What is something unique and special about your child with trisomy that you wish more people knew?

Tirzah had a cleft lip and palate, but a cleft specialist was able to find a bottle that would work for her mouth. She was so tiny but very precious and sweet, just a really good baby. She loved to be swaddled and held. She was such a blessing to us.

Why do you believe raising awareness about trisomy conditions is important, and how can others make a difference?

Every person is made in the image of their Creator and has great value and worth. Most of Tirzah’s doctors had never seen a T13 baby before and were really clueless on what to do or what to tell us to expect.

During Trisomy Awareness Month, what message would you like to share with the world about your family’s journey and the trisomy community?

God values all life, and even though Tirzah was born with T13, she was perfectly loved by her Creator. Her precious life will never be forgotten. She is healed and whole in heaven, and we will see her again one day.