Mar 10, 2013 / 12:03 pm
Laura Thompson had been through the emotional rollercoaster before when she was told by doctors that her daughter was going to be born with a cleft palate before being born without one, and now, in her doctor's office, she gets news that her son will face a life of uncertainty due to a rare physical condition.
It was almost two decades ago when she was on her back in the doctor's office getting an ultrasound about a week before Christmas when her doctor told the expectant mother that he saw a fibular malformation called Fibular Hemimelia. It is the developmental anomaly characterized by the absence or gross shortening of all or part of the limb.
"I guess we all doubt our inner strengths until we are faced with this kind of a situation," Thompson said. "The doctor walks in with x-rays and said we have problems that we have to talk about, and at this point you are not sure what is going on or what needs to be done. It is tough when you find out that your baby is not perfect."
Jake Wesley Thompson was born on May 18, 1996, to his parents Curt and Laura Thompson, on a day that would end up testing her Catholic faith and taking it to heights she never knew was possible.