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

Chapman was so aware! He had the best clenched fists ever. His hands were my favorite! His eyes would just stare right into your soul. He knew when Mommy and Daddy were in the room! He turned towards the tv every time we watched church from home. He loved his big brother and they became quite the duo! Chapman will forever be a part of our lives and our family!

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

Every family needs to know that a trisomy diagnosis does not mean incompatible with life! These children are precious and very compatible with love and life! They’re perfect just as they are! God makes no mistakes!

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

Chapman was our little Champ! Born a month early at just 3lbs, we were prepared for death. He defied every expectation and was born crying, ready to nurse! He came home on hospice care and was given an NG tube at 2 weeks old. He thrived and continued to amaze all medical professionals! He lived for 20 beautiful weeks. We were so blessed by him! He taught us about surrendering to God’s plan above all else and that the power of prayer can change lives. Chapman was proof that God can still do miracles! We were grateful for our sweet boy!