How come everyone is telling me that the brain fluid can not move or swish back and forth ?
I had a CT scan got back the results and they keep saying nothing has changed! Now that is certainly not what my body is telling me.
I have tried over and over again to explain as simply as I can what is happening. The doctor takes out the CT scan and tells me that the brainfluid is not moving anywhere . I cannot be any clearer, "The brainfluid most certainly can move and it does move. Do you know when I heard how a tsunami starts and where it ends up that is exactly the way the fluids in my brain are working. Working too much with my head in a downwards possition the brain fluid moves forward. Then once I have sat down for around 10-20 minutes the brainfluid swishes from back to front. Making me want to vommit and losing my balance. Showing me the scan results means absolutely nothing. This is a photo nothing more or less. A second or minute photo! Now if you were able to take a moving photo of what the brain is doing then and only then you could convince me. I am not impressed. I know exactly what and how I am feeling. I am not a child. Even when I was a child the adults didn't beleive anything I said.
Guess how that turned out.......I did have water in the brain. Only after turning 32 yrs old I finally proved my point.
I will not be around for the next 32 yrs to prove this point. However , I do have respect for the Neurologists. Its just the way they go about trying to prove me wrong that burns a hole in my soul.
Just because your equipement is not yet advanced enough to see it happen., does not mean that the patient do not know what is going on. I know that they are hesitating to do anything for me because of the dangers involved.
I am truely grateful that they have learned so much already. I will be continueing with the homeopathic helpers. I will come in for a scan once in awhile. For the rest , I can only say sit back and watch. I knew a lot of fluids had drained. There is a lot of nerve damage left to which no one can fix.
My hearing is taking a backwards leap. I just pray that my eyes do not follow. I have been lipreading for a while now.
My brain is not registering sounds, there is nothing wrong with my ears as the specialist had pointed out.
I used to hear the stent shut on and off.
I can only register the difference when it turns on that I need to use the lu more often.
The doctor also explained that patients with a hydrophaelus often have incontinence! Hence the reason when I sit to urinate when I feel the pressure on the bladder , I cannot feel any pressure once I sit on the toilet. I have two years left in which I will find out what happens next!