11/20/2023
Welcome to our page in honor of Ellie Kate! It's hard to believe Our Precious Girl would be turning 18 year old on December 4th. As many of you know, Ellie suffered from the same rare and terminal genetic disease as Lucy - Non-Ketotic Hyperglycinemia, or Glycine Encephalopathy. Ellie Kate died from NKH complications on December 23, 2012.
The purpose of this page is to honor our Daughter, to share her stories, to share God's faithfulness and the many struggles which come along with caring for medically fragile children.
To commemorate EK's 18th birthday, we invite you to join us in giving to our fellow NKH families around the world. We are a small, tight-knit community and as you can imagine, the needs are great. Each Christmas Season, NKH families are encouraged to fill out an application for, "Ellie Kate's Wish". Monies raised go directly to the chosen families with practical, immediate and medical needs.
Check out our Go-Fund-Me page here: https://thewonderfullymadelife.blogspot.com/
We know this is a busy season of giving and gratefulness and we appreciate your thoughtfulness in donating to this worthy cause, on behalf of our Beloved Daughter.
Mike and Ryan
