<![CDATA[Patient Innovations]]>f13dca25-a11c-5e58-9aaa-16374fa248e3Fri, 20 Mar 2026 11:01:44 +0000Captivate.fmPatient Innovationshttps://artwork.captivate.fm/147cd52d-09f7-433e-9feb-9003e2bc9195/NkND0vcT0ZDFhG-qg4T9GGnp.pngPatient InnovationsPatient InnovationsPatient InnovationsPatient Innovations explores the connections between patients receiving treatment for a variety of serious health conditions, the caregivers working directly in the field and the innovators working to solve these life altering issues. Patient Innovations brings to life the very real struggles and triumphs happening right now in the world of healthcare. Brought to you by the nonprofit Healthcare.MN, join us each month for a new exploration into a different condition and the people working to make a change.https://www.healthcare.mn/podcastfalseepisodicnopodcastNasopharyngeal CarcinomaNasopharyngeal CarcinomaIn this episode of Patient Innovations, Rashmi and Shannon dive into one of the most overlooked challenges in healthcare: rare disease detection, focusing on nasopharyngeal carcinoma (NPC), sometimes called nasal cancer. NPC forms deep in the upper throat behind the nose, and its early symptoms—persistent congestion, nosebleeds, ear fullness, hearing changes, or headaches—can feel minor and easily dismissed. Yet for many patients, these subtle signs lead to delayed diagnosis, fragmented care, and life-altering consequences. This conversation grounds NPC in lived experience, clinical insight, and innovation—highlighting where delay happens and how we can do better.

The episode brings together three powerful perspectives:

Michael Arulfo, Chief AI Officer and CTO at Cadre, shares his personal journey with NPC—from early symptoms that were easy to overlook to navigating diagnosis and treatment. His story reflects the emotional toll of uncertainty, moments of feeling unheard, and the importance of persistence and patient advocacy when something doesn’t feel right.

Dr. Amy Anne Lassig, head and neck surgeon at Hennepin Healthcare, offers clinical clarity on why NPC is often diagnosed late. She explains how its location makes early detection difficult, how symptoms overlap with more common conditions, and how risk factors like Epstein-Barr virus can inform clinical suspicion. She also shares how clinicians approach treatment and the challenges of navigating rare cancers within complex care systems.

Dan Que Pham, co-founder and CEO of Oncodea, highlights innovation in early cancer detection. She discusses how advances in blood-based diagnostics, nanophotonics, and AI are working to identify cancer earlier, reduce delays, and expand access to timely, life-saving care.

Key takeaways from the conversation include:

Rare diseases like NPC are often missed because early symptoms appear common and non-specific.

Delays in diagnosis are shaped by both clinical complexity and system-level gaps in awareness and pathways.

There is no one-size-fits-all journey; patient advocacy and persistence play a critical role in getting answers.

Clinicians must balance probability with possibility, especially when symptoms persist without resolution.

Innovation in early detection has the potential to significantly improve outcomes and reduce disparities.

Listening to patient stories is essential to improving recognition, reducing delay, and saving lives.

Links & Resources:

Nasopharyngeal Carcinoma & Rare Cancer

American Cancer Society: https://www.cancer.org

National Cancer Institute: https://www.cancer.gov

Head & Neck Cancer Care

Hennepin Healthcare: https://www.hennepinhealthcare.org

Innovation in Early Detection

Oncodea: https://oncodea.com

#PatientInnovations #RareDisease #NasopharyngealCarcinoma #CancerAwareness #PatientVoices #HealthcareInnovation #EarlyDetection #HealthEquity #AIinHealthcare #HealthcareMN

]]>In this episode of Patient Innovations, Rashmi and Shannon dive into one of the most overlooked challenges in healthcare: rare disease detection, focusing on nasopharyngeal carcinoma (NPC), sometimes called nasal cancer. NPC forms deep in the upper throat behind the nose, and its early symptoms—persistent congestion, nosebleeds, ear fullness, hearing changes, or headaches—can feel minor and easily dismissed. Yet for many patients, these subtle signs lead to delayed diagnosis, fragmented care, and life-altering consequences. This conversation grounds NPC in lived experience, clinical insight, and innovation—highlighting where delay happens and how we can do better.

The episode brings together three powerful perspectives:

Michael Arulfo, Chief AI Officer and CTO at Cadre, shares his personal journey with NPC—from early symptoms that were easy to overlook to navigating diagnosis and treatment. His story reflects the emotional toll of uncertainty, moments of feeling unheard, and the importance of persistence and patient advocacy when something doesn’t feel right.

Dr. Amy Anne Lassig, head and neck surgeon at Hennepin Healthcare, offers clinical clarity on why NPC is often diagnosed late. She explains how its location makes early detection difficult, how symptoms overlap with more common conditions, and how risk factors like Epstein-Barr virus can inform clinical suspicion. She also shares how clinicians approach treatment and the challenges of navigating rare cancers within complex care systems.

Dan Que Pham, co-founder and CEO of Oncodea, highlights innovation in early cancer detection. She discusses how advances in blood-based diagnostics, nanophotonics, and AI are working to identify cancer earlier, reduce delays, and expand access to timely, life-saving care.

Key takeaways from the conversation include:

Rare diseases like NPC are often missed because early symptoms appear common and non-specific.

Delays in diagnosis are shaped by both clinical complexity and system-level gaps in awareness and pathways.

There is no one-size-fits-all journey; patient advocacy and persistence play a critical role in getting answers.

Clinicians must balance probability with possibility, especially when symptoms persist without resolution.

Innovation in early detection has the potential to significantly improve outcomes and reduce disparities.

Listening to patient stories is essential to improving recognition, reducing delay, and saving lives.

Links & Resources:

Nasopharyngeal Carcinoma & Rare Cancer

American Cancer Society: https://www.cancer.org

National Cancer Institute: https://www.cancer.gov

Head & Neck Cancer Care

Hennepin Healthcare: https://www.hennepinhealthcare.org

Innovation in Early Detection

Oncodea: https://oncodea.com

#PatientInnovations #RareDisease #NasopharyngealCarcinoma #CancerAwareness #PatientVoices #HealthcareInnovation #EarlyDetection #HealthEquity #AIinHealthcare #HealthcareMN

]]>092cd6ad-09c9-4199-ad2d-111c39a04f17Fri, 20 Mar 2026 06:00:00 -050001:09:57falsefull318183Menopause and Hormone Replacement Therapy (MRT/HRT)Menopause and Hormone Replacement Therapy (MRT/HRT)In this episode of Patient Innovations, Rashmi and Mary dive into one of the most debated and misunderstood topics in women’s health: Menopause and Hormone Replacement Therapy (MRT/HRT). Menopause is a natural life transition, yet for many women it brings disruptive symptoms, limited access to care, and widespread misinformation. This conversation grounds menopause and hormone therapy in lived experience, clinical science, and innovation—cutting through fear and confusion.

