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Headaches and pain following anterior cervical discectomy.
I am 2 years post-op anterior cervical discectomy with fusion to relieve compression on spinal cord at c5/c6 level. Had lots of pain and progressive leg weakness, right arm pain, and unable to write + loss of balance. I have had 18 months of constant neck pain since the surgery, worse in the night and on wakening. Every morning waking with severe headache and pain radiating from back of head to over eyes and sometimes down one side of face. This feels like a combination of nerve pain and a peculiar sensation, as if the bones at the back of my neck are being stretched from the inside.
Finally, after 18 months, the stretching pain has eased but I still have the headaches 2-3 times a week. On my 2 year check with the Neurosurgeon he said the pain could have been due to the titanium cage having been too big and that my pain should continue to improve, or it is just that my body has taken longer to adjust to surgery.
I also still have difficulty swallowing and have always felt that something is pressing against my throat, and I have a weak voice, my arm pain is worse than before the surgery. My legs are now stronger and the neck pain I had prior to the surgery has gone.
Do you think these headaches will go and the swallowing improve. If not do I have any other options. I was realistic about the surgery and did not expect miracles after having had this problem for over 24 years (now 48), but I am finding the pain so debilitating. I have a desk job which does aggravate the symptoms. Also, will there be any long-term effects of the cage being too big.
Thank you
Finally, after 18 months, the stretching pain has eased but I still have the headaches 2-3 times a week. On my 2 year check with the Neurosurgeon he said the pain could have been due to the titanium cage having been too big and that my pain should continue to improve, or it is just that my body has taken longer to adjust to surgery.
I also still have difficulty swallowing and have always felt that something is pressing against my throat, and I have a weak voice, my arm pain is worse than before the surgery. My legs are now stronger and the neck pain I had prior to the surgery has gone.
Do you think these headaches will go and the swallowing improve. If not do I have any other options. I was realistic about the surgery and did not expect miracles after having had this problem for over 24 years (now 48), but I am finding the pain so debilitating. I have a desk job which does aggravate the symptoms. Also, will there be any long-term effects of the cage being too big.
Thank you
After reading everyone's comments I'm freaked. I had ACDwF last November. Everything seemed to be going extremely well until this past weekend. I have no idea if it is related, however over the weekend, the glands under my neck become swollen and I begun to run a low grade fever. Physically I was feeling fine until I layed down Monday night. I noticed discomfort once again in my neck. As of today the pain has increased and is now back in my shoulder and the top part of my arm.
Before surgery, the one thing my neurosurgern couldn't explain was the fact that the nerve damage (and spurs) were on the left side yet all my neck/shoulder/arm pain was on the right. ??? Prior to surgery xrays and MRIs of my neck and shoulder showed no issues with the right side. The right side is where the pain has returned.
I'm not sure if the pain is a result of increased activity or if it stems for other issues. I'm honestly sure sure if I'm up to starting the doctor and xray thing back up to only be told the xrays look fine. Pain meds have always been a last resort for me because I am in alcohol recovery and no better than to tempt fate. However the thoughts of living once again in the pain I was in 24/7 prior to surgery seems even less of an option.
I guess my question is has anyone done okay after surgery to later have the pain return and then the pain leave again?
Is it worth going back to the doctor to be told all has been done or could something else be going on? Which obvious I wouldn't know without returning to the doctor ...
Before surgery, the one thing my neurosurgern couldn't explain was the fact that the nerve damage (and spurs) were on the left side yet all my neck/shoulder/arm pain was on the right. ??? Prior to surgery xrays and MRIs of my neck and shoulder showed no issues with the right side. The right side is where the pain has returned.
I'm not sure if the pain is a result of increased activity or if it stems for other issues. I'm honestly sure sure if I'm up to starting the doctor and xray thing back up to only be told the xrays look fine. Pain meds have always been a last resort for me because I am in alcohol recovery and no better than to tempt fate. However the thoughts of living once again in the pain I was in 24/7 prior to surgery seems even less of an option.
I guess my question is has anyone done okay after surgery to later have the pain return and then the pain leave again?
Is it worth going back to the doctor to be told all has been done or could something else be going on? Which obvious I wouldn't know without returning to the doctor ...
A related discussion, Headache in back left side of head was started.
Angels2halos,thank you for your words of encouragement. I have 4 herniated discs but I'm told only one is causing the neck pain and right arm/hand problems and the bone spurring has to go because it is what's causing the numbness and weakness in my left arm and hand. I'm 43 yrs old and I've had several surgeries including laparoscopy and a c/section. I'm an RN who has assisted in the OR on many ocassions and I'm not normally squeamish but the idea of having my neck cut open and cutting instruments hovering around my spinal column and voice box (I'm a 1st sporano in my church choir) have me more nervous than any other procedure I've dealt with. Not having surgery is not an option though unless I want to continue with this pain and the progression of numbness and loss of coordination in my hands (not good attributes for a nurse.) I'm just so thankful donor bone grafts are available.
I'd like to know what helped the most as far as recovery goes. My husband won't be very helpful (just not in his nature) and my 11 year old son will do what I ask but most of the time I will be alone. Any suggestions on what supplies to have on hand to make the recovery go as smoothly as possible?
I'd like to know what helped the most as far as recovery goes. My husband won't be very helpful (just not in his nature) and my 11 year old son will do what I ask but most of the time I will be alone. Any suggestions on what supplies to have on hand to make the recovery go as smoothly as possible?
