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.
Report from our February meeting
We had a wonderful time in Birmingham when patients, parents, and carers spent time meeting each other, with lots of learning from all the experts around us. Read our report.
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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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Recipes
Light and Fruity Mince Pies
These light and fruity mince pies are easy to make and work out at less than 1g fat each.
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In partnership with the rare disease community





