Episodes

  • The Complex Medical Mama: Caregiving, Advocacy, and Seeing Healthcare Through a Different Lens

    The Complex Medical Mama: Caregiving, Advocacy, and Seeing Healthcare Through a Different Lens
    Oct 16 2026

    What changes when a patient advocate becomes the mother of a critically ill child? Julie Croner joins Ursula Mann and co-host Anne-Marie Hayes to share her experiences with psoriatic arthritis, avascular necrosis, complex regional pain syndrome, and melanoma—and how her youngest daughter’s six-month hospitalization gave her a different understanding of caregiving.

    Julie reflects on the patient communities that helped her find a path forward, the emotional impact of illness on the whole family, and her work at Health Union helping others turn lived experience into meaningful advocacy.

    Highlights With Timestamps

    • 00:33 — Meet Julie Croner: Patient leader, mother of four, and the “complex medical mama.”
    • 04:40 — Childhood symptoms and the search for answers: Repeated knee surgeries and the difficulty of accepting psoriatic arthritis at a young age.
    • 07:19 — Facing avascular necrosis: A devastating diagnosis and uncertainty about her mobility and future.
    • 08:43 — Finding the patient community: How online connections offered support and helped Julie discover information about treatment options.
    • 11:57 — Becoming an active partner in care: Tracking symptoms, identifying patterns, and sharing her findings with doctors.
    • 12:56 — The mental health impact of chronic illness: Depression, panic attacks, and asking for professional support.
    • 14:45 — Melanoma and rediscovering herself: An early skin cancer diagnosis, an unexpected singing performance, and the beginnings of her blog.
    • 18:30 — Becoming a complex medical mama: Pregnancy uncertainty and her youngest daughter’s early feeding difficulties.
    • 21:19 — A medical emergency at five weeks old: Influenza B, pneumonia, and complications that led to two months on a ventilator and six months in hospital.
    • 23:34 — Illness affects the whole family: A new understanding of her parents’ caregiving experience and supporting Ellie’s siblings through trauma.
    • 25:46 — “It’s just a bad day, not a bad life”: Finding moments of hope during difficult seasons.
    • 26:45 — Turning lived experience into a career: Julie’s transition from IT consulting to patient community leadership.
    • 29:05 — Recognizing the value of patient expertise: Fair compensation, collective knowledge, and why advocates should not undervalue their contributions.
    • 30:28 — Building confidence as a patient leader: A certification resource for responsible storytelling and advocacy.
    • 32:21 — Finding joy in family life: Togetherness, new experiences, and a shared love of Disney.

    Links and Resources

    • Julie’s blog: It’s Just a Bad Day, Not a Bad Life — Her personal story and advocacy journey. itsjustabadday.com
    • Social Health Network — A community for patients, caregivers, and healthcare professionals. socialhealthnetwork.com
    • Patient Leader Certification Program — Free training to strengthen storytelling, credibility, and advocacy skills. socialhealthnetwork.com
    • Patient Voice Partners — Learn more about Amplify and opportunities to share your patient or caregiver experience.

    Disclaimer:

    The views and opinions expressed by guests on Amplify are their own and do not necessarily reflect those of the podcast, its hosts, Patient Voice Partners, or its affiliates.

    Medical Disclaimer:

    The content shared on Amplify is for informational and educational purposes only.

    Nothing discussed on this podcast—including stories, experiences, perspectives, or commentary from hosts, guests, or contributors—should be interpreted as medical advice, diagnosis, or treatment recommendations.

    Always seek the guidance of your physician or other licensed provider with any questions regarding your health, medical conditions, or treatment options.
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    35 mins
  • Beyond Asking the Doctor: Bringing the Patient Voice Into Clinical Research

    Beyond Asking the Doctor: Bringing the Patient Voice Into Clinical Research
    Oct 9 2026
    40 mins
  • When Lived Experience Becomes a Calling: Building Advocacy Around IBD and Better Care

    When Lived Experience Becomes a Calling: Building Advocacy Around IBD and Better Care
    Oct 2 2026

    What does it take to turn lived experience into lasting change for patients? Gail Attara joins Ursula Mann and Anne-Marie Hayes to share how growing up with a mother living with Crohn’s disease shaped her commitment to advocacy. Together, they explore the impact of inflammatory bowel disease beyond the gut, the importance of medication coverage, and the work behind patient organizations. Gail also offers candid insights into funding, accountability, and what meaningful collaboration requires to build better, more individualized care.