The episode brings together three powerful perspectives:

Karen Bannon, spiritual care leader and educator, shares her personal menopause journey—from unexpected symptoms and their impact on daily life to navigating decisions around hormone therapy. Her story reflects the emotional toll of feeling unheard and the importance of informed, patient-centered care.

Dr. Jewel Kling, Professor of Medicine and nationally recognized menopause expert at Mayo Clinic, offers clinical clarity on what’s happening biologically during perimenopause and menopause. She unpacks how evidence around hormone therapy has evolved, addresses common misconceptions, and explains how clinicians personalize treatment based on timing, risk, and individual goals.

Ashlie Beiter, founding partner and VP of Marketing at Winona, highlights innovation in menopause care. She discusses how telemedicine and education-first models are expanding access, reducing stigma, and helping women navigate hormone therapy with confidence and trust.

Key takeaways from the conversation include:

  1. Menopause is a major life transition—not a niche issue—and symptoms can significantly affect quality of life.
  2. Hormone therapy requires nuance, not fear, with newer research clarifying safety, timing, and personalization.
  3. There is no one-size-fits-all approach; informed, individualized care is essential.
  4. Access to accurate information and trained clinicians remains a gap, one that innovative care models are helping to close.
  5. Listening to women’s stories is critical to improving care and normalizing menopause conversations.

Links & Resources:

Menopause & Hormone Therapy

The Menopause Society | Homepage: https://www.menopause.org

Choosing a Healthcare Practitioner | The Menopause Society: https://www.menopause.org/for-women/choosing-a-healthcare-practitioner

Mayo Clinic — Menopause & Hormone Therapy: https://www.mayoclinic.org

Female Sexual Health

Prosayla | Female Sexual Health Education: https://www.prosayla.com

Related Podcast

Read. Talk. Grow. Podcast — Guides at Mayo Clinic: https://readtalkgrow.mayoclinic.org

Innovation in Care

Winona — Menopause Care & Education: https://bywinona.com

#PatientInnovations #Menopause #HormoneReplacementTherapy #WomensHealth #MidlifeHealth #HealthEquity #PatientVoices #HealthcareInnovation #MenopauseCare #HealthcareMN

]]>In this episode of Patient Innovations, Rashmi and Mary dive into one of the most debated and misunderstood topics in women’s health: Menopause and Hormone Replacement Therapy (MRT/HRT). Menopause is a natural life transition, yet for many women it brings disruptive symptoms, limited access to care, and widespread misinformation. This conversation grounds menopause and hormone therapy in lived experience, clinical science, and innovation—cutting through fear and confusion.

The episode brings together three powerful perspectives:

Karen Bannon, spiritual care leader and educator, shares her personal menopause journey—from unexpected symptoms and their impact on daily life to navigating decisions around hormone therapy. Her story reflects the emotional toll of feeling unheard and the importance of informed, patient-centered care.

Dr. Jewel Kling, Professor of Medicine and nationally recognized menopause expert at Mayo Clinic, offers clinical clarity on what’s happening biologically during perimenopause and menopause. She unpacks how evidence around hormone therapy has evolved, addresses common misconceptions, and explains how clinicians personalize treatment based on timing, risk, and individual goals.

Ashlie Beiter, founding partner and VP of Marketing at Winona, highlights innovation in menopause care. She discusses how telemedicine and education-first models are expanding access, reducing stigma, and helping women navigate hormone therapy with confidence and trust.

Key takeaways from the conversation include:

  1. Menopause is a major life transition—not a niche issue—and symptoms can significantly affect quality of life.
  2. Hormone therapy requires nuance, not fear, with newer research clarifying safety, timing, and personalization.
  3. There is no one-size-fits-all approach; informed, individualized care is essential.
  4. Access to accurate information and trained clinicians remains a gap, one that innovative care models are helping to close.
  5. Listening to women’s stories is critical to improving care and normalizing menopause conversations.

Links & Resources:

Menopause & Hormone Therapy

The Menopause Society | Homepage: https://www.menopause.org

Choosing a Healthcare Practitioner | The Menopause Society: https://www.menopause.org/for-women/choosing-a-healthcare-practitioner

Mayo Clinic — Menopause & Hormone Therapy: https://www.mayoclinic.org

Female Sexual Health

Prosayla | Female Sexual Health Education: https://www.prosayla.com

Related Podcast

Read. Talk. Grow. Podcast — Guides at Mayo Clinic: https://readtalkgrow.mayoclinic.org

Innovation in Care

Winona — Menopause Care & Education: https://bywinona.com

#PatientInnovations #Menopause #HormoneReplacementTherapy #WomensHealth #MidlifeHealth #HealthEquity #PatientVoices #HealthcareInnovation #MenopauseCare #HealthcareMN

]]>da0ece7e-6d22-4a39-b224-c342f74a4f8dThu, 05 Feb 2026 06:00:00 -050054:27falsefull317173Chronic Pelvic PainChronic Pelvic PainIn this episode of the Patient Innovations Podcast, Rashmi Kandwal and Mary MacCarthy explore one of the most complex and underrecognized conditions affecting millions of women: chronic pelvic pain. Defined as pain in the lower abdomen or pelvis lasting longer than six months, chronic pelvic pain can stem from a wide range of causes — from uterine dysfunction and neuropathic pain to hormonal and mood-related conditions. Because the condition is multifaceted, effective treatment almost always requires an integrated, multidisciplinary approach.

The conversation begins with patient guest Kaleigh Karlen, a high school science teacher from Denver whose personal journey highlights the day-to-day realities of navigating symptoms, stigma, delayed diagnosis, and fragmented care. Kaleigh shares what has helped her most — including pelvic floor therapy, electrical therapy, and lifestyle changes talks about Beating Endo, a book that helped her understand the link between endometriosis, inflammation, and diet. Her story offers a candid look at how CPP affects mental health, work, relationships, and identity, and the hope that emerges when patients finally feel heard.

The clinical perspective comes from Dr. Kaitlin Baily, a Doctor of Physical Therapy specializing in pelvic health. Dr. Baily explains why chronic pelvic pain is so difficult to treat and underscores how many of her patients experience meaningful improvement through evidence-based pelvic rehab. She dispels common misconceptions, emphasizes the role of consistent PT, and outlines why multidisciplinary care is essential for long-term recovery.

