4 years ago
Tysabri news…

There’s some news on the ms society website today that this may be approved as a first line treatment rather than having to try the injectables first. That has to be good news…

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Here’s the link to the story:-
http://www.mssociety.org.uk/ms-news/2013/02/tysabri-become-potential-first-line-therapy-ms
Although it doesn’t impact me, SPMS, I should imagine that swapping frequent injections for a once monthly infusion would seem preferable……

I start Tysabri on Monday ……….was diagnosed in march and it’s my first type of any treatment……….I’m a bit nervous as I’m JCV positive but looking forward to an improvement in my relapse rate had 3 in 11 months.

Libby

I was diagnosed December 2011, and in February 2012 I was put straight on tysabri as my first medication.

I started Tysabri I have SPMS not sure yet if works have only had one dose. got afew of the side affects, felt a little better for one day han felt like shit again. still early days going for second dose this thursday.

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