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Data is a tool that provides facts and statistics as a framework for observing various phenomena, which is then used to make decisions. However, it is not the phenomena itself, this misunderstanding is contributing to various health inequities and a relational gap between communities and practitioners. We will be discussing this gap in order to create a better understanding of the uses of data in health justice.
How communities ideally use the scientific method for their own health justice.
The responsibilities of practitioners in health justice.
How we create an ecosystem of trust between communities and practitioners.
Format
Virtual Workshop held on zoom. To be sent a link please register below.