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I'm a bit nervous. My daughter and I are traveling to NYC Saturday for a week and it's the first time I am outwardly using assistive devices like my cane and I just bought a walker. I am really hoping it goes well. I don't get a lot of exercise and I also have a desk job.

About to get on a plane for the first time in years and the first time since my diagnosis, I used to love flying but now I’m very anxious and want to just stay home. Too many uncertainties.

Evening all Im from the UK and thinking to go on a 4 day holiday to New york in March, I know this is a stupid question but can you go abroad there with MS or possible MS diagnosis to America? Thank you x

Just wondering ,has anyone travel while taking meds? I am taking Teriflunomide tablets and want to do some traveling . I have double checked if I can have the meds in the country I want to go to . But I more thinking like the touristy part. Like the all the walks or hiking.

Hi All, I am newly diagnosed with relapsing remitting MS. Decided I am not going to let this stop plans for traveling that I have always wanted to do. Planning on going to South America towards the end of the year but there seems to be some controversy about travel vaccinations and MS. Looking for s...

Hi, I had some problems when traveling and wondered if anyone had similar or could offer suggestions, or at least just want to vent my frustration!... I was diagnosed a few months ago (although for a year before was experiencing symptoms). I am still physically fully able, however often get pins a...

How do you navigate travel during treatment when your immune system is reduced? Specially air travel to larger city’s like New York, London or Paris with lots of people and infection risks? Always with 95 mask?

Hello All, been a while, largely due to the following. So, i'm off to South America in about 6ish weeks, for work primarily, then following up with a (in my belief much needed) break. i'm going backpacking down to Argentina then back up through Chile to Bolivia and to Peru before coming back home....

Hi all. Recently diagnosed with relapsing remitting and considering treatment options. My favoured option at the moment is Lemtrada. I'm just wondering what experiences people have had with travelling and getting travel insurance afterwards. I love backpacking and don't recessarily want this to stop...