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Fresno child battles rare form of Spinal Muscular Atrophy

The living room of Zaira De La Cruz's home has been turned into a makeshift hospital room.

Family works to develop treatment for their toddler

Mary Saladino started a foundation is hoping to raise nearly $3 million dollars needed to test and produce a treatment for her little boy.

Savannah: Rare disease kills baby, her parents fight for a cure

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