Spinal Surgery :: Fractured Facet Joint
Jun 2, 2015
8 months after my L1 compression fracture, another doctor (fired the first one) found out that one of the T12 facet joints is fractured (broken off in 2 pieces). I should have been operated on after the fall, but it's too late now.
Could someone tell me what this could cause (what kind of pain)? I have local pain, and severe pain in the iliac area, after being active for a while, or after sitting for a while.
I can sleep at night, but after 5-6hrs, I wake up because of the pain, can't continue to lay down. Very painful.
also, I still can't lay down on my back on a hard surface.
I'm scheduled for a nerve ablation T12-L1, both sides this Friday and Monday. I'm scared because of all what I read...
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I had five facet joint injections in my neck yesterday and I am in a lot of pain.
I have a lot of stiffness and can not move my head that well without being in pain. Anyone else experience this?
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I had back surgery in March 2013 that left me with mechanical instability, acquired spondylolisthesis and lots of pain.
I have 2 ortho spine surgeons telling me that I need a bi-level spinal fusion surgery to repair the damage, but after the botched first surgery, the thought of another surgery scares me to death. Plus, since surgery is what spine surgeons do, the recommendation seems obvious.
I also started seeing a new pain management doctor (we moved to a new state) and he is suggesting that I consider a spinal cord stimulator trial, with surgical implantation if we find that it helps the pain.
So...I'm left confused. I see the positives and negatives of each, but I'm just not sure if one makes more sense over the other. I think that my spondylolisthesis will worsen over time and could pose a threat of nerve damage, while the spinal cord stimulator is designed to mask pain and does nothing to address the instability.
I'd love to know if anyone else has faced a similar decision...or has thoughts, ideas, comments, suggestions for considering one over the other.
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Since 3 yo I have had pain in my back and up until I was 12 they said that it was growing pains! they then said I had wear and tear at l3/4 and suffered everyday since but been a pain I know that's there but didn't stop me I just grit my teeth and get on! Every few years I have a flare up of it and knocks me for a few weeks then back to usual bearable pains!
April 2013 woken to numbness /tingling legs and feet 3 days later horrendous back pain and it hasn't left since! Been 15 month of living hell! I've tried pt many many times over the years and always made my pains worse! I've eventually seen PM who said they will do facet joint injections in July however I am due to fly on holiday 5wks later! I can't imagine coping on holiday being the way I am atm however if I get worse then I won't be able to go!
Anybody had facet joint injections? Any good for you ? All experience welcome please
I was taken 300mg X2 daily pregabalin (lyrica). 250mg x 3 naproxen daily and 30mg oxycodone 2x daily they have cramped my meds to now 50mg x2 lyrica, 60mg x1 duloxetine and 30 mg X2 oxycodone! All the meds do is take the edge of the pain but if having a flare up then nothing helps!
I have to use crutches constantly just can't walk without at least one because it causes to much pain in my lumber,hips, groin and my legs sometimes give way!
The things I have been diagnosed with are, ddd, spondylosis, osteoarthritis, fibromyalgia. (They said I have loss if disc height and osteophytes too)
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Has anyone breastfeeding had facet joint injection i've been told by 1 surgeon i can feed after 2 days another said 2 weeks and another not to feed again anyone any ideas which is right.
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I've been suffering with lower back pain (left side) and an MRI has shown a slight bulge on one disc, an impacted disc below it and degenerative disc disease in the facet joints. None of this is serious and the pain is like toothache when it flares up. I've been referred for physio, third session later, and am due to have facet joint injections, under X-ray guidance, on Monday. Has anybody had these done? Are they worth it or should I put them off and give the physio a chance first?
I'm not afraid of needles, but had a steroid injection in my wrist some time ago and reacted to the fluid which felt like it was scalding from the inside out right up my arm, this lasted about 10mins or so and then wore off. So I am nervous about this procedure.
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Update on my silent migraine - having seen new orthopaedic consultant today regarding possible SCM or silent migraine diagnosis - we hopefully move on a step as he thinks my symptoms might be being caused by facet joint syndrome in the back of my neck. The good news is he is arranging some injections to help with the issue hopefully easing the dizziness and maybe stopping the weird head stuff that you get with silent migraines. All sounds promising but I'm not holding my breath. Maybe this could be your diagnosis too ?
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I wanted to know if anyone had facet joint spine injections or Epidural injections for pain management, whilst taking Remicade?
I would really like to hear from you if it went fine and if you had any negative reactions, such as an infection, or any other adverse reaction after the injections?
