Skip to main content

At Last!!


Baby Gavin arrived into this world at 7:02 pm tonight! Megan pushed only 15 minutes, and he is perfect! He looks just like his sisters- which means, he looks just like his daddy. He weighed 8lbs 1.5 oz and is 20.25 inches long. He has a head of blond hair and very long fingers and toes. His little cry sounds just like Girlie and Julia. Here are some pictures of the sweet boy for you to enjoy!





Comments

Anonymous said…
He he so beautiful!!!!
March 4, 2008 at 10:28 PM
Anonymous said…
thanks for the update tali!

hugs to the newest baby in your extended family,

the nam fam
March 5, 2008 at 6:46 PM
Anonymous said…
so sweet!
March 6, 2008 at 11:38 AM
Post a Comment

Popular posts from this blog

Diagnosis and Grace

Friends- "God is our refuge and strength, a very present help in trouble" Psalm46:1 Much has happened since I last wrote only 2 short days ago. We found out much later that night a new diagnosis, that our sweet boy has leukemia . We were not completely shocked but we were certainly shaken. After I posted about what was going on at Shady Grove, and we waited a bit more for some results, and we were informed that we needed to take Jack to Children's Hospital in DC for further testing with specialists. This raised our concern level quite high as you can imagine, that even with a snow storm coming, we were needing to make this trip. I began to google the combination of things they had found in the tests done on our little boy (swollen spleen, low platelet count , swollen lymph nodes) and came up options that were NOT Lyme disease, although a few of these symptoms did also look like Lyme. As a result of the google quest, I came across some concerning outcomes, one of the most
57 comments
Read more

.Results and Re-Admission.

I am so happy to share that the results from the bone marrow biopsy came back with the results we had hoped and prayed for! They said they found less than 0.1% Leukemic cells in his bone marrow!!! So this is such great news! The prognosis is a good one, and now we get to keep marching on into the next 3 years of making sure the Leukemia does not come back and he is fully in remission! Thank you all so much for all the prayers said on our behalf! I also have the happy report of how last night and this morning went as well... So last night, we woke Jack up at 11:30 to feed him one last time before midnight. He was so sweet and groggy but ate a bunch of nuggets and french fries. We gave him a bottle and put him in bed at midnight and hoped for the best... well, he did not wake up again until 4:45... which was AMAZING for us and him! That was a long stretch for the little guy! After that he cried for a while and Jordan tried distracting him with books and holding him for a while. Jordan w
18 comments
Read more

.Please Pray.

It is hard to believe it has been a month since we first heard the words Leukemia from the Doctors at Children's Hospital. Is it possible for the days to be both long and fast and the nights to seem like they will never end, and yet they are all too short? Many days, by the time is is 5:30 or 6, I feel like I am about to loose my mind! Jordan coming home is the sweetest sight for me, and the boys! I think it is a universal law, that dinner time, no matter the circumstances of life you are in, is just tricky if you have children! And this month has been no exception. There are two reasons why I title this post as .Please Pray. One is that tonight is THE LONG ONE....after midnight, Jack is not allowed to eat until 10 or 11 am after his procedure. If you have been following the blog or talked to us, you know that this is no small feat. He has for the past 3 weeks been awake every 2 hours or so with several nights being every 20 minutes asking for food to eat- which he has eaten all of
16 comments
Read more