Download the How to talk to family and friends about your FCS guide today.

Living with familial chylomicronemia syndrome (FCS) symptoms like severe abdominal pain, nausea, or fatigue can be frustrating—and trips to the ER can add even more stress and uncertainty.36

That’s why we created the How to talk to family and friends about your FCS communication guide. It’s a simple, practical tool to help you explain what you’re feeling, how it affects your life, and why support matters.

Excerpt from How to talk to family and friends about your FCS: