Guest guest Posted February 27, 2010 Report Share Posted February 27, 2010 in New Mexico wrote: > I had a new set of scans done today and my doctor showed me that the next procedural step for controlling my spine pain is a fusion from L.3 through S.1. > He says the recovery period is about 9 months. I would like input from those of you who have had similar fusions. How bad was it? > My recovery time was less than six weeks but I followed my doctor's directions. I think the cramps from the instrumentation straightening my trunk was the main thing and depending on what it is being done for is a consideration. A year for fusion determination and bone growth. My spinal fusion was done for functionality so that I could walk, as my vertabrae disc were gone and they were sittting on top of each other with no cushsion. Bennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2010 Report Share Posted February 28, 2010 Yes, Bennie, my discs are reduced or gone throughout my spine because of Ehlers-Danlos syndrome, and L4 and L5 have collapsed on one side, making them trapezoidal so they have slid out of line. I think my main concern is that if I don't get the fusion done the vertebrae will slide further and completely pinch off the spinal canal and the few nerves that are still going through it at that level. I certainly don't want leg paralysis! But if I can, I want to wait at least a couple of years. Also, my regular spine doctor is talking rods and screws rather than bone - I don't know if that makes a difference. I see the surgeon in about two weeks. >Bennie wrote: > > My -- vertebrae disc were gone and they were sitting on top of each other with no cushion. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2010 Report Share Posted February 28, 2010 pavolady wrote: > > Yes, Bennie, my discs are reduced or gone throughout my spine because of Ehlers-Danlos syndrome, and L4 and L5 have collapsed on one side, making them trapezoidal so they have slid out of line. > > I think my main concern is that if I don't get the fusion done the vertebrae will slide further and completely pinch off the spinal canal and the few nerves that are still going through it at that level. I certainly don't want leg paralysis! > > But if I can, I want to wait at least a couple of years. Also, my regular spine doctor is talking rods and screws rather than bone - I don't know if that makes a difference. I see the surgeon in about two weeks. > Pavolady, I have them all, you have to have to put something in there to screw the rods to and they usually do a laminectomy and put in cages or artificial discs, and then rods and screws, I had impingement so it was time. My L 4. L 5 were gone. So , I had from the back with cages , rods and screws. I had Zimmer BAK cages. Spine Health and Spine Universe have videos on these. Bennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2010 Report Share Posted February 28, 2010 Millie wrote: > Hi , I had a 3 level/360 spinal fusion from L2 to L5 in Nov.of 07, spinal surgery or any other surgery unless in an emergency situation is a very personal decision, you need to have that conversation with yourself and say, " Can I live with this pain and uncertainty through out my life? " , then do the pros and cons list, and your decision will be made clearer for you. All, I agree it is a personal opinion and also go to several doctors. I could not walk, and it was for functional reasons. I also went to orthopedic surgeons and nuerosurgeons and went to neurosurgeon as for me, I wanted my nerves looked at more than bone and checked his bio and who he trained under, how many he had done. So, it takes and investment in doing so while you are in pain. Most surgeons will say after two level fusions, the success rate goes down and they did do with me so I had to make this decision with a lot of thought and research. Good Luck no matter what choice you chose. Bennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2010 Report Share Posted February 28, 2010 I have a friend with EDS (Ehlers-Danlos syndrome). It mostly affects her legs and knees now, but she is only 22 or so. The EDS contributed to your spine problems? Thanks, Anne in TX Quote Link to comment Share on other sites More sharing options...
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