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

CSL Chief Operating Officer Paul McKenzie during a podcast interview
Episode 5: CSL’s COO Shares the 3 "C"s of Management

24 September 2019

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.

CSL Behring Chief Communications Officer Anthony Farina with Uplifting Athletes Executive Director Rob Long
Episode 4: Taking on a Cause With No Offseason

20 August 2019

Nonprofit organization Uplifting Athletes wants to connect 30 million football fans with 30 million rare disease patients. Hear Executive Director Rob Long explain why.

Tahirah Austin
Episode 3: Growing Up with Sickle Cell Disease

18 June 2019

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.

Movie poster for "Do Something: The Jeffrey Modell Story"
Episode 2: From Heartache Comes Hope

21 May 2019

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.

World Haemophilia Day
Episode 1: World Hemophilia Day

16 April 2019

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.