Enjoying the Small Things

Enjoying the Small Things

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AOL Parentdish Interview

March 23, 2010 By Kelle

I was interviewed by AOL’s Parentdish last week.

Interview can be found on following link:

Blogger Kelle Hampton Touches World With Story of Down Syndrome – ParentDish

Happy Tuesday!

Filed Under: Designer Genes 126 Comments

A Celebration of Life

March 22, 2010 By Kelle

Yesterday was World Down Syndrome Awareness Day.
And I never thought I would ever be ‘celebrating’ it.
But yesterday, I did.

I woke up sad. The forecast predicted rain and storms in the evening and this was supposed to be my girl’s special celebration.
But more than that, I think I was afraid.
I was afraid I would get to the beach holding my white-gowned girl and see all these people together — the people who have been there for us through all of this — and it would hit me again. The loss of that dream and the sadness for what she may not have.

And as the morning dragged on, fear gripped a little deeper until I faced it hard. I looked that fear square in the eyes and told it to beat it.

This is a happy day. This is a glorious celebration. This is our testament to all of these people and to so many more that Nella is a blessing. Nella is a rockstar. And Nella is going to do great things. Today is beautiful.



And beautiful it was.

Beginning with this necklace (Thank you, Betsy) my dad gave me.

Three little copies of that beautiful 21st chromosome. How I love them.

The rain cleared just in time for our gathering and, as our car pulled into the very back parking lot of that quiet beach, my throat tightened hard. There were so many people standing there. Our people. And the cars just kept rolling in. And, as we climbed out to greet those we love, I was taken by how happy it was. No sadness. Just this amazing aura of celebration. Gratitude. And Life…in it’s purest, most beautiful form.

Did I cry?
Oh, yes.
I cried the happiest tears.
And a little bit of sad ones too.
I cried when my friend sang “Somewhere Over the Rainbow” and I cried when Katie read the line in the Welcome to Holland poem that says “the pain of that will never, ever, ever go away.”
But, mostly, I cried tears of thankfulness for the amazing blessing of the girl I held in my arms and what she has done, is doing and will do for our family and our friends.

And as the sun went down and the whole lot of us stood there celebrating this beautiful amazing life we’ve been waiting for, I couldn’t help but be proud. …Of the amazing journey these eight weeks have brought us.

I am happy to be here…in Holland.

And we were blessed to have friends from Holland attend last night…and they made me an honorary resident…

…and blessed Nella with her first real pair of beautiful, pink, perfect wooden shoes.


Thank you, Jan & Francien!

It was perfect.

And just kept getting better.

After sunset, we gathered for a party.
Here I was all day, afraid of the evening being sad.
Oh, it was anything but.

There was so much life last night.
There was laughter. And Music. Candles. Huddles of warm bodies in every corner of the room. Wine glasses toasting and baby trade-offs. I couldn’t stop smiling and thinking this was exactly what it’s supposed to be.
A celebration of beautiful, amazing, unexpected Life.

My favorite moment of the evening?

The sky lanterns (thank you Aunt Janie for the idea!)

We gathered poolside. We listened to her song. And we watched as these big beautiful illuminated lanterns were ignited and set free. We watched as the dark sky welcomed their warm glow as they drifted far above us…slowly and beautifully.

Okay, I cried then too.

The night went on as did the celebration.

And 3-21 will go down as a triumphant festival of big, beautiful Life.

Yesterday was World Down Syndrome Awareness Day.
And I was proud to be celebrating it.

We are so thankful for our family. For the two brothers who provide so much love for these girls. For our spirted little firstborn. And for our precious, amazing little bunny.

Yes, Nella is a blessing.

And Nella is a rockstar.

Happy World Down Syndrome Awareness Day to all of the amazing families we share this journey with! And thank you to everyone who has embraced this new journey with us. We can’t wait to see all the good stuff that extra chromosome’s gunna give us.

And to anyone interested, the sky lanterns are earth friendly and can be found here. They are worth every penny.

Filed Under: Designer Genes 280 Comments

Rockstars and such.

February 28, 2010 By Kelle

It has recently been brought to my attention that, two years ago, on this very blog, on the eve of my thirtieth birthday, I wrote the following in my post:

“I took all the twenties and kissed them good-bye tonight…tucked them away in boxes with all their sweet memories and sorrows…

…and once the twenties were safely stored and a proper farewell was said, I brought out the new box. I can’t see in it yet, but I can tell just by the outside that there is beauty inside. Sorrow too…yes, I’m sure. But there is in every box, and this one seems to come with more coping skills. More growth. More experiences. More challenges. More love.
I can’t wait.”


Little did I know…behind the flaps of that mysterious box was, indeed, love.

Quite prophetic, really.

I’m almost ready to cut my hospital bracelet off…almost. It’s just that it’s the last physical link to this entire experience and I still think about it like crazy…the shock still, I guess, and I’m wanting this thought process to die down because it is consuming.

