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TSA’s Management Committee

TSA’s voluntary Management Committee help guide the organisation and focus its activities. Many of the members of the Committee have experience of living with TSC. If you would be interested in volunteering with TSA, please contact us.

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Debbie Crosby

Debbie and her husband Anthony have two beautiful daughters, Alana and Sophie. Alana was diagnosed with TSC at 7 months old and has autism, a developmental delay and epilepsy. Through TSA, Deb and Anthony have met many other families in the same situation as them. Deb decided to join the committee so she too could help other families.

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Michael Jones
Vice President

Michael has extensive business and not-for-profit experience gained with a number of different organisations, most recently Asthma Australia. Michael does not have a personal connection with TSC but was moved to make a difference for people living with the condition.

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Nova Young

Nova lives with a family member who has TSC and this has inspired her to want to make a positive contribution to the TSA Community. Nova has significant financial experience across many industries and is a Chartered Accountant and member of the Association of Corporate Treasurers.

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Alison McIvor

Alison has a personal connection to TSC through her family. Alison’s background includes the financial services and not-for-profit sectors, where she has worked for many years in a range of marketing, business development, management and operations-focused roles. She is happy to share her experience to benefit TSA.

Rob Rossano

Rob Rossano
Committee Member

Rob is a Senior Consultant with many years of experience in facilitation, training, coaching and managing organisational change. He has facilitated several major events and been a very successful fundraiser for TSA. Rob has two beautiful children, Roxie (who lives with TSC) and Teddie.

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Sze-Ann Woon
Committee Member

Sze-Ann lives in Perth, Western Australia and joined the Committee in 2022. She is an Infectious Diseases Physician and has a young son, Karamo, who was diagnosed with TSC at 3 months of age. As a parent and a doctor, Sze-Ann understands the difficulties of navigating the health system and would like to do more to advocate for children like hers with rare conditions.