My MS diagnosis story: "It took me a long time to realise that it was okay not to be okay"
When Carla was diagnosed with MS in 2008, she felt like she’d lost control of her “body and future.” Here she explains how the Kubler-Ross Curve helped her come to terms with her MS diagnosis and to stay positive.Read more
"Live life to the fullest and accept any challenge that makes you look twice"
Trudi Lampart-Macdonald from Kent took part in our Jump in June skydiving month last year and raised around £1,000 to help fund the MS Trust’s work. Here she tells us why it meant so much to her to be able to take on this challenge.Read more
On the box: Hollyoaks set to tackle MS storyline
In this blog, Lydia from the MS Trust comms team highlights the importance of having people with MS on primetime TV, but also looks at the difficulties of portraying such a complex condition in a drama.Read more
Getting to know my MS
Heather tells us how she and her family are dealing with her recent MS diagnosis and why she has decided to take on the Bath Half Marathon.Read more
A whole new world for me
Sarah was still getting to grips with her own MS diagnosis when she decided to throw a garden party to raise awareness and funds.Read more
Making our voices heard
Mags Lewis was diagnosed with MS in 1994. After a career as a manager in the NHS, she’s now the Green Party disability spokesperson, and hopes to stand as the party’s candidate for Leicester at the next general election. She tells Open Door why she thinks it’s important for people with MS to get involved and make a difference.Read more