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Innhold levert av Ronda F Jefferson. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Ronda F Jefferson eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.
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The Importance of Diverse Representation in Clinical Trials

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Manage episode 367968820 series 2923408
Innhold levert av Ronda F Jefferson. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Ronda F Jefferson eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.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 episoder

Artwork
iconDel
 
Manage episode 367968820 series 2923408
Innhold levert av Ronda F Jefferson. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Ronda F Jefferson eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.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 episoder

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