Talking to Doctors about ME # (when they get condescending)

Full "Talking to Doctors/Convincing People" video playlist:
• Talking to doctors abo...
When they get condescending, I get a little condescending right back. If they are pushing treatments linked to outdated and debunked research, I make it clear that that is exactly what they are doing.
I make sure to say "outdated and debunked" and then say "but doctors who are up on CURRENT research by institutions like Stanford and Harvard and Columbia university and aware of the new CDC guidelines (or NICE guideline in the UK) will use other treatments.
Other treatments are covered in "Talking to Doctors #2" • Talking to Doctors abo...
AUTHORITY/PROOF for DOCTORS
The CDC website: www.cdc.gov/me...
Stanford's Center: med.stanford.e....
Harvard's center: endmecfs.mgh.h....
Colombia University's Center: www.publicheal...
About the deeply flawed Pace Study (and CBT and GET):
(research) www.qeios.com/...
www.statnews.c....
www.npr.org/se....
www.npr.org/se....
Stanford's Blood Test:
med.stanford.e...
MRI differences: translational-...
About the Gut Microbiome: www.ncbi.nlm.n...
RESOURCES FOR DOCTORS
U.S. ME/CFS Clinician Coalition Resources for Doctors: mecfsclinician...
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Essentials of Diagnosis and Management (Mayo):www.mayoclinic...
Resources for Medical Providers Caring for People with Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome (U.S. ME/CFS Clinician Coalition) mecfsclinician...

[@MicheleLuff]

Thank you Corey for all of your efforts! Keep up being a pioneer for those that can't.

[@corey-me-cfs]

thank you!

[@KidCity1985]

Thank you, please keep doing this. 🥰

[@raggedblossom508]

Re. the PACE trial, I read somewhere (don't remember where) that it was underwritten by a medical insurance company. Does anyone know any more about that?

[@corey-me-cfs]

I have heard rumors, but haven't seen the facts on that.