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My Breastfeeding Badges of Honor

Speaking the Language of Mr. Emmett John ~ Round 2

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I don't know where to begin.

Yesterday I took Mr. Emmett John for his 18 month well-baby check-up with Dr. H. Tomorrow I will take him to the Audiologist to have his hearing tested. Physically, he's doing well. He isn't sick. Motor skills are right on track. He's still channeling Jack-Jack, which is absolutely exhausting. I honestly don't know how he does it. One minute he's right next to you then he's gone and there are 6 of him everywhere! On the bright side, his constant movement doesn't seem to be having any effect on his growth...

The Stats

Head Circ: 48.8cm (75%)

Length: 35.25in (98%)
Weight: 26lb 1oz (41%)

I spoke with Dr. H about my growing concerns about Emmett John's lack of language. He doesn't talk, period. He babbles, which basically means he makes the noises that don't pertain to anything. For Emmett John, MaMa doesn't hold any signifigance for him towards me. Neither does DaDa, BaBa or any of the rest of them. He just says them.

He doesn't seem to hear us either. Our house is set up in a circle - front room (living room), hallway, kitchen, dinning room - all in a circle. The other night Emmett John was sitting on the couch in the front room and I snuck around so I was about 2 feet behind him then I clapped. I clapped so hard my hands instantly turned red and I moved Emmett John's hair. He didn't even move. He didn't startle, flinch or anything else. We call out to him from across the room and he doesn't respond. Loud noises, quiet noises...it doesn't matter because he doesn't seem to hear any of them. The only ones that he sometimes seems to hear are high pitched cell phones.

I mentioned his complete lack of a startle reflex to Dr. H when Emmett John was about 5 months old. At the time though, he had so many other things going on that we needed to figure out that it was lost in the shuffle. Plus his hearing test at the hospital when he was born so Dr. H felt that the "wait and see" approach was probably best. I allowed myself to be poo-pooed into silence and ignored my mother's instinct. Here we are 13 months later.

Tomorrow we are going to the Audiologist for his first hearing test, the OAE. It's the regular hearing test to see if he can hear at all. After that Dr. H has referred him to the local children's hospital for the sedation hearing test, the ABR. He is also referring us to Help Me Grow for early intervention. Help Me Grow will help us to get started with Speech Therapy, Sign Language classes so that we can communicate until we find out what is going on and even there after. He's also referring us to Gavin's Developmental Neurologist so that he can be evaluated for Autism.

Dr. H said that Autism is on the bottom of his possibilities list; however, with the family history via Gavin and the significant speech delay he wants to be sure that all of the bases are covered. That way if he does happen to be Autistic we have early intervention in place, whereas Gavin was unable to benefit from those services. I agree with Dr. H, I don't think that he's Autistic. I think he's deaf. However, I will feel better knowing. Especially if the hearing tests come out a-okay.

I'm not going to lie here guys, I'm terrified for my baby.

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Tuesday Toot

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Two of Gavin's major doctor appointments down.

Of course, that's not saying anything about the rest of the month. Let's just not go there right now, shall we?

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Google it...

6:16:00 PM Posted In , , , , , , Edit This 0 Comments »


I haven't done a Google it in what feels like forever. So, I figured, "Hey, I'm in a blogging mood. Emmett John is sitting on Rob and watching the penguins. The boys are upstairs playing. Why not?!" Any away we go!


