Gabe's story: Life with a rare genetic disorder

As they care for their 4-year-old son, who has a genetic disorder so rare that it doesn't even have a name, a West Michigan family is finding ways to bring the world to him. (Jan. 10, 2019)

[tatianaflores]

What a precious boy who will never be forgotten

[sarah.]

Update: Gabe died in 2022 at the age of 7.

[sugar-free-centz]

This is sickening. The fact that parents who claim to be loving do this to their kids is so wrong. How incredibly selfish on their part. Torturing him in a miserable existence year after year, just so they can feel good. That's not love, that's horrendous.