PPCM (Peripartum Cardiomyopathy) Online Support Group

Our vision is for everyone affected by cardiomyopathy to lead long and fulfilling lives. We are the specialist national charity for people affected by cardiomyopathy. We provide support and information services, work to raise awareness of the condition, campaign for better access to quality treatment and promote research.How we use your information.  All personal information given to Cardiomyopathy UK is only held and used in accordance with the Data Protection Act 2018. We do not share our mailing lists...

Cardiomyopathy UK

Are you affected by Peripartum Cardiomyopathy (PPCM)?  Come along and meet the community.

This meeting will be hosted by Midwife Volunteer Rebecca Jarman. This session is for anyone who has been diagnosed or is a loved one of someone with PPCM.This is a great opportunity to meet others with PPCM, ask questions and share experiences.You can join the session from your computer, tablet, smartphone or by phone. All sessions are free of charge but you will need to book to secure your place.The session will take place online - a link and password will be sent to you.Please note this meeting is not suitable for healthcare professionals seeking information about PPCM, please contact Cardiomyopathy UK separately in this instance (contact@cardiomyopathy.org), and we will be happy to help.If you have any questions, please email the charity's Services team at services@cardiomyopathy.org. Julia or Christie will reply within office hours.

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PPCM (Peripartum Cardiomyopathy) Online Support Group

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