News & Events

Check out presentations from Johns Hopkins CF Center patient and family educational events.

Patient & Family Day / Educational Events

 

Living as an Adult with CF: A Commentary on Identity, Mental Health and the Future

Patient and Family Education Day
April 20, 2024
Tré LaRosa discusses living with cystic fibrosis

 

Update in Clinical Trials in CF – Focus on the New Era of Genetic Based Therapies

Patient and Family Education Day
April 20, 2024
Dr. Christopher Goss discusses the latest research in the development of therapeutics for cystic fibrosis

 

Partnership Enhancement Program: Sharing What Matters with the Care Team

Patient and Family Education Day
April 20, 2024
Karen von Berg discusses how to optimize patient and family experiences in Cystic Fibrosis Clinic

 

An Adult Perspective on Cystic Fibrosis

Patient and Family Education Day
November 12, 2022
Jeff Breslin provides his insights on living with cystic fibrosis

 

Below the Diaphragm: A 2022 Research Update on CF Reproductive Health

Patient and Family Education Day
November 12, 2022
Dr. Traci M. Kazmerski discusses male and female reproductive health for people with cystic fibrosis.

 

Beating the Odds: Cultivating Resilience in Your Life

Patient and Family Education Day
November 20, 2021
Chris MacLeod discusses living with cystic fibrosis and the value of resilience. He is the author of Beating the Odds.

 

CF Therapeutics: Great Strides & Future Directions

Patient and Family Education Day
November 20, 2021

Dr. Jennifer Taylor-Cousar discusses current and future cystic fibrosis therapeutics

 

CF Warrior Project

Patient and Family Education Day
November 7, 2020

Andy Lipman discusses living with cystic fibrosis and the creation the CF Warrior Project

 

CF Research: Now that We Have Modulators, What’s Next?

Patient and Family Education Day
November 7, 2020.
Dr. Patrick Flume presents the latest in cystic fibrosis research.

 

An Adult Perspective of Cystic Fibrosis

Family Education Day – November 23, 2019
Chad Riedy provides his perspective on living with cystic fibrosis and his advocacy for people with cystic fibrosis.

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