The Emory backbone specialist said. "I see a few problems with your  back but 
none of which would cause the symptoms you have explained to me. You  should 
not be Here, you should go see a neurologist. I'm not a specialist in  that 
field but you might have some thing viral in your spinal cord. So get you  an 
appointment with  a neurologist. There is nothing I need to do for  you".   
   Now here we go back home and make an appointment with a  neurologist. Of 
course that is another 2-3 weeks to get in his office.
   By this time I'm starting to show Some improvements with my  balance and 
occasionally only use 1 cane to walk with at times.
   I have my visit with the neurologist which was very young like  just out 
of medical school. He checks me out and pokes me with a needle all over  
finding out that I was totally numb and I remember being very surprised my self 
 and 
even questioned him on the fact " are you sure your using a sharp  needle?"  
He just smiled and said Yes.  Thank goodness " I guess" that  I could feel the 
vibration from the tuning fork on my big toes. The doctor looks  at my MRI's 
and says I need you to go get another MRI. I'm like isn't the three  you have 
now good enough? He said  not really cause this one needs to be  done with 
Contrast. So Now that takes another week.  I remember telling my  wife "ok this 
is it, this is my last MRI, I'm not having another one" I have  never been so 
tired of being shoved in a tube in all my life.  
   I was asked to have a nerve test done on my next scheduled  visit after 
the Contrast MRI and Wow oh Yeah that was fun. Having the living day  lights 
shocked out of you for 45 minutes straight uh huh yeah fun time  there!
   Ok now I'm laying on the table "with smoke rising from my  charred body 
from the voltage test"lol and the doctor comes in says I'm going to  have a 
listen to your muscles,Ok, He proceeds to jab me with a needle  and  said "hmmm 
you have the thickest skin I've ever seen, Let me get a longer probe"  So I get 
to listen to my own muscle move on Loud speaker in the office.  Interesting. 
He finishes up , leaves, comes back sits down beside me and says "  You have 
Transverse Myelitis".
   Rather than him going into great detail (which now I know  would have 
taken him forever to fully try and explain the illness) he said do  you have 
internet access? I said yes and he wrote down the name of my illness  and said 
look 
it up on the internet and you will be able to read a lot of  information 
about it. And boy he was right, the info. is vast on the  subject.
 
       Of course the doctor told me their was  no cure for the illness and he 
could perscribe me Neurontin for my nerve burning  pain.  On my next visit 
with him I told him the Neurontin was causing me  horrible nightmares, all of 
which I had never experienced before , and I mean  horrible nightmares.  He 
then 
switched me to Lyrica and although it does  not make the constant burning and 
needle feelings go away. Lyrica does help to  lower the intenseness. 
       I now am able to walk without a cane  and do physical labor work to 
some degree. I get fatigued a lot quicker these  days and still feel very 
uneasy 
on ladders and depending on how hard I'm pushing  myself sometimes the 
burning effects start hitting me hard. When I talked to the  doctor about this 
he 
said for me to rest more in between my work so my spinal  cord want over heat 
so 
bad.  He is right, sometimes I can feel the heat  inside my back from my 
spinal cord. My body still has a lot of numbness and I  still cannot feel hot 
or 
cold on most of my body,  but some sensations have  come back on my hands and 
the tops of my arms. 
    The doctor told me that it will take 2 years for me to  know how much 
recovery I will have. He said most likely ever how you are 2 years  after 
having 
TM that is how you will most likely stay. He also told me that 1/3  of the 
people that get TM are paralyzed for life. 1/3 have certain problems from  TM 
and 
just have to live with it after 2 years. And the other 1/3 heal after 2  
years and never even know they had TM with no symptoms at all.   
 
                     I can only hope that one day their will be a pill to 
take and make this illness  go away.
 
                                                                              
         Gaylon, in Georgia



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