Nine years ago, Bill Vick was diagnosed with Idiopathic Pulmonary Fibrosis. With no available cure and few treatment options available, Bill embarked on his journey with IPF with the idea that the more you learn, the more you’re in control. He founded PF Warriors, a volunteer support group made up of patients, caregivers, and medical professionals—and ultimately discovered a new outlook on life.
“Dying is easy; it’s the living that’s hard.”
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