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in reply to: 3 years of sciatica #6019
Thanks again for your help Dr. Corenman. I will show this thread to my doctor when I next go for a meeting and see what he says. You have offered some new ideas for me. Thanks again. Any opinion and insight such as that which you offer on this site is so helpful.
in reply to: 3 years of sciatica #5992symptoms:
Variable/changeable over the period since my microdiscectomy (which was November 2010 – 17 months ago)
Pain in lower back. (sciatic) Pain radiating from right buttock through leg thigh, hamstring, groin (occasionally), through calf, permanent pain at the bottom of right foot. (this foot pain was not permanent before the microdiscectomy… it was occasional)
I get ‘minor’ muscle spasms in my leg, often feel cramp in it and generally there is mild pain. The pain is not terrible and is generally bearable. However, it prevents me from exertion or exercise, as this can aggravate it or even cause a relapse. It is restrictive and this is what I would like to fix. I had trained to be a ski instructor and played soccer as well as keeping fit… but have not really been able to do any of this for 3 years now.average intensity of the pain is currently 1-3 most days, but has probably been up to a 7-8 at worst. I had a bad relapse in August and it has been slowly, but progressively better since then, but I think this is largely because I have ceased any kind of exertion, for fear of relapsing again, as well as having paid for treatments including a steroid injection, physiotherapy and an ablation.
Walking/sitting/lying… I am currently ok with. Pain is always there. not much difference in each… however, walking is better, perhaps because it takes my mind off it… but whilst jogging it begins to return to mind.
I have no x-rays. Might these be a good idea? I have had 3 MRI scans: 1 in 2010 and 2 in 2011.
Thanks.
in reply to: 3 years of sciatica #5971Hi Doctor,
Thanks again for replying to my message. This site is very helpful and interesting, with lots of useful information for people such as myself trying to improve back problems.
I found my most recent MRI report and have pasted it below. It is from September 2011 and was taken because I had experienced a strong relapse around 9 months post microdiscectomy. I am inclined to believe that the bulge may have receded a little and improved since then, as overall the pain has lessened and I am more mobile and able than previously and am close to how I was prior to the relapse. (I could be wrong, but this would be my humble guess)
MRI report-
“Findings: . The conus and cauda equine appear normal. There is normal lumbosacral vertebral alignment. No vertebral collapse or focal bone marrow lesion is identified. Disc dehydration with loss of height is present at L5-S1. At this level there is a prominent annular bulge slightly more pronounced on the right side but no obvious nerve root compression. The annular bulge extends into the exit foramina on both sides with contact between the bulging disc and L5 exit nerve root on the right side. Minor bulging is also present at L1-L2 also slightly more prominent on the right side with distortion of the thecal sac and slight compression of the adjacent nerve roots. The exit foramina appear otherwise intact. The articular facet joints appear normal.
Conclusion: Disc bulging at L1/L2 and L5/S1 more pronounced on the right side.”
The trouble is I have residual sciatic symptoms from the microdiscectomy that preceded this relapsed bulge in September and have remained to today, whilst I have largely recovered from the relapse.
This is why I was asking about piriformis syndrome. I have had several expensive treatments to attempt to relieve or solve these problems, but they have remained almost unchanged ever since the op. I was wondering if perhaps they were targeting the wrong thing or had missed something. I accept that piriformis syndrome is probably very rare, so I’m guessing I could be clutching at straws there, but I have already beat the odds of recovery from the microdiscectomy. My surgeon said that this operation had a 90% success rate and I don’t really feel I have come into the successful category.
From the information and suggestions that you gave me, I could fit my symptoms partially into most of them, as described on your site, but perhaps the best fitting one would be lateral recess stenosis. My symptoms are not terrible right now, but have been permanent since the op, with variable pain in my leg & buttock and a permanent pain on the bottom of my foot. My real desire, if achievable, is to get back to being active. I could live with pain if I could get my active life back, but at the moment I am fearful of doing anything too active, in case something happens again.
If you have any thoughts regarding the MRI report, or ideas for treatments that I might try, or investigate I would be very grateful. I have also heard of a company called Regenex that are doing stem cell treatment. I have considered this, but I approach it with caution, as it may be too early stage according to some who I have spoken to.
Many thanks again for your assistance and website.
in reply to: 3 years of sciatica #5917Hi Doctor. Thank you so much for your speedy and helpful reply. All information on this issue is so helpful. I will read further around your site and will reply tomorrow as I am trying to fix this problem. Thanks again.
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