My Real Life

October 9, 2009

Real Good People

Filed under: Uncategorized — Amy @ 6:39 am
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I want to take a moment to make a shout out to an organization that made our hospital stay much more enjoyable than it could have been.

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The Starlight Foundation is a non-profit organization that supports hospitals and sick children.

At the hospital where we were staying, the Starlight Foundation was responsible for the playroom.

Now, we couldn’t take advantage of the playroom until the third day, as Baby Monkey was tethered to the wall, however, we were able to take toys and bring them to our room.  And, on the third day, when he was un-tethered from the wall, we spent a few hours there as we waited for results.

Check this place out.

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They had books, games, instruments, toys, computers, a craft station, a big screen tv for playing movies or video games, a Wii, Nintendo DS, GameBoy, trains, trucks, cars, blocks…basically anything a small child or teenager could want. 

The one thing that kept going through my head while we were in the hospital was that I was so grateful that Baby Monkey wasn’t sick.  Because there were a lot of kids there that were.  There were many kids who had been there before we got there and were nowhere near ready to go when we left.  There were kids who are there at least once a week for one treatment or another.  Other kids who come in and can never really go home.

It breaks the heart.

So, the Starlight Foundation exists and it helps those kids make a really crappy situation bearable.  It doesn’t cure them, but it certainly helps them forget, even if just for a short while.

My friend, Michaela, used to work for Starlight.  I remember the amazing things she used to talk about the foundation doing. 

So, if you are thinking about any charitable donations in the coming year, I would encourage you to keep the Starlight Foundation in mind.

October 8, 2009

Real Relief

Filed under: Uncategorized — Amy @ 7:27 am
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Three days in the hospital and the results are good.

EEG clear.  MRI clear.

This means we don’t know anymore than we did on Sunday, but we do know what it isn’t, and at this point, that’s major.

I’m not going to bore you with every detail of the stay, but I do have a few things to say.

First of all, the bravery of Baby Monkey leaves me speechless and moves me to tears.

Despite the fact that he is terrified of loud noises (remember this post?) he didn’t even flinch when they hooked him up to the 20 EEG wires with glue and a loud dryer.  He just lay there, like this…

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..and occasionally made silly faces like this…

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Once the wires were on and the head was wrapped in bandages and he was tethered to the wall for three days, his smile never left his face.  He stayed busy with the toys they brought him and the books and game we brought from home.

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QUICK PLUG FOR HOSPITAL FOOD

So, let’s be honest…any food that I don’t have to prepare tastes fabulous.

However, the food at this hospital was unbelievable.

Here’s Baby Monkey and his breakfast from Day 2.  Waffles covered in whipped cream with strawberries, bacon, vanilla yogurt, an orange, milk, blueberry muffin, orange juice, and corn flakes.

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And here’s my lunch from the same day.  Is this not one of the most beautiful fruit platters you’ve ever seen?

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Yeah, it was all fantabulous.

Back to our regularly scheduled brag about Baby Monkey.

On day 3 when they used a very smelly solvent and scissors to get it all off of his head, he smiled his way through it.

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Every doctor and nurse and hospital staff member that he came in contact with said that he was the most laid-back, best behaved patient they had ever treated.  They couldn’t believe that, at 3, he took it all in stride.  I was so freaking proud of that boy.  Particularly when they couldn’t find a vein for the IV and they just kept jabbing away until they got it and while he didn’t smile at that, he also didn’t make a fuss.  Just snuggled into Mommy and dealt.

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And, of course, in the end, he smiled all the way home.

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October 6, 2009

Day One

Filed under: Uncategorized — Amy @ 6:52 am
Tags: , , , , ,

So, day one is done and Baby Monkey did great.
We played games, read books, did puzzles, watched movies and had a mice day together.
He’s a trooper.
They wanted him to be sleep deprived as that often triggers seizures, so we were up until 2 am.
The only bad part was that his pulse oxygen monitor kept coming off of his finger while we slept, waking me up with loud beeping every half hour. So, I’m more than a little sleep deprived! The good news is that once he was out, he was out.
We’ll be here until Wednesday. It’s a nice hospital. I’ve only been in the one where I gave birth to all the monkeys. They sent us here because they said thee wouldn’t be as many sick kids and it is quieter. They were right
So, I’ll let you know how today and tomorrow go. They decided to do the MRI last, so I won’t know those results for awhile.
Thanks to you all for your well-wishes. They are much appreciated!!!

