Back and Neck Pain Exchange
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You need to find out why your body didn't fuse before you think about another surgery.
?Vertebroplasty: injected bone cement
Reduce pain: L4-S1 is stressed when you flex and extend spine or hold something away from your body. multiply the wt of object x 10 for lbs of stress you place on that area /cervical x 3. So when you pick up your 9 lb Gbaby, it is putting 90 lbs of pressure in an already weakened area. Sit down and hold her close to you; support her wt on your lap.
Did the doc let you go to PT? Strengthen abdominals? learn to take care of your back?
Try a molded back brace made for you. by Orthotist/prosthetist to stop excess movement?
I can not believe it when I hear surgeons respond like you describe. He should have at least tried to find out what the problem was or referred you to someone who would. I hope you live near a big city so that you can see a different better Orthopod. Research for good one/compassionate with lots of referrals from satisfied clients.
If you have a failure to fuse, mechanical stress over time will cause more problems at surgical site and vertebra above.
Best of Luck
A partial list of reasons for continued pain include: disunion or failed fusion, hardware impinging nearby tissue, nerve damage, bone damage, osteoarthritis, fibrosis (scar tissue) that impinges nerve roots, unresolved stenosis, spinal collapse (vertebra self-fused), osteophyte (bone spur) impinging tissue or nerve root and instability.
It sounds from your description that your fusion is not as solid as it should be at eight months. This is somewhat unusual, particularly with hardware.
My first question is what type of fusion did you have? Did your surgeon use autologous donation? Cadaver donation? What was the source of your graft? My fusion was as hard as any bone in my body at six months. But, I had autologous donation. That is, my surgeon harvested bone from my hip and grafted it onto my spine. Today, many surgeons prefer to us rods, cages, pins, pedicle screws and other metal hardware. Sometimes older is better; and that might be the case with traditional spinal fusion. With hardware, there is always the risk that the metal implants will one day compress nearby nerve roots. Did you have this discussion with your surgeon before surgery? He should have asked which type of fusion you prefer.
There is a chance that you have spinal nerve root damage, from the surgery or from before the surgery. It can take a very long time for damaged nerves to heal - up to a year. Sometimes they never heal, as in my case. You can hope that this is the case and that you will see some improvement in the next few months.
There is no significant treatment or cure for damaged spinal nerve roots, advanced fibrosis, osteophytes or osteoarthritis. You can treat the symptoms with long and short-acting narcotics, anti-depressants (to inhibit the reuptake of Seratonin) and anti-convulsants (for neuropathic pain secondary to spinal nerve root damage). The best results are from using all of these medications simultaneously. I understand that you don't like using narcotics. But, that might be all that can help you manage your pain and remain productive. If you have instability, arthritis, osteophytes or fibrosis (scarring), PT is likely to exaccerbate the pain, not improve it. The only cure for instability is fusion (again).
Spine surgery is only 50% successful for pain relief (80% for improved function). I'll bet your surgeon didn't tell you that before surgery. Nor is it likely that the surgeon provide medications that you require. More surgery might or might not help (it could make it even worse).
Finally, I understand how frustrating it might be when you can't pick up a grandchild without pain. But, please know that you are indeed fortunate compared with many others. I am forced to remain horizontal virtually all of the time. I can't sit upright or stand for more than a few minutes. Some people are unable to sit, stand or care for their bodily needs. Many others are permanently paralyzed. I say this only for perspective. As bad as it can seem, many others are more disabled and in more pain.
At this point, you want to hope that it was just nerve damage.
Good luck
I had a spinal fusion with instrumentation in 2005. The dr. prescribed a 'bone growth stimulator'. I am a smoker, they used bone from my own hip for the fusion, but the stimulator worked wonders. My fusion was complete within 8 months. In fact, it worked a little too well, I now have bone growth problems because of bone growth pressing on other nerves. If your fusion hasn't taken yet, as your doc abt the stimulator. Everyone I've talked to who used on had positive results.
A am 47, was hit by the car when I was 41, fusion at 44...way too mush pain to discuss again. I have 3 grandsons and can understand your frustration. Have you tried a TENS unit? It uses electrical current to fool your nerves into not feeling pain, great device. Even after 6 years I use mine on a regular basis. Sometimes it's the only thing that works. Pain meds are a frustration, but, unfortunately, they are a way of life for me. I could not get through the day without the massive doses of morphine, vicodin, ultram, lyrica, flexeril, and robaxin. The help of a good pain doctor is a must. You have to find one you are comfortable with and one who has some empathy for your condition. They are hard to find, but worth the effort. I would try to avoid any further surgery, but get another opinion if that is the path you feel you need to go on.
