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Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Est. Listeners
Based on iTunes & Spotify (publisher stats).
- Per-Episode Audience
Est. listeners per new episode within ~30 days
1,001 - 10,000 - Monthly Reach
Unique listeners across all episodes (30 days)
5,001 - 25,000 - Active Followers
Loyal subscribers who consistently listen
501 - 5,000
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
Recent episodes
The “Last Mile” in Cancer Care: What It Takes to Turn Innovation Into Access
Apr 29, 2026
37m 59s
Reading the Signals: How One Successful Organization Knew It Was Time to Change
Mar 31, 2026
31m 22s
Shaping the Future of AI: A Leadership Moment for Patient Advocacy
Feb 26, 2026
46m 29s
Rebuilding Trust: What the Autism Community Teaches Us About Vaccine Confidence
Jan 22, 2026
39m 07s
A Year of Transformation: What Patient Advocates Taught Us About Evolving to Deliver More for Patients
Dec 11, 2025
51m 56s
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 4/29/26 |  The “Last Mile” in Cancer Care: What It Takes to Turn Innovation Into Access | When someone is diagnosed with cancer, the expectation is that care begins quickly and smoothly. In reality, many patients and caregivers find themselves navigating a complicated system, juggling access barriers, approvals, and logistics before treatment even begins. In this episode of Patient Advocacy Voices, host Eric Racine is joined by Meagan O’Neill, Executive Director of the Association of Cancer Care Centers (ACCC), alongside co-host Rachel Solomon of Sanofi. Together, they explore how... | 37m 59s | ||||||
| 3/31/26 |  Reading the Signals: How One Successful Organization Knew It Was Time to Change | A highly respected patient advocacy organization with a trusted identity and decades of impact made a bold decision to change – the reasons behind this decision matter for every organization. For many advocacy leaders, brand identity is deeply tied to trust and recognition. But as science evolves and patients’ needs become more complex, organizations must ask themselves: are we reaching all the patients we’re meant to serve? In this episode of Patient Advocacy Voices, host Eric Racine i... | 31m 22s | ||||||
| 2/26/26 |  Shaping the Future of AI: A Leadership Moment for Patient Advocacy | How can patient advocacy leaders ensure that artificial intelligence truly serves the people it is meant to help? As AI rapidly reshapes the healthcare system, patient advocates have both an opportunity and responsibility to influence how these technologies are designed, governed, and implemented to transform patient health. In this episode of Patient Advocacy Voices, host Eric Racine welcomes back Randy Rutta, President and CEO of the National Health Council (NHC), alongside Fabrice Bocquill... | 46m 29s | ||||||
| 1/22/26 |  Rebuilding Trust: What the Autism Community Teaches Us About Vaccine Confidence | How do we rebuild trust in vaccines when fear and misinformation stand in the way, especially for autistic individuals and their families? In this episode of Patient Advocacy Voices, host Eric Racine is joined by co-host Heather Entenmann, U.S. Public Health Engagement Lead at Sanofi, for a thoughtful conversation on vaccine confidence, trust, and inclusion. Together, they welcome two leading voices in public health and advocacy: Danielle Hall, former Vaccine Education Lead at the Autism Soci... | 39m 07s | ||||||
| 12/11/25 | A Year of Transformation: What Patient Advocates Taught Us About Evolving to Deliver More for Patients | 2025 was a year of transformative change and opportunity across the patient advocacy community, Sanofi, and for patients. In this special year-end episode, host Eric Racine, joined by Adam Gluck, Head of U.S. & Global Specialty Care Corporate Affairs, and all Sanofi Season 2 co-hosts, revisit the most powerful conversations and lessons from the 2025 season while exploring the year’s defining theme, transformation. We are living through an unprecedented moment where sweeping shifts i... | 51m 56s | ||||||
| 11/24/25 | The Sanofi Patient Community Promise: Moving Beyond Patient Centricity Talk to Real Actions for Patients, Feat. the Crohn’s & Colitis Foundation | What does it take to move from patient-centric talk to patient-driven action? In this episode, we go inside Sanofi’s Patient Community Promise, a commitment to truly integrate patients throughout every part of its global organization. Host Eric Racine is joined by Sanofi co-hosts from around the world: Kersten Sharrock, Amy Akers-Teets, Catherine Coulouvrat, and Nick Taylor. They share how the Patient Community Promise was co-created with more than 80 patient advocacy leaders, how Sanof... | 53m 26s | ||||||
| 10/30/25 | Evolving for Impact: How March of Dimes Adapted Beyond Polio to Tackle Today’s Healthcare Challenges | How does an advocacy organization with a historic legacy transform and lead on the most pressing issues facing its constituents today? Host Eric Racine and co-host Robin Johnson sit down with Cindy Rahman, President & CEO, and Erin Jones, Senior Director Legislative & Strategic Counsel, at March of Dimes. From its historic role in eradicating polio to its modern fight for the health of all moms and babies, March of Dimes evolves by mobilizing data, storytelling, and collaboratio... | 31m 38s | ||||||
