Sickle Cell Podcast Series-COVID & Sickle Cell Care
Social Entrepreneurship Now Podcast
Release Date: 04/08/2021
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
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
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)
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
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
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
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
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
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
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.
info_outlineIn this episode, Alix and John continue with our conversation around sickle cell patient care and specifically regarding COVID and vaccination. Questions asked are: What do folks want to know about COVID? What is COVID-19? What are the benefits and risks of the vaccine?
What we discussed further:
- Seeking and finding trusted sources of information
- The toll of social isolation for people with SCD
- The development of the COVID-19 vaccine and hesitation to get the vaccine
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]