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The Importance of Diverse Representation in Clinical Trials

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Manage episode 367968820 series 2923408
Content provided by Ronda F Jefferson. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Ronda F Jefferson or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

On this episode, I will be speaking with Erica Courtenay-Mann, an advocate for patients with Sarcoidosis. She gives talks regarding what it's like to live with chronic illnesses & she is involved in the Women of Color Committee and the ACTe Now! Patient Committee. She is a strong voice to raise awareness about the importance of clinical trials, especially in communities that are underrepresented. With each step taken towards more inclusive clinical trials and the data gained from them, we grow closer to a better understanding of how “snowflake" diseases progress.

Links for further information:

https://www.stopsarcoidosis.org/

Mayo Clinic - Information on Clinical Trials and Sarcoidosis Research

Congress Enacts Legislation Requiring Guidance on Clinical Research Diversity and Modernization | Ropes & Gray LLP

Contact Info -

Podcast: See the Invisible: Living with an Invisible or Rare Disease

Contact: Email: Seetheinvisible2020@gmail.com

Twitter: Ronda F Jefferson (@CInvisible2020) / Twitter

Facebook: SeetheInvisible2020 | Facebook

Instagram: Ronda Jefferson (@seetheinvisible2020) • Instagram photos and videos

YouTube: SeeTheInvisible - YouTube

  continue reading

54 episodes

Artwork
iconShare
 
Manage episode 367968820 series 2923408
Content provided by Ronda F Jefferson. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Ronda F Jefferson or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

On this episode, I will be speaking with Erica Courtenay-Mann, an advocate for patients with Sarcoidosis. She gives talks regarding what it's like to live with chronic illnesses & she is involved in the Women of Color Committee and the ACTe Now! Patient Committee. She is a strong voice to raise awareness about the importance of clinical trials, especially in communities that are underrepresented. With each step taken towards more inclusive clinical trials and the data gained from them, we grow closer to a better understanding of how “snowflake" diseases progress.

Links for further information:

https://www.stopsarcoidosis.org/

Mayo Clinic - Information on Clinical Trials and Sarcoidosis Research

Congress Enacts Legislation Requiring Guidance on Clinical Research Diversity and Modernization | Ropes & Gray LLP

Contact Info -

Podcast: See the Invisible: Living with an Invisible or Rare Disease

Contact: Email: Seetheinvisible2020@gmail.com

Twitter: Ronda F Jefferson (@CInvisible2020) / Twitter

Facebook: SeetheInvisible2020 | Facebook

Instagram: Ronda Jefferson (@seetheinvisible2020) • Instagram photos and videos

YouTube: SeeTheInvisible - YouTube

  continue reading

54 episodes

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