Looking for
something specific?

Hi, I'm wondering what side effects people have experienced with Tysabri infusions? I had my 8th infusion on Friday, and I'm feeling so dizzy! This is a first for me, previously I've felt a bit tired for a day or so after, but not dizzy. Other than this dizziness my experience with Tysabri has be...

I've been on Tysabri for 6 months and my MRI results came back looking good. I have been feeling unwell for 2 days and this makes me spiral down into dark thoughts and what ifs🥺 does it usually work for a long time?!

Hi everyone, I've just had a relapse while on Gilenya so I'm going to be changing treatment to either Tysabri or an antiCD20 molecule like Kesimpta. I was wondering whether it gets progressively more difficult to find a vein for iv access once a month while taking Tysabri? Also, does anyone have ex...

So I start tysabri this week…anything I should know or prepare for?

Hi All, Quiet new to this but I've been reading all the posts and the responses and everyone has been so supportive towards each other. I have my first Tysabri treatment coming up soon and I was wondering what I should take with me to pass the time? (Abit of a foodie) can I take snacks to eat and ...

My wife was just diagnosed with MS, symptoms started showing over a month ago. First a slur developing into a loss of words and brain fog, plus loss of left arm and leg usage. The neurologist wants to put her on Tysabri, what can anyone tell me about it? Thank you in advance

I have just had my 55th Tysabri infusion. I had my bloods taken last time around. I was told today that I am still jc-. I am feeling blessed. Tysabri has been so good for me.

Hello all, I’m recently diagnosed with MS, it’s a bit of a relief to get a diagnosis if I’m honest. It ties up a few strange loose ends and means I don’t have prostate cancer or a brain tumour! I have had several MRIs, second one was brain and spine with dye and it was after that that I got my f...

Im so nervous to start tysabri as i had a bad skin rash from steroid infusion which has sort of gone after 3-4 months taking antibiotics but still ruined my face I just want to be able to dance and walk without thinking about it So im 50/50 about taking dmt drugs has anyone had a skin rash on face t...

Hi im really confused as im about to start Tysabri infusions because i have a new active lesion in my brain. I have rrms since 2008 Has any obe taken this drug and how did they find it ?

I got diagnosed with MS in October and started on Tysabri in December however, I tested positive for the JC Virus. Did any body else test positive at the start of their treatment and still continue with Tysabri?

Hi guys, I had the new Tysabri injection form rather than the infusion the other day and would recommend it! Especially if you hate sitting around waiting for it to finish...it's much quicker than the infusions. :)

Hi everyone, I have recently been diagnosed with RES MS as I have had 3 relapses since the disease onset in June. I am due to start treatment very soon, hopefully in January. I have been told that I need to choose between Lemtrada or Tysabri (depending on whether i'm JC +/-). Please can you advise m...

Hi guys... I've been on two treatments since my diagnosis (Rebif and now Tysabri) Rebif didn't work out for me so changed to Tysabri and is working wonders for me. Tysabri is given intravenously but recently I have been given the opportunity to have the treatment through injections to speed up the...

Hi all! I’m really excited I found a forum like this - I’ve been trying to find a solution and I was wondering if perhaps someone here has insight - I live in the US and I’m currently on Tysabri (switched from Tecfidera) for over two years and it’s working well. I am supposed to receive the infusion...

Hello, has anyone any experience with coming off Tysabri and moving to Ocrevus. My consultant is very keen on me switching due to PML. Just wanted some advice / to hear people's experiences. Thank you 😊

Thoughts anyone?? https://pubmed.ncbi.nlm.nih.gov/36639226/

Hi, my partner had COVID in February 2022 and the week after that she started feeling the weakness in her legs. In a matter of months, she was completely immobile. She was diagnosed with MS in June 2022. The treatments started with Steroids, then moved to 6 doses (one every 28 days) of Tysabri (Nat...

Any advice❓Tips? Please share👋

I was just wondering if anyone else here is on Tysabri? I have been on it for two years and at risk for the complications that Tusabri can bring - but have chosen to stay on it as it is working so far. I also have just had my first dose of it through subcutaneous injections. Has anyone else had e...