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Explore every episode of the podcast The HDSA Podcast

Dive into the complete episode list for The HDSA Podcast. Each episode is cataloged with detailed descriptions, making it easy to find and explore specific topics. Keep track of all episodes from your favorite podcast and never miss a moment of insightful content.

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1–15 of 15

TitlePub. DateDuration
S4:E1 - Let's Talk About HD with Tam, Allison & MaryAnn23 Apr 202600:27:32

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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. 

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S3:E1- Let's Talk About Volunteering with HDSA12 Feb 202500:22:07

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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.


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S2:E5 Let's Talk about the HD ELPFDD Meeting02 Dec 202400:24:15

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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!

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S2:E4 - Let's Talk About POWERHD18 Oct 202400:22:30

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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!

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S2E3: Phyllis Foxworth & Dr. Victor Sung11 Jun 202400:37:52

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 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.   

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S2E2: Leora Fox, PhD & Kelly Andrew Part 208 May 202400:39:11

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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.   

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S2E1: Leora Fox, PhD & Kelly Andrew18 Apr 202400:42:18

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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.  

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Episode #3: Maryann Emerick, Dr. Jim Gusella and Dr. Marcy MacDonald 30 Mar 202300:49:23

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In this episode HDSA's President & CEO Louise Vetter is joined by MaryAnn Emerick;   Dr. Jim Gusella and Dr. Marcy MacDonald.

Maryann is  HDSA's Manager, Youth & Community Services and an HD family member.

Dr. Gusella is a Professor of Neurogenetics at the Department of Genetics at Harvard Medical School.

Dr. MacDonald is a Professor of Neurology at Mass General Hospital.


To learn more about Huntington's disease, please visit HDSA.org. 

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Episode #2: Chris Cosentino & Robi Blumenstein28 Feb 202300:53:31

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In Episode #2, Louise Vetter is joined by Chris Cosentino & Robi Blumenstein. 

Chris Cosentino is HDSA's Director of Marketing & Communications and has been with the Society since 2014. 

Robi Blumenstein is President of CHDI and in 2002 organized CHDI Management to provide management services to non-profit organizations engaged in Huntington’s disease research.

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Episode #1: Arik Johnson & Teresa Srajer26 Jan 202300:38:06

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In this episode HDSA's President & CEO Louise Vetter is joined by Arik Johnson, PsyD and Teresa Srajer. They discuss the launch of the new HDSA Podcast, the 38th Annual HDSA Convention and a behind-the-scenes look at the Huntington's Disease Society of America. 

Dr. Johnson is HDSA's Chief Mission Officer and former Chair of HDSA's Board of Trustees. 

Teresa is an HD family member, long-time volunteer and HDSA's newly appointed Chair of HDSA's Board of Trustees. 

To learn more about Huntington's disease, please visit HDSA.org. 


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S4:E2 - Let's Talk About HD Awareness Month with Tam, Allison & MaryAnn18 May 202600:27:30

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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.

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S4:E3 - Let's Talk About HD Awareness Month Part 229 May 202600:35:11

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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.

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S4:E4 - Tell Allison What She Missed at the HDSA Annual Convention10 Jul 202600:47:20

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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. 

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S4:E6 Let's Talk About the Grey Area : Part 214 Aug 202600:17:55

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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.

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S4:E5 Let's Talk About the Grey Area: Part 111 Aug 202600:31:31

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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.

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