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A courageous tale comes to an end: Baby with rare genetic disorder passes away close to Christmas

Most people don’t contribute to the world over a lifetime what Charlotte Joy Norris did in just two short years.    Born with a rare genetic.

Kelsea mccolleyJoyce mccolleyKyle norrisMelanie hollifieldUniversity of north carolinaReception centerTuscola high schoolMarine corpsCam hollifieldNorth carolinaRutherford countyWells eventBaby charlotteCharlotte joyCharlotte joy norrisNeimannpick disease

2-year-old Charlotte Joy dies from rare genetic disorder

The family of a little girl battling a rare genetic disorder is mourning after the 2-year-old died Sunday, Dec. 17, 2023.

Melanie hollifield windsorCharlotte joyHealth medical pharmaMelanie hollifieldHuman interestGenetic disorderCongenital disordersLipid storage disordersRare diseasesSphingomyelin phosphodiesterase

The courageous tale of Charlotte Joy: Rare genetic disease can t stop one Haywood family and their daughter from helping other children

Charlotte Joy is a hero; she just doesn’t know it yet. Her parents, Kyle Norris and Kelsea McColley, were thrilled when they found out Kelsea was preg.

United statesKelsea mccolleyElizabeth jalazoJoyce mccolleyMelanie hollifieldKyle norrisSteven laffoonNational neimannTuscola high schoolPick disease foundationMarine corpsChapel hillTar heelsCam hollifieldNational neimann pick disease foundationWylder nation

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