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All Access DNA
All Access DNACreating Community for Rare Disease ParentsBuilding 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 with a rare genetic condition and the creation of her podcast, The Rare Life. She emphasizes the importance of building a community for parents facing similar challenges, the emotional impact of being a carrier of a genetic condition, and the role of advocacy in medical care. Madeline shares her experiences with grief, resilience, and the need for self-care, while also outlining the future goals of her nonprofit organization to support families in the N...
2026-01-2756 minAll Access DNA
All Access DNAWhat's my biological age again? Latest on longevityAging, genetics, and lifestyle. In this conversation, Daniel Tausan discusses the concept of longevity, focusing on biological age, biomarkers, and the interplay between genetics and lifestyle. He emphasizes the importance of understanding biological age as a measure of health rather than just chronological age. The discussion covers various biomarkers, the significance of blood tests, and how lifestyle choices impact aging. Daniel also touches on the role of telomeres, lifestyle habits for longevity, and the latest breakthroughs in longevity science. Philosophical perspectives on aging and the future of longevity research are explored, highlighting the importance of quality of life and...
2026-01-1349 minAll Access DNA
All Access DNAReplay- A patient and a physician: How is hEDS diagnosed?Flexibility, pain, and fatigue are part of hypermobility EDS. In this conversation, Dr. Taylor Kerrins discusses Ehlers-Danlos Syndrome (EDS), particularly hypermobile EDS, covering its definition, symptoms, diagnosis, and management strategies. He shares personal experiences with the condition, the challenges of obtaining a diagnosis, and the importance of physical therapy and exercise. The discussion also touches on genetic testing and available support resources for patients. Taylor emphasizes the need for ongoing research and understanding of EDS, highlighting the complexities of the condition and the importance of community support.   Key Takeaways: EDS is a connective tissue d...
2025-12-2341 minAll Access DNA
All Access DNAHow do I know if something is safe during pregnancy?Teratogens. Medications. Infections. Safe in Pregnancy. In this conversation, we explore the safety of exposure to certain things during pregnancy such as alcohol, beauty products, and yes even Tylenol. We learn more about how an agent or exposure is evaluated as being teratogenic as well as resources for pregnant individuals with questions.   Key Takeaways: Teratogens refers to an exposure (drug, chemical, infection, radiation, or substance) that can interfere with growth or development of an embryo or fetus.  Every pregnancy has a background risk of 3% for birth defects, unrelated to exposures or family history. The ti...
2025-12-1640 minAll Access DNA
All Access DNACancer and privacy: What are the risks for transgender individuals?Transgender and gender diverse cancer care, privacy, community safety. On this episode of All Access DNA, we talk to Dr. Mittendorf about hereditary cancer considerations for people who are transgender and gender diverse. We discuss management guidelines, cancer risks and how knowing hereditary cancer risk may inform medical decisions. The conversation also delves into the significant concerns surrounding the privacy of medical data for transgender individuals. It highlights the fear of being identified as trans in medical records and the potential repercussions of such identification, especially in light of recent legal actions involving healthcare providers.    On...
2025-12-0949 minAll Access DNA
All Access DNAWhat does it really mean to grow up with Spina Bifida?Patient zero, memoir, understanding. In this conversation, Steven Crane shares his personal journey living with spina bifida, discussing the challenges he faced from birth through adulthood. He reflects on the support from his family, the medical treatments he underwent, and the impact of his condition on his life. Steven emphasizes the importance of advocacy, understanding, and resilience, and how he found purpose through writing about his experiences. He also addresses the complexities of navigating multiple health conditions and the role of healthcare providers in supporting patients.   Key Takeaways: Spina bifida is a multifactorial condition w...
