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Yeah, it’s been one of those days.  It is about 85 degrees in my house and the kids had doctors appointments today.  No worries though, it was just school physical time.  Madison weighed in at 60.6 pounds and she is 49 1/2 inches tall.  (We are going to Great America in a couple of weeks, so I am going to have to check out what rides this will allow her to ride.  My mom is a little worried, because Madison only has about 11 more inches to grow to be taller than her!).  This year they gave us her BMI reading which is 84%.  Healthy weight is 5%-85%, so she just made it under the wire.  However, if you’ve ever seen Madison, you’d know how thin she is, so I’m just like whatever with the BMI thing.  Will is 40.4 pounds and 42 inches tall.  His BMI was 52%.  Needless to say, we aren’t worry about the BMI.  Unfortunately, Will ended up with 2 shots.  It was that or he’d have to get 5 come kindergarten.  I choose 2 today and next year he’ll get the other 3.  Poor kid.

And that leads us to the headboards part of the title of this post.  Bill and I have been talking about when we move Will out of his toddler bed.  The first thing you have to take into account is that his room is only 9′ x 11′.  He has no closet.  I would also like him to be able to play in his room.  Of course, that does not give us a whole ton of options.  Right now, the toddler bed works.  However, if he keeps growing like a weed, it won’t!  I am thinking that headboards for full size beds or even king headboards, just aren’t going to work in his room.  The kicker is that with his crib, we actually have the full size headboard.  Honestly, I am thinking we will just have to check out moreheadboards.com and find a twin size headboard and then get him a new mattress.

How long to you wait to move your kids out of their toddler beds?  What size bed did you move them to?  What size bed would you think I should get for him considering how small that room is?

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Well, actually Madison can. She had an eye doctor appointment last night.  I changed her from the pediatric ophthalmologist to the eye doctor Bill and I go to.  It’s just down the street, and it’s covered under our vision insurance (whereas her ophthalmologist was not).  The amazing thing is that we’ve been going to the other place for 2 years, and I learned more about what’s up with Madison’s eyes last night!

Now, we ended up at the ophthalmologist when Madison was 3, because she had a lazy eye.  The glasses were to correct it.  What I was never told was that she has a refractive error in her eyes, so she’ll always wear glasses.  She’ll always have to wear glasses.  Unlike adults, they also don’t give them the full prescription right away either.  They slowly work their way up.  This explains why every single year her prescription has changed.  Also, until they get her to her full prescription her depth perception sucks.  For us, this explains a lot.  We couldn’t figure out why she can’t catch.  Well, that explains a lot.  If you don’t have depth perception that would make it quite difficult.

Now, we wait for her new lenses.  These still aren’t her full prescription, but her new doctor has already told us that she’s putting Madison on an accelerated schedule to get her up to where she needs to be.

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I finally got Will in for his 2 year checkup.  He’s a growing boy!  He’s 29 lbs 3 oz and 36 3/4 inches (which means he put on I think like 3 lbs and almost 3 inches in 6 months).  Except for his speech, he is right on target with everything.  His doctor agreed that he is speech delayed, and we got a referral for early intervention.  I called and am expecting a call in the next 2-3 days to set up his evaluation.  He also got a shot and didn’t even cry!  He’s been a happy, active boy all day since, so the kids needs more shots.  LOL

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I keep getting asked what happened on our Disney trip, so I thought I’d better finally get this post up.  The day before we left for Disney, Will (my 20 month old) was throwing up.  I called the doctor and was told it was a 24 – 48 hour bug.  By the next day, he seemed fine.

When we were boarding our flight, Madison threw up at the airport.  The decision we made right then made us the worst parents ever!  Seriously.  We figured that since Will beat it, Madison would get over it in 24 hrs too.  How wrong we were.

When we got to Florida, she looked like hell.  She threw up on the Magical Express (Disney’s transportation to the resorts).  However, here’s the weird thing (and will had it too), they both were completely fine between puking episodes.

Saturday morning she only threw up once.  We had her drinking all day and all night (over night she drank half a bottle of water).  Sunday morning was our undoing.

See, we thought she’d perk up if we took her to Magic Kingdom.  How wrong we were!  She just looked worse and worse, so we took her to the first aid clinic there.  They couldn’t treat her but called to get us transfered.  What I didn’t realize is that they were taking us to Urgent Care.  On the way there, I filled out the paperwork and even wrote on there we were there for dehydration and the flu.  At this point, she had thrown up only once.

We sit at Centra Care for 2 FREAKING HOURS!  Now, remember I have a puking kid, so we ask for a bag.  They give us attitude but hand us some bag they got from like a drug sample person.  Madison throws up, and we used it.  Bill went up to get another bag, and we were told “she could use the bathroom”.  Now, I have a sick 5 year old who couldn’t walk because her legs her so bad but she could use the bathroom.  Bill didn’t tell me that’s what they said till after we left which is probably good since I would have had a fit.  Then, after sitting there 2 hours, Madison had to use the bathroom.

We get called back and are told we need a urine sample.  I tell them there is no way they are getting that.  She is dehydrated and she just went!!!!!!  I’m like did you not read what I put on her admitting forms!  Then they refuse to treat her.  I KID YOU NOT!  After sitting there 2 hours with a severly dehydrated child, they won’t treat here.  When I have a fit (which I had every right too), the nurses cop an attitude with me.  Bill even noticed the attitude I got (and he normally noticed nothing).  So now we are walking out the door, and Bill says “Are you charging us for this?”.  They are like “no”.  He responds “then where is our copay?”  Basically, if he wouldn’t have asked for it back, we wouldn’t have gotten it back, since the girl who had to refund it back did not know how to do this!

