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.

Rare Disease Genetics. Clear Next Steps.

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 accelerates the diagnosis of rare diseases and understanding of next steps by creating a supportive health platform that is accessible to all. 

A step-by-step infographic with a purple line and icons, showing the process: untangled line, get tested, understand results with people and speech bubble icon, take next steps with arrow icon, and completion with checkmark icon.

Introducing the Emerge™ Platform

Diagram of a DNA double helix inside a circle with the text 'Get Tested' beneath it.
Line drawing of a woman with shoulder-length hair wearing a uniform, encased in a circle, with the words "Find Providers" below.
A screenshot of a website or presentation slide with purple text and icons, including a lightbulb symbol, and points about understanding results, genetic information, and sharing with a care team.

* EveryLife Foundation for Rare Diseases Delayed Diagnosis Study

** EveryLife Foundation for Rare Diseases; Sept, 2023