About Us
MS Research has merged with fellow MS charity, The MS Trust.
The MS Trust is a prominent Multiple Sclerosis charity, who train MS health professionals and provide support services including a helpline to people living with MS and their families. By joining forces as one charity, the now combined Multiple Sclerosis Trust is in a stronger position to deliver robust scientific research, while now linking with clinical practice.
Together, we can create greater impact for people with MS.
Find out more about this exciting collaboration at the news section of our website.
We are still funding research
The merging of MS Research and MS Trust is an exciting opportunity for two charities to come together and create greater impact for people with MS. We will continue to provide the support that researchers and MS professionals seek from MS Research, with greater reach and resources than before.
Please stay tuned for updates and sign up to the MS Trust’s newsletters.
Do you have a question?
If you have any queries regarding how this merger affects your funding application, a donation, or your fundraising efforts, please get in touch. Our team will be happy to discuss any concerns you may have.
This website will be transferring to the MS Trust in the coming weeks.
Visit MS Trust website for more information or
For support with MS Call the MS Trust Helpline on 0800 032 38 39 or for anything else, email
MS Research is dedicated to furthering understanding of Multiple Sclerosis to develop better treatments and in the hope of one day finding a cure.
To do this, we fund robust research in all apsects of MS. We also fund education bursaries for MS professionals and provide treatment courses to help improve the lives of people living with the condition.
Multiple sclerosis (MS) is a progressive condition which causes nerve damage in the brain resulting in varying levels of lifelong disability, each year thousands are diagnosed with MS, this condition does not discriminate – men, women and children of all ages and ethnicity can be affected. In the UK MS is one of the most common causes of disability affecting young people.
We believe research is vital to:
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find better answers to the problems those who have MS and those close to them face every day
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maximise vital opportunities to bring us closer to an eventual cure
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help to overcome the inadequacies and inequalities of treatment
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further understanding of MS and its impact.
Our Aims
We have three main aims:
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Listen to people with MS and those who share their lives
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Learn more about the problems they face everyday
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Act to alleviate those problems