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Meet Our Board of Directors

The EDFA Board of Directors is committed to supporting families and carers of people with an eating disorder. All current EDFA directors have lived experience as carers.

David Quilty

Acting Chair

David Quilty has experienced firsthand the struggle of supporting a child with an eating disorder. He is passionate about EDFA and the vital role it plays in the family and carer journey.

Jennifer Paterson

Deputy Chair

Jennifer Paterson is passionate about EDFA as a way to advocate for better services, promote evidence-based research for better treatment, and give families and carers a community to feel educated and empowered.

Jane Rowan

Executive Director

Jane is a senior communications, marketing and stakeholder engagement leader with over 20 years of management experience across various sectors including health.

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Fiona Mitchell

Director

Fiona Mitchell is a parent of a child living with a life-threatening chronic illness who was diagnosed with an eating disorder in her late teenage years.

Genevieve Pepin

Director

Professor Pepin is an experienced mental health occupational therapist and a proficient academic. Built on almost 20 years’ work in the area of mental health and eating disorders in Canada and in Australia and including partnerships with national and international leaders in the field, Prof Pepin has established herself as a significant contributor to eating disorders research.

Janis Carren

Director

Janis is an experienced executive with a demonstrated history of working in the entertainment, sports, and tourism industries. She brings extensive public sector and commercial experience from working in various Western Australian statutory authorities over a 30-plus year career.

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Nick Steele

Director

Nick Steele is an accomplished senior executive with over 23 years of experience in public health systems in both the United Kingdom and Australia. With a profound background in engaging and collaborating with health service executives, clinicians, and external providers, Nick excels in developing innovative funding models that promote service and system sustainability, ultimately leading to improved patient care.

Palmyra De Banks

Director

Palmyra De Banks is a distinguished General Practitioner with an extensive background spanning over two decades in the healthcare sector. She currently serves as the Clinical Director and Head of Performance at ForHealth Group, showcasing a remarkable commitment to advancing healthcare practices and elevating patient well-being.

Kathryn Hutchins

Director

Kathryn Hutchins has accrued over 20 years of business leadership experience, holding senior executive positions in Operations, People, and Culture within various industries. For the past decade, Kathryn has been dedicated to the early education sector, recognising the crucial role early education plays in the development of young children. Before this, she worked in a senior human resource position in the financial services industry.

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Kyra Bennett

Treasurer

Kyra Bennett is the Treasurer and Company Secretary of EDFA. She is a seasoned finance executive having worked in investment banking for more than 25 years. She is a mother of two and in her spare time enjoys holidays, family time, fitness and cycling. She strongly believes in the need for, and benefits that flow from, the EDFA model of carer support.

A message from the Chairman

A Message to all Parents and Carers

Carers and families play an instrumental role in supporting and caring for a loved one living with an Eating Disorder. A carer may be a parent, child, sibling, grandparent, partner, friend, neighbour, or other individual in the person’s life. Carers are an essential but often overlooked component
of the health care system and require support and assistance to effectively carry out their role.

The impact of an eating disorder is not only felt by the sufferer, it is also felt by a sufferers’ entire family and circle of support. The impact may lead to caregiver stress, loss of family income, disruption to family relationships and a high suicide risk for the sufferer. 

I have first-hand experience of the initial shock and trauma of caring for a loved one for an eating disorder. When my eldest daughter was diagnosed with Anorexia Nervosa a number of years’ ago, our family was desperate for information and support, and we found it very difficult to source.   

Our health system is very focused (as it should be) on supporting the health of a sufferer. However, there is also a real need in our community to support the carers. Carers are an integral part of the team required to support an eating disorder sufferer on their journey to recovery. EDFA plays a vital role in providing support and education to carers.

EDFA has an incredible group of volunteers who are making a real difference in the lives of many carers and their families. All of our peer support volunteers have lived experience. I am constantly amazed at how our volunteers and our members support and educate each other through their lived experience.   Our volunteers and members go the extra mile to make sure families and carers get the support they need and deserve because we know how frightening, confusing, distressing and exhausting caring for a loved one with an eating disorder is.

Carers’ needs and preferences for support vary, though may include information and knowledge, skills-based training, financial support, community-based support, co-ordination or case management services, advocacy training and services, assistance to overcome barriers to paid employment, and support for physical and psychological wellbeing.

Whilst we cannot cover all these needs, EDFA has three key programs to support carers: operating a national network of strive support groups for carers accessible to both city and regional communities; running carer eating disorder education sessions accessible to both city and regional communities; and through a training program on a treatment modality known as ‘temperament based training with supports (TBT-S)

The name strive stands for support, teach, reassure, inform, validate and empower. This very much represents what EDFA stands for. 

Finally, EDFA is a not for profit lived-experience volunteer supported organisation, where we fundraise to support the delivery of our programs. Without the generous financial support of our members and donors we would not be able to provide the support we do. On behalf of EDFA, I would like to thank our members and donors for their continuing support. 

David Garvey

Chairperson

Eating Disorders Families Australia

EDFA's Strategic Plan

EDFA’s 2024 – 2028 Strategic Plan – available for download here

EDFA's Constitution

EDFA’s Constitution – available for download here 

Annual Reports

2023 Annual Report – available for download here 
2022 Annual Report – available for download here