Advertise on podcast: The HDSA Podcast

Send us Fan Mail Join Tam, Allison, and Maryann for a conversation about the Biologics License Application (BLA) update and what it means for the Huntington’s disease community. Together, they break down the terminology, discuss questions on the minds of individuals and families impacted by HD, and offer perspective on navigating hope and uncertainty as the community follows the path toward potential new treatments. Don't forget to follow us on social media!

Send us Fan Mail In this episode of the HDSA Podcast, we sit down with Dr. Kae Bendixen to discuss the importance of medical advocacy and how individuals and families impacted by Huntington’s disease can play an active role in their healthcare. The conversation explores how to prepare for medical appointments, communicate effectively with healthcare providers, ask the right questions, and ensure that your concerns, needs, and goals are heard. Dr. Bendixen also shares practical guidance for navigating the healthcare system and building collaborative relationships with your care team. Whether you are living with HD, supporting a loved one, or serving as a caregiver, this episode offers helpful strategies for becoming a more confident and informed advocate throughout the care journey. Don't forget to follow us on social media!

Send us Fan Mail In this episode of the HDSA Podcast, hosts Tam, MaryAnn, and Allison are joined by special guest Erin Paterson for an open and informative conversation about in vitro fertilization (IVF) and preimplantation genetic testing/Diagnosis (PGD) for families impacted by Huntington’s disease. Emily shares her perspective and experience while the group explores what the IVF and PGD process can look like, why individuals and couples may consider these options, and some of the emotional, financial, and practical realities that can come with family planning in the HD community. As always, the conversation is candid, compassionate, and centered on helping families better understand the choices that may be available to them. Whether you are considering IVF and PGD, supporting someone who is, or simply want to learn more about reproductive options for families affected by Huntington’s disease, this episode offers an approachable starting point for the conversation. This podcast is for educational purposes only and is not intended to provide medical advice. Individuals considering IVF, PGD, or other reproductive options should speak with qualified medical and genetic counseling professionals. Don't forget to follow us on social media!

Send us Fan Mail In Part 2 of Grey Area, the HDSA Podcast team continues the conversation with researchers Chris Kay, PhD, and Jessica Dawson, PhD, diving even deeper into the complexities of Huntington’s disease genetics. The conversation explores why HD may be diagnosed more often today, what researchers are learning about loss-of-interruption variants, and why a CAG repeat number may not always tell the full story. Chris and Jessica also explain the limitations of current diagnostic testing, the role of genetic counselors and HD specialists, and ongoing research aimed at better understanding sequence variants in people with reduced penetrance CAG repeats. The group also discusses research-based testing underway through the HD Biobank at the University of British Columbia and why continued research could help improve how these complex genetic results are understood in the future. Join Tam, Allison, Marianne, Chris, and Jessica as they continue navigating the fascinating—and sometimes unexpected—grey areas of Huntington’s disease genetics. Don't forget to follow us on social media!

Send us Fan Mail What happens when a Huntington’s disease genetic test result doesn’t look the way you expect? In Part 1 of Grey Area, the HDSA Podcast team is joined by researchers Chris Kay, PhD, and Jessica Dawson, PhD, to explore the complexities of HD genetics. Using a Reddit post as the starting point, the group breaks down CAG repeat lengths, intermediate alleles, reduced penetrance, inheritance, and why genetic test results aren’t always as straightforward as they may seem. Join Tam, Allison, Marianne, Chris, and Jessica for a fascinating and approachable conversation about the “grey areas” of Huntington’s disease genetics—and the questions that can send even HD researchers down a rabbit hole. Don't forget to follow us on social media!

Send us Fan Mail Allison couldn’t make it to Convention, so Tam and Maryann are filling her in on everything she missed! From powerful sessions and community moments to key updates, inspiring stories, and behind-the-scenes highlights, this episode recaps the energy, connection, and hope that made this year’s HDSA Annual Convention so meaningful.  Don't forget to follow us on social media!

