The MS Society would like to hear your views and experiences about ways information about MS can best be made available in health and social care settings, and the support that you need in order for it to happen.
By completing our survey https://www.surveymonkey.com/s/mssocietyinfopoints you will contribute to forming recommendations for the future of our work (completing the survey may take between 5 and 10mns).
The MS Society provides practical and financial support (including quality reviewed information free of charge) to help health and social care professionals provide information about MS where, when and how people affected by MS need it so they can take active steps to manage their MS and live life to the fullest.
Do contact the local information services coordinator if you have any question regarding this survey or MS Society’s work or would like to go through the questions by phone – 020 8438 0705 or by email informationcentrescoord@mssociety.org.uk.