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.

Richard Sprenger is a journalist with MS, on a journey into the heart of the wellness industry to find alternative ways to manage his condition outside conventional healthcare. In a series of films for the Guardian, Richard invites us to investigate everything from gut health to goat yoga, to find out what might help him manage his MS.

Alex was a young student when his MS diagnosis came out of the blue. In this article, he tells us how he coped with the diagnosis by actively changing his lifestyle and finding a whole new career and passion in the process.

John opens up on life with childhood sweetheart Mary and her secondary progressive MS.