if so how long did it last.
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I am not sure how long it takes the soft tissue to heal to a point where it does not hurt when you are not walking. Or is what I am feeling nerve pain. I started PT this week and am PWB. My doctor thinks I will be in a shoe in 3 weeks and I don't know at this rate how that could be possible. I am icing a majority of the day for sure after I do my PT exercises.
It has been quite a while since I have been on here. I had surgery on Mar 14 to repair a tendon and release the nerve that runs on the top of my foot. I have had severe nerve pain since the surgery. I could only get so far in rehab - because of the severe nerve pain. I had a cortisone shot about five weeks ago - it was somewhat helpful. I can finally let a sheet rest on the top of my foot.
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However, it is my right foot. It is extremely painful to drive - and basically impossible for me to be able to drive more than 25 miles without pulling over to alleviate the pain from the nerve. I still cannot wear anything more than sandals as I cannot let anything touch the top of my foot. Now mind you, it has improved some. It used to be the entire top of my foot. Now it is mainly the toes and about 3 inches up from my toes - it is so severe it has put me in tears more than once. I have been living with some friends of mine - about 25 miles from where I work. The problem is that I own a house about 52 miles from work - one way. There is no way I can drive that far - and don't think that will get better anytime soon.
I see my surgeon again on 8/16/13. I am willing to try another cortisone shot - but someone else has strongly recommended I cut the nerve to alleviate the pain. If he cuts the nerve - I will not have any feeling on the top of my foot for the rest of my life. I have asked him if I would be able to drive, etc....and he commented that cutting the nerve might actually make driving/pain worse?
It started 9 months ago with a back pain, got diclofenac from doctor, then got sharp pain down left leg, went back and he said just take the diclofenac. It didn't improve so went privately to a physio, he said I was rotating my leg so sent me to a podiatrist and I paid £300 for insoles but they didn't do any good. Went privately to a chiropractor and osteopath -no help. Finally after another 6 weeks I went to NHS physio and he thought it might be a disc, had useless exercises to do while waiting for appointment with consultant then waited for MRI scan then another 2 weeks to see consultant. Diagnosed with 2 large prolapses, one of which is completely squashing sciatic nerve. In a lot of pain and can't get much sleep. Still working as don't want to lie around bored at home all day, luckily it's a part time sitting down job. Consultant says I can have op if I want but I've decided to try pain clinic first as he said it will get better eventually, so will try epidural steroid injection in 2 weeks time. Fingers crossed, existing on co-codamol at moment, others have side effects.
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I am 7 and a half weeks post op after a Lapidus & an Akin procedure. I was in cast until last week and have managed a tennis type shoe and a sandal on so far.
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The swelling has been bad as expected with full weight bearing, but the real pain is in the ball of my foot and my big toe does not lie flat, but rather sits elevated. I think the ball of the foot under the big toe is swollen so that may be the cause? I can only walk for a few minutes properly before the pain becomes too much and I am limping and walking on the outside of my operated foot. I can usually cope with pain so know this must be fairly severe.
I am doing my toe bending exercises and think that already the range of motion is not too bad.
I am nearly 6 weeks post op decompression of L4-5 and have severe nerve pain returned in both legs. Up to now all I have been told is it is early days, but as time goes on, it is getting worse. Has anyone else any experience with this problem. I can't get an appointment with the surgeon for another 6 weeks and am getting very frustrated.
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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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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.
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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.
I am on week 4 after my surgery. I am wondering if there is anyone that could give me some hope. Right not walking of going PWB on my foot seems like light years away. I am having severe nerve pain and my foot still brings me to tears on occasion. I am taking Ibuprofen to help with the pain and down to two Percocet a day. When did you notice a huge improvement in your pain and will the pain be mostly gone by the time I go into my boot.
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I have had lower back pain for years. It always gets worse when lying down for long periods or bending over for long periods. I've also had sciatic pain in my left leg for years. It comes and goes. Recently I have started to get the same pain in my right leg. The sciatic pain as gotten severe. I also have some other new symptoms. One new symptom is searing pain in my knee sometimes when I'm standing or when I bend my leg all the way in. The other is sharp pain in my pelvic area. Are these connected? Can you please possibly tell me what is going on? The only notable health history I have is ovarian cysts.
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I've been reading older messages regarding this topic because i have been having this problem since my surgery in September 2013! Doctor has no idea why i'm still in pain and my physio therapies don't get nowhere. So i'm a lot desperate! Can anyone help me, pls? Is it sesamoiditis? Is it tendonitis? Who has experienced any of these and can advise me what to do?
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