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Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS). |
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#11 | ||
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i saw ent today and will be getting the final test to prove that the inner damage is causing the constant dizziness and bumping into things so that is one test that can help you... also even though the mri/cat show not break or bleed there is further brain mri that can be done that pinpoint the damage done in the injured area. it must be requested specifically and is not usually done as it costs more and they are only looking for breaks/bleeds...
that is some that i know anyway , i hope you get your answers ![]() Quote:
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#12 | ||
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Hi I'm not crazy, I sent you a personal message and now realize that you could not reply as you are so new.
I am not crazy either - though at times and in the early days I did wonder. I am now 9 years post injury - thats why I haven't been posting lately - I seem to take a month at this time to have a good "wallow". I am in Auckland. The best testing/report/info I have had was a QEEG - with a neuropsych at Parramatta - Rosemary Boon - the only evidence on paper! I was referred to her by somebody I came across via the internet - who has now moved to Aus. I have had 2 hour psych tests that have come out with above average and exceptional which of course leads to the result that there is nothing wrong and have been told that anybody would be happy to have your results - too bad that I had to sleep for the remainder of the day and for days afterwards. I have been constantly told that my symptons far out weigh the MINOR nature of my injury. I firmly believe that some of the specialists I have been referred to have increased my stress levels and effectively made my condition worse. It appears that if you can walk and talk by stringing a few words and sentences together you have very minor TBI. I have had to remind many that I have cumulative head injuries, beginning with a fall from a horse at 14 yrs, ko playing hockey at 16, ko car accident at 21 and on and on it goes. The head injury that has had the worst effect was when I was 45, hit my head on a hanging basket and about 20 days later hit my head on the door frame of a taxi when I was going into the city with an armful of files. I struggled to keep working - part time for approx 7 years - barely hanging on - I was lucky I had such a good employer. I firmly believe that if my injury had been acknkowledged immediately I had not constantly had to "prove" it AND if I had been 10 years younger I would like to think that I would have had a full recovery - as I considered I had from the previous injuries. Anyway I have waffled on long enough - I am tired. Mark is a wonderful source of information and his timing is much like mine - Mark I remembered recently that my mother had told me I had rolled off her bed when I was a baby and vomitted badly - makes you wonder if that set the scene way back in 1956! Anyway Mr I'mnotcrazy, should you wish to contact me you will find my phone no under BM Stone, Arthur Street in the Auckland city listings. I must admit that I now talk better than I write! Lynlee Last edited by Lucy; 07-21-2010 at 04:42 AM. Reason: grammar |
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#13 | ||
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Junior Member
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Small discovery that encourages me that the root cause of my ongoing problems is in my ear: I just had a cold, and while recovering from the cold I was stuffy and congested for a couple of days; they were the best days I've had since I hit my head. Balance and equilibrium were noticeably better. I was comfortably staying awake longer and even had a bit of an appetite.
This encourages me that I'm on the right path in pursuing middle/inner ear problems. Is there ANY other explanation? Waiting to hear back from an ENT who will review my previous CT scan looking for SCD, and arrange a new scan if the old one isn't detailed enough. Aside from SCD, are there other things that the ENT should be looking for? Thanks! |
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#14 | ||
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wow...a bad cold is your best day? That should tell someone something for sure! Look for postings on here from BeccaP. She has some rare inner ear issue that her doc was trying to treat with injecting her own blood back into her ear canal or something like that? sorry I don't remember the name of it, but search postings by BeccaP and you should find it.
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#15 | ||
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"Ultra high resolution CT scan of the temporal bones (0.6 mm cuts) with axial, coronal, and sagittal reconstructions. W=400, L=900. Evaluate for superior or posterior canal dehiscence" Thankfully they were negative. I was diagnosed with a Perilymph Fistula. The doctor I'm working with is trying something called a "blood patch" (they take blood from your arm and inject it into your middle ear then let it clot to try to stimulate healing). If this doesn't work, they consider surgery. My patches don't seem to be holding so I wonder if my injury was too old when we tried it (8 months out). I'm speculating on that. I know I'm on the right track though, because when my ear is full the symptoms are markedly improved. After the last patch (I've tried it twice), even when my ear drained, I felt almost normal until the patch broke. Right now it is better than before the treatment but the symptoms are still there. I'm out of the US so won't be able to see the doctor again until mid autumn, so I have to be patient until then. If you read over my previous posts you'll see that this wasn't the only issue, I had brain, hormone and neck stuff going on and I've worked from several different angles with a great neurologist and chiropractor. The ENT I'm working with told me that some of my eye symptoms are brain related and not the ear problem. I'm so much better now, it's been almost a year since my injury. Hang in there and don't give up, no one here thinks you're crazy! ![]() Best wishes! Last edited by BeccaP; 08-12-2010 at 04:14 AM. |
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