Living With MS

Discussing all aspects of Multiple Sclerosis, various treatments, including accurate information regarding Tysabri.

Wednesday, November 23, 2011

My Tysabri Diary...

Happy Thanksgiving everybody! I completed my 67th Tysabri infusion yesterday, and everything went fine.

At this time, I would like to wish everybody a joyous Thanksgiving, with good food, spending quality time with your loved ones, family and friends.

In addition, I would like to share the following E-card from Jacquelin Lawson...,

Enjoy your holiday!


Love, Lauren :)


  • At 3:37 PM, Anonymous Anonymous said…

    hey lauren. I woke up monday morning with an abundance of energy. Did a 15 min workout on wii fit and still had some left over energy to clean up a bit - my wife was shocked lol.

    So its now saturday an i still feel real good and have been doing a 15 min workout all week - i really wasnt expecting any improvements for a while but the tysabri seems to have helped!

    ALmost looking forward to my next infusion now lol


  • At 5:31 AM, Blogger Debra said…

    I'm trying to make a decision whether or not to start Tysabri. I admit I have some fears, even though my CJ virus blood test result was negative. I need some feedback on the any negatives, too. Also, comparisons in energy vs. previous meds taken. Thanks.


  • At 11:03 PM, Anonymous Anonymous said…

    debra - its changing my life !! i was good for 3 years pretty much but this year went down hill big time - even bought a wheelchair.

    I've had 2 infusions and the results I've had are amazing to say the least. HEAPS more energy - working out a bit in the morning - did a list of chores around the house today that i would never had done a few months back. I was negative for the JC virus blood too. I was on rebif before tysabri.

    i honestly wish i had been on tysabri much earlier... i have/had the same fears as you - but the way i was going backwards i couldn't see that i had anything to lose.


  • At 12:14 PM, Blogger deej said…

    Hi Lauren, I stopped Tysabri a year ago after 4 years because I had been feeling Worse for awhile and was afraid of getting PML.I admire your bravery for staying on Tysabri and wish you the Best. I have pursued CCSVI and got soome relief, but I have a problem that CCSVI docs cannot fix yet, so that is the end of CCSVI treatment for me. Good luck to you always.


Post a Comment

<< Home