I step into the role of Chair of the LE&RN New Zealand Chapter with a strong belief in the power of collaboration and the importance of shared voices in creating meaningful, lasting change. With a background in social work, my work as a health coach specializing in lymphatic health and wellbeing, and my own diagnosis of lymphoedema in 2012, this advocacy is both professional and deeply personal.
Since my diagnosis, I have been dedicated to raising awareness, sharing education, and fostering connection through online platforms and, more recently, my blog. This work has led to the formation of private support groups in New Zealand and internationally, creating a sense of community for individuals who previously felt isolated in their experiences.

While individual support is essential, significant systemic gaps remain. Limited awareness continues to contribute to delayed diagnoses, restricted access to comprehensive care, insufficient education and resources, and a lack of emotional support. As a result, many people living with lymphatic dysfunction face life-altering inequities, often compounded by misunderstanding, stigma, or discrimination.

This is why aligning with LE&RN is so meaningful. As a global organization with strong professional leadership and access to evidence-based education, research, and resources, LE&RN provides a powerful platform to amplify voices in New Zealand while connecting our community to an international movement for change.

Advocacy work requires persistence and patience and can often feel like steadily chipping away at a rock face. Yet through shared commitment and collective action, we can ensure that those affected by lymphatic disease are seen, heard, recognized, and valued.

As Chair of the New Zealand Chapter, I am committed to identifying systemic challenges, reducing barriers, and working collaboratively to build pathways toward solutions that truly reflect the needs of individuals living with lymphatic conditions.