2025-11-2537 minAll Access DNA
All Access DNAHow does someone tell the story of genetic risk?Narrative medicine, story telling, BRCA and breast cancer. In this conversation, Sarah shares their personal journey with being a BRCA1 carrier and experiences with breast cancer. She discusses the emotional weight of genetic risk, the complexities of identity as a previvor, and the importance of narrative in understanding and coping with illness. Sarah also reflects on their professional background in medical anthropology and genetic counseling, emphasizing the need for patient-centered care and the power of storytelling in healthcare. The discussion touches on themes of grief, hope, and the ongoing nature of living with a genetic condition, culminating in Sarah's...
2025-11-1840 minAll Access DNA
All Access DNACan a DNA test help your heart health?Heart disease and lack of genetic testing. In this conversation, Ana Morales discusses the critical signs of genetic heart disease, particularly focusing on early onset conditions and the importance of recognizing red flags such as elevated cholesterol and complications during/after pregnancy. She emphasizes that these health issues should not be ignored and highlights the need for awareness and proactive health management.   Key Takeaways: Having early onset heart disease of any kind is not normal. Early onset is defined as less than age 60. Severely elevated cholesterol, especially if it runs in families, is concerning. O...
2025-11-1146 minAll Access DNA
All Access DNAIs childhood obesity genetic?Weight management, epigenetics, and childhood obesity. In this conversation, Dr. Evan P Nadler discusses the complexities of childhood obesity, emphasizing that it is a disease influenced by genetics, maternal health, and lifestyle factors. He highlights the importance of understanding the role of epigenetics and the in utero environment in the development of obesity. The discussion also covers the myths surrounding childhood obesity, the impact of genetics versus lifestyle choices, and the potential benefits of genetic testing. Dr. Nadler advocates for a comprehensive approach to treatment, including lifestyle changes and medical interventions, while encouraging parents to seek help and to...
2025-11-0447 minAll Access DNA
All Access DNACan my DNA tell me what diet is best for me?Diet, genetics, and lifestyle. In this episode we talk to Natalie Samson, a genetic counselor with certification in Integrative and Functional Nutrition who is also a certified Integrative Health Coach. We talk about the role of genetics and molecular/biochemical pathways that affect diet and weight. Natalie tells us about the role of genetic testing in nutrition management and functional health as well as the importance of working with a trained professional when considering this type of testing. We also discuss nutrigenetic testing for children and the integration of nutrigenomics into mainstream medicine.   Key Takeaways:
2025-10-2842 minAll Access DNA
All Access DNAHow does grief inspire genetic action & awareness?Grief, genetics, and accessible testing. In this episode, Matt Goldstein shares his personal journey through grief after the loss of his daughter, Javi, who was diagnosed with Tay-Sachs disease. He discusses the impact of this experience on his career, leading him to focus on preventive genetics and the mission of JScreen, an organization dedicated to providing genetic testing and support. We explore the importance of preconception carrier screening, the advancements in genetic technology, and the emotional aspects of navigating grief and loss. Matt emphasizes the power of genetics in preventing diseases and the support systems available for families.
2025-10-2130 minAll Access DNA
All Access DNAHow 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.” Today’s episode of All Access DNA features Rome Madison. Rome’s podcast- Genetics for Healthcare- aims to educate patients about genetic information and its relevance to their healthcare. Rome shares his personal journey from a sales background to podcasting, emphasizing the need for patient advocacy and access to genetic information. We explore the balance between commercial goals and ethical responsibilities in healthcare, the challenges of navigating insurance coverage for genetic tests, and the role of technology in improving patient access to precision...
2025-10-1428 minAll Access DNA
All Access DNAHow can men benefit from genetic counseling?Prostate cancer, male infertility, and underserved populations. Brittany Szymaniak discusses the complexities of hereditary cancer risks, particularly focusing on prostate cancer and the role of BRCA genes. She emphasizes the importance of genetic counseling and testing, especially for men, and addresses the challenges in male reproductive health and infertility. The discussion also covers insurance aspects related to genetic testing and the significance of family communication regarding genetic results. Brittany highlights the need for increased awareness and research in men's health genetics, particularly for underrepresented populations. Key Takeaways: BRCA1 and BRCA2 mutations can affect both men and...
