Hi there, everyone
I’ve suffered with pain in my back and left leg intermittently for 30 odd years (I'm 47 now). After a very bad car accident in 94 and following much cynicism from many docs over many years I was finally diagnosed with a prolapsed disc at L5/S1.
I had spinal fusion and a nerve decompression in 97 which worked for a while until boney overgrowth bothered the sciatic nerve again. I subsequently had a second decompression in 98 which was unsuccessful. The pain had exacerbated to the point that I was in constant agony, taking a shed load of meds and wheeled about in a chair unable to do simplest of tasks for myself,
After many nerve blocks, facet joint injections, and seeing chiropractors, osteopaths, acupuncturists, followed an intensive pain management programme and a host of other stuff I have been left with bad days where I'm completely immobile or better days when I walk with a crutch. The pain varies from unbelievable agony to being bearable, but it's always there in my back, buttock and leg. I've been told there's nothing else that can be done for me except for pain management so I've been left taking daily: gabapentin, mexilitine, baclofen, meptazinol, diclofenac, tramadol and when it's worse I add methadone, diazepam and dihydrocodeine into the mix. I do stretches and pilates when I can which seems to help.
I'm going thru a hell of a relapse which has lasted now about 2 mths and even on all these meds, the pain's breaking through. My regular osteopath (of 8 yrs) has recently left England, but even he couldn’t help this time. The guy he recommended me to referred me back to my GP for further investigations i.e MRI GP’s cut back on some of my meds and added MST (slow-release morphine) I’m now at the max dose of 50mg twice daily which is just about controlling the breakthrough pain. I’m still stuck in bed lying on my side with a pillow btw my legs, can’t sit up (I kind of lean to one side) for more than a few mins, can’t walk at all, even the good old tens doesn’t help.
I was actually looking for some advice for help out there, when I was directed to this amazing group of people by the wonderful ‘heart as big as the sun’ RichT. I’ve read thru just about every thread from pg1 to 33. Your stories have had me sobbing into my orange-juice, so angry at yr docs/surgeons the air round my bed has been VERY ‘blue’ You’ve had me laughing out loud, which is hard because that hurts, I so wish I’d been a fly on the wall the day 1 of you ( Fran I think ) socked yr doc and if ever your boxing gloves come out of retirement…I’ve a bit of a list myself if you wouldn’t mind! I’ve learnt so much but my head has been left spinning with all your knowledge and you’ve saved my sanity at many a moment.
Now I’d have loved to be able to get to The Bonati Institute to have LSS but my pennies don’t stretch that far. I’ve found out about a surgeon a ‘Mr Martin Knight’ who performs Minimally Invasive Surgery here in the UK at ‘The Spinal Foundation’ (check out their website if you have time). I’ve read just about all I can find on Mr Knight and it all sounds/looks pretty impressive,
I’d like to pick your brains if you wouldn’t mind, a) has anyone heard of/about him over at your end of the pond and b) in an fool-proof way ( honestly I’ve read Pina3013’s post 3-4 times but my mind still goes blank) could someone perhaps explain what either of these procedures are, I think I’m on so many pills that you literally have to hold my hand and show me the pretty pictures.
Minimally Invasive Lumbar Spinal Surgery
Lumbar Endoscopic Laser Decompression and Foraminoplasty
Thanks for allowing me to ramble on for so long. I’d like to say, continued success for those who have had their surgeries and are doing well. Much luck to those who are about to have their surgeries and to those of us who are still fighting, fingers-crossed, one day we too will be pain free.
Noelle