When I was first told about Hudson’s possible diagnosis (which was confirmed via blood test several days later) of Down syndrome….I remember the fear and uncertainty that crippled my heart as I held my newborn baby. What would his life be like? How would people treat him? Would he go to school? Will he have friends? Will he ever find love? ⠀
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And then he looked up at me with those big blue/green eyes, and his soul locked onto mine. God whispered gently in my heart that He had it all figured out and I just needed to obediently follow and expect big things from this little man. Those fears melted away. ⠀
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Almost 2 years into this journey, and I now know my initial fears were so irrational! Yes…he will lead a fulfilling and beautiful life like others. Yes….He may experience adversity but he will be strong enough because God will give him bravery and courage! Yes…he will go to school just like other kids his age (and he may need some extra help). Yes…he already has friends and I found more friendships than I even knew possible in this community! And yes….he will find love. Love from people all over this big world….and maybe one day as an adult, romantic love as well. ⠀
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I feel GRATEFUL for Down syndrome. Yep – grateful. The love of God shines through Hudson – he truly is an angel on this earth. Huddy shows our family the value of loving ALL people, working hard every day, extending grace, doing all things with kindness, compassion for every human being because we all have value, and how a hug, wave or high five can make a REMARKABLE impact on a fellow human being. ⠀
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Today we celebrate that extra chromosome. Hudson is so much more than Down syndrome….but it’s also what makes him special. That 3rd copy of that 21st chromosome. We didn’t plan for it….we didn’t know it would be the journey God planned for me and for my family….but we are so grateful to be a part of this light, this love, and this special community. ⠀
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Happy World Down Syndrome Day! May your life be blessed by people who carry the love of God and live it out every single day like many of our friends with Down syndrome.
