Winter appeal for MS research

To give everyone affected by MS hope for tomorrow, we need your help today.

An MS diagnosis doesn’t just affect one person, it ripples out. It affects our whole world and the people we share it with. We need to make new progress for people affected by MS now – and create a world without MS for everyone.

As part of this year’s Christmas MS appeal, you’ll hear from Moira and Nicola. As mother and daughter their MS diagnoses are only a generation apart, but their experiences couldn’t be more different.

You’ll also hear from Francine, who was diagnosed with MS shortly before Christmas, almost 30 years ago. She shares the highs and lows of life with MS and how love has carried her through.

Their stories, among so many others, are what drives us towards hope and our vision of creating a world free from MS.

With your help, we’re funding bold and ambitious research. Such as Dr Kellie Horan’s research which is helping us understand which nerves are lost in MS and why. And Dr Sophie Fawson’s clinical trial of an app to help people with MS manage fatigue. Your support could help fund more research like Dr Ben Jacobs’. He’s looking at whether we can predict MS even prevent it in future generations.

The ones you love

Read more about the lives of people affected by MS, and the ones they love.

We’re mum and daughter both living with MS

Moira, 60, and her daughter Nicola, 28, both live with multiple sclerosis (MS). This Christmas, they’re sharing their stories of diagnosis and hope across the generations.