It takes an average of 6 years to diagnose a rare disease*.
We believe that is 5.9 years too long.
A timely diagnosis is essential when there are potentially disease-altering or life-saving treatments available. Even in the absence of FDA-approved therapies, timely diagnosis can have a profound impact on the management of irreversible symptom progression**.
Jura Health aims to accelerate the diagnosis and understanding of rare diseases by creating a supportive health platform that is accessible to all patients and healthcare providers.
This is just the beginning.
Introducing the Emerge™ Platform
Jura Health combines whole genome sequencing (WGS) with on-demand genetic counseling and next steps in one report in as early as 4 weeks.
* EveryLife Foundation for Rare Diseases Delayed Diagnosis Study
** EveryLife Foundation for Rare Diseases; Sept, 2023