Laminectomy And Synovial Cyst - Reviews Or Feedback?
May 21, 2013
In January 2013 I started having left leg pains and started taking ibuprofens or store brand pain killers. Over the last 3 months the pain has become chronic, numbness in my big toe and foot, tingling, and pain in my buttock. This is only happening in my left leg. To make a LONG story short. The MRI showed a cyst pressing against my spine causing the pain. Initially my chiropractor thought is was a disc issue causing my sciatic nerve issues. My neurologist suggested a laminectomy Surgery however his concern was if I need fusion. I had an x-ray done that indicated there is some slipping. The neurologist gave me his best guestimation of how long that area of my back would last without the fusion. If he could have given me a high % that the fusion is necessary I would be at peace with it. Decisions, decisions. I was told the recovery is about 4 -6 weeks and longer with the fusion Do you have any knowledge on either procedure?
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I am a 65 year old female soon to have a L4/L5 Laminectomy with resection of Synovial Cyst (L4/L5) I need more information about the surgery, and what to expect as far as recovery time, etc.
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Hello,
I'm new on this board. On October 1st 2015 I had decompression surgery (L2-L4), a laminectomy and removal of a synovial cyst that was very high up on the spine (L2)- it was compressing the cauda equina in a bad way. Since then I have had a lot of nerve pain in my groin (both sides), hamstrings, plus sciatica down my right leg from the hip to the toes (according to the neurosurgeon, this is a 'small hernia' due to stenosis and a trapped nerve on S1/L5/L4 that he will operate on when the pain gets too much for me). Not sure if the sciatica is related to the cauda equina syndrome, but imo the cause of both is spinal stenosis. The nerve pain got less throughout the months (except for the sciatica) but the last weeks it's returning again more, on both sides. I had an MRI done two months ago for the sciatic pain and the doctor saw 'something' on the L2 facet joint that could be a new synovial cyst, or else it's scar tissue, he wasn't sure. My gut feeling is that the cyst is growing back and pressing on the cauda equina again- or could it be that i'm still recovering from the first surgery (now 6 months ago)? I sure hope it's the latter, as it was a big operation and the surgeon said that fusion may be next, as the facet joints move too much and in this way the liquid will keep forming new cysts. Ugh. Mid August I will have a new MRI to see whether the synovial cyst is back or not.
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i am having a posterior lumbar 4-5 laminectomy with synovial cyst removal on August 27,2015. I have a 5 day trip to Germany planned 6 &1/2 weeks later.
I now know the recovery to be longer than the one week I had thought. I know it is at least 6 weeks, after my pre surgery intake with the wonderful nurse I have. Does anyone have feedback about a 8 hour plane ride to Europe with only 6 weeks recovery time? Thanks
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I am on the waiting list for a new hip and I am a bit worried that I won't be able to do normal young person activities with my new hip. I am 37 years old and have been doing Zumba for years now and I really want to go back to it at some point. I also live in a flat so have stairs to deal with everyday.Will this be a problem?
I would really like to talk to some people of a similar age who have had the op and hear about their experiences of having a hip replacement.
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I have (5-6) small multi cervical fibroids and one approx 7cm pedunculated, in consultation with a very supportive medical practitioner I have decided to have, well it is my only option now because of the size of one the pedunculated one, a myomectomy. I feel ok about the decision as my periods are getting increasingly heavier and I know have constant lower back pain, which may be related to the fibroids. I need to have 4 injections every 4 weeks to try and shrink the fibroids to a more manageable size, however, this will bring on menopausal type symptoms. I have been given a prescription for Livial, which I am loathe to take. Has anyone had this procedure recently or within the past few years? I am concerned and a bit worried, to say the least, about having the procedure as most of the testimonials I have read appear to be generally dissatisfied, as the side effects were severe.
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I am currently on Harvoni for my Hep C and I wanted to ask has anyone had the virus return or a unsuccessful treatment?
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I havn't been on here for awhile and I wanted to know how the folks who have finished Harvoni are doing.I have 1 more week of my 6 month treatment of Harvoni and being a former relapser with sovaldi-olysio I wanted to hear from the hard to heal non responders who are 1A like myself.Are you folks staying negative?I feel like I am going to be losing my best friend next week cause another relapse is always in the back of my mind.
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I'm scheduled to get one of these , a mechanical one in about five weeks time , and seeing I know little about this surgery and the after effects, I'm trying to find out as much as I can through the internet.
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I'm due to go in for surgery on Wednesday and a bit terrified as I always feel like I am choking when I eat food and the only way I can cope is by getting sick....not being able to do this after surgery has me freaked out bit time. Just hoping that the positives of having this done will take away the feeling of having food lodged in my throat and I can have a normal life. I've had this condition since I was 16 and I'm 39 now. Hopefully I will get better after this. Anyone going through this too or have gone through this and come out the other side? Could use some positive vibes right now.
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I'm a 30-year old woman with three medium-large uterine fibroids. At the time of my last ultrasound (July 2013), my uterus was at the size of about 14 weeks. I have another ultrasound coming up at the end of this month but, given how much I can now see/feel my fibroids when lying on my back, I suspect that they've grown.
I'm weighing my different treatment options, and I'm currently leaning toward uterine artery embolization. Has anyone out there undergone this treatment? What was your experience with it?
