OBITUARY: Zoe Jayne Orcutt |

OBITUARY: Zoe Jayne Orcutt

October 4, 2006 – February 1, 2013

Zoe Janye Orcutt was born October 4, 2006 at Elkhorn, WI. When Zoe was 8 months old, she was diagnosed with Angelman Syndrome, a rare neuro-genetic disorder that causes developmental delays, lack of speech and walking and balance difficulties. These children are known for their sweet demeanor and happy faces, and Zoe’s smile never failed to light up a room. She was a beacon of happiness and love that far overshadowed her physical limitations. Zoe did not know hate, evil or greed. She was created the way God intended for us to be. She only knew love. Zoe touched the lives of everyone who met her. Her younger brother Deaken loved to play with her and was the recipient of an abundance of wonderful hugs, kisses and an occasional tug at his hair.

Zoe loved water, the wind, bubbles and animals, and she especially loved music. Zoe loved to dance, using her walker to move with grace and pure joy.

Zoe’s parents, Dusty and Cyndee were dedicated to giving their daughter the most life had to offer. Theirs and Zoe’s diligence and perseverance resulted in Zoe surpassing every threshold her therapists and teachers had set for her.

Although Angelman children rarely develop spoken language, Zoe had her own unique silent voice that spoke the language of unconditional love.

A true Angel in life, Zoe was called by God on February 1, 2013 with her parents at her side. When Zoe was diagnosed with the brain tumor that gave her a few precious remaining days, her grandparents Steve and Evelyn Yonker, Suzi Browne, Betty and Doug Moscrip, Francine Titherington, and many family members and friends gathered to surround Zoe with their love.

Zoe has been welcomed by the angels in heaven, where she will spread her wings to sing and dance for eternity.

A memorial service will be held on Saturday, February 23rd at 1:00 PM at Sierra

Community Church.

In lieu of flowers, the family asks that donations be made to the Angelman Syndrome Foundation

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