A dermatologist examining a woman's face with a magnifying glass, both depicted on a purple-tinted background.

It takes an average of 6 years to diagnose a rare disease*.

We believe that is 5.9 years too long.

Four people walking outdoors in autumn, two women on either side of a young boy in a stroller, holding his hands, with a man pushing the stroller behind them. All are smiling, surrounded by yellow fall foliage.

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

Diagram showing DNA entering a microscope, followed by icons representing human, brain, network, and a document, then an arrow pointing to a report or paper.

Jura Health combines whole genome sequencing (WGS) with on-demand genetic counseling and next steps in one report in as early as 5 weeks.

* EveryLife Foundation for Rare Diseases Delayed Diagnosis Study

** EveryLife Foundation for Rare Diseases; Sept, 2023