Right now I'm wishing I hadn't stumbled on this site. I'm scheduled for ACD&F with bone spur removal on Monday, Sept. 18th. I spent months thinking my neck, back and shoulder pain were caused by incorrectly exercising but when my arms started having electrical current sensations and my hands became numb I realized there had to be more to the story. Dreading surgery, but feeling it would be the only way to obtain relief, I agreed to the procedure. I was certain that after Monday my symptoms would become progressively less noticeable and I would eventually feel better than I have in years. However, after reading the posts at this site, I'm really concerned about the future. Has anyone had total relief from symptoms and return to normal function after discectomy and fusion? Are those people all too busy running around feeling great to chat online? Is it only those of us with debilitating pain who sit at the computer commiserating???
L-Hawk, I have had great relief and the Doc said that it may be just muscle spasms still at my throat. I've also been a little emotionally upset for those few days. I'm very independent and am not able to even pick up my son, this is probably the worst part of the surgery. Recovery seems long at the time, but when your released from the Neurosurgeon as I was yesterday, it seems like it was just yesterday. I do believe that the people that are just fine won't be writing in to here, because they have no questions and are feeling good. Well, I am on here to bring some positiveness and a little advice. I may be only 27 but I'd like to help with any advice and experience I have had.
My Neurosurgeon did not require me to have a cervical collar. I have just lived the last 3 weeks as if I had one on. I think the collar would extend my neck up to far and be uncomfortable. I have one and have not needed it since I asked for it. I also have hardware and everything is still in place and the swelling is, I think gone. So I just wanted to tell the ones that are nervous (rightfully so) that there is hope, don't be to discouraged. I'm really GLAD I went through with it, the before pain was not worth it. A little noise in my throat is nothing, in fact I had posted before that I also had to have Laparoscopic surgery a week ago, and I must say the co2 that they bloat your belly with was more painful than my throat was uncomfortable.
There will definitely be throat pain after ACD, due to everything being moved aside and manipulated. I found it to be worse at night. So, just keep some fluids next to you at all times for about the first week and a half.
If anyone else has any questions I will answer from my experience, I am not a Doc however I like and pay attention to most medical things and have read alot.
L-Hawk and everyone else who is about to have the surgery, keep us posted and let us know how it went. Take care.
Last words (I think) PILLOW, PILLOW, PILLOW that's key.
Don't get behind on pain meds, no matter how good you feel.
Be positive, have someone around, you may feel alone and helpless at times. Don't pick up anything, don't look up, or down, or side to side for a few weeks.
You are all in my prayers.
My Neurosurgeon did not require me to have a cervical collar. I have just lived the last 3 weeks as if I had one on. I think the collar would extend my neck up to far and be uncomfortable. I have one and have not needed it since I asked for it. I also have hardware and everything is still in place and the swelling is, I think gone. So I just wanted to tell the ones that are nervous (rightfully so) that there is hope, don't be to discouraged. I'm really GLAD I went through with it, the before pain was not worth it. A little noise in my throat is nothing, in fact I had posted before that I also had to have Laparoscopic surgery a week ago, and I must say the co2 that they bloat your belly with was more painful than my throat was uncomfortable.
There will definitely be throat pain after ACD, due to everything being moved aside and manipulated. I found it to be worse at night. So, just keep some fluids next to you at all times for about the first week and a half.
If anyone else has any questions I will answer from my experience, I am not a Doc however I like and pay attention to most medical things and have read alot.
L-Hawk and everyone else who is about to have the surgery, keep us posted and let us know how it went. Take care.
Last words (I think) PILLOW, PILLOW, PILLOW that's key.
Don't get behind on pain meds, no matter how good you feel.
Be positive, have someone around, you may feel alone and helpless at times. Don't pick up anything, don't look up, or down, or side to side for a few weeks.
You are all in my prayers.
I also wanted to add, a good pillow is key to being comfortable. I go into Neurosurgeon today, hopefully I find out what is wrong with my throat. Good Luck to anyone that is about to have this surgery. Don't set your expectations too high, too quick.
Hello, i'm 27 yrs old and 3 weeks post-op for ACDw/fusion. Everything seems to be fine, I had lots of unrelieving neck pain for 9 months before I found out I had a ruptured disk causing spinal cord compression and swelling. 2 1/2 months before surgery it started affecting the muscles in my neck than to serious pressure headache for a month. That headache is GONE:) My problem right now is that I feel like there is something poking me in my throat sometimes. I'm also the only one who makes my house go-round and have a 7yr old daughter who is a great help with my 20 month old son. I don't have the support that I once thought, or wished that I had. Two weeks after surgery I had to have unexpected, emergency laparoscopic surgery. I don't think that i'm enough rest and relief from everyday life, could this be the reason for the throat problems (stress)? Other than that, I feel good.
