Just to keep you updated on David.
OPERATION DAY: DAY ZERO. The surgery went "without a hitch!" We arrived at the hospital around 6 a.m., and the operation "actually started" by 9:20. I was so happy and relieved to talk to the doctor around 2 p.m. when he was all sewn up again!
Relatively speaking, he had a pretty good night. Some nausea. They woke him up every hour to poke and bother, so sleep was pretty choppy. But he looks better than yesterday right after surgery, and the pain has so far been kept in check. Of course each hour/half-day will bring new challenges.
We have felt so much support from everybody. Thank you for fasting and praying in his behalf. I think there is more power in those 2 things than we realize.
Tuesday, DAY 1: A lot of people came in and out. Nurses check vital signs every couple of hours. The Dr. checks in, the anesthesiologist, the "C.A."--can't remember what that one stands for. Also the Pain Management guy.
He is encouraged to breathe deeply every hour, with a plastic tube thing, to expand his lungs and keep them active. They stopped the constant flow of morphine this morning; now he has only the pump. (When he's uncomfortable, he can press the pump button. He doesn't press it very much.) He hasn't complained or been in TOO much pain. Maybe he got Mom's "high tolerance" for pain after all. We hope.
They took out the drain tube that was collecting fluids from his back. Now the body should start absorbing that fluid, they say.
They say the more active the kids are after surgery, the quicker they feel comfortable doing things. They encouraged him to sit up today: the nurse brought in a big recliner-type chair, and they got him sitting up on the bed and then into the chair. Upright is better than laying down, they say. Once in the morning and once late afternoon, for a total of 3 1/2 hours in the chair. For "Day 1," that is great, they keep saying.
The movement made him nauseous but they put a dramamine-type patch behind his ear. He hasn't been nauseous since. Movement wipes him out completely. His eyes droop and he's out for 60-90 minutes after exerting the energy.
He has "air-boots" on his calves, pumping air like a blood-pressure cuff. It's supposed to keep the circulation active in his legs while he's lying there so much.
Another HUGE blessing is that he's in a room by himself! For now. No guarantees, of course, that he'll stay here the whole time. There are only 6 single rooms on the floor, and they are reserved for kids who will be here for extended (long, long) periods of time, or contagious kids.
He has been drinking water and apple juice this afternoon. Maybe we try crackers tomorrow. :)
Tuesday, March 9, 2010
Here We Go...
Posted by Kari at 5:50 PM 4 comments
Friday, February 19, 2010
Winter Break Week!
Here's an old concept in New England: the public schools get TWO spring breaks: one in February, one in April. (Now you know why we go to school through the end of June, here.)
I think maybe because winters are so long here, they like to give people the chance to vacation away where it's warm, or vacation to somewhere where there's really good skiing. They have resorts here, of course, but no huge mountains.
(Now that I've offended all the New England skiers, I'll backpedal a bit with "Your national parks are beautiful--great hiking trails everywhere! Cross-country skiers have it made, too! It's even fine to learn to downhill ski here. It's just not the Rockies.")
So, for those of us who do NOT plan big, expensive vacations to Carribbean waters, we stay in town for the week. (Frank, of course, does not get the week off. He works, same as every week. A thousand thanks for that, Frank.)
To give us all some variety, I put on my Activities Director hat. One day we played indoor mini golf, another day we went to Disney on Ice. We also visited Boston's Institute of Contemporary Art (ICA), and tonight we'll try Rock Climbing at a rock climbing gym.
Here are a few pics from the ICA, the INSTITUTE of CONTEMPORARY ART. It's right on Boston Harbor, and some of the top floor even hangs out over the water.

