Patient Centered Care Advocacy Group

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The Patient Centered Care Advocacy Group is focused on generating publicity that spotlights discrimination and harm faced by patients with chronic Lyme disease due restrictions imposed by the Infectious Diseases Society of America (IDSA) guidelines for diagnosis and treatment of Lyme disease. Our goal is to increase awareness among the public, the media, the medical establishment, and most importantly, the policy makers who have the power to root out corruption and reform the system that shapes federal policy on Lyme disease and associated tick-borne illnesses.

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