Wow! Christmas Break was a little hectic! We began our journey back to KY by loading two kids (under the age of 20 months!), 4 suitcases, a diaperbag, purse, stroller, carseat...need I go on... into the car and headed to the airport. I think next time we travel I am going to make a strict "no shoes policy" for everyone. I mean come on- I am not hiding a bomb in Ava's shoes. And if airport security even had an idea of how long it took us to convince her to even put them on, they would have mercy on us. So here we go... first take off mommy and daddy shoes, belt, empty pockets, large jewelry. Then onto the kids- Ava gets out of her carseat and runs like a toddler who has sipped one cup too many of fermented apple juice through the security point- only to be escorted back to me so that I can remove her shoes. All the while Daddy is working on getting Tal out of his carseat without waking him- not an easy task when his sister is screaming at the top of her lungs while I try and put her shoes BACK ON! So we are already exhausted and we haven't even begun! I once had someone tell me to just sleep on the plane- they obviously don't have children! Once we got past security, having already explained to many people that we need the water to make the formula and the liquid tylenol for teething, we were on our way. The plane rides- yes we had a connection- were uneventful for the most part. It was great to be home!
Ava Ryan playing with her buddy, Cooper

Ava and Cousin Emma at the bowling alley- Ava thinks if she holds the i-pod up to her ear that she'll be able to hear the music

Maguet grandchildren- look how tall Ava is!!



Granna holding Tal on his 1st Christmas

Mommy-Anne (great grandmother), Daddy Buck(great grandfather), and Baby Talmage
Ava and Mommy just hangin out
We also found out that Talmage has a rare metabolic disorder called galactosemia. This is a disease where the body lacks the enzyme to break down lactose (to make it as simple to understand as possible) and therefore he cannot have any form of milk product or he could get very sick. After a lot of tears and many nights spent on the internet (only to find out worst case senario information) we took him to an endocrinologist for further blood testing. The results were more than we could hope for. We found that he has a variant form of galactosemia called duarte galactosemia. Basically, this type only requires that he be on soy formula for the first year of life, then after another blood test and a "milk test" he should be able to be on a normal diet for the rest of his life. We were so lucky and relieved that he didn't have Classic Galactosemia which is the type where all dairy would have to be removed for the duration of his life. So we dodged a huge bullet. I always wondered why Matt and I were in TX and now I think that I have my answer- TX is only one of a very few states that test newborns for metabolic disorders twice (once at birth and again at 2 weeks). Had we been in KY, we might never have found this given that it didn't show up on his first test, and could have a very sick little boy on our hands.
So now we are back in TX and back in the swing of things. Being a mother of 2 young children is not an easy task. The house is always a mess, it is never quiet, and someone is ALWAYS hungry! But I wouldn't have it any other way. I enjoy seeing them grow and change everyday and know that I will never have a chance to get back these precious moments. So I am trying to drink it all in and take lots of pictures which I will post very soon!












































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