Information on FCS
Patient/Caregiver Support and Information
- FCS Foundation is a US based patient community
- Website: www.livingwithfcs.org
- Facebook: www.facebook.com/fightFCS
- Action FCS is a UK based patient community
- Website: www.actionfcs.org
- Facebook: www.facebook.com/ActionFCS
- Canadian Organization for Rare Disorders (CORD) is interested in hearing from FCS patients living in Canada that may be interested in getting involved
- Website: www.raredisorders.ca
- LPLD Community on RareConnect is sponsored by the EURORDIS and is an on-line based community where FCS patients can connect with others from all over the world
- Asociación hipertrigliceridemia familiar is a patient community based in Spain:
- Association de l’hyperchylomicronémie is a Canadian-based patient community (French):
- Hyperchylomicronémie familiale is a French-Canadian patient community:
- Association Francophone Hypertriglycéridémies Majeures Génétiques is a patient community based in France
- Website: www.afhymage.com
