Through education, research, and shared experience, PPCM support groups empower patients and families with knowledge, connection, and hope at every stage of the journey.
A private Facebook support community for people affected by peripartum cardiomyopathy. Members offer one another understanding, hope, and connection as they journey through diagnosis, treatment, and life beyond PPCM.
A collaborative group of clinicians and researchers across the United States and Canada dedicated to improving care for women diagnosed with peripartum cardiomyopathy. The Network maintains a contact list of clinicians who offer specialized expertise in PPCM.
A nonprofit organization dedicated to raising awareness, educating families, and supporting people affected by Peripartum Cardiomyopathy. Their work focuses on community outreach, educational materials, workshops, storytelling platforms, and supportive services.
A campaign from the American Heart Association provides education, support, and community engagement to improve awareness of heart disease in women.
Many women with PPCM will also be diagnosed with preeclampsia. The Preeclampsia Foundation provides education and support to improve outcomes for women and families affected by preeclampsia.
