By Kelly McKenna My name is Kelly McKenna, and I’m a single mom to two amazing kids. One of them is an eight-year-old boy who has Fanconi anemia (FA). Logan’s medical journey started during my pregnancy at the 20-week anatomy...
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Peter Pless
Board Member | MD
Father of Julia
Peter Pless is board certified in Internal Medicine and Dermatology, has a private practice in dermatology and is active on the medical staff at the Meadville Medical Center in Meadville, Penn. He is a clinical instructor at Lake Erie College of Osteopathic Medicine in Erie, Penn. and a lecturer for the Nurse Practitioner Program at Edinboro University.
As a parent of two daughters, one a young adult with Fanconi anemia, his interest on the board is to help advance the goals of the founders. Notably, this entails increasing understanding of FA so that treatment and preventable strategies can improve the quality of life for those who have this disease. His goal is to direct funding, with the help of scientists, to support research studies.
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By Sarah Borden Our lives changed forever the day we learned our son Eli was diagnosed with Fanconi anemia. Just days earlier, we had celebrated his fourth birthday with family and friends, blissfully unaware of the journey ahead. When faced...
“If I had waited another six months, my story wouldn’t be the same.” Katherine was born into a world shaped by loss. Her older sister, Gracie, was diagnosed with Fanconi anemia (FA) shortly after the family moved to the United...