The episode closes with an innovation-forward discussion featuring Dr. Yingchun Zhang, Co-founder and President of HillMed and Professor of Biomedical Engineering at the University of Miami. Dr. Zhang introduces HillMed’s EMG imaging system, which produces a clear and comprehensive map of muscles and nerves to pinpoint optimal treatment and injection sites. This precision mapping is designed to support better outcomes, faster recovery, and more comfortable patient experiences, and reflects how patient feedback continues to shape HillMed’s research and design.

Together, these three perspectives paint a comprehensive picture of a condition that is too often misunderstood and undertreated — and they spotlight the hope, progress, and innovation emerging in this space.

#ChronicPelvicPain #PatientInnovations #HealthcareMN #PelvicPain #PublicHealth #ChronicIllness #HealthEquity #PatientStories #HealthcareInnovation #Resilience

]]>In this episode of the Patient Innovations Podcast, Rashmi Kandwal and Mary MacCarthy explore one of the most complex and underrecognized conditions affecting millions of women: chronic pelvic pain. Defined as pain in the lower abdomen or pelvis lasting longer than six months, chronic pelvic pain can stem from a wide range of causes — from uterine dysfunction and neuropathic pain to hormonal and mood-related conditions. Because the condition is multifaceted, effective treatment almost always requires an integrated, multidisciplinary approach.

The conversation begins with patient guest Kaleigh Karlen, a high school science teacher from Denver whose personal journey highlights the day-to-day realities of navigating symptoms, stigma, delayed diagnosis, and fragmented care. Kaleigh shares what has helped her most — including pelvic floor therapy, electrical therapy, and lifestyle changes talks about Beating Endo, a book that helped her understand the link between endometriosis, inflammation, and diet. Her story offers a candid look at how CPP affects mental health, work, relationships, and identity, and the hope that emerges when patients finally feel heard.

The clinical perspective comes from Dr. Kaitlin Baily, a Doctor of Physical Therapy specializing in pelvic health. Dr. Baily explains why chronic pelvic pain is so difficult to treat and underscores how many of her patients experience meaningful improvement through evidence-based pelvic rehab. She dispels common misconceptions, emphasizes the role of consistent PT, and outlines why multidisciplinary care is essential for long-term recovery.

The episode closes with an innovation-forward discussion featuring Dr. Yingchun Zhang, Co-founder and President of HillMed and Professor of Biomedical Engineering at the University of Miami. Dr. Zhang introduces HillMed’s EMG imaging system, which produces a clear and comprehensive map of muscles and nerves to pinpoint optimal treatment and injection sites. This precision mapping is designed to support better outcomes, faster recovery, and more comfortable patient experiences, and reflects how patient feedback continues to shape HillMed’s research and design.

Together, these three perspectives paint a comprehensive picture of a condition that is too often misunderstood and undertreated — and they spotlight the hope, progress, and innovation emerging in this space.

#ChronicPelvicPain #PatientInnovations #HealthcareMN #PelvicPain #PublicHealth #ChronicIllness #HealthEquity #PatientStories #HealthcareInnovation #Resilience

]]>1a6f9c5f-4116-45b6-9291-1b72df0ee924Fri, 05 Dec 2025 06:00:00 -050047:27falsefull316163Long CovidLong CovidWhat is Long COVID—and why does it persist for some people but not others? Why do symptoms vary so widely—from fatigue and brain fog to shortness of breath and heart palpitations? And how are clinicians and public health leaders working to better understand and support those affected?

In this episode of Patient Innovations, Rashmi and Mary kick off the new season diving into one of the most complex health challenges to emerge in recent years—Long COVID, a condition with no known standard of care and a growing need for awareness, research, and compassion.

Our guests bring deeply personal and professional perspectives to this evolving condition:

  • Senator Lindsey Port, Minnesota State Senator, shares her lived experience navigating life, work, and treatment with Long COVID—and the struggles she’s faced with insurance coverage and care access.
  • Dr. Ruby Tam, physician with the ME/CFS Clinic, runs a free clinic that offers a clinical perspective on what she’s seeing among patients, how her team helps them manage symptoms, and why treating Long COVID remains such a challenge.
  • Kate Murray, from the Minnesota Department of Health, discusses one of the nation’s first statewide public health initiatives focused on Long COVID research and awareness—and the power of collaboration in driving progress.

Key Takeaways:

Long COVID is real—and it’s life-altering for many.

While symptoms vary, the most common include fatigue, brain fog, shortness of breath, and post-exertional malaise. For some, recovery is slow and unpredictable.

Be your own champion.

Patients often face skepticism or delayed diagnosis. Listen to your body, document your symptoms, and connect with clinicians who understand post-viral conditions. If one provider isn’t listening—find another, and then another.

Find your community.

Join care and support groups to learn, connect, and navigate insurance or access challenges. Long COVID remains widely misunderstood and under diagnosed—but community can help bridge those gaps.

Certain groups are more affected.

Women, Hispanic and Latino communities, older adults, and those with underlying health conditions are at higher risk. Stressful living conditions can also worsen symptoms, as stress often manifests as inflammation.

Innovation and collaboration are key.

Minnesota’s public health initiatives and clinical partnerships are leading the way in building awareness, research, and resources for those living with Long COVID. There’s a long road ahead, but progress is happening—join the movement and access available support.

Links & Resources:


#LongCOVID #PatientInnovations #HealthcareMN #PostCOVIDCare #PublicHealth #ChronicIllness #HealthEquity #PatientStories #HealthcareInnovation #Resilience

]]>What is Long COVID—and why does it persist for some people but not others? Why do symptoms vary so widely—from fatigue and brain fog to shortness of breath and heart palpitations? And how are clinicians and public health leaders working to better understand and support those affected?

In this episode of Patient Innovations, Rashmi and Mary kick off the new season diving into one of the most complex health challenges to emerge in recent years—Long COVID, a condition with no known standard of care and a growing need for awareness, research, and compassion.

Our guests bring deeply personal and professional perspectives to this evolving condition:

  • Senator Lindsey Port, Minnesota State Senator, shares her lived experience navigating life, work, and treatment with Long COVID—and the struggles she’s faced with insurance coverage and care access.
  • Dr. Ruby Tam, physician with the ME/CFS Clinic, runs a free clinic that offers a clinical perspective on what she’s seeing among patients, how her team helps them manage symptoms, and why treating Long COVID remains such a challenge.
  • Kate Murray, from the Minnesota Department of Health, discusses one of the nation’s first statewide public health initiatives focused on Long COVID research and awareness—and the power of collaboration in driving progress.

