Jill Holdren has a background in environmental science and public health/epidemiology and has experience managing state-wide public health programs, international consortiums, and non-profits, as well as thinking about and analyzing public health data. She is active as a patient and research advocate representing the hereditary breast and ovarian cancer community. She is focused on supporting the empowerment and autonomy of self-organized patient communities, understanding and communicating the critical role peer support plays in the healthcare continuum, and helping individual patients and patient communities work with research and healthcare institutions as full partners, rather than subjects.
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