This past year has been tough on all of us. But imagine being diagnosed with a lifelong condition such as multiple sclerosis in the middle of it all. In this episode the MS Trust chat to two young women, to find out how they coped with their MS diagnosis in the middle of a pandemic.

Many people with MS struggle with fatigue during the best of times, but lockdown made things several times worse. In this episode we meet Ant Chapman, a musician and educator who worked all the way through lockdown remotely. We talk about his MS journey and how getting creative and starting to stream music making sessions on Twitch helped him get through lockdown.

During 2020 we had to learn to live with the new norm where everything moved to online. But how does that work when you are expecting a baby? In this episode we chat to Jenna and Annie, two ladies with MS who both found out they were expecting during lockdown.

During 2020 many people found themselves on furlough, or being made redundant. In this episode we speak to Amy, who started not one but 2 new jobs during 2020. Amy also runs an online support group for young people with MS and we chat about how that was a great help during the year.

Did MS or the pandemic make you rethink your career path? In this episode of "Me MySelf and I" we talk to Will and Diva, two performers who used their MS diagnosis as a catalyst to change direction in their working lives.

Guest presenter, Will, raids our archive to talk about disease modifying drugs (DMDs). Featuring input from MS nurse advisor, Nikki Embrey, Will covers key questions including how to tell whether a treatment is working and how long to stick with a DMD that is causing side effects.

In this Carers Week special we hear from Martin who was diagnosed with MS around 40 years ago and his wife Lizzy, who offers support through unpaid care. We also chat with Roma from Carers in Hertfordshire about what help and support is available for carers across the UK.

Guest presenter and MS Trust volunteer, Will, continues raiding our MS archives. This time he's talking about pain and multiple sclerosis. Featuring input from consultant nurse in pain management, Sue Barnes.

There are over 40,000 people living with advanced MS in the UK. In this episode we talk to Paru and Rob from the MS Trust about why we are raising funds to place more health professionals in the NHS. We also talk to MS Champion Nicki Hare about what life with advanced MS is like and what MS champions do to help.