ME Society of Edmonton

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ME Society of Edmonton The M.E. (Myalgic Encephalomyelitis) Society of Edmonton is a not for profit that advocates, supports and educates those affected by ME/CFS.

The ME Society of Edmonton does not recommend any medications, but you can discuss any of them with your physician if yo...
10/09/2026

The ME Society of Edmonton does not recommend any medications, but you can discuss any of them with your physician if you believe they are appropriate for you.

10/07/2026
What does sleep dysfunction in ME/CFS feel like to you?  It is often unpredictable: one night you may feel "tired but wi...
10/05/2026

What does sleep dysfunction in ME/CFS feel like to you? It is often unpredictable: one night you may feel "tired but wired" and cannot sleep, while the next night you may have hypersomnia. It is extremely frustrating!

Instead of diagnosing dysautonomia as the illness, it could be ME/CFS as the illness represented by the entire elephant ...
09/27/2026

Instead of diagnosing dysautonomia as the illness, it could be ME/CFS as the illness represented by the entire elephant in this meme. It depends on which specialist you see as to what diagnosis you may receive, or whether you get a diagnosis at all. The doctors are only looking within their specialty. The pieces of the puzzle from each specialist are often not put together into a diagnosis of the entire elephant, or ME/CFS. The neurologist uses the acronym FND, which refers to Functional Neurological Disorder.

What does post-exertional malaise (PEM) or post-exertional symptom exacerbation (PESE) feel like to you?
09/25/2026

What does post-exertional malaise (PEM) or post-exertional symptom exacerbation (PESE) feel like to you?

ME/CFS Support GroupDate:  Wednesday, September 9, 2026 (link below)Time:  2:00-3:30Join us for our monthly ME/CFS Suppo...
09/08/2026

ME/CFS Support Group
Date: Wednesday, September 9, 2026 (link below)
Time: 2:00-3:30

Join us for our monthly ME/CFS Support Group. Everyone is welcome! Please make yourself comfortable for our meeting. Our Support Group meets on the second Wednesday of each month from 2:00 PM to 3:30 PM.
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Zoom link: https://us06web.zoom.us/j/83792782697?pwd=z9fZ2pCFiDN1zo2yqbwgo6atoIySwp.1
Meeting ID: 837 9278 2697
Passcode: 663990

08/15/2026

What is your experience of post-exertional malaise (PEM)? ME Research UK Survey https://tinyurl.com/PEMsurveyME

ME Research UK wants to present its work and the realities of ME/CFS in ways that are relatable to supporters. The lived experiences of those affected convey the reality of the disease in the most direct way possible. We are collecting anonymous quotes from individuals with confirmed or suspected ME/CFS about various core symptoms to be used at our discretion online, in print, and for internal organisational education.

Share your experience of PEM: https://tinyurl.com/PEMsurveyME

*For privacy purposes, we will not be using information from social media comments on this post – therefore if you wish to participate, please follow survey link*

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Edmonton, AB

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