    Episode Highlights

    • 02:25 — Why healthcare cannot be one size fits all: Gail’s red-stiletto analogy illustrates why policies must reflect different patient needs.
    • 03:22 — Three decades of advocacy: Gail introduces the two organizations she leads and explains the origins of the Gastrointestinal Society.
    • 04:19 — When lived experience becomes a calling: Her mother’s experience with Crohn’s disease—and the blame she faced—helped shape Gail’s advocacy.
    • 08:01 — New hope in IBD treatment: Moving beyond symptom management toward therapies that can change the course of disease.
    • 09:00 — Trusted education and medical collaboration: How gastroenterologists help review patient resources and support advocacy.
    • 10:20 — IBD beyond the gut: Exploring mental health, the gut–brain connection, and the broader burden of chronic illness.
    • 11:48 — Medication approval versus coverage: Why an available treatment may still be out of reach for the person who needs it.
    • 12:18 — Why patient organizations matter: Helping people navigate healthcare, access reliable information, and evaluate an organization’s credibility.
    • 19:11 — Ethics and independence: Gail discusses fundraising boundaries and her organizations’ approach to product endorsements.
    • 22:53 — Making patient voices part of drug reviews: Gail reflects on advocating for patient-group submissions to the Common Drug Review.
    • 25:41 — Care that recognizes individual needs: Why treatment coverage must account for differences between patients.
    • 28:05 — Behind the scenes of collaboration: Funding pressures, unequal workloads, and fair compensation.
    • 31:09 — Supporting patients in everyday life: Employer education and free resources bring digestive-health information into workplaces and communities.
    • 36:57 — Advocacy in action: Helping connect a patient needing an intestinal transplant with political support.
    • 39:47 — What authentic collaboration requires: Respect, addressing harmful behaviour, and returning to a shared mission.

    Links and Resources

    • Connect with Gail Attara on LinkedIn
    • Gastrointestinal Society and Canadian Society of Intestinal Research
    • GI Society Programs and Services
    • Patient Voice Partners — Learn More or Join Patient Voice Connect

    About Gail Attara

    Gail Attara is Chief Executive Officer and Co-Founder of the Gastrointestinal Society and President of the Canadian Society of Intestinal Research. With three decades of leadership in patient advocacy, she champions trusted digestive-health education, patient involvement in healthcare decisions, and better access to appropriate treatment. Her family’s experience with chronic illness helped shape her commitment to keeping patients at the centre of care.

    Disclaimer:

    The views and opinions expressed by guests on Amplify are their own and do not necessarily reflect those of the podcast, its hosts, Patient Voice Partners, or its affiliates.

    Medical Disclaimer:

    The content shared on Amplify is for informational and educational purposes only.

    Nothing discussed on this podcast—including stories, experiences, perspectives, or commentary from hosts, guests, or contributors—should be interpreted as medical advice, diagnosis, or treatment recommendations.

    Always seek the guidance of your physician or other licensed provider with any questions regarding your health, medical conditions, or treatment options.
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    45 mins
  • When Pregnancy Suddenly Becomes Life-Threatening: Bonnie’s Story of HELLP Syndrome

