Tysabri diaries (open)
To aid those who may have been prescribed Tysabri® or those thinking of asking their Neurologist to prescribe Tysabri® we at the MS-UK have enlisted the help of a number of people with MS who are now currently taking Tysabri® to provide some insight into how they went about getting the drug and how the monthly infusions have changed, or not, their condition.
If you are currently taking Tysabri®, and would like to join our panel of "Diarists" please contact us by clicking here.
Opinions expressed are those of the authors and do not reflect the opinions or policies of MS-UK. MS-UK is an unbiased organisation and the content displayed here is done so in the spirit of free speech. Please click here for more information.
Annaoc (Updated 21/11/12)
Claire (Updated 25/02/13)
Christine (Updated (05/11/12)
Kirsty (Updated 23/05/13)
Krissie (Updated 26/03/13)
Lisa (Updated 18/10/12)
Mandy (Updated 01/03/13)
Natasha (Updated 09/01/13)
Neil (Updated 08/01/13)
Nicki (Updated 26/04/13)
Nutty (Updated 17/04/13)
Richard (Updated 19/01/12)
Simon (Updated (26/02/13)
Sonya (Updated 10/09/12)
Sue Lawrence (Updated 02/05/12)
Tony (Updated 09/03/12)
