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Additional links and resources for sHTG & FCS
National Support
Look for this icon to read expanded content about living with FCS.
The FCS Foundation is a US-based patient patient advocacy group for people living with FCS:
- Website: livingwithfcs.org
- Facebook: facebook.com/fightFCS
Organizations outside the US include:
- Canadian Organization for Rare Disorders (CORD)
- LPLD community on RareConnect
- Association de l`hyperchylomicronémie
- l’hyperchylomicronémie familiale