T21 Compass™ ← Back to home

About

Our story

When our child was born with Trisomy 21, we did what most families do. We searched. Late at night, between appointments, in hospital hallways. Good answers existed, but they were scattered across textbooks, guidelines and forums, and none of them knew our child.

So I wrote the book I wished someone had handed us, and then we built Compass to make it answer back. Every answer points to where it came from, so you can check it, print it, and bring it to your care team.

This is a small project made by people who live it. It will keep getting better, and we will keep telling you exactly what it can and cannot do.

Samuel Solomon · Author & founder

Start with a question