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Being a first time mom, I'm trying to get all of the input I can. Every post I see on here about breastfeeding is positive. With everything, there are always 2 sides. My question is, who planned on breastfeeding but didn't continue and why? Is there anyone who is unsure or doesn't plan on breastfeeding? Please don't give abrasive responses about how breastfeeding is the only way. I just want to see this aspect from all, unbiased points of view.
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I just received my first shipment of harvoni in the mail. My dr is starting me on a 12 week treatment plan. I was excited to hear about this new medicine that has little side effects and a high cure rate. But now that I actually have the medicine in my hands, I'm extremely nervous. If there is anyone out there that has tried harvoni can you please share your experience?
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A few weeks ago, I saw a specialist who does laser surgery and infrared coagulation for hemorrhoids. He took a look at my backside, and recommended that I get laser surgery. So I scheduled it, and got 4 days off from work approved by my boss for the surgery and recovery.
But now that the surgery date is drawing near, (this coming Tuesday) my hemorrhoids don't feel as swollen or painful as they did when I first scheduled the appointment with the doctor. A month earlier, my hemorrhoids were KILLING me. But now my bowel movements are pretty much pain-free. I looked at my backside using a mirror, and it doesn't look as bad back there as it had a month ago.
So now I'm thinking: Should I still go through with this scheduled surgery? I'll be paying a lot out of pocket for it because I have a pretty high deductible on my insurance. Is it worth it to go ahead and get the procedure done anyway to prevent them from flaring up again? The doctor told me in our initial appointment that once you get the laser procedure done, your hemorrhoids won't come back. Anyone else who's had it done find that to be true?
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I'm 48 and would like feedback on the TURP surgery...
I've had issues with my prostate over the past 2 years. Last October it was 3.9 cm x 4.9 cm. An now its measured at 5.9 cm x 5.7 cm during the past year I've noticed I was getting 5-8 times a night and during the having to rush to the restroom with no time spare, in the past 4 months I've had to force my urine out. Called doc he ordered urodynamics test, it showed that my bladder has no reaction when I'm full of urine. Doc said MY prostate is so large it's shutting off my urethra tube. So he said I need the TURP surgery. .
I'm so unsure about this because I've had penile implant surgery this past Jan. and if I have the TURP I'll lose my ejaculation...
I also would like to know how to do all with not being able to cum?
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Impression: Moderate L4/5 disc bulge and a left medial synovial cyst. Significantly compressing the left thecal sac and contributing to moderate central canal and left greater than right lateral stenosis.
I have had progressively worsening low back pain and upper leg and butt pain.
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I had a laminectomy with removal of a synovial cyst exactly 17 days now and feel wonderful. Last weeks follow up visit actually was an eye opener because i found out I was doing too much, like bending for example, and I am really suppose to take it easy so the scar tissue can form a strong bond.
My cyst was large and sitting on the nerve root. As soon as it was removed the compressed nerve popped right back up, all good news.
I am wondering how soon before i can start doing other things besides resting and walking. I understand the golf is not happening for at least another 6 weeks and that's ok, but can I swim or when can i ride a bike?
I have basically no pain aside from a little muscle spasms.
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I have sever back pain and haven't been able to work since August. I am unable to stand, sit or walk for long periods of time. It hurts to sneeze, cough, bend or pick anything up. The pain is constant, stabbing at times and it feels like I have a rock in my spine. They have done facet and epidural injections. I take an anti-inflammatory, muscle relaxer and Norco (3 times a day). They tried to put me on Neurontin but it made me too sick. I have had every test done imaginable and basically what I have is degenerative disk disease with mild broad-base bulge. Bilateral facet arthropathy and ligamentum flavum hypertrophy. Indentation of the thecal sac in L4-L5. L5-S1 bilateral arthropathy. L3-L4 bilateral ligamentum flavum hypertrophy and a left nerve sleeve cyst (synovial cyst).
My surgeon wants to do a foraminotomy because I have radiculopathy on L4-L5 and then do a spinal cord stimulator for the pain. He isn't worried about the cyst...said it isn't the reason for my sever back pain. From what I have been reading, all of my symptoms sound like its the cyst causing at least some of the pain. Am I wrong to second guess his opinion? I just don't want to have these surgeries done and then later down the road turn around and have to have the cyst removed.
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I'm scheduled for surgery next month to remove a synovial cyst in my lower spine. The pain is present only when standing and walking for long periods, but debilitating when it occurs. I've read so much on this site, I thought I would get some of your views.
My neurosurgeon plans to do a laminectomy to reach the cyst which he says is quite large. We debated about whether a fusion is necessary to prevent the cyst from recurring. There is a difference of opinion among surgeons. Two that I've had review my X-rays say I have some degeneration in the disk and should have a fusion. A third says to take the risk and avoid the fusion. Eventually my surgeon convinced me I should have this done in order to return to an active life vs sitting on the couch. He does minimally invasive surgery and does not use a cage or pedicle (sp?) screws as he believes they put too much stress on other disks. Instead he showed me a very simple clamp he has used successfully. Has anyone heard of this - alternative?
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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 ten days post cyst surgery, no fusion, just cyst removal. I have some numbness still in my foot. Is that normal?
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