Hi everyone,
I’m looking for a scientifically sound and medically credible resource (preferably a printable document or website) that I could show to a doctor in my family who has no prior knowledge of ME/CFS.
He’s a 60-year-old general practitioner, open-minded and willing to read, but like many doctors of his generation, he has never been properly educated about ME/CFS. He claims he has “never seen a case” in practice – which I suspect means he probably did, but like in many countries (especially here in Poland), patients were misdiagnosed or dismissed as having psychosomatic issues due to the lack of biomarkers or clear diagnostic criteria at the time.
I’d like to give him something concise, serious, and free of pseudoscience – something written in the language of medicine: evidence-based(or at least sounding reasonable/common sense), preferably endorsed or authored by established institutions (e.g., CDC, NICE, NIH, etc.), possibly including:
Ideally, this could be something I could translate (e.g., with AI) and print out for him to read, or a web page that is easy to follow for a medically trained reader.
Any suggestions? I'm sure this could be helpful for others trying to bridge the gap with health professionals unfamiliar with ME/CFS.
Thanks in advance!
I’m looking for a scientifically sound and medically credible resource (preferably a printable document or website) that I could show to a doctor in my family who has no prior knowledge of ME/CFS.
He’s a 60-year-old general practitioner, open-minded and willing to read, but like many doctors of his generation, he has never been properly educated about ME/CFS. He claims he has “never seen a case” in practice – which I suspect means he probably did, but like in many countries (especially here in Poland), patients were misdiagnosed or dismissed as having psychosomatic issues due to the lack of biomarkers or clear diagnostic criteria at the time.
I’d like to give him something concise, serious, and free of pseudoscience – something written in the language of medicine: evidence-based(or at least sounding reasonable/common sense), preferably endorsed or authored by established institutions (e.g., CDC, NICE, NIH, etc.), possibly including:
- an overview of the current understanding of ME/CFS (pathophysiology, diagnosis, impact)
- diagnostic criteria (e.g., IOM/NAM 2015, NICE 2021)
- information about post-viral onset, PEM, and why it is not psychological
- management approaches (even if limited), with an emphasis on pacing and the dangers of graded exercise
Ideally, this could be something I could translate (e.g., with AI) and print out for him to read, or a web page that is easy to follow for a medically trained reader.
Any suggestions? I'm sure this could be helpful for others trying to bridge the gap with health professionals unfamiliar with ME/CFS.
Thanks in advance!