New guides launched: how to campaign for access to MS medicines

We're pleased to launch a set of brand new guides on how to campaign for access to MS medicines in England, Wales, Scotland and Northern Ireland.

The guides aim to help people affected by MS make the best possible case for access to medicines which have been proven effective, including:

  • how medicines are made available on the NHS
  • how to navigate local NHS systems and
  • how to raise awareness of the issue

Give us your feedback!

The MS Society believes that everyone with MS in the UK should receive the right medicine at the right time, no matter where they live.

If you’ve found these guides useful then let us know by commenting below, or contact the campaigns team at campaigns@mssociety.org.uk or call 020 8438 0700. 

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I thought we'd be automatically told and made aware of new drugs for MS but it seems not.

 

The MS Society always aims to bring you the latest news on research for new drugs and their availability. http://www.mssociety.org.uk/ms-news/2012/08/ms-drug-gilenya-now-availabl...

it important guides for health
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