I am a PhD student with MS and am conducting my research on the topic of psychological support in MS (something that as a patient myself I feel is lacking!).

I'm interested in knowing...

What has been your experience of psychological support in MS?

What kind of psychological support would you like for living with MS?

I'm also particularly interested in people's use of forums like this as a means to get support which is why I'm specifically reaching out here.

If you are happy to help out then you can complete this online survey here by clicking the ‘start’ button at the bottom of the page. https://research.reading.ac.uk/neurodegenerative-diseases/multiple-sclerosis/

Or you can go directly to the survey here: https://forms.gle/5YTssp4pDVFciYEe9