Professor Fiona Stanley AC
Fiona is a globally recognised epidemiologist who has spent most of her career in child and maternal health and birth disorders like. She established the Meningitis Centre in 1992 with the help of Bruce Langoulant. She is also a founding member of the Telethon Kids Institute and was named Australian of the Year in 2003.
Bruce Langoulant AM
Bruce is the Chairman of Meningitis Centre Australia and has been the head of the not for profit for almost a quarter of a century after he was asked to join by our Patron Professor Fiona Stanley. Bruce’s daughter Ashleigh contracted Pneumococcal Meningitis at the age of six months. 25 years later he and his family have successfully lobbied for the introduction of several meningitis vaccines on to the National Immunisation Plan including, and Pneumococcal.
Barry has spent a lifetime in media and communications and joined Meningitis Centre Australia 14 years ago in 2002 as CEO to help MCA achieve its goal of eliminating meningitis in Australia. In 2004 he played an important role in MCA's campaign to have the Australian Government add the pneumococcal vaccine to the National Immunisation Program.
Dr Anita Campbell
Dr Anita Campbell is an Infectious Diseases Specialist and the medical lead of the newly created Stan Perron Immunisation Service at Perth Children’s Hospital. She is also a mother to two young children, which provides a further level of insight when working with families.
Dr Campbell’s experience in paediatric health has been strengthened by varied experiences in both remote and metropolitan settings across three different states in Australia. She has maintained a strong commitment to ongoing medical education and in 2015 was selected to complete the Postgraduate Diploma of Paediatric Infectious Diseases with the University of Oxford.
Her aim is to continue to advocate for child health through education, immunisation, and research.
Jane King is the Head of Membership Development, at Artsource, the peak body for visual arts in Western Australia. She brings skills in financial management, governance, and private sector fundraising to Meningitis Centre Australia.
In 1991, Jane's son Andrew, contracted. Happily, Andrew survived but Jane’s quest, is to promote more awareness of all types of meningitis and the vaccines available.
Sarah knows firsthand about meningitis after her daughter Siobhan contracted Meningococcaldisease at the age of seven months whilst on a family holiday in Ireland. Siobhan underwent intensive therapy, survived the disease and is now studying to become a nurse. Sarah is passionate about educating more people about meningitis and making people more aware that people can die within 24 hours if they don’t get medical assistance.
Dr Catherine Gangell
The passion to improve health outcomes drove Catherine to pursue a successful career in Paediatric Respiratory disease research, before moving to a research governance role at a leading WA university. Her pursuit for the improvement of health in the community is a goal she wishes to achieve through Meningitis Centre Australia. Catherine brings her research background, governance knowledge and board expertise to the Centre.
Linda has worked for Meningitis Centre Australia for over 10 years as the Administration Manager. She brings her knowledge of administration and the day to day management of a not for profit agency, to the board.
Lisa is the Communications Manager of Meningitis Centre Australia. She has spent over 12 years in the media as a radio and TV journalist and a Government Media Adviser. She liaises with stakeholders and clients on a regular basis and also runs the communications and social media department of the charity.
Madeline Cross is a Business Development Manager in Wollongong NSW. She brings experience in advertising, marketing, sales and communications.
In June 2017, Madeline's youngest son Dean contracted Pneumococcal Meningitis and passed away within hours. Madeline's mission is to assist Meningitis Centre Australia to promote awareness of meningitis and to help educate about the importance of understanding the signs and symptoms of this deadly disease.
Desiree Scofield is a mother of two young children. Her eldest child Robbie contractedwhen he was just 5 and a half months old. He ended up losing all his limbs and has undergone multiple surgeries ever since. Desiree is a crusader who would like to get the ACWY and vaccines on to the National Immunisation Plan so that other parents don’t have to go through what she experienced with Robbie.
Iain Buchan is the father to Robbie and also little Luna and joins his partner Desiree in campaigning to protect the most vulnerable, young children, from the scourges of, by pushing for the ACWY and Men B vaccines to be put on the National Immunisation Plan. Iain also works in the banking industry and brings his financial experience to the not for profit organisation.