We next get sent to Celebrations Hospital.  I tell them our sob story which of course I get told that too bad so sad, it doesn’t bump you anywhere near the front of the line.  Now, remember, we have a 1 year old we have to keep occupied while this is all going on AND I know she is dehydrated.  We’ve done this before when she was 2.  What happened was she got the throwing up flu and ended up in the hospital dehydrated.  Her counts went off the charts, and we ended up at a geneticist.  At that time, we were told it was a fluke.  Not so much a fluke anymore.  AND TWO HOURS MAKES A HUGE DIFFERENCE WHEN YOU ARE DEALING WITH SEVERE DEHYDRATION AND METABOLIC ACIDOSIS!  Okay, sorry for yelling, but if we wouldn’t have lost that time (that is, if Disney wouldn’t have sent us somewhere that couldn’t treat her and if that damn Urgent Care would have read their form), she may not have gotten as sick as she did.

I can’t complain too much about Celebrations Hospital.  We only ended up in the waiting room for about an hour.  The doctor tells me what I know and that they need a urine sample.  Umm, the kid is dehydrated, you just told me that, and how do you expect me to get her to pee.  I swear I could smack these people upside the head.  Here’s what she looked like:

Yes, she looked that bad.  So they hook her up to an IV and then we get kicked out of that room.  They take us to a room that has about 15 other people in it.  Basically, it looked like a holding area.  Now, again, we have a 20 month old with and are told that Bill and Will can’t come into that room.  Seriously.  So Bill spent the next 5 hours walking the hospital with Will.  Andddd to make matters worse, he had to cab it back (which Disney did not reimburse), since nobody bothered to tell us that the free transportation ended at 6.  We sat and sat and sat in that room.  I kept asking for her test results and kept getting told the nurse was too busy.  After being in there at least 4 hours, I am told that they are waiting on a urine sample.  Sigh.  And nobody could have told me that 2 hours prior?  Soooo I take Madison to the bathroom.  She refuses to walk because her legs hurt.  Do you think they give me a wheelchair?  No.  I had to carry a 50 lb kid from one end of the ward to the other.  I was a little pissed about that.  Soooo I had to carry a 50 lb kid and her IV with no help.  She did pee and I was told her CO level was 10.  Now, your CO level should be 24.  We are now told that have to spend the night.

Now, you’d think this wouldn’t be a problem.  Think again.  The Celebrations hospital (which is where we were sent) doesn’t treat kids.  Yeah you heard me.  If you have a scrape or a broken arm, you can get treated.  If you have to spend any amount of time there, well you are screwed.  We got sent (by ambulance) to another hospital 25 miles away.  Now, remember, we are there on vacation.  That is a $53 cab fare each way.  We have no car seats either.  It took another 2 – 3 hours for them to even get us into a another hospital.  What a freaking joke.

So we get to the other hospital at about 2 am.  Now, I haven’t eaten or drank anything since the day before.   At least the nurses here were able to at least give me a soda to drink.  We were sent to the Florida Children’s Hospital in Downtown Orlando.  This is the next day:

Now, she actually looks a lot better than she was here.  We didn’t get to go home, because her potassium was low, and they couldn’t get it back up.  She was on a potassium IV drip all day, and that still didn’t raise it.  That night they had to give it to her orally (I missed this.  Bill decided he wanted to stay the second night with her).  She also ended up with EKG too.

She did get out the third day (with 2 days left of our 7 day vacation).  She looked like hell.  We stayed and finished our vacation.  When we got home, she had to go to our pediatrician who ran a bunch of tests.  Madison is still complaining her legs hurt.  Now, the first time we ran these, her liver enzymes were elevated.  She was retested last week and those enzymes are back to normal.  Woohoo!

Now, we are still waiting on the records from Florida (its only been almost a month since I requested those records and we are still waiting).  My pediatrician needs those to determine our next step.  We need to see if her test results mimic what happened when she was 2 to determine what our next step is.  My fear is that we are going to end up in the hospital every time she gets the throwing up flu.  The pediatrician even said that there is no way she should have had a CO level of 10.  Her body should have been shutting down, and it wasn’t.  She shouldn’t have been still peeing, and she was.  They also told me that her blood was acidic (which would be metabolic acidosis).  We aren’t going to be lucky that she’ll get this once every 3 years after she starts school.

I’ll be writing another post about what we actually got to do at Disney, but that’s the medical update. Would we go back? Actually, yes. I will be writing another post about what fun we did have after she got out of the hospital. We still had to take it easy but we were able to salvage a little.

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I had to bring Will into the doctor due to some weird episodes we were having with him, and before I went to post how that went, I realized that I never got around to telling you all about the kids last checkup! This was Madison’s 5 year old checkup and Will’s 18 month checkup.  Both needed shots, so it was lots of fun.  We had a really bad snow day that day, so Bill ended up being able to come with us (he tried driving into work — made it less than 2 miles in an hour and half and he wasn’t even on the expressway yet!).  Now, I had this on a little piece of paper I lost, so I am doing this from memory. 

Madison is 46 lbs. and 44 1/2 inches tall.  Will is still 26 lbs. and is 34 inches tall now.  The doctor is fine with where they both are at in their development, and except for the shots, it was a good visit.

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