Share Your Story

We would like to hear from you.

At Aceragen, we address rare, orphan diseases that typically have no available treatments, and strive to develop novel therapies to positively impact the lives of patients and families.

  • If you are a healthcare professional who has diagnosed or is managing someone with this condition, we would like to hear from you.
  • If you are living with Farber disease, or caring for someone who is, we would like to hear from you so we can better support the global Farber community. We would love to better understand how you were diagnosed, what your symptoms are and how living with Farber impacts your life. You may be able to provide us with important information.

A Diagnosis Story

Santi’s story illustrates how symptoms of Farber disease were missed at first but became impossible to ignore as the condition rapidly progressed.

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Suspect Farber Disease? No-Cost Genetic Testing Available.