Thanks,
Angels2halos
Thanks,
Angels2halos
After living with horrible neck pain for years, about 2 1/2 years ago I had a partial discectomy/laminectomy of C6-C7. The surgeon removed the bulging disc material and stitched up the rest of the disc, and cut-out the back of the verbrae to make more room for the spinal column (this is what a laminectomy is). What I didn't know was that a laminectomy would lead to an unstable spine. A few months ago at work I was inpecting plumbing and was in an awkward position and came up fast and hit my head hard. Immediately I felt the burning pain from my forehead, to the top and back of my head, down my neck, shoulders, and arms. I tried seeing a chiropractor for a few months - no lasting relief. I went to a Ortho Surgeon who sent me for an MRI. After reading the MRI it was apparent - when I hit my head it caused C6 and C7 to collapse into each other and they are rubbing against each other, and the disc is completely blown - and compressing my spinal column. I also have four bone spurs at that area due to the bones rubbing against each other. I am now scheduled to have a Discectomy/Fusion of C6-C7 in a couple weeks. What makes me angry is this: if my first surgeon had just done a FUSION with the Discectomy/Laminectomy - I wouldn't have had spinal instability and wouldn't be in the predicament that I'm in now. Beware of a laminectomy - it leads to unstable spine and possible future spinal surgery.
In October of 05 I visited my reg doctor due to migrains which I developed and lasted for weeks. This was my 2nd time in experiences these over this type of duration. I also explained that I had pain in my shoulder area, and numbness/tingling in my right thigh. He refered me to get a CT Scan and to follow up with a Neurologist. The Neuro refered me for a MRI on my L-spine and to see a EYE specialist. My CT scan came back normal. The eye specialist refered me for an MRI of my brain and orbits - normal. I did not follow up with the eye doctor. L-spine showed DDD at multi levels and was refered to a neurosurgeon and a EMT of my lower. The surgeon refered me for anther MRI of my R shoulder and C-spine as well as a EMT of my upper. I was also refered for PT but prior to starting it was canceled prior to starting upon the results of my MRI/EMT.
I had a 'Anterior Cervival Fusion with plating on C5/C6/C7 in July of 06. This surgery was performed for several reasons; Severe DDD in those areas, compression of the roots and Edema of the cord at C6/C7, spondylosis with myelopathy, cervical radiculopath, ect, ect....This is all due to bad genes, I did not have any injury that I can directly relate any of this to. I had a 2nd opinion prior to surgery and was told the exact same thing - recomended surgery to relieve the pressure on my cord/roots and to hopefully stop the pain which it causes. I had all the tests; CT Scan of my head; MRI of my brain, orbits, L-spine, C-spine, and right shoulder;EMT on my upper and lower extremities.
I am 7 weeks post op right now and still in my Aspen collar for another week. I was out of work for the first 4 1/2 weeks after surgery and have now been back for 2 1/2. The time I was off work I had ZERO pain and symptoms which I indured daily pre op. I am an automotive designer working at a desk on Unigraphics (software) on a 40 hour schedule - 8 hours a day. My pain and symptoms are BACK and for the first time admitted that I wish I wouldnt have had this performed. I was told at my 4 week post op surgeon appointment that I had damangened my nerve at both levels and that I would be symptom-matic untill the nerve heals completly, or 'scabs' as I understand it.
My pain is a radient (warmth) pain in my right shoulder/scapula area and has moved into my upper arm and has progressed towards a painfull hand - I find it hard to grasp items or even make a fist. I never had any pain on my left side till recently. It is starting above my left upper shoulder, at a height even with my collarbone.
I also have a bad lower back and was told that it is a matter of time before something would have to be done for that. In addition to that I have a torn tendon in my right shoulder that he wants to keep an 'eye' on.
It is hard for me to 'complain' about these symptoms to anyone, because I know that people are sceptical of injuries that one can not directly see, and my wife has MS so this is so minor when related to her.
thanks for all of your time, I feel for all of you............
I had a 'Anterior Cervival Fusion with plating on C5/C6/C7 in July of 06. This surgery was performed for several reasons; Severe DDD in those areas, compression of the roots and Edema of the cord at C6/C7, spondylosis with myelopathy, cervical radiculopath, ect, ect....This is all due to bad genes, I did not have any injury that I can directly relate any of this to. I had a 2nd opinion prior to surgery and was told the exact same thing - recomended surgery to relieve the pressure on my cord/roots and to hopefully stop the pain which it causes. I had all the tests; CT Scan of my head; MRI of my brain, orbits, L-spine, C-spine, and right shoulder;EMT on my upper and lower extremities.
I am 7 weeks post op right now and still in my Aspen collar for another week. I was out of work for the first 4 1/2 weeks after surgery and have now been back for 2 1/2. The time I was off work I had ZERO pain and symptoms which I indured daily pre op. I am an automotive designer working at a desk on Unigraphics (software) on a 40 hour schedule - 8 hours a day. My pain and symptoms are BACK and for the first time admitted that I wish I wouldnt have had this performed. I was told at my 4 week post op surgeon appointment that I had damangened my nerve at both levels and that I would be symptom-matic untill the nerve heals completly, or 'scabs' as I understand it.
My pain is a radient (warmth) pain in my right shoulder/scapula area and has moved into my upper arm and has progressed towards a painfull hand - I find it hard to grasp items or even make a fist. I never had any pain on my left side till recently. It is starting above my left upper shoulder, at a height even with my collarbone.
I also have a bad lower back and was told that it is a matter of time before something would have to be done for that. In addition to that I have a torn tendon in my right shoulder that he wants to keep an 'eye' on.
It is hard for me to 'complain' about these symptoms to anyone, because I know that people are sceptical of injuries that one can not directly see, and my wife has MS so this is so minor when related to her.
thanks for all of your time, I feel for all of you............
To follow up above, I am only 35 years old....
