MS Around The UK

You've got MS, why not try the 3 Peaks Challenge! Natalie was a great laugh and very open too. #MS #3peakschallenge #multiplesclerosis

Talking about all sorts, MS Life 2016 and why she's a bit unsure of the Paleo Diet. Not very often we get to speak to an MS Nurse, it's a great listen!

Picture the scene...... You are studying in the UK and head back home to the States for a wedding, then you can't see. From there it's just a downward spiral..... Got it? Nicole lived it! Listen to her here.

Today we got to speak to an all action MSer, if there is a fitness class then chances are Vicky will be in it! Welcome to City 8, Coventry! #MS #multiplesclerosis #Coventry

MSaroundtheUK went on holiday again to America again to speak to a lady who said she wasn't very good at talking....We'll let you be the judge of that one! #MS #multiplesclerosis #usa #America

Imagine being diagnosed and having no one your own age to talk to about it. What do you do? Set up a Facebook group for people your own age of course! MSaroundtheUK got the exclusive about this fantastic new group! #MS #multiplesclerosis #Facebook #makingadifference

She has represented MSers all over the UK with her dancing on 'The People's Strictly'. But there's more to this woman than meets the eye, grab a cuppa and have a listen to the fascinating Trishna Bharadia! You can follow here here too: Twitter: @TrishnaBharadia Facebook: www.facebook.com/trishnabharadia2015 #peoplesstrictly #ms #trishnabharadia

Less than a year from diagnosis and do you know what saved her??? Maria shares all with us, Must listen!

Oh when the Saints, go marching in..... We spoke to a friend of MSaroundtheUK: Jill in Southampton to find out about her take on MS. Another person who thought they had a tumour!!!

If you have MS you need to listen to this and join the register! Take it away, Rod! #MS #multiplesclerosis #ukmsregister #register #swanseauniversity

MsaroundtheUK has spoken to America before and today we were really flexing our podcast muscles by heading down under, to speak to a MS legend. An inspirational MS legend at that, her story is not for the faint hearted! #MS #multiplesclerosis #carolcooke #paralympian #inspirational #inspired #hardwork

"You haven't got a brain tumour.... but you HAVE got Multiple Sclerosis" Tasha from London talks about the time she couldn't walk and was left blinded by MS, amongst other things. Everyone who has MS will be able to relate to something in this interview. #MS #multiplesclerosis #London #MSfamily #winning

Imagine being told you have MS, then being told to get on with it?! Could you cope with that? It's a tale that everyone needs to hear. #MS #multiplesclerosis #cambridge #msaroundtheuk #msfamily

We had the opportunity to speak to a lady who has been called the 'Accidental Activist' in the press and has become an award winner for her efforts to make life easier for people with MS. How could we not speak to her? This is Shana Pezaro and she is a real sweetheart! #MS #Brighton #Multiple Sclerosis #MSfamily #MSer

MsaroundtheUK is branching out tonight... across the pond! When we were searching Twitter we came across this couple. Both married to MS but also married to each other! Husband and wife, both living with MS, using our experiences to empower others. Engaging public speakers and book authors . Check them out on Twitter @DanJenDig #ms #USA #mulitplesclerosis #acrossthepond #msfamily #msaroundtheuk

Bike the UK for MS is taking on a challenge that will probably leave the participants saddle sore for years to come. How would you fancy cycling the length of the UK taking in 3 countries as you go? Raising money for the MS Society, what a challenge! www.biketheukforms.org

The MS awards celebrate and reward the hard work and dedication of people who make a difference in the MS community.  Nominations for the MS Society Awards 2016 are now open. All nominations must be received by 5pm on Friday 19 February 2016.

Part of the MSaroundtheUK challenge was to also speak to organisations who make the lives of people who have MS a bit easier. We spoke to Suzanne Crighton from Mutual Support a Forces based MS organisation to find out what they offer... #MS #Multiplesclerosis #mutual-support #charity

I thought we could use the podcast to speak to other people or companies or organisations, after all we are all in this together. A quick search on twitter brought me to MS UK, but who are they and what do they do? Ryan is here to answer all our questions. #MS #multiplesclerosis #MSUK #charity

What's it like to be hanging for a diagnosis for 2 years?!!! That's exactly what Lucy Wallace is going through right now and she took time out to speak to us. Is there light at the end of the tunnel? #MS #multiplesclerosis #diagnosis

MS diagnosis when you're 21, still in denial years on. This is a story we can all relate too. Speaking to Bobby in Bangor. #MS #multiplesclerosis #msfamily #Bangor

Who has heard of the MS hug? Have you ever heard of Tysabri the drug that stops episodes? Well, Mary Burke has and she joined us to talk about MS in Liverpool. #MS #Multiplesclerosis #Liverpool #MSfamily

What's it like to have MS and be in Aberdeen? What do we even know about Aberdeen? The lovely Kirsty Ewen was there to give us the update! #MS #multiplesclerosis #aberdeen #msfamily