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Hi all, I was diagnosed last month and had my appointment with the MS team on Tuesday. The DR has strongly suggested for me to have Tysabri as my DMT. Although I'm happy to follow his recommendation, I'm not going to lie... The risks with JC virus does worry me, even though I know they will monito...

Wow! Been on tysabri for 4 years already 😯

Anyone else on tysabri and gets sick all the time?? I’m on my third infusion and the second time I’m sick 🫠

Anyone on Tysabri? and what are you’re thoughts about it…I’ve been on it a year now

How do I know if it’s working???

What are your thoughts on this? I’ve been told I’ll be out on this and next week I’ll be seeing MS nurses about the next step and booking me in for IV’s.

Sooooo.... im finally starting my DMT next week. Any tips or advice before I start natalizumab subcut? Both anxious & weirdly excited so any words of wisdom welcomed! 😘

I was diagnosed in April of this year and due to the number and location of lesions, recommended infusion Tysabri once a month. I had my first infusion and felt like I had a hangover for a month with some heaviness in my legs. My second infusion was a week ago and three days after my infusion I woke...

Just came back from my ms appointment with the neurologist and I'm gonna be starting Tysabri potentially after blood tests? Is this a good medication? As I have no idea what's best treatment. I've looked at some of the potential side effects and worried as I already have some of the issues it says...

I’ve just started tysabri, it’s been good so far but my body still aches so I’m just wondering if I could still use cannabis?