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June 6, 2017 by Ines Martins, PhD

Lupus Patients Will Have a Chance to Sit Down with Treatment Developers and Regulators

American lupus patients will get an unusual chance in person or online to tell therapy developers and regulators what future treatments ought to do for them. Three national organizations are sponsoring the Washington-area gathering on Sept. 25, which those unable to make the trip can participate in by watching a…

July 6, 2016 by Ines Martins, PhD

Lupus Advocates in New York Cheer Passage of Bills Advancing Disease Education and Access to Treatment

The Lupus Agencies of New York State (LANYS) announced two advocacy triumphs this legislative session — passage of the Lupus Education and Outreach Bill and a bill revising Step Therapy protocols — in both the state Senate and Assembly. If signed by Gov. Andrew Cuomo, the bills will become law in New…

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