Monday, September 28, 2009
Happy 3 Month Birthday Jaylynn!
Happy 3 Month Birthday beautiful sweet girl! You are such a sweet baby. Smiling and cooing. You even like Daddy now. You still love cuddling with Jasmine but have found a friend in James too. Jenna and Jacob keep you laughing. I love that big toothless grin. We are so blessed to have you.

Wednesday, September 23, 2009
Jaylynn already thinks she can talk
She's going to talk sooo early. *sigh*
Miss Blue Eyes
Look at Jaylynn's eyes. Can you believe how blue they are? Gorgeous. I hope she keeps them. Well I wouldn't be sad if they turned green. ;-)

And three other sweet pictures

And three other sweet pictures
Friday, September 18, 2009
Fabulous Friday Foto
I'm totally stealing the Fabulous Friday Foto idea from my friend Alida. Such a cute idea and another great reason to post pictures of my adorable kiddos! So here is today's fabulous foto. A sweet moment with Jenna and Jaylynn. Love those smiles!

Wednesday, September 16, 2009
A Smile to Light Up a Room
You could have the worst day ever and come home to your kids with their smiles and hugs and it's all better. Jaylynn's smile definitely makes everything all better. Those cheeks. I think I'm spotting dimples too. Melt. My. Heart.

After Tracy commented about Jaylynn looking more like Jenna, I had to go find this picture. Wow! Check it out! This is Jenna at 3 months old.

After Tracy commented about Jaylynn looking more like Jenna, I had to go find this picture. Wow! Check it out! This is Jenna at 3 months old.

Happy 4th Birthday Jenna!
Jenna, our punkin. Happy 4th Birthday sweet girl. I know I always say it but where has the time gone? It seems like just yesterday that Daddy was wheeling me upstairs only to miss you being born while parking the van. You are an amazingly funny and opinionated child. You make us laugh all the time with your funny faces and hilarious things you say.
We love you so much Jenna. Thank you for all the laughs you give our family.

These are more like Jenna!


Some of my favorite pictures of Jenna over the last 4 years (in no particular order).
Click here for the posts labeled with Jenna's name.
Birthday cake time! **Nothing fancy. She's getting her fancier cake on Sunday when Opa, Oma and Uncle Boo come over.**
Daddy singing "you look like a monkey and you smell like one too" made her crack up.

Blowing out the candles

On Sunday, Oma & Opa came over for cake and to watch the Redskins game. Jenna opening up all of her Barbie gifts from Oma & Opa.
Opening her Barbie movie which came out the day before her birthday. She actually cried when she saw the commercial on her birthday and she hadn't gotten it.

We love you so much Jenna. Thank you for all the laughs you give our family.
These are more like Jenna!
Click here for the posts labeled with Jenna's name.
Birthday cake time! **Nothing fancy. She's getting her fancier cake on Sunday when Opa, Oma and Uncle Boo come over.**
Daddy singing "you look like a monkey and you smell like one too" made her crack up.
Blowing out the candles
On Sunday, Oma & Opa came over for cake and to watch the Redskins game. Jenna opening up all of her Barbie gifts from Oma & Opa.
Opening her Barbie movie which came out the day before her birthday. She actually cried when she saw the commercial on her birthday and she hadn't gotten it.
Monday, September 14, 2009
RIP Patrick Swayze
The other Mom
Jasmine is also known as being the other mom in the house. I often call her Little Mama. I always say that if something happens to me tomorrow that Jasmine would take right over for me and take care of everyone. Very rarely do I actually ask her to help. She most often asks what she can help with or just does it on her own. She is a tremendous help to me. You can obviously tell from the pictures how much Jaylynn loves her big sister. Look at the hold Jaylynn has on her! She almost always calms down whenever Jazzi picks her up.
**Don't mind Jazzi's towel on her head. She had just gotten out of the shower.**
Sunday, September 13, 2009
We are so mean!
It was bed time tonight. We told Jenna it was time for her to go to bed. Now I will be the first to admit, I am super lucky with my kids when it comes to bed time. I may here a groan or two but I've never had to fight with my kids when it's time for the sand man to come. So we got the usual groan from Jenna, followed by stomping into her room and some grumbling under her breathe ~ loud enough for us to hear her talking but not loud enough to know what she said. I did catch the word dumbest though. (Some may call this the Jacqueline attitude and I'm still trying to figure out how my parents didn't kill me.)
We called Jenna back into our room to inquire about her choice of words. After a few back and forth words of trying to get her to tell us, we were finally informed that bed time tonight was "the dumbest, worst thing ever to do." Being the totally mature parents that we are, Jamie hid behind his blanket laughing his butt off. I bit my cheeks while trying to tell Jenna that while she may think that she still had to go to bed.
Jenna is so lucky that I have that same attitude and can so relate to how the whole world is against her. I sympathize with my girl. I think that's the only way she has made it close to her 4th birthday.
We called Jenna back into our room to inquire about her choice of words. After a few back and forth words of trying to get her to tell us, we were finally informed that bed time tonight was "the dumbest, worst thing ever to do." Being the totally mature parents that we are, Jamie hid behind his blanket laughing his butt off. I bit my cheeks while trying to tell Jenna that while she may think that she still had to go to bed.
Jenna is so lucky that I have that same attitude and can so relate to how the whole world is against her. I sympathize with my girl. I think that's the only way she has made it close to her 4th birthday.
Saturday, September 12, 2009
Jaylynn's Zebra Friend
Jaylynn loves her zebra buddy. I also think Jaylynn knows she's numero seis so she has got to start talking earlier to be heard in this house!
Friday, September 4, 2009
Jacob's heart
Jacob went to the cardiologist this morning. Our pediatrician thought it would be best that he go. He's always had a slight heart murmur. He also has pectus excavatum. Jacob's is not severe. You wouldn't even notice it really unless you were looking for it. His left side of his chest is bigger than his right. Those two things separately aren't a big deal but together could mean something.
We went in and they did an EKG right there. Everything looked normal on that but he said there is about 10% of kids that still have something wrong. He did an echo cardiogram as well to check everything out. Jacob is one of those 10%.
He has aortic stenosis. Here's the medical description of it: The aorta is the main artery leaving the heart. When blood leaves the heart, it flows from the lower chamber (the left ventricle), through the aortic valve, into the aorta. In aortic stenosis, the aortic valve does not open fully. This restricts blood flow.
He also has a bicuspid aortic valve. The medical description of it: A bicuspid aortic valve is an aortic valve that only has two leaflets, instead of three. BUT Jacob's is a bit different. He has three leaflets but they aren't sized equally (which they should be) and two are starting to fuse together (which is not good at all and should not be showing up in a 5 year old).
Jacob's condition is considered a mild to moderate case at this point. Because the doctor has no baseline for him right now, he has to go back in 6 months to have all the tests run again. He has no idea if he was born with it or if it's changed over time.
We really have no idea what the future holds for Jacob at this point. We'll have a better understanding in 6 months to see if there is any change. He will eventually one day need valve replacement surgery. Again, in 6 months, we'll know better when that would be.
As of now, he's not restricted in anything he does. He does have to have antibiotics before any medical procedures including going to the dentist. That will be for the rest of his life. Later on, he will more than likely never be able to do contact sports (and I'm not signing him up for t-ball or football any time soon either). If he receives a hard hit to the chest, it could cause damage. He also couldn't be a power lifter either (sorry Schwarzenegger, who has had three valve replacement surgeries because of this) as this would put too much pressure on his heart. If we notice him getting tired easily while he plays or complaining his chest hurts, he needs to come back before the 6 months.
All the other kids have to go in. This is genetic and comes from either Jamir or I. We both have to go in and get tested as well.
So while we are devastated by the news, we are grateful that we know about it so now he can be monitored. We are praying that none of the other kids have it.
And just because he's so darn cute....