I had C5 C6 and C6 C7 ACDF, donor bone, and titanium plate last Thursday, 8-17. So far, my recovery is better than I expected. All of the horrors of recovery that I prepared myself for so far have not come to pass. I don't have swallowing problems and I was very afraid of that one. My sister is an RN and she advised me to eat cold things such as popsicles, Icees(sp), if I have any difficulty because that would help swelling in the throat. I am putting iodine on the incision for 10 days and keeping it covered per dr instructions, the only small problem I have is when it starts to absorb, I get stinging, relieved by putting ice on it. I have a cervical pillow that I bought from the chiropractor years ago and I'm using that. I will go for x-rays next week, follow up with the neurosurgeon next Friday, expect to start physical therapy 3 weeks post op. My neurosurgeon is also prescribing a bone stimulator to ensure my fusion will be solid. He does this with EVERY patient that has a 2 or more level fusion. I'm being very careful to 'loaf' which is extremely hard for me. I intend to be gentler on myself than what the doctor advises to have the best outcome for me. I don't want to compromise my recovery in any way.
My symptoms prior to surgery were nerve pain into my head (both sides of neck, and left side of head), collar bone pain, pain down between my shoulder blades, left foot nerve pain, left shoulder, arm, hand, and finger pain. My right hand started to develop the familiar finger pain this summer and the neck stiffness increased. I didn't have to do anything to aggravate the symptoms. Carrying a handful of weeds in my left hand made my left bicep hurt. I put up with all of this discomfort for years, being told I have a neuropathy, take Neurontin, Baclofen, and anti-inflammatories. I did the med route, the chiropractor, and physical therapy.
I love to work out in the yard and we have 1/3 acre. Pushing a lawn mower, using the weed whacker, sweeping, and all that goes into taking care of your yard would make my neck hurt for a week or more. Carrying groceries into the house, housecleaning, even driving caused me discomfort. This year I had 2 episodes of left arm weakness that scared me. After helping a neighbor with some yard work, when I was undressing to take my shower, my left arm felt different and when I showered, it continued. A couple weeks later the same thing happened after I did some yard work at my home. My arm recovered from the weakness, but I didn't want to ignore it so I discussed it with my primary doctor.
I did my research, found out my own primary doctor had the same surgery, only 1 level, and talked to other people who had the surgery. My brother had a 2 level after a car accident years ago. My mother fell down the stairs a couple years ago and cracked a vertebrate that resulted in wearing a halo for a long time. All of these people are feeling great now. I was terrified of this surgery but the 2 things that eased my mind was that my primary doctor advised me not to wait too long, she did and has permanent muscle wasting in her right arm and some tingling. The second thing was the OR nurse who would care for me in the OR had the same thing done and she said it was the best decision for her.
For me, attitude makes a difference. I think I was in good physical shape prior to surgery because of all the yard work and activity level that I maintained in spite of my problems. (I always figured I'd hurt either way so I may as well reap some benefits of activity.) My neurosurgeon says I can return to running in 6 months. I'm starting to go for walks to 'get out of the house' and I hope my good luck continues, I have a strong faith in the Lord, who is the only one who truly knows how much I have put up with, and I believe that OR nurse was a gift from him to ease my mind further. If you are Catholic you know St. Therese, 'the little flower'. She told the Lord she wanted to do good on Earth after her death and she always uses roses as her sign. My sister sent me flowers and did not know what the florist chose. There were 12 roses in the bouquet, three big Red ones and 9 pink rose buds. My mother (a strong believer in St Therese) sent me a plant; it came from "A Bed of Roses" flower shop.
I empathize with everyone who suffers from chronic pain and health issues, I have had my share since 29, and I
My symptoms prior to surgery were nerve pain into my head (both sides of neck, and left side of head), collar bone pain, pain down between my shoulder blades, left foot nerve pain, left shoulder, arm, hand, and finger pain. My right hand started to develop the familiar finger pain this summer and the neck stiffness increased. I didn't have to do anything to aggravate the symptoms. Carrying a handful of weeds in my left hand made my left bicep hurt. I put up with all of this discomfort for years, being told I have a neuropathy, take Neurontin, Baclofen, and anti-inflammatories. I did the med route, the chiropractor, and physical therapy.
I love to work out in the yard and we have 1/3 acre. Pushing a lawn mower, using the weed whacker, sweeping, and all that goes into taking care of your yard would make my neck hurt for a week or more. Carrying groceries into the house, housecleaning, even driving caused me discomfort. This year I had 2 episodes of left arm weakness that scared me. After helping a neighbor with some yard work, when I was undressing to take my shower, my left arm felt different and when I showered, it continued. A couple weeks later the same thing happened after I did some yard work at my home. My arm recovered from the weakness, but I didn't want to ignore it so I discussed it with my primary doctor.
I did my research, found out my own primary doctor had the same surgery, only 1 level, and talked to other people who had the surgery. My brother had a 2 level after a car accident years ago. My mother fell down the stairs a couple years ago and cracked a vertebrate that resulted in wearing a halo for a long time. All of these people are feeling great now. I was terrified of this surgery but the 2 things that eased my mind was that my primary doctor advised me not to wait too long, she did and has permanent muscle wasting in her right arm and some tingling. The second thing was the OR nurse who would care for me in the OR had the same thing done and she said it was the best decision for her.
