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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...

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.

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.

All MS patients are entitled to a disabled bus pass that gives them free bus travel Current symptoms and benefits are not considered, you just need to send a letter from your consultant that confirms your diagnosis and 2 passport pics. This do not apply to Scotland and all you need to do is cont...

Hi all, I am looking for some advice from any MS sufferers who have or still do a great deal of globe trotting. First of all I have always dreamed of traveling the world but as always things get in the way! However, since my diagnosis nothing else seems to matter to me but making this happen. As a...

Hi All, I have been browsing for a while and finding it really useful to read all the conversations on here, so first of all....thank you! A bit about me- I have recently received a diagnosis of Optic Neuritis and been told by the Optometrist that the most likely cause is MS. I am currently await...