Key Takeaways:

Long COVID is real—and it’s life-altering for many.

While symptoms vary, the most common include fatigue, brain fog, shortness of breath, and post-exertional malaise. For some, recovery is slow and unpredictable.

Be your own champion.

Patients often face skepticism or delayed diagnosis. Listen to your body, document your symptoms, and connect with clinicians who understand post-viral conditions. If one provider isn’t listening—find another, and then another.

Find your community.

Join care and support groups to learn, connect, and navigate insurance or access challenges. Long COVID remains widely misunderstood and under diagnosed—but community can help bridge those gaps.

Certain groups are more affected.

Women, Hispanic and Latino communities, older adults, and those with underlying health conditions are at higher risk. Stressful living conditions can also worsen symptoms, as stress often manifests as inflammation.

Innovation and collaboration are key.

Minnesota’s public health initiatives and clinical partnerships are leading the way in building awareness, research, and resources for those living with Long COVID. There’s a long road ahead, but progress is happening—join the movement and access available support.

Links & Resources:


#LongCOVID #PatientInnovations #HealthcareMN #PostCOVIDCare #PublicHealth #ChronicIllness #HealthEquity #PatientStories #HealthcareInnovation #Resilience

]]>49b550af-9b62-4214-99d3-24155528d4f1Fri, 24 Oct 2025 06:00:00 -050058:59falsefull315153Multiple Sclerosis (MS) – Living, Treating, and Curing TogetherMultiple Sclerosis (MS) – Living, Treating, and Curing TogetherIn this episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal explore Multiple Sclerosis (MS)—a complex neurological disease that affects nearly 3 million people globally, including over 1 million Americans. MS disproportionately impacts women, and studies show higher prevalence in northern states like Minnesota, which has the highest rates in the country.

Guests include:

  • Mary Johnson, MS patient and advocate
  • Dr. Jessica Stulc, Director of MS Treatment & Research, Minneapolis Clinic of Neurology
  • Kathleen O’Donnell, President, Upper Midwest Chapter, National MS Society

Together, they shed light on early symptoms, lived experiences, the current state of MS research, and the power of advocacy, partnerships, and community in creating hope for those impacted by MS.

]]>In this episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal explore Multiple Sclerosis (MS)—a complex neurological disease that affects nearly 3 million people globally, including over 1 million Americans. MS disproportionately impacts women, and studies show higher prevalence in northern states like Minnesota, which has the highest rates in the country.

Guests include:

  • Mary Johnson, MS patient and advocate
  • Dr. Jessica Stulc, Director of MS Treatment & Research, Minneapolis Clinic of Neurology
  • Kathleen O’Donnell, President, Upper Midwest Chapter, National MS Society

Together, they shed light on early symptoms, lived experiences, the current state of MS research, and the power of advocacy, partnerships, and community in creating hope for those impacted by MS.

]]>e66c0e46-34df-448c-9694-4c11f9f7e3e7Mon, 21 Jul 2025 06:00:00 -050054:34falsefull214142Spinal Cord Injury (SCI): Resilience, Recovery & NeurotechSpinal Cord Injury (SCI): Resilience, Recovery & NeurotechIn this powerful episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal go beyond stats and symptoms to explore the lived experience of spinal cord injury—and the groundbreaking technologies transforming recovery.

Nearly 18,000 people in the U.S. are diagnosed with a spinal cord injury each year. Today’s episode features two voices at the forefront: a hockey player's unshakable will and a scientist's drive to innovate.

Featured guests:

Jack Jablonski – Former Minnesota hockey standout and current LA Kings digital media specialist. Jack shares how his life changed after a 2011 spinal cord injury—and how he’s advancing recovery through his personal journey and the Jack Jablonski Foundation.

Dr. Parag Gad – CEO and Co-Founder of SpineX, Dr. Gad explains how his team’s non-invasive neuromodulation therapies (like SCONE™) are helping patients regain function—and what FDA Breakthrough Device designation means for the future of care.

In this episode, you’ll hear about:

  • Living with and training through paralysis
  • How neuromodulation is redefining recovery
  • Jack’s mission to help others BEL13VE
  • The hope that drives patients and innovators forward

Want to collaborate or sponsor? Email rashmi@healthcare.mn.

Next up: Multiple Sclerosis—closing the gap in care.

Support spinal cord injury research through the Jack Jablonski Foundation. Every donation fuels progress toward life-changing breakthroughs.

#SpinalCordInjury #Neurotech #JackJablonski #PatientStories #ParalysisRecovery #HealthcareInnovation #SCI #SpineX #PatientInnovations #HealthcareMN #BEL13VE

]]>In this powerful episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal go beyond stats and symptoms to explore the lived experience of spinal cord injury—and the groundbreaking technologies transforming recovery.

Nearly 18,000 people in the U.S. are diagnosed with a spinal cord injury each year. Today’s episode features two voices at the forefront: a hockey player's unshakable will and a scientist's drive to innovate.

Featured guests:

Jack Jablonski – Former Minnesota hockey standout and current LA Kings digital media specialist. Jack shares how his life changed after a 2011 spinal cord injury—and how he’s advancing recovery through his personal journey and the Jack Jablonski Foundation.

Dr. Parag Gad – CEO and Co-Founder of SpineX, Dr. Gad explains how his team’s non-invasive neuromodulation therapies (like SCONE™) are helping patients regain function—and what FDA Breakthrough Device designation means for the future of care.

In this episode, you’ll hear about:

  • Living with and training through paralysis
  • How neuromodulation is redefining recovery
  • Jack’s mission to help others BEL13VE
  • The hope that drives patients and innovators forward

Want to collaborate or sponsor? Email rashmi@healthcare.mn.

Next up: Multiple Sclerosis—closing the gap in care.

Support spinal cord injury research through the Jack Jablonski Foundation. Every donation fuels progress toward life-changing breakthroughs.

#SpinalCordInjury #Neurotech #JackJablonski #PatientStories #ParalysisRecovery #HealthcareInnovation #SCI #SpineX #PatientInnovations #HealthcareMN #BEL13VE

]]>24aca631-cad7-4f27-b78f-ea0d2af658f8Sat, 07 Jun 2025 06:00:00 -050043:29falsefull213132Heart Health: Heart Valve InnovationsHeart Health: Heart Valve InnovationsIn this spring episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal explore the vital role heart valves play in keeping us alive—and what happens when they don’t work as they should. With 2.5% of the U.S. population affected by heart valve disease and 40,000 babies born each year with congenital heart defects, the need for innovation is more urgent than ever.

