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2023 Patient Community discussion series

Up to 1 MILLION Americans are living with Lynch syndrome.

Unfortunately, 95% of them don’t know it.

Lynch syndrome is not rare, it is undiagnosed.
We want THAT to change.

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Each session features a Living with Lynch patient video content followed by live discussions around each topic. Held May through August 2023, we engaged an expert moderator to facilitate conversation with patients, medical professionals and other experts, patient advocates, and online attendees.

Navagating Cultural Barriers to Lynch Syndrome Diagnosis and Care
58:16

Navagating Cultural Barriers to Lynch Syndrome Diagnosis and Care

After a Lynch Syndrome Diagnosis
01:00:02

After a Lynch Syndrome Diagnosis

Lynch Syndrome as a Family Diagnosis
57:49

Lynch Syndrome as a Family Diagnosis

Genetic Testing for Lynch
01:16:34

Genetic Testing for Lynch

Coping with a Lynch Syndrome Diagnosis
56:59

Coping with a Lynch Syndrome Diagnosis

Being a Previvor
57:45

Being a Previvor

Managing Annual Cancer Screenings
56:24

Managing Annual Cancer Screenings

Speaking with Children about Lynch Syndrome & Listening to Your Family
57:52

Speaking with Children about Lynch Syndrome & Listening to Your Family

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