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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...

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...

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...

I used to take Copaxone and would pack the syringes in ice to keep cold when traveling. Now years later I don’t take MS meds but I just don’t want to travel. My daughter wants me to visit her in Phoenix; it is a 5 day drive which I don’t want to do and I don’t want to fly either. I have become rathe...

Trying to convince my older children of my disease PPMS is like telling them I will grow and eye on my finger in a few minutes 🥴 I have younger ones who witnessed my decline however the older ones I am making my way to see, not so much! Yes they have families and all I just only worry about if thi...

I'm planning on going travelling next year around South America and I'm not sure how I'm going to manage my MS medication and follow up appointments. Has anyone went travelling for long periods of time living off-grid? How did you manage the MS side of things?