chat reminder for Monday, August 4

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Forum Moderator

Date Joined Jan 2007
Total Posts : 3571
   Posted 8/3/2008 12:57 PM (GMT -6)   
Hey everyone,
I would like to invite everyone to MS chat.  We start around 4 pm pacific, 5 pm mountain, 6 pm central, and 7 pm eastern time.  I hope you all come for fun and information.  See you there.
If you have never chatted before, you just need to click on the word "chat" in the blue bar in the upper right of this page.  Select the Multiple Sclerosis room and sign in!
We have no topic for tomorrow.  Bring questions and topics as you would like.

Gretchen       co-moderator MS board       diagnosed with MS July 2006

mystery reader
Regular Member

Date Joined Jun 2007
Total Posts : 257
   Posted 8/4/2008 10:55 AM (GMT -6)   
Not sure if I am going to make it tonight. If not, I will be back in a few weeks.
Barb/mystery reader
Diagnosed April 2007
Started betaseron --  May 2007 -- experienced allergic reactions after 2 weeks
Started copaxone -- June 2007 -- stopped after 4 1/2 months;experienced  severe 5 IPIR's
Started tysabri -- December 2007
Stopped tysabri -- April 2008 (developed antibodies/severe reactions)

New Member

Date Joined Aug 2008
Total Posts : 1
   Posted 8/4/2008 1:54 PM (GMT -6)   
Hello Everyone, cool
I am obviously new up here. I was searching the web, and saw this.
I was DX'd in 2000 with  RR MS, and have now graduated to 2ndary Prog.
MS. and will be starting on Novatrone in the next 2 weeks when they
can schedule me in.
I am on Rebif.
I have been on Avonex, wow that was a ride.  And on Copaxone, and that
seem to keep the MS at bay, and the silly Doc took me off of it thinking
that my MS was "going away"
yep we all know that there are those Drs, that have to graduate at the
"bottom of their class" and I have found several of them.  confused
Anyway. I am with one that seems to know what he is doing as long as I
keep him on task.  tongue
I also have several other health issues, a silly ole' back disease that keeps
me busy.
Had a fight with cancer last year, and lost the battler with IBS last year
as well and almost lost my life with it. I really enjoy life now after 07.
I will try to get up on line tonight. Which is 7pm, Minnesotan, time, depends if the skies clear up and we take the boat out and how the hubby
feels, he does dialysis 3 x a week, oh yeah, if anyone had a spare kidney
they don't mind losing he is in need of only 1. yeah .... Just got off the
phone with him he is going in now for his spin cycle. He works full time.
As I did up until 2 weeks ago when I was laid off.
Anyway I hope to talk to you all and hope everyone is having a good
summer and staying cool.
Take care.
"although my legs may not always carry me to the dance floor my heart
always will"
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