FND RESEARCH

TOGETHER WE WILL SEARCH FOR BETTER TREATMENTS THROUGH SCIENTIFIC RESEARCH

FND SCIENTIFIC REGISTRY

You are about to enter the FND Hope Scientific Registry. The Genetic Alliance hosts the FND patient registry and stores your data securely amongst thousands of other individuals battling illness. If you have not done so already please visit the FND Scientific Registry Question and Answer page to learn about the registry. For any additional questions or concerns please email us at contact@fndhope.org.

THE FND SCIENTIFIC REGISTRY DATA IS CURRENTLY BEING ANALYZED.

AN UPDATED REGISTRY WILL BE AVAILABLE IN 2022.

HAVING TECHNICAL ISSUES WITH THE SCIENTIFIC REGISTRY?

1. Be sure you are registering on a computer and not a mobile phone or tablet. This scientific registry was designed to be completed on a computer and is not compatible with mobile phones/tablets.

2. Have you read all the other FAQs?

3. Still have an issue? Please submit your issues to the Genetic Alliance via Give Feedback.