My First Tysabri Infusion living with Multiple Sclerosis

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Uploaded by on Dec 27, 2007

My first Tysabri infusion for Multiple Sclerosis. I was pretty nervous.

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Uploader Comments (spikegrl1000)

  • I was dignosed in 2006 and I'm on Tysabri and I felt the same way as you did (PML)and everything but it's worked out great for me I really hope its working for you.

  • Thanks Jaye! I went and it was fine. HOw long have you been on Tysabri?

  • Ive been one Tysabri since Dec. 2006.I was dignosed in July 2006.I've never been on anything eles..

  • That's cool that you've only been on Tysabri. I wish my doc would have done that instead of having me try all the other crap! Anyway, I hope you're doing well and I'll keep trying to update as much as possible! Thanks and Peace, Steph

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  • ~My Friend Has PML and is very bad now because of Tysabi 111 people are ~~DEAD because of it, Dont Take it!!

  • @kadenlover11 your an idiot

  • I mean girl*

  • yeah I am sure your comment made the guy of the video feels really better now just as me who also suffers from ms. NOT.

  • im sorry for your loss, may he rip

  • hva MS too with simiilar smptoms thanjk you for sharing your story . i d be happy to share , and I feel like throwing everything out to be honest but I am too scared to get worse well done for starting the tyusabri tell us how it goes for you and happy new yeart

  • Glad I found your videos! I didn't know of MSWorld before reading the comments here. Glad it was mentioned, because I'm now enrolled and it's an amazing resource! Hope you are doing well! :)

  • I was on Avonex and hated it, made me sick as fuck liver problems and all. copaxone never did anything for me but give me bumps and infections, my skin couldn't handel it.. After this steroid treatment I am going the herbal rout, gonna see how that works, I was diganosed in 2000 so i have been down the medicatation road and all the meds thats the problems from the meds cause.. lol fun aint it.

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