No one knows your body like you do. Advocate for the care you deserve.

If you feel like you’re not being heard by your doctors—Your health, your voice, your choice: A guide to self-advocacy for people with familial chylomicronemia syndrome (FCS) is intended to provide you with the tools to help you speak up and take control.

Being your own advocate could be the most powerful step you take in getting answers.

Because FCS is a rare genetic condition that is often missed or misunderstood—even by medical professionals—self-advocacy isn’t optional.36 It’s essential.

This guide gives you the tools to:

  • Speak up with confidence in medical appointments
  • Ask the right questions and push for deeper testing
  • Explain your condition clearly to family, doctors, and employers
  • Understand your rights as a patient
  • Build a support system that has your back

Whether you’ve just been diagnosed with FCS or have been living with symptoms for years, this guide is intended to provide you with tools to take ownership of your health journey.