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.

Gideon, who trained as an Orthodox rabbi while living with secondary progressive MS, talks about the Jewish celebration, Hanukkah (the Festival of Lights) and how he’s adapted to life with multiple sclerosis.

Emily was diagnosed with MS in 2010 when she was still physically, very active. However since being diagnosed, she now struggles with mobility issues and uses a wheelchair to get around. We chat to her about how she finds exercising helps with her MS

Nick, was diagnosed with relapsing remitting multiple sclerosis at the start of the first lockdown. In this story we talk to him about how he coped with his diagnosis and how running helps him with his MS.

MS affects not only you, but those around you as well. When is the right time to discuss your MS with your children? How should you open the conversation?