Lynch Syndrome Series
In recognition of Lynch Syndrome Awareness Day on March 22 each year, The Positive Gene Podcast is featuring a five-part series exploring what it means to live with Lynch syndrome; from diagnosis and treatment to advocacy, prevention, and long-term survivorship.
Note: This episode includes brief discussion of depression and suicidal thoughts. Please listen with care. Support resources are included below.
Episode Overview
In this episode, Sara Kavanaugh speaks with JJ Singleton, a young adult colorectal cancer survivor and advocate living with Lynch syndrome.
Diagnosed at just 27, JJ shares the experience of noticing symptoms but not initially acting on them, the reality of navigating cancer treatment in a rural setting, and what it meant to later learn his diagnosis was connected to a hereditary cancer condition.
This conversation goes beyond diagnosis. JJ speaks openly about the mental health challenges that came with long-term treatment, including periods of deep depression, and how therapy, connection, and advocacy helped him find a path forward.
Today, JJ uses his experience to support others through advocacy, peer connection, and patient advisory work, helping ensure that the realities of young adult cancer are better understood.
This episode offers both perspective and practical insight for patients, families, and those supporting individuals navigating hereditary cancer risk.
Key Takeaways
Resources Mentioned in this episode:
Mental Health Support
Lynch Syndrome & Hereditary Cancer
Young Adult & Peer Support
Why This Episode Matters
JJ’s experience highlights that hereditary cancer is not limited by age, geography, or expectation.
His voice brings attention to:
Listen & Share
If this episode resonates, consider sharing it with someone who may benefit—from patients and families to healthcare providers and advocates.
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