Devon, living with FCS and Fin, father and carer
Patients & Carers
Where Science Meets Life
We are committed to researching and developing medications in cardiometabolic, pulmonary, liver, neuromuscular, and other therapeutic areas, bringing hope to those who need it most.
Jill, founder of Action FCS and living with FCS in the UK, and Jon, husband and carer
Patient Centricity & Advocacy
Together with advocacy organisations, we’re amplifying voices, raising awareness, addressing needs of the communities we serve, and developing therapies that make a real difference in people’s lives.
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Fin, father & carer, and Devon, living with FCS
Patient Stories
Hear from real patients living with Familial Chylomicronaemia Syndrome (FCS) as they share their journeys of diagnosis, treatment, and hope. Discover how these individuals and families are reclaiming their lives and becoming advocates for better care.
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About Arrowhead
We’re taking on hard-to-treat diseases by silencing the genes that cause them.
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Spotlight on FCS Paper
Providing perspectives from patients and caregivers who experience living with Familial Chylomicronaemia Syndrome (FCS).
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Triglyceride Resources
Disease education and management for patients living with high triglycerides.
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