September 17, 2009

Update on Real Scary

Filed under: Uncategorized — Amy @ 7:12 am
Tags: , , , , , ,

So, today was the day that we went to the neurologist with baby Monkey.  Real Man had a doctor appointment in the morning, so we sent him to nursery school and then picked him up before lunch.

Since we had no idea what he was going to have to endure at the hospital, we decided to treat him with lunch at Wendy’s.  That went over very well. 

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Not only was he thrilled to be there, but Real Man actually got the chicken sandwich from the commercial.  You know how your burger/sandwich never looks like it does on the big board over the counter or like it does in the commercials?  Well, for the first time ever, Real Man got the dream sandwich. 

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We can never go back, however, because anything after that sandwich will be a let down.

After lunch, we headed to the hospital for the appointment.

We went up to the neurology wing and sat in the waiting room.  Off of the main waiting room was a sign that said “Children’s Playtime Waiting Room.”  How exciting!

We drew Baby Monkey’s attention to it and went in with him. 

We were greeted with this sign on the wall:

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Ooookkkeeee. 

I get it.  I do.  Swine flu.  Sick kids all playing with the same toys.

So, Baby Monkey played with the one toy that was left.  The one toy that every sick kid who goes in there touches, bites, drools on, sneezes on, coughs on, and bleeds on.

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Ah, he’s tough.  He’ll survive.

We get to the hospital, they do the routine check-up stuff like height and weight and then load him up with a bunch of stickers.  They send us up to the neurologist.

So, we met with the neurologist and he asked a bunch of questions and then had Baby Monkey do some neuromotor things like play with little toys, run after a ball, catch a ball and throw a ball.

He said that it was probably a seizure, but that it seems like a one-time deal right now.  He wanted us to get an EEG to rule out anything like epilepsy.  He said if the EEG was clear, and it doesn’t happen again, then we should just relax and pretend like it never happened.  If the EEG shows something, we’ll deal with that.  If the EEG shows nothing, but it does happen again, then we’ll need to come back for MRI and further tests to look for abnormalities in the brain, growths, etc.

So, he calls down to the EEG lab and says he’s going to use his charm to get us in right away so we don’t have to come back.  He tells them “I’ve got an adorable 3 year old here who I’d like to get an EEG for immediately.”  He said that he was sure Baby Monkey would be able to withstand the 40 minutes of the EEG and they said, “Okay…send him down.”

So, we head down to the EEG lab.   We sit down and at first, Baby Monkey just sits there, quietly, looking around.

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Then, he starts putting the stickers on his head, pulling them off, saying “Ouch” when they pull his hair, then putting them back on his head again.

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This continues for about ten minutes. 

Then, the woman who has been watching him the whole time we were there says to us “You know there is a children’s waiting room just around the wall.”

We didn’t know.

We stand up, take three steps, peek around a wall and lo and behold, a beautiful children’s waiting room, complete with actual toys.

Cool toys.

First there was this thing on the wall.

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I think I almost had a  seizure watching this thing spin.

Then there was this awesome magnetic table.

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There were magnets underneath and you had to move the boats around using the magnets.  That was fun.

There were other toys, as well.  Lots with magnets.  I thought that was interesting in a lab where they did lots of electromagnetic testing.  Interesting choices.

Anyway, then we go in.

Now, let me say this:  Lest any of you think that my child was getting a major neurological exam and all I could think about was taking pictures for my blog, the following pictures were taken at the request of Baby Monkey.  He kept wanting to know what he looked like.

First, with the Sharpie marker on his head.

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Then, with all the wires attached.

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He did great.  The test was 40 minutes.  Part of it was just him laying there, watching a video.  Then, he had to blow a shiny pinwheel for 5 minutes.  Then, he had to have a strobe light flashing in different intervals for another 5 minutes. 

There were lots of squiggly lines on the screen and neither Real Man nor I have a clue what any of them mean.  The neurologist said we can call on Friday for the results.  Story of our life right now…hurry up and wait.

So, as of today, I have no more answers for anyone than I had yesterday.  But, I can tell you that Baby Monkey is an absolute trooper and a pleasure to be with, under any circumstance.

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