For me, attitude makes a difference. I think I was in good physical shape prior to surgery because of all the yard work and activity level that I maintained in spite of my problems. (I always figured I'd hurt either way so I may as well reap some benefits of activity.) My neurosurgeon says I can return to running in 6 months. I'm starting to go for walks to 'get out of the house' and I hope my good luck continues, I have a strong faith in the Lord, who is the only one who truly knows how much I have put up with, and I believe that OR nurse was a gift from him to ease my mind further. If you are Catholic you know St. Therese, 'the little flower'. She told the Lord she wanted to do good on Earth after her death and she always uses roses as her sign. My sister sent me flowers and did not know what the florist chose. There were 12 roses in the bouquet, three big Red ones and 9 pink rose buds. My mother (a strong believer in St Therese) sent me a plant; it came from "A Bed of Roses" flower shop.
I empathize with everyone who suffers from chronic pain and health issues, I have had my share since 29, and I
Well I just had my 3 wk followup. X-Rays looked good, though its too early to tell if fusion is happening or not. At least the bone graft, plate and screws are still where the doc left them. No need for the collar anymore, just cant lift more than 20lbs for the next month till my next appt.
If you're looking for a positive discectomy story I think I have to qualify. I've been working since 4 days after surgery(graphic designer), and have no problems. No more headaches, no more numbness, no more arm or shoulder pain, no more swallowing pain. The only pain I have is a slight pinching between the shoulder blades if I turn my head certain ways. It almost doesn't qualify as pain its so minor. And I'm only 3 weeks post-op so I'm fairly confident that it will go away as I continue to heal.
Hope this gives hope to somebody else in need of the same surgery as me. I literally feel as good as new only 3 weeks out!
If you're looking for a positive discectomy story I think I have to qualify. I've been working since 4 days after surgery(graphic designer), and have no problems. No more headaches, no more numbness, no more arm or shoulder pain, no more swallowing pain. The only pain I have is a slight pinching between the shoulder blades if I turn my head certain ways. It almost doesn't qualify as pain its so minor. And I'm only 3 weeks post-op so I'm fairly confident that it will go away as I continue to heal.
Hope this gives hope to somebody else in need of the same surgery as me. I literally feel as good as new only 3 weeks out!
I had ACDF with donor bone on June 30, 2006. Prior to the surgery, I couldn't do much for eight hours at a time. My left arm was losing strength pretty rapidly and the pain worsened with each passing day.
Had my first appointment with the ortho guy. He popped my MRIs into the viewer, did some tests on me, then popped the x-rays into the viewer. I'm no doctor (pretty sure I ditched every anatomy class I had), but even my untrained eye could easily see the gigantic lumps protruding into the spinal column, which definitely had a compressed look to it on those x-rays.
Doc said normally he likes to try a few things - physical therapy, other options - but with the amount of strength I had lost, he was recommending surgery.
I have an acquaintance who sells disc replacements. Through his network, he checked out the doctor for me and assured me he had a good rep and was not one of those docs who is "quick to cut." I decided to have the surgery.
Surgery @ 7:00am on Friday, June 30
Turn off morphine drip @ 7:00pm same day
Released from hospital @ 7:00am next morning
No need for pain killers after Sunday, July 2
Wore the collar for two weeks. Went in for my followup and stitch removal (no stitches - just glue...they simply peeled it off). Was told I'd have to wear the collar four more weeks.
I have had no pain since a day or two after surgery. My left arm is still weak but nothing that some exercise will not be able to cure. The only issue I had was a TMJ-related issue. The collar would push up into my jaw while sleeping. This stressed the tendons and/or ligaments in my TMJ and caused a small amount of pain.
I voluntarily quit wearing my collar at the seven week mark because I was tired of my jaw and inner ear hurting. It's been a week and the jaw/ear pain is still there but not as bad.
Last remaining issue I have is something I don't even consider an issue. Due to having my neck in that collar for near eight weeks, the muscles in my shoulders and neck are reluctant to move. They've had it easy for a while and don't want to work now. Again, just something I'm pretty sure can be handled with a little stretching and exercise.
Back to work slinging cards tonight. No worries, no trepidation -- soooo ready to get the hell out of the house!
I may be one of the lucky ones, or maybe too dumb to know better (it was my first surgery, first stay in a hospital - ever), but I'd do it again in a heartbeat. I feel just as well as I did before I started having the aches and pains, the x-rays look great. Life is good!
Had my first appointment with the ortho guy. He popped my MRIs into the viewer, did some tests on me, then popped the x-rays into the viewer. I'm no doctor (pretty sure I ditched every anatomy class I had), but even my untrained eye could easily see the gigantic lumps protruding into the spinal column, which definitely had a compressed look to it on those x-rays.
Doc said normally he likes to try a few things - physical therapy, other options - but with the amount of strength I had lost, he was recommending surgery.
I have an acquaintance who sells disc replacements. Through his network, he checked out the doctor for me and assured me he had a good rep and was not one of those docs who is "quick to cut." I decided to have the surgery.
Surgery @ 7:00am on Friday, June 30
Turn off morphine drip @ 7:00pm same day
Released from hospital @ 7:00am next morning
No need for pain killers after Sunday, July 2
Wore the collar for two weeks. Went in for my followup and stitch removal (no stitches - just glue...they simply peeled it off). Was told I'd have to wear the collar four more weeks.
I have had no pain since a day or two after surgery. My left arm is still weak but nothing that some exercise will not be able to cure. The only issue I had was a TMJ-related issue. The collar would push up into my jaw while sleeping. This stressed the tendons and/or ligaments in my TMJ and caused a small amount of pain.
