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.
In a new blog, a person with MS chronicles her journey taking part in a clinical trial. This is part one in which Hellie spots a request for people to participate in a clinical trial.
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.
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”.
Paul Kosinski pushed himself out of his comfort zone to take part in our Jump in June skydiving month.
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.
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.
Jo Sopala, Director of Health Professional Programmes at the MS Trust, has signed up to run the British 10K in July and wants you to join her.
The weather's picked up, the BBQs are out and the ice-cream van is making its tuneful way up our road. This can only mean one thing: the holidays are hurtling towards us. As a general rule, breaks away are meant to be a relaxing experience. But when MS comes as part of the package deal, this isn't always the case. Caroline, who blogs at Mildly Scrambled, was diagnosed 14 years ago and has picked up a few holidaying tips along the way.