All Access DNA
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#67- What are the ethical considerations of genetic testing in…
#67- What are the ethical considerations of genetic testing in…
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What is DNA anyway? Should I consider genetic testing? Can my genes tell my future? All Access DNA answers the questions you have about genetics, healthcare, and popular issues in precision medicine as it relates to our daily lives. We may even veer into territory that is no longer science fiction but science reality. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic medicine and research. Join us as we empower everyone to know more about DNA in an entertaining format.
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De nyeste 20 af 71 episoder
- #67- What are the ethical considerations of genetic testing in children? · 40 min. · Episode 67Bioethicist Curtis discusses the complexities of genetic testing in children, including ethical considerations, parental rights, and privacy issues. He emphasizes the importance…
- How do viruses work and what makes mRNA vaccines so powerful? · 34 min. · Episode 66Virologist Trudy Rey explains the complex world of viruses, their genetic makeup, how they infect cells, and the future of mRNA technology in vaccines and cancer treatment. For…
- MTHFR Gene: What’s real, what’s not and what does it actually mean? · 39 min. · Episode 65In 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 clinical…
- #64- Should we select embryos based on chance? · 36 min. · Episode 64Dr. Betty Cohn discusses the complexities, ethical considerations, and current state of polygenic embryo screening and risk scores, highlighting the scientific, ethical, and…
- #63-How can you cure ALS & FTD in a race against time? · 53 min. · Episode 63In 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. Discover…
- #62- Is the healthcare experience keeping genomic medicine out of reach? · 32 min. · Episode 62In 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? · 40 min. · Episode 61Carissa 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? · 45 min. · Episode 60In 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 · 33 min. · Episode 59Dr. Jeremy Koenig shares how he came to performance genomics through his own athletic background, and the conversation explores how genetic information can inform training…
- #58-Could epilepsy & seizures be genetic? · 39 min. · Episode 58In 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 fundamentals of…
- #57-What is Fragile X syndrome & why is it underdiagnosed? · 37 min. · Episode 57Dr. Emily Allen, a genetics researcher, explains the complexities of Fragile X syndrome, its genetic basis, and the importance of advocacy and ongoing research. Discover how…
- #56-Why is communication important in genetic care? · 38 min. · Episode 56Dr. Marleah Dean Kruzel explores the critical role of communication in healthcare, emphasizing how effective dialogue between clinicians and patients can improve health outcomes…
- #55-Heart health & Connective Tissue: What is Marfan syndrome? · 34 min. · Episode 55Maya Brown-Zimmerman shares her personal journey with Marfan syndrome, the importance of early diagnosis, and navigating life with a connective tissue disorder. She discusses…
- #54-Genetic News Updates with DNA Dispatch · 11 min. · Episode 54We 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? · 32 min. · Episode 53In this insightful interview, genetic counselor Andy McCarty discusses the rise of private practice in genetics, the nuances of direct-to-consumer genetic testing, and how to…
- Tortured Hope: What is it like growing up at risk for Huntington’s Disease? · 41 min. · Episode 52Lori 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 · 40 min. · Episode 51In 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 genetic…
- Therapeutic Abortion Explained: Heartbeat Laws, Genetic Testing, and Hard Decisions · 34 min. · Episode 50In this conversation, Kate talks to Shannon Wieloch about the complexities surrounding therapeutic abortions, particularly in the context of heartbeat laws and genetic…
- Bonus-Rare Disease & Treatment Delays: Hope for Sanfilippo syndrome · 45 min. · Episode 2In 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 discusses…
- Living with Sickle Cell Disease: Turning Pain into Advocacy · 49 min. · Episode 49Chronic pain, invisible illness, Black health. In this conversation, Wunmi Bakare shares her profound journey living with sickle cell disease, detailing the challenges and…