2025-10-0734 minAll Access DNA
All Access DNAPatient to Physician: How is hEDS diagnosed?Flexibility, pain, and fatigue are part of hypermobility EDS. In this conversation, Dr. Taylor Kerrins discusses Ehlers-Danlos Syndrome (EDS), particularly hypermobile EDS, covering its definition, symptoms, diagnosis, and management strategies. He shares personal experiences with the condition, the challenges of obtaining a diagnosis, and the importance of physical therapy and exercise. The discussion also touches on genetic testing and available support resources for patients. Taylor emphasizes the need for ongoing research and understanding of EDS, highlighting the complexities of the condition and the importance of community support.   Key Takeaways: EDS is a connective tissue d...
2025-09-2340 minAll Access DNA
All Access DNAIs childhood cancer genetic?Pediatric cancer and genetic testing. In this conversation, Sarah Scollon discusses the complexities of childhood cancer, particularly the genetic factors that may contribute to its development. She explains the differences between tumor and germline testing, the importance of identifying children at risk for hereditary cancer syndromes, and the evolving guidelines for genetic testing in pediatric oncology. The discussion also touches on the psychosocial aspects of genetic counseling, informed consent, and the implications of genetic testing for families. Sarah emphasizes the need for ongoing research and the importance of communication with families about genetic risks and testing options.  
2025-09-1631 minAll Access DNA
All Access DNACan patients with mitochondrial conditions afford to wait for the FDA?Navigating child heart failure and mitochondrial disease. Dr. Heather Gatcombe shares her personal journey as a physician and mother navigating the complexities of mitochondrial disease and heart failure in her son. She discusses the challenges of diagnosis, the emotional toll of medical crises, and the journey through heart transplant. Dr. Gatcombe emphasizes the importance of understanding mitochondrial disease, the role of advocacy, and the potential future of mitochondrial medicine, including the impact of new treatments and the need for continued support and awareness.   Key Takeaways: Mitochondrial disease can be difficult to diagnose due to it...
2025-09-0942 minAll Access DNA
All Access DNAHow did a mom turn an autism diagnosis into advocacy?Neurodiversity advocacy and a genetic condition associated with autism. In this conversation, Jacalyn Lee shares her journey into advocacy, driven by her experiences as a mother of a child diagnosed with DEAF1 Associated Neurodevelopmental Disorder (DAND). She discusses the emotional complexities of receiving a diagnosis, the importance of community support, and the establishment of the DAND Alliance to raise awareness and promote research. Jacalyn emphasizes the critical role of genetic testing in understanding neurodevelopmental disorders and offers resources for families navigating similar challenges. The conversation concludes with key takeaways on advocacy, awareness, and the importance of checking in on...
2025-09-0237 minAll Access DNA
All Access DNAHow can DNA help me make better medication choices?How does genetics influence individual responses to medications and what is pharmacogenomics? Jeri explains the significance of pharmacogenomic testing in personalizing medication management, highlighting its potential to improve patient outcomes and reduce adverse effects. Through real patient stories, the discussion emphasizes the importance of genetic information in prescribing practices and the challenges faced in integrating pharmacogenomics into routine healthcare. We talk about how pharmacogenomics can help in prescribing medications for pain, depression, and acid reflux as well as other conditions.   Key Takeaways: Pharmacogenomics is the study of how genetics affect medication response. Genetic testing c...
2025-08-2632 minAll Access DNA
All Access DNAWhat is Wolfram syndrome? with It Happened to MeIt is a podcast crossover with It Happened to Me: A Rare Disease & Medical Challenges Podcast! It Happened to Me is also part of the Gene Pool Media Network In this podcast, patient advocates Cathy Gildenhorn and Beth Glassman share their medical challenges living with rare diseases and are joined by fellow advocates and experts on the show.   For this episode, Beth Glassman interviews her co-host Cathy Gildenhorn about her rare disease, Wolfram Syndrome.  Co-host Cathy Zacks Gildenhorn has devoted much of her life to improving the lives of others and con...
