Send us a text

In this episode of the Ask Dr. Mia podcast, Dr. Mia invites her husband, Dr. Alex Fertman, to discuss the nuances of palliative care and hospice, particularly in the context of dementia. They explore the differences between these two forms of care, the challenges families face when dealing with dementia, and the difficult decisions surrounding feeding tubes and end-of-life care. The conversation emphasizes the importance of understanding what constitutes a 'good death' and the dynamics within families as they navigate these tough discussions. Dr. Alex shares valuable insights on how families can prepare for serious illness and the significance of having open conversations about healthcare decisions.

As an Assistant Professor in Palliative Medicine, Dr. Alex Fertman provides care to patients during serious illness. He works with patients and their families to provide care for the whole person, with particular focus on alleviating symptom burden and coordination of complex care. Dr. Fertman address all aspects of a person’s health, and collaborates with an interdisciplinary team consisting of counselors, chaplains, social workers, and pharmacists to provide excellent and comprehensive care. He enjoys active clinical teaching on inpatient rounds with students, residents, and fellows about palliative care and the art of being a great palliative care consultant.

Chapters

00:00 Introduction to Palliative Care and Hospice
03:46 Understanding Dementia and Its Challenges
07:08 Navigating Feeding Decisions in Dementia
09:58 The Concept of a Good Death
12:47 Family Dynamics in End-of-Life Care
16:05 Advice for Families Facing Serious Illness

Support the show

Video on Ask Dr. Mia YouTube channel
Transcripts on www.miayangmd.com. Transcripts are automatically generated and may contain minor inaccuracies.
Email: ask@miayangmd.com
Opinions expressed are exclusive of Dr. Mia Yang and not reflective of her or guest speaker's employers or funders.

Send us a text

In this episode of Ask Dr. Mia, Rohan Ramakrishna, co-founder of Roon, discusses the innovative healthcare technology platform designed to provide patients with reliable medical information.

Roon aims to bridge the gap between patients and healthcare experts, offering personalized guidance and 24/7 support. Rohan shares insights into the journey of building Roon, the importance of expert vetting, and the platform's commitment to keeping the service free for users. The conversation also touches on the global reach of Roon and its future aspirations to expand access to healthcare information worldwide.

Rohan Ramakrishna is a professor of neurosurgery at Weill Cornell Medicine and New York Presbyterian hospitals and the Co-Founder of Roon. He attended medical school at the University of Pennsylvania. He then completed training in neurosurgery at the University of Washington and MD Anderson Cancer Center.

Like & Subscribe. Follow Dr. Mia on social media @askdrmia

Chapters

00:00
Introduction to Roon and Its Purpose

02:57
The Journey of Building Roon

06:03
The Unique Features of Roon

09:14
Expert Vetting and Content Quality

11:51
User Engagement and Feedback

14:57
Global Reach and Future Aspirations

#Roon, #healthcare technology, #patient information, #expert guidance, #caregiver support, #medical information, #health app, #user experience, #global access, #mental health

Support the show

Video on Ask Dr. Mia YouTube channel
Transcripts on www.miayangmd.com. Transcripts are automatically generated and may contain minor inaccuracies.
Email: ask@miayangmd.com
Opinions expressed are exclusive of Dr. Mia Yang and not reflective of her or guest speaker's employers or funders.

Send us a text

In this episode of the Ask Dr. Mia podcast, Dr. Mia interviews Amanda Gengler, a sociology professor and author, about her personal experiences as a caregiver for her mother with Alzheimer's and her young son. They discuss the complexities of navigating the healthcare system, the emotional labor involved in caregiving, and the challenges of family dynamics. Amanda shares insights on advocacy, the impact of her mother's recent fall, and the strategies she employs to manage stress and communication within her family. In this conversation, Amanda Gengler shares her experiences navigating the complexities of caring for a parent with dementia while also raising her child. The discussion delves into the emotional challenges of family dynamics, the importance of communication with children about illness, and the unique burdens faced by the sandwich generation. Amanda reflects on the surprises and difficulties encountered in her caregiving journey, emphasizing the need for open conversations about death and dying.

Disclaimer: There were audio issues with this episode and some of the interview was edited out. For the full unedited video check out the Ask Dr. Mia Channel on YouTube. Link below;

https://youtu.be/iBrJKKqWoJw?si=67JXHVSFq-v1YNjY

About Amanda Gengler, Ph.D

An associate professor of sociology at Wake Forest University who completed her PhD in Sociology at Brandeis University and a Masters degree in Social Work at the University of Wisconsin-Madison. She is the author of the book, "Save My Kid" How Families of Critically-Ill Children Cope, Hope, and Negotiate an Unequal Healthcare System, and her current research examines the emotional dynamics of routine pediatric care. She regularly teaches undergraduate courses on the Sociology of Health and Illness, the Sociology of Birth and Death, and the Sociology of Care Work.

Support the show

Video on Ask Dr. Mia YouTube channel
Transcripts on www.miayangmd.com. Transcripts are automatically generated and may contain minor inaccuracies.
Email: ask@miayangmd.com
Opinions expressed are exclusive of Dr. Mia Yang and not reflective of her or guest speaker's employers or funders.