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Our Team

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Our Team

Who we are

Parents of Hemi Heroes,
united in purpose.

A dedicated team of parents supporting hemispherectomy children and their families across Australia.

Kelly Wilton

President

Kelly is mum to Mikey, who underwent a left hemispherectomy in 2017 for HHE Syndrome. Her lived experience and professional advocacy work drive her passion for leading the Foundation with empathy and purpose.

Kelly Wilton

President

Kelly serves as President of the Hemispherectomy Foundation Australia and brings both lived experience and strong advocacy skills to her role.

She is the mother of Mikey, who underwent a left hemispherectomy in 2017 to treat seizures caused by HHE Syndrome (Hemiconvulsion–Hemiplegia–Epilepsy Syndrome). Walking alongside her son through this journey has given Kelly a deep appreciation of the strength, resilience, and support families need when facing life-changing surgery.

Her professional background at Source Co. has equipped her with valuable expertise in community engagement, advocacy, and supporting families through complex challenges.

Kelly is passionate about ensuring that no family feels alone in their hemispherectomy journey and is committed to building a strong, connected community across Australia. Through her leadership, Kelly works to raise awareness, provide practical support, and amplify the voices of families, driving the Foundation’s mission of hope, resilience, and connection.

Phone:‭+61 455 580 475‬
Email:kelly@hemispherectomyaustralia.org.au

Carolyn Pinto

Secretary

Carolyn is mum to Freya who had a right hemispherectomy in 2010 for Rasmussen's Encephalitis. With her background in health and disability policy and research in both government and at the Murdoch Children's Research Institute, she brings both insight and expertise to the Foundation.

Carolyn Pinto

Secretary

Carolyn brings both personal insight and professional expertise to her role as Secretary of the Hemispherectomy Foundation Australia.

She is the mother of a young adult daughter who underwent a right hemispherectomy in 2010 as a result of Rasmussen's Encephalitis, giving her a deep understanding of the challenges and resilience involved in this journey.

With a long career in government health and human services—spanning policy, program design, implementation, and management—Carolyn has dedicated her professional life to improving systems of care and support. She is now a Research Associate at the Murdoch Children’s Research Institute (MCRI), where she contributes to advancing knowledge and outcomes in children’s health.

Her combined experience as both a parent and a professional makes Carolyn a passionate advocate for families navigating hemispherectomy, ensuring their voices are heard and their needs are supported.

Phone:+61 403 431 360
Email:carolyn@hemispherectomyaustralia.org.au

Kylie Hockley

Treasurer

Kylie is a founding member and mum to Gemma, who underwent a left hemispherectomy in 2006 for Rasmussen’s Encephalitis. She works as a Medical Secretary in Sydney and brings both lived experience and organisational expertise.

Kylie Hockley

Treasurer

Kylie is a founding member of the Hemispherectomy Foundation Australia and serves as Treasurer, bringing a strong commitment to both the mission and community of the Foundation.

She is the mother of Gemma, who underwent a left hemispherectomy in 2006 at the age of seven due to Rasmussen’s Encephalitis. Kylie’s lived experience as a parent has given her valuable insight into the challenges families face and the importance of hope, support, and connection.

Professionally, Kylie works as a Medical Secretary in Sydney, where her skills in organisation and administration complement her role on the Board.

As a founding member, she has been instrumental in shaping the Foundation from its earliest days and continues to play a key role in ensuring its sustainability and growth. Her combination of dedication, personal perspective, and professional skills make Kylie an invaluable advocate for families navigating the hemispherectomy journey.

Email:kylie@hemispherectomyaustralia.org.au

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HFA supports children, young people and families impacted by hemispherectomy surgery.

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Registered Charity

HFA is a registered charity with the Australian Charities and Not-for-profits Commission (ACNC)

GET IN TOUCH

info@hemispherectomyfoundation.org.au
PO Box 6474 Rouse Hill NSW 2155
ABN 69370311647

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