| 9/25/25 | From Invisible to Empowered: Advocacy Strategies from PDSA to Drive Early Recognition, Patient Connections, and Innovation | When patients are living with a misunderstood condition, and healthcare providers may not always have the answers, advocacy organizations have the power to step in and help close the gaps. In this episode, host Eric Racine and co-host Elizabeth Franklin sit down with Caroline Kruse, President & CEO of the Platelet Disorder Support Association (PDSA), whose personal experience with ITP, a rare autoimmune disease, profoundly shapes how she leads. From helping patients and clinicians recogni... | 33m 55s | ||||||
| 8/21/25 | From Unmet to Unforgettable: Inside CHES’s Approach to Patient Programs that Stick | Successful patient advocacy groups often start with a simple but powerful question: What do our patients need that no one else is delivering? The CHES Foundation took this approach head on, turning gaps in care, education, and belonging into innovative, measurable programs for the rare bleeding disorders community. In this episode, host Eric Racine and co-host Jane Smith sit down with Janet Brewer, Co-Founder & Executive Director of the CHES Foundation, to explore how CHES builds solution... | 25m 34s | ||||||
| 7/8/25 | Culture Change: What Leaders Need to Know to Help Improve Mental Health in Their Organizations and Communities | In this episode of Patient Advocacy Voices, host Eric Racine and co-host Marco DeThomasis, People Business Partner, Specialty Care at Sanofi, sit down with Schroeder Stribling, President & CEO of Mental Health America (MHA). Together, they explore how data, early intervention, and workplace culture can help address America’s growing mental health crisis. From national trends to practical tools, this conversation blends strategy with humanity – offering advocacy and business leaders insigh... | 29m 36s | ||||||
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| 6/12/25 | How to Close the Gap Between Scientific Innovation and Patient Access in the U.S. Healthcare System | Why do life-changing medical innovations often struggle to reach the patients who need them most? In this episode of Patient Advocacy Voices, Esther Krofah of the Milken Institute moderates a powerful conversation with senior Sanofi leaders across immunology, vaccines, diabetes, and policy on the systemic barriers that stand between scientific breakthroughs and ensuring access for patients in need. The conversation was recorded in February 2025 at the Sanofi Patient Advocacy Council. You’ll h... | 24m 28s | ||||||
| 5/19/25 | Building Awareness, Driving Change: Inside APFED’s Strategy for Rare Disease Advocacy | How do you drive awareness for a rare disease with a name that’s difficult to even pronounce and a wide range of symptoms that mimic other conditions? In this episode, host Eric Racine and co-host Preeya George-Guiser sit down with Mary Jo Strobel, Executive Director of the American Partnership for Eosinophilic Disorders (APFED), about the organization’s strategic approach to rare disease advocacy. Mary Jo shares how APFED blends creativity, strategy, and a patient-centered approach to raise ... | 37m 10s | ||||||
| 3/27/25 | How the Shifting U.S. Health Policy Landscape is Impacting the Patient Community | How will the shifting U.S. healthcare policy landscape impact patients? It’s an important topic that many patient advocates are thinking about today. This month’s special episode features a thought-provoking panel discussion recorded during the Sanofi Patient Advocacy Council meeting in Washington, D.C., where panelists dove into this topic. Adam Gluck, SVP and Head, U.S. and Specialty Care Corporate Affairs at Sanofi moderated the panel, which featured Randy Rutta, CEO of the National Heal... | 22m 29s | ||||||
| 2/18/25 | Scalable Solutions: How the American Lung Association Evolves to Meet the Needs its Community | Get ready for an inspiring conversation about the power of passion, purpose, and partnerships in evolving patient advocacy to meet the changing needs of a community! In this episode, Harold Wimmer, President and CEO of the American Lung Association, shares insights from his incredible 46-year journey with the organization. Harold reveals how the American Lung Association grew successful regional initiatives into powerful, national programs that deliver critical resources and support to lung p... | 26m 49s | ||||||
| 1/7/25 | Springboard to Season 2: How Advocacy Leaders Make a Difference for Patients, Science, and Policy | Patient Advocacy Voices is dedicated to helping US advocacy groups strengthen capabilities in service to patients and their mission. Season 2 continues and will provide deeper insights and more pragmatic tips from patient advocacy leaders and visionaries. In this special episode to start the new season, host Eric Racine is joined by all his Sanofi co-hosts from Season 1 to recall the powerful stories and lessons learned from advocacy leader guests. Insights are recapped on vital topics ... | 46m 10s | ||||||
| 12/10/24 | How to Innovate and Collaborate to Advance Patient-focused Priorities – The National Health Council | With more than 100 years of experience, the National Health Council knows how to bring patient advocacy groups and other organizations together to advocate for patients’ interests. How do they stay at the forefront of a patient-focused US healthcare system? They innovate and collaborate. In this episode, Sanofi host Eric Racine and cohost, Demi Anastasiades, lead of US Public Affairs and Patient Advocacy for Immunology at Sanofi, are joined by Randy Rutta, CEO of the National He... | 22m 12s | ||||||
