Hi everyone. I'm pretty new to the board and I just found this area for surgery questions. So forgive me if I've repeated myself from another posting.
Since this surgery is so new, there is not a lot of research and postoperative information available. I've been trying to journal anything I find about postoperative incidents/complaints. Not to cause problems, but to be able to take it to my PM Dr. & my general Dr. to let them know I am not alone. The neurosurgeon who did this to me, I've never went back to since my 2 week follow up after surgery.
I am looking for others who have had this surgery and their experiences. I had mine done in Oct. 09, I'm 10 months postop, and not in good shape at all. And from what I understand, I've not fused. I now have pain in my lower lumbar, right leg, right hip, right glute that is constant every minute of every single day. At times, it will also go down into my right foot. I do get some pains on my left side, but it's definitely very significant more so on my right.
I am a 41 yr old Mom of 3 who was extremely physically active before all of this. I'm down to doing nothing other than a brief walk, which I am thankful in that sense. At least I'm able to walk where as others aren't. Believe me, I know there are others worse off than me. But this is not what I signed up for. This was suppose to be this new miraculous surgery according to my surgeon. I'd be back to work in 2 weeks tops.
Now I live day to day and dread the pain as soon as I open my eyes. I still do my exercises I learned in PT. I take Tramadol and this isn't even close to helping. When I tell them I need something different and stronger they look at me like I'm asking for a kidney. I have a Tens Unit, I ice, I also heat sometimes but it's usually ice.
I returned to work 10 weeks postop against the advice of my PT. I HAD to. Financially I couldn't even pay my house pmt., let alone my bills. I have missed a lot of time at work because of all this. I was told a few months ago they may have to take the hardware out? Um, that's not even an option for me, I'll lose my job. I was told I could get on disability, but I must work. I have a desk job and I love what I do. It's better for me to be here than it is for me to be at home thinking about all the pain I'm in.
So here I am wondering if there are others like me. Am I the only one suffering after this miraculous AxiaLIF surgery that is so highly spoken of? Am I the only one who can't get the pain meds she needs to have some releif from pain?
Thanks everyone for taking the time to read this novel.. lol