This episode is the second of a series where Kathy talks to MSers from around the world about their diagnosis and treatment experiences, to see how they differ from our own.

Kathy's guest today is Robert Joyce, who lives in a beautiful part of the world, Connemara in Ireland. Now aged 50, Robert was diagnosed with MS while he was living and working in England at the age of 23. Although his fatigue meant that he couldn't continue working at the same rate, over the years he has owned several businesses, operated as a business consultant, and was the head of a sporting organisation in Ireland.

However, following a minor car accident his MS, which had been in remission for nearly a decade, returned and since then his life has to be lived in 30-minute blocks

Topics covered include:

Robert's story of diagnosis in England, and subsequent treatment in IrelandHis experience of working with a chronic illness in Ireland, USA, UK, Norway, Spain, Turkey and SwitzerlandThe accident which bought his MS out of remissionThe symptoms which mean he has to live in thirty-minute bursts of activity

Resources mentioned in this episode (clickable links):

Robert’s website A 30 Minute LifeRobert on TwitterRobert on InstagramTemperature conversion! To change Fahrenheit to Celsius, deduct 32, then multiply by 5, then divide by 9To change Celsius to Fahrenheit, multiply by 9, then divide by 5, then add 32

 

** Sign up for the FUMS Friday Night 6 Pack at FUMSnow.com. And for more information about Patients Getting Paid, please visit FUMSnow.com/PatientsGettingPaid.

**If you get value from the FUMSnow Podcast Show, please consider leaving a rating or review wherever you get your podcasts. Reviews are really important and help to spread the word about what we do. It’s quick and easy to do and we have some instructions here. Thanks for your time and support!

**Don’t forget to join us on the FUMS Facebook Pageand on Twitter at FUMS. Have an idea for a topic or someone to interview? Perhaps YOU?? Send me an email at [email protected].

And remember to speak to this stupid disease as it deserves: tell it FUMS every day!!

Twitter Mentions