Hayley who lives with MS, talks candidly about the importance of being seen in her wheelchair in order to spark a change in accessibility.

Helena talks frankly about her MS bladder and bowel problems and well-being, and why she finally sought help.

Andy Reynard blogs about his footballing days and how foot exercises and an electric bike keep him moving in the face of MS.

Niti finds resilience and strength through running, whilst living with relapsing remitting MS and endometriosis.

Guest blogger Andy goes outdoors with tips for mowing the lawn, dog walking and supermarket shopping.

Dr Cora Sargeant explores how she and her loved ones take on MS monsters through podcasting, creative writing and psychology.

Mike was diagnosed with MS 36 years ago and held an active career in the army for much of that time. Here he tells how the group Mutual Support have helped him.

Author, blogger and relapsing remitting MS-er Andy Reynard shares his top tips for an easier life. Humour included.

Sometimes I feel like I’m the only black man with MS, so I’m making it my mission to create a safe space for black men with MS to be vulnerable.