Living with Multiple Sclerosis - getting a Tysabri infusion
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Hello Lauen Parrott I to am a MS recipient and I've been taking Copaxone for a year. I heard of the medication Tysabri from my neurologist today, so I decided to do look at some articles and video footage on it. Your story is both inspirational and intreging; so thank you for your week by week observation of being on that medication for the 1st time.
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@OneManTagTeam Good luck!!
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1st November 2010 & I'll be going through this for the first time too
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i will thank you...lauen parrott
rentas813 6 months ago
@rentas813 Great! I wish you the best!
laurenvparrott 6 months ago
well i was on copaxone it did not work for me i was getting relapses and more lesions, let see if tysabri works for me i just stated 0n 8/4/11 i will keep you posted....
rentas813 7 months ago
@rentas813 Yes, please keep me posted! I wish you the very best!!
laurenvparrott 7 months ago
Hi Lauren, i was just diagnosed with MS, and my neurologist prescribed me to take rebif injections 3 times a week, i havent started taking it yet, im kinda scared of giving myself injections,in your opinion do you feel that the tysabri infusion is better?
Trinna2003 1 year ago
@Trinna2003 Hello! I started giving myself Copaxone injections. Tysabri is definitely a lot easier, but your neurologist knows your case the best. I would listen to them - I actually gave myself shots for 5 1/2 years - you get used to it, trust me! I wish you the best with everything!!
laurenvparrott 1 year ago