Helpful Links

National Support

Patient/caregiver support  and information for FCS patients and caregivers

FCS Foundation is a US-basesd patient community

Website: www.livingwithfcs.org
Facebook: www.facebook.com/fightFCS

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.

Website: www.rareconnect.org/en/community/lipoprotein-lipase-deficiency

Association de l`hyperchylomicronémie is a Canadian-based patient community (French):

Facebook: www.facebook.com/Association-de- l’hyperchylomicronémie-262283483810867

l’hyperchylomicronémie familiale is a French-Canadian patient community:

Facebook: www.facebook.com/Hyperchylomicron%A9miefamiliale-135780279829722

Show References

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National Support

Patient/caregiver support and information for FCS patients and caregivers

Show References

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Patient/caregiver support  and information for FCS patients and caregivers