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A few q's from a newbie
Hi, this is my first post. I have Chiari 1 dx about 6 years ago. Went to neuro for check-up recently and doc suggested surgery. I have a cervical/thorasic MRI coming up to check for syrnix. If I do have syrnix I plan to have surgery, if not I may try to 'deal with' the Chiari until I absolutly need the surgery. So here are my Q's.
1. For anyone who has had syringomyelia once it was found how rushed were the docs to see that surgey was done? 2.Do most insurance companies cover either or both chiari/syringomelia. I have Atena. When called they want the code for the surgery. However, while this surgery is not elective I need to know whether they cover it before I consult a neurosurgen, otherwise I am paying a neurosurgen for a consultation for a surgery I can't get because if don't cover it. I hope that made sense.:o Thanks for any input and info. |
Welcome to the forum Cattea! :) NT is a great place for making new friends and finding information as well as sharing with others. I hope you'll find the answer to your question and maybe make some new friends as well. Take care. :hug:
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I just wanted to welcome you to NT!:)
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Welcome to the forum!
My best advice is this - ask for contrast with your MRI, so if you do have SM, it will better show up. Mine would not have without contrast. Can't advise on surgery. My docs can't even spell syringomyelia. They can't even say it. LOL. Don't know where you are, I'm near Toledo OH. I was dx in '04. My syrinx is (was) T5-T8 about 3mm wide. My sx were hard to peg because I have other health issues, but one for sure was I could not tell hot/cold in my hands. I also suspect the hand/arm tingling and numbness after lifting (as in lifting 15-20 lbs, bringing in groceries) is due to this. All I really do about sm is try not to provoke it - no serious physical stuff. Last I read, they did not operate on syrinx under 6 mm wide and surgery was getting less popular at any rate. I admit I don't keep up on this stuff though. |
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