Walls of Jericho - the story of a Mother and her son with Cockayne Syndrome

Walls of Jericho - the story of a Mother and her son with Cockayne Syndrome Believing in God's promises whilst raising a child with Cockayne Syndrome. CS is an extremely rare, progressive and degenerative disease.

This page is my personal story of growing and grappling with faith while facing devastating diagnosis. Welcome to Walls of Jericho! My name is Nicole and I am the mother of three school aged children. My middle child, Toby is 6 years old and has Cockayne Syndrome - an extremely rare, degenerative and progressive disease. I felt led by God to share our story. I will share my thoughts, experiences a

nd emotions, and what God is doing in my life as I learn to walk alongside Him through the darkest of valleys. I am not a pastor, theologian or bible scholar. I am a woman of faith and a mother who thanks God daily for the gifts of grace and mercy because heaven knows I need them! This is a page that I pray will support others as they learn to grow and grapple with their faith. Judgement is not welcome here but prayer and loving support of one another is! God bless you all xx
**If you'd like to donate to Toby to assist him with ongoing medical treatment and attending the International Conference on Cockayne Syndrome in UK please visit our Go Fund Me page. Any amount is so very appreciated. https://gofund.me/d2853662

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Perth, WA

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