Featured guests:

  • Kris Bauerschmidt, entrepreneur and medical device leader, shares his journey receiving a mechanical heart valve and what life is like post-surgery.
  • Dr. Maan Jokhadar, Cardiologist at Mayo Clinic, explains how heart valve care has evolved, when to repair vs. replace, and why anticoagulants like Warfarin are still necessary.
  • Dr. Mayra Guerrero, Mayo Clinic Interventional Cardiologist and board member of the Heart Valve Society, discusses global collaboration in research and what innovations give her hope.

In this episode you will hear about: 

  • Living with a mechanical valve
  • Evolving heart valve treatments
  • Research priorities and future tech
  • Why heart health starts with awareness

Have ideas on collaboration or want to sponsor Patient Innovations? Reach out to rashmi@healthcare.mn.

Next up: spinal cord injuries—featuring a Minnesota hockey legend's powerful recovery story.

#HeartValveHealth #Cardiology #PatientStories #HealthcareInnovation #MayoClinic #HeartValveSociety #PatientInnovations #HealthcareMN

]]>In this spring episode of Patient Innovations, co-hosts Mary MacCarthy and Rashmi Kandwal explore the vital role heart valves play in keeping us alive—and what happens when they don’t work as they should. With 2.5% of the U.S. population affected by heart valve disease and 40,000 babies born each year with congenital heart defects, the need for innovation is more urgent than ever.

Featured guests:

  • Kris Bauerschmidt, entrepreneur and medical device leader, shares his journey receiving a mechanical heart valve and what life is like post-surgery.
  • Dr. Maan Jokhadar, Cardiologist at Mayo Clinic, explains how heart valve care has evolved, when to repair vs. replace, and why anticoagulants like Warfarin are still necessary.
  • Dr. Mayra Guerrero, Mayo Clinic Interventional Cardiologist and board member of the Heart Valve Society, discusses global collaboration in research and what innovations give her hope.

In this episode you will hear about: 

  • Living with a mechanical valve
  • Evolving heart valve treatments
  • Research priorities and future tech
  • Why heart health starts with awareness

Have ideas on collaboration or want to sponsor Patient Innovations? Reach out to rashmi@healthcare.mn.

Next up: spinal cord injuries—featuring a Minnesota hockey legend's powerful recovery story.

#HeartValveHealth #Cardiology #PatientStories #HealthcareInnovation #MayoClinic #HeartValveSociety #PatientInnovations #HealthcareMN

]]>5203c400-6fb3-4a90-b06c-129c7f2b98f8Sat, 17 May 2025 06:00:00 -050043:55falsefull212122Sleep ApneaSleep ApneaIn this episode of Patient Innovations, we hear from Robert J. Proulx, who is receiving care for sleep apnea. Then Dr. Runji Varghese, a sleep medicine physician at Hennepin Healthcare and Medical Director at the Minnesota Regional Sleep Disorders Center, and Sarah Chiapetta, head of product at GEM Health in White Bear Lake, Minnesota, share clinical information and innovation from their organizations.

For resources and support, check out the American Sleep Apnea Foundation at https://www.sleephealth.org/. You can learn more about Dr. Varghese's center at https://www.hennepinhealthcare.org/specialty/minnesota-regional-sleep-disorders-center/. To learn more about the GEM Health solution go to https://www.mygemsleep.com/.

#sleepapnea #PatientAdvocacy #PatientInnovationsPodcast 

]]>In this episode of Patient Innovations, we hear from Robert J. Proulx, who is receiving care for sleep apnea. Then Dr. Runji Varghese, a sleep medicine physician at Hennepin Healthcare and Medical Director at the Minnesota Regional Sleep Disorders Center, and Sarah Chiapetta, head of product at GEM Health in White Bear Lake, Minnesota, share clinical information and innovation from their organizations.

For resources and support, check out the American Sleep Apnea Foundation at https://www.sleephealth.org/. You can learn more about Dr. Varghese's center at https://www.hennepinhealthcare.org/specialty/minnesota-regional-sleep-disorders-center/. To learn more about the GEM Health solution go to https://www.mygemsleep.com/.

#sleepapnea #PatientAdvocacy #PatientInnovationsPodcast 

]]>dd74e2ca-287b-4167-b99b-ea3ca400080eWed, 02 Apr 2025 06:00:00 -050051:16falsefull211112ALS / Lou Gehrig’s DiseaseALS / Lou Gehrig’s DiseaseIn this episode of Patient Innovations, we dive into Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease—a progressive neurodegenerative condition that affects nerve cells in the brain and spinal cord.

Joining us in the studio are:

  • Mark Bearman – An ALS patient with a genetic mutation, sharing his personal journey.
  • Dr. Sam Maiser – Chair of the Department of Neurology at Hennepin Healthcare, offering medical insights.
  • Jennifer Hjelle – Chief Community Engagement Officer for the ALS Association, discussing advocacy and resources.

ALS, which currently has no known cure, often begins with muscle weakness in the hands, feet, arms, or legs before progressing to other parts of the body. As nerve cells die, movement becomes more difficult, eventually impacting chewing, swallowing, speaking, and breathing.

The Ice Bucket Challenge became a historic movement, raising millions of dollars for ALS research. These efforts contributed to the development of the first drug showing significant potential in treating genetically induced ALS.

 Learn more, find resources, and support advocacy efforts at The ALS Association – dedicated to finding a cure for ALS. 

]]>In this episode of Patient Innovations, we dive into Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease—a progressive neurodegenerative condition that affects nerve cells in the brain and spinal cord.

Joining us in the studio are:

  • Mark Bearman – An ALS patient with a genetic mutation, sharing his personal journey.
  • Dr. Sam Maiser – Chair of the Department of Neurology at Hennepin Healthcare, offering medical insights.
  • Jennifer Hjelle – Chief Community Engagement Officer for the ALS Association, discussing advocacy and resources.

ALS, which currently has no known cure, often begins with muscle weakness in the hands, feet, arms, or legs before progressing to other parts of the body. As nerve cells die, movement becomes more difficult, eventually impacting chewing, swallowing, speaking, and breathing.

The Ice Bucket Challenge became a historic movement, raising millions of dollars for ALS research. These efforts contributed to the development of the first drug showing significant potential in treating genetically induced ALS.

