Meet Sutton – Newborn screening success story“I’m very thankful that Greenwood Genetics is there to walk with us through the process of getting diagnosed, getting treatment,…Read More
Meet Sam – Navigating a lifelong disabilityGGC has cared for Sam since his diagnosis of Fragile X syndrome at age two. “When you go through this…Read More
Meet the Emery Family – Turning tragedy into purposeThe Emery family has endured the unthinkable – the loss of a child. But their son’s legacy lives on through…Read More
Meet Robin, a GGC patient and employeeRobin Fletcher is a genetic counselor in GGC’s Diagnostic Lab who found herself on the other side as a patient…Read More
Meet McCall – A long-awaited diagnosis changed everythingMcCall’s family had explored every possible avenue to help their struggling son. After seven years, GGC was able to deliver…Read More
Meet Emmy – Managing mom’s condition led to two healthy boysEmmy was diagnosed with PKU at birth and moved to SC after college. She knew that her dietary management was…Read More
Meet Mabry – Overcoming ChallengesMabry’s first infantile spasm at eight months came out of nowhere and was frightening. Her parents weren’t sure what was…Read More
Meet the Hunt Family – Managing PKU x2 with grace and supportMeet the Hunt Family! Two of their children, Madison and Levi, were diagnosed with PKU by newborn screening. GGC’s Metabolic…Read More
Meet Esther – Being cared for at a Rett Syndrome Center of ExcellenceEsther was referred to GGC around a year of age after her parents and pediatrician identified concerns with her development.…Read More
Meet Reuben – Lifetime support and careReuben has been part of the GGC family for nearly all of his life! He was diagnosed with propionic acidemia…Read More
