When Shayla was born in 1970, her parents thought they were bringing home a healthy baby girl. Within 24 hours, she was admitted to the hospital and diagnosed with Maple Syrup Urine Disease (MSUD) — the same rare genetic disorder that had already claimed the life of their son.
MSUD, named for the sweet smell it causes in urine and ear wax, must be diagnosed immediately after birth to prevent irreversible brain damage. At the time, very little was known about the condition — especially in northern Indiana.
Shayla’s mother learned through trial and error. Treatment required a strictly monitored diet and specialized medical formula. There were no local physicians with enough experience to guide them through daily challenges, and the burden of managing a rare disorder often felt isolating and overwhelming.
For years, they prayed for access to specialized care closer to home.
That prayer was answered with the establishment of the Community Health Clinic.
Today, Shayla is cared for by a dedicated team that includes a physician, dietitian, and staff who understand the complexities of MSUD. Her treatment has improved, and her family no longer walks this journey alone. When questions arise, someone knowledgeable is just a phone call away.
“We appreciate the CHC and its exceptional standard of care,” her parents share. “May God bless all who are involved as they serve our community and beyond.”
