Just an Update! My daughter Melani Grace is now 9 months & time is flying by! But after meeting with my Nuerologist, I've got to start treatment again next month. I was previously had the Ocrevus Infusions and now changing over to Tysabri. At least this time for treatment, will be a little different to where I'll only to have to go twice a month, instead of every 2 weeks; like before. Has anyone had the Tysabri Infusions? If so, did you have any changes or side affects?
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Marz91
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Hi. Marz91! So glad to hear that you and Melani Grace are doing well. It's good that you're getting back on meds! I've never been on Tysabri, but I know my old neurologist thought it was a great drug. I've pretty much only heard two things about it from folks on here, and those are that they're on it and they really feel like it's working for them, or they had to quit because their JC virus level got to be too high (to prevent PML, which as you probably know is a very serious adverse event) and their doctors took them off of it. In which case they're usually very unhappy because they really liked it. Your doctor can explain in more detail how they'll monitor your blood work to help prevent PML.
You have to really be good about getting your infusions once a month, though. It may be hard with a little one to go that often, but I'm sure you know how critical it is to prevent new lesions, relapses and disability down the road.
Good luck with the Tysabri! I think you'll like it. Let us know how it goes!
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