What Silly Socks Don’t Tell You

At school yesterday, we wore our silly socks for World Down Syndrome Day. Today is actually WDSD, but since there isn’t school on Saturday, we celebrated on Friday. As the other teacher assistants and I walked down the hall to pick up our students from the bus, we talked about our socks. I said that, on some level, I didn’t really like this celebration, because every day should be a celebration of individuals with Down syndrome. Then I thought, What a humbug I am for saying that.

When Wil was younger, I was very into this celebration. But back then, I was also new to this journey with Down syndrome, and I think I was celebrating his diagnosis as much for myself as I was spreading awareness.

When Wil was born, I needed celebration. I needed to hear that everything was going to be okay. I sought that out hard. Any celebration of Down syndrome I could find, I clung to. But then, over time, the celebrations began to come on their own. They were not big, worldwide, put-posters-on-the-wall-at-school-and-shout-it-out-on-social-media kinds of celebrations. They came in the form of Wil saying a new word, demonstrating a new skill, taking a new step, making a new friend, or a friend showing him a new form of kindness.

These were the celebrations that only those who live this life up close get to see. There is no fanfare outside our circle, but the feeling of celebration is more powerful because of that. The earlier pain of what we once believed we had lost was transformed into new forms of joy.

Don’t get me wrong. Rocking our silly socks is fun. It’s a creative, accessible, enjoyable way to spread joy and awareness. It’s a way to come together, point out our silly socks, and smile and laugh.

But for a new mom, those funky socks may look good from a distance, and that’s exactly what they are: joy at a distance. And joy at a distance is a good thing. But when you are carrying the pain of hearing your child’s diagnosis, you need something to hold on to. You need a kind of joy you can actually grasp, and silly socks, even when they symbolize joy, just aren’t enough.

You need another parent who has gone through what you are just beginning to hear say, “This journey will be full of joy, even if you don’t realize it yet.” That kind of statement is ethereal, yes. It may feel like trying to grasp a cloud. But you can breathe in the spirit of it with everything you have, breathe it down deep, and hold it within you. When it is shared deeply and personally, it is not just a passing date. It is not just a pair of socks. It is a promise, and your heart knows it.

It has been 19 years since I first heard those words. I may not have them exactly right, but the essence of the message is still within me. And that promise has come true over and over and over again. It continues to.

So I wear my fun socks. I do celebrate this day. Spreading awareness will always be vitally important. But the essence of true awareness, the essence of the true value of individuals with Down syndrome, is known deep in our hearts. It is learned through lived journeys. It is learned through experience. It is learned through promises given to us, and through the promises we share with others.


(WDSD is on 3-21 representing 3 copies of the 21st chromosome. If you hold up socks, they resemble chromosomes.)

Discarding “Popular” Wisdom

“The first problem for all of us, men and women, is not to learn, but to unlearn. We are filled with popular wisdom of several centuries just past, and we are terrified to give it up.”

Gloria Steinem may have had women’s rights on her mind with this quote, but it rings very true for our friends with Down syndrome. I was so scared when I received Wil’s diagnosis. Why? Because of an outdated belief system handed down to me from centuries just past. I had no other frame of reference; it was what I knew and the unknown is a scary place.

When I opened my mind; when I truly looked at Wil and accepted anything and everything to come — all the knowns and most importantly the unknowns — is when my world first cracked open, then burst open, and love flowed in place of the fear.

HAPPY WORLD DOWN SYNDROME DAY!! #WDSD2023

How We Celebrate

Wil chose not to wear green today. Just because he was told to. I wouldn’t be surprised to find him dressed in green tomorrow; because it would be his choice. Wil did follow the color code on Valentine’s Day. He had been coveting Elizabeth’s neon pink shirt and she let him borrow it for the occasion. And, Wil is all about the love ❤

During Spirit Week at school he makes up his own mind to play or not to play. If it’s wear black day, he may purposely avoid black — or go all in with hat, shirt, undies, pants, socks and shoes in black. If one of those pieces — even the undergarments — is not black, he may abandon the whole outfit even if we have minutes to leave for school. However the last time the school had Dutch Day, he spent careful time the night before selecting which Dutch shirt, which Dutch hat, and what pants and socks would go with.

On World Down Syndrome Day 3/21 (representing 3 copies of the 21st chromosome), ironically he has refused to wear his crazy socks on certain years. And believe me, he has a drawerful to choose from. He’ll wear his snowflake socks in July if they match his shorts. He wears his blue star socks whenever singing the Star Spangled Banner in choir. He has socks that look like a fish is swallowing your leg, which he said he’ll wear this 3/21, but I won’t know for sure until seconds before we leave for school if that choice will stand.

Wil could care less that you are wearing crazy socks on a certain day of the year. He’d get more joy out of your socks if you wore snowflakes in July!

Wil loves the Buddy Walk because it’s a big celebration of people in-person, coming together to enjoy a great day outdoors. Wil’s not out to make a calendar or societal-driven statement. Wil’s about making friends and living life fully his way.

Let’s celebrate Friendship over counting chromosomes. Let’s celebrate who we are behind the date on the calendar and behind the clothing. Let’s celebrate how different we are, and how different we aren’t. No matter what you wear, or what day you wear it, Wil will love you anyway, every single day of the year.