Gabby Gingras has a disease so rare she's the only person her parents and doctors can find in the U.S. suffering from it. Like any other three-year-old, Gabby takes her share of slips and falls. Her reaction to each is predictable — at least for her family.
For no matter how hard Gabby hits the ground, she will not shed a single tear. Hard as it is to fathom Gabby Gingras feels no pain. There is no cure, nor will she outgrow it.
You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You can vote in polls in this forum