I love my kids, that really goes without saying. I love them every moment of every day.
But I also love being their mother.
I love the silliness of it
Like dancing in the aisle of super market because a fun song come on
Wearing the kids fun hats
Belting out theme songs, just because
(or in the case of my father - IT'S GROUNDHOG DAY!! At 7am, every.. single.. day - it was an improvement on GOOD MORNING VIETNAM!)
I love the silliness of dancing however my body feels like moving at the moment
You know that saying Dance like no one is watching - my new saying is dance like your kids are watching
Or even better - dance like you dancing with your kids!
I love the silliness of getting on the floor for some crawling contests
My kids think I am the most talented artist ever!
Be jealous of my stick figures! And I can (mostly) stay inside the lines
Needless to say I have the best decorated car on the block!
I never wanted a black car - but it makes the best canvas!
So today I am succumbing to the silliness of motherhood!
It's a good day.
A Journey with Love and Laughter
Read about our family as we journey through life as a family, with siblings, school and spina bifida, and lots of fun and laughter along the way!
More About Our Family
Showing posts with label our kids. Show all posts
Showing posts with label our kids. Show all posts
Friday, April 20, 2012
Monday, November 29, 2010
O Christmas Tree…
Every year we pick out the most beautiful Christmas tree. And after we defrost it’s time to decorate!
Katheryn thought the tree was great! Especially when we put all this stuff on it! That she can pull off and hide all around the house. At the moment we have most of the decorations on the top 4 feet of the tree, not so much on the bottom 3 ft.
And Nick is happy to play with whatever he can get his hands on! And by this I mean crawling over to get whatever he can get his hands on. He is army crawling all over the place! And sometimes getting his hips and knees helping as well.

So it might look like Katheryn is helping to decorate - but really it's the other way around. She LOVES those candy canes! I've actually taken off the hooks so she can carry and collect them around the house.
And a couple of really happy kids! Even if they do look kinda goofy in these pictures!
Katheryn liked that we had a TREE in the house! And playing with the branches that were taken off.
Then I take over. Decorating the tree, decorating the house, listening to Carols and teaching the kids all my favourites.
And Nick is happy to play with whatever he can get his hands on! And by this I mean crawling over to get whatever he can get his hands on. He is army crawling all over the place! And sometimes getting his hips and knees helping as well.
So this is the finished product!
And a couple of really happy kids! Even if they do look kinda goofy in these pictures!
Monday, October 18, 2010
Today I am a mother....
I think in my post yesterday I was a nurse.
And I even feel a little guilty about that. I feel that I should have a post praising my Nickolas and all of the other children and families who are here today. Not 'defending' someone took all of the good out of our lives. Who reminded us that there are people out there who thinks that a child with spina bifida deserves to die, or to never be born.
But I also had to recognize that I once faced that agonizing choice. The trial by fire. But I emerged unscathed. I triumphed. And I have the scars to prove it! (I was thinking that metophorically, then thought yes I do have my c-section scar.) And Nickolas has his scar. His scar that I am so proud of.
But today I am posting about love and joy and a choice to take a step of faith. Today I am posting about the amazing mothers and children that I have loved reading about and getting to know. I am proud to be a mother of a child with spina bifida. I am proud to have made my choice.
Today I am a mother and I am proud.
Spina bifida is about so much more than doctors appointments, medical jargon and surgeries. It is about love, hope and faith. It is about laughter and joy. It is about a child who teaches the parents what it is like to live. It is about miracles and much much more than milestones and accomplishments.
It is about being aware and proud and about redefinitions. It is about finding a family who knows exactly where you are and where you are going. It is about finding confidence and courage that you didn't know that you had.
That is what spina bifida is to me.
This is what every mother who blogged over the weekend about how much they were devastated and disgusted about what had happened in our community. I think this is the blog that I should have written as a mother.
Please look at other mothers who took this opportunity to express their joy at their children who also have spina bifida, who are not defined by a medical diagnosis, and are the best things that happened to their parents.
Joanna and Jet
Jill and Kingsley
Nicole and Annabelle
?Jen and Charlie (sorry I couldn't find your name - bad me!)
Selina and Madison
Kimberly and Jonathan
Star and Tanner
Sara and Ruth
Stephanie and Nathan
Cassie and Caleb - definitely check out Cassie's site - she is showcasing different kids with SB every day this month! - Nick was there with all of his superstar buddies!