I voluntarily quit wearing my collar at the seven week mark because I was tired of my jaw and inner ear hurting. It's been a week and the jaw/ear pain is still there but not as bad.
Last remaining issue I have is something I don't even consider an issue. Due to having my neck in that collar for near eight weeks, the muscles in my shoulders and neck are reluctant to move. They've had it easy for a while and don't want to work now. Again, just something I'm pretty sure can be handled with a little stretching and exercise.
Back to work slinging cards tonight. No worries, no trepidation -- soooo ready to get the hell out of the house!
I may be one of the lucky ones, or maybe too dumb to know better (it was my first surgery, first stay in a hospital - ever), but I'd do it again in a heartbeat. I feel just as well as I did before I started having the aches and pains, the x-rays look great. Life is good!
Wow! I was scared before i astatrted readin these..now im really really confused!! I don't unerstand some of the problems that are associated e/ this procedure..Where are the Good stries that are involved w/ this operation?? I am being told that you are in-n-out like a cheese burger... I am thinking abour doint the dugery in a few weeks. Iam being told theres no other way to fix the problem...With all the advances in medicine today you would think they could do this w/ a laser so theres no scars or plate, screws etc>> that is why i decided to write thisI have reallly been searching the web for as much info on this as possible. Can someone enlight me on this?? It seems theres alot more of negatives than positives w/ this?? Please help me understand this...Thanks--db
Wapy if your fusion did not take I would be very concerned. You ddfinately do NOT need to be skiing etc.
I am fused at c5/6 and 6/7. I get pain on the right side of my neck radiating up the right side of my head similar to a migrane. This happens most days.
I figure I will just live with it. My concern is I am 56 in good health otherwise and wonder what my neck will be like if I live to my late 70's or mid 80's since most of my family has lived to be in thier late 80's to late 90's. Good genes.
I am fused at c5/6 and 6/7. I get pain on the right side of my neck radiating up the right side of my head similar to a migrane. This happens most days.
I figure I will just live with it. My concern is I am 56 in good health otherwise and wonder what my neck will be like if I live to my late 70's or mid 80's since most of my family has lived to be in thier late 80's to late 90's. Good genes.
Waby if your fusion did not take I would be very concerned. You ddfinately do NOT need to be skiing etc.
I am fused at c5/6 and 6/7. I get pain on the right side of my neck radiating up the right side of my head similar to a migrane. This happens most days.
I figure I will just live with it. My concern is I am 56 in good health otherwise and wonder what my neck will be like if I live to my late 70's or mid 80's since most of my family has lived to be in thier late 80's to late 90's. Good genes.
I am fused at c5/6 and 6/7. I get pain on the right side of my neck radiating up the right side of my head similar to a migrane. This happens most days.
I figure I will just live with it. My concern is I am 56 in good health otherwise and wonder what my neck will be like if I live to my late 70's or mid 80's since most of my family has lived to be in thier late 80's to late 90's. Good genes.
I am 40 years old and10 days postop now from an anterior cervical discectomy with fusion at C6/C7. I had a variety of pain from my neck down my left arm over 6 weeks, some of it quite debilitating...particularly in the shoulder area. At times it felt like I had dislocated my shoulder. I also had numbness develop in my index finger and thumb and less noticeably my entire left arm. A large loss of strength in my left triceps and chest was my ticket tosuregry however, as the doctors all said it could become permanent without surgery.
Immediately after surgery all of the arm/shoulder/neck pain I had before was gone. All that was left was a slight numbness to the finger and thumb, and of course some weakness still in the left side which no doubt will go away with a little physical therapy. It feel a ton stronger already regardless. Surgery was on a Thursday and I was back to work(desk job) 4 days later on Monday(unfortunately).
The surgery did cause some severe difficulty swallowing for the first 4 days or so, and then gradually lessening to be almost unnoticeable right now at 10 days. I had on again/off again headaches for the first 4 days as well, but not so severe that the pain meds didn't control them. The numbness in my finger/thumb went away after a few days post op. Needless to say I am incredibly happy with the results. I was lucky in that everything else in my spine checked out and this appears to have been a singular anomaly.
Right now Im just waiting on my followup appt. to see whether the fusion is happening or not.
Immediately after surgery all of the arm/shoulder/neck pain I had before was gone. All that was left was a slight numbness to the finger and thumb, and of course some weakness still in the left side which no doubt will go away with a little physical therapy. It feel a ton stronger already regardless. Surgery was on a Thursday and I was back to work(desk job) 4 days later on Monday(unfortunately).
The surgery did cause some severe difficulty swallowing for the first 4 days or so, and then gradually lessening to be almost unnoticeable right now at 10 days. I had on again/off again headaches for the first 4 days as well, but not so severe that the pain meds didn't control them. The numbness in my finger/thumb went away after a few days post op. Needless to say I am incredibly happy with the results. I was lucky in that everything else in my spine checked out and this appears to have been a singular anomaly.
Right now Im just waiting on my followup appt. to see whether the fusion is happening or not.
I am 40 years old and10 days postop now from an anterior cervical discectomy with fusion at C6/C7. I had a variety of pain from my neck down my left arm over 6 weeks, some of it quite debilitating...particularly in the shoulder area. At times it felt like I had dislocated my shoulder. I also had numbness develop in my index finger and thumb and less noticeably my entire left arm. A large loss of strength in my left triceps and chest was my ticket tosuregry however, as the doctors all said it could become permanent without surgery.
