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Hi Kccb
I wound up in Columbia Missouri, Mayo clinic sent me there for treatment. Try Columbia University medical center, 1 hospital drive in Columbia. They do lots of research and it is also a teaching institute. I engaged in a trial study there, and found the care to be excelent. This facility was better, than in St.Louis, Barns hospital. I wish you all the best. ginnie
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I am in St. Louis and just received my MRI results. Starting in square one… I would love to understand personal experience with the local neuro docs. Have a consult next week with a doc that has repaired 4 cord herniations. 4.---to say I am very concerned would be an understatement. |
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About Fusions
Hello to both of you. I hope you get in to see the right kind of doctors. How you do, really depends on just how severe the cord compression is. I would never wait 6 months to see if it got worse. If you are having trouble walking, seek out that neuro surgeon that you can trust. You don't want the vertebra to get worse. If all other methods of help have been exhausted, go for the surgery. I have had two fusions, different area, and had a good outcome. ginnie:grouphug:
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Thank you ginnie. With this diagnosis comes a tear in the dural lining that surrounds the spinal cord and brain; the tear allows the spinal cord itself to kink or slip through the opening causing a variety of symptoms in both kind and intensity. The more I read, the more concern I have, but finding the correct neuro doc is imperative. Thus the main reason for my posts here. I don't believe the surgery relates to fusion or disc management but instead freeing the cord from its entrapment and repairing the dural sac tear. Some of the more recent literature reports 130 (with one reporting 176) or so documented cases world wide. I'd really like to find the docs with the most experience in repairing this type of lesion.
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I am still looking for someone to connect with who is on this same journey I am on. Anyone reading this thread who has a you spinal cord herniation PLEASE contact me. |
hello after a year
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I was lucky as it was the risk of being paralyzed. I came out ok and only have to worry if the below hardware vertabre would fail. I also came to NT to connect with others going through this. do u have a good support team near you? Having that shoulder near by, can ease the whole of your being and help. Please do contact me at any time with anything u think I can help with.:grouphug: I am out of the USA right now, but have a tablet. I hope your progress can get better. None of this is easy, and we are forever changed for going through spinal fusions and herniations. not to mention a great deal of pain. Let me know how you are anytime. |
Mommy How are you????
I read this post just now & was following Mommy and saw she was going to have surgery in May 2012.
If your here, I would really like to hear from you to see how everything went and if your ok. I hope the very best for you and hope to hear from you very soon. |
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5 years 5 months post Spinal Cord Herniation repair. Anyone here following this forum with this diagnosis? Ambulatory without a device almost always. Symptoms still present in some forms but continuing to improve... MRI tomorrow for 5 year f/u... new symptom, dizziness with thoracic extension. |
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