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.
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