Hi, I have just found this site and I am looking forward to talking to you all. I am 35 years old, I was diagnosed with MS 17 years ago and for the most part I have been really well. For the first 7 years I was on an injection treatment, Avonex and for the past 10 years I have been on Tysabri. I am now changing treatment as I have entered a high risk category for PML due to the length of time I have been on Tysabri and I am JC Virus Positive. I am due to start Mavenclad (cladribine) in May. What are peoples views on Mavenclad? Is it the wonder drug that people say it is? Is it tough starting on it?
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