To my fellow Canadians with M.E./CFS:
Are you also single, and/or without family or carers?
Do you have difficulties being taken seriously by your doctor’s or specialists?
Do you have challenges accessing appropriate treatment, and healthcare?
What about accessible, affordable housing? If so, and you feel able to share a little bit about who you are, and where you live, and how you cope, I’d love to hear from you.
I’m interested in finding out more to see if we can’t lobby the powers that be to improve things for those of us living alone with #MyalgicE.