01 July 2009

There's No Place Like Home, There's No Place Like Home ...

Now that we've recovered and caught up on some much needed sleep, we thought we'd better send out a post with an update.

First and foremost, we can not stop saying thank you to everyone who sent good thoughts our way, prayed for Cole, our doctors, nurses, and us. We are so so touched with everyone's generosity and love for our sweet and special son.

We finally made it out of the hospital last Friday (what seems like a month away) and have spent the last few days just recovering and trying to get back to our semi-normal life. The doctors were very pleased with the progress he's made, his head and incision look good. We head back to the doctor next week to get the shunt stitches removed and probably another CT scan -- pretty soon we'll have hit the two dozen mark on the CT scans. Cole is slowly returning to his old self - smiling more and more, laughing, playing with more toys, squealing. And his pal Ellie is glad to have him home, once she got done smelling him ALL over. As we expected, we took a few steps back with regards to sitting up and rolling over, but we're confident we'll be right back there soon.

He's still in some pain when we pick him up in certain positions. But that's to be expected with all of the work they did in his noggin. And he's still got some fluid sloshing around. We're on a strict routine to switch him from side to side about every two hours -- don't want to lose that beautiful new head shape. And that tends to cause some puffiness in one side or the other (depending on the side he's on). We've noticed a little bit of a droop in one eye (we saw some of it in the hospital but because he was so swollen, we couldn't decide if it was longer term effect) - we're waiting to see if it sticks around or is more like the palsy incident we had after his last shunt installation. It may be something we have to watch for and advice the surgeons on subsequent shunt installations ... hopefully years and years from now.

And he's still on his seizure medication as a precaution, because it's one of those meds you have to be slowly taken off (vs just stopping). We were able to switch him from Prevacid (for his reflux) to Zantac (thanks to his good and willing doctors and the good advice of one of our hydroparents). And he's been off his more serious pain meds (Lortab) for several days and we're only using Motrin every other day -- so hopefully we can be completely off of that as well. And his hair is really beginning to come back fast.

And with Cole doing much better, Shawn was able to return to group (thanks to his colleagues that filled in for him over the last two weeks), which meant a trip out to Grandma Jacquie's and Grandpa Keith's. Next, we're ready to where the therapists can start their routine ... a really positive step.
Thanks again to everyone - you mean the world to all of us.

7 comments:

Sara said...

Yay! Glad you are finally home. What a cutie! Not sure if I could smile if it was me in his shoes. What a trooper. We are keeping you in our prayers.

Colleen said...

You two make me feel like I was on vacation as a parent! I'm amazed at the faith and strength the two of you have! I just look forward to celebrating all the success of medical and faithful work. You two are an inspiration to anyone who is going through difficult times. I continue to pray for your family and wait and watch for the next update. Thank you! Colleen

The Heuristic Hall said...

Happy home! His is a lucky boy to have such amazing parents!

Anonymous said...

Shawn and Teri! what wonderful news! i am so happy to see that he pulled through so well. i can't wait until i can get back home to hold my little nephew! you guys rock. love and kisses!
-Penny

Eric and Lara said...

I love that smile. Good to hear your home and well.

Nicole said...

Your blog is amazing and inspiring, just like you! Glad you are home and doing well. Cole is blessed to have such loving parents!

jackelyn said...

I came across your blog, from a friend of yours and so glad to hear that he is doin better. MY son AJ is scheduled to have his cranial reconstructing done the of AUG at primary and dr. Walker is also his nuerosurgeon i would love to hear if you have any tips or advice im scared out of my mind. AJ is 7 months old with hydro,in case you were wondering. If you have the time please contact me at jackelyngaray@yahoo.com thank you and take care