 Learn more, find resources, and support advocacy efforts at The ALS Association – dedicated to finding a cure for ALS. 

]]>dd9e85c4-5b13-4cab-8540-04e162547f86Tue, 04 Mar 2025 06:00:00 -050056:20falsefull210102Organ TransplantOrgan TransplantIn this episode, we explore the journey of organ transplantation—what it takes to make transplants possible, the latest advancements in the field, and the powerful stories of those whose lives have been forever changed.

Our guests include:

  • Ben Williams – Kidney transplant recipient, NFL Players Association Chapter President, and former US NFL football player (including the Minnesota Vikings) who transitioned to the NFL Europe/World Football League. Ben Williams Foundation is on a mission to educate on kidney disease: https://benwilliamsfoundation.org/
  • Dr. Vanessa Humphreville, MD, FACS – Liver, kidney, and pancreas transplant surgeon and associate professor at the University of Minnesota School of Medicine.
  • Kate Kishish – Transplant coordinator at LifeSource, one of 56 Organ Procurement Organizations (OPOs) in the country. LifeSource serves the second-largest geographical region, covering Minnesota, North Dakota, South Dakota, and parts of western Wisconsin, with a mission to save and heal lives through organ donation and transplantation.

Organ transplantation is a life-saving procedure in which a donor’s organ is surgically placed into a recipient whose own organ has failed or been damaged. While thousands of lives are transformed each year through organ donation, the need for organs continues to far exceed the available supply. Join us as we explore the science, the human impact, and the critical need for awareness and action in organ transplantation. Learn more about how to become a donor at LifeSource.

]]>In this episode, we explore the journey of organ transplantation—what it takes to make transplants possible, the latest advancements in the field, and the powerful stories of those whose lives have been forever changed.

Our guests include:

  • Ben Williams – Kidney transplant recipient, NFL Players Association Chapter President, and former US NFL football player (including the Minnesota Vikings) who transitioned to the NFL Europe/World Football League. Ben Williams Foundation is on a mission to educate on kidney disease: https://benwilliamsfoundation.org/
  • Dr. Vanessa Humphreville, MD, FACS – Liver, kidney, and pancreas transplant surgeon and associate professor at the University of Minnesota School of Medicine.
  • Kate Kishish – Transplant coordinator at LifeSource, one of 56 Organ Procurement Organizations (OPOs) in the country. LifeSource serves the second-largest geographical region, covering Minnesota, North Dakota, South Dakota, and parts of western Wisconsin, with a mission to save and heal lives through organ donation and transplantation.

Organ transplantation is a life-saving procedure in which a donor’s organ is surgically placed into a recipient whose own organ has failed or been damaged. While thousands of lives are transformed each year through organ donation, the need for organs continues to far exceed the available supply. Join us as we explore the science, the human impact, and the critical need for awareness and action in organ transplantation. Learn more about how to become a donor at LifeSource.

]]>429040cd-e61c-4afb-b9fd-e70f2f28f8adThu, 06 Feb 2025 06:00:00 -050001:02:20falsefull2992Understanding Depression: Stories of Struggle, Support, and StrengthUnderstanding Depression: Stories of Struggle, Support, and StrengthThis episode of Patient Innovations delves into the realities of living with depression, featuring personal stories, expert insights, and organizational perspectives.

Guests:

  • Julie Berggren shares her journey with depression, the challenges she faced, and the tools that have supported her mental health.
  • Dr. Talee Vang, award-winning psychologist and Vice President of Health Equity at Hennepin Healthcare, emphasizes the role of cultural sensitivity, equity, and access in effective mental health care.
  • Shannon Stauff, COO of Cadre, a mental health app, discusses her journey in the mental health space and how Cadre, a MN based startup is making a difference in addressing depression and other mental health issues  

]]>This episode of Patient Innovations delves into the realities of living with depression, featuring personal stories, expert insights, and organizational perspectives.

Guests:

  • Julie Berggren shares her journey with depression, the challenges she faced, and the tools that have supported her mental health.
  • Dr. Talee Vang, award-winning psychologist and Vice President of Health Equity at Hennepin Healthcare, emphasizes the role of cultural sensitivity, equity, and access in effective mental health care.
  • Shannon Stauff, COO of Cadre, a mental health app, discusses her journey in the mental health space and how Cadre, a MN based startup is making a difference in addressing depression and other mental health issues  

]]>f27b5c70-31fd-4bbb-9a15-3a6518a6cb90Fri, 03 Jan 2025 06:00:00 -050055:45falsefull2882Multiple MyelomaMultiple MyelomaIn this episode, we explore Multiple Myeloma, a rare and complex blood cancer, with insights from experts and a patient navigating the journey firsthand. Together, they share the challenges of diagnosis, advancements in treatment, and hope through innovative care.

  • Ron Thiessen – A patient sharing his courageous story of resilience.
  • Dr. Joseph Maakaron – A leading oncologist, Assistant Professor of Medicine at the University of Minnesota, and Clinical Investigator in the Bone Marrow Transplant Division and Stem Cell Institute.
  • Jeff Liter – CEO of Luminary Therapeutics, a clinical-stage company transforming care with allogeneic cellular therapies.

This conversation highlights the strength of the Multiple Myeloma community and the transformative impact of cutting-edge research and personalized care.

#MultipleMyeloma #BloodCancerAwareness #PatientInnovations #HealthcareAdvances

Additional Resources:


]]>In this episode, we explore Multiple Myeloma, a rare and complex blood cancer, with insights from experts and a patient navigating the journey firsthand. Together, they share the challenges of diagnosis, advancements in treatment, and hope through innovative care.

  • Ron Thiessen – A patient sharing his courageous story of resilience.
  • Dr. Joseph Maakaron – A leading oncologist, Assistant Professor of Medicine at the University of Minnesota, and Clinical Investigator in the Bone Marrow Transplant Division and Stem Cell Institute.
  • Jeff Liter – CEO of Luminary Therapeutics, a clinical-stage company transforming care with allogeneic cellular therapies.

This conversation highlights the strength of the Multiple Myeloma community and the transformative impact of cutting-edge research and personalized care.

