For a newbie, this is so overhwelming.....
Overwhelming
I want to post a reply because I have been reading about Tysabri and would like to communicate with others on the drug. I had my second infusion on January 17 and it kicked my butt for three days. Pain, sleeplessness, and of course worry. Can I expect the infusions to get easier? I have RRMS disagnosed for 8 years. Copaxone was my durg of choice until Tysabri came back. I am so unsure about using this site, but I will get better.
- msladyinca
- Family Elder
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DonnaJ, Noreen, and Pete....
Hi Donna...
I've had 4 infusions, with my 5th coming up.
Also Donna, if you go to http://www.mspatientsforchoice.org/, you can read other Tysabri Patient Progress Reports.
Hi Noreen and Pete,
I am so very happy for you both (and Donna too), that you now have a superior efficous medication (Tysabri) to help you fight your MS.
If any of you (or any Tysabri users here that I missed-and I'm sure there are many of you), would like to share your Tysabri experiences on the http://www.mspatientsforchoice.org/ website, which will be helping other MS'ers looking for Tysabri info, please send me a PM with your email address, or send me an email directly at LGLBGL2003@AOL.com for further information
Noreen and Pete, thanks for the Lot# and Exp. Date of your Tysabri vials... keep them coming for each infusion you receive...wooohooo!
Take care all,
Lauren
I've had 4 infusions, with my 5th coming up.
These are probably side effects and will more than likely pass as your body gets accustomed to Tysabri (as a few others have reported this too, and they said that it passes in a couple of days as well - and it doesn't happen with each infusion)...your worry is more than likely adding to your sleeplessness (I'm just guessing as I'm not a dr.) Try not to worry as it causes stress and stress + MS don't mix well, as we all know.Pain, sleeplessness, and of course worry
Also Donna, if you go to http://www.mspatientsforchoice.org/, you can read other Tysabri Patient Progress Reports.
Hi Noreen and Pete,
I am so very happy for you both (and Donna too), that you now have a superior efficous medication (Tysabri) to help you fight your MS.
If any of you (or any Tysabri users here that I missed-and I'm sure there are many of you), would like to share your Tysabri experiences on the http://www.mspatientsforchoice.org/ website, which will be helping other MS'ers looking for Tysabri info, please send me a PM with your email address, or send me an email directly at LGLBGL2003@AOL.com for further information
Noreen and Pete, thanks for the Lot# and Exp. Date of your Tysabri vials... keep them coming for each infusion you receive...wooohooo!
Take care all,
Lauren
Feel free to visit my Blog and leave me a comment, I'd love to hear from you! 
http://lauren-livingwithms-aolcomlglbgl ... gspot.com/
Co-owner of a MS Support Group
http://lauren-livingwithms-aolcomlglbgl ... gspot.com/
Co-owner of a MS Support Group
