We are thrilled to announce the launch of our "Dispelling Myths" campaign, a vital initiative aimed at tackling the misconceptions surrounding ME/CFS and Long-COVID. These conditions affect millions, yet misinformation can lead to stigma, misunderstanding and even harmful treatments. Our goal is to provide evidence-based content and foster a supportive community for those impacted. What You Can Expect: Over the next six weeks, we will publish a series of blog posts, each desi

The holidays are a time for joy, but for those of us with ME, FM and/or Long-COVID, they can also be a recipe for exhaustion and symptom flares. That's why we've created a free "Living with ME/Long-COVID" email series module dedicated to helping you navigate the holidays with energy to spare. Register for our "Living with ME/Long-COVID" email series now . Note if you have signed up for our email series, you do not need to sign up again. Need an energy boost?  Jam out to our

"I feel like this series is a life-line for people with ME or Long-COVID who are faced with healthcare and social support systems that provide so little access to knowledgeable help and meaningful support." Christina Wiebe Our new educational series, including 12+ helpful, informative modules, is now being sent directly, by email, to people across the province. Information is fact-based, up-to-date, and developed by experts, patients and caregivers. Includes friendly, easy

For an audio version of this article, click on the red SoundCloud arrow. Introduction and diagnosis Symptom management and referral ME W ebinar for physicians Complex Chronic Diseases Program FAQ page In order to support you with your primary care provider, our website hosts information on Introduction and diagnosis and Symptom management and referral . This information is aimed at health care providers. Our Introduction and Diagnosis page contains links to The National

For an audio version of this article, click on the red SoundCloud arrow on the right. Applicable links My MLA and ME program L etter to Minister Dix and Ministry of Health staff We continue to advocate for all British Columbians living with ME in our ongoing communications with sitting MLAs, Health Minister Dix and Ministry of Health staff. In addition to our successful and ongoing My MLA and ME program, we also communicate our concerns in other ways. As demonstrated in

For an audio recording of this article, click the SoundCloud link arrow. Summary notes of the May 12 webinar Accompanying survey Examining the Unmet Needs of British Columbians living with Myalgic Encephalomyelitis On May 12, 2022, in recognition of International ME Awareness Day, the ME|FM Society of BC was pleased to host a virtual event: Sounds Like ME - a community conversation. During the event, Society Co-chair Hilary Robertson provided an update on Society work and

The connection between Long COVID and ME is evolving. In an effort to collect information on this developing topic, there is a new page to our website out today. ME and long covid resources - hosts a collection of published research on ME and Long COVID, collected accounts from researchers and experts, and a series of media pieces covering “long-haulers” developing ME/CFS. Please visit, read and share.

We express our gratitude to ICanCME Research Network for sharing this informative Journal of Orthopaedic and Sports Physical Therapy episode with us. Episode description: More than 10 million people across the world are living with the long-term consequences of COVID-19. But the crushing fatigue experienced by so many with long COVID—the postexertion malaise—is not new. People have lived with postviral illness and postexertion malaise, and they've faced stigma and harm for d