My Life Beyond Neurofibromatosis - Federighi, Guillaume
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A fictional graphic novel adventure story offers a kid’s-eye view of living with, and beyond, neurofibromatosis.

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Produktbeschreibung
A fictional graphic novel adventure story offers a kid’s-eye view of living with, and beyond, neurofibromatosis.
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Autorenporträt
G.W. Page was diagnosed with a rare genetic condition called Neurofibromatosis (NF) as a baby, after his mom noticed some new birthmark-type spots on his legs. When he was 3 years old, an MRI revealed a large tumor in G.W.'s brain, requiring surgery to remove it. At age 9, G.W. has an extensive team of doctors who routinely monitor him for new tumors or other NF-related problems, which can be very unpredictable. With his positive outlook and fierce courage, even as the youngest of his siblings, he sets a big example for his family about choosing how to react when things go wrong or we're afraid. He loves playing sports, creating art, fishing, fantasy football, cooking with his dad, and being a goofball with his big sisters. When he grows up, G.W. hopes to become a professional sports analyst.   Guillaume Federighi (AKA Hey Gee) is a French and American author and illustrator. He began his career in 1998 by exploring the world of street art and graffiti in different European capitals. After moving to New York, Hey Gee developed a reputation for a direct and instantaneous style of graphic design and illustration that brings out unifying ideas, creates distinctive characters, and affects all generations. He is also the owner and creative director of Hey Gee Studio, a full-service creative agency based in New York City.   Medical editor, Dr. Babovic-Vuksanovic is a pediatrician and clinical researcher in genetics at Mayo Clinic. She leads several collaborative studies looking at children, adolescents, and young adults with neurofibromatosis 1 and progressive plexiform neurofibromas as well as adult patients with neurofibromatosis 1 and extensive plexiform and paraspinal neurofibromas. Dr. Babovic-Vuksanovic is passionate in her work toward a better understanding of various genetic syndromes and metabolic disorders, aiming to improve diagnosis, treatment, and outcomes for patients with these conditions.