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I've never heard of this being done - normally when a fusion is done the disc is removed and hardware is put in-place.
Fusion surgeries have a high rate of success and the outcome is to stabilize the spine. Fusion surgeries can only hope that the pains will be reduced and/or completely gone.
I had a single fusion L5-S1 done in 2008 - my surgery was a success as I did fuse 100%. However, damage in my spine area was more severe than they had hoped as they couldn't do anything to reduce my pains.
It could be that your surgeon may have removed the artificial disc if it was noted that this disc was not put in-place or maybe it was moving around.
At any rate, it would be beneficial to address this question with your surgeon. I have been on this support group since 2006 and have never heard of this type of procedure done if the hardware was placed to help stabilize the spine and artificial disc.
Once you do see your surgeon, please let us know exactly what happened during ur surgery. Take care - Joy
I'd be VERY intersted to know whether this works for you. I don't have spinal stenosis but still curious since I've asked around and can't seem to find anyone else who has actually had it.
I just found this discussion - I hope you're doing really well now, five months after your surgery. Would you be willing to update your progress?
I had the Charite implanted at L5 - S1 in 2005 and am currently considering fusion to deal with the pain and arthritis. I'd be very grateful to hear how your fusion surgery has affected you.
Thanks much,
KjB63
please remember that with any back surgery there is no guarantee it will work. and fusion surgeries are done to help stabilize the spine. they do have a success rate of about 45-65% for stabilizing and fusing. There is no guarantee that back surgeries will reduce/eliminate pains.
You can click on my name or pic and read my story. I had single fusion L5-S1 done in 2008. my surgery was a success as it relates to stabilizing and fusing, however they could not do anything to my pains in my lower back or the nerve damage in both my legs.
I'm not trying to discourage you from the surgery, but you should research fusions on the internet and ask numerous questions to your surgeon. I'm glad I had mine done (had a lot of damage to the disc) and would do it again if I had to.
Hope this helps - oh and we have not heard from Catpardue since this posting - we do hope he/she is doing well.
take care - Joy
My son has a Charite' disc in his back since they first started implanting them. That was in Nov. 2004 and I certainly hope they have improved since then. He has pain 24/7 that has caused psychiatric break a few years ago and his life is at a standstill. That said... he also has nerve pain down both legs and was on Gabapentin for this part of the pain. He also uses Duragesic transdermal and tramadol for supposed arthritis as well as psychiatric meds as well. The neurologist recently put him on Nucynta for the nerve pain in his legs and it has done wonders for that. Unfortunately, it doesn't relieve any of the other pains and issues, but it DOES work for the nerve pain in the legs. I notice you say you have nerve damage in your legs. I don't know if that entails pain or not, but just wanted to mention Nucynta in case you do have pain from nerve damage and haven't tried it yet. My son KNOWS he is addicted to most of his meds and I really thought he would not report a change in the nerve pain, but he did and has taken himself off the Gabapentin. Now, it seems the main issue is anxiety; don't know whether the back pain causes it or not. Not much seems to work on the anxiety or the back pain. Please check into Nucynta (they did have a 2 week free trial script in November/December...maybe still do) and I hope it helps!
I hope you son can find something to help with the anxiety - just about anything can cause it and most people that have severe chronic pains tend to have anxiety attacks.
I do have pains in my legs along with the nerve damage - the Gabapentin really does help with mine. I can tell a difference if I miss a dose (take 3600mg a day~~1800 in morning and 1800 at nite) so I know when I start having leg pains that I have missed my dose and its usually the nite dose.
I do take some heavy narcotics already 240mg morphine day; 120mg oxycodone; .25mg xanyx when needed; Soma 4X daily and 3600mg Gabapentin daily. With my hubby's Union plan, based on quarterly hours worked, we have to pay for meds out of pocket and submit claims for reimbursement so I need to have generics prescribed.
The combination I am on has been working great for the last 4 yrs. I know here soon I will be looking at having the pain pump implant done as I am at the highest dosage and cannot be changed.
thanks for the info - hope you son finds his medium~~
Take care ~~ God Bless ~~
~~ Joy ~~
Right now I rely on ice, Lidoderm patches and also have a spinal cord stimulator and it does help more than any meds so far to a point. Once the nerve flares go past level 6-7 then forget about it - nothing will touch it.
I also have anxiety and depression issues and found that meditation (my therapist showed me a great one that involves breathing and loosening all the muscles systematically) and wellbutrin work best but still can't handle much in the way of over stimulation - like going out in crowded places without high anxiety.
Most of us on this board are addicted to our meds - I don't know how we wouldn't be considering the narcotics involved. Thanks so much for sharing this info - I will look into Nucynta.
I should maybe start my own, but now I am wondering how many people have had to have the fusion after the replacement and about how long did the replacement last? Trust me, I've put alot of miles on mine and I have not found any long term studies as to the life span of these. Are the problems just with that particular brand? Mine is different, then again, was done overseas. I am only 30 and do not want to go through anymore with this.the original post was over 10 months ago and don't believe we have had any new updates from this member.
You may want to do a GOOGLE search on disc replacement problems and/or complications and see what it shows. You may find a forum that would have more posts from people who have problems etc.,
please keep us posted what you do find~~
Take care ~~ God Bless ~~
~~ Joy ~~
I am curious as to the stem cell injections you will be having. Do you live in the US? I had thought they were not approved for the mid/lower spine?! My primary doc has a notice in his office about stating that they can do these in the upper neck/head area but not the mid/lower spine.
I know yoiu mentioned not being able to take some of the meds listed above and wonder if you are referring to Gabapentin? I know when I first started on this med it did make me feel a "groggy/drunk" feeling but that went away after the first week of taking it. Then as I dosed up (slowly increased dosages) I hardly had any side effects.
It has been 5 yrs since my fusion and I have DDD in my entire spine, blown out T11 & T12 left facet joints and also at L4 & L5 both sides, blood vessel tumor at T9. It seems once you have injured your back and have an operation a domino effect happens.
Do keep us posted on the stem cell injections and how you are doing.
Take care ~~ God Bless ~~
~~ Joy ~~
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