Lately, I’ve found myself reminiscing while scrolling through my social media photos. Each snapshot holds a special place in my heart. I tend to capture moments and replay them in my mind like a true sentimentalist. However, I can’t help but notice that for every picture of my oldest or youngest child, there are six or seven featuring my middle child. Yes, I know how that sounds—sacrilege, right? My middle child also happens to have Down syndrome.
I’ve come to accept myself and my choices, embracing both the good and the imperfect. I’m aware of how others perceive me, and I’m not blind to the potential whispers about “her poor other children” who might feel overshadowed by their brother’s endless spotlight. I realize that some might think I’m too obvious in showcasing my “favorite.” Perhaps these critics exist only in my mind, but I recognize the patterns in my posts—the videos and adorable moments that flood my feed, all centered around the one child with an extra chromosome.
Yet, I know all my children are incredibly precious. You may not see it, but I do. You might find the child who looks a bit different, drools occasionally, or doesn’t speak as clearly to be intimidating. That’s why I choose to share my son Caleb, who is my shining star and my wonderful resource. By sharing his journey, I hope to enlighten others and dismantle misconceptions surrounding disabilities. It’s my way of contributing to a bit of change in the world, not just for Caleb, but for all children like him.
This is why you’ve been inundated with images of a baby I initially found intimidating. It’s a journey we’ve shared, and I hope you’ve grown alongside us. I aspire for Caleb’s story to resonate with everyone, so when you see someone in a wheelchair, you think of him. I want people to understand that every child with a disability has a family that adores them. I hope the world acknowledges the incredible talents possessed by individuals with disabilities and that they receive applause instead of pitying glances.
I believe that my “exploitation” of Caleb’s journey helps others recognize that there are countless individuals who don’t view him or others with disabilities merely as diagnoses, but rather as miracles deserving of love and respect. And this approach seems to be working. I’ve received numerous heartfelt messages from people who thank me for helping them see beyond the label of disability. Many have shared how witnessing Caleb’s milestones, like taking his first steps, has made them more compassionate.
As more people connect with Caleb’s story, they discover articles they wouldn’t have read before simply because they now know someone with Down syndrome. My advocacy has become theirs, and it fills my heart with joy to see them share articles on social media.
As long as Caleb continues to achieve amazing things (and he will), I’ll keep sharing those moments. I have no qualms about it. Because not only is he charming, witty, and delightful, but he is also here to teach us all. His life is an open book meant to be shared, learned from, and celebrated.
He is not just my gift; he is a gift to the world, here to foster compassion, acceptance, and love. Yes, he’s the beautiful boy I’m proud to showcase, and I’m unapologetic about it.
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Summary: This article explores the author’s experience as a parent of a child with Down syndrome, highlighting the joy and love their child brings to their life and the importance of sharing this journey to foster understanding and compassion in the world. The author embraces their child’s uniqueness and aims to change perceptions about disabilities.