7 Oct 11:06:50 PM www.google.ca i believe that faith has brought us here...cheerios commercial ~ I can't believe that people are still looking up this commercial. Okay, honestly I'm more surprised by the fact that people are still watching commercials. I figured everyone was recording television to skip the commercials by now.
7 Oct 05:11:37 AM www.google.co.in i love my baby and cant live without him ~ Me too. Isn't it great? :)
3 Oct 10:09:11 PM www.google.com 4 year old boy refuses to potty train attachment parenting ~ I hadn't considered this but now I'm starting to wonder...maybe this is Elliott Richard's problem.
2 Oct 02:00:22 AM www.google.com things i can't live without ~ I just covered this not too long ago as my Thursday 13! Go check it out.
1 Oct 08:24:27 PM blogsearch.google.com vincent d'onofrio ~ Oh how I *heart* him! And oh how y'all have devastated me by informing me of his leaving the show. I won't watch it once he's gone. I refuse. What's his face just isn't that good at "crazy". I'm sorry but he's not. Vincent fans know what I mean. And now because it's my blog and I can....
30 Sep 01:51:49 AM www.google.com micropreemie autism high functioning ~ Hhhhhhmmmmmm...interesting. I don't know if there's a connection but I'd be interested in doing my own search to find out.
29 Sep 02:02:55 PM www.google.com have you ever had a cheerio ~ I've seen one. Have you? Just in case you haven't check out my badge at the top right of my blog...the background is a whole bunch of them.
24 Sep 12:26:14 PM www.google.com johnemmett.blogpot.com ~ I was curious so I checked this blog out. It was a temporary blog. There are no posts. And the profile is empty. Bummer.
21 Sep 06:53:04 PM www.google.pl masochistic torture ~ And again we find ourselves discussing Mr. Emmett John's future with our fine military. Assuming, of course, that there is a United States of America and a military to speak of once he's of age. Who knows...we may be American Socialist Nation by then. But we won't go there just now.
18 Sep 06:19:29 PM www.google.com cant live with them... cant live without them... but for more than 2 weeks!!! even years!!! ~ I assume the "cant live without them" part brought you to my blog. Although I'm not entirely sure what this person was searching for. Men maybe? ;) lol
17 Sep 06:23:06 PM www.google.ae i remember when we were asking each other ~ What?! "I remember when we were asking each other" WHAT?!?! What were you asking each other?! Why do these people torture me like this?! I'm curious by nature and these searches...oy! It's killing me! lol
16 Sep 02:04:11 PM www.google.se cheerio governor ~ There's a Cheerio Governor?! Wow. I mean we have a Cheerio Mayor here in Cheerioville but we don't have a Governor because those are for a state as a whole. But that's cool.
13 Sep 06:35:11 PM www.google.com length of first cheerios commercial ~ Another interesting search. I wonder if this was for curiosity sake or for a report or project or something.



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Gavin's 7 Rules

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Gavin's 7 Rules

1.) No internet. Especially YouTube as it is grossly inappropriate for anyone under the age of 18 in my opinion. But basically, no internet at all. He cannot even watch you on the internet because he doesn’t understand the difference.

2.) No video games. This includes computer, internet, console (Wii, PS2, PS1 etc.), handheld (Game boy, DS, PSP etc.) or $5 cheapie hand-held games. If it's digital and a game, the answer is No. This also includes watching others play video games. He cannot even handle being a spectator.

3.) No fighting. This includes martial arts battles, sword fighting, toy guns and weapons of any kind. This also includes imaginary Pokemon battles. He is unable to set or follow limits in these situations and therefore cannot be involved in these situations.

4.) No shopping or presents unless Rob & I approve it in advance. This includes window shopping online, window shopping in the stores or catalogs.

5.) No play dates. This includes cousins, play lands at fast food establishments, parks etc. Gavin CANNOT interact with most other kids (for their own safety as well as Gavin’s).

6.) Be on time. If you say you will be here to pick him up or drop him off at 1:00pm then be here at 1:00pm not hours later.

7.) When in doubt as to if something falls under a rule, ASK FIRST! It only takes a simple phone call to double check that you have the correct information, which will prevent major issues later on. As much as we all love Gavin, he isn't the best source for information so please, please, please always ask first.


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Life...Ever Changing

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Everyday in the Cheerio household brings about a new sort of "normal". I use that term loosely of course. Our lives are in a constant state of flux. Mostly because of Gavin, not that I'm saying everything is his fault because it isn't. It's just that a majority of the time our lives revolve around Gavin and his needs. Some days the flux is caused because of me and my needs. However, mostly, our lives revolve around Gavin. His moods. His needs. His whims. His fits of anger. His fits, period. His appointments. Him, in general.

I feel like as soon as we get one thing under control here. One thing stablized. Everything else hits a huge wave and smashes into a million pieces. Then we are left clinging to that one thing we managed to stablize while we scramble to gather the other million pieces and try to put them back together. Only it feels as if we are trying to put them back together, in the dark, without glue, without directions and honestly, without any real idea of what they were in the first place. All the while that one stablized thing, whatever it was, is slipping away so slowly that we don't notice until it's gone.


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3 sick boys, 2 ped appts, 1 fibro flare & a baby on the way

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(You're supposed to sing the title to the tune of "The 12 Days of Christmas".)

3 Sick Boys

Yes, you read that correctly all three of my boys are sick, again. Isn't that always how it seems to go in the Cheerio household though? I'm not sure if it's better this way or not. I guess it is. I know it would definitely be much easier without the #1 down there. But I digress.

