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We took MS to Parliament with an exhibition on research, read the featured stories and the objects people picked to represent what MS means to them.
Find out more about our new email service for anyone who has been newly diagnosed with MS.
Read more about a recent change to membership requirements for your group's coordinating team members
Read about the impact this project is already having for people with MS in Wales and how there is still some time left for more people to get support.
Get in touch
Don't forget we always want to hear from you - send us your stories: [email protected]
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