Severe Foot Pain After Microdiscectomy L5-S1
Jul 25, 2015
I had a microdiscectomy almost 4 weeks do to the disc pinching my sciatic nerve. The pain before the surgery went from my left butt cheek down to my foot, and felt like someone was sticking a knife in my hip and calf. Since the Surgery I have had severe nerve pain in my left foot in the ball of my foot to my toes. I am currently on gabapentin pills and gabapentin cream. I was just looking to see if anyone had any ideas what could help get me off the recliner. Or any ideas whether this would go away or how long this usually lasts.
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I have pretty severe Achilles pain in my left foot. The pain is most severe in the morning, and it clicks all day and I have never heard the 'pop' that other people talk about.
Guessing its not a full rupture however it is really limiting in what I can do. I have been to the GP surgeries and clear for several occasions I am a Due for a ultrasound scan, but the whole process is taking really long I haven't been able to do sports since October.
there are many of you who have suffered with the same pain, do you have any advice as I am at a loss and it's getting quite depressing.
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I just had a lumbar microdiscectomy yesterday on the L5-S1 disc. Right after I woke up and got up to walk in hospital I noticed the bottom of my right foot feels asleep. I never had this problems before. The reason why I had the surgery was from sciatic pain down my right leg going into my calf. I have had back problems with a herniated disc for 2.5 years. My latest flare up was sciatic pain for 3 months straight, I had a spinal injection, was in physical therapy, on pain meds and had no relief. I finally made the decision to go through with the surgery. My leg pain is completely gone, back incision hurts, but my main concern is the bottom of my foot is numb. Has anyone had this problem? I called the spine surgeon this morning and waiting for his call back. I was unable to speak with him after surgery because I was his 4th surgery of the day, he spoke with my husband when I was in recovery.
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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 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.
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.
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I had a microdiscectomy back in December 21, 2015 right before my 18th birthday ( today marks the 4 month post surgery mark ). I still have pain running down my right leg ( upper glut and sometimes in my calf muscle ). Before the surgery I have had the disc pinching on my nerve for nearly 10 months.... It ruined my summer and I couldn't do what most of my friends were doing... My parents were too scared that something would go wrong with the surgery, so we tried Physical Therapy for about 2-3 months. My pain was getting worse and worse. After a lot of convincing I got my parents to allow me to get the surgery ( No regrets at all ). I would rate my pain before my surgery as 9/10 and now after my surgery I rate it as 5-7/10. I can't even remember how it feels to have no pain... It is constant and doesn't go away ( I feel better when I lie down on my back or stomach ).. I feel better when I sleep on the ground rather than on my, what used to be comfortable, bed.... I am starting to lose hope on ever feeling better... Everytime I walk I have pain in my upper right glut ( every time I extend my right foot ) and sometimes it goes down my right leg to my calf.... I still can't bend down without a massive amount of pain running down my right leg... I can't even sit down for longer than 30 minutes because I start to have a lot of pain in my calf, which makes going to school really hard.. Are there any patients that have had this type of surgery and felt better in more than 6 months?
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I had L4/L5 microdiscectomy and laminectomy about 4 months ago. I had on and off low back pain for 6-7 years but it became unbearable couple of years back. Prior to surgery I had buttock pain and I couldn't walk or stand without pain. I am recovering pretty slowly. I am off pain meds and I walk 45 mins a day and do gentle back stretches as advised by the surgeon. The surgeon said that I had a big herniation and he removed about 60-70% of the disc. Is it common to have that much removed?. Will I be able to recover fully or will i need more surgery like fusion in the future. I am just 27 yrs old and I don't want to live in pain.
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I am early on after my discectomy (day 3), but I am concerned. I see many people have immediate pain reduction, I woke up and still had my preop pain. Now it's just pain deep in my thigh and the surgical pain. I am also worried because I still can't stand up straight! I haven't been able to stand straight for two months following a car accident that reherniated my l5s1. The original injury was resolved to an acceptable level without surgery. It was interesting that the car accident immediately stopped all nerve pain in my right leg that I learned to live with, but it moved to the left leg!
