I’m a mom to a child with a rare genetic condition called FOXG1.
The simplest way to describe it: a tiny “bug” in the code — a small piece of a gene is missing.
It sounds small, but at 6 years old, my child still can’t speak, walk, or sit independently.
I’m starting this page to share our life and hopefully support other parents.
And one thing I truly believe: never give up. There is always hope