#MultipleMyeloma #BloodCancerAwareness #PatientInnovations #HealthcareAdvances

Additional Resources:


]]>4a09e197-41df-4b08-aeae-bdfccb363b8eTue, 10 Dec 2024 06:00:00 -050055:05falsefull2772DiabetesDiabetesIn this episode, we delve into the realities of diabetes with three insightful guests. Angie Kruger shares her journey of managing Type 2 Diabetes (T2D), Dr. Pankaj Shah, an endocrinologist at Mayo Clinic, offers expert insights into the medical aspects and challenges of diabetes care, and Stacey Pugh, CEO of Endogenex, discusses innovations in T2D treatment and Minnesota's role as a medtech hub. Together, they explore the importance of lifestyle adjustments, early detection, and the latest therapies transforming diabetes management. Tune in for valuable insights on the future of diabetes care and tips for living well with T2D.

Disclaimer: This episode is intended to inform and explore innovations; it does not promote or endorse any specific products or companies.

]]>In this episode, we delve into the realities of diabetes with three insightful guests. Angie Kruger shares her journey of managing Type 2 Diabetes (T2D), Dr. Pankaj Shah, an endocrinologist at Mayo Clinic, offers expert insights into the medical aspects and challenges of diabetes care, and Stacey Pugh, CEO of Endogenex, discusses innovations in T2D treatment and Minnesota's role as a medtech hub. Together, they explore the importance of lifestyle adjustments, early detection, and the latest therapies transforming diabetes management. Tune in for valuable insights on the future of diabetes care and tips for living well with T2D.

Disclaimer: This episode is intended to inform and explore innovations; it does not promote or endorse any specific products or companies.

]]>b21655b1-c825-4ab0-8ab4-6db79de1fed0Tue, 05 Nov 2024 09:00:00 -050058:03falsefull2662Sickle Cell Disease (SCD)Sickle Cell Disease (SCD)In this episode of Patient Innovations, we explore the complexities of Sickle Cell Disease (SCD) through the lens of personal experience, medical expertise, and community advocacy. Our guests include Dennik McBride, a courageous sickle cell warrior, who shares her personal journey living with the condition. Dr. Ashish Gupta from the University of Minnesota,  Dr.Gupta largely cares for children and young adults with sickle cell disease who need transplant based therapies. In the episode he provides insight into the latest research and treatment advancements;This episode highlights that there are many challenges, including the implementation of standard guidelines, for adults with sickle cell disease. These include, but not limited to, access to primary and specialty care, transition of care as well as comprehensive sickle cell care. We also have Rae Blaylark, Executive Director of the Sickle Cell Foundation of MN, who highlights the importance of community support, advocacy, and resources for those affected by SCD. Together, they discuss the challenges patients face in navigating healthcare, the impact of SCD on marginalized communities, and the promising future of treatments like gene therapy and bone marrow transplants. 

For resources and support, The Sickle Cell Foundation can be accessed at  www.sicklecellmn.org . You can calso follow them @sicklecellmn on LinkedIn, FB, IG and Twitter (X).

#SickleCellAwareness #HealthcareEquity #PatientAdvocacy #PatientInnovationsPodcast #SickleCellFoundationMN #GeneTherapy #HealthDisparities

]]>In this episode of Patient Innovations, we explore the complexities of Sickle Cell Disease (SCD) through the lens of personal experience, medical expertise, and community advocacy. Our guests include Dennik McBride, a courageous sickle cell warrior, who shares her personal journey living with the condition. Dr. Ashish Gupta from the University of Minnesota,  Dr.Gupta largely cares for children and young adults with sickle cell disease who need transplant based therapies. In the episode he provides insight into the latest research and treatment advancements;This episode highlights that there are many challenges, including the implementation of standard guidelines, for adults with sickle cell disease. These include, but not limited to, access to primary and specialty care, transition of care as well as comprehensive sickle cell care. We also have Rae Blaylark, Executive Director of the Sickle Cell Foundation of MN, who highlights the importance of community support, advocacy, and resources for those affected by SCD. Together, they discuss the challenges patients face in navigating healthcare, the impact of SCD on marginalized communities, and the promising future of treatments like gene therapy and bone marrow transplants. 

For resources and support, The Sickle Cell Foundation can be accessed at  www.sicklecellmn.org . You can calso follow them @sicklecellmn on LinkedIn, FB, IG and Twitter (X).

#SickleCellAwareness #HealthcareEquity #PatientAdvocacy #PatientInnovationsPodcast #SickleCellFoundationMN #GeneTherapy #HealthDisparities

]]>de8deb85-6466-43e9-8232-dd89ffafa57fTue, 15 Oct 2024 10:30:00 -050054:17falsefull2552This Podcast Journey so FarThis Podcast Journey so FarIn this special episode of Patient Innovations, we're flipping the script! Our hosts, Rashmi Kandwal and Mary MacCarthy, step into the guest spotlight as our production engineer, Sam Devine, takes on the role of interviewer.

Join us as we delve into the motivations and challenges behind launching the Patient Innovations podcast. Rashmi and Mary share personal stories, discuss the highs and lows of their podcasting journey, and offer a behind-the-scenes look at what it takes to bring healthcare innovation stories to life.

Whether you're a longtime listener or new to our show, this episode provides an intimate glimpse into the passion and dedication driving Patient Innovations. Tune in to learn more about the dynamic duo at the heart of the podcast and their vision for the future.

Key Topics:

  • The inspiration behind starting Patient Innovations
  • Personal and professional challenges faced by the hosts
  • Memorable moments and lessons learned from past episodes
  • Future aspirations and upcoming topics for the podcast

Guests:

  • Rashmi Kandwal, Co-Host
  • Mary MacCarthy, Co-Host
  • Sam Devine, Production Engineer (Interviewer)

]]>In this special episode of Patient Innovations, we're flipping the script! Our hosts, Rashmi Kandwal and Mary MacCarthy, step into the guest spotlight as our production engineer, Sam Devine, takes on the role of interviewer.

Join us as we delve into the motivations and challenges behind launching the Patient Innovations podcast. Rashmi and Mary share personal stories, discuss the highs and lows of their podcasting journey, and offer a behind-the-scenes look at what it takes to bring healthcare innovation stories to life.

Whether you're a longtime listener or new to our show, this episode provides an intimate glimpse into the passion and dedication driving Patient Innovations. Tune in to learn more about the dynamic duo at the heart of the podcast and their vision for the future.

