Spinal Steroid Block Injection 3 Weeks Ago But Still Pain
Sep 30, 2014
I was told by my doc i have bulging discs and micro fractures in the bottom of my spine l5 i suffer with chronic pain from it both in my back and down both legs. I had a steroid block injection 3 weeks ago in the facet joints and they worked for a bit but now the pain is back with a vengeance! Is this normal? Im at my wits end i am taking morphine for the pain but doesn't touch it. I'm 26 years old and have tried everything so far. Apparently the facet joints are rubbing the wrong way? I really don't understand.
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I've had this painful condition for a few months after falling and breaking a wrist. I thought it was as a result of the 'jarring' at the time but it got worse not better and, yesterday, I re-visited my consultant who diagnosed frozen shoulder and explained the long term nature of this. I've agreed to try the steroid injection. Does it work?
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I'm after some advice, anecdotes etc. Two years ago I sprained my ankle quite badly and it never really healed. It has bothered me quite a lot since, particularly after walking and running but seven weeks ago I broke the head of the fibula on the other leg and the ankle has become very angry as a result of having to take almost all my weight for so many weeks.
I mentioned it to my orthopaedic consultant at my last appointment, was x-rayed and it was then explained that there is a two year old avulsion fracture there; the bone and ligament never reattached. As well as this, I also have sinus tarsi syndrome. The ankle is very painful and unstable and he strongly recommends a repair. I have a podiatrist friend who suggests strapping, rehab and a steroid injection.
Has anyone had anything similar and what route did you go down with what result?
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I had dynesys done from S1 to L4 back in 2011. A year or so later a screw removal was done to the right side. The original problem was because L5 disc had collapsed. New MRI has shown the L5 and L4 both degenerated and L5 disc is bulging to the right side which is causing alot of pain around to the right hip. In the last 4 weeks u have had a couple of scares and immense pain I am due to see consultant on 23Rd May I think I am gonna possibly just gonna be fobbed off with a nerve root injection I am worried it's not gonna work any advice please does anyone think that this would be the right course of action for me to take??
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took a 2nd dose of oxycodone 3 hrs ago and my pain is only gotten worse i'm crying and shaking - called my doc at 630am -1 hour ago before i was crying and shaking he told me to take 2 aleve and the 2 oxy every 4... is this normal or should i call back?
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Can a nerve root block eliminate musculoskeletal pain?
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I had double bunion surgery 7 months ago. With my right foot the pain is making it vert hard for me to get my foot flat onto the ground. I have had xrays and a scan and that show everything seems to have healed ok however due to the pain I am walking on sides of my feet this is causing other issues with alignment etc... So I am off to have a nerve block put into my back to help with this and hopefully get me walking. Sometimes talking to the surgeon is difficult as he does not really know what is going on. Has anyone had a nerve block put into their back for the same sort of reason and if so how was it done and did it help?
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I'm a 38 year old with ankle and foot problems all my life. I was born with flat feet and I was always spraining my ankles. I acquired PTTD/Flat Foot on my left about a year ago and finally was diagnosed by an orthopedic foot and ankle expert. He recommended surgery and after a second opinion I decided I might as well get this taken care of so that I can go back to a normal life of walking through the streets of Europe.
I had my surgery about 2.5 weeks ago and I wanted to lend advice to those about to take on this crazy surgery. Firstly, the morning of surgery when the anesthesiologist was performing the nerve block it hurt like hell and made me even more panicked about the surgery. The relaxing medication they gave me did nothing to settle my nerves. I woke up from surgery a few hours later and I could feel all sorts of shocking pains coming from my foot. I asked if I should be feeling all the pain and they said that the nerve block failed. The anesthesiologist was busy for another hour and so I writhed in pain (crying hysterically) for the hour and vomited multiple times due to the extra anesthetic they gave me due to the failed nerve block.
Once the new anesthesiologist came she figured out that my nerve split into two and the other guy had not seen this split. After she was finished it was completely numb and I was worn out. I was sent home. Over the next day I vomited profusely, found out that I cannot breath when I take Oxycontin, I lost balance and fell on my foot and I was taking anything I could get my hands on for constipation. I finally found the foul tasting milk of magnesia and I can now go to the bathroom every few days.
