Dr Terri Lewis is a clinical educator with more than 30 years of experience in the development and administration of community rehabilitation and counseling programs.

Terri’s insights into the machinations of the medical system come from both her professional career and her role as a mother.

When Terri’s child experienced pain, it was by and large dismissed by doctors as if children were from a different planet where the species didn’t experience pain.  By ignoring what Terri’s son was reporting, doctors contributed to a worse and more painful - and needless - outcome for him.

In our interview, Terri shares both the formal and personal aspects of her experiences with the health care system --- a medical system that is not focused on the patient as they purport, but focused on cutting patient-doctor appointment time and decreasing other costs while maximizing profits. A system Terri aptly describes as ‘drive-by medicine’.

Connect with Dr Terri Lewis:

Tennessee Pain Care for All

https://www.facebook.com/groups/219464761765372

Fungal Meningitis Survivors

https://www.facebook.com/groups/meningitisoutbreaksurvivors

Twitter

https://twitter.com/tal7291

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.