MS research

Research matters. But so does lived experience.

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Why MS research matters

MS research is constantly evolving. New treatments. Better understanding of symptoms. Improved approaches to care.

Progress is happening. But research only works properly when it reflects real life.

That’s why we actively work alongside researchers to ensure the voices of young adults living with MS are included, not as an afterthought, but from the start.

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Why research needs young adults

Most people are diagnosed with MS in early adulthood. Yet research, services and conversations don’t always reflect what that stage of life looks like.

MS Together team

Projects we’ve supported

We’ve recently collaborated with researchers on projects including:

Menstrual-related worsening of MS symptoms

Many women in our community report changes in symptoms linked to their menstrual cycle, but this isn’t always widely discussed or understood.

We supported research exploring menstrual-related symptom changes, helping ensure the experiences of young women living with MS were represented clearly and honestly.

Because if people are experiencing it, it deserves to be studied.

Read more about this research

How we work with researchers

We can support research by:

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Sharing surveys with our community

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Providing lived experience insight

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Offering co-production input

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Contributing to panels and advisory groups

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Helping shape research questions so they reflect real needs

We are particularly interested in projects focused on:

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Mental health

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Identity and adjustment

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Employment

Hormonal change

Hormonal impact

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Quality of life

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Young adult experiences

Are you a researcher?

If you’re working on a project relevant to young adults living with MS and would like to collaborate, we’d love to hear from you.

Contact: hello@mstogether.org

Get involved in research

Research helps improve understanding, treatment and support for people living with MS. By taking part, you can help shape the future of care and ensure that the experiences of young adults are represented.

There are many ways to get involved, from surveys and advisory panels to clinical studies and trials.

You can explore current opportunities through trusted organisations:

Taking part in research is always voluntary, and you can choose opportunities that feel right for you.

Looking for support?

Research shapes the future. Support helps today.If you’re 18–35 and living with MS, you can explore our community and services below.

People living with MS at an event