MS is CHRONIC

Barney Black

Welcome to MS is Chronic. If you have Multiple Sclerosis, are on a journey that is leading to an MS diagnosis or know someone with MS this podcast is for you. Having MS impacts people emotionally and physically. These episodes are with people living with, the often unpredictability, of MS day to day. Telling their story with honesty, openness, humour and stoicism. Sometimes the language can be a little blue. And the topics covered are from the heart, intimate and very personal. This is not science, medical or health advice. It is regular folk sharing their own experience and from time to time the chat moves from MS into the normal humdrum day to day of life. As the series develops guests will include perspective of family and friends of those with MS. I’ll have professionals share their knowledge insight and advice too. If you’d like to be a guest in future series please get in touch. Thanks, Barney Black

  1. 13h ago

    Season 3 - Episode 5: Annette McGarvie

    Welcome to MS is Chronic. My latest guest is Annette McGarvie. Who I met through our local MS Support group. Annette’s story starts with a fall and a broken nose. Which ultimately leads to a diagnosis of Multiple Sclerosis.  The journey from an MRI to the day of diagnosis Annette shares with a range of emotions many listeners will be familiar with. You’ll hear Annette share how she copes and what it means to have access to the local MS Support group where she meets like minded people who ‘get it’ and lnow what it means to have MS. Annette is also a member of SB Elevate, which is Scottish Ballet’s dance programme. The aim to support the physical, mental and social wellbeing of people living with Multiple Sclerosis (MS).   This programme, which is the first of its kind in the UK, was developed in partnership with MS specialists, University of Florida, Georgetown University, MS Society Scotland and MS Revive. SB Elevate® has been made possible by the generous support of Baillie Gifford (Scottish Ballet’s Neurological Dance Health partner), our trusts, foundations, and patrons.   If you have Multiple Sclerosis, are on a journey that is leading to an MS diagnosis or know someone with MS, this podcast is for you. MS impacts people emotionally and physically. These episodes are for people living with, this often unpredictable, chronic illness. Telling their story with honesty, openness, humour and stoicism. Sometimes the language can be a little blue. The topics covered are from the heart, intimate and very personal. This is not science, medical or health advice. It is regular folk sharing their own experiences. The chat ebbs and flows from MS into the day to day of life. If you’d like to be a guest in future series, please get in touch. Thanks, Barney Black     Source: The MS Society UK website: https://www.mssociety.org.uk/about-ms/what-is-ms What is MS? Multiple sclerosis (MS) is a condition that affects nerves in your central nervous system. That's your brain and spinal cord. In MS, the coating (called myelin) that protects your nerves is damaged. This causes a range of symptoms like blurred vision and problems with how we move, think and feel. Once diagnosed, MS stays with you for life, but treatments and specialists can help you to manage the condition and its symptoms. More than 150,000 people in the UK have MS. In the UK people are most likely to find out they have MS in their thirties and forties. But the first signs of MS often start years earlier. Many people notice their first symptoms years before they get their diagnosis. MS affects about two and half times as many women as men. People from many different ethnic backgrounds can get MS.  Fampridine (original brand Fampyra) What is fampridine? Fampridine is a tablet that can help some people with MS walk quicker. It’s the only drug with a licence to improve walking speed in MS. You can’t get fampridine from your GP. Only someone with specialist knowledge of MS can prescribe it, like a neurologist. How do I take fampridine? You take two tablets a day, one in the morning and the second in the evening, with 12 hours between each dose. You take it without food and on an empty stomach. Your doctor will tell you more about how meal times should fit with taking this drug. The tablet is made in a way that lets the drug into your bloodstream at a steady rate over a long period of time. That’s why you must swallow the tablet whole and not suck, chew, crush or break it. Doing that would let too much of the drug into your bloodstream too quickly. If that happens, side effects are more likely, such as the risk of a seizure. This is also why you need to take the drug without food and on an empty stomach. How does fampridine work? It’s not known for certain how fampridine works. But we know that fampridine keeps potassium in your nerves. Potassium is a mineral in your body that it needs to work properly. The movement of potassium in and out of cells helps signals move along nerves, which stimulates muscles to work. By keeping potassium in nerves, fampridine makes them work better, with the result that you can walk faster. A Fae The Scheme Production Music by The PFJ - M Lee, B Black, D Sissons, C Mclaren

  2. 08/02/2025

    MS is Chronic Season 3: Episode 2 Trishna Bharadia

    Welcome to MS is Chronic.  Now into Season 3 and another fabulous guest. Trishna Bharadia MFPM(hon) Multi Award-Winning Patient Leader and Patient Engagement Professional. Trishna will be familiar to many people in the MS community. Diagnosed with RRMS in 2008 Trishna very quickly became an MS Adovocate and Patient Leader in the MS Community and Asian MS. (From MS Society website) Asian MS Asian MS is a national support group that offers tailored and culturally-sensitive services for Asian people with MS, their carers, friends and family. It's aimed at people whose heritage originates from South Asia. We aim to: raise awareness and dispel ignorance of MS in the Asian community bring people within the Asian MS community together through various channels and means raise money for services to help people affected by MS from the Asian community represent the views and support needs of Asians affected by MS within the MS Society and wider MS community which is part of https://www.mssociety.org.uk/  Asian MS offers: information and education webinars literature on MS in English literature on MS in Asian languages guidance and support for living a healthy lifestyle with MS, contextualised for the Asian community Support and connection to the MS community: virtual chai and chat meet ups social media community telephone support newsletter Find Asian MS on Facebook Find Asian MS on Instagram Find Asian MS on LinkedIn   Trishna includes, public speaking, campaigning, peer review publications and media work in the work she does across the MS community.  A highlight for Trishna was being part of the 2015 Peoples Strictly For Comic Relief. Trishna was nominated by her sisters and it led to an amazing experience for Trishna. It also gave Multiple Sclerosis the highest profile so far on telly. Leading to connections and wider awareness. Millions of viewers across the world tuning in. The links below are to Trishna's website - please do take the time to have a look.   https://www.trishnabharadia.co.uk/  This is a great listen and I am sure you will enjoy what Trishna has to say. As always, likes, shares, comments and follows help others hear MS is Chronic episodes. Happy Listening, All the best, Barney Black Produced by Barney Black Music by Mike Lee  A Fae The Scheme Production