We went in and they did an EKG right there. Everything looked normal on that but he said there is about 10% of kids that still have something wrong. He did an echo cardiogram as well to check everything out. Jacob is one of those 10%.
He has aortic stenosis. Here's the medical description of it: The aorta is the main artery leaving the heart. When blood leaves the heart, it flows from the lower chamber (the left ventricle), through the aortic valve, into the aorta. In aortic stenosis, the aortic valve does not open fully. This restricts blood flow.
He also has a bicuspid aortic valve. The medical description of it: A bicuspid aortic valve is an aortic valve that only has two leaflets, instead of three. BUT Jacob's is a bit different. He has three leaflets but they aren't sized equally (which they should be) and two are starting to fuse together (which is not good at all and should not be showing up in a 5 year old).
Jacob's condition is considered a mild to moderate case at this point. Because the doctor has no baseline for him right now, he has to go back in 6 months to have all the tests run again. He has no idea if he was born with it or if it's changed over time.
We really have no idea what the future holds for Jacob at this point. We'll have a better understanding in 6 months to see if there is any change. He will eventually one day need valve replacement surgery. Again, in 6 months, we'll know better when that would be.
As of now, he's not restricted in anything he does. He does have to have antibiotics before any medical procedures including going to the dentist. That will be for the rest of his life. Later on, he will more than likely never be able to do contact sports (and I'm not signing him up for t-ball or football any time soon either). If he receives a hard hit to the chest, it could cause damage. He also couldn't be a power lifter either (sorry Schwarzenegger, who has had three valve replacement surgeries because of this) as this would put too much pressure on his heart. If we notice him getting tired easily while he plays or complaining his chest hurts, he needs to come back before the 6 months.
All the other kids have to go in. This is genetic and comes from either Jamir or I. We both have to go in and get tested as well.
So while we are devastated by the news, we are grateful that we know about it so now he can be monitored. We are praying that none of the other kids have it.
And just because he's so darn cute....
Wednesday, September 2, 2009
Jaylynn's 2 Month Check-Up Stats
Jaylynn had her 2 month check-up today. :-( I hate the 2 month check-up. Too many shots. Poor girl was screaming and Jenna was a mess. We survived though and now she is conked out.
She is growing great and doing really well. The doctor didn't have any concerns.
Jaylynn now weighs 9 lbs 10 oz and 22 inches. She's had a busy few weeks of growing. I was finally noticing her getting heavier and filling out her car seat better. I have no clue what percentile she is. I don't get hung up on those. My kids will grow the way they grow and as long as they stay on their own up curve of growth, I'm not worried.
And here's a picture of her from her 2 month *birthday* (yes, I know I just posted it but she's so dang cute).

Jaylynn's 2 Week Check-Up Stats
She is growing great and doing really well. The doctor didn't have any concerns.
Jaylynn now weighs 9 lbs 10 oz and 22 inches. She's had a busy few weeks of growing. I was finally noticing her getting heavier and filling out her car seat better. I have no clue what percentile she is. I don't get hung up on those. My kids will grow the way they grow and as long as they stay on their own up curve of growth, I'm not worried.
And here's a picture of her from her 2 month *birthday* (yes, I know I just posted it but she's so dang cute).
Jaylynn's 2 Week Check-Up Stats
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