Immediately after surgery all of the arm/shoulder/neck pain I had before was gone. All that was left was a slight numbness to the finger and thumb, and of course some weakness still in the left side which no doubt will go away with a little physical therapy. It feel a ton stronger already regardless. Surgery was on a Thursday and I was back to work(desk job) 4 days later on Monday(unfortunately).
The surgery did cause some severe difficulty swallowing for the first 4 days or so, and then gradually lessening to be almost unnoticeable right now at 10 days. I had on again/off again headaches for the first 4 days as well, but not so severe that the pain meds didn't control them. The numbness in my finger/thumb went away after a few days post op. Needless to say I am incredibly happy with the results. I was lucky in that everything else in my spine checked out and this appears to have been a singular anomaly.
Right now Im just waiting on my followup appt. to see whether the fusion is happening or not.
Immediately after surgery all of the arm/shoulder/neck pain I had before was gone. All that was left was a slight numbness to the finger and thumb, and of course some weakness still in the left side which no doubt will go away with a little physical therapy. It feel a ton stronger already regardless. Surgery was on a Thursday and I was back to work(desk job) 4 days later on Monday(unfortunately).
The surgery did cause some severe difficulty swallowing for the first 4 days or so, and then gradually lessening to be almost unnoticeable right now at 10 days. I had on again/off again headaches for the first 4 days as well, but not so severe that the pain meds didn't control them. The numbness in my finger/thumb went away after a few days post op. Needless to say I am incredibly happy with the results. I was lucky in that everything else in my spine checked out and this appears to have been a singular anomaly.
Right now Im just waiting on my followup appt. to see whether the fusion is happening or not.
Hello, I have been told by my nurosurgeon that I needed an anterior cervical disectomy w/ fusion. The doctor insisted that if I didn't get surgery that I would end up paralyzed. After he said the word "surgery", all I heard after that was just a loud noise in my head. I am deathly frightened, it was always the other guy getting chopped, not me. Now, it is my turn to get chopped. I tried to research as much as possible about the surgery and it's procedure on the internet. I even went to an exhibition here in NY called "bodies" to get a better understanding and examine exactly where and how the surgeon would actually perform the operation on my neck.
Abouit 5 months ago I had total numbness and weakness in my left arm and leg leg which also effected my left knee making it hard to walk. I went to see my chiropractor and after some readjustments to my spine and some meds from my ortho doctor, I felt 100% better. Now this nerosurgeon wants to chop me like last week, and very insistant he was in pushing the paralysis issue. He told me that he has been doing this for over 10 years and he is an expert. I felt like telling him "so what? I've been masturbating 3 to 4 times a day since I was a little kid and now I'm 44, but that doesn't make me an expert in doing it to other people!" Is he just looking for some pay day to purchase a new car or something? Should I also get alawyer as well? I discussed this issue with my family and close friends and they all insisted that I get a 2nd and 3nd opinions immediately which I am. Infact, I am seeing another neurosergeon and paying him out of my own pocket for his consultation. I suggest anyone else do the same, get a 2nd and 3rd if need be, a 4th if you can.
After logging on to this sight, all I've read is one horror story after another after another. I've stared going to the gym and I enjoy it alot working out on the heavy weights because of the way it transforms your body and makes it stronger and sheds off the unwanted pounds. But now, after reading all these horror stories I will not be able to go back to the gym ever again to work out nor will I even be able to go back to work ever again as well. So what knid of alternative is this surgery anyway? Not one comment that I have read is even positive at all! Are there any successful post surgical people out there at all? And "you" "sugarfairy", for Christsakes man, how bad is your situation? You claim to have had this problem "24" years? I just recently started having them! And DML50, StillHurtin, Wapy, Nataraj and you, FibroFlogger, holy ****! No ******* way!This is a fucken nightmare1 If you told me that I only had "one" of "two" choices to save my life, "one" being forced to put a uniform back on and fight in Iraq for 13 months or "two" go for the surgery, I would go to Iraq for 13 months because I know that I can have an effect on my own outcome. But with surgery, your outcome is dependent upon the skill of your doctor and luck if everything goes well and there's no complications or screw ups.
Please, please, please, if any of you have any type of encouraging words for me or if you know of people had had this surgery and back on their feet with "NO" problems please, write to me and let me know, (***@****) it seems only the folks who are writing here are the ones hurting after the so called needed operation! Please, any comments at all, I don't drink and now I've started drinking in order to numb out the fear and anxiety.
Abouit 5 months ago I had total numbness and weakness in my left arm and leg leg which also effected my left knee making it hard to walk. I went to see my chiropractor and after some readjustments to my spine and some meds from my ortho doctor, I felt 100% better. Now this nerosurgeon wants to chop me like last week, and very insistant he was in pushing the paralysis issue. He told me that he has been doing this for over 10 years and he is an expert. I felt like telling him "so what? I've been masturbating 3 to 4 times a day since I was a little kid and now I'm 44, but that doesn't make me an expert in doing it to other people!" Is he just looking for some pay day to purchase a new car or something? Should I also get alawyer as well? I discussed this issue with my family and close friends and they all insisted that I get a 2nd and 3nd opinions immediately which I am. Infact, I am seeing another neurosergeon and paying him out of my own pocket for his consultation. I suggest anyone else do the same, get a 2nd and 3rd if need be, a 4th if you can.