Kari and Toby this site also has postings from other moms as well - great central resource!
Mom Dugan and Brenden - sorry I couldn't find your name!
I am SURE there are more postings out there. On top of whatever is on BabyCenter and facebook.
And because it's Monday - Lets talk about some meterstones!
-babbling - FINALLY - dadada and bababa are the favorites
-getting on his hands and knees - when he is angry or excited
-resting on his knees and playing with something elevated
-following directions - putting a ball in a basket when asked
-Eating table food
-actually eating any food he can get his hands on - he's our little land shark!
-Not falling over AT ALL when sitting
-Reeeeeaching forward for things until he is allllmost over onto his belly
-Knowing what he wants - if he wants to put his fingers in your ear, he pushes your head away
-Sleeping (mostly) through the night
-Cut his 5th tooth!
-started on milk! (Goats milk - great for the constipation problem) though a sippy cup
-entered into a battle of wills with his mother (has alot to do with the above point)
Sorry no pictures!
I was crazy busy last week, I presented my Master's (of Nursing) Research at a conference (and won an award) - Yay for me! And things have not settled down since!
I promise picture this week!
And I even feel a little guilty about that. I feel that I should have a post praising my Nickolas and all of the other children and families who are here today. Not 'defending' someone took all of the good out of our lives. Who reminded us that there are people out there who thinks that a child with spina bifida deserves to die, or to never be born.
But I also had to recognize that I once faced that agonizing choice. The trial by fire. But I emerged unscathed. I triumphed. And I have the scars to prove it! (I was thinking that metophorically, then thought yes I do have my c-section scar.) And Nickolas has his scar. His scar that I am so proud of.
But today I am posting about love and joy and a choice to take a step of faith. Today I am posting about the amazing mothers and children that I have loved reading about and getting to know. I am proud to be a mother of a child with spina bifida. I am proud to have made my choice.
Today I am a mother and I am proud.
Spina bifida is about so much more than doctors appointments, medical jargon and surgeries. It is about love, hope and faith. It is about laughter and joy. It is about a child who teaches the parents what it is like to live. It is about miracles and much much more than milestones and accomplishments.
It is about being aware and proud and about redefinitions. It is about finding a family who knows exactly where you are and where you are going. It is about finding confidence and courage that you didn't know that you had.
That is what spina bifida is to me.
This is what every mother who blogged over the weekend about how much they were devastated and disgusted about what had happened in our community. I think this is the blog that I should have written as a mother.
Please look at other mothers who took this opportunity to express their joy at their children who also have spina bifida, who are not defined by a medical diagnosis, and are the best things that happened to their parents.
Joanna and Jet
Jill and Kingsley
Nicole and Annabelle
?Jen and Charlie (sorry I couldn't find your name - bad me!)
Selina and Madison
Kimberly and Jonathan
Star and Tanner
Sara and Ruth
Stephanie and Nathan
Cassie and Caleb - definitely check out Cassie's site - she is showcasing different kids with SB every day this month! - Nick was there with all of his superstar buddies!
Kari and Toby this site also has postings from other moms as well - great central resource!
Mom Dugan and Brenden - sorry I couldn't find your name!
I am SURE there are more postings out there. On top of whatever is on BabyCenter and facebook.
And because it's Monday - Lets talk about some meterstones!
-babbling - FINALLY - dadada and bababa are the favorites
-getting on his hands and knees - when he is angry or excited
-resting on his knees and playing with something elevated
-following directions - putting a ball in a basket when asked
-Eating table food
-actually eating any food he can get his hands on - he's our little land shark!
-Not falling over AT ALL when sitting
-Reeeeeaching forward for things until he is allllmost over onto his belly
-Knowing what he wants - if he wants to put his fingers in your ear, he pushes your head away
-Sleeping (mostly) through the night
-Cut his 5th tooth!
-started on milk! (Goats milk - great for the constipation problem) though a sippy cup
-entered into a battle of wills with his mother (has alot to do with the above point)
Sorry no pictures!
I was crazy busy last week, I presented my Master's (of Nursing) Research at a conference (and won an award) - Yay for me! And things have not settled down since!
I promise picture this week!
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