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The MS Society is the UK's largest charity for people affected by multiple sclerosis (MS).
We are a membership organisation but provide services to all.
The Society funds MS research, runs respite care centres, provides grants (financial assistance), education and training on MS. It produces numerous publications on MS and runs a freephone specialist
Helpline
.
We are committed to bringing high standards of quality health and social care within reach of everyone affected by MS and to encourage and support medical and applied research into its cause and control. We have
a vision and mission
for action across the UK.
With a network of
branches & regions
across the UK, the Society has a
National Centre
in London and national offices in (External)
Northern Ireland
,
Scotland
and
Wales/Cymru
.
Comments, Compliments or Complaints
The MS Society is committed to providing high quality services. We want MS Society services to achieve the highest services in all that they do, no matter what the service is or where it takes place. One of the ways in which we can continue to improve is by listening and responding to feedback.
If you have any comments to make about the MS Society please follow this procedure
Comments, Compliments and Complaints (60 kb)
Please follow the link to find the latest information from the meetings of the Board of Trustees.
Information on the policy and guidelines for relations between the MS Society and the pharmaceutical and allied industries can be downloaded below. image: [pdf]
Policy on relations with the pharmaceutical industry (72 kb)
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