Monday, April 1, 2013
Happy Spring Break: Quick Post With More to Come
We have just got home from the conclusion of a wonderful Easter weekend with family. The kids ate great, played great, slept great, with some minor car ride hiccups on the way home due to Wee Pie's busted lip. His face and the back of a chair met. It wasn't a pretty sight. We thought for a minute we would be at the emergency room today, but it was bloodier and nastier than it was deep.
The car ride was also lengthened due to our overwhelming urge to visit the fictional town of "Woodbury" from our favorite show, The Walking Dead. (Yeah, we are dorks like that.) We weren't able to get out and sight see due to an unhappy babe in the back, but now we know where it is filmed. I am excited to go back and actually look around next time we visit family.
So more on Easter with pics and posts to come. Let's officially ring in the Spring Break and let the fun and laziness around the house begin. First stop, laundry all day tomorrow to catch up along with dinner at Loves Seafood later tomorrow night with Aunt BT and Uncle Mike. Did I mention we got home tonight and I realized we have only a smidgen of milk and no laundry detergent? Oh Well! Who Cares?! Its Spring Break!
Wednesday, March 27, 2013
Thursday, March 21, 2013
World Down Syndrome Day and Lots of Socks
Happy World Down Syndrome Day! Celebrated on 3/21 to signify the trisomy on the 21st chromosome. I spread the word by mouth and facebook to wear funky socks for the lots of socks campaign.
I got to school and was greeted with some sock wearing companions waiting on the kids to get off the buses. Socks on their pants, toe socks, and pants rolled up with funky socks showing. I was ready to spread the word and explain my socks, but only one person asked me why I was wearing my socks. Not even my students noticed. So I was a little disheartened reflecting on it as I rode home. But then I logged onto facebook and found this...
And this from Grayson's Aunt BT...
And this...
And this from Wee Pie's other aunt, Aunt Nikki...
All the pics and posts were full of comments and questions about the lots of socks campaign, Down syndrome, and of course wonderful compliments for Grayson's pure sweetness. Thanks so much from all the supporters of the campaign and the day to raise awareness for Down syndrome. It made my day to see others sharing information and support for our DS community. Lots of love!
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My Socks |
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"Rocking my socks today ;)" (from my friend Sarah) |
And this from Grayson's Aunt BT...
And this...
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"Happy to celebrate recognition of world down syndrome day" (from my friend, Jodi) |
And this from Wee Pie's other aunt, Aunt Nikki...
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"It's Down Syndrome Awareness Day! Over 400,000 people have DS including one of my favorite nuggets, my nephew Grayson. I am so proud of him and can't wait for his sloppy kisses at Easter." |
All the pics and posts were full of comments and questions about the lots of socks campaign, Down syndrome, and of course wonderful compliments for Grayson's pure sweetness. Thanks so much from all the supporters of the campaign and the day to raise awareness for Down syndrome. It made my day to see others sharing information and support for our DS community. Lots of love!
Wednesday, March 20, 2013
Monday, March 18, 2013
Still Not Sweatin' It or My Way of Sharing World Down Syndrome Day (3/21) or Our Trip to the Zoo
Why am I not sweatin' the petty stuff or pettin' the sweaty stuff?
Because I am beginning to learn that I just shouldn't. I have spent the last 2 years in a state of worry. I've spent them in a state of woe or even mourning, but I don't think that is the true description for it. I've just been different. Not myself. Sometimes I didn't even like myself. I would be in the moment, not being myself, knowing I wasn't being myself, and yet I still acted not myself! It was frustrating. I cried to Drew about it, my mom, my close friends. Why couldn't I just be me again? What happened to me? Is this what I was going to be like forever? Is this what a stressed out mom, teacher, parent of a special needs child, and wife acted like? I lamented who I used to be, I grieved over who I was becoming, and I longed for the old me.