| 11/21/24 | How Might We? How Fresh Perspectives Can Change Outcomes in Overlooked Conditions | When it comes to meeting healthcare’s biggest challenges, sometimes the best approach begins with curiosity. Dr. Jean Wright, MD, MPH, Chief Executive Officer of the Chronic Obstructive Pulmonary Disease (COPD) Foundation, has made an immense impact on the COPD community and knows firsthand how to bring new solutions that move the needle for poorly understood patient communities. In this episode, Sanofi host Eric Racine is joined by Kate Tighe, Head of US Public Affairs and Patie... | 27m 02s | ||||||
| 10/10/24 | Transforming the Pace of Medicine Development Through Partnerships with the Patient Advocacy Community | From leveraging existing resources to filling gaps with innovative tools, partnerships throughout the healthcare industry can help meet the needs of more patients and drive impact in an accelerated way. In this episode, Eric Racine is joined by Vicky DiBiaso, Global Head of Patient Informed Development and Health Value Translation at Sanofi, and Sara Loud from the Accelerated Cure Project, to discuss the transformative efforts of the Patient Advocacy Leaders in Drug Development Industr... | 31m 50s | ||||||
| 9/16/24 | Taking a Business Approach to Advocacy and Philanthropy - How a Venture Philanthropist Invests to Impact Peoples’ Lives | David Panzirer, a trustee of the Helmsley Charitable Trust, discovered his calling when his daughter was diagnosed with type 1 diabetes (T1D). A businessperson at his core, David views healthcare grants as investments, and his team continuously develops a deep understanding of the ecosystem as a key success factor to maximize their impact. Learn from one of the most significant players in the field of venture philanthropy, his team’s portfolio approach to healthcare investments, and their sin... | 16m 36s | ||||||
| 8/21/24 | Long-Term Impact: Aggregating Data to Accelerate Innovations for Patients | To help make an impact for patients, it's important to have a comprehensive understanding of how a disease impacts their day-to-day lives. Michael Osso, Chief Executive Officer of the Crohn's & Colitis Foundation knows this well. He and his team created a comprehensive research ecosystem that harnesses data– from reported anecdotes to clinical data, biosamples and more – to help researchers, patients, advocates and care teams get a holistic view of inflammatory bowel diseases (IBD) and dr... | 14m 06s | ||||||
| 7/9/24 | An Advocate's Journey to Put Patients at the Forefront of Research | Patient advocacy groups have become a powerful force engaging with clinical researchers. The National Bleeding Disorders Foundation (NBDF) has been one of the best at driving a research agenda that matters to patients, yet they still saw areas for improvement. Maria Santaella, Vice President of Research Strategy at NBDF, realized the importance of including patient voices at the very start of and throughout the research process. This is what it takes to ensure researchers understand the unmet... | 13m 36s | ||||||
| 6/4/24 | Building a Leader: How to Grow with Your Patient Advocacy Group | What does it take to grow a patient advocacy group from the ground up to become a driving force for patients in the US? Learn how Julie Block, President and CEO of the National Eczema Association (NEA), defined a bold long-term vision and learned to trust her team to stay true to the plan. Defining a five-year strategic blueprint, NEA took a broad view of stakeholders throughout the healthcare ecosystem, enabling them to set bold goals for what could be achieved through partnerships. Julie’s ... | 21m 29s | ||||||
| 5/20/24 | The First Cancer Center on Native Land – From Promise to Reality | What does it take to improve access to specialty care for vulnerable and underserved populations? What if the starting point is a complete lack of specialty care services? When Kim Thiboldeaux, CEO of the Northeast Business Group on Health, was told there was no cancer or specialty care on Native American reservations, her first reaction was shock, then it quickly turned to advocacy and action. After years of hard work and perseverance, the first cancer center on native land was opened on the... | 18m 25s | ||||||
| 4/25/24 | Many Voices, One Goal: The Power of Alliances | Cancer can be an isolating condition, so Meredith Cowden has made it her mission to ensure other patients are not alone. Meredith, a cancer survivor living with chronic graft versus host disease (cGVHD), responded to adversity by forming the Meredith A. Cowden Foundation with her family to support and advocate for fellow transplant patients. The key to Meredith’s success is her ability to advocate and form a successful alliance of advocacy groups that strengthens their ability to help and adv... | 20m 51s | ||||||
| 4/8/24 | Capturing Data to Evaluate and Communicate Impact | Impact is a word we often use in patient advocacy. We know it’s important to the patients and communities being served, and that it also matters to the funders of advocacy programs. But how do you capture impact, when do you start, where does the information come from, and how should it be communicated? Sanofi host Eric Racine and co-host Elizabeth Franklin discuss this with our guest, Aicha Diallo, patient advocacy leader and senior director of programs at the Patient Empowerment Network (PE... | 17m 40s | ||||||
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