It affects around 5,500 women a year in the UK (that's about 0.7% of all pregnancies), while in parts of South America the incidence has settled at around 4-5%: it's a geographically diverse condition! Although ICP is not life-threatening to the mother-to-be, there are concerns for the baby as it is associated with fetal distress, spontaneous premature labour and, in very severe cases, stillbirth.
We know therefore that it can be a very worrying and distressing condition to have so as a charity we provide support and information to people affected by ICP, raise awareness of the condition, and promote and fund research into it. We have active Facebook groups (for during and after an ICP pregnancy) that you can go to for support or to ask questions and we can provide one to one support via email. Our replies to you will be based on research and personal experience. You can find out more about our support here: https://bit.ly/OurSupportForYou
We believe it is important that you have the most up to date scientific information about the condition so what is written on our website about ICP is verified by researchers, scientists and doctors. Jenny Chambers, Founder of ICP Support, is also part of the Maternal and Fetal Medicine Group - a London-based research group investigating ICP. Jenny remains in contact with the charity as our research advisor and can be contacted if you are interested in taking part in research ([email protected]). Please share this page with friends, family and health professionals and help us achieve our vision that every ICP baby will be born safely. NB: Any photos we post on here will always be with the permission of the people involved and, if required, with the permission of the organisation (such as a hospital or company) too.