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Location: Blogs The cure4treebeard Blog |
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| Posted by: Daddy |
9/25/2009 6:18 AM |
JT has absolutely been LOVING Kindergarten. It's been so good to see. He comes running out of the school everday shouting, "Mommy, look in my backpack at what I did today!" He just seems to love learning new things and is soaking it all up like a sponge. He's also making some friends. I am so happy for him in this arena - it's been long in coming. Overall my little boy is growing up right before my eyes. What a blessing - I remember when he was a baby and we didn't buy clothes in the next size bigger because we were afraid he might not live to make it to that size and now look at him. From the deepest parts of a momma's heart - thank you Jesus!
On the medical front, JT and I are currently staying in room 534 at Cincinnati Children's hospital. A couple of days ago a little black spot showed up on JT's lip and one on his hand. After our last scare Brian suggested I take some pictures and e-mail to our doctors in cincy. I did that yesterday morning and then around 11:00am I got the call from our nurse practitioner to get to the hospital right away. UGH! Quickly I called a friend to see if she could watch Justy until Brian got home from school (Thanks Mindy!) and then got home to pack up JT and me. We made it to Cincy in record time and got a direct admit to the BMT floor. They drew a CBC and blood cultures and initiated IV antibiotics - the big guns. His CBC came back totally normal. We've got to get to the bottom of this. Driving to Cincy on the drop of a dime is unsettling for our whole family and JT truly does not like being in the hospital much anymore (especially when he feels just fine.)
I'll post more after rounds, but for now we're just hanging out playing Rush Hour. Thanks for checking in. |
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Raise money for the National Foundation for Ectodermal Dysplasias simply by clicking your mouse! GoodSearch.com (powered by yahoo.com) is donating money to charities for use of their search engine. To use it, install the GoodSearch toolbar to the top of your browser screen and then type in the charity (National Foundation for Ectodermal Dysplasias) and then search as you would on Google.com or Yahoo.com. The NFED gets a monetary donation for every search! The more folks that know about this, the greater the donation to NFED, and hence the more money there is to fund research on Jacob's condition and others like his. Thank you!
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