Elliott Richard

Elliott Richard was first. For all the "gory details" see this post here. He will finish up his antibiotics tomorrow. Yippee! Because even though he's on the "bubble gum" meds that most kids love he's 3 and a terrorist and therefore he enjoys being difficult.

Things were just starting to return to "normal" (not a term that usually applies to our household). Meaning that Elliott Richard was sleeping in his bed rather than on the couch in the living room with Daddy. He was sleeping through the night again. Wasn't super whiney or clingy. He was himself again. He seems to be doing much better. Although he's developing a cough, but I'll get to that in a moment.

So things were starting to look up...and then...

Emmett John

Emmett John, never one to be out-done in anything, was next. Friday afternoon he spiked a fever. By Friday night, his fever was 102.8. By Saturday morning it was 103.2 so off to see Dr. Beth we went. No ear infection or strep. It was just a virus. She said to let it run it's coarse and by Monday the fever should be gone. If Monday morning the fever was still there or his cold symptom had returned, I was to bring him back in.

So we suffered the weekend. No one slept. Emmett John screamed a lot. I considered clawing my eyes out and super-gluing my ears shut. But decided against it in the end. We all survived (I use that term loosely).

Monday morning, always the over-achiever, Emmett John still had his fever and his cold symptoms had returned with avengance so off we went to see Dr. M. But really, let's be honest here, what's a week in the Cheerio household without a visit (or two or three - keep reading) to the pediatricians' office? He checked out our young bebe and thought for sure he had strep throat so he did the swabs - rapid and 48hr. Both ended up coming back negative.

So now he's just a super-clingy grump. He doesn't really want to eat. But he downs water and juice like they are going out of style. He's exhausted but won't sleep. Wants to snuggle but doesn't want held. My fellow mommies out there know this drill well. *sigh*

Gavin

Then of course, Gavin had to jump on the bandwagon. Although truthfully, it's not like he had much of a choice, with two sick little brothers the odds were stacked against him in a major way. So a week or so ago Gavin developed a cough. As the week went on the cough got worse. The problem that Patty brought to our attention at our appointment on Tuesday was timing. The cough started about the same time that Dr. R increased Gavin's dose of Zyprexa. Patty was worried that the Zyprexa was possibly that Gavin is over-medicated and it's causing decreased respiratory function. Of course, I mean what else would you expect from a Cheerio Child?!

So I called and made an appointment with Dr. M. The appointment was actually going to work three ways. Here's what they are and why:

a.) If Gavin is over-medicated, the dose will be changed.

b.) If Gavin is sick, hopefully it's something that will be fixed with anti-biotics.

c.) Everytime Gavin gets a tickle in his throat he proclaims that he has asthma, which he does not.

So I was hoping to find answers to all three of those when we met with Dr. M. Although truth be told, Dr. H has already told Gavin on numerous occasions that he does not have asthma. Heck, even his original pediatrician Dr. Mike told him he didn't have asthma. But he's still convinced that he does.

So we went. We saw. We talked. Some of us more than others. Dr. M asked Gavin a bunch of questions to rule out asthma, which he was able to do, again. Then as Dr. M and I were talking about the cough - when it came on, the meds he's taking etc - Gavin kept jumping in with random Aspie statements. "I like pancakes." Things that given the given the context of the conversation really didn't make much sense. Gotta love those Aspies. :)

Dr. M checked him out and let us know that:

a.) He is not over-medicated. Huge relief there.

b.) He is sick.

c.) He also does not have asthma, although I don't know that this will put an end to the debate.

Apparently, Gavin has some funky form of bronchitis. The normal anti-biotics won't work on it because of the cell walls or something. And the anti-biotic they would normally prescribe is Zythromax or something in that family but Gavin is allergic to those. Even if he weren't he can't take them because they increase the levels of the Zyprexa in his blood stream. So he's on an anti-biotic I've never heard of before, which after three boys (especially Emmett John) I didn't think that was possible. lol And I have to take him back on Monday so that Dr. M can listen to his lungs and make sure that he's improving etc.

Back to Emmett John

Now we get to go back to the pediatrician today. In the last 24hrs Emmett John has developed a rash that started on his back so I thought it was heat rash. Then it began to creep. It creeped to his sides, stomach and now it's creeping down both arms and legs. So I called and talked to Paula, one of the lovely nurses, and she talked to Dr. M. He said that he felt Emmett John should be seen because of Gavin and Elliott Richard both being sick. So at 4:15pm we will be back at the pediatrician's office. This time we get to see Dr. H though. Yippee! So we'll see what that brings us. Oy vay.