But I am slowly coming to realize that I will never be that person again. A lot has happened in my life in the past two years. I had Marloe, got pregnant with Grayson 6 months later while still learning how to be a mommy, then found out at birth that Grayson had Down Syndrome. I can't be the same person after going through all of those life changing events in less than two years. I am just now realizing that a year and a half later. I am beginning to accept who I am now, in the present.
The lamentation over the past me is slowly staying where it should stay...in the past. I like this newness. I like the feeling of accepting where I am in life...Finally! I feel fresh, excited, like anything is possible. Bring it on Spring! I welcome your growth. I am going to grow with you.
March 21st marks World Down Syndrome Day. This is a day to raise awareness for people with Down Syndrome. But for me, every day is Down Syndrome Day. This is my life. I want to raise awareness every day. I want to tell my story to the world. That's why I started this blog. Its been so therapeutic to just get my thoughts out and maybe someone, somewhere is learning more about people with Down syndrome because they clicked my link or found me in this great big "web." I hope so. I know reading other parents of Down syndrome children's blogs like Noah's Dad, Pudge and Biggie, and The Bates Motel has helped me. They have inspired me to share our life. Of all the resources, books, pamphlets, and websites out there on raising children with Down syndrome, other parents' stories have been the most helpful.
I have a special needs son, a typically developing daughter, and a wonderful husband who I share my crazy life with. I have a great supporting community of family, friends, and co-workers. And yes, Grayson has delays. He has therapies. Yes, I have to explain to strangers and acquaintances why he isn't walking yet or what living with a child with Down Syndrome is all about. But I don't care. I want to do that. I love talking about my children. Above all the diagnosis and chromosome counting, Grayson is my child, my son. He is my wonderful, curly haired, blue eyed, funny, stubborn, snotty, slobbery, and loving son.
And now more pics of Our Trip to the Zoo
Hopefully I will post my Wordless Wednesday and make a post on 3/21, but if not
Happy World Down Syndrome Day! I'm loving all of my world Down syndrome days for the rest of my wonderful life!
Grayson didn't want to turn around to take the picture. |
Me preggers with Grayson and really really a Blondie! |
The lamentation over the past me is slowly staying where it should stay...in the past. I like this newness. I like the feeling of accepting where I am in life...Finally! I feel fresh, excited, like anything is possible. Bring it on Spring! I welcome your growth. I am going to grow with you.
March 21st marks World Down Syndrome Day. This is a day to raise awareness for people with Down Syndrome. But for me, every day is Down Syndrome Day. This is my life. I want to raise awareness every day. I want to tell my story to the world. That's why I started this blog. Its been so therapeutic to just get my thoughts out and maybe someone, somewhere is learning more about people with Down syndrome because they clicked my link or found me in this great big "web." I hope so. I know reading other parents of Down syndrome children's blogs like Noah's Dad, Pudge and Biggie, and The Bates Motel has helped me. They have inspired me to share our life. Of all the resources, books, pamphlets, and websites out there on raising children with Down syndrome, other parents' stories have been the most helpful.
I have a special needs son, a typically developing daughter, and a wonderful husband who I share my crazy life with. I have a great supporting community of family, friends, and co-workers. And yes, Grayson has delays. He has therapies. Yes, I have to explain to strangers and acquaintances why he isn't walking yet or what living with a child with Down Syndrome is all about. But I don't care. I want to do that. I love talking about my children. Above all the diagnosis and chromosome counting, Grayson is my child, my son. He is my wonderful, curly haired, blue eyed, funny, stubborn, snotty, slobbery, and loving son.
And now more pics of Our Trip to the Zoo
Marloe giving tokens to a wildlife project. |
Grayson watching tortoises. |
Family Shot with Nana (my mom) |
Nice people offered to take one of all of us. |
Now if only we were all cooperating...Marloe! |
Taking a break on the playground. |
Such a Little Sweetie! |
Happy World Down Syndrome Day! I'm loving all of my world Down syndrome days for the rest of my wonderful life!
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