hi, i was just wondering if anyone on this board has PARS DEFECT if u do, it would mean a lot to me if u would e-mail me and we could talk. thanks alot

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In response to having a pars defect, yes I have and I have had two surgeries.I've been through hell-34 years old in the body of an 80 year old-It's difficult-and I struggle alot-since 1998 to be exact-I would be more than welcome to talk to you and exchange our experiences.I have noone who I am able to talk to that can relate-it has put a hardship on my social life-
But I'd be happy to talk to you- Brea

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Brea

I was in a car accident last Septemer. I;ve tried and tried to get a lower back MRI since but only finally got it two weeks ago. The MRI showed a fracture in L5 and possible pars defects at L4/5 and L5/S1. I looked up a little bit about it and I sort of understand it, but I'd like to know more. You both have it. For instance a lot of people get fusion which seems reasonable to stop the slippage of the spine but that teds to be reserved for level 3, 4 or 5. At the same time I hear these people talking about how its degenerative, how the continue to get worse. If thats true why not get surgery at a 1 or 2 and save yourself some of the pain a loss?

I am 48 and have been diagnosed with a Pars Defect. I am told that I was probably born with it. Pain relievers and physical therapy have not helped to relieve the pain. My neurologist is suggesting surgery to remove bone that has moved and is pushing against nerves and stabilize or restore a bridge between the vertebral bodies on either side of the pars defect. He says that ultimately bone forms the bridge, but for the several months that it takes for the fusion of bone chips and/or artificial bone placed at the time of surgery, stabilization with (metal) instrumentation (rods, screws, hooks, etc.) is necessary. I have the same question: why wait?
I would welcome information from someone who has had this same problem and surgery. Thanks.
CL