For all of you who are living with Myalgic Encephalomyelitis in Canada – please take a moment to engage with your MP’s and your MLA’s, and if you can, get them on board. We need funding and education and a substantial.chamge in the approach to this disease and to do that, we need a voice.
We are #MillionsMissing and we must #selfadvocate
If you’re tired of this view then please take part in whatever way you can.
http://www.millionsmissingcanada.ca/faq-meet-my-m-p-campaign/
