SHREVEPORT, La. (KTAL/KMSS) — A mother fighting for her 3-year-old daughter is on a mission to raise $6 million for a potential treatment awaiting FDA (Federal Drug Administration) approval.

Lydia, a bright, fun and loving little girl living with a rare and terminal genetic disorder called Sanfilippo Syndrome, often referred to as childhood Alzheimer’s, was diagnosed at just 18 months old, her mom says there’s now a glimmer of hope.

“A week and a half ago, we found out that a potential treatment option could become available,” Morgan said. “The pharmaceutical company is sending the medicine to the FDA for approval, and while that process could take a year or more, they plan to make extra doses for children waiting in the meantime.” The treatment has shown promising results in reducing to

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