In this episode, we sit down with Tucker’s mom to talk about their journey with Epidermolysis Bullosa (EB), a rare condition often called “butterfly skin.”

She shares what life looks like behind the scenes — the challenges, the strength it takes to keep going, and the love that fuels everything. Tucker may be small, but his story and spirit are incredibly powerful.

This conversation is raw, real, and a reminder of how strong families can be when facing the unimaginable.