Emergency care is meant to be a safety net—a place to turn when symptoms escalate or a crisis hits. But for individuals living with ME , FM, or Long-COVID , visits to the ER can often feel more like an uphill battle than a lifeline. This post explores the unique challenges our community faces in emergency settings, shares lived experiences from across British Columbia, and offers practical tools to help prepare for and navigate these often difficult situations. Ongoing Strugg

The ME|FM Society of BC expresses profound disappointment with the 2025 BC Budget’s continued neglect of over 87,000 British Columbians living with Myalgic Encephalomyelitis (ME), 136,000 with FM and 118,000+ for those living with ME post COVID.  Despite years of advocacy and explicit recommendations from the Select Standing Committee on Finance and Government Services, this budget ignores the urgent needs of a community facing systemic healthcare barriers, stigma, and a loom

The ME|FM Society is revamping the My MLA & ME program for the new Legislative session – and you’re invited to be a part of it . People with myalgic encephalomyelitis know too well what it is to live with a misunderstood disease. From gaslighting to lack of awareness, we are practiced at advocating for ourselves in medical settings. But what does it look like to bring those advocacy skills to the political realm?  Since 2020, the Society has run its My MLA & ME campaign, supp

Welcome back, myth-busters! In our second installment of the 'Dispelling Myths' campaign, we're diving deeper into the intricate world of ME/CFS and Long-COVID. Today, we're tackling two prevalent misconceptions that often leave patients feeling misunderstood and frustrated. Ever heard someone say, 'If you could do it yesterday, why can't you do it today?' or 'Isn't that just a middle-aged woman's condition?' Buckle up as we challenge these oversimplifications and shed light

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 Travel Assistance Program (TAP) offers financial relief for BC r esidents traveling for non-emergency medical services not available in their communities. Residents must have MSP enrollment and a referral to an MSP enrolled medical specialist for services outside their community. Key Points: TAP does not cover personal expenses like meals or accommodations. Your travel must not be covered by third party insurance. Before travelling, you will require: a completed TAP form

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

Good news! If you are a Person With Disabilities (PWD), with a valid Disability Tax Credit certificate, you will be able to apply to the Canadian Dental Care Plan (CDCP) using the online tool starting on June 27, 2024. For information on services covered, see here . In order to qualify, you must not have access to dental insurance have an adjusted family net income of less than $90,000 be a Canadian resident for tax purposes have filed your tax return in the previous year