My pain was managed by a morphine twice a day while in the splint, but now that I am in the cast my heel is killing me especially at night and the dr gave me hydrocodone which didn't touch the pain last night. Is it normal to have more pain at this point?
When will I be fairly pain free and when will I be able to leave the house? I live in Santa Barbara and i have an ocean view so I should not be complaining but i am feeling pretty horrid and ready to get out. When I think about leaving I worry about falling again and having my throbbing leg down.
Am I alone in all of this? Many experiences I have been reading say that after 5 days everything was hunky dory.
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I had an l4/l5 fusion 11 weeks ago. During the day I'm doing really well. Starting my phased return to work and going on my exercise bike. Have little discomfort during the day other than if I reach incorrectly or sit for too long etc.
I am really struggling at night. As soon as I get into bed in any position I am in immense pain. I struggle to sleep and wake up constantly through the night. My physio has changed all my exercises to ensure nine involve laying down so at least now I only have to worry about night times.
Has anyone else had this problem?? Anyone got any advice?? Am taking ibuprofen during the day and codydramol at night but doesn't seen to help.
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i had depo provera for the first time on Monday. so for 5 days now, and ever since i got it i've been having pain when i urinate like burning. sometimes it's not as bad. I thought it was getting better but its not. what should i do? what's the doctor going to do?
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I had a shot of cortisone for tarsal tunnel today. My pain is normally not constant. The pain occurs intermittent behind the ankle bone there is a sharp pinching. Since yesterday it was horrible and pinching like crazy. I could barely walk normal today so i went to podiatrist. For the past few months I had been seeking treatment ( ART, graston, chiro and ultrasound). I've also been doing strength exercises.
When you experienced the TT was it always constant and did cortisone ever help. If it helped how long before you noticed a difference.
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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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After a L5-S1 in October, I am left with residual left foot and partial leg nerve pain. In addition to numbness, my leg aches. My MRI looks clean, but neurosurgeon referred me to neurologist for possible nerve root injections. He also suspects the it may be radial sympathetic nerve issue. If nothing else, he's willing to take hardware out to see if that helps. I keep falling with my left foot so "numb," so I am frustrated. Is the device that scrambles pain. (can't think of it now) good for nerve pain? (Pain extends to my left lower back.) Has anyone had nerve blocks for nerve pain? I wouldn't have had surgery if I had known my mobility would have been compromised so much.
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Lisa here...Before my S1-L5 fusion, I had some foot pain caused by waiting two weeks to have a laminectomy/discectomy in my L 4 and 5 discs after a herniation (5 years ago). After my fusion - about 7 weeks ago - I have had terrible burning pain, sensations that feel like I am being bitten on a toe or have tape in between my toes. At night the pain is worse. Walking intensifies the pain and weakens my ankle and leg. I can't wear any of my shoes. Does anyone have any experience with this? I've called my neurosurgeon and he wants an x-ray. Suggestions? Comments?
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I'm 5 months post op from MIS fusion of l4/l5 and in pain.
Had microdiscectomy at the same level november 2013 without any relief. The back pain only got worse. The disc was completely dehydrated and I was offered the fusion 6 months later. Not that much pain after the operation but it has increased a lot. Severe back pain in the lower back and all the way up to the shoulders.
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Does nerve pain on the feet and calves go away after spinal surgery? I've been suffering from burning nerve pain since my back surgery. I had a laminectomy and fusion at t22 l1.
What can I do to help. Other imaging?
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I had this unit put in in Dem. 2013 but because of the lead trying to push through the back of my neck it had to be revised in August 2014. Was doing great until January 19, 2016 when the lead again pushed entirely through the skin on back of my neck. Now my insurance company will not approve for me to have another unit put back in. I was free 90% of the time with my unit in and now I am back to having so much pain in this area. It makes it very hard to have any quality of life except to wait around for another horrible burning pain that takes 3 mores days to overcome each time. Has anyone else had their insurance refuse this especially when it worked great?
