What is something unique and special about your child with trisomy that you wish more people knew?
Bella has a smile that could melt anyone’s heart. She’s full of sass and knows exactly how to push the limits—doing something she shouldn’t, then flashing the biggest smirk when she gets caught, especially if she’s kicking her brother. But beneath that mischievous streak, she’s the most affectionate little girl, always ready for snuggles. She’s the perfect mix of feisty and lovable, keeping everyone on their toes while stealing their hearts at the same time.
Why do you believe raising awareness about trisomy conditions is important, and how can others make a difference?
I think these precious babies are too often labeled as burdens when, in reality, they are anything but. Every child I’ve met with trisomy has been the sweetest, each with their own unique personality. And the idea that they are “not compatible with life” couldn’t be further from the truth—these children are compatible with life. They bring joy, love, and so much light into the world.
During Trisomy Awareness Month, what message would you like to share with the world about your family’s journey and the trisomy community?
The beginning of our journey was filled with trauma and heartbreak. I was told my baby girl wouldn’t survive her first month, and when I asked, “What if she does?” the doctor simply replied, “Then bring her to see me.” In the NICU, all I heard was, “I’m so sorry.” But looking back now, if I had known what our future would hold, I would have never felt sadness when she was born—I would have been filled with pure joy. She is the little blessing our family needed. We needed her.
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