2025-08-1916 minAll Access DNA
All Access DNAWhy make a movie about BRCA? with Love, Danielle filmExploring Hereditary Cancer and the Making of "Love, Danielle". In this conversation, Devon Sidell and Amy Byer Shaneman discuss their new film, 'Love, Danielle' which explores the emotional and physical challenges faced by individuals with BRCA gene mutations. They share their personal stories, the impact of preventative surgeries, and the importance of genetic testing. The film aims to raise awareness and provide support for those navigating hereditary cancer risks, while also addressing family dynamics and the emotional weight of such decisions. The discussion highlights the need for better resources and education surrounding genetic testing and cancer prevention.  
2025-08-1235 minAll Access DNA
All Access DNAWhat is IVF with pre-implantation genetic testing (PGT)?Considerations in genetic testing and IVF. In this conversation, Natalie Richeimer discusses the intricacies of pre-implantation genetic testing (PGT) as part of in vitro fertilization (IVF). She explains the different types of PGT, its accuracy, limitations, and the ethical considerations surrounding genetic testing. The financial burden of IVF and PGT is also addressed, highlighting the lack of insurance coverage and the high costs involved. Richeimer emphasizes the importance of genetic counseling in navigating these complex decisions and shares her personal experiences with IVF, underscoring the emotional impact on patients. The conversation concludes with a call to action for patients...
2025-08-0538 minAll Access DNA
All Access DNAPodcast Awards & New SeasonHey hey DNA! We are celebrating our first season by being nominated for the Podcast Awards! Please help us win the title as Best Health Podcast. Just head over to podcastawards.com and click the blue button that says “Signup to Vote Now” and fill out your info. Then a CRUCIAL step is to check off the box that says “Please consider me as one of the listeners that will be randomly selected to vote on the final slate in August”. This means you, our listener, will get to vote in the final round of voting! Once y...
2025-07-0801 minAll Access DNA
All Access DNAIs autism genetic?In this conversation, Dr. Chaya Murali discusses the importance of understanding autism, the role of genetic testing, and the impact of misinformation surrounding vaccines and autism. She emphasizes the need for families to seek reliable resources and support while navigating the complexities of neurodivergence. The conversation also highlights the emotional aspects of parenting children with autism and the importance of empathy in medical practice.   Key Takeaways: Many genetic conditions can co-occur with autism, highlighting the need for genetic evaluations. Autism is partially genetic, but environmental factors also play a role. Current genetic testing can i...
2025-06-2451 minAll Access DNA
All Access DNADoes genetics influence sex and gender?In this conversation, Kim Zayhowski discusses the distinctions between sex and gender, emphasizing that sex is biological while gender is a social construct. She explores the complexities of chromosomes, the fluidity of gender identity, and the implications of societal norms on individual expression. The discussion also touches on the weaponization of scientific terminology in policy-making, the intersection of transphobia and misogyny, and the importance of recognizing diverse gender identities. Zayhowski advocates for active allyship and resistance against discriminatory policies, highlighting the importance of empathy and understanding in fostering a more inclusive society.   Key Takeaways: S...
2025-06-1744 minAll Access DNA
All Access DNAHow do budget cuts impact genetic medicine?In this conversation, Eric Green discusses the role of the National Human Genome Research Institute (NHGRI) in leading the Human Genome Project and advancing genomic research. He shares his journey at NHGRI, highlighting the significant progress made in genomic medicine, including the All of Us Research Program, which aims to collect genomic and health data from a diverse population. Dr. Green emphasizes the importance of public sector involvement in data sharing and the challenges faced in genomic research. He also addresses the potential impact of funding cuts on future research initiatives. Dr. Green discusses the importance of public advocacy...