2 Ped Appointments

Yeah, it was 2 ped appts if you only counted Emmett John with Dr. M on Monday and Gavin with Dr. M yesterday. However, if you count Emmett John with Dr. Beth on Saturday and now Emmett John today. The grand total is now 4 ped appts but that doesn't work with my title at all. ;) lol

1 Fibromyalgia Flare

Yeah, that would be me. Of course, who else would it be. I love living in Ohio. Really, I do. Lately though, this weather, it's killing me. The ups and the downs - the weather is just crazy and it's downright killing me. I've been flaring off and on for nearly 2 weeks now. But that's another post entirely, believe me.

A Baby on the Way

Okay, so he's not so much "on the way" anymore because I started this post 5 days ago and let's face it, that's kind of a long time for active labor! (Ouch!) On Thursday, August 6th my cousin Sam went into labor with her second child, first boy. If you would like to see his stats and a picture of him head on over to her blog. Try and prepare yourself though ~ seriously.

Welcome to the World and to the Family, Mr. Evander Benjamin!



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Google It

9:13:00 AM Posted In , , , Edit This 2 Comments »
25 Jul 10:16:31 AM www.google.com ear infection antibiotics
24 Jul 07:11:17 PM www.google.ca i believe that faith has brought us here
23 Jul 09:24:12 PM www.google.com dryer cheerios
23 Jul 03:12:52 PM www.google.com compassionate weaning
22 Jul 06:55:16 PM www.google.com cheerios confession
19 Jul 11:40:58 AM www.google.com johnny sado
17 Jul 05:02:56 PM www.google.com weaning cold turkey
17 Jul 08:19:25 AM www.google.com excema from cheerios
17 Jul 12:01:26 AM www.google.com aspergers stop the screaming chores
15 Jul 12:30:17 PM www.google.com i had biweekly biophysical profile and autism
9 Jul 03:09:48 PM www.google.com cheerios and farting
7 Jul 11:47:25 AM www.google.ca john emmett physician chronic pain
2 Jul 06:09:53 PM www.google.pl masochistic puppy

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Google It!

3:06:00 AM Posted In , , , Edit This 0 Comments »
who is the actress in the cherrios commerical (Google) ~ I have no idea but I'm fairly certain you won't find her here.
i got excema from eating cheerios (Google) ~ Holy cow! I figured Cheerios were one of the blandest foods available. Sorry to hear about your luck.
i believe in faith has brought us here (Google) ~ Some days I feel this way. Some days I feel all out of faith. I'm not sure which of those days today is.
karate in 2009 (Google) ~ That would be true of Gavin.
mommy sado (Google) ~ I am not the sado! Mr. Emmett John is the sado.
confessions cheerio box (Google) ~ I think this is me...maybe...then again, maybe not.
cheerioconfessions.blogspot.com (Google) ~ This is definitely me. :)
cheereo side effects (Google) ~ I may actually have to Google this myself because I'm intrigued.
torture sado (Google) ~ This would be Mr. Emmett John again.
cherrio confessions (Google) ~ Yup, definitely me again.
interesting m&m facts (Google) ~ Probably not what you were looking for. I wasn't referring to the candy. I was talking about my Mini-Miracles (M&M's).
sado story (Google) ~ Again, probably not what you were looking for...
cheerios smelly fart (Google) ~ lmao...that's all I've got...
london mccalling (Google) ~ Exploring Holland or the blog formerly known as London McCalling.
fun facts about m&m (Yahoo) ~ Again just random fun facts about my babies, not candy.
autism signs 6 weeks old (Yahoo) ~ I don't think I even knew what Autism was when Gavin was 6 weeks old.
freesealpoint kittens (Google) ~ Ah yes, the Twins. I miss them. I pray everyday that they have a better life where ever they ended up.
razor blade torture (Google) ~ Um...Emmett John is skilled in many types of sado masochistic torture, however, he's never been known to use razor blades! He kind of lacks the fine motor skills for that. Geez.
cheerios commercial - brother and sister (Google) ~ I have a brother, Zach. He's graduating from high school today.
torture specialist (Google) ~ Hello Mr. Emmett John!
sado-masochistic (Google) ~ Mr. Emmett John again.
what is sadomasochistic torture (Google) ~ Ask Emmett John. He was born knowing the definition. It's quite disturbing really.
sado masochism tylenol (Google) ~ Wow. Tylenol is really branching out aren't they?
block castles (Google) ~ This is a reference to Gavin.
cheerios commercial moving house (Google) ~ A moving house, huh? Yeah, this could very easily be a reference to Gavin as well.



