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Hey everyone 👋 Before reading on, can I ask a favour. Can you comment down below with your relationship status? (Just one word will do)👇 It’d be cool to know so we can make more podcasts focused on what you need! I recently guested on the MS Trust podcast which explored how MS affects dating, rel...

https://podcasts.apple.com/us/podcast/ms-diagnosis-journey/id1613922867 This is an excellent podcast that talks to people with MS and Each person describes their initial symptoms, and how they finally or quickly became diagnosed. It’s nice to hear the stories of others who are passing through the s...

Hi everyone! My friend Alex is on a new podcast with MS blogger Ardra Shephard (@MS_trippingonair on Instagram), who I’m sure some of you already follow! The podcast is all about life with MS, as well as the perspective of someone who’s partner has MS (this episode featuring be a nice shoutout ...

Hello 👋 I'm Jordan and I've been diagnosed with MS in the past couple of weeks. I'm trying to process the news but I'm feeling pretty good at the moment. I'd like to gather more info about MS and living with MS. What books, podcasts, blogs etc. would you recommend? 😀

This is not a commercial exercise, it is a mission, and one which I hope might give comfort to fellow MSers. My weekly podcast can be found on all your favourite platforms perfectpitch.buzzsprout.com and following is easy! I hope you may enjoy it the way others have. Nick

Hello my shifties! I'm producing podcasts for the MS Trust. They recently ran this piece: https://mstrust.org.uk/research/research-updates/210802-multiple-sclerosis-dating-romantic-relationships and that one: https://mstrust.org.uk/news/dearbhlas-story-dating-and-ms We'd like to do a podcast epi...

To mark MS awareness week, we have put together a special clips edition of Multiple Shenanigans. Multiple Shenanigans is a video podcast about the funny side of life with MS (honest there can be one) and features myself, a comedian and improvisor and Lytisha, a poet. Lytisha and I have both have...

Multiple Shenanigans- The Red Snow Episode The new Multiple Shenanigans is now live! We we mainly talk about snowy adventures in this one. We've both had MS for a good while now, but sometimes MS can just exist in the background. Our mishaps in the snow lead us to ask if MS can make you stubborn...

Hello! Our latest episode of Multiple Shennanigans, 'Green Memories', came out on 24th. It talks about our experiences of living with MS (for 10 + years) and we laugh about some of the funny sides to it all. This is probably the most medical/ serious that we're ever gonna get, as it discusses diag...

Today we release the first (pilot) episode of MS related video podcast Multiple Shenanigans. It will be released at 4pm. Here's what it's about: A poet and a comedian both with Multiple Sclerosis meet to chat, life, escapades and the funny side of their chronic illness. And they laugh. A lot. Bec...

Hello! We have just launched a comedy podcast about having MS and would love to share with you. Myself and co-host Lytisha have both has MS for 10+ years, so have a fair bit to chat about, but also to laugh about. Because sometimes you just have to! Anyway, here is the trailer, feel free to share a...

Hi all, Really interesting and informative podcast on the causes, mechanisms and potential future treatments. https://podcasts.google.com/?feed=aHR0cHM6Ly93d3cudGhlZ3VhcmRpYW4uY29tL3NjaWVuY2Uvc2VyaWVzL3NjaWVuY2UvcG9kY2FzdC54bWw&episode=NWQ3MTExNzM4ZjA4MjUxNDg3OWVlNmRl Hope you enjoy! Birdbo...

Did anyone hear this podcast that was aired earlier this week? https://www.bbc.co.uk/programmes/p06p32gz It starts about 10 mins 30 seconds in and and focuses on the story of Nick and Tracy Gaskin. Nick has PPMS, and he met Tracy when she became one of his carers. The story in the podcast talk...

Hi! I’m Kathy Reagan Young, founder of FUMSnow.com and the FUMS Podcast Show. I’m interested in interviewing English-speaking MS’ers from several different countries about your diagnosis and treatment experiences in your country. I think it will be really interesting to see the difference in care...

http://msentials.podbean.com/?source=pb My friend Philip and I started a podcast. We discuss lifestyle strategies as well as challenges that come up in our own experiences with MS. I was diagnosed in 2012 but had my first symptoms in 2007 and Philip was diagnosed earlier this year and had his first...

Hi guys, did anyone hear the podcast / radio programme on MS broadcast on Radio 5 Cambridgeshire last week? They had a guy talking about being on a trial of a drug that resets your immune system in the hope that it comes back minus the MS aspect (he said he hasn't had any symptoms since). Quite he...

People asked me about my Podcast but I couldn’t figure out HOW to reply back, so I’ll make a whole new post… here’s my Podcast link I hope it works … https://anchor.fm/j-fingers

I can NEVER find anything for ppl like us with MS so imma make a podcast just so if there’s ppl out there like me you can listen to me & not feel so alone. That’s my goalh