Action on Postpartum Psychosis is the national charity for women and families affected by postpartum psychosis (PP). PP is a severe mental illness which begins suddenly following childbirth. Symptoms include hallucinations and delusions, often with mania, depression or confusion. Over 1400 women experience PP each year in the UK (1 to 2 in every 1000 mothers). An episode of PP can be very frightening for women and their families. Most women go on to make a full recovery, however the journey to full recovery can be long and difficult.

We run an award-winning peer support service, connecting women and families throughout the UK to recovered volunteers, via: an online peer support forum; one to one email support; meeting a volunteer programme (video and in person); social groups and creative workshops.

We develop patient information for women who have experienced PP and their families, co-produced by women, families, specialist clinicians and leading academic experts.

We offer training to frontline health professionals in PP and Managing SMI in pregnancy, co-produced and co-delivered by academics, clinicians and women with lived experience.

We facilitate research into the causes of PP, treatments and what helps families to recover.

We promote greater public awareness of PP in the general public, work to address stigma and misinformation, and campaign for improved perinatal mental health services.

Action on Postpartum Psychosis (APP) is a registered charity, hosted by the University of Birmingham and we are grateful for their support. We also thank The Big Lottery, Comic Relief and individual women and families for supporting our project. For information about how to support us, please click here.


Postpartum psychosis: our personal experiences

PP Insider Guides

APP has produced a series of downloadable guides with the help of women who have experienced postpartum psychosis (PP), their partners and health professionals. Learn more

My postpartum psychosis story: a short animated film


Sign up to receive updates

Joining the APP Network is a brilliant way to…
  • Find out how you can help mums and families affected by postpartum psychosis (PP)
  • Receive our enewsletters with information about our projects and research into PP
  • Be a part of a national network of people who have been affected by PP
  • Hear about events, workshops, conferences and opportunities to take part in research studies
  • Help us to change things for the future
Click here to sign up to the APP Network >

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