We offer many services for Manitobans (and others) with ME/CFS. Send us an email if you’d like more information. You don’t need a ME/CFS diagnosis to use our services.
A monthly Zoom support group where you can talk to other Manitobans with ME/CFS to discuss strategies and give and receive support.
A Discord server where you can connect with other Manitobans with ME/CFS. Email us if you’d like an invite link.
A yearly event for May 12th, the day of ME/CFS Awareness. In 2026 we organized an art exhibit of masks created by members like you!
Weekly Zoom meetings for socializing and body doubling. Socializing Zooms are at 8:00 PM on Monday and 1:00 PM Wednesday for an hour. Body doubling starts at 2:00 on Wednesdays. Send us an email if you’d like the Zoom link.
Every month we have an in-person social meeting. This is typically lunch at a restaurant. For more details sign up for our newsletter.
A monthly newsletter letting you know what we're up to, and highlighting Manitoba ME/CFS news.
We can mail you a physician package, documents to give your doctor to educate them about ME/CFS
We keep a list of doctors in Manitoba who are knowledgeable about ME/CFS. The document also includes tips for working with unknowledgeable or unsupportive doctors. Michael keeps it up-to-date as we hear about more doctors.
If you'd like one-on-one support from a board member, send us an email. We can also schedule a phone call.
Michael can join you at a doctor's appointment, to advocate for you, or to take notes if brain fog makes it difficult to concentrate.
We have a small library of books about ME/CFS that you can borrow. Currently they're all hard copies but we are planning on adding digital books.
Michael has written documents summarizing some of the aspects or co-morbidities of ME/CFS, such as POTS and MCAS.
Michael has written an "ME/CFS 101" document for people who are new to the illness.
If you have ideas for other ways we can support the community, let us know!