Sarah Borscha
Sarah Borscha, age 6, was born with Apert’s syndrome, a rare genetic disorder that disrupts normal bone growth and causes malformations of the skull, face, hands and feet. The medical costs associated with Sarah’s care are enormous.
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Sarah Borscha, age 6, was born with Apert’s syndrome, a rare genetic disorder that disrupts normal bone growth and causes malformations of the skull, face, hands and feet. The medical costs associated with Sarah’s care are enormous.
Tina Witowsky, age 20, suffered a brain trauma, similar to a massive stroke, four years ago. Following months of critical care, multiple surgeries, and intensive rehabilitation, Tina was able to come home, but she needs extensive in-home services and supports, which her private health insurance stopped covering.
Claire Smith, now 5 years old, was born with a rare genetic syndrome whose symptoms include multiple, severe physical, developmental, and intellectual disabilities. Claire’s family has private health insurance, but because of its bureaucratic barriers, her parents have had to struggle to obtain the care Claire needs.
Kay Dickerson, age 57, is a Hurricane Katrina survivor. After the storm, Kay and her husband, Tom, relocated to Portland, Oregon. During her intake at the welcome center, Kay, who had long been uninsured, was diagnosed with anxiety, depression, PTSD, high blood pressure, and diabetes.
Darius, age 9, was born with periventricular leukomalacia, a brain injury that causes frequent seizures, as well as central apnea, a condition that often causes him to stop breathing. He also has mild cerebral palsy, which impairs his mobility, balance, and reflexes.
Latrita McFadden noticed from the beginning that her son, Anthony Burke, always walked on his tiptoes. He began to complain that his knees hurt, but doctor after doctor said he would grow out of it.
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