Support us

Interested in supporting us? Please consider donating. We are a proudly non-profit and non-compromised 501(c)(3) organization and all donations are tax deductible.

Your donation will help keep all of our resources running and contribute to the development of new projects to support those wading through their diagnostic odyssey.

We have made a deliberate decision to not monetize our app so that it is available and accessible to all. So if you use the app and like it, please consider donating.

Mobile App

Have you or your child had whole exome or genome sequencing? Did it find a VUS: variant of uncertain significance? Sometimes the VUS is benign and sometimes it's the cause of your medical concerns. Often times there just aren't enough cases or information to allow clinicians or geneticists to make a definitive diagnosis.

We've created an app to help you connect to other families like yours. Families with the same gene or gene variant finding who are looking for answers. All you need to do is sign up with an email, provide the gene name from your test results, and the gene variant if possible, and away you go. If there's a match, the app will ping you. Then you exchange contact info you feel comfortable sharing and connect with your match independently - off app - to protect your confidentiality and privacy.

The app is not just for those still waiting for a diagnosis. If you have been diagnosed with a rare single gene disorder, we are hoping to build a big enough user base to allow for meaningful connections of all kinds. And interested in sharing your data with the academic and research community? Or would like to be involved with future research opportunities? in so that you can participate. It's your data. You decide.