I am just getting concerned since I see so many posts where people wake up painless and can walk freely. I can walk for maybe 2 minutes then i am in really bad pain, and i'm hunched over while walking. Should I be concerned? Any insights from people with less than storybook recoveries?
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I am currently 8 weeks post op from a very extensive flat foot reconstructive surgery . I was excited to start partial weight bearing this week starting w 25 percent in a boot.
My problem is I have sharp pains coming from the bottom of my heel which I am thinking may be from the screws from the calcaneal osteotomy. This is making it very difficult to put any pressure on my foot when weight bearing ?
Has anyone experienced this ? Did it go away on its own? Was there anything that helped this . I am afraid I will not be able to proceed the wt bearing with this continued heel pain.
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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.
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.
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I'm 5 months post op, Is they any light at the end of the tunnel for me?
I'm still in pain especially my right calf, feels like constant cramping.
I can walk ok, as soon as I stop I can't stand up straight due to my right leg feeling very tight.
It was a herniated disc at l5, s1 nerve.
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Week 5 post microdiscectomy on L5/S1. Numbness and pain on my leg and toes is gone BUT currently experiencing numbness and sharp shooting pain on my left testicle making it difficult to have an erection.
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I have suffered with plantar fasciitis in my right foot for about a year now.
It originally started after a knee operation and a torn calf muscle after an accident.
The pain in my right foot is so unbearable that I opted for a steroid injection last year. I watched some of the youtube videos to see that some numb the area first then inject.. Not my GP...Straight in with the steroid and it was so painful I kept saying "Oh my god oh my god". Well it didn't work and I know that I will NEVER have another one. The pain is more than before.
My left foot has now got a pain across the top of the foot.inferior extensor retinaculum I think it's called.
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It is my right foot only. Heel pain, and basically all of my foot. I wear inserts plus an extra heel cushion. I been to the foot doctor and gave me a antibiotic and he recommended icing and heating and stretching bottom of foot. Any other suggestions?
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I had PTTD reconstructive surgery on Feb. 24th. I am still NWB and in the hard cast.
I have been good about icing and elevating, and now the swelling is rarely an issue. However, now that the cast is much looser, I am very aware of the feeling that my foot is turning inwards... as in...It feels like i'm "standing" on the outside of my foot. If I prop the foot up so that the bottom of my foot is all fully touching the bottom of the cast, I have significant pain along that outside area from what feels like right under my ankle to just below the ball of my foot. Is there any chance that I am healing "crookedly" due to the cast being loose? Although I can't put weight on it, just straightening my leg completely will cause that "rolling out" and pain.
On an unrelated note:
Is there anything that I can do for nerve pain at this point in my recovery? I am no longer taking the "heavy" pain medication. I am just taking Advil and Tylenol. I am finding, however, that these do nothing for the nerve pain. Is there anything that I can do besides going back to narcotics? I'm wary of taking them for too long, but the real issue is that I would rather be clear-headed.
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I'm a long time sufferer of low back pain (20 years, I'm 42). I believe I've given my diagnosis & previous treatment rundown on a previous post, but I'll post it here again, hopefully short and sweet:
Last MRI (Feb. 2012)
Bulging L4-L5, Herniated L5-S1 (Central Annular Tear, 6mm protrusion)
Previous MRI in 2008 showed basically the same as above.
I have tried most therapies & treatments, including but not exclusively:
Acupuncture, TENS, PT, ESI in 2008 & 2012, Prolotherapy, Mackenzie Stretching, Chiro, Massage.
Some of my main activities that I've had to scale back to, and serve as productive exercise:
Walking everyday, inversion table, swimming, Mackenzie stretching.
I used to do martial arts and grappling and have not done so in a couple years now.