    When Pregnancy Suddenly Becomes Life-Threatening: Bonnie’s Story of HELLP Syndrome
    Sep 25 2026
    Pregnancy complications can affect a woman’s health long after delivery—but those connections are not always recognized.In this episode of Amplify, Ursula Mann and Anne-Marie Hayes speak with Bonnie about her experience with HELLP syndrome, a rare and potentially life-threatening pregnancy complication involving the blood and liver. At 36 weeks pregnant, Bonnie developed high blood pressure, a severe headache, and vomiting, leading to an urgent induction and the early delivery of her first child.At the time, Bonnie believed that delivering her baby marked the end of the danger. Years later, however, she experienced a major cardiac event and was diagnosed with atrial flutter. Despite her continuing symptoms, traditional cardiac tests and risk assessments repeatedly classified her as low risk.Bonnie shares how she eventually learned about the connection between hypertensive disorders of pregnancy and an increased risk of cardiovascular problems later in life. She discusses the relief of finally having her experience validated, the importance of including pregnancy history in cardiovascular assessments, and the difficulties patients face when their symptoms do not fit established clinical models.Through her advocacy and collaboration with healthcare researchers, Bonnie is helping bring the patient perspective into medical education, research, and conversations about women’s heart health. She also offers practical advice for communicating with healthcare professionals, preparing for medical appointments, and remaining “stable but alert” when managing long-term health risks.Episode Highlights with Timestamps09:49 – Understanding HELLP syndromeUrsula explains what HELLP stands for, its relationship to preeclampsia, and why it can become a medical emergency for both mother and baby.12:39 – When Bonnie realized something was wrongBonnie describes feeling unusually tired, heavy, and unwell before her 36-week prenatal appointment.14:21 – An urgent and unexpected deliveryAfter developing a severe headache and vomiting, Bonnie was admitted to the hospital and induced before she had even packed a hospital bag or attended prenatal classes.17:25 – Navigating subsequent pregnanciesBonnie discusses the closer monitoring she received during her second and third pregnancies, as well as complications that were not initially connected to her history of HELLP syndrome.20:40 – Why delivery may not be the end of the storyBonnie explains what she later learned about the potential long-term effects of hypertensive pregnancy disorders on cardiovascular health.23:26 – The missing question in cardiovascular careBonnie shares why healthcare professionals should ask women presenting with cardiovascular symptoms about their pregnancy history.27:18 – Bringing the patient voice into cardiology educationBonnie reflects on participating in cardiology rounds and helping medical professionals understand how standard risk assessments can overlook pregnancy-related risk factors.30:15 – Becoming “stable but alert”Bonnie explains how she manages her health through regular medical follow-ups, blood-pressure monitoring, medication adherence, and awareness of changes in her body.37:49 – A message for expectant mothersHer practical advice is simple but important: attend every prenatal appointment, complete recommended blood work, and do not delay seeking care when something feels wrong.38:14 – Giving women permission to care for themselvesBonnie encourages families and loved ones to help mothers make space for rest, movement, stress management, and their own healthcare needs.40:30 – Practical tools for patient self-advocacyFrom writing down symptoms to carrying a card with essential medical information, Bonnie shares ways patients can communicate more clearly during stressful medical appointments.49:23 – A major cardiac event years laterBonnie recounts waking with an unusual sensation in her chest, initially dismissing it, and eventually learning in the emergency department that she was experiencing atrial flutter.51:19 – When the tests say everything is fine—but the patient is notDespite experiencing a serious cardiac event, Bonnie’s traditional assessments continued to categorize her as low risk, leaving her frightened and searching for answers.53:41 – Finally finding the missing connectionBonnie describes the relief of meeting a physician who recognized that her cardiac problems could be connected to her pregnancy complications years earlier.55:34 – Why reassurance is not always enoughBonnie explains the fear and uncertainty patients experience when standard tests are normal but severe symptoms continue—and why clear communication about what to do next matters.Disclaimer: The views and opinions expressed by guests on Amplify are their own and do not necessarily reflect those of the podcast, its hosts, Patient Voice Partners, or its affiliates.Medical Disclaimer:The content shared on Amplify is ...
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    41 mins
  • 20 Years in the Fight: Kathy Barnard on Melanoma, Advocacy, and Innovation

    20 Years in the Fight: Kathy Barnard on Melanoma, Advocacy, and Innovation
    Sep 11 2026

    Episode Summary

    When Kathleen “Kathy” Barnard noticed two small spots on her arm, she had no idea they would lead to a diagnosis of metastatic malignant melanoma—and a prognosis of just three to six months.

    In this episode of Amplify, Kathy shares the extraordinary story of how persistence, family advocacy, compassionate-access treatment, and emerging immuno-oncology gave her another chance at life. She also speaks candidly about the gaps she encountered throughout her journey, from an initially dismissed concern and missing medical records to financial barriers and unequal access to treatment.

    Those experiences became the foundation for the Save Your Skin Foundation, a patient-led organization that has spent 20 years supporting people affected by melanoma and other skin cancers while advocating for prevention, research, clinical trials, innovative treatments, and more equitable cancer care across Canada.

    Kathy’s story is a powerful reminder that lived experience can expose weaknesses in healthcare—and become a driving force for meaningful change.

