#25- Patient Perspectives & Preferences with Risk and Uncertainty

In this episode we are talking about uncertainty and risk along with patient preferences for communication.

Segment 1: The attitudes of individuals with or at risk of adult-onset genetic conditions on reproductive genetic testing: A systematic review

Shanice Allen is a PhD student from the Sheffield Institute for Translational Neuroscience (SITraN) at the University of Sheffield. The aim of her research is exploring the attitudes and experiences of individuals with or at-risk of genetic MND on reproductive genetic testing, and explore how and if clinicians discuss these options with these individuals. This will help us identify any barriers to accessing reproductive services.

LinkedIn: https://www.linkedin.com/in/shanice-allen-9a89661a5/

 

In this segment we discuss:

- The attitudes toward reproductive genetic testing in adult-onset genetic conditions.

- Experiential knowledge and perceived disease severity in shaping reproductive decision-making.

- Ethical themes including guilt, eugenics, and concerns about pregnancy termination.

- Findings supporting more tailored, longitudinal genetic counseling approaches.

 

Segment 2: Assessing patient communication preferences for reclassified variants of uncertain significance in a general genetics clinic

Eden Brush, MS, CGC is a pediatric and inpatient genetic counselor in the Division of Clinical Genetics at Columbia University Irving Medical Center. She completed her graduate training at Columbia University as part of the class of 2024. She is passionate about rare disease advocacy, narrative medicine, and disability justice.

 

In this segment we discuss:

- Patient communication preferences for reclassified variants of uncertain significance (VUS) and patient-driven practice insights

- Factors that emphasize the utility of shared responsibility, the need for standardized recontact systems, and the importance of equity-focused implementation strategies.

- How VUS reclassification type impacted patient-preferred disclosure methods. 

 

Would you like to nominate a JoGC article to be featured in the show? If so, please fill out this nomination submission form here. Multiple entries are encouraged including articles where you, your colleagues, or your friends are authors.

 

Stay tuned for the next new episode of DNA Dialogues! In the meantime, listen to all our episodes Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Dialogues”. 

 

For more information about this episode visit dnadialogues.podbean.com, where you can also stream all episodes of the show. Check out the Journal of Genetic Counseling here for articles featured in this episode and others. 

 

Any questions, episode ideas, guest pitches, or comments can be sent into [email protected]. 

 

DNA Dialogues’ team includes Jehannine Austin, Naomi Wagner, Khalida Liaquat, Kate Wilson and DNA Today’s Kira Dineen. Our logo was designed by Ashlyn Enokian. Our current intern is Stephanie Schofield.