In this special series, we sit down with Mandy Daly, the inspiring Founder of the Irish Neonatal Health Alliance, to delve into the realities of patient advocacy in 2024.

In the first part, Mandy shares her perspectives on the evolving challenges patient advocates face today. From financial constraints and travel demands to communication hurdles, we explore how these barriers shape their ability to influence decision-making and drive meaningful change.

Join us on this journey as we uncover the resilience, determination, and impact of patient advocates working tirelessly to improve healthcare outcomes for all.

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In the second part of our interview series with Mandy Daly, Founder of the Irish Neonatal Health Alliance, we dive into the personal side of advocacy. Mandy opens up about moments when her voice, as a patient or advocate, wasn’t heard or valued.

Through her experiences, we’ll explore what could have been done differently to foster inclusion and respect in decision-making processes. This conversation highlights the importance of meaningful engagement and the lessons we can all learn to amplify patient voices.

Join us as we uncover the realities, challenges, and opportunities for growth in patient advocacy.

You can always pause the videos, come back and watch again, or re-watch them at your convenience.

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In the third part of our interview series with Mandy Daly, Founder of the Irish Neonatal Health Alliance, we look ahead to the evolving role of patient advocates in a value-based healthcare system.

Mandy shares her vision for how future advocates can excel in this transformative landscape and discusses the critical support and training needed to empower them. From skill development to systemic change, this conversation highlights the steps required to build a stronger foundation for patient advocacy in the years to come.

You can always pause the videos, come back and watch again, or re-watch them at your convenience.

You can make the screen larger by clicking on the four small corners in a square box at the bottom right. To return to the main page, simply press Esc.

In the fourth part of our interview series with Mandy Daly, Founder of the Irish Neonatal Health Alliance, we delve into the essential elements that will shape the next generation of patient advocates.

Mandy shares her insights on thriving in a value-based healthcare system, highlighting the importance of equipping advocates with the right tools, training, and support to make a lasting impact.

This discussion sheds light on the pathways to success and the collaborative efforts needed to ensure patient advocates remain a vital force in driving healthcare innovation and inclusivity.

Join us as we envision a future where advocacy and value-based care go hand in hand.

You can always pause the videos, come back and watch again, or re-watch them at your convenience.

You can make the screen larger by clicking on the four small corners in a square box at the bottom right. To return to the main page, simply press Esc.

In the fifth part of our interview series with Mandy Daly, Founder of the Irish Neonatal Health Alliance, we focus on transforming patient engagement from symbolic gestures to meaningful collaboration.

Mandy discusses the critical steps needed to ensure that patients are not only heard but actively involved in shaping healthcare decisions. She also explores the key elements required to build genuine partnerships between patients and healthcare professionals, fostering trust, mutual respect, and shared decision-making.

Join us as we uncover what it takes to create a truly patient-focussed healthcare system.

You can always pause the videos, come back and watch again, or re-watch them at your convenience.

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In the final part of our interview series with Mandy Daly, Founder of the Irish Neonatal Health Alliance, we address one of the most pressing issues in healthcare today: ensuring equality in patient engagement.

Mandy shares her thoughts on how society can create opportunities for all patient groups—regardless of socio-economic background or disease type—to have their voices heard. She also sheds light on the challenges of achieving equal access to shared decision-making and how we can work together to overcome these barriers.

Join us as we close this inspiring series with a call to action for a more inclusive and equitable future in patient advocacy.

You can always pause the videos, come back and watch again, or re-watch them at your convenience.

You can make the screen larger by clicking on the four small corners in a square box at the bottom right. To return to the main page, simply press Esc.