Multiple Voices: your stories of living with MS
The MS Society can represent you so much more effectively if we have your real life stories of living with MS. As well as helping us to illustrate issues of concern, your experiences can guide how we work in the future. We want to hear from family members and carers of people with MS, of all ages.
Tell us how being a family member or a carer of someone with MS has affected you. We want to hear from everyone, young and not so young!
For instance,
- what are the problems you have experienced and how have you overcome them, if at all?
- What are the best bits about being a carer; what are the worst?
- What could the MS Society do to better support you and others in similar circumstances.
- What have been your experiences of seeking support locally?
These are just a selection of the sort of things you might want to tell us about. It's your slot, so over to you!