    Episode Highlights

    • Episode Highlights
      • 00:33 — Why melanoma deserves greater attention
      • 02:44 — The early signs that started Kathy’s journey
      • 04:44 — Receiving a metastatic malignant melanoma diagnosis
      • 08:04 — How healthcare gaps revealed the need for patient advocacy
      • 09:30 — Treatment, difficult side effects, and the team that inspired her
      • 11:21 — Learning the cancer had spread and facing a three-to-six-month prognosis
      • 12:19 — How Kathy’s son helped find another treatment option
      • 14:13 — The remarkable response to an innovative treatment
      • 17:02 — Kathy’s advice for patients and families facing cancer
      • 19:50 — The beginnings of the Save Your Skin Foundation
      • 20:48 — Immuno-oncology and the fight for treatment access
      • 23:39 — How patients can become advocates for themselves and others
      • 26:58 — Prevention, collaboration, and the All.Can initiative
      • 33:29 — Why cancer research and treatment access must be equitable across Canada
      • 36:19 — Life beyond cancer: pickleball, travel, and connecting with patients

    Links and Resources

    • Save Your Skin Foundation — Patient support, education, prevention, advocacy, and resources for melanoma, non-melanoma skin cancers, and ocular melanoma
    • All.Can International — A global initiative working toward sustainable, efficient, and patient-centred cancer care
    • Melanoma Canada — Information and support services for people affected by melanoma and skin cancer
    • Canadian Cancer Society: Melanoma — Information about melanoma, risk factors, signs, diagnosis, and treatment
    • Government of Canada: Skin Cancer — Skin cancer information and prevention guidance

    Disclaimer: The views and opinions expressed by guests on Amplify are their own and do not necessarily reflect those of the podcast, its hosts, Patient Voice Partners, or its affiliates.

    Medical Disclaimer: The content shared on Amplify is for informational and educational purposes only.

    Nothing discussed on this podcast—including stories, experiences, perspectives, or commentary from hosts, guests, or contributors—should be interpreted as medical advice, diagnosis, or treatment recommendations.

    Always seek the guidance of your physician or other licensed provider with any questions regarding your health, medical conditions, or treatment options.
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    40 mins
  • When Caring for Patients Comes at a Cost: The Complex Reality of Chronic Hand Eczema

    When Caring for Patients Comes at a Cost: The Complex Reality of Chronic Hand Eczema
    Jul 17 2026
    This episode is part of Amplify’s special three-part series on Chronic Hand Eczema, sponsored by LEO Pharma Canada. Across this series, we’ve explored Chronic Hand Eczema through three deeply connected perspectives: the lived experience of patients, the professional realities of healthcare workers, and the clinical understanding of a condition that is often underestimated. In the first episode, Amy Wright shared what it is like to live with Chronic Hand Eczema — how painful, visible symptoms can affect everyday routines, family life, confidence, and emotional well-being. Her story reminded us that behind every diagnosis is a person navigating moments that others may not always see. In the second episode, Marley Gregorio brought forward the healthcare worker perspective, highlighting how Chronic Hand Eczema can affect nurses and care providers whose hands are central to their work. From repeated handwashing and glove use to the emotional burden of struggling with symptoms while caring for others, her episode showed how this condition can become a serious workplace and quality-of-life issue. In this final episode of the series, Dr. George Christodoulou joins the conversation to connect these experiences to the broader clinical picture. He discusses why Chronic Hand Eczema can be difficult to manage, why early recognition matters, and how the condition can create barriers not only for patients, but also for healthcare professionals who are expected to continue caring for others while managing their own pain and discomfort. Chronic Hand Eczema is often dismissed as “just a skin condition,” but for many people, it can be painful, persistent, visible, and life-altering. It can affect work, relationships, sleep, mental well-being, social participation, and a person’s ability to feel comfortable in their own skin. Together, these three episodes highlight the complex reality of Chronic Hand Eczema: it is a patient experience, a healthcare worker issue, a clinical challenge, and an important conversation about awareness, support, and quality of life. This final episode brings the series together by asking us to look more closely at the impact of Chronic Hand Eczema — especially when caring for patients comes at a cost. In This Episode, We Discuss: Why Chronic Hand Eczema can be difficult to manage How symptoms can affect daily life, work, and emotional well-being The added burden for healthcare workers who rely on their hands every day Why early recognition and proper support are important How Chronic Hand Eczema can become a barrier to both receiving and providing care The importance of listening to patient and healthcare worker experiences Why greater awareness is needed to improve understanding and support Episode Highlights 00:03:20 — Why Chronic Hand Eczema is complex to diagnose Dr. George Christodoulou explains why Chronic Hand Eczema can be difficult to identify, with different causes, triggers, and contributing factors. 00:06:28 — Common symptoms patients experienceThe conversation covers symptoms such as itching, pain, cracking, dryness, flaking, and how these can affect quality of life. 00:09:06 — When everyday actions become painfulDr. Christodoulou shares how cracked and irritated hands can make simple moments — like washing hands, holding food, or shaking someone’s hand — uncomfortable or painful. 00:10:52 — Why treatment is not always simpleThe episode explores why Chronic Hand Eczema often requires more than one approach, including managing inflammation, repairing the skin barrier, and addressing triggers. 00:14:30 — The impact on work and daily lifeDr. Christodoulou discusses how Chronic Hand Eczema can affect a person’s ability to work, especially in jobs that involve frequent handwashing, irritants, or manual labor. 00:20:00 — Access to treatment across CanadaUrsula outlines how drug approval and reimbursement pathways can influence whether patients are able to access treatment options. 00:24:53 — How coverage can shape care Dr. Christodoulou shares how insurance and affordability can affect which treatment options are available to patients. 00:29:30 — The long-term burden of chronic diseaseThe conversation looks at how living with a chronic condition over time can affect work, relationships, mental health, and overall life opportunities. Dr. George Christodoulou is a board-certified dermatologist by the Royal College of Physicians and Surgeons of Canada and the American Board of Dermatology. He obtained his MD and completed his 5-year dermatology residency at McGill University, and then he went on to complete a Mini-MBA in Physician Business Leadership from the Schulich School of Business at York University. Dr. Christodoulou is fluent in English, French, and Greek. He practices general medical and surgical dermatology with an additional interest in cosmetic dermatology and clinical research. He primarily focuses inflammatory ...
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    35 mins
  • More Than Skin Deep: The Unseen Impact of Chronic Hand Eczema on Nurses at Work

