PPCM awareness saves lives and promotes recovery.
Advocacy Groups and Educational Websites
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Peripartum Cardiomyopathy (PPCM) Survivor Support - FacebookMission Statement:link to Advocacy Group:
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Peripartum Cardiomyopathy NetworkMission Statement:
The Peripartum Cardiomyopathy Network (PCN) is a network of physicians, nurse practitioners, physician assistants and nurses at clinical sites across the United States and Canada dedicated to both clinical care and investigation of peripartum cardiomyopathy (PPCM). Information about the ongoing REBIRTH trial can be found here.
link to Advocacy Group: -
LetsTalkPPCMMission Statement:
The mission for LetsTalkPPCM is to eradicate peripartum/postpartum cardiomyopathy as a life-threatening heart disease found in pregnancy by advancing research, treatment, education, short films, and awareness.
LetsTalkPPCM offers PPCM Workshops and Screening Training for birth workers and health care providers. We provide free PPCM Patient Advocate Support, BNP Blood Testing, and Postpartum Exams to help bridge the gap in this area.
We encourage women who've experienced: High blood pressure, Preeclampsia, Multiple births, Heart murmur, Hyperemesis gravidarum, Fertility treatments, Covid-19, and Family history of heart disease to request a BNP blood test during and after pregnancy.
Through PPCM screenings and timely intervention, serious problems can often be avoided.
Contact:Brianna Henderson, PresidentAdvocacy Group Email:link to Advocacy Group: