Back in the saddle: How my dressage dream became a reality
When Diane Green was diagnosed with progressive MS, she thought her riding days were over. But now, 17 years later, Diane and her horse Winnie have their sights set on the Paralympics in 2020. Diane shares her inspiring story.Read more
Ian's story - "I just put the exhaustion down to being 50"
Ian, diagnosed with primary progressive multiple sclerosis last August, tells us about his journey with MS and offers some advice for others in a similar situation.Read more
How an MS diagnosis helped me find my creative side
Carole has been living with MS for 15 years. She tells us how channelling her creative side has helped her “see the good in things again”.Read more
Can you dance the cog fog away?
Many people with MS experience 'cog fog', which is when you sometimes struggle with things like memory, attention span and concentration. In this blog, Helena, who was diagnosed with MS 11 years ago, talks about her own experience of the dreaded cog fog, and why she's determined those 'fuzzy brain days' won't stop her doing the things she loves.Read more
"Writing poetry helped me come to terms with my MS diagnosis"
An MS diagnosis left Phil feeling ‘stunned and scared’, but writing about some of the emotions he experienced in a poem helped him come to terms with the diagnosis.Read more
Sharing my MS story was empowering
Having kept her MS secret for eight years, MS Trust supporter Jenna decided to open up about life with the condition earlier this year – and says it was the best decision she’s ever made. Here she tells us about the empowerment she felt sharing her story and raising awareness of MS.Read more