All Access DNA Episodes
Want to know more about your DNA? Curious about how your genes impact your health? All Access DNA honestly answers the questions you have about genetics, healthcare, and popular issues in genomic medicine. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic health and research. Join us as we bring you understandable, scientific information about genetics.
New episodes every Tuesday!
Genetic News Updates with the DNA Dispatch
We review current news in the genetic healthcare world and its impacts on you in the The DNA Dispatch presented by All Access DNA. In this episode we cover the Olympics, life insurance and AI use of genetic data.
I bought a DNA test, now what?
Many people turn to direct-to-consumer genetic tests out of curiosity or necessity. But what happens when the results are confusing or alarming?
Tortured Hope: What is it like growing up at risk for Huntington’s Disease?
Kate talks to Lori Jones, an author, about her book “Spared: A Memoir of Risk and Resolve” and navigating uncertainty with Huntington’s disease.
What does this genetic diagnosis mean? Living well with uncertainty
Kate talks to Anna Chassevent about what living well can mean and how to make meaning in uncertainty.
Therapeutic Abortion Explained: Heartbeat Laws, Genetic Testing, and Hard Decisions
Kate talks to Shannon Wieloch about the complexities surrounding therapeutic abortions, particularly in the context of heartbeat laws and genetic counseling.
Rare Disease & Treatment Delays: Hope for Sanfilippo syndrome
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.
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 and triumphs she faced from childhood through adulthood.
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?
Creating Community for Rare Disease Parents
Building support, navigating the emotional journey of having a medically complex child.
What’s my biological age again? Latest on longevity
Aging, genetics, and lifestyle. Latest on longevity science.
How does grief inspire genetic action and awareness?
Grief, genetics, and accessible testing.
How do podcasts give patients the genomic lowdown?
“The more innovation happens, it doesn’t mean a thing if patients can’t have access to it.”
How can men benefit from genetic counseling?
Prostate cancer, male infertility, and underserved populations.
A patient & a physician: How is hEDS diagnosed?
Flexibility, pain, and fatigue are part of hypermobility EDS.
Can patients with mitochondrial disease afford to wait for the FDA?
Navigating heart failure and mitochondrial disease.
How did a mom turn an autism diagnosis into advocacy?
Neurodiversity advocacy and a genetic condition associated with autism.