Newly diagnosed survey

1. What were your initial feelings after you were diagnosed with MS? *

2. At the point of diagnosis were you given any further information by your medical team? (e.g. about MS, possible therapies, signposting to support) *

If yes, please specify

3. On reflection, what information and signposting do you feel should have been offered at the point of your diagnosis? *

4. Post-diagnosis, did you conduct your own research into MS treatments, therapies and support? *

If yes, what resources did you find the most beneficial? (e.g. MS charities, websites)

5. Emotionally, how have you coped since your MS diagnosis and what support have you accessed that has helped you? *

6. What advice would you give to others who have just been diagnosed with MS? *

7. Is there anything else you would like to share with us and the wider MS community about your diagnosis and life with MS? *

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Newly diagnosed survey

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