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!
((((hugs))))
Love, Lauren :)
posted by Lauren @ 10:48 AM
4 Comments:
At 3:37 PM,
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
mark
At 5:31 AM,
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.
Deb
At 11:03 PM,
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.
mark
At 12:14 PM,
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.
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