Guest guest Posted April 13, 2004 Report Share Posted April 13, 2004 In a message dated 4/12/2004 3:33:16 PM Eastern Standard Time, Mdmssmile@... writes: I wonder what the percentage is in the normal and the EDS population for nonunions in fusions? My neck (post 6 months) has not totally fused and I used a bone stimulator 24/7 for the first 3 months. How about if we make a poll on CEDA's polls (Yahoo Groups) and actually ask these questions? And then, if need be, we can follow it up with another poll. It seems to me, that over the years, many people have questioned the same issue & many of them have done so recently. It would be much easier than doing it this way. We can just ask if you've had a non fusion...... maybe pick a few different areas, ask if you used a bone stimulator, etc., etc., etc. ___________ OK everybody,,,,,,,,,,,,,, I just became brave & just created a poll. Your identity is protected, you can check off more then one response & you can see the results as you vote & go back to the poll on CEDAYahoo Groups, I'm pretty sure, so you can see the other repsonses as they come in. It is ALL about fusions & non-fusions , which is really the same as a non-unions. I hope it works. I tried to set it up as logically as possible. And then, afterwards, we can follow up with each other, through CEDA or person to person/offline or online, or whatever. ___________ Personally, I now have a non fusion in my ankle. It was " supposedly " fused after 4 months, but when I constantly complained of pain, the Doc decided to remove the screw (he said the screw can often cause an irritation) & that made it 100 times worse. Then, after months of complaining, he did X-rays that were supposedly negative. I said I didn't care, that he had to look more. So he did an MRI & again it was negative & again I said " Do more. " ___________ I said that, because, # 1, I don't give up & #2, a CT shows more bone & all along I said that it was bone pain & it was deep inside. After 50 operations, I think I know my body & I know what different kinds of pain feel like & what it generally means & unfortunately, I have never been wrong, although I would have loved it, if I had been wrong this time. ___________ The CT showed a 95% non fusion. Then we went with an AFO & that stupid bone stimulator. He said I could try the bone stimulator for as long as 9 months (that was in late November) & when the pain continued to worsen, I insisted after @5 months that he do a repeat CT, to at least see if we were headed in the correct direction. Believe it or not, he argued with me. He wanted to wait the 9 months. I won the argument (not a big surprise, huh?) & we recently did the repeat CT. Well, well, well..... What a surprise..... It now shows a 100% non fusion!!!!! Ask me.... do I want to non fuse his head? I'll let you know, as I'm due to see him today & if I feel well enough, (due to other problems), I'll let you know. But first you should check out the poll. I shall try to create a link to it, right from this page. You can either click on them or cut & paste the link in to your top line: http://health.groups.yahoo.com/group/ceda/surveys?id=1204441 Yahoo! Groups : ceda Vote : IF you have had a fusion, did you have a successful fusion or did you never fuse or did you devel.. If it doesn't work, you can just go to Yahoo.com & go to your groups & you'll see CEDA & YOU SHOULD CHECK THE POLLS COLUMN ON THE LEFT & then you should see the poll about non-fusions. The Poll question is: " If you have had a fusion, did you have a successful fusion or did you never fuse or did you develop a non fusion? " Can you tell I'm not used to doing this?? You may see my votes, I'm really not sure. If you do, simply click on my boxes & it will take my answers away. And then just go down the list & click everything that applies TO YOU & be sure to scroll down to the bottom & press " VOTE " so that your vote counts. And it will probably show my email address as boop4@..., but it might say foundit1999@.... I think I did right. At least I tried........ Good luck to all, Luv Ya, Quote Link to comment Share on other sites More sharing options...
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