I wouldn't do the spinal tap at this time either.   Maybe, if you were
having new symptoms, but your not. 

 

Sandy Brassil

 

________________________________

From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] 
Sent: Tuesday, June 26, 2007 5:47 PM
To: [EMAIL PROTECTED]
Cc: [email protected]
Subject: Re: [TMIC] from Gary

 

Sally,

I think  I agree with your statement

 

"Unless you feel like you're having another attack, it seems to me that
the original 'attack' of TM is long past and you're just dealing with
the aftermath of the attack and treatment meds, like most of us."

 

I think my neuro's idea is that if the spinal tap shows MS then I can
take treatment to help prevent further MS attacks.  He said that he
hopes it was just a "one time" lesion brought on by a virus but the
spinal tap will show if it is MS and treatment right away would stem any
tide of MS.


My opinion is that iwhat happened to me is just  a one- time idiopathic
occurrence as I have had no brain or spinal changes in three years (
I've had MRIs) and so forget the spinal tap.  Of course, if I get "hit"
down the road with MS I'll wish I had listened to him--so I'm in a
quandry.  I do have good insurance so could just get the spinal tap but
still......

 

Thanks for your input.

 

Gary

        ----- Original MeUnless you feel like you're having another
attack, it seems to me that the original 'attack' of TM is long past and
you're just dealing with the aftermath of the attack and treatment meds,
like most of us.ssage ----- 

        From: [EMAIL PROTECTED] 

        To: [EMAIL PROTECTED] 

        Cc: [email protected] 

        Sent: Tuesday, June 26, 2007 5:26 PM

        Subject: Re: [TMIC] from Gary

         

        Gary, 

        I'm no expert here but this sounds concerning to me.  It was my
impression that the spinal tap they did in the ER was to establish if
there was a viral cause of the TM (or was it bacterial? - sorry I always
get the 2 confused).  They even put me on meds just in case and sent the
sample to the mainland to have it tested.  When it came back negative,
they stopped the meds.  I always kind of raise my eyebrows at doc's
giving meds 'just in case'.  

        Unless you feel like you're having another attack, it seems to
me that the original 'attack' of TM is long past and you're just dealing
with the aftermath of the attack and treatment meds, like most of us.
It sounds like she wants to treat you as if the inflammation in your
spinal cord just started, rather than recognizing that it was just the
culprit that originated all the problems you have now, leaving you with
a myriad of symptoms to deal with!  It sounds like she's read something
about TM and remembers this piece, but doesn't understand where all the
pieces fit!  But I well may be wrong, here, and welcome differing
opinions!

        I was fortunate that the neuro who was in the ER had seen a case
of TM before and had the 1,000 mg/day for 5-days routine of
methyl-prednisone started within 13 or 14 hours of my sudden paralysis.
Within 3 days I could wiggle a muscle in my knee, and went from there.
On the other hand, she doesn't seem to know anything about the aftermath
of symptoms I deal with, and seems to think if I can stand up and walk,
everything's fine.  But hey, you can't have everything!  At least I'm
not still paralyzed!

        Good luck,
        Sally

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