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Down with the month of MAY!

1:52:00 PM Posted In , , , , , , , , , , , , Edit This 1 Comment »
Historically, for the past 7 years the month of May has sucked. And not just sucked in the terms of "Oh wow, this is kind of lame" sucked. It has sucked in terms of "Next year I am skipping the month of May", sucked in terms of "deep space vacuum" sucked. (little nerd girl joke there - sorry) Every year I go into the month of May with the mindset that this year will be different. This year May will not suck. Every year since my Grandma M died on May 11, 2002; May has sucked. Positive mindset or not. Until this year.

This year things were shaping up a bit differently. This year May 1st through the 10th was great. We had our normal bumps and bruises but nothing major. May 11th was a little sad for me but nothing I couldn't handle. We made it through May 12th through the 17th. The first 17 days of May were normal (for us), calm (for us) and completely unlike May for the past 7 years. Then I picked Gavin up from school on Monday, May 18th. Allow me to explain.

Monday, May 18th, 2009

The day started out normal and innocently enough. Gavin was feisty and angry, nothing new. However, he wasn't hungry even though he went to bed without dinner the night before since he chose to pitch a massive meltdown during dinner rather than eat. This seemed slightly odd to us but we figured maybe he wasn't really hungry the night before. Maybe it had all been a power struggle. So we went about our day and then I picked him up from school at 3:00pm. Gavin decided that he didn't want to do his work, much like every other day. Only on this day he decided to try and physically intimidate one of his teachers. He tried to hit her. She stopped him. He also spent a lot of time physically assaulting himself, which led her to trying to prevent this behavior. While lecturing Gavin on our way home my sister called me. It would appear that the poo-cloud was raining on our family as a whole, not just us. That's her story though. Just trust me when I say that it's the nightmare of mothers with teenage daughters everywhere.

Tuesday, May 19th, 2009

This morning I was helping Gavin get ready for school and a thought occurs to me. Here's the conversation I had with Gavin. I'm serious.

Me: Gavin, you weren't hungry when you woke up yesterday were you?
Gavin: Nope.
Me: Is that because you ate something that wasn't food? (Gavin, like most Autistic kids, has PICA.)
Gavin: Yup.
Me: Was it the strings from your blanket? (He's been known and seen Dr. H for pulling the threads out of his comforter (yes, he insists on sleeping with it even when it's 70+ outside - that would be the sensory integration disorder) and eat them.)
Gavin: No.
Me: (having a light bulb moment) Did you eat your toothpaste? Is that why you went through it so quickly?
Gavin: Yes.
Me: What other things do you eat that aren't food?
Gavin: Paper. Strings. Toothpaste. But not toe-jam. Well, not anymore. But I used to. (I kid you not.)
Me: What paper?
Gavin: The paper on my desk.
Me: Why would you do that?
Gavin: Well, I was hungry!
(Now Rob and I had checked out his desk Monday night - separately. Rob thought I had cleaned it off. I thought Rob had cleaned it off. And we both forgot to mention it to the other one. Rob and I would later figure out there were roughly 12-24+ sheets of paper (copies, construction paper, art paper, art projects, cardboard, paper scraps etc covered in copier ink, crayon, marker, color pencil, pencil, pen, glue etc) not to mention a bunch of little plastic "gumball machine toys". All of these things are now gone.)



After this conversation I took Gavin to school. A.) Because Dr. H's office didn't open until 8:00am and I didn't know what he was going to want me to do. and B.) Because at the time I didn't realize just what was on the desk. So a little while later I called Dr. H's office and spoke with a nurse. She said she would speak with Dr. H and call back but I should call Poison Control in the meantime just to be safe. So I called Poison Control and they said that given Gavin's age and size the crayon etc wasn't a concern. Their bigger concern was the amount of paper and whether or not it was going to cause a bowel obstruction. (Oy.) They told me to follow whatever Dr. H said to do.

