“You get left behind and lost in a complex world of rare care”: equity in access to rare disease care—learnings from the Australian Rare Disease Awareness, Education, Support, and... by Elizabeth Emma Palmer, Krista Recsei, Lauren McKnight, Natalie Roberts, Adam Jaffe, Gareth Baynam, Yvonne Zurynski, Michelle Farrar, Louise Healy, Nicole Millis, Yvonne Zurynski

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'Integrating Ethics and Equity with Economics and Effectiveness for newborn screening in the genomic age: A qualitative study protocol of stakeholder perspectives. by Didu S Kariyawasam, Joanne Scarfe, Christian Meagher, Michelle A Farrar, Kaustav Bhattacharya, Stacy M Carter, Ainsley J Newson, Margaret Otlowski, Jo Watson, Nicole Millis, Sarah Norris

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