    More Than Skin Deep: The Unseen Impact of Chronic Hand Eczema on Nurses at Work
    Jul 3 2026

    Sponsor Acknowledgment

    This episode is sponsored by LEO Pharma. LEO Pharma is a global research-based pharmaceutical company dedicated to advancing the standard of care for people living with skin conditions, their families, and society. Sponsorship helps support the Amplify podcast, but the conversation, perspectives, and final content are produced independently by Patient Voice Partners and its guests. We thank LEO Pharma for supporting conversations that elevate patient experiences and increase awareness of chronic skin conditions.

    Episode Summary

    Living with Chronic Hand Eczema is about far more than dry or irritated skin. For many people, it affects their work, sleep, confidence, relationships, and overall quality of life.

    In this episode of Amplify, hosts Ursula Mann and Anne Marie speak with Marley Gregorio, critical care nurse, nursing researcher, and Vice President of the Canadian Association of Critical Care Nurses (CACCN), about the often-overlooked realities of Chronic Hand Eczema among healthcare professionals.

    Marley shares insights from national nursing research highlighting the significant burden Chronic Hand Eczema places on healthcare workers. The conversation explores the physical pain of repeated hand washing, the emotional toll of stigma and embarrassment, barriers to diagnosis and treatment, and the difficult decisions some nurses face when symptoms impact their ability to work.

    The discussion also highlights the importance of empathy, awareness, and understanding different lived experiences. Many people living with Chronic Hand Eczema feel isolated, but as Marley reminds us, they are not alone. Through advocacy, education, and continued research, there is hope for better recognition, better support, and better outcomes.

    In this episode, you'll learn:

    • Why healthcare workers face a higher risk of Chronic Hand Eczema
    • The hidden impact of Chronic Hand Eczema on daily life, mental health, and self-confidence
    • How stigma and assumptions can affect people living with visible skin conditions
    • Why early diagnosis, education, and workplace support matter
    • The importance of listening to different perspectives and lived experiences
    • How advocacy and research are helping drive change across healthcare systems
    • Why hope, community, and awareness are essential for improving care

    If you or someone you know is living with Chronic Hand Eczema, this conversation is a reminder that support exists, your experiences matter, and you are not alone. This episode is sponsored by LEO Pharma.

    Links & Resources

    • Patient Voice Partners
    • Canadian Association of Neonatal Nurses (CANN)
    • LEO Pharma
    • CHE Nurses Report

    Marley Gregorio

    Marley is a critical care nurse who works in a large acute care and academic hospital in Southwestern Ontario. She also is the Vice President of the Canadian Association of Critical Care Nurses (CACCN) and a first year PhD student in Nursing at the University of Ottawa. She is passionate about education, research and advocacy within nursing.


    Medical Disclaimer:

    The content shared on Amplify is for informational and educational purposes only.

    Nothing discussed on this podcast—including stories, experiences, perspectives, or commentary from hosts, guests, or contributors—should be interpreted as medical advice, diagnosis, or treatment recommendations.

