When farmers Emily Padfield and Mark Warner applied for a new TV show promising an “off-grid experience in the Alaskan wilderness", they never once imagined they would actually end up appearing on the show, let alone winning it! We caught up with Emily to hear more about the couple’s experience on the BBC2 show ‘Win the Wilderness’ and why it was her MS that persuaded them to take on this ‘crazy’ adventure.

Don, 86, is a carer to his wife Sandie. He shares his experiences of caring for a loved-one with MS.

Just over a year ago we published a diary entry about Inclusivity and Diversity at the MS Trust. In this piece we take a look at what's changed since then and what we still need to do.

MS blogger Martin Baum was diagnosed with MS nearly forty years ago. Here he reflects on the impact his diagnosis has had on the festive period over the years.

The Cellist is a new ballet inspired by the life and work of renowned British cellist Jacqueline Du Pré, who lived with multiple sclerosis. Choreographed by the award-winning Cathy Marston, it has proved a particularly personal and poignant journey for Cathy as her mum also has MS. The Cellist premieres at the Royal Opera House on February 17 and will be screened at cinemas across the UK on February 25. Ahead of the premiere, we caught up with Cathy to hear more about the inspiration behind the work, what made Jacqueline Du Pré so special and the importance of raising awareness of MS.

Lucy Phillips was diagnosed with relapsing remitting MS in 2016 – just three months before her wedding day. Here, Lucy talks dealing with loneliness, finding support, and staying positive.

Receiving a diagnosis of MS is never easy. But being told you have MS in these extraordinary times could mean a whole new level of uncertainty and worry to deal with. We hear the experiences of people who have been diagnosed with MS during lockdown, and share some tips to help.

The MS Trust were deeply saddened to hear that former Trustee and dear friend, Sandy Burnfield passed away at the end of last week.

Megan Roberts is the Head of Health Professionals Programmes at the MS Trust, supporting MS health professionals to provide the best possible care for people with MS. We caught up with Megan to find out about the impact of Covid-19 on MS services, how the MS Trust is helping to bridge the gaps in MS care and what she loves most about her role.