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CSL Behring Podcast: World of Promise

CSL Behring presents the World of Promise podcast series, focused on biotechnology and its promise to transform the lives of people and patients around the world living with serious and rare diseases.

Logo for World of Promise podcast from biotechnology leader CSL BehringEach episode features conversations with leading medical experts, patients or other people involved in the field of biotechnology, with a goal of, "providing engaging and useful content to people with rare and serious diseases and their families, health care providers and others interested in learning more about these topics. The format of a podcast allows us to go more in-depth on these topics that are so critically important to our patients,” says Anthony Farina, CSL’s Chief Communications Officer, who is also the show’s host. 

World of Promise is available on Apple Podcasts, Spotify and other podcasting platforms.

Episodes

Date Title Description Link
28 May 2021 Episode 19:  How Technology Is Changing Vaccines Our VP of R&D for Seqirus, CSL's vaccine business, explains how the company is leveraging knowledge about COVID-19 vaccines to improve influenza vaccines. Listen
12 April 2021
Episode 18: Adapting to Change  Two doctors/leaders in the hemophilia space discuss changes in hemophilia treatment and how this past year has changed everything. Listen
30 March 2021
Episode 17: Taking Risks, Overcoming Doubts

In honor of Women's History Month, this episode features two female CSL leaders sharing their career journeys, the obstacles they've overcome and offer advice for other women working in biotechnology. 

Listen
4 March 2021
Episode 16: The Case for Career Development

CSL’s Chief Human Resources Officer Elizabeth Walker explains why the company wants employees to invest in themselves. 

Listen
29 January 2021
Episode 15: Protecting Public Health During the Pandemic Hear what Dave Ross, a leader from our flu vaccine business Seqirus, has to say about the twin threats of influenza and COVID-19.  Listen
7 January 2021 Episode 14: Digital Transformation and Rare Disease Patients For more than 30 years, Mark Hill has worked in digital technology for large, global biotech and pharmaceutical companies. Now, as CSL's Chief Digital Information Officer, Mark chats about his experiences and where he sees digital transformation taking biotechnology in the future.  Listen
7 October 2020
Episode 13: It's International Plasma Awareness Week  Willy Pardinas, General Manager and Vice President of CSL Plasma, world leader in plasma collection, discusses the importance of plasma donation to people around the world living with rare and serious diseases.  Listen
21 July 2020
Episode 12: Suffering in Silence: Rare Disease Awareness & Management in Asia-Pacific A new report by the Economist Intelligence Unit takes a look at the challenges facing patients living with rare diseases across five Asia-Pacific economies. Listen to hear the editor's thoughts on the report.  Listen
15 June 2020
Episode 11: Super Bowl MVP Discusses His Family’s Battle Against Sickle Cell Disease  The Steelers legend Santonio Holmes - and Dad to a son with the disease - talks about his foundation that helps families cope.  Listen
3 June 2020
Episode 10: Why We Do Clinical Trials Hear from Deirdre BeVard, CSL Behring’s Senior Vice President of R&D Strategic Operations, about how clinical trials benefit patients, why they are so critical to the advancement of biotechnology and how they are being impacted by COVID-19.  Listen
14 April 2020
Episode 9: Celebrating 30+ Years of World Hemophilia Day  As the COVID-19 pandemic continues around the world, rare disease patient groups continue to provide support and outreach to their communities, and community is more important than ever for those with bleeding disorders. Listen
1 April 2020
Episode 8: Lessons from COVID-19  Tony Strickland, Head of Enterprise Security at CSL Behring, talks about being on the front lines of company security during these unusual times.  Listen
20 February 2020
Episode 7: Chasing the Cure  Dr. David Fajgenbaum was diagnosed with a rare disease in medical school. Rather than give up hope, he began researching it and remarkably, his research led to remission. He went on to write a book about his journey and how he is now living his life “in overtime.“  Listen
29 January 2020
Episode 6: The “Palpable Passion” of Patient Focus  Chief Medical Officer Charmaine Gittleson explains how CSL works closely with patients to listen their needs and brings together the palpable passion of employees from across the organization to better understand how each employee can take a part in addressing those needs.  Listen
24 September 2019  Episode 5: CSL’s COO Shares the 3 "C"s of Management
Early in his career, CSL's Chief Operating Officer Paul McKenzie discovered the three “C”s, a concept that he says has been critical to his success as a leader. Listen to learn how he creates, channels, and conserves energy.
Listen
20 August 2019
Episode 4: Taking on a Cause With No Offseason  Nonprofit organization Uplifting Athletes wants to connect 30 million football fans with 30 million rare disease patients. Hear Executive Director Rob Long explain why.  Listen
18 June 2019  Episode 3: Growing Up with Sickle Cell Disease  June 19 is World Sickle Cell Day. In honor of this day and the more than four million people around the world living with this genetic blood disorder, podcast host Anthony Farina sat down with a person living with Sickle Cell Disease to talk about the challenges she faces, and has faced, as a person with the condition.  Listen
21 May 2019
Episode 2: From Heartache Comes Hope  When young Jeffrey Modell continually begged his parents to “do something” about his primary immunodeficiency, it broke their hearts. In 1987, one year after Jeffrey’s death, the Modells founded a foundation in their son’s name. Now the Modell's story is the subject of a documentary being released on June 11. Host Anthony Farina asks the Modells about Jeffrey, the film and the foundation's work.  Listen
16 April 2019
Episode 1: World Hemophilia Day  In our first episode, Host Anthony Farina interviews Dr. Andra James of Duke University. Her research and publications pertain mainly to the care of women with blood and bleeding disorders, with a special focus on von Willebrand Disease. With World Hemophilia Day on April 17, Dr. James talks about von Willebrand Disease, and how it relates to the more well-known disease, hemophilia.  Listen