Well as if all of this wasn't more fun than a barrel of monkeys (it wasn't) I also woke up with a very sore throat Tuesday morning. So while waiting to hear back from Dr. H I called my Dr. N and made an appointment for that morning. So Trisha, Emmett John, Elliott Richard and I left. We dropped Elliott Richard off at Grandma G's fully intending to pick him up on the way home. Then Trish and I went to my appointment while Rob waited to hear from Dr. H. I had a sinus infection, strep throat, and upper respiratory infection. I suppose anything worth doing (or having) is worth doing well.

While I was sitting at Dr. N's office, Dr. H called Rob...personally. Dr. H had already called the head of gastroenterology at the local children's hospital who said to keep an eye on Gavin. As long as he was asymptomatic there was no need to bring him in. That was before we realized everything that had been on his desk and was now missing. Once Rob explained the desk contents et al Dr. H said he wanted us to pick Gavin up from school and take him straight to the children's hospital emergency room. He said they would be the best equipped to handle Gavin and his situation. So Rob, Trish, Gavin, Emmett John and I made our way to the Emergency Room.

All told we spent 2-3 hours there. They "probed" him to be sure he wasn't blocked. Gavin loved that, let me tell you. They did x-rays to be sure that he hadn't swallowed anything made of metal, which turned out clear. Thank God. Then the Attending had to check his nose to make sure he hadn't shoved anything up there. He thought he saw a marble up there so that led to another procedure, which led to Gavin being wrapped like a burrito - something we'll be using for blood draws in the future. In the end, all was clear. The paper will pass. If there were toys, they were made of plastic, didn't appear to be causing any poisoning, and seemed to be passing with the paper. If he became sick, started vomiting, complaining of stomach pain or still hadn't pooped in 3-5 days we were to call Dr. H for a follow-up. Luckily none of those things happened. And the paper seems to be leaving the building.

Wednesday, May 20th, 2009

You know, I don't remember what happened on Wednesday. Oh wait! Yes, I slept as much as humanly possible to try and feel somewhat human again. It didn't work. And when Rob picked Gavin up from school we learned that Gavin had cussed in school. However, when asked about it, he lied. This led to a giant meltdown. As Gavin was melting down, Rob and I gutted his bedroom. We stripped it of every piece of paper we could find. Every tiny toy. Every big toy. Every everything that could fit in his mouth.

While we were doing this, Jenn was watching Elliott Richard and Emmett John. And the phone rang. It was Grandpa G calling from the local hospital. Apparently, Grandma G had been outside gardening. When she stood up, she heard a *snap*. All she did was get up and she broke her ankle. Dad sounded pretty freaked out on the phone. She's okay. But she's pretty shaken up because she truly didn't do anything except stand up and her ankle snapped.

Thursday, May 21st, 2009

We woke up. Things were moving along fine. The morning was calm and quiet. Gavin went off to school without incident. Mr. Emmett John and I laid down at about 9:00 am for our usual morning nap. (Yes, my fibro is that bad that I have to take naps - usually more than one - everyday.) The house phone rang but no one answered it. Then my cell phone rang. It was the school. When the school calls, it's never good news. I answered and spoke with the school guidance counselor. Now it's important to keep in mind that I drop Gavin off at school at 8:00am. The school was calling at about 9:00am. During that hour Gavin did little else besides meltdown. All because his teachers had the nerve to ask him to write his name and do his work. He refused. You're surprised, I know. He melted down for 45 minutes. Finally, the guidance counselor decided to try and help him by holding his hand with her hand and physically helping him to do his work, not force him to do it but actually help him. This led to Gavin throwing his pencil across the room. Before holding his classmates "hostage" by blocking them from leaving the room. Then when they did get the class evacuated the guidance counselor was getting ready to give Gavin the chance to get himself under control or she was calling me. She was about to offer his that chance, when he threw the pencil at her head and missed her by about an inch. At that point, she'd had enough and she told him that she was calling Mom. She left the room expecting him to continue with his meltdown. He didn't. He followed her and cornered her in the office, ordering her not to call me. By the time Rob and I arrived at the school Gavin, the Principal, and Mr. B (the IEP Coordinator) were locked in the office with another teacher Ms. J sitting outside as a watchman. In the end, we took him home early. He spent the day in his room without toys or anything fun to do. We had plans to do his work he was missing by coming home early but the day took a very different turn once we arrived home.