2025-06-1051 minAll Access DNA
All Access DNAWhy would someone have a third trimester abortion?In this conversation, Dr. Shelley Sella discusses her book “Beyond Limits: Stories of Third-Trimester Abortion Care” and her experiences in providing third trimester abortion care. She emphasizes the importance of understanding the circumstances that lead individuals to seek such care, the emotional and psychological aspects involved, and the need for compassionate support. The discussion also touches on the legal implications surrounding abortion, the safety of the procedures, and the necessity for empathy and understanding in the healthcare system. Key Takeaways: Third-trimester abortion care is often stigmatized and misunderstood. The emotional and spiritual aspects of care are inte...
2025-06-0338 minDemystifying Genetics
Demystifying GeneticsFrom Rural Roots to Genetic Advocate. Demystifying Genetics with Kate Wilson.In the season finale of Demystifying Genetics, host Matt is joined by fellow genetic counselor and podcaster, Kate Wilson, the voice behind All Access DNA. They delve into the evolving landscape of genetic counseling, exploring Kate's personal journey from rural beginnings to becoming a passionate advocate for equitable access to clinical genetics. This episode highlights the disparities within healthcare systems, the importance of accessible genetic information, and how Kate is breaking norms with her dual role as a counselor and a science communicator. Tune in for a compelling discussion on the responsibilities and opportunities for genetic counselors beyond traditional...
2025-06-0253 minAll Access DNA
All Access DNAReplay: Should I delete my 23andMe data?This is a replay of our bonus episode that was released on March 28, 2025 and prior to Regeneron Pharmaceuticals purchasing 23andMe. Regeneron entered the asset purchase agreement on May 19, 2025 and states it plans to maintain the consumer genetics business. Regeneron also stated it would prioritize the privacy, security and ethical use of 23andMe's customer data. See more about the announcement here. In this episode, we explore the complexities of genetic data privacy, particularly in light of 23andMe's recent bankruptcy filing. Anya Prince discusses the implications for customer data, the legal protections in place, and the unique risks associated...
2025-05-2738 minAll Access DNA
All Access DNAWhat are sex trait variations and how do we support intersex individuals?In this conversation, we delve into the complexities surrounding intersex and transgender identities, focusing on medical ethics and the importance of patient autonomy. Our guest, Kaitlyn Brown, discusses their advocacy for the intersex community, emphasizing the importance of trauma-informed care in healthcare settings. We talk about the differences between intersex and transgender identities, the prevalence of intersex conditions, and the challenges faced by parents of intersex children. The discussion highlights the complexity of genetic definitions and the need for better understanding and support within the healthcare system. It highlights the ongoing legislative challenges that threaten the rights and healthcare...
2025-05-2058 minAll Access DNA
All Access DNAHow does DNA solve crimes? with DNA Today podcastWe are featuring an episode from another podcast on Gene Pool Media, DNA Today. True crime dominates the podcasting world, but what about the genetic aspects behind these cases? In this episode of DNA Today, we dive into the pivotal role of DNA in forensic science with Dr. Henry Erlich, a pioneer in DNA analysis and a key figure in developing polymerase chain reaction (PCR) technology. His work has transformed the criminal justice system, from solving cases to overturning wrongful convictions. Dr. Henry Erlich has authored over 450 publications and spent decades applying DNA analysis to criminal investigations...
2025-05-1347 minAll Access DNA
All Access DNAHow does music tell the story of genetic hearing loss?In this episode, Kate talks to Matt Hay about is book, “Soundtrack of Silence”. Matt opens up about his experience with neurofibromatosis type 2 (NF2), a genetic condition that led to profound hearing loss- and ultimately, the creation of his memoir, “Soundtrack of Silence: Love, Loss, and a Playlist for Life”. We explore his and his wife’s journey with IVF and preimplantation genetic testing, how they faced life-changing diagnoses together, and why his wife is the true hero of his story. Matt tells us how music shaped his life and how he continues to connect with it after hearing loss, the...
