Humour and writing help author come through three major health shocks.

When hand tremors caused by multiple sclerosis forced Iza to give up her love for photography, she didn't realise it would lead her to a whole new passion.

Roxy Murray talks about her MS diagnosis journey and the importance of sharing her own experiences to ensure that other ethnically diverse individuals don’t face the same difficulties and delays.

The personal experiences of someone with relapsing remitting MS who takes the DMD, Kesimpta (ofatumumab).

The Black MS Foundation provides a platform for black people and people of colour with MS to share their experiences, meet others and raise awareness. We caught up with Founder, Natalie to hear about her own multiple sclerosis journey, which led her to set up the group.

What is it like to have a lumbar puncture? A woman who underwent a lumbar puncture during her diagnosis for MS (multiple sclerosis) shares her personal account of the process.

Tim was diagnosed with multiple sclerosis in 2009. Since then Tim, and his wife Caitlin, have been dedicated to raising funds for and supporting the MS Trust. Here, they talk about their fundraising efforts and what led Caitlin to become the Chair of Trustees.

Yeoman Warder, or Beefeater, Andy Merry talks about his diagnosis of multiple sclerosis in 2016, and how he has since gone on to scale the highest mountain in Western Europe.

While everyone around her seems to be starting a family, Edith considers what impact having children when you've got MS, will have.