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I am new to the board and am now one year out from lumbar fusion. I am a very physical person and a Personal Trainer as well. My low back pain has all but disappeared however neck and shoulder pain,stiffness and numbness are very concerning !!! I am currently treating with acupuncture and muscle relaxers. I also am a chronic migraine sufferer and believe this is partially being caused by cervical issues.
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My brother is on disability. He has a bulging disk in his neck that is making him dizzy. He has fallen several times because of this and frequently has to sit down. His insurance company won't cover the surgery. Is there anything I can do or something he can do to ease the pain? It makes me so sad that he is in such pain and can't afford to get help.
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I was diagnosed as having a synovial cyst by a neuropsychiatrist. I had a procedure where he went in and drained the cyst along with that I had a steroid injection. Apparently he did not get much out of the cyst. The pathology report came back negative on what he did manage to get out.
On day two post procedure the pain starting coming back. Each day the pain level increased to where I am now a level 8 and sometime 9 and can barely stand the pain. My lower right back just above the buttock feels like there is pressure and is very achy. The deep achy pain goes into my right buttock and wraps around the lower groin area. The achy pain goes down my right leg and into my foot. It is a pulsating deep ache and I can hardly stand it. It also feels numb at times and I get pins and needle tingling. When I get up from laying down or sometimes sitting (when I can sit) I get this sharp excruciating pain in my right groin that doubles me over. I have to stay still in the doubled over position to let it subside before I can straighten up and walk. Sometimes the groin pain just hits me out of nowhere when I am standing.
On my follow up visit with my physiatrist he recommended I have a consult with a neuro spine surgeon. My appointment with the surgeon is in a couple of days. I feel very fortunate to get into see this surgeon who is very hard to get in to see. He is rated as "one of the best" in a very large healthcare system where I work.
I am taking 1500mg of gabapentin along with 6 ibuprofen a day. I am also taking hydrocodone. I fight the pain and only take on the average one pain pill a day because I don't like the groggy feeling.
My question is, has anyone else with a synovial cyst had all of these symptoms? Is the groin pain related to the compression on the nerve from the cyst. I appreciate any feedback and would love to hear from someone who has had these symptoms.
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I am a 40 year old male that has had two back surgeries. First Surgery February 2014 Lumbar Spine Posterior Discectomy Micro-discectomy on L4 & L5. Surgery failed no improvement. My Second surgery March 2015 Anterior lumbar interbody fusion (alif) surgery on L4, L5, & S1 with cage implants and bone grafts harvested from my own hip bone. I experience sciatica on my right leg and most frequent on left leg ;shooting pain down my right/left hip/buttocks, goes down the back of the leg. The last 3 years left foot numbness. My worst pain is in bed getting up is very painful. Before my ALIF surgery I suffered from sciatica foot numbness and pain in mostly my left leg region. After 6 weeks post ALIF surgery or so I started getting pain in my buttock/hip region. This actually started during my physical therapy. At first I was doing water therapy this is when it started. My last day of water therapy I was literally about to go to ER from P.T clinic. From there on it just had gotten worst, no real improvement. I went back for more P.T sessions stretching and other exercises . What Physical Therapist did notice that my hip motion was very limited and not much improved happen during all my sessions about 40 or so. Its being about 10 months after surgery and 4 months of P.T. and pain on hips doesn't go away. I have to be careful going up or down stairs. Getting out of bed or moving around in bed its a battle. I have spoken to my surgeon and he says it will take more time for recovery and possible have to live with this pain as a fact of life. I have also spoke to other doctor s and pretty much same response. Once thing I just found out recently is about Hip Bursitis. I was diagnosed with Arthritis. My surgeon keeps on saying its my Arthritis causing pain but prior to ALIF surgery I never had this buttocks pain , specially getting in and out bed. I was wondering if anyone has had same symptoms after spinal fusion surgery having Hip Pain From Arthritis or Hip Bursitis?
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