Lost Women of Science

Lost Women of Science

I was on a zoom conference, I was bored. it was about using my zoom account, so it wasn’t extremely engaging. I continued to listen while I wandered away from the conference and was looking on the zoom page that recommended podcasts. One caught my eye…actually the word Cystic Fibrosis jumped out at me for obvious reasons. Then I saw the Lost women of science podcast and read the description. It was about science pioneer, Dr. Dorothy Anderson. I didn’t know anything about her, how could I not know anything about her? .Thanks to Dr. Anderson, CF was diagnosed. Next, I read a description about the podcast and listened to every episode about Dr. Anderson, over and over again. Host and Executive producer Katie Hafner does a wonderful job telling the story with her voice, and the voice of others. Hafners co-executive producer, Amy Scharf is with us today to talk about all that they uncovered about Dr. Anderson’s life.

Amy is a bioethicist at Memorial Sloan Kettering Cancer Center in New York City. Amy is also the Chair of Board of Children’s Aid, a non-profit that provides comprehensive social, educational, and health services to children in NYC’s underserved communities and an Advisory Board member of the Johns Hopkins University Berman Institute of Bioethics.

We’re honored to talk with her.

Lost Women of Science Website: https://lostwomenofscience.org/

Lost Women of Science Podcast Season 1: https://lostwomenofscience.org/season-1

For more information on The Bonnell Foundation find us at: https://thebonnellfoundation.org/

Thanks to our sponsors:

Vertex Pharma - the science of possibility. https://www.vrtx.com

Viatris: https://www.viatris.com/en

The original music in this podcast is performed by Kevin Allan, who happens to have Cystic Fibrosis. You can find him on Facebook here: https://www.facebook.com/KevinAllanMusic

This podcast was produced by JAG in Detroit Podcasts: https://jagindetroit.com/

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Thanks to our sponsors:

Vertex: https://www.vrtx.com

Viatris: https://www.viatris.com/en

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Watch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

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Episoder(208)

The Anomaly: living off donated organs and dark humor by Inka Nisinbaum

The Anomaly: living off donated organs and dark humor by Inka Nisinbaum

What would you do if you didn't know what your future held? For people living with cystic fibrosis, uncertainty is often a constant companion. Inka Nisinbaum faced one of the biggest unknowns of her l...

27 Jul 47min

Ireland's Rising Golf Star, David Howard, who happens to have CF

Ireland's Rising Golf Star, David Howard, who happens to have CF

Luck of the Irish.   Irish international amateur golfer David Howard  doesn't seem to need luck with all the talent he has. We had an inspiring conversation about chasing big dreams while living with ...

20 Jul 44min

CF Scholars: Stories of Determination

CF Scholars: Stories of Determination

Dreams and Determination: Meet four Inspiring students, Living with cystic fibrosis. One of the greatest joys of The Bonnell Foundation is helping young adults living with cystic fibrosis pursue their...

13 Jul 53min

Turning family loss into hope: Kate O'Donnell's story

Turning family loss into hope: Kate O'Donnell's story

I thoroughly enjoy doing my podcasts. It’s the one thing I truly miss from my television news reporting days — interviewing extraordinary people every single day. Through The Bonnell Foundation, I now...

6 Jul 44min

Jon Gay on Radio, Podcasting, and the Art of Storytelling

Jon Gay on Radio, Podcasting, and the Art of Storytelling

Jon Gay and I had a great time recording this podcast because we not only talked about podcasting, but also reflected on our years in the broadcast business and what people should know before starting...

29 Jun 48min

Running changed and saved her life - Katie O'Grady inspires

Running changed and saved her life - Katie O'Grady inspires

"Many people have their own thing that lights them on fire, for me, it's running" say Katie O'Grady.  CF modulator drugs changes are a game changer for people living with cystic fibrosis. Katie O’Grad...

22 Jun 38min

Final Breath, First New Life: Jillian’s Transplant Journey

Final Breath, First New Life: Jillian’s Transplant Journey

“Take in your final breath before your first new one.”  Those were the words Jillian heard before her double lung transplant—words that would mark the end of one life chapter and the beginning of anot...

15 Jun 26min

Rare, But Not Invisible: Chrisy and Dr. Kingzett talk advocacy.

Rare, But Not Invisible: Chrisy and Dr. Kingzett talk advocacy.

Chrisy and Dr. Kingzett, two women I met when we were all trying to raise our rare voices a little louder. Christine “Chrisy” Klavitter and Dr. Kristen Kingzett are both rare disease advocates, but mo...

8 Jun 58min

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