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MEET THE ALANIZ FAMILY
Hi! We’re the Alaniz’ and we are SO happy you are here! We began Walk With Noe in 2021 to honor the one year mark of our daughter, Noella’s, diagnosis with 18q deletion syndrome. Since then we have had a goal to turn our small fundraiser into a non-profit that could prayerfully make in impact in the lives of families with children with rare diseases.