Tuesday, March 1, 2011
Bath Time
Yesterday morning, when Owen and I made it to the hospital, Henry was napping. So, we started out playing in the playroom. It's a huge room full of toys and more toys for patients and patient's brothers. Owen loves it... and really loves Diane, our child life person. Every day, "where's Diane". She is so wonderfully helpful with both kids. What a great job!
After Henry woke up we saw this: a kid desperate for a bath.
Friday, February 25, 2011
Owen
One year ago today, we brought Henry home from the hospital. The sixteen days he spent in NICU after he was born seemed to be an eternity... Here were are fifteen days into this hospitalization, and it seems like we have an eternity to go...
More pictures, more days...
Here's Henry and Lucas playing with a mirror, an idea from speech therapy to help him out. I think Henry is more in love with the pink rattle/teething toy, than the mirror. It's his new security toy.
Taking in the view from our room

The packaging doesn't taste as good as real food.
More pictures, more days...
Here's Henry and Lucas playing with a mirror, an idea from speech therapy to help him out. I think Henry is more in love with the pink rattle/teething toy, than the mirror. It's his new security toy.
Monday, February 21, 2011
Routines
We are starting, ever so slowly, to develop a routine. Each morning, we bring Owen to the hospital and spend a few hours as a family of four. Here are a few pictures from the past few days.
On Saturday, Henry started the "big gun" chemotherapy. We dressed him up for the occasion.
Tiffany was in town for the weekend, hence a family of four picture. Owen is in love with the green "swabbies" that we use to give some mouthwash to Henry. He brushes his teeth endlessly with them. (that's what's in his hand)
Beautiful eyes.
Owen showing off his shinny teeth.
Brothers.
Hospital life is tough.
Self-portrait.
This is one of the many chemo drugs Henry gets through his IV. This is the prettiest one. Looks like Cool-Aid.
Bob-Bob feeding Henry his FAVORITE food... pudding.

Overall, he's tolerating chemo better than we thought. No puking yet, just maybe a little more tired, but still playing... still my sweet Henry. Our oncologist is happy with how well he's doing... so far, he's doing well. And that's all I can focus on. Today, this weekend was a good weekend. Today was a good day.
On Saturday, Henry started the "big gun" chemotherapy. We dressed him up for the occasion.
Friday, February 18, 2011
Caring Bridge
We have started another blog, this one dedicated to Henry and his hospital journey. It's through Caring Bridge. A huge plus is that I can update it via my phone, yes, there's an app for that, so easier to update at the hospital...
If you care to take a peek:
www.caringbridge.org/visit/henryfriedler
If you care to take a peek:
www.caringbridge.org/visit/henryfriedler
Fun times
Being in The Children's Hospital has a few perks. One is Music Rx, a part of Children's Cancer Association. Wonderful volunteers go room to room three times a week and play music and sing, and leave musical toys with the kids to play with. Then, we will rotate toys next time we see them.
Henry is loving this drum. (note, he has both hands back because we got central IV access yesterday!)
He looks so big! But the hair does add a few inches.
Henry is loving this drum. (note, he has both hands back because we got central IV access yesterday!)
Coolest Ever
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