Our research priorities
At the MS Society, we believe in a future free from MS. And research is how we’ll get there.
But research is a marathon, not a sprint. Big breakthroughs take many years, even decades. And that can be incredibly frustrating.
That's why it’s so important we have a clear research strategy. To help us make smart decisions about what we fund. And make sure we’re investing in research that has best chance of leading to real progress.
Our 2025–2029 Research Strategy
Manage the impact of MS. Stop it from getting worse. Prevent it before it starts.
Our Research Strategy sets out our research priorities for the next five years. It’s our roadmap for delivering the Stop MS pillar of our organisational strategy.
It’s shaped by the voices of people living with MS and built on the momentum of recent discoveries. It sets out what we believe we can achieve in the next five years while driving towards our long-term vision.
Our research priorities
Our strategy focuses on three priorities that reflect what matters most to people living with MS. We’ll invest in high-quality research to:
- Manage the impact of MS holistically to improve quality of life
- Find new treatments to stop MS getting worse for everyone
- Drive towards the possibility of preventing MS in future generations
These priorities are underpinned by strong national and global research partnerships, and a clear focus on turning discoveries into real-world impact.
MS affects mood, memory, energy, pain, mobility, and more. And improving how we understand and manage the impact of these symptoms is so important for quality of life.
Since the launch of our previous strategy, more effective DMTs means many people with MS are experiencing fewer relapses and slower progression. And they’re living longer. So now we need to go beyond just individual symptoms. And take advantage of advances in technology to make progress.
We’ll focus on improving well-being and quality of life by managing the impact of MS in a way that focuses on the whole person. This could include research that:
- Supports mental health and wellbeing
- Explores non-drug approaches to symptom management like lifestyle changes
- Looks at new ways to support rehabilitation and make it part of everyday care
- Develops digital tools to make sure everyone can access support
- Finds new routes for research to be turned into real-world services
Our aim is to find treatments that can slow, stop, and one day even reverse, the build-up of disability in MS for everyone.
Since the launch of our previous strategy, we’ve seen significant changes in the treatment landscape:
- Two new treatments have been licensed for people with active primary and secondary progressive MS: ocrelizumab and siponimod.
- For the first time, two phase 3 trials – HERCULES and ORATORIO-HAND - have shown drugs are able to slow disability progression in people with non-active primary and secondary progressive MS
- We now understand that MS progression can happen without relapses (the concept of PIRA or smouldering MS)
We must keep the momentum going. And step it up.
We’ll support research that deepens our knowledge of the mechanisms of progression. This could include research that:
- Expands our understanding of PIRA and smouldering MS
- Studies the effect of ageing, and the role of female hormones, on progression
- Develops new models of how MS gets worse over time
- Takes advantage of the wealth of data provided by Octopus
And we'll support research that develops and tests new approaches to slowing or stopping progression, which could include:
- Getting the right treatment to the right person at the right time, known as precision medicine
- Delivering combinations of treatments that work on different aspects of MS, and putting together drugs that could work better together than on their own
- Looking at non-drug approaches, like managing other health conditions and lifestyle changes
- Identifying signals in the body (called biomarkers) that could be used in clinical research
And of course, we’ll continue backing world-leading clinical trials, like Octopus. And programmes that turn lab research into new ways to protect nerves and promote myelin repair in people with MS.
We want fewer people to develop MS in the future. To make this a reality, we first need a better understanding of who’s at risk of MS and why. And how we can act on those risk factors.
Since the launch of our previous strategy, the research community have generated huge momentum around the prevention of MS, with breakthrough papers on EBV and its causal role in MS. And the concept of identifying and even treating MS before someone develops it clinically (known as the MS prodrome) is gaining traction.
Now, developing and testing ways to prevent MS must be a global effort. And we have a key role to play.
We’re seizing momentum in the research community with our UK Prevention Taskforce. And we’ll support research that:
- Gives us a clearer picture of how people affected by MS feel about risk
- Identifies early signs that someone has a higher risk of MS
- Works out how to support people who are at risk of MS to take part in studies
- Helps us understand what we need to do to run successful prevention trials in the future
To speed up progress across all three priorities, we need the right people, the right tools, and the right partnerships.
We’ll continue building a growing, skilled and diverse MS research workforce, that’ll produce tomorrow’s leaders and breakthroughs. We’ll develop strategic collaborations and influence other funders to support MS research.
And we’ll involve people with MS at every stage, to make sure solutions are accessible, inclusive and based on lived experience. We’ll focus on:
- Building a thriving community of early career researchers
- Improving diversity and inclusivity in our research programme
- Developing greater capacity in data science, to make the most of developments in AI and other digital technologies
- Playing a vital role in national and international collaborations, like the International Progressive MS Alliance, and creating partnerships with organisations from other health condition
- Using our influence to leverage new funding into MS research
Equity, Equality, Diversity and Inclusion in Research
MS affects everyone differently. Your biology, environment and life circumstances all influence how your MS develops, how you experience symptoms, and how you respond to treatments.
But research doesn’t always reflect this complexity. And that means it can fail to address the needs of the whole MS community.
We’re committed to funding inclusive research that improves the lives of everyone affected by MS. You can read our progress so far in our 2021-2024 EEDI in research progress report.
Now, our new EEDI Action Plan for Research 2025-29 sets out how we’ll make meaningful changes to achieve our EEDI goals for the next five years:
- An MS research workforce where everyone has equal access to funding, opportunities and career progression
- Advisory and funding panels that draw on diverse experience to make inclusive and unbiased decisions
- Funded research that actively considers the diversity of the MS community and provides opportunities for people from all backgrounds to take part
- People affected by MS from all walks of life helping to shape our research programme through our Research Network
If we can do this, we open the door to better science, and ultimately to treatments and care that truly work for everyone.
James Lind Alliance priority-setting
In 2013, we carried out a project to put people living with MS at the heart of our research programme. We worked with people with MS, families and health care professionals to find the top 10 MS research questions. This work was supported by the James Lind Alliance.
These questions supported our Research Strategy 2018-2022. You can download that strategy and 2023-2024 Research Strategy Extension documents from the sidebar.
Since then, we've made big steps towards answering many of these questions. And we've continued to work closely with people with MS to develop our new strategy, and make sure any unanswered questions are included.
- Which treatments are effective to slow, stop or reverse the accumulation of disability associated with MS?
- How can MS be prevented?
- Which treatments are effective for fatigue in people with MS?
- How can people with MS be best supported to self-manage their condition?
- Does early treatment with aggressive disease modifying therapies (DMTs) improve the prognosis for people with MS?
- Is Vitamin D supplementation an effective DMT for MS?
- Which treatments are effective to improve mobility for people with MS?
- Which treatments are effective to improve cognition in people with MS?
- Which treatments are effective for pain in people with MS?
- Is physiotherapy effective in reducing disability in people with MS?
We've done this in a number of ways, including funding new research projects every year through our open grant round.
We also brought together researchers, health care professionals and people with MS to discuss some of these priorities as part of our Clinical Trials Network.
These groups looked at things like the best way to:
- test the benefits of vitamin D supplements
- find the best treatments for fatigue
- and to understand the benefits of early treatment with aggressive DMTs
You can read more about the impact of our research and the difference it makes.