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Scott Simpson에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Scott Simpson 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
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Maya Dusenbery: Author of "Doing Harm: The Truth About How Bad Medicine and Lazy Science Leave Women Dismissed, Misdiagnosed, and Sick"

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Manage episode 281516231 series 2540386
Scott Simpson에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Scott Simpson 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.

When author Maya Dusenbery started to experience pain after a viral infection, she was introduced to a medical system that mostly marginalizes women and dismisses diseases that predominantly affect women.

This of course will come as no surprise to any female that has a disease the medical system does not readily recognize. If that disease doesn’t have a biomarker yet, doctors will often attribute women’s physical symptoms as psychological in origin. This is known as medical gaslighting and its origins can be traced back to the cocaine fueled thinking of Sigmund Freud and beyond.

In spite of medicine and research claiming to be self correcting institutions, Maya lays out the problems embedded in research, diagnosis and treatment and identifies 2 cracks - or what Maya calls ‘gaps’ - in the health care system: A knowledge gap and a trust gap, and the feedback loop that sustains them.

In this interview, we unpack Maya’s experience with the health care system and why it prompted her to take a deep dive into exposing the systemic gaps in women’s access to appropriate research data and treatment protocols.

Connect with Maya Dusenbery

https://www.mayadusenbery.com/

https://twitter.com/mayadusenbery

Buy Maya’s book on Amazon

Be a podcast patron

Support Medical Error Interviews on Patreon by becoming a Patron for $2 / month for audio versions.

Premium Patrons get access to video versions of podcasts for $5 / month.

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.

  continue reading

94 에피소드

Artwork
icon공유
 
Manage episode 281516231 series 2540386
Scott Simpson에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 Scott Simpson 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.

When author Maya Dusenbery started to experience pain after a viral infection, she was introduced to a medical system that mostly marginalizes women and dismisses diseases that predominantly affect women.

This of course will come as no surprise to any female that has a disease the medical system does not readily recognize. If that disease doesn’t have a biomarker yet, doctors will often attribute women’s physical symptoms as psychological in origin. This is known as medical gaslighting and its origins can be traced back to the cocaine fueled thinking of Sigmund Freud and beyond.

In spite of medicine and research claiming to be self correcting institutions, Maya lays out the problems embedded in research, diagnosis and treatment and identifies 2 cracks - or what Maya calls ‘gaps’ - in the health care system: A knowledge gap and a trust gap, and the feedback loop that sustains them.

In this interview, we unpack Maya’s experience with the health care system and why it prompted her to take a deep dive into exposing the systemic gaps in women’s access to appropriate research data and treatment protocols.

Connect with Maya Dusenbery

https://www.mayadusenbery.com/

https://twitter.com/mayadusenbery

Buy Maya’s book on Amazon

Be a podcast patron

Support Medical Error Interviews on Patreon by becoming a Patron for $2 / month for audio versions.

Premium Patrons get access to video versions of podcasts for $5 / month.

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.

  continue reading

94 에피소드

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