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

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Chana Masala

Delicious combination of spices, chickpeas and mushrooms.

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