2025-05-0641 minAll Access DNA
All Access DNAIs cancer genetic?In this conversation, Barry Tong discusses the complexities of cancer genetics, emphasizing the intersection of genetic factors and public health. He explains how cancer arises from both genetic predispositions and environmental influences, and the importance of personalized risk assessments. The discussion also highlights the role of family history in cancer risk, and the challenges faced by patients navigating a cancer diagnosis, and the need for accessible genetic services in underserved communities.  Key Takeaways: Public health aspects are crucial in understanding cancer. Misconceptions about cancer origins can hinder patient understanding. Personalized risk assessments are essential for effective c...
2025-04-2932 minAll Access DNA
All Access DNAWhy is newborn screening at risk?In this conversation, Kevin Alexander shares his personal journey living with PKU (phenylketonuria) and his passion for newborn screening advocacy. He discusses the importance of dietary therapy, the challenges of navigating insurance coverage for treatment, and the critical role of newborn screening in early detection. We discuss the recent policy changes enacted without warning by the current administration and how that impacts newborn screening practices. Kevin shares personal stories and experiences that highlight the need for advocacy and community involvement in maintaining and improving the newborn screening system.  Key Takeaways: PKU is an inborn error of m...
2025-04-2248 minAll Access DNA
All Access DNAIs Parkinson's Disease genetic?In this conversation, Priscila discusses Parkinson's disease, its genetic and environmental factors, and the role of genetic counseling. She highlights the PD Generation study, which aims to increase awareness and understanding of Parkinson's disease, particularly in diverse communities. Priscila emphasizes the need for inclusive research and the role of language access in genetic counseling, sharing her personal motivations for advocating for better access to care and information for all individuals affected by Parkinson's disease. Key Takeaways: Parkinson's disease is a neurodegenerative disorder affecting movement. The causes of Parkinson's are multifactorial, involving genetics and environment. Genetic testing...
2025-04-1538 minAll Access DNA
All Access DNAAre eye color and vision hereditary?In this conversation, Naomi Wagner (she/her) discusses the intersection of ophthalmology and genetics, focusing on how genes influence eye development and diseases. She explains the complexity of inherited eye conditions, particularly retinitis pigmentosa, and the ongoing research in ocular genetics. The discussion also explores the inheritance of eye color and the importance of understanding vision impairment in society. Takeaways: Ophthalmologic or ocular genetics explores how genes affect eye health. Inherited conditions can be complex and multifactorial. Blindness and vision loss vary greatly among individuals. Eye color inheritance is influenced by multiple genes. Gene therapy shows...
2025-04-0836 minAll Access DNA
All Access DNACancer & Chemo: Could DPYD testing save lives?In today’s episode, Karen Merritt shares her personal journey of advocacy for DPD deficiency awareness following her mother's tragic experience with chemotherapy. The discussion delves into the importance of genetic testing for DPYD mutations before administering certain chemotherapy drugs, the challenges in raising awareness among healthcare professionals, and ongoing advocacy efforts to include DPYD testing in national guidelines. The conversation highlights the critical need for patient education and informed decision-making in cancer treatment as well as updates in guidelines to ensure patient safety. Takeaways: Karen Merritt became an advocate after her mother's death due to DP...
2025-04-0142 minAll Access DNA
All Access DNAShould I delete my 23andMe data?In today’s episode, we explore the complexities of genetic data privacy, particularly in light of 23andMe's recent bankruptcy filing. Anya Prince discusses the implications for customer data, the legal protections in place, and the unique risks associated with genetic information. The discussion also covers the challenges of data de-identification, customer rights regarding data deletion, and the potential for data breaches. The conversation concludes with reflections on the global landscape of genetic data privacy and the importance of understanding personal values in relation to data sharing. Key Takeaways: 23andMe's bankruptcy raises concerns about customer data. New ow...
