June 12, 2025 // 11:30 AM (BST)
Giving voice: Breaking barriers for men with lymphedema
This MOH Talk aims to spotlight the often overlooked experiences of men living with lymphedema, focusing on the challenges they face in accessing appropriate compression solutions and having their needs acknowledged. The topic addresses an important gap in awareness: ensuring men not only receive the right compression therapy but also feel confident and supported in wearing it. By amplifying these voices, we hope to foster a more inclusive approach to care in the veno-lymphatic field.
Agenda
- Dr. Garry Cooper will present findings from a systematic review, survey and patient diaries, highlighting key insights and how healthcare professionals can improve communication and care delivery.
- Matt Hazledine, a participant in the study, will share his lived experience with lymphedema and reflect on what helped and what still needs to change from a patient’s point of view.
Speakers
Dr. Garry Cooper, UK (LinkedIn)
Clinical Nurse Specialist in lymphoedema
An award-winning Queen’s Nurse, recognised by the Queen’s Nursing Institute for his exceptional contributions to primary care. He holds a PhD focused on the lived experiences of men with non-cancer-related lymphedema, particularly in the areas of self-management, identity, and support needs.
His research emphasizes the value of active listening and reveals how clinicians can refine their language to better support patients insights drawn directly from interviews, surveys, and patient diaries. Dr. Cooper brings a compassionate, evidence-based perspective to improving care for a population often overlooked in traditional lymphedema services.
Matt Hazledine, UK (LinkedIn)
Author and founder of Lymphoedema United
Matt was diagnosed with lymphedema in 2011 after getting a severe bout of cellulitis that hospitalised him for 2 weeks. Since then, he has tried everything to reduce his swollen leg, including two types of surgery.
In 2021, Matt decided to share his experiences and tips to help others with this lifelong condition, by writing a book, joined by over 20 experts ‘How to Live Better with Lymphoedema – Meet the Experts’ and creating Lymphoedema United, a patient-based website with everything you’d need to know and who to know to get trusted information and guidance.
Moderator
Katy Stevens, UK (LinkedIn)
Clinical Advisor at SIGVARIS GROUP Britain