Jean shares with the Rare Collective® her insights, experiences and advice that has helped countless others in our community become more effective in serving patients and organizations.
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Jean Campbell reflects on why the patient voice needs to be not just heard but acknowledged.
In this series, David Lapidus talks with members of the Rare Collective to debunk common myths surrounding rare diseases. In this post, Jean Campbell talks about when orphan drug companies should begin interacting with the patient community.
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