Key Topics:

  • The inspiration behind starting Patient Innovations
  • Personal and professional challenges faced by the hosts
  • Memorable moments and lessons learned from past episodes
  • Future aspirations and upcoming topics for the podcast

Guests:

  • Rashmi Kandwal, Co-Host
  • Mary MacCarthy, Co-Host
  • Sam Devine, Production Engineer (Interviewer)

]]>b84edb05-4bc1-4c81-ae3c-9255a61fb87eTue, 06 Aug 2024 10:00:00 -050020:34falsefull1441Addiction and Substance AbuseAddiction and Substance AbuseIn this episode, hosts Rashmi and Mary dive deep into the critical issues of addiction and substance abuse, exploring various aspects of mental health. They are joined by three distinguished guests:

Duffy Fallon

A person in recovery, Duffy shares his personal journey and insights into how his experiences have shaped his work in the mental health field.

Sue Abderholden

The Executive Director of NAMI Minnesota , Sue brings her extensive expertise and advocacy experience to discuss the broader impact of mental health issues on communities and the importance of support systems.  NAMI MN offers both online and in-person support groups for adults living with Mental health and their families.

Dr. Jungjin Kim

Mental Health and Addiction Service Line Chief at the   University of Minnesota Medical School , Dr. Kim provides a clinical perspective on addiction, discussing treatment options, research advancements, and the challenges faced by healthcare providers.

]]>In this episode, hosts Rashmi and Mary dive deep into the critical issues of addiction and substance abuse, exploring various aspects of mental health. They are joined by three distinguished guests:

Duffy Fallon

A person in recovery, Duffy shares his personal journey and insights into how his experiences have shaped his work in the mental health field.

Sue Abderholden

The Executive Director of NAMI Minnesota , Sue brings her extensive expertise and advocacy experience to discuss the broader impact of mental health issues on communities and the importance of support systems.  NAMI MN offers both online and in-person support groups for adults living with Mental health and their families.

Dr. Jungjin Kim

Mental Health and Addiction Service Line Chief at the   University of Minnesota Medical School , Dr. Kim provides a clinical perspective on addiction, discussing treatment options, research advancements, and the challenges faced by healthcare providers.

]]>bad7ab55-905a-467e-8941-cb43d4842c45Fri, 31 May 2024 06:00:00 -050050:12falsefull1331Alzheimer's DiseaseAlzheimer's DiseaseIn April 2024 Mary MacCarthy and Rashmi Kandwal focused on learning about care and innovation in Alzheimer's Disease. They talked with Kanada Yazbek who has been living with dementia for many years, Susan Perriott who is the CEO of the Alzheimer's Association of Minnesota and North Dakota and Dr. Joseph Gaugler, Director of the University of Minnesota's Center for Healthy Aging and Innovation, School of Public Health. 

To contact Kanada or the Alzheimer's Association of Minnesota or North Dakota, email mnnd-info@alz.org. Call them anytime day or night at 800-272-3900 for help and to get connected to many resources.

To contact Dr. Joseph Gaugler and team, email fltz@umn.edu.

To access the Minnesota Senior Linkage Line, go to https://mn.gov/senior-linkage-line/

To register for the free Caring for people with Memory Loss conference at the University of Minnesota on June 1, 2024: https://www.sph.umn.edu/events-calendar/caring-for-person-with-memory-loss-conference/

#alzheimers #medicalalley #healthcaremn #memoryloss

]]>In April 2024 Mary MacCarthy and Rashmi Kandwal focused on learning about care and innovation in Alzheimer's Disease. They talked with Kanada Yazbek who has been living with dementia for many years, Susan Perriott who is the CEO of the Alzheimer's Association of Minnesota and North Dakota and Dr. Joseph Gaugler, Director of the University of Minnesota's Center for Healthy Aging and Innovation, School of Public Health. 

To contact Kanada or the Alzheimer's Association of Minnesota or North Dakota, email mnnd-info@alz.org. Call them anytime day or night at 800-272-3900 for help and to get connected to many resources.

To contact Dr. Joseph Gaugler and team, email fltz@umn.edu.

To access the Minnesota Senior Linkage Line, go to https://mn.gov/senior-linkage-line/

To register for the free Caring for people with Memory Loss conference at the University of Minnesota on June 1, 2024: https://www.sph.umn.edu/events-calendar/caring-for-person-with-memory-loss-conference/

#alzheimers #medicalalley #healthcaremn #memoryloss

]]>7e0c73b6-6d96-40fa-85b1-b48eb7a7da17Thu, 02 May 2024 06:00:00 -050059:28falsefull1221Colorectal CancerColorectal CancerDive into a discussion on Colorectal Cancer, the 3rd most common cancer in the US and worldwide.

In this episode of Patient Innovations, Rashmi and Mary speak with three remarkable guests:

  • Meghan Wallace: A recent survivor, Meghan shares her journey from diagnosis to treatment and being cancer-free.
  • Dr. Subree Subramanian: Professor in the Department of Surgery at the University of Minnesota and co-founder/CSO at EV Therapeutics Inc. Dr. Subramanian discusses cutting-edge immunotherapies to boost the patient’s own immune system.
  • Dr. Ajay Prakash: An award-winning medical oncologist trained at NYU. Dr. Prakash sheds light on existing therapeutic pathways, patient experiences, and the future of colorectal cancer research.

Tune in to explore the latest innovations and research in colorectal cancer treatment.

#colorectal cancer #healthcareMN #cancerdrugs #patientjourney #Immunotherapy #innovations #UniversityofMN #early screening #devinefoxproductions

]]>Dive into a discussion on Colorectal Cancer, the 3rd most common cancer in the US and worldwide.

In this episode of Patient Innovations, Rashmi and Mary speak with three remarkable guests:

  • Meghan Wallace: A recent survivor, Meghan shares her journey from diagnosis to treatment and being cancer-free.
  • Dr. Subree Subramanian: Professor in the Department of Surgery at the University of Minnesota and co-founder/CSO at EV Therapeutics Inc. Dr. Subramanian discusses cutting-edge immunotherapies to boost the patient’s own immune system.
  • Dr. Ajay Prakash: An award-winning medical oncologist trained at NYU. Dr. Prakash sheds light on existing therapeutic pathways, patient experiences, and the future of colorectal cancer research.

Tune in to explore the latest innovations and research in colorectal cancer treatment.

#colorectal cancer #healthcareMN #cancerdrugs #patientjourney #Immunotherapy #innovations #UniversityofMN #early screening #devinefoxproductions

]]>3e1cf016-3223-43c3-ae91-7646aee9a71eFri, 12 Apr 2024 06:00:00 -050042:39falsefull1111TrailerTrailerPatient Innovations Trailer.

]]>Patient Innovations Trailer.

]]>8434e5d0-b6a1-4194-95da-c7cc5fc39a61Fri, 29 Mar 2024 06:00:00 -050006:13falsetrailer