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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Virtual meeting

Tuesday October 20th, 7pm-8.30pm
Meet Dr Charlotte Dawson, consultant in metabolic medicine, Queen Elizabeth Hospital, Birmingham.

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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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Recipes

Chicken and Sweet Corn Noodle Soup

Tasty soup that’s easy to make.

View recipe

News from Action FCS

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