Amy Thompson, Founder of MS Together, talks about what led her to set up the group and how it has led to new friendships this World Friendship Day.

Lisa, who was diagnosed with MS in 2008 tells us about how creativity and a little help from Spud the hamster helped her get through tougher times.

Emily, also known as The Wibbly Dinosaur, discusses her feelings on mobility aids and how using a wheelchair provides her with the freedom to continue doing the things she enjoys.

The Government have announced that from 19 July 2021, social distancing restrictions will finally be lifted. Many people are dubbing this as 'Freedom Day'. However, as Carla King discusses in her latest blog piece, many people with MS are feeling more apprehensive than jubilant at this news.

After over 20 years of living with multiple sclerosis, MS blogger Martin Baum asks what happens when a symptom turns out to be nothing to do with MS after all?

Father of daughters, Dan talks about life with MS and how transparency has been key when talking to his children about the condition.

These pages look at how being active can help people with MS. As everyone's MS is different, so is their capacity for exercise. Whether you feel able to practice some gentle stretches or train for marathons, you will find that adding exercise to your life in a safe way will bring benefits.

Services for you from the MS Trust. Find our Helpline, our Map of MS Services and links to our broadcast channels.

Adam, who was diagnosed with MS eight years ago, and his wife, Sharon, share their MS caring journey as well as some tips for people in a similar position.