  3. 05/31/2025

    Season 3 - Episode 1: Ben Parker

    Thank-you for dropping in to this latest episode of MS is Chronic. Season 3: episode 1 https://open.spotify.com/show/5LVRa7QkIUIgnoU2nVTmpb?si=69540d7b470a462e First a request from me to you 😊 Please like, share, comment and follow MSisChronic podcast and help these episodes reach the widest audience possible. Thank-you. A couple of weeks ago I had the pleasure of getting to know the wonderful Ben Parker aka The Wheelie King. When I heard about Ben’s challenge to wheel himself from the South East of England (Lowestoft) to South West of England (Lands End) I was super keen to have him share his story. What a fabulous it is. Many topics get covered in this episode in addition to the epic challenge Ben will undertake in July. Ben’s childhood, his time as a bus driver where he began to experience his first Multiple Sclerosis symptoms. His journey to becoming an inspiring maths teacher and loads more. Throughout the episode Ben tells of a few people that have influenced his life and been a positive impact: His other half Louise. His art teacher and head of year Mrs. Oliver from secondary school. Childrens author and comedian James Campbell (he has a show at this years Edinburgh Fringe) https://www.jamescampbellauthor.com/home  Paralympics GB Wheelchair racer Richard Chiassaro https://www.richardchiassaro.com/  Ben is raising money and awareness for two organisations. Click on the links to find out more and you can donate to Bens Just Giving Page here. Help him smash his target for two great causes! https://www.justgiving.com/team/wheelieking?utm_medium=TE&utm_source=CL  Andys Man Club  https://andysmanclub.co.uk/about/origin-story/  No Child Without (Harlow) https://www.nochildwithout.co.uk/  Believe it or not we do talk about Multiple Sclerosis, Tysabri, Secondary Progressive Multiple Sclerosis, MRI scans and stuff like that. Ben can be followed here: X @Wheelieking2025 Instagram https://www.instagram.com/wheelieking2025/# Tik Tok https://www.tiktok.com/@wheelieking2025 With each episode I ask my guests to nominate a song for the accompanying playlist to this podcast MuSic is Chronic – Ben picks a couple of belters... https://open.spotify.com/playlist/1dkwko354172LXNic352QF?si=24495a9d45a54d1f I loved doing this episode and I believe you’ll enjoy it too. Enjoy. B A Fae The Scheme Production Produced by Barney Black Music by Mike Lee

  4. 04/02/2025

    Season 2 - Episode 6: Bev Malcolm: "Just a lassie from Lancashire"

    Thank-you for choosing to listen to the latest episode of MS is Chronic. This is season 2 episode 6. With a fabulous guest Bev Malcolm. I met Bev through the MS Society Perth and Kinross group. And we have been trying to get together for a while to record this episode. When we met to record Bev was still recovering from a broken hip. In addition to dealing with her MS. And I am very grateful to her for the time she gave. You'll hear her story as a girl from Blackpool that moved to Bournemouth and ended up in the Fair City of Perth. Bev introduced me to the Scottish Ballet’s dance programme, SB Elevate® and shared that she is a member of local choir as well as a key member of the MS Societ Perth and Kinross group too. A very inspiring lady. Enjoy the episode and if you would like to take part or know someone who would like to take part that would be fabulous. Just let me know. Happy Listening.   The intro and outro Music in this episode is by Perth musician Mike Lee. This is a 'Fae The Scheme' production   https://scottishballet.co.uk/move-with-us/dance-classes/sb-elevate/  Which aims to support the physical, mental and social wellbeing of people living with Multiple Sclerosis (MS). This programme, which is the first of its kind in the UK, was developed in partnership with MS specialists, University of Florida, Georgetown University, MS Society Scotland and MS Revive. SB Elevate® has been made possible by the generous support of Baillie Gifford (Scottish Ballet’s Neurological Dance Health partner), our trusts, foundations, and patrons". MS Society Perth and Kinross Group  https://www.facebook.com/profile.php?id=100076069987270&__tn__=%2Cd

About

Welcome to MS is Chronic. If you have Multiple Sclerosis, are on a journey that is leading to an MS diagnosis or know someone with MS this podcast is for you. Having MS impacts people emotionally and physically. These episodes are with people living with, the often unpredictability, of MS day to day. Telling their story with honesty, openness, humour and stoicism. Sometimes the language can be a little blue. And the topics covered are from the heart, intimate and very personal. This is not science, medical or health advice. It is regular folk sharing their own experience and from time to time the chat moves from MS into the normal humdrum day to day of life. As the series develops guests will include perspective of family and friends of those with MS. I’ll have professionals share their knowledge insight and advice too. If you’d like to be a guest in future series please get in touch. Thanks, Barney Black