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.

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Webinar: Tips and tricks for cooking without fat

Thursday 23rd November 2023, 5pm – 6pm GMT. Join this webinar for tips and tricks for adding variety and taste to the severely restricted FCS diet.

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The Facts about FCS

Learn more about FCS and its diagnosis

Symptoms of FCS

Learn more about the symptoms of FCS

Medications for FCS

Learn how FCS is treated

Get involved

Recipes

Oat and Veg Bites

Make them with any combination of fruit or vegetables.

View recipe

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In partnership with the rare disease community

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