Multiple Sclerosis Society
About us
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 Northern Ireland and Scotland.
Latest Press Releases
- Misconceptions make life more tough for people with MS
- Stem cell therapy may halt and even reverse disability in people with relapsing remitting MS
- Majority of UK doctors opposed to legalisation of euthanasia
- Sativex shows significant spasticity improvement
- Respite care investment needs close scrutiny
- Care charges risk leading people with MS into poverty
- Embryo Bill decision offers hope to people with MS
- MS Society welcomes Government Social Care review
- Sainsbury Trust funds “vital” MS research
- MS Society event highlights childhood MS

