The MS Trust website provides evidence based information for people with multiple sclerosis, their families and friends and for all health professionals who work with them.
The MS Trust is an independent charity, funded primarily from fundraising. The MS Trust website also provides information about our work, the services we provide and the various ways members of the public can support us through fundraising.
Any grants to support specific projects are cited on the relevant pages. A summary of our income and expenditure is published in our annual report.
All information published on this website is accurate at the time of publication and all sections are regularly reviewed. Pages prepared under the Information Standard show the date the page was published and will be reviewed within three years.
The content, design and navigation for this website are developed in consultation with relevant users of the site and are periodically reviewed by people with MS. If you would like to be involved in this process, please contact us.
Where information relevant for people with MS in the UK or for the health professionals who work with them is available from an external source, we may at our discretion link to their online resources. We endeavour to keep this information up to date but are not responsible for the information on these third party websites. Links to external websites should not be taken as endorsement of any kind.
The MS Trust endeavours to ensure the content of this website is accurate and up to date but does not accept any liability for error or omission.
The contents of this website constitute information only and should not be construed as advice. Decisions on how to act on this information are the responsibility of the individual and not the MS Trust. The information on this site is not intended to be an alternative to seeking professional help and advice.
Information may be changed or updated without notice. If you want to re-use the information on our website see our copyright policy.