Sophia LeClaire was diagnosed with Congenital Disorder of Glycosylation (CDG)- Rare metabolic disorder, a genetic condition with an as yet undetermined defective gene resulting in metabolism problems and an enzyme deficiency. Sophia is legally blind, developmentally delayed, unable to sit, stand, walk, crawl or use her arms and legs.
Sophia requires constant attention, care and support from her loving and attentive family as well as caregivers.