WEDDING DECORATIONS 2012
WEDDING DECOROLOGY 2012
Showing posts with label entertainment ideas. Show all posts
Showing posts with label entertainment ideas. Show all posts

Saturday, September 24, 2011

Wallpaper




There is a picture on my- James’ iPad- of James smiling. It’s from his newborn shoot. There are two different pictures of him on the iPad. One is the smiling picture from his newborn shoot. He’s looking at the camera from his side and his eyes are wide open, mouth open, gawking at the lens. During the shoot we paused several times to try to lull him to sleep. The best, or most classic, newborn pictures are those of the sleeping, innocent child. They are designed to capture the child at his most innocent, before age and time wash away the wonder of a sleeping baby and leave you with a smiling child. James refused to sleep during his newborn shoot. We tried feeding him, rocking him, warm blankets. He knew better than to sleep, even at 11 days old. James didn’t have time to be that kind of baby. I think he knew that. He never napped much, he was always wide awake. His eyes were incredibly alert, just as they are in that picture. He always seemed so much more engaged than I thought a baby would be. Perhaps it is only that I was his father and I need reasons, explanations to provide some theme so I can justify things in retrospect. But I think it was more. The other picture on the iPad is the wallpaper picture. He’s smiling at the arboretum, sitting in front of the tulips, a hand outstretched to grab one. Joy came so easily to him, to my wonder and relief.

My Dad bought the iPad while we were in the hospital. James loved to play with phones, my Dad thought that the iPad would be something fun for him to play with during chemo. James had a tactile fascination for how responsive the touch screens were. He marveled at how easily he could manipulate them. The iPad was something we could use to entertain him during the hundreds of hours we’d spend in the hospital while James got his treatments. We eagerly loaded it up with every children’s app we could think of. Doodling apps, PBS Kids, Disney, Rattles, and more. We researched the “top” kids apps and downloaded them all in James' hospital room, liberally abusing the Hospital's free Wifi. We consulted the nurses for advice.

The apps mock me now. Eveytime I turn the iPad on to fire up hulu or check my e-mail, I feverishly scroll to the last screen where I’ve stashed all the non-kid apps. Past Elmo, the Christmas Rattle, and the Doodler James once used to trace lines across the screen. I don’t always make it. Sometimes I’ll be a touch slow, click on the doodle app and wonder that my son was once alive enough make the doodles here. I e-mail them to myself, over and over again, because I always want them at the top of my inbox, as if he just drew them the over day. If I spend all my time on James I won’t do anything else. I won’t ever delete those apps of course. I won’t do anything to materially alter the IPad, that’s inconceivable. It belonged to James, and is therefore sacrosanct.

The iPad is just one reminder. A symptom of a larger, intractable problem. A reminder of a hope, dream, and future I once had that will never be. No hours of chemo, no need to worry about ways to entertain him through long hours. No need to worry about infections. The hard work I spent studying the notebooks the chemo nurses gave us, harder than I ever studied for any exam, wasted. All of this made still more frustrating because I spent time on that instead of with him. All of these are reminders that there is nothing left of James to hold onto. The feel of his hair, the tenuous strength of his fingers grasping yours. All of that is gone, with his piercing eyes. There’s nothing to hold onto. I’m left with his newborn photo, James stubbornly mocking the photographer and refusing to sleep.

That’s not to say that there aren’t comforts. We have had a great many. James has left a legacy far greater than anything we dreamed possible. I am moved by the responses that his story has generated. Still, when I’m flicking through the touch screen to avoid laying eyes on the doodle app, I can’t help but wish I was reading a blog about someone else’s life. Someone else’s child, and not writing about my own. I would never wish what happened to James on anyone else. No one should experience this. I just wish it didn't happen at all.

As always, thank you for your prayers. They are a continuing source of strength.

Tuesday, June 28, 2011

MRI Results

The MRI results came back this evening and they are great! Dr. Sacco feels very confident that he got out about 95% of the tumor. The remaining 5% (which could actually be less!) should be able to be taken care of with the chemo/radiation treatments that we will do next. We are SOOOOO thankful for this amazing news. I can't tell you how much of a weight has been lifted off my shoulders!

We have moved down to the floor now, and will stay here until further notice. We should meet with our neuro-oncologist tomorrow to confirm that we won't need anymore surgery in the near future, but we feel strongly that she will agree with Dr. Sacco. The next step is waiting for the pathology results that will most likely take until the end of the week!

At this point we are really living day-to-day. Sometimes it's hour-to-hour. We aren't looking at the big picture that all of this means, because honestly it's just too overwhelming. Right now we know that our sweet boy is doing well and is happy. And that is all we can ask for today!

My dad got James a portable dvd player that we can use in the hospital and when we go to chemo. James has never watched movies before, so I wasn't sure how he would react. Our pediatrician was here the other day and I had turned it on for James to watch Cars. I started apologizing to her because I know that TV watching is terrible for your child. She told me that throughout this journey I am going to be doing alot of things that I never thought that I would do as a parent. I need to do whatever I can to get through it, and she thought the dvds were a great idea.

Speaking of dvds, does anyone have ideas about how to entertain an 8 month old during chemo treatments?! If you have ideas, I'd love to hear them. So far I have movies. That's the only thing on my list!

And finally, dear friends, let me thank you for everything. I know I sound like a broken record, but I could not be going through this journey without the wonderful, caring, supportive friends and family in our lives. I truly feel that prayer lifts us up and carries us when our hearts are too heavy to hold. Thank you for sustaining me and breathing life into me when I wasn't sure I had breath left. There is not an hour that goes by that I don't reflect on your kind words of encouragement. You are such a blessing to me and I am so very grateful for you.