    Always seek the guidance of your physician or other licensed provider with any questions regarding your health, medical conditions, or treatment options.
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    33 mins
  • Chronic Hand Eczema: A Nurse’s Story of Pain, Work, and Family

    Chronic Hand Eczema: A Nurse’s Story of Pain, Work, and Family
    Jun 19 2026
    Sponsor Acknowledgment This episode is sponsored by LEO Pharma. LEO Pharma is a global research-based pharmaceutical company dedicated to advancing the standard of care for people living with skin conditions, their families, and society. Sponsorship helps support the Amplify podcast, but the conversation, perspectives, and final content are produced independently by Patient Voice Partners and its guests. We thank LEO Pharma for supporting conversations that elevate patient experiences and increase awareness of chronic skin conditions. Episode Summary What happens when the very hands you rely on for work, caregiving, and everyday life become a source of pain? In this episode of Amplify, Amy Wright shares her personal journey living with chronic hand eczema while working as a neonatal nurse practitioner and raising two young children. Amy opens up about the physical discomfort, emotional impact, workplace challenges, and advocacy efforts surrounding this often misunderstood condition. From delayed diagnosis and painful flare-ups to navigating triggers and advocating for safer workplace products, Amy offers an honest look at the realities of living with chronic hand eczema and why greater awareness, prevention, and support are urgently needed. Episode Highlights 03:23 – Amy shares when she first noticed something was wrong and how her symptoms began during an international trip. 05:13 – How the pandemic dramatically worsened her condition through constant handwashing and disinfectant exposure. 08:34 – The long road to diagnosis and the frustration of limited treatment options. 10:22 – What Amy learned from patient communities that she didn't learn in the healthcare system. 14:28 – The physical symptoms of chronic hand eczema—and why it's much more than "just dry skin." 16:20 – The emotional impact of visible skin conditions, including embarrassment, stigma, and everyday interactions. 17:37 – A mother's perspective: when chronic hand eczema affects the simple act of touching your children. 20:22 – How everyday products, from soap to shampoo, can become unexpected challenges. 24:15 – The reality of managing chronic hand eczema while raising young children. 28:25 – What coworkers, employers, and healthcare organizations can do to better support those living with the condition. 31:24 – Amy discusses advocacy efforts aimed at improving workplace safety and awareness. 35:29 – The hidden economic burden of chronic hand eczema on individuals and healthcare systems. 38:40 – Amy shares what she's most looking forward to outside of work and advocacy. Links & Resources Patient Voice Partners https://patientvoicepartners.com/ LEO Pharma https://www.leo-pharma.ca/en-caCanadian Association of Neonatal Nurses (CANN) https://cann.ca/ CHE Nurses' Report https://caccn.ca/wp-content/uploads/2025/05/2025-04-Final-SDEL2406_CHE-Nurses-Survey-Whitepaper_612x792_EN_S04.pdfDr. Amy Wright, RN, PhD, NP-Pediatrics, NCC-BC, is a distinguished leader in neonatal nursing and an acclaimed researcher dedicated to advancing health equity and cultural safety. As an Assistant Professor at the Lawrence Bloomberg Faculty of Nursing, University of Toronto, she bridges the gap between high-level academia and frontline clinical excellence. Dr. Wright’s program of research, funded by the CIHR and SSHRC, focuses on the experiences and needs of Indigenous parents with young children. Her work is deeply rooted in community-engaged approaches, advocating for Trauma- and Violence-Informed Care (TVIC) and the elimination of structural barriers within the healthcare system. Clinically, she maintains an active practice as a Neonatal Nurse Practitioner in the NICU at McMaster Children’s Hospital, ensuring her research remains grounded in the realities of patient and family care. A tireless advocate for the profession, Dr. Wright serves as the President of the Canadian Association of Neonatal Nurses (CANN) . Her contributions have been recognized nationally, including being named one of the "150 Nurses for Canada" by the Canadian Nurses Association, solidifying her reputation as a pivotal voice in neonatal health and advocate for Indigenous cultural safety. Medical Disclaimer:The content shared on Amplify is for informational and educational purposes only.Nothing discussed on this podcast—including stories, experiences, perspectives, or commentary from hosts, guests, or contributors—should be interpreted as medical advice, diagnosis, or treatment recommendations.Always seek the guidance of your physician or other licensed provider with any questions regarding your health, medical conditions, or treatment options.
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    35 mins