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I had a series of 8 facet joint injections into lumbar and sacral joints two days ago. This was supposed to be a test to see if the doc was in the correct area. So, no steroids yet, just anesthesia. However, after 2 days, my pain has not returned. Don't get me wrong, I am NOT complaining, just puzzled. How could this be? Has anyone had this test done and how long did it take the pain to return?
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After 13 ish weeks off work with back pain I visited an osteopath who finally told me I have a problem with my facet joints caused by my hyper lordosis. I've been given exercises but that's about it, looking to try and find out if anyone else has experienced this and has any advice? I can't do anything through the day without being confined to the couch in the evening in a lot of pain. I'm doing yoga to try and help too but I have a holiday to Florida booked for September and the last thing I want is it ruined by being in so much pain.
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I recently had facet joint and caudal injections for an L5/S1 herniation with nerve compression. It blissfully worked for 5 days but now back to the same state as before the injections (classic symptoms of this type of herniation). I have my follow up appointment tomorrow and wondered what the chances are of a 2nd round of injections working? Would be good to know others' experience of this.
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Hello, I read about root nerve block and the like, what I was offered is an epidural steroid injection, is that the same?? And X-ray led or without X-ray (?)The doctor said he would give me a steroid injection around my tailbone as it is safer (further away from spinal cord) and it is without X-ray.
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Has anyone had facet joint injections c2, c3, or know how many years is safe to keeping burning the nerves? Or weak muscle and occipital pain to where to skull is out of place and you have to snap it back into place with swelling and pain. Or know anything about cervicalgia? Or steroids in the facet joints in the occipital, c1 joints? When does steroids injection start to soften the bones?
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Anyone who can advise me on how this procedure is done? I am having it done next tuesday and from what i can tell from the letter i have received, is that i will only be having a local anesthetic. I am worried i will feel the injections ( I have read that some discomfort can be felt) and i would rather have a general anesthetic. Has anybody had injections in their spine under general anesthetic? Many thanks in advance for your help
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Just had my procedure and in recovery now, waiting to be discharged!
I have severe prolapse of L4/L5 with bilateral impingement of nerve roots. This results in severe back pain and constant sciatica. Worse on my right side.
Whole process took less than half an hour and I feel just fine after. Was offered sedative, but refused as I'm personally cool with stuff like this and very relaxed/able to keep still.
Very little pain during the actual procedure. In fact the worst bit was the initial injection of local anaesthetic!
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Can anyone please tell me how long it takes for these blocks to take effect,had them done a week ago and still in bad pain,MRI report said severe deep space narrowing at L4-5,have had 3 microdiscectomy and 12 epidurals over the past 9 years.
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My L4-L5 synovial cyst that I had removed two months ago has recurred again - this was the 2nd removal, so I've now grown 3 synovial cysts from the same dysfunctional facet joint.
One surgeon has recommended removing the bad facet joint which is causing the cysts and doing a microscopic fusion just at that level on that one side. I have no instability and no back pain issues elsewhere, so this is sounding like my best option, and not a very extensive surgery. I was wondering if anyone has had a fusion with a facet joint removal and how it worked out.
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I have CS in my neck and am in constant chronic (pain for the past three years). I am sick of being in pain.
My first visit to the NHS pain clinic was interesting, as the consultant informed me that I need to have Facet Joint Injections into the top part of my neck, which he plans to do in April !
I asked the consultant if there are any potential dangers from this procedure and he informed me that me that nothing can go wrong !
I got home ran a web search on Facet Joint Injections and am really horrified to read that there are rare - but very serious potential dangers from this procedure ... I feel that the NHS consultant has not explained the potential dangers to me.
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I had no idea what Excruciating Pain was. Does Radiofrequency Ablation in the facet joint nerve work?
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I had TLIF spinal surgery in 2010. Went as well as could be expected, but I have a very weak back and live with constant pain. I body won't accept strong painkillers, so was prescribed Amitriptyline. Came off them due to nose bleeds and feeling like a complete zombie. Although it was good to get a good night sleep!!! Doc then put me on Gabapentin 300 mg 3 times a day. Had no pain relief and so doc has now upped me to 600 mg 3 times a day, plus zapain in between.
I worry about taking so much, but I need something to take the edge off my pain. I've read a lot of negative reviews about Gabapentin. Will have to see how I get on.
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I am 40 and have grade 1 l5 s1 spondylolisthesis. When I read forums, all I see is people having to be on painkillers, fusion surgeries that don't work, people who can not work, have children (pregnancy) and so on because of this condition. I am so terrified I will end up in a wheelchair or without a social life. There is so little information about the condition online. Please, please, can someone give me some hope that you can live with this condition, perhaps by doing exercises, yoga, pilates etc? Please tell me I can avoid surgery, have a pregnancy to term without complications from spondy. I feel so alone. I hope all of you are having a good day.
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