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Regular Member

Date Joined Aug 2004
Total Posts : 274
   Posted 9/27/2007 7:36 AM (GMT -6)   
has been about 3 months since i saw neuro. and he allowed me to stop injections of rebif. neuro. was unsure, but agreed. after this time, i find having the ivig (intravenous imunogamaglobulin) alone is definitely still keeping me going. notice an increase in energy and rise in spirits. have a 3-hour drip two days/month. had a port installed as veins were collapsing. anyone else on ivig? linda

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Date Joined Jan 2007
Total Posts : 3571
   Posted 9/27/2007 4:23 PM (GMT -6)   

Hey Linda,

I have been hearing good things about ivig.  My doctor offered it to me instead of steroids for my next flare.  I didn't enjoy the steroids too much lol.  I am glad it is working for you.  I am so glad you are feeling good on it. 

love and prayers


diagnosed: MS  July 2006
A person without a sense of humor is like a wagon without springs.  It's jolted by every pebble on the road.
Henry Beecher

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