Our strategy is built on three pillars. The second is to be heard. We want to raise public awareness and create a stronger voice to challenge inequalities. To advocate for treatments, care, support and financial security that people with MS deserve.
Improving awareness of MS
There are around 150,000 people in the UK living with MS. While nearly nine in ten people in the UK have heard of MS, less than a third know what risk factors are associated with it. And only one in five adults know at what age you’re most likely to be diagnosed with MS.
We’re committed to raising awareness across society. So there’s greater understanding of MS and its impact, and increased support for people with MS.
Lobbying for improved access to treatments and care
With our community, we’re pushing for the health and care services people with MS deserve. We’re challenging identified inequalities and exclusion and calling for improvements. So that everyone with MS can access the tailored care, treatment and support they need.
Advocating for improved financial security
We’re pushing to address employment barriers and improving access to welfare support for people with MS.
“But I also want to be honest about the realities of MS, and the debilitating impact it can have – particularly the longer you have it. I’m not ready for what progression is starting to do to my body. I think there’s so much still to be done to maintain and improve quality of life for those of us living with it.
“I hope sharing my experiences might inspire and empower people to get involved with the work of the MS Society, whether that’s through donating or sharing their own story, too.”
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Share your story
Just like MS, every MS story is unique.
We'd love to hear about your MS stories, from diagnosis to how you told loved ones and employers. Maybe you have found an interesting way to manage your symptoms or want to tell us about the challenges you have faced?
We're always on the look out for stories about life with MS to share with the community. So get in touch.