I have a hard time now with doing things that I HAVE to do, like working around the house or sitting in my car to drive to work as a couple examples. I cannot do any type of sports that have ANY kind of flexion movement. (I'm able to swim because my back is in extension position)
I've been reading some posts regarding folks who've had the microdiscectomy procedure done, and I've met with many neuro and ortho surgeons during my long journey. I've also begun to research BMSC treatment as well, as this is proving to be very promising, but is still in the very early stages of acceptance and use in the States. I've always opted to not have an invasive procedure because of fear of it not helping and possibly making things worse.
However, I'm just tired of the conservative approach not working and I'm tired of not being able to fully live my life.
Believe me, I understand there are many that are worse off than me and I wish I could help you because I know how bad chronic pain is and what is does to you physically AND mentally.
All the doctors I've ever seen look at me (at 5'9, 150 lbs, lean and "looking" healthy), and I pass all the "strength" tests they give me. They tell me to go conservative, which I fully respect. However, just because I look healthy and can pass them pushing on my legs and feet while I resist, and I'm not losing bladder or bowel control doesn't mean that the slightest move or overdoing it won't put me down again.
Case in point, (After 2 years since my last episode and the walking and my conservative exercising not giving me the progress I'm expecting after 2 years), I decided to, (at the recommendation of a sports med doctor), to go see a well respected and very highly recommended, (by friends), PT Strength and Conditioning coach. He put me through an initial PT type evaluation and I had my first session last night. Well, about half-way through, something wasn't feeling right. We scaled down the workout, (which was pretty conservative already), to just stretching at that point. Long story short, I'm now back to stabbing pain, radiating leg pain and tingling, and standing crooked and not being able to sit down.
I'm really beginning to seriously consider surgery, or possibly explore BMSC treatment for the disc(s). I'm sure since it's been 2 years from my last one, I'll need another MRI before doing anything.
My question is, what would you do if you were in my shoes?
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I have had a lumbar L5S1 mico on feb 14 of this year. Now I am having sharp pain in my back under my right shoulder blade by the T7. Plus this makes my back tighten up and spasm. Any thoughts out there. I know it has to do with the injury but does anyone know what this is... btw not the gallbladder I don't have one anymore. This pain is at its worst when I am lying down and if I rotate to the right side the pain will be so sharp it stops me in my tracks...any help would be great. I also got my S! nerve checked and it is relieved from the surgery but I am left with the numbness in the foot, calf, and upper thigh and also told this might be permanent.
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I'm having a lot of pain on the outside bottom of my left foot. It came on pretty suddenly and has gotten worse over the past three days. It's not that swollen, but I do have very poor circulation to my hands and feet. I now have some bruising on ankle and shin that are specific to the areas that start feeling pain when it really starts hurting. In the morning it feels better but it only takes a little bit of walking for all the pain to come back.
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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.
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?
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I am looking for information on pain, burning, numbness, and kind of pounding on the outside of my foot, it appears to be tender to the touch on the outside and the top half of my foot is numbness.
This problem was first noticed after physical therapy where the therapist was trying to increase the range of motion of my ankle. The problem doesn't effect or bother me walking and it seems to start when I am at rest at the end of the day and it is effecting my sleep. At first icing helped and I guess it still does somewhat, the condition isn't getting worse, but its not improving.
I am recovering from RSD and chronic compartment in my left leg and foot,I had been out of work for six months and have been back for 4 weeks under restrictions, and I am hanging on barely as I am having issues with pain load bearing and extremely tight calf's, when my left calf gets real tight
it gets more painful and my knee feels like it is hyper extending. I really like my job and want to be there and maybe it was to early to go back.
My pain management;
Aleve - Sometime it helps with muscle aches otherwise is useless. I have taken hundreds and hundreds of them.
Norco 10/325 - Helps reduce pain. Can't use at work.
Cymbalta 30mg - Just started taking three weeks ago for chronic pain.
Haven't had enough time on it to report any results. The side effect of drowsiness makes me want to sleep.
Kevin
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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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