Action FCS is the UK charity for people affected by Familial Chylomicronaemia Syndrome (FCS)
FCS is an ultra-rare genetic condition. People with FCS can't eat fat as they don't have the enzyme which breaks it down, or what enzyme they have doesn't work properly.
FCS in Children: Webinar
Watch our webinar FCS in Children
Recorded on Wednesday 26th April 2023
Join us to hear our four speakers to learn more about managing FCS in childhood.
Get support from your community
Learn more about FCS and its diagnosis
Learn more about the symptoms of FCS
Learn how FCS is treated