Send us Fan Mail In this episode of Let’s Talk About HD, hosts Tam Maiuri and MaryAnn Emerick are joined by Paul, Hannah, Rachel, Emily, Jenna, and Mariana for a meaningful conversation about Huntington’s disease, community, connection, and the experiences that shape the HD journey. Together, they share personal perspectives, reflect on the importance of support, and highlight the power of open conversation in helping families feel seen, heard, and less alone. This episode reminds us that every HD story matters—and that by talking about HD, we continue to build awareness, understanding, and hope. Don't forget to follow us on social media!

Send us Fan Mail Let’s Talk About HD Awareness Month with Tam, Allison & MaryAnn In this episode of Let’s Talk About HD, we recognize Huntington’s Disease Awareness Month with a meaningful conversation featuring Tam, Allison, and MaryAnn. Together, they reflect on the importance of raising awareness, and discuss how storytelling, advocacy, and community support help shine a light on the experiences of HD families. Throughout the conversation, Tam, Allison, and MaryAnn highlight why awareness matters, not only in May, but all year long, as HDSA continues working to provide help for today and hope for tomorrow for everyone impacted by Huntington’s disease. Don't forget to follow us on social media!

Send us Fan Mail Meet the new hosts of the HDSA Podcast: Tamara Maiuri, PhD, Associate Director of Research and Patient Engagement; Allison Bartlett, Esq., Senior Manager of Disability Programs; and MaryAnn Emerick, LMSW, Senior Manager of Youth & Community Services. Together, they bring expertise, insight, and a deep commitment to the Huntington’s disease community.  Don't forget to follow us on social media!

Send us Fan Mail In this insightful episode, Neekia Davis, Teresa Srajer, Beth Hoffman, and Dom Thomas dive into the importance of volunteering and how you can get involved in supporting the Huntington’s Disease Society of America (HDSA). They share personal experiences, tips for making an impact, and why volunteers are the heart of the organization. Whether you're looking for ways to give back or just curious about HDSA’s mission, this conversation is packed with inspiration and practical advice. Don't forget to follow us on social media!

Send us Fan Mail In this insightful episode, Neekia Davis and Phyllis Foxworth dive deep into the highlights and critical discussions from the ELPFDD Meeting on November 13th. They break down the key takeaways, and provide an inside look at the collaborative efforts shaping the next steps. Join us as they outline action plans, share community feedback, and discuss strategies for addressing the pressing challenges and opportunities identified during the meeting. Whether you attended the ELPFDD or are catching up on what you missed, this episode is packed with valuable insights to keep you informed and engaged in the journey ahead. Tune in to stay in the know and discover how you can contribute to the path forward! Don't forget to follow us on social media!

Send us Fan Mail In today's episode, we're thrilled to take a deep dive into POWERHD with special guests Erika Boulavsky, MSW, LCSW, Community Outreach Specialist at HDReach, and MaryAnn Emerick, LMSW, Manager of Youth & Community Services at HDSA. Tune in for an insightful conversation! Don't forget to follow us on social media!

Send us Fan Mail  In this episode, HDSA's President & CEO Louise Vetter is joined by Phyllis Foxworth and Dr. Victor Sung to chat about the changing landscape of research.  Phyllis is the Senior Manager, Advocacy at HDSA Dr. Sung is the Director of the HDSA Center of Excellence at The University of Birmingham, Alabama, and the former chair of the HDSA Board of Directors.  To learn more about Huntington's disease, please visit HDSA.org.    Don't forget to follow us on social media!  Don't forget to follow us on social media!

Send us Fan Mail In this episode, HDSA's President & CEO Louise Vetter is joined by Leora Fox, PhD and Kelly Andrew to chat about Somatic Instability and how to get involved in research opportunities. Leora is the Assistant Director of Research and Patient Engagement at HDSA. Kelly is the Coordinator of Research and Mission Programs at HDSA.  To learn more about Huntington's disease, please visit HDSA.org.    Don't forget to follow us on social media!

Send us Fan Mail In this episode HDSA's President & CEO Louise Vetter is joined by Leora Fox, PhD and Kelly Andrew. Leora is the Assistant Director of Research and Patient Engagement at HDSA. Kelly is the Coordinator of Research and Mission Programs at HDSA.  To learn more about Huntington's disease, please visit HDSA.org.   Don't forget to follow us on social media!