2025-03-2838 minAll Access DNA
All Access DNAColon cancer: What is Lynch syndrome?In this episode of All Access DNA, Dave Dubin discusses his foundation, Alive and Kick’n, which he started after being diagnosed with Lynch syndrome. He explains the importance of awareness and advocacy for Lynch syndrome, a hereditary condition that increases the risk of colon and other cancers. The discussion covers the differences between sporadic colon cancer and hereditary forms, the significance of genetic testing, and the personal journey of dealing with cancer at a young age. Dave emphasizes the need for proactive screening and the role of advocacy in improving awareness and support for those affected by Lynch sy...
2025-03-2541 minAll Access DNA
All Access DNACan someone own my genes?In this conversation, Ellen Matloff, a certified genetic counselor and CEO of My Gene Counsel, discusses the implications of gene ownership and patents, particularly focusing on the BRCA gene patent case against Myriad Genetics. She shares her journey from being a cancer genetic counselor to becoming an individual plaintiff in the gene patent case. We discuss the challenges faced in the legal battle and the impact of the Supreme Court's decision in 2013. The discussion highlights the importance of access to genetic testing, the intersection of law and genetics, and the implications of gene patents for research and innovation in...
2025-03-1839 minAll Access DNA
All Access DNAWho has surgery to prevent colon cancer?In this episode, Dan “Dry Dock” Shockley shares his journey with attenuated familial adenomatous polyposis (AFAP), a hereditary condition that increases the risk of colon cancer. He discusses the discovery of his condition, the importance of genetic counseling, and his proactive approach to managing his health. Dan emphasizes the importance of advocacy, education, and the need to destigmatize living with an ostomy. He talks about the role of humor and resilience in facing health challenges and highlights his commitment to educating medical professionals about rare diseases. His mantra, 'Always forge ahead with a purpose,' encapsulates his approach to life...
2025-03-1136 minAll Access DNA
All Access DNAWhat is prenatal genetic testing?In this episode of All Access DNA, we talk to Samantha Stover, a reproductive genetic counselor, about prenatal diagnostic testing. We discuss Sam’s journey into genetic counseling, and the differences between screening and diagnostic testing methods such as chorionic villus sampling (CVS) and amniocentesis. The conversation also touches on the conditions that can be detected through these tests and the benefits, risks, and limitations of genetic testing. Sam emphasizes the importance of informed consent, patient autonomy, and the emotional challenges faced by patients. She discusses the variability in insurance coverage and the necessity of understanding each patient's unique si...
2025-03-0453 minAll Access DNA
All Access DNAWhen is rare disease not so rare?In this conversation, Susanna Smith shares her personal experience with CADASIL. The discussion explores the evolving definitions of rare diseases, the importance of accurate classification, and the implications for research and treatment. We cover how insights from rare diseases can inform our understanding of more common conditions. Susanna discusses the complexities of living as a 'previvor'—someone at risk for genetic conditions without symptoms. She explores the emotional and practical implications of genetic testing, the challenges of navigating healthcare and insurance, and the importance of patient advocacy. Susanna also shares insights from her podcast, 'Genetic Frontiers,' which delves in...
2025-02-2539 minAll Access DNA
All Access DNAHow does family history shed light on sudden cardiac death?In this conversation, Dr. Susan Weiss Liebman discusses her memoir, 'The Dressmaker's Mirror,' which intertwines her personal journey with a genetic search for a mutation linked to her niece's sudden death. She emphasizes the importance of genetic testing, the cultural heritage of her Jewish family, and the challenges faced in communicating genetic information to family members. We delve into the importance of genetic testing, particularly in relation to cardiomyopathy and other heart conditions. Dr. Liebman emphasizes the need for education among healthcare providers and the role of genetic counseling in improving patient outcomes. Key Takeaways: ...
