We want to hear from you if you live in Canada with one or more of:
Myalgic Encephalomyelitis (ME/CFS)
Fibromyalgia (FM)
Lyme Disease
Post COVID/Long-COVID that meets the diagnostic criteria for ME.
Living with these complex, chronic and often debilitating illnesses isn't easy. You deserve safe, effective care. By sharing your needs and experiences, you can help doctors, clinics, governments, media and funding agencies in BC understand what's working - and what needs to change.
Every response brings us closer to better care and outcomes for the people affected by these conditions.
Together, we can push for real change. Your insights are the key.
If you experience challenges with the survey, please email us at techsupport@mefm.bc.ca.
There are 6 multiple choice questions
plus a place to type in your own thoughts.
You can skip any question you like.
It helps even if you only fill in part of the survey.
Please add your voice by December 22.
*This survey has been developed and is being conducted by four collaborating patient support,
education and advocacy groups in BC: The ME|FM Society of BC, the National ME/FM Action
Network, the M.E. Victoria Association, and the BC Lyme Society.
** All data collected is anonymized/aggregated and no individual personal data will be
identifiable. Submitting this survey constitutes consent to use your data.
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