Скачать или смотреть Jenna Payne trailer: Stupid Stuff Doctors Say: You’re depressed because your unmarried and childless

Pretty much everyone who’s had a chronic or complex illness will have a story to tell about some of the most ignorant and arrogant - and dangerous - utterations made by physicians.
I’ve spoken with a lot of health care workers and patients from a wide variety of health care systems, and regardless of their geographic location, the god complex physician culture is rampant in their institutions and is a significant cause of medical error, harm and death.
When Jenna Payne’s health took a nose dive, she encountered countless doctors that dismissed or denigrated or shamed her physical symptoms. Turns out Jenna wasn’t faking her symptoms, and she didn’t need a husband and baby. What Jenna needed was a competent physician.
In our interview, Jenna takes us on a journey from the United States to Russia, and from health care to health harm.
Connect with Jenna Payne:
www.jennapayne.com
  / jenna_payne  
https://kypsel.com/comics/zompire-vix...
   / dirjennapayne  
www.disastercapitalproductions.com

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Be my Guest
I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer.
If you are a survivor, a victim’s surviving family member, a health care worker, advocate, researcher or policy maker and you would like to share your experiences, please send me an email with a brief description: [email protected]

Need a Counsellor?
Like me, many of my clients at Remedies Counseling have experienced the often devastating effects of medical error.
If you need a counsellor for your experience with medical error, or living with a chronic illness(es), I offer online video counseling appointments.
*For my health and life balance, I limit my number of counseling clients.*
Email me to learn more or book an appointment: [email protected]

Scott Simpson:
Counsellor + Patient Advocate + (former) Triathlete

I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard.
I have been living with HIV since 1998. I was the first person living with HIV to compete at the triathlon world championships.
Thanks to research and access to medications, HIV is not a problem in my life.
I have been living with ME (myalgic encephalomyelitis) since 2012, and thanks in part to medical error, it is a big problem in my life.

Counseling / Research
I first became aware of the ubiquitousness of medical error during a decade of community based research working with the HIV Prevention Lab at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, here and here.
Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions.

Patient Advocacy
I am co-founder of the ME patient advocacy non-profit Millions Missing Canada, and on the Executive Committee of the Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
I am also a patient advisor for Health Quality Ontario’s Patient and Family Advisory Council, and member of Patients for Patient Safety Canada.
Medical Error Interviews podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system.

My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.