ME|FM Society of BC

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Asad Ali

Great group of people striving to help others live a more healthy and fulfilling life! Kudos to the team!

Christina Thiele

The ME|FM Society of BC is an amazing organization that truly cares about the well-being of people with ME and FM. They provide a supportive space for people to connect and learn, and are making a real difference in the lives of those with these illnesses. Their commitment to raising awareness and educating healthcare professionals is making a real difference, and I'm proud to support them.

Leslie

The ME/FM Society of BC really provides me with hope and empowerment. They have multiple programs and initiatives to help people struggling with Myalgic Encephalomyelitis and Fibromyalgia to live a better life, and champion our voices in the many unmet needs we have for basic ADL's Activities of Daily Living.. They strive to make a better today and tomorrow for us.. And for myself, it helps feeling heard, seen, and championed... Thank you.. Huge gratitude. I also get a feeling of empowerment and belonging, by volunteering with their My MLA and M.E Initiative.. Helping to build bridges of awareness, compassion, understanding and advocacy... This initiative is changing the understanding of living with chronic illness, and the many supports we need to live well with dignity and quality of life. The ME/FM Society of BC also runs events and support groups, as well as articles and blogs, etc.. Which really helps with the constant isolation. Even for those of us able to interface well in the community, it is still isolating to be unseen with these invisible illnesses... So a huge thank you to the board of directors, and volunteers that are helping to move things forward. If you are a philanthropist, or know someone who is... Or simply wish to be of help, please consider donating annually as this organization desperately needs to grow allowing for more advocacy, more training in the community, and more hands on resources for folks in the autoimmune community... Please don't forget us after the pandemic... Remember that word immunocompromised... Because we live that, and we need support for folks living with Myalgic Encephalomyelitis and other related autoimmune illnesses. We desperately need government support, and research... As these diseases impact thousands of people province wide... And globally, the research is lagging. God bless the ME/FM SOCIETY of BC.

Kristyna Vogel

The ME/FM Society if BC is a non-medical dysfunctional charity made up of those struggling with ME/FM and their support. The organization is known to have lack of leadership at the top - this absence of leadership and professionalism has led to qualified board members leaving rather than be associated with this group. It is my experience that rather than provide the support they initially set out to provide, has fallen to making petty and baseless accusations against actual doctors widely recognized as allies and experts in this field of medicine; besmirching the reputation of said doctors working hard and providing medical support to actual ME/FM patients. Accusations made without ANY first person experience with said doctors.