2025-02-1846 minAll Access DNA
All Access DNAShould I consider genetic testing for dilated cardiomyopathy?In today’s episode, Greg Ruf (he/him) talks about his diagnosis of dilated cardiomyopathy, genetic testing, heart failure, and patient advocacy. He explains the formation of the Dilated Cardiomyopathy Foundation, emphasizing the need for awareness, education, and support for patients. The discussion also highlights the genetic factors associated with the disease, the challenges in diagnosis, and the critical importance of genetic testing to identify at-risk individuals. Greg also addresses the barriers to awareness and testing in the medical community, advocating for better recognition and understanding of genetic cardiomyopathy. He highlights the necessity for patients to be proactive about th...
2025-02-1138 minAll Access DNA
All Access DNAAre Leukemia and Lymphoma Hereditary?In this conversation, Sarah Bannon discusses the complexities of inherited blood cancers, particularly leukemia, and the evolving role of genetic counseling in understanding and managing these conditions. She highlights the historical context of genetic research in blood cancers, the importance of family history in assessing risk, and the advancements in genetic testing that have led to better identification of hereditary cancer syndromes. The conversation also covers the implications of genetic testing results for patients and their families, the challenges faced in the field, and the rewarding aspects of working in this emerging area of genetic counseling. On...
2025-02-0441 minAll Access DNA
All Access DNAHow Accessible is Genetic Testing?Skip to 03:19 min for episode start if you want to bypass intro. In this episode of All Access DNA, host Kate Wilson interviews Deanna Darnes about the intricacies of genetic counseling and testing. We discuss Deanna's journey into the field, the various reasons individuals seek genetic testing, the challenges faced in accessing these tests, and the complexities surrounding insurance coverage. The conversation also highlights the differences between direct-to-consumer testing and tests ordered through healthcare providers, emphasizing the importance of understanding the logistics and implications of genetic testing. In this conversation, Deanna Darnes discusses the complexities and limitations...
2025-01-2841 minAll Access DNA
All Access DNADo I need prenatal genetic screening?In this conversation, Blair Stevens, a prenatal genetic counselor, discusses the importance of prenatal genetics, focusing on screening and testing options available to expectant parents. The conversation covers the differences between screening and diagnostic testing, the types of conditions that can be detected, the accuracy of tests like NIPT or cell free DNA screening, and the role of genetic counselors in guiding families through the process. Additionally, the discussion touches on the emotional aspects of receiving test results and the importance of understanding insurance coverage for these tests. On This Episode We Discuss: ...
2025-01-2129 minAll Access DNA
All Access DNAWhat is a genetic counselor?In this conversation, Holly, a genetic counselor, discusses the multifaceted role of genetic counselors, their training, and the importance of genetic counseling in healthcare. She explains the process of genetic counseling, the significance of family history, and the nuances of genetic testing. Holly also addresses the challenges and rewards of being a genetic counselor, emphasizing the emotional aspects of the job and the importance of patient advocacy. The conversation concludes with practical advice on how to find a genetic counselor and the significance of seeking help for genetic concerns.   On This Episode We Discuss: T...
2025-01-1442 minAll Access DNA
All Access DNAWhat does a geneticist do?In this episode, Dr. Anna Hurst discusses the multifaceted role of geneticists in healthcare, the diagnostic process for genetic conditions, and the importance of understanding dysmorphology. She explains the evolution of genetic testing, the significance of genetic counseling, and the challenges faced in the field, including insurance issues. She shares her personal journey to becoming a geneticist, emphasizing the importance of specialized training and the need for more professionals in the field.    On This Episode We Discuss: Integration of genetics into healthcare The importance of family history in genetic evaluations and risk assessments The ro...
2025-01-0747 minAll Access DNA
All Access DNAComing Soon- All Access DNAFor more information about this episode, visit allaccessdna.podbean.com, where you can also stream all episodes of the show. This link is also in the show notes for easy access.   Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com   Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health.   Please rate and review the podcast on Apple, Spotify, or whe...
2024-12-3101 minAll Access DNA
All Access DNAIntroducing All Access DNAWhat 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. New episodes every Tuesday! Learn more (and...
2024-11-2000 min