After logging on to this sight, all I've read is one horror story after another after another. I've stared going to the gym and I enjoy it alot working out on the heavy weights because of the way it transforms your body and makes it stronger and sheds off the unwanted pounds. But now, after reading all these horror stories I will not be able to go back to the gym ever again to work out nor will I even be able to go back to work ever again as well. So what knid of alternative is this surgery anyway? Not one comment that I have read is even positive at all! Are there any successful post surgical people out there at all? And "you" "sugarfairy", for Christsakes man, how bad is your situation? You claim to have had this problem "24" years? I just recently started having them! And DML50, StillHurtin, Wapy, Nataraj and you, FibroFlogger, holy ****! No ******* way!This is a fucken nightmare1 If you told me that I only had "one" of "two" choices to save my life, "one" being forced to put a uniform back on and fight in Iraq for 13 months or "two" go for the surgery, I would go to Iraq for 13 months because I know that I can have an effect on my own outcome. But with surgery, your outcome is dependent upon the skill of your doctor and luck if everything goes well and there's no complications or screw ups.
Please, please, please, if any of you have any type of encouraging words for me or if you know of people had had this surgery and back on their feet with "NO" problems please, write to me and let me know, (***@****) it seems only the folks who are writing here are the ones hurting after the so called needed operation! Please, any comments at all, I don't drink and now I've started drinking in order to numb out the fear and anxiety.
I had anterior cervical fusion surgery in November of 05 (8 Months ago) between C5 and C6. They put in a cadaver bone and a plate. Yesterday they did an xray and there is no fusion happening at all. There was sliver of some new bone down the back side but it had cracked. The PA I saw was unclear as to what the implications would be if I did not have a second surgery through the exterior of the neck. They said I fall into the 5% of those out there who do not fuse. I am a healthy, athletic non smoker of 43 - I dont take anti inflammitories etc...I have been diagnosed with Osteopenia but I am taking the proper meds for that. The pain is there but minimal. What are the risks of living with this unfused? I want to go back to skiing, biking etc...
Hi there, I had an anterior cervical discectomy around 1 mth ago (june '06). I have also had headaches since surgery & pain on moving & swallowing etc. Also, numbness in my right hand/arm has not improved, neurosurgeon told me it could take 12-18 mths to return, if it returns at all. The disc between c5/c6 had herniated/slipped & was trapping nerve root at spinal cord. I didnt have fusion & didnt get an implant due to the fact that I am a police officer & would have been unable to return to operational duties had I had implant. I was told I would feel instant relief from pain & as yet I havent! Feel a bit put out, as I'm still in a lot of pain & can still only turn my neck a maximum of 90 degrees, despite doing exercises I was given by physio every day. I asked my Dr when I would start to feel better & he said that was like asking "how long is a piece of string!". I feel as if I have gone thru with surgery needlessly, resulting in a scar I didnt need! Am hoping I'll improve soon & will update this as & when I feel like a new woman! Fingers crossed...
Hi, boy I thought I was the only one with these miserable headaches and pain since my anterior discectomy and fusion of c5-6/6-7 with bone grafts in fall of 2003. The headaches are dibilitating and no meds seem to help. I also have degenerative disease and was found after a MVA. My lumbar l3-4/4-5/s1 are all damaged and or bulging. I have an unexplained burning stabbing pain now off to the right of L5 and burning pain 1/2 down the right leg. I am trying facet joint injections, they don't seem to have any effect on the pain. I don't know if injections of steroids into the cervical fused areas would help, does anyone know? I don't want to be doped up on narcotics, I have a very sensitive affect with meds. With my work I need to function and that just is not happening lately. I already lost one job due to the pain and disabling effects. Any suggestions? Thanks
I would like to talk to someone that had went throught this before I had. C-4,5 and c-6,7 Had the ACD w/f. The First one in Jan,2000 Then again in Oct,03 .I am still having severe back and neck pain on more days than not, When I sit or stand for a period of time my back pain and my neck feel like there on fire.The numbness in my hands is still there on most days and sleep forget about it. I get about 3-4 hours a night if I'm lucky just no way to get comfortable. And after 3 years I have tried everything. What I'm wondering is does it ever stop. or get easier.
I had a Ant. C5-6 Discectomy/fusion a year and a half ago, after numbness/tingling in both hands and fingers and pretty bad neck pain. I'm a nurse, so not feeling my hands was very hard at work, couldn't start IV's, and ended up getting stuck by a dirty needle one night without even knowing it... so I finally decided to have surgery. The numbness and tingling were gone immediately, the neck pain was better. Things were slow to heal, but better for about a year, then I noticed the neck pain returned slowly, down my shoulders a bit, intermitently. Then I was in a very mild car accident about 5 weeks ago, and gradually I've regained numb and tingling hands and fingers again. Not that I've even been back to the doctor, accept the eval the night of the accident, but I don't want surgery again, the thought of going through that long recovery again. I had forgotten until reading everyone's accounts about the shoulder blade pain, the trouble swallowing for so long, etc. I feel lucky to have had such an easy time, and it still seemed so miserable as it was! A fusion can really be messed up by the slightest little bump, my car accident was hardly even a tap, and here I go again. I'll just keep living with this until I can't stand it I guess, or my neck is too painful. I also have a new baby at home, and I don't want to miss out on taking care of him for a month or more, because picking him up would be out of the question after surgery, and I don't know who I would get to help while my husband was at work for a month.
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