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I'm going on my first big holiday since my diagnosis and I can't stop crying. I've had 3 days of being told my 3 year delayed honeymoon been cancelled and starting to make alternative plans, coming to terms with that, then today being told we are flying in 48 hours. I'm just so scared! It's the firs...

Hi all, how risky is it taking a folding electric wheelchair on a flight (putting it in the hold)? I’m planning on flying & taking my etech w/chair but wondering if it’s safer to use assistance in both airports & then hire a chair in Spain at my destination? I’ve read about how equipment is handled...

Hi everyone hope you are well. We are looking to plan a holiday to Thailand was wondering if anyone has any experience with taking meds over there? I am on baclofen, norflex, anti inflams, pain killers, anti nausea (will be leaving opioids at home can hopefully wear norspan patch?). I have medical c...

Question on what do I need to do when traveling abroad. I’m going to Turkey in august . What do I need to do at the airport ? I.e medication ( does it need to be labelled ) do I need paperwork of my diagnosis . Any advice on what to do with the heat ,ways to cook myself down . This is first holida...

Hello, hope you're all well/as well as can be expected! I was wondering if anyone had any advice regarding travel insurance? I have RRMS if it makes a difference. I have visions of it costing loads to be fair Thanks, have a cosmic weekend.

Is anyone else on the Octopus trial and been told they can not get travel insurance to cover them? I’ve just tried to renew my policy and because the medication is not regulated or used as standard for MS, I cannot get cover? Has anyone else had this problem or is there a travel insurance company t...

Hi guys! One of my best friends lives in Hong Kong and last year I booked a ticket to go see her for this coming march, I have had a rough time with my ms recently and although I am starting to feel much more mobile & stable I am petrified to go. I experience really bad numbness in my legs at time...

Hi, hoping someone could help me. I'm due to go on a bucket list holiday, whilst I'm currently still mobile and taking a long haul flight of 20+ hours. I've read conflicting reports about whether compression socks are needed. My concern, and that in the reports stated that if you have tingling\sen...

As most probably know with regards to travel insurance is ridiculous for people with MS. I was wondering if anyone has sites that they know of where you can get cheap(ish) travel insurance?

Hey I’m due to start my infusions next wed but the travel cost is going to be about £50 to Oxford and back and by taxis and national express coaches, The hospital said they don’t provide transport does anyone know of any help I can get with the costs I haven’t applied for pip yet as it hasn’t been ...