Kate talks to Shannon Wieloch about the complexities surrounding therapeutic abortions, particularly in the context of heartbeat laws and genetic counseling.

Abby Milburn shares her journey as a mother of a child with Down syndrome and Sanfilippo syndrome, a rare neurodegenerative disease. She discusses diagnosis challenges, advocacy efforts, and the importance of research and policy changes to support children with rare diseases.

Chronic pain, invisible illness, Black health. In this conversation, Wunmi Bakare shares her profound journey living with sickle cell disease, detailing the challenges and triumphs she faced from childhood through adulthood.

Primary Care and Genetics: Bringing DNA Into Everyday Healthcare. Primary care is often the first stop in healthcare—but where does genetics fit in?

Building support, navigating the emotional journey of having a medically complex child.

Aging, genetics, and lifestyle. Latest on longevity science.

Heart disease and lack of genetic testing.

Weight management, epigenetics, and childhood obesity.

Diet, genetics and lifestyle.

Grief, genetics, and accessible testing.

“The more innovation happens, it doesn’t mean a thing if patients can’t have access to it.”

Prostate cancer, male infertility, and underserved populations.

Flexibility, pain, and fatigue are part of hypermobility EDS.

Pediatric cancer and genetic testing

Navigating heart failure and mitochondrial disease.

Neurodiversity advocacy and a genetic condition associated with autism.

How does genetics influence individual responses to medications and what is pharmacogenomics?

It Happened to Me: A Rare Disease and Medical Challenges Podcast

Hereditary Cancer and making the film “Love, Danielle”

Considerations for genetic testing in IVF