We can provide emotional support and information on: symptoms; current research; diagnosis; treatments; accessing services, support and benefits; and getting in touch with the MS community.
Whatever your question or connection to MS we’re here to listen. We are not medically qualified and we’re not benefits advisors: we can't tell you what to do, but we can give you information and explore your options with you. The information we provide is always up to date and based on current evidence.
Every year, we speak to thousands of people affected by MS, including
• People newly diagnosed with MS
• Partners or friends of people with MS
• Carers and young carers
• Health and social care professionals
• People who have suspected MS but no diagnosis
Who to contact