In this back to school themed episode we speak to Suzy, a teacher with MS and Nick, a dad to three boys who was diagnosed with MS at the start of lockdown. With schools going back after the summer holidays, we discuss everything from the challenges of home schooling to talking to children about multiple sclerosis.

We chat to neuro-physiotherapist Jody Barber about how mobility problems may present in MS and what to do if you think you need a mobility aid. Jody also discusses the psychological barriers people may face when needing to use one for the first time.

In this episode we chat with blogger, Emily, who was diagnosed with relapsing remitting MS in 2010. Emily shares her experience of using walking aids and discusses how using a wheelchair helped change her life.

Guest presenter and volunteer, Will, is back to delve into another area of our MS archives. In this episode he turns his focus to balance and dizziness in multiple sclerosis, and shares ways to help manage these symptoms. Featuring input from Neuro and Vestibular Physiotherapist, David Herdman.

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.

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.

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, 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.

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.

During the pandemic many people with MS were told to shield. But what was it like for the keyworkers with MS? In this episode we chat to Mel, about her experiences of working as a nurse during lockdown. And speaking of nurses, we also chat to MS Trust CEO David Martin, about what happened to the MS Nurses and the MS Trust Nurse program during 2020.