Amy was diagnosed with MS at just 17. Here she tells us about the challenges of being diagnosed at such a young age, living with an 'invisible' condition, and why she's determined MS won't stop her.
David, whose mum has MS, talks about his project with the Fixers campaign to create a short film to help other young people talk about MS.
Our day job is an important part of our identity, and being diagnosed with MS shouldn't mean giving up the things that make us who we are. But the unpredictability of MS may mean that you have to make some adjustments to how you approach work. In this guest blog, Carla, who was diagnosed with MS in 2008, suggests some simple changes you could make to help manage work life and MS.
MS awareness week is coming and we’re excited to announce that we’ll be launching MSTV, our new YouTube channel designed to help young people affected by MS.
Radio 1 DJ Scott Mills, whose mum has MS, offers his advice for young people navigating the ups and downs of growing up when you have a parent with MS.
Teresa and Des have set themselves a mammoth challenge of running 1000 miles in 2018 to support people living with MS.
Zoe tells us why she and her partner Rob ran The Big Half for the MS Trust to help support people affected by MS.
When Yvonne adopted her dog Bonnie, she could never have imagined the positive difference she’d make to her life. Last year Yvonne trained Bonnie up to become an Assistance Dog, and the benefits have been endless, as she explains in this guest blog.
A few years after her diagnosis of multiple sclerosis, Elaine had to come to terms with using a wheelchair. In this inspirational guest blog she discusses her own journey of acceptance, the reaction of others, and the positive and negative sides of life in a wheelchair.