The Power of the Mind.
It’s amazing what control we really do have over our thoughts and what tactics we use to control it. Like, seriously, envisioning myself as a rockstar really makes me think I am one. And I tell myself every day I am going to rock this day out. Even when I want to cry and stay in bed. It becomes such a challenge to myself to see exactly what I am capable of and usually, the more down & out I feel, the more I rock it out. And that doesn’t just pertain to this whole D.S. thing. It’s all the crap in life…just rock it out.

My sister says picture a person who models what you’re going through exactly how you’d want a role model to show it. Then become that person.

And that, I try to do.

With all that said, this blog has been the most necessary form of therapy for me and while I have had questionable views on various forms of socialization in the Internet before, I shan’t any longer. I may not update my Facebook status every two hours with what I’m eating or where I’m going, but I will give credit where credit is due…and that is the pure good in human kind and the soul balm you all have been in your comments and e-mails…even phone calls from ‘strangers’. I have come to ‘know’ so many of you and have been slowly healed by the photos and stories you have sent.

Do I read all the comments? You betcha. Every one of them. Often in the middle of the night from my phone while I am nursing the wee babe, but I have read them. And they are so incredibly touching. There’s just so many good people who really do care about others who are hurting. And so many good mamas and daddies out there who are all striving for the same thing. Who love their babies and want to suck every bit of popsicle juice out of this Lifecicle.

And who knows…the Facebook updates may come…

Kelle Hampton is going to the bathroom. Kelle Hampton is nursing her baby. Kelle Hampton is laughing because updating in third person is really funny.

I actually forgot, for a minute, what I used to write about on here because I’ve been using this as total therapy lately. I’m beginning to bore myself. We’ll get back to funny, random, beautiful moments eventually. And, for God’s sake, I’ll turn the sappy music to something more fun soon, but there’s so many clicks still being made to the birth story post and Play that Funky Music, White Boy doesn’t really jive with that kind of seriousness.

Needless to say, I’m craving that propeling force of Moving-on.

And let me make a tangent here for a moment to clarify the Holland thing. To all the beautiful Dutch readers, I would LOVE to visit Holland someday and my slander of wooden shoes was only referencing one of my crazy analogies brought on by this poem, a poem I actually think is beautiful…just a bit skewed as it likens having a special needs child to traveling to Holland as opposed to Italy. The only thing I have a problem with is the ending…that special needs’ parents will always grieve never getting to Italy…to which I say…GO THERE! No one said it was an imprisonment to one particular place. Perhaps it may take a little more effort to get there, but never say never.

In other news…

Our puzzle has been complete these past couple days because our much-loved Daddy is here, filling all the empties we’ve had while he’s been away.

And we’ve been talking a lot lately about how our family is fueled by togetherness, and I’ve needed that so much more lately…because nothing is more important than family. And, I guess the absence of that feeling has fueled it even more and caused us to dig deeper into what life is really about and what goals we will make efforts to strive toward. With us, it always leads to each other. To our kids. And to the little moments we make with them…moments that carve deeper impressions than money ever can.

I love our daddy.

This weekend was again somewhat chilly for Southwest Florida standards, so we cozied up inside enjoying cozy things like homemade lemon poppyseed scones (okay, I lied. They weren’t homemade. They were these from Cost Plus, but, with a smattering of butter, they were amazing), and long afternoon naps.

Nella is getting amazing with her neck muscles…something that’s apparently delayed with D.S. A little tummy time and the girl becomes a freaking rocking horse, froggy legs all hoisted behind her and that precious little head just a stretchin’. That’s because she’s a rockstar, you know.

And Miss Lainey. Her head cold gives her the cutest stuffy voice, but it comes at the expense of a very runny nose which, if you’re not watching, gets wiped on couch arms, dish towels and, um…Nella’s clothes. But she’s still a rockstar too.

And she hasn’t left Brett’s side since he’s been home.


And, perhaps this is the world’s most boring post…because I’m beating a dead horse here…but I had a bit more emotional blah-blah I had to spew before I get over the hump to more thought-out posts.

I did promise a few F.A.Q.’s. though.

A: Where do you get the knits?

My mom has made a lot of them and then people found out I’m in love with homemade baby knits, so they’ve bought them for me for gifts. But I have, over the course of taking newborn photos and obsessively scouring Etsy shops while pregnant, stocked up.

Some favorite Etsy shops:

Huggabeans
The Bee’s Nest
Wanderlust Creations

B. Lainey’s Clothes

I get a lot from the coolest consignment shop here in Naples, Once Upon a Child, which is totally stocked with fantastic finds.
And then Baby Gap, Children’s Place, Costco (yes, Costco) and wherever else we might happen to find something on sale.

C. What does Brett do?

He sells software.

D. How do you find time to do everything?

I don’t. I can only juggle so many balls and, while I choose to keep one up, another falls. And when I pick that one up, another falls. And so on. However, I always make time for babies. For snuggling them, loving them, holding them…even if it’s while I’m doing something else.

Which brings me to bed time. The girls are jammied and ready and all the balls get dropped at this time of night while I cherish my favorite task of all. Inhaling their goodness…their littleness…and the opportunity of moments I can never get back years to come.

My littles await.

Tell Facebook Kelle Hampton is loving her girls.

Filed Under: Coping, Designer Genes, Fashion 355 Comments

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