My name is Faith Alexandra Stone. My parents
are Robby and Trinsy; and, my big sister's
name is Fallon.
A pre-natal sonogram showed an abdominal
abnormality and led to a diagnosis of cystic fibrosis (CF) before I was born. Shocked and saddened, my parents prayed for me and my health, and decided to name me Faith to represent their commitment - with God's help - to my care. I was born at Johns Hopkins University Hospital - an accredited CFF care center - where I continue to be treated. I had surgery when I was a day old to correct an intestional blockage, and spent five weeks in neonatal ICU. My diagnosis led to the discovery that not only my parents but also my sister Fallon are symptom-less carriers of the defective CF gene.
Ironically, it was good that I was diagnosed with CF before birth so my treatment began immediately. Many children are mis-diagnosed for years and suffer the consequences to their lungs and digestive systems. With a daily regimen of enzymes and other medication, inhalants, and twice-daily physical therapy to help keep my lungs free of congestion, I've remained relatively healthy. But, without a lot of help for the Cystic Fibrosis Foundation, some day I will be very sick.
