clifffaith
TUG Member
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- Feb 24, 2016
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I'm throwing the topic out there hoping to hear the experiences, good and bad, of fellow Tuggers.
Four years ago last month I started having back issues. First my back was "out" for about three weeks (I'd had two, maybe three "outages" over the previous ten years, always lasting less than four days). Then two months after that I started feeling a knot in my right butt cheek. Of course I Googled "right butt cheek pain" and it seemed like I likely had sciatica, and I did some exercises that seemed to relieve the knotted feel. But by the six month mark I found I had a 35 minute window of opportunity to get cats fed and breakfast on the table, before pain in my right leg forced me to sit down for a few minutes.
At that point I got myself to my GP who wrote me a Rx for flexeril and sent me for a course of physical therapy. When that offered no relief she sent me for an MRI which showed a bulging disc. Off to the spinal surgeon who said "meh, come back if it gets worse" and the rheumatologist who prescribed two more drugs (Tramadol & Diclofenac) and put me on a routine of cortisone injections, just under the skin of my tailbone, every three months. About eighteen months ago the pain was racheting upward and I had my first epidural steroid injection from a pain doctor I was referred to, administered while I was awake. I didn't see any improvement and at the followup appt the next week I told him so. Bastard looked me in the eye and called me a liar. I did not go back to him, and just kept limping (literally many days) along.
By last Memorial Day I could not walk from the car to a store without using my husband for support, so finally broke down and bought a cane. Rheumatologist sent me for a new MRI and said we have to try another epidural because insurance company won't pay for surgery until we've exhausted all other avenues. Saw a new pain Doctor at the end of August who gave me multiple precise epidural injections while I was knocked out. Blessed relief! 100% pain free by third day after procedure. Then at seven weeks and two days we were taking a small stroll on vacation and all of a sudden my right leg "says hello, I'm back". I waited until the cane level pain returned, and a few days before Christmas had another epidural which basically didn't really take. Had to continue to use the cane the first week, then the pain subsided to misery instead of agony levels. Packed the folding cane for our annual two weeks in Hawaii at the end of January, and by the third day of the trip (just over a month from the last epidural) I was back to using it.
So last Wednesday pain Doctor does a different procedure where he threads a "noodle" along the spine to administer the steroids. I'm quite a bit more comfortable, but not pain free, and feel I need to be sure my cane is available in the car at all times, just in case.
This doctor's mantra is NO SURGERY, NO SURGERY, NO SURGERY. Next step, and I strongly suspect that's where we are headed, is an external "electric impulse" device that will then be implanted under the skin if they can get it working for me. My understanding is that the device attempts to reroute and/or disrupt the brain/nerve pain signals.
So I'm wondering what has worked, or at least given some relief, to others. My Chinese pain Doctor says "meh" to acupuncture and acupressure. Tonight's NBC Nightly News mentioned both, as well as yoga. I see ads for the Laser Spine Institute, my rheumatologist says I don't want to go that way because nerves are severed to bring relief. When asked for a referral to a back specialist, my GP says I'm in excellent hands with the current doctors.
Four years ago last month I started having back issues. First my back was "out" for about three weeks (I'd had two, maybe three "outages" over the previous ten years, always lasting less than four days). Then two months after that I started feeling a knot in my right butt cheek. Of course I Googled "right butt cheek pain" and it seemed like I likely had sciatica, and I did some exercises that seemed to relieve the knotted feel. But by the six month mark I found I had a 35 minute window of opportunity to get cats fed and breakfast on the table, before pain in my right leg forced me to sit down for a few minutes.
At that point I got myself to my GP who wrote me a Rx for flexeril and sent me for a course of physical therapy. When that offered no relief she sent me for an MRI which showed a bulging disc. Off to the spinal surgeon who said "meh, come back if it gets worse" and the rheumatologist who prescribed two more drugs (Tramadol & Diclofenac) and put me on a routine of cortisone injections, just under the skin of my tailbone, every three months. About eighteen months ago the pain was racheting upward and I had my first epidural steroid injection from a pain doctor I was referred to, administered while I was awake. I didn't see any improvement and at the followup appt the next week I told him so. Bastard looked me in the eye and called me a liar. I did not go back to him, and just kept limping (literally many days) along.
By last Memorial Day I could not walk from the car to a store without using my husband for support, so finally broke down and bought a cane. Rheumatologist sent me for a new MRI and said we have to try another epidural because insurance company won't pay for surgery until we've exhausted all other avenues. Saw a new pain Doctor at the end of August who gave me multiple precise epidural injections while I was knocked out. Blessed relief! 100% pain free by third day after procedure. Then at seven weeks and two days we were taking a small stroll on vacation and all of a sudden my right leg "says hello, I'm back". I waited until the cane level pain returned, and a few days before Christmas had another epidural which basically didn't really take. Had to continue to use the cane the first week, then the pain subsided to misery instead of agony levels. Packed the folding cane for our annual two weeks in Hawaii at the end of January, and by the third day of the trip (just over a month from the last epidural) I was back to using it.
So last Wednesday pain Doctor does a different procedure where he threads a "noodle" along the spine to administer the steroids. I'm quite a bit more comfortable, but not pain free, and feel I need to be sure my cane is available in the car at all times, just in case.
This doctor's mantra is NO SURGERY, NO SURGERY, NO SURGERY. Next step, and I strongly suspect that's where we are headed, is an external "electric impulse" device that will then be implanted under the skin if they can get it working for me. My understanding is that the device attempts to reroute and/or disrupt the brain/nerve pain signals.
So I'm wondering what has worked, or at least given some relief, to others. My Chinese pain Doctor says "meh" to acupuncture and acupressure. Tonight's NBC Nightly News mentioned both, as well as yoga. I see ads for the Laser Spine Institute, my rheumatologist says I don't want to go that way because nerves are severed to bring relief. When asked for a referral to a back specialist, my GP says I'm in excellent hands with the current doctors.