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.
View 1 RepliesSince 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)
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.
View 2 RepliesI'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.
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?
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?
View 2 RepliesHello, 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.
View 2 RepliesHas 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?
View 2 RepliesI 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?
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
View 10 RepliesJust 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!
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.
I've only recently been put on the medication, can you tell me if any of you have had any of the side effects? and how long before I start to look and feel normal again?
View 1 RepliesMy wife has had migraines every day since January 2014. The last 9 months have been very difficult. We have tried many types of medication/treatments.
Currently she is trying Gabapentin (600mg per day).
Does anybody know how long it can take for Gabapentin to have an effect?
Is it possible for Gabapentin to make migraines worse?
I have been in depression for quite a few years now with one adversity following other. Have been on Mirtazapine 15 mg for 5 days now. How long does it take to show benefits?
Resorted to meditation for healing self and keep myself going personally and financially. Now felt unable to carry on and felt like doing something drastic.
Went to the doctor last week to tryy out medication and was prescribed Mirtazapine 15 mg.
Slept well the 1st day but was restless the next. Hit the treadmill in the evenings from 3rd day for the fear of staying awake and the mind wandering. This helped me tire out and sleep, but feel totally down, frustrated, hopeless and angry during the day.
I have been on a gluten free diet for about 4 weeks now. I had originally went on this diet because I am having the same symptoms and someone that may have a gluten sensitivity bad headaches, feeling very fatigued, joint pain, depression, numbness and foggy brain I was to a point where I couldn't get the word out of my mouth that I was trying to say and that's the point where I really started to research some things. I went to a neurologist and had an M.R.I. done all came back negative the Dr. said there is nothing wrong with me. Quite frankly I can't believe this so I started doing my own research since I wasn't going to get help from that Dr. I do plan on getting a second opinion done here soon, But none the less frustrating. So I found that pretty much all the symptoms that describe a gluten sensitive individual is everything I felt as well, so I thought I might as well give this a shot. I started this diet 2 weeks in I noticed that the numbness went away for the most part the pain still lingered the foggy brain hasn't shown its ugly face still fatigued and still had the headaches. So now 4 weeks in the numbness and the pain has been coming back more frequently and the headaches are still around foggy brain is still gone for now. But as the numbness and pain intensify and start showing up more often now it kind of makes me think am I really having to do this diet, and for the record I am not one of those people that cheat diets nor thinks its okay to cheat a diet especially with this kind of health dependency. I have been very strict with this hence why the frustration with it seeming like its not helping so high. I have done my research on the hidden gluten what to look for etc I actually try to buy only certified gluten free foods that say on the packages. I mean if all I have to do is change my diet to a gluten free one and it changes my life for the better because of this i'm all on board not just half way. Some places I read 6 weeks others say 6 months before you start to add wheat back into your diet to see if it affects you in a negative way, of course only if you feel like its not working for you. I definitely don't want to do this to soon because any chance that this is helping me I would hate to ruin that. At first I thought it was helping me, But not so sure anymore.
View 1 RepliesI have been using a lotion called dalacin t topical lotion from about october 2007, it really improved the big spots i used to get on my back, and it helped my face a little, but not much.So i went back to the doctors and she prescribed me with Oxytetracycline, which i take 2 tablets 2 times a day, so in total 4 a day. I have been on them for a month on this monday coming up (18th), that will then be a month, i think the doctor told me they would take about 3 weeks to a month to have a visual effect, im just hoping they do work! how has everyone's experience been with this medication? how long did it take for it to start working?
View 2 RepliesHad 6 facet injections today now i can't bend down at all am i so much pain also worried about painkillers
Tried to speak to the doctor about it but he seemed like he was in a rush and didn't have time for my questions.
I have a L5/S1 disc bulge which is pinching the sciatic nerve (have been suffering for 18 mths)Shown on MRI Last month I was given a caudal epidural injection, I experienced increased pain and brain fog for a couple of weeks but my pain is still persisting. Yesterday I seen another specialist but he says I have sacroiliac pain instead because I had normal ankle reflex. Having read up about it I'm not sure as I don't get hip/groin pain and my pain radiates below the knee into my feet and toes. He suggests I have sacroiliac and facet injections. I don't know what to do for best, I would love nothing more than to be pain free but don't want to put myself through anymore unnecessary extra pain.
View 1 Replies8 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...
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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