A podcast talking about multiple sclerosis from someone living with it. We're not talking about new medicines or diets (for the most part), we're talking about how it felt when you got diagnosed, what it was like during an MS hug; things we've experienced that we can't explain to regular people without that look. It's new to the podcast world, so it'll start off with my experiences, but it will grow. Join me in my rants as I talk about my life with MS and how annoying it can be. Support this podcast: https://anchor.fm/RantMS/support
Hi guys, I can't believe I took so long to set up another episode. This one is more on covid-19 and having fears about it. As always, I'm just ranting...
Part 2 and I kinda break my happy attitude around the end. Emotions swell up for me during big flare-ups apparently, and I did have to stop for a mome...
It happened after so long. The feeling of losing control of my body. Let me share with you a little of what's happening. --- This episode is sponsored...
Have you wondered what you could do for exercise living with MS? I'll be talking about cycling for the most part in this episode --- This episode is s...
Random episode, saw the date and realized it was 7 years ago that I was diagnosed with multiple sclerosis. --- This episode is sponsored by · Anchor: ...
Pretty self explanatory, this episode will deal with me coming to terms with using mobility devices. --- This episode is sponsored by · Anchor: The ea...
This episode will deal with my experiences with doctors and the medicines they've put me on. Find me on Twitter at OchoJoJo or send me an email at och...
This episode will be taking about the beginning of my MS story. This podcast will mainly be about ranting about MS; be it about the beginning, feeling...