I have the e-mail here and I also every day check the TM Message board.  I try 
to help out with a few answers now and then to the new people who come on board 
with TM.  There are more and more of us all the time.  At least there is 
somewhere to turn for answers for our questions about this condition which 
doesn't seem to have a lot of answers coming from the doctors when you are 
first diagnosed.  Just the diagnosis and that seems to be it in the beginning.  

It sure was comforting to me to find this TM Association website and to my 
husband too.  He was the one at home for 2 months with me in the hospital and 
he tooled around on the computer and found the site. 

This past week I have been very sick with the Norovirus the vicious stomach 
virus that is going around all over the place.  I ended up in hospital on 
Sunday night/Monday morning after throwing up for about 6 straight hours.  I 
ended up having 2 1/2 bags of intravenous given to me to 'top up my fluids'.  
This is now 7 days later and I'm almost feeling 'human' again.

In the beginning I was not able to take any of my pain meds and it took me 
until yesterday to finally have my legs back to the numbness that I'm used to.  
The rest of the week they were terrible with the old pain, touchiness etc all 
back with a vengeance.  It has made me realize that the pain meds do work for 
me and I know the strength that I need to take.  I'm ever so grateful to have 
the access to them.

In Canada we are having problems with too few hospital beds and too little 
staff there to run the hospitals so after the ambulance took me to the hospital 
at 5 a.m. on Monday morning I still had to sit in a very uncomfortable 
wheelchair in the ER waiting room for another 4 1/2 hours holding my barf bag 
and having my hubby wheel me to the bathroom over and over again.  It was not a 
very good day.

I was on the actual bed in the ER for another 8 hours being 'topped up with 
fluid' until they sent me home once I could handle water by mouth.  

It has been a bad week.  

Hope no one else out there with TM (or anyone for that matter) gets this awful 
virus.  Even the doctor told me it was a very vicious one.  Not deadly (but you 
almost wish you were dead) but vicious. 

Heather in cold and snowy Calgary 
where I'm still recovering and eating only very liquid diet.  oh yum. 
  ----- Original Message ----- 
  From: [EMAIL PROTECTED] 
  To: [email protected] 
  Sent: Saturday, January 13, 2007 10:45 AM
  Subject: Re: [TMIC] slow


  Plus there is a TM message board or bulletin board now, too, and I think 
perhaps a lot of people prefer that format -- they can go to the category they 
have specific questions about.

  Barbara H.
  http://barbarah.wordpress.com/

  In a message dated 1/13/2007 12:17:21 PM Eastern Standard Time, [EMAIL 
PROTECTED] writes:
    Well, we've been on this list since 97 September and haven't skipped a 
beat, or missed a step, or something like that ...... ;>):>):>)   Almost ten 
years,  wow....!!!

    True, there are lots more info out there, but I still think the 
ask-and-respond between e-pals works wonders.

    Regards from Elvisland,    Bobberino
    ------------------------------------------- 
    From: "wim from holland" <[EMAIL PROTECTED]>
    To: <[email protected]>
    Sent: Wednesday, January 10, 2007 4:51 PM
    Subject: [TMIC] slow


    > Maybe it is a good sign. Ten years ago there wre a bunch of people dayly 
on 
    > the net with all kinds of questions. The good sign can be that doctors 
now 
    > know so much more over TM that the people have the most answers they need 
    > already for TM.
    > 
    > The fact that they don't need this group to communicate about this 
subject 
    > and with there problems, can mean that they have people around them for 
    > support.
    > 
    > Internet is faster, people have learned to Google, more info is available,
    > 
    > still I have my doubts.....
    > 
    > Wim from Holland




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