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.
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Learn more about FCS and its diagnosis
Learn more about the symptoms of FCS
Learn how FCS is treated
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In partnership with the rare disease community