Exercise is a must as much as medication. Keep your core strengthened, if nothing else, it makes a huge difference on what you are able to do on a daily basis. Learn your limitation, but don't let them rule you...attitude is important as well. So, keep your chin up. find good doctors that are willing to help you, don't let the future scare you, just take one day at a time.
Good luck!!!!
Pain free and 60--grandmother of 7
nanabiddy
I had a fusion on C6/C7 July 16, 2009 from an injury that occured Jan. 07. Before my SX I had severe neck pain/spasms as well as the constant sensation of pins and needles going all the way down my left arm, into the hand (all fingers included) and the same sensation occasionally in my right arm and into my pinky and ring finger. Since the surgery I do not have as much pain/spasms in my neck and shoulders (though pain is still presant...so maybe after 3 yrs I have simply gotten used to it????) BUT I will say that the "pins and needles sensation" (and in turn loss of strenth that goes along with that wonderful feeling, have not subsided at all in my left arm/hand and have actually increased in my right arm/hand (to the point that the right bothers me more than the left).
I have just recently had a 2nd MRI done and just this past Thursday had to suffer through a CT Milogram. I have an appointment with my surgeon this upcoming Monday so he can go over all the results with me but another surgery is a strong possiblility at this point. I will tell you that I just saw my pain management doctor yesterday and he told me that he hates to see someone as young as I am (31 years old now- 30 at the time of surgery) have a fusion because it almost never fails that within 10 years I will have to have another due to the fact that the disks either above or below the fusion have to work that much harder to compensate for the lack of movement in C6/C7.
On a brighter note, I have recently met with a lady that owns a pilates/yoga establishment and she seemed rather knowledgable as she was reading over my latest MRI report. She stated that she has had people in MUCH worse condition than me come to her and get wonderful results. Mind you, they are not over night but I have heard nothing but good things regarding pilates and GENTLE yoga. Kay (the owner that I spoke with) told me about one client who had 6 diks that were all buldging and herniated and couldn't even walk when he first went to her. It has been a long road (about 5 years) but he is now able to play tennis again. Looking at his MRIs, nothing has changed as far as the bulging/herniated disks but he is no longer in pain which is the ultimate goal.
On one last note, if you are finding that you back pain is causing extreme lower pack pain (as mine has) I have a suggestion. I threw out my lower back a week ago from last Sunday and up until this last Sunday I was laid out in bed on constant ice and when I did have to get up I could barely walk and was completely hunched over. I went to Bed Batha and Beyond and spent the best $200 of my life on a product called Back2Life. Look up the website to get more info. It runs in 12 minute sessions and the first night I bought it I had to get help to set it up because I was in so much pain but once it was all done. I ran two sessions in a row and for the first time in a week I got up and was with VERY LITTLE pain I could stand up straight and walk quicker than the 90 year old pace I had been walking for that last week. I have used it everyday since I got it, 3 sessions at a time and sometimes more than once a day and have not had any lower back pain since. Seriously, if I could marry that machine I would! lol.
Anyway, I hope this info is able to help you and if you would like to discuss this further you can find me on hotmail.com under desrae1. If you do write me just make sure to specify in the subject line who you are from WebMD so I don't delete you on accident.
Good luck!!!!!I wish I never had it done. This has caused severe chronic pain, and I can not do so many things. Another spine doctor wants to do a revision. He gives me a rosy positive story of success - just like the spine doctor who did my surgery.
Another spine doctor and my ortho surgeon said that my chances of a successful second surgery is very low because my arthritis and degenerative disc disease is progressing. Even if the fusion would fuse, I probably would still have pain - and it could be worse..
I wish I could give you a better answer. I can not give you advice. I can only tell you my story. Best wishes that another doctor can help you.
Thanks
IMHO, If you're still in pain after more than a year, do what I did and look for another doctor. My doctor was the greatest until he sliced me up. After which he completely ignored me and my problems.
But don't expect miracles after such a long time. Unless your doctor is trying to hide something (like mine, but I doubt yours is) you'll be subjected to more MRIs, CAT scans, and dye injections into the spine to fine more detailed information.
Good luck.
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