From the top floor, you can see the bridge and the skyline. Yesterday it was clear and sunny--really pretty. (The long, skinny picture is from the ICA website , and the boat/bridge picture is mine.)
Teresa and Kara tried their hands at creating contemporary art: see Teresa's mound of flowers on a base, and then here at home she let Komodo explore the artwork.
P.S. Just got back from the Rock Climbing Gym--awesome! The kids have so much energy, they could probably have stayed longer and longer. Me? I'm beat! I think everybody had fun. Friday night is "Family Night" and they cut rates a little for you. Here's a picture from their website:
Well, it's Friday! (After a week of Saturdays, that doesn't mean that much.) Have a happy weekend! Kari
Posted by Kari at 11:25 PM 4 comments
Sunday, February 7, 2010
No Snow for Us, Knock-on-Wood
Hola!
After reading
about the frenzy the D.C./Virginia/Maryland area was in this weekend, it is with more than a little relief that I tell you that it missed us. We were too far north for THAT storm! It's been sunny and clear in Massachusetts for a few days now.
Our consultation with David's doctor was Thursday. We had lots more questions for him, and he answered them all. He was almost offended when I asked "Would you have your son have this same surgery?" He gave a very quick "OF COURSE--do you think I'd recommend something I wouldn't do on my own kids?" Made me chuckle a little.
This doctor has done over 1000 of these surgeries. Not that he still counts, he tells us! It's just that for the first 5 years you DO have to count, and report on your surgeries, to get into some National Association or other. He just knows that his numbers have not gone down from those first five years, so he can estimate.
The good part is that David's curve is very basic, and "simple." And he has good bone structure: plenty of room on each spine segment to attach the rods to the sides of his spine. They'll go in the back, which is "quickest recovery," as opposed to going in from the side.
He'll spend 5-7 days in the hospital. After 1 day, they have him sitting up. After 2-3 days, he is standing and
walking around. By 5 days or so, he'll be walking up stairs. That's the criteria for going home: to be able to walk up stairs by yourself.
He'll go in to give blood for himself (should he need it during the surgery) tomorrow, and then it's quiet for a couple of weeks.
Then a pre-op day the first week of March, and the surgery will be March 8.
Now you know the calendar!
Onward to Monday--have a great week, Kari
Posted by Kari at 6:24 PM 5 comments
Sunday, January 31, 2010
Red Letter Day
Hola!
It's January 31st! YESSSS!!!!!!! Last year and this, January 31st is a Red Letter Da
y. (BTW, 'Red Letter Day' is a term from as early as 1490, referring to when church festivals were written on the calendar in RED. More recently, it simply means "a special day.")
Of course it is (Frank's sis) Dana's birthday, a Red Letter Day in itself: Happy Birthday, Dana!
But otherwise, it marks the fabulous fact that:...(drumroll please) We Have Made It Through January!!!!!!!!!
That is a VERY b
ig deal. It means the BULK of winter is behind us now. December and January can be tough in New England! From what I read, MANY states have had some weird and harsh weather this month. But now, January is over.
IN OTHER NEWS. You may remember that David just got braces, including an obnoxious "bite plate,"that literally keeps his molars from meeting in the back. Amazingly, he can eat almost anything now. I don't know how. His teeth still don't meet in the back, for chewing. But he's learned to make it work, wearing that "bite plate." It will be Teresa's turn, in 10 more days.
DIGITAL FRAME. I finally set up my Christmas Present: Frank got us a digital frame. We can watch a running slide show of 35 photos. Awesome! 
MRI. (These are Internet photos, not David, but it may as WELL be him. Exact same set-up. David did not wear socks. I sat in a hard rocking chair off to the right.)
I sat in the room while David lay perfectly still for a torturous 45 minutes Friday, for Pete's sake! (I have no idea how smaller children do that--they must have to sleep through it.) Both of us received ear plugs to dull the constant pounding that went on al
most the WHOLE TIME. It's a pretty amazingly huge machine, and all I could think was, "that piece of equipment costs more than my house!" Frank chuckled when I said that. In actuality -- I looked it up -- those machines can cost anywhere from $1-$3 million. (WAY less than our house...ok, just kidding)
We will meet with his orthopedic surgeon this coming week, to pummel him with questions.
RUBIK's CUBE. David figured out this puzzle, and likes to compete with himself, on how fast he can solve it. This has made Teresa interested in it, so she has been practicing, t
oo. Some toys are indeed timeless.
Have a good first-week-of-February, Kari
Posted by Kari at 4:34 PM 3 comments
Sunday, January 24, 2010
Braces 'R' Us
Each week I wonder where the week went...these days it's doctors, dentists, and orthodontist appointments!
Last July we started the process of choosing an orthodontist...David and Teresa are the lucky recipients of this service right now.

David got braces last Tuesday. Go ahead, groan...such memories, for those of us who have had them. Bonus points for those of us (myself included) who have had them twice. Ouch.
The top teeth have a funky close overbite that would make them pop OFF the lower front braces. So for the first 3-4 months, he gets an ADDITIONAL retainer thing that keeps his teeth from closing together all the way. This makes it nearly impossible for him to EAT.
So basically, he is learning to talk and eat again. Let's all think of soft things to eat, shall we?


If you can think of any other good, soft foods, please let us know. Right now he's eating very s-l-o-w-l-y, too. (Finally, somebody in the family eats slower than Frank!)
Posted by Kari at 7:43 PM 4 comments
Saturday, January 16, 2010
David's Spine
Hi!
I'm giving an update on David's back--some people ask how he's doing wearing the brace, so thank you for thinking of him. I also have 2 friends whose kids have scoliosis, so maybe if this information can be helpful to them, or a time comes when they ask for specifics, I can send them to this post.
David has been wearing the brace for about 8 months now. He wears it about 17 hours a day: when he sleeps, and when he's at school. He takes it off after school and puts it back on again before bed. He also has PT exercises to strengthen the muscles. The idea is that as he grows, by wearing the brace his back will grow more UP than more curved.

Just a heads up, that it's probably coming, and
just to keep David in your prayers! He's so even-keeled, he didn't even get upset about the prospect of surgery and a hospital stay. He said he would prefer to do it before summer, so he can heal and maybe participate in cross-country again in the fall.Posted by Kari at 2:49 PM 7 comments
Sunday, January 10, 2010
Just a Smattering
Let's see...this week! Sometimes it's hard to keep track of them...all the days run together.

SKIING: BRRR! Yesterday we took the kids to the same ski resort we went to last year, Wachusett Mountain. It was cold: 15-20 degrees all day! They see
med to remember how, and get more comfortable with it, as the day went on. And
even though it was c
old, they came home saying they had a good time. (SUCCESS!) I
didn't take the camera this time but here are some from last year: the resort, and the kids still look about the same.
ent to the dentist! Clean teeth, and thankfully no cavities. And just
a "think about it" on my old, old filling that takes up half my tooth...my dentist recommends a crown, of course with a smile. (Cha-ching! Does anyone ELSE hear cash flowing from my bank account into my mouth?)Just a smattering of the week. Hope yours was safe and inspirational, in one way or another! Kari
Posted by Kari at 6:06 PM 1 comments
