All Access DNA

MTHFR Gene: What’s real, what’s not and what does it actually mean?

In today's conversation, Kate Wilson welcomes Emalyn Cork to explore the complexities of the MTHFR gene, a topic that has sparked curiosity and confusion alike in both cl

#64- Should we select embryos based on chance?

Dr. Betty Cohn discusses the complexities, ethical considerations, and current state of polygenic embryo screening and risk scores, highlighting the scientific, ethical,

#63-How can you cure ALS & FTD in a race against time?

In this episode, Yentli Soto Albrecht, PhD, shares her personal journey with ALS and FTD, her scientific research, and her efforts to accelerate the search for a cure. Di

#62- Is the healthcare experience keeping genomic medicine out of reach?

In this episode, Megan Johnson discusses the disparities in genomic healthcare, focusing on how healthcare experiences influence participation and trust, especially among

How does Jack's Basket celebrate people with Down syndrome?

Carissa shares her inspiring journey of parenting her son Jack, diagnosed with Down syndrome, and how it led to the creation of Jack's Basket—an organization dedicated to

#60: How do I know if I have a hereditary bleeding disorder?

In this episode, we explore bleeding disorders, their symptoms, diagnosis, and management, with expert Kaylee Dollerschell. Learn how these conditions affect individuals,

Are athletics in my DNA? Genetic testing & performance coaching

Dr. Jeremy Koenig shares how he came to performance genomics through his own athletic background, and the conversation explores how genetic information can inform trainin

#58-Could epilepsy & seizures be genetic?

In this interview, we learn what epilepsy is, its causes, and the role of genetics in diagnosis and treatment. Beth Sheidley, a genetic counselor, explains the fundamenta

#57-What is Fragile X syndrome & why is it underdiagnosed?

Dr. Emily Allen, a genetics researcher, explains the complexities of Fragile X syndrome, its genetic basis, and the importance of advocacy and ongoing research. Discover

#56-Why is communication important in genetic care?

Dr. Marleah Dean Kruzel explores the critical role of communication in healthcare, emphasizing how effective dialogue between clinicians and patients can improve health o

#55-Heart health & Connective Tissue: What is Marfan syndrome?

Maya Brown-Zimmerman shares her personal journey with Marfan syndrome, the importance of early diagnosis, and navigating life with a connective tissue disorder. She discu

#54-Genetic News Updates with DNA Dispatch

We are talking about current events in genetics, including Olympic sex testing, genetic privacy in insurance, and legal challenges faced by genetic testing companies. It

What should I know about buying a DNA test?

In this insightful interview, genetic counselor Andy McCarty discusses the rise of private practice in genetics, the nuances of direct-to-consumer genetic testing, and ho

Tortured Hope: What is it like growing up at risk for Huntington’s Disease?

Lori Jones shares her personal journey with Huntington's disease, exploring its symptoms, family impact, and the importance of community and research. Lori shares with us

What does this genetic diagnosis mean? Living well with uncertainty

In the realm of genetic counseling, understanding and support are crucial for families facing daunting medical news. When I sat down with Anna Chassevent, a seasoned gene

Therapeutic Abortion Explained: Heartbeat Laws, Genetic Testing, and Hard Decisions

In this conversation, Kate talks to Shannon Wieloch about the complexities surrounding therapeutic abortions, particularly in the context of heartbeat laws and genetic co

Bonus-Rare Disease & Treatment Delays: Hope for Sanfilippo syndrome

In this heartfelt interview, Abby Milburn shares her journey as a mother of a child with Down syndrome and Sanfilippo syndrome, a rare neurodegenerative disease. She disc

Living with Sickle Cell Disease: Turning Pain into Advocacy

Chronic pain, invisible illness, Black health. In this conversation, Wunmi Bakare shares her profound journey living with sickle cell disease, detailing the challenges an

Should Genetics Be a Routine Part of Primary Care?

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

Creating Community for Rare Disease Parents

Building support, navigating the emotional journey of having a medically complex child. In this conversation, Madeline Cheney discusses her journey as a parent of a child