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Hi I am waiting on knee surgery after badly breaking my leg now they say that I probably will not walk again. I was wondering how or if people travel ? Still don't know if I will be able to transfer which I guess will be crucial? Probably the only option are cruises. Anybody who does travel I woul...

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...

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...

Hey! I have RRMS - I really want to go travelling again but lost a lot of my circle of friends when I was diagnosed- does anyone on here solo travel? How do you find it? Any firms/companies you recommend?

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?