AJHAWES wrote: Heading in surgery on Monday @ 0800
Not sure what the waiting list is like down in NSW, but it's a long wait up here in QLD (even to get back in to see the neurosurgeon after all scans have been done).auto clickerword unscramblerjumble solver
As if I don’t have enough problems with my lumbar spine, my neck and mid spine have decided to cause me issues. Cervical spine self fused at three levels, cord being compressed, Nuerosurgeon has injected without much relief so it’s off to see the orthopaedic surgeon in December
hi, havent been around for awhile, but i have a cervical fusion, and i have spinal cord stim, i really recommend that anyone considering the implant really think about your pain, is is nerve pain, muscle pain, bone pain - where is it coming from?? because the stim will ONLY address nerve pain, i thought my stim would be the way to get my life back, wrong! it only helps with the nerve pain, and dont get me wrong, my night nerve spasms were 100/10 and they are now well managed with the odd spasms 3-4/10 but can lay down put the stim on diff mode and sorted, HOWEVER, i am plagued by the day to day pain from having muscle pain, bone pain, disc bulges etc ... the stimulator does nothing to manage these pain, and so i am still taking all the same meds, i need to spend most of my day in bed, as sitting and standing are not good for my pain
at the end of the day, i am still glad i have the SCS and it helps manage my nerve pain well, i just thought it would fix everything, it is marketed that way and that is the part that needs to be changed
Hi Pam. My neck has self fused, it was causing a lot of pain and a visit to a orthopaedic and Nuerosurgeon plus a MRI showed only one level that had not fused at the time, it has since then fused and my neck pain has lessened considerably. Movement is very restricted, very little down, no upwards and I have to keep stretching the left and right to keep as much movement as I can.
My lower lumbar is where my Nuerosurgeon has recommended a stimulator implant but I’ve held off for your very reasons, not all my pain is nerve related and I’m very reluctant to go down the implant road. I have injections twice a year but even they are hit and miss, even after having bone scans to show up the ‘hot’ spots.
I’m so used to pain it takes an acute attack to get me onto the strong pain relief. I wish you well.