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Sickle Cell Podcast Series-Intersection of Race & Health

Social Entrepreneurship Now Podcast

Release Date: 03/11/2021

Season 2 Sickle Cell Podcast: Kendra Hogenson show art Season 2 Sickle Cell Podcast: Kendra Hogenson

Social Entrepreneurship Now Podcast

Welcome to Season 2 of our Sickle Cell Podcast, the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.   This podcast is a collaborative work between the Metropolitan Seattle Sickle Cell Task Force and the Social Entrepreneurship Now podcast where our guests speak up and out about creating equity, diversity and inclusion from where they are.  Season 2 of the Sickle Cell podcast journey is co-hosted...

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Season 2 Sickle Cell Podcast: Ken West show art Season 2 Sickle Cell Podcast: Ken West

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Season 2 Sickle Cell Podcast: Dr. Michael DeBaun show art Season 2 Sickle Cell Podcast: Dr. Michael DeBaun

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Season 2 Sickle Cell Podcast: Andre Harris, PhD(c) show art Season 2 Sickle Cell Podcast: Andre Harris, PhD(c)

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Season 2 Sickle Cell Podcast: Dr. Stephanie Ibemere show art Season 2 Sickle Cell Podcast: Dr. Stephanie Ibemere

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Sickle Cell Podcast Season 2: Dr. Cliff Takemoto show art Sickle Cell Podcast Season 2: Dr. Cliff Takemoto

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Sickle Cell Podcast Season 2: Ice Dean show art Sickle Cell Podcast Season 2: Ice Dean

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Sickle Cell Podcast Season 2: Mariam Lawal's Story show art Sickle Cell Podcast Season 2: Mariam Lawal's Story

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell.

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Sickle Cell Podcast Season 2: Meet our Co-Host Karim Assalaam show art Sickle Cell Podcast Season 2: Meet our Co-Host Karim Assalaam

Social Entrepreneurship Now Podcast

The Social Entrepreneurship Now Podcast is the only podcast dedicated to understanding and appreciating the voices of patients, caregivers, healthcare workers and community-based organizations perceptions of racial bias in the healthcare system for people living with sickle cell. 

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Meet Skillbank Founder Mehak Vohra show art Meet Skillbank Founder Mehak Vohra

Social Entrepreneurship Now Podcast

Meet Mehak Vohra, female Founder and Entrepreneur of Skillbank a dynamic entry level marketing organization whose mission is to empower people and unlock potential through education.  In our podcast together, Mehak speaks to her experience around why she dropped out of college and why she started SkillBank.

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More Episodes

Thanks for listening in to the Social Entrepreneurship Now podcast where our guests speak up and out about creating equity, diversity and inclusion in the systems they are in.  This is a special series with the Metropolitan Seattle Sickle Cell Task Force and our sponsors the Rotary Clubs of Ballard, Magnolia Mercer Island and Seattle. 

In this special series we will bring together sickle cell patients and healthcare providers and use SC as a lens to explore racial bias in the U.S. healthcare system.  Please subscribe to the podcast @ www.diversityandinclusioncoach.com to keep listening as our guests share their perspective, pain points and journey. 

Special Guests are: John Masembe and Alix Dassler

Show Highlights:

  • John explains how life rotates between home and school and how life can seem somewhat directionless when you have sickle cell. 
  • John now looks at journey as not a weakness, but as a survivor.  John explores how surviving is about resilience through duress.  He also discusses how sickle cell is a disability.  
  • Alix is a Nurse Practitioner who works with patients with sickle cell at the Odessa Brown Children's Clinic in Seattle, WA.  She identifies as white and female and wanted the audience to understand why it matters to say this up front.  
  • Alix further explores privilege, racial equity and duality of being white and her patients being black and brown. 

For more information about sickle cell and to connect with our show guests, please go to the Metropolitan Sickle Cell Task Force @  www.mssctf.org 

For more information about Nikki, please email: [email protected]