My wife goes to her neuro once a year, or less.

Bobberino
  ----- Original Message ----- 
  From: john snodgrass 
  To: transverse myelitis 
  Sent: Tuesday, January 15, 2013 6:37 PM
  Subject: Re: [TMIC] Face book


  as far as going to the neuro unless there are circumstances that would cause 
you to have to have help 6 month visits are normal.theres not much they can do 
anyway.managment of symptoms can be done by primary care after you find out 
what works best



------------------------------------------------------------------------------
  From: Linda Egli <le...@sbcglobal.net>
  To: "Butcher, Bernie (S&FS)" <bernie.butc...@honeywell.com> 
  Cc: "tmic-list@eskimo.com" <tmic-list@eskimo.com> 
  Sent: Tuesday, January 15, 2013 3:35 PM
  Subject: Re: [TMIC] Face book



  I was offered Copaxone by my neurologist about 2 years ago.  He had a study 
showing the drug could prevent TM from progressing to MS.  However the study 
was by the manufacturer of  Copaxone so I declined to take it.  One question - 
when  saw my neurologist Dec, 2011,  I was told he no longer needed to see me 
unless there was a problem.  Is this normal not to be followed at least yearly? 
 I do see my Primary care doctor 3-4 times a year.



------------------------------------------------------------------------------
  From: "Butcher, Bernie (S&FS)" <bernie.butc...@honeywell.com>
  To: Linda Egli <le...@sbcglobal.net>; "tmic-list@eskimo.com" 
<tmic-list@eskimo.com> 
  Sent: Tuesday, January 15, 2013 10:54 AM
  Subject: RE: [TMIC] Face book



  I agree. I was diagnosed with TM in 2002 and MS in 2008. I think it was MS 
all along. I stopped getting the flu shot in 2002, and no flu. (just lucky I 
guess). I had a transplant in 1993, and my immune system is knocked down by the 
anti-rejection meds. My doc and my neuro say to get the shot, but I don’t.  
it’s my belief that they just don’t know, they don’t really know what causes 
TM, they don’t know what causes MS, and they don’t really know what effect the 
flu shot has with my condition. 
  So, I’ll take my chances. I’m taking Copaxone injections for MS.

  BERNARD BUTCHER
  Honeywell Engineering
  516-577-5868
  From: Linda Egli [mailto:le...@sbcglobal.net] 
  Sent: Tuesday, January 15, 2013 11:10 AM
  To: tmic-list@eskimo.com
  Subject: Re: [TMIC] Face book

  I have had TM for 9 years , & was told by my neurologist to never get another 
flu shot or any other type of  immunization (ex: tetanus or chicken pox).  He 
thought the flu shot was what precipitated my TM.  I worry about catching the 
flu, but everyone knows not to come around me if they have any type of illness. 
 I also pretty much stay at home & avoid crowds in the winter, so far no flu.  
I agree with Gary.  I got a bad cold a few months ago & it about did me in.  I 
can't imagine what the flu would do.  I miss the old group on TM, but I just 
don't trust Facebook.  The TMIC list is my contact with other TMers. Nice to 
see some conversation on this site.
  Linda E. in East Texas


------------------------------------------------------------------------------

  From: Gary Thomas <gbthomas8...@sbcglobal.net>
  To: Transverse Myelitis list <tmic-list@eskimo.com> 
  Sent: Tuesday, January 15, 2013 8:25 AM
  Subject: Re: [TMIC] Face book

  I used to get flu shots but stopped after getting TM in 2004.  I have not had 
the flu.....until this season!  I got it at around Christmas and am still not 
up to full strength (which is not that great anyway due to the fatigue I 
already had from the TM). 

   So, I am rethinking, should I get the shot next year, or not?  Fortunately, 
I did not pass the flu to my 87-year-old dad who always gets the shot but 
forgot this time, or my pregnant daughter and her family visiting us while I 
was sick, or my wife who has not gotten the shot either.  I think her 
chiropractor is not for getting it.  I don't think my doctor or neurologist had 
anything against getting the shot.  I guess I'll have a year to think about 
it???  

  The worst part about the flu was that my grandkids were here from Georgia and 
I did not get to do much with them.  

  Gary in Niles, MI
    ----- Original Message ----- 
    From: Robert Pall 
    To: jcs...@yahoo.com ; tmic-list@eskimo.com 
    Sent: Tuesday, January 15, 2013 8:11 AM
    Subject: Re: [TMIC] Face book

    I get the Flu and Pneumonia shot and have never gotten the flu in the past 
15 years. And The TMIC_LIST is pretty much the only one I read...it is too bad 
that so many of our group has gone to facebook...I guess you can't stop 
progress!~

    Rob in New Jersey



    -----Original Message-----
    From: john snodgrass <jcs...@yahoo.com>
    To: transverse myelitis <tmic-list@eskimo.com>
    Sent: Mon, Jan 14, 2013 10:59 pm
    Subject: Re: [TMIC] Face book

    i had the flu shot and the pneumonia shot the same time and i still cant 
play the violin!

----------------------------------------------------------------------------

    From: Dalton Garis <malugss...@gmail.com>
    To: Pat Cooley <patticoole...@gmail.com>; pjv1...@chartermi.net 
    Cc: tmic <tmic-list@eskimo.com> 
    Sent: Monday, January 14, 2013 9:31 PM
    Subject: Re: [TMIC] Face book

    I still listen and read.

    Because I still have TM and always will.  By the Way, that mustard cure has 
greatly reduced seizures for me.  Now, I only get them every 10 days or so.

    DG
    Dalton Garis
    Flushing, Queens
    New York, USA
    Mobile: 718-838-0437

    From: Pat Cooley <patticoole...@gmail.com>
    Date: Monday, 14 January 2013 8:33 PM
    To: <pjv1...@chartermi.net>
    Cc: tmic <tmic-list@eskimo.com>
    Subject: Re: [TMIC] Face book
    Resent-From: <tmic-list@eskimo.com>
    Resent-Date: Mon, 14 Jan 2013 17:33:21 -0800

    Patti I think you made the right decision.  You have to do what is best for 
you and your family.  You need to protect your mom, hubby & grandchildren.

    Patti C. in Wisconsin
    On Mon, Jan 14, 2013 at 5:39 PM, <pjv1...@chartermi.net> wrote:
    I've noticed some talk of people comng back to the tmic list for 
discussions and wondered just how many people actually look at this site 
anymore.  The onky discussion I have is that I received my first flu shot last 
Wednesday since my 9 years with TM.  We had two deaths from the flu in our area 
and I had a fear of carrying the flu to my 86 year old Mom, my diabetic hubby, 
or my grandchildren.  My fears of being a carrier outweighed my fear of a 
reaction.  I called my Neurologist and asked if he had any objection to me 
getting the flu shot.  His answer was go ahead and get it.

    Patti V - Michigan 










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