While we were at the school, Rob's little sister, Jenn, babysat Elliott Richard and Emmett John. Now as I was leaving that morning to take Gavin to school, I saw a red female pitbull she was either currently nursing or had recently stopped nursing pups without a collar or tags limping through the neighborhood so I called the county dog warden. I made it very clear that she did not appear aggressive just scared and possibly injured. I just wanted her reunited with her pups and I didn't want her hit by a car. So while we were gone the dog warden showed up at our house where he is greeted at the door by Maggie Sue, our tan female Boxer/American Bulldog non-nursing with collar and tags non-limping secured dog. Jenn answered the door and Elliott Richard takes Maggie by the collar saying "bad dog...stop barking". The dog warden told her that Maggie was a pitbull and she was going to "bite that baby". So when we got home from dealing with Gavin and the school we now had to deal with the county dog warden or risk losing our beloved Maggie. Rob called them and was on the phone for what seemed like forever. In the end we had to produce copies of the paperwork from the vet stating that she isn't a pitbull and that our vet had done a temperament test on her. We also had to present her to the head dog warden for an examination to prove that she isn't a pitbull. In the end, he sided with us and ruled that she is in fact a Boxer/American Bulldog mix. Thank God for small favors!

If he had ruled against us, we would have had two choices. In our county, if you own a pitbull mix you have to have a $100,000 insurance policy, a 6 foot fence surrounding your yard and if we ever took her for a walk she would have to be on a 6 foot chain leash with a muzzle. So if he had ruled against us, we either had to find a way to afford the new fence and insurance policy. Or we were going to have to return Maggie to the humane society. Luckily, we don't have to think about that...ever again. :) When Rob left to take her to see the dog warden though. I was devastated. I am not a dog person. Period. But I am absolutely a Maggie person and the idea of having to give her back broke my heart.

Of course, what week of chaos is complete without a visit to Dr. H for Mr. Emmett John? (Have I mentioned this is his third appointment in as many weeks? We've been busy, Mr. Emmett John and I, but that's another post.) I had to take Emmett John to see Dr. H at 2:00pm because he's had diarrhea for almost 3 weeks. He isn't sick. He isn't on any medications. At first we thought it was a side effect of the Zyrtec he was taking for his allergies so we expected it to clear up once it was out of his system. It hasn't. Now it's also gotten to a point where he's loosing weight because of it. So now we find ourselves back in the familiar land of Emmett John being sick and us not knowing why. I dropped off a stool sample at the local hospital so they could run a half dozen different tests to try and find the cause. We won't have the results back until Tuesday though since Monday is a holiday.

And so Thursday comes to an emotional close. All of the up-and-down up-and-down this week so far has made me nauseous. And I usually love roller coasters.

Friday, May 22nd, 2009

We finished out the week with a fairly calm day, by the rest of week's standards anyway. Gavin went to school where the Head of the local MST program sat in his classroom and observed him for an hour or so. He was in the office for 3-4 times in that hour, so Gavin did not disappoint. Which believe it or not, for once we were actually worried that he would hold it together and keep all of his bananas, thereby having a pretty good day. It would figure, wouldn't it? A woman comes to the classroom just to see his behavior and he has a wonderfully well-behaved day? lol That didn't happen though. Thank God again.

Then at 2:00pm Rob and I met Patty at Dr. R's office for an appointment with him to discuss what to do with Gavin.

They would like him to have some pretty heavy duty, in depth psychological testing done. The problem is that this particular testing is an art when given to adults but to give it to children and interpret it correctly is even more of an art. So it's even more difficult to find someone who not only performs the test but is good at it. Dr. R is going to find the people who perform the test. And Patty will review them and pick out just the right one.

Then we discussed medications. Dr. R said he doesn't like to pick a medication and work his way through the doses. Then if it doesn't work, move on to the next medication. However, in Gavin's case he said he doesn't see any other choice. So we left his Depakote alone, although he needs more blood work done. (Thankfully Rob and Grandpa G are taking him this time.) We also left his Klonopin alone. Dr. R did make the decision to increase Gavin's Zyprexa in the hopes that it would calm him down. Right now, all it's doing is doping him up, which I suppose is better than nothing. Although truthfully I don't want him to go through life doped up. At the same time, I can't have him lashing out at people and trying to assault others.

We also discussed if Rob and I should consider a different school for Gavin. I love his school. I think the world of everyone there. However, Rob and I are wondering how long Gavin is going to be able to stay there. Also most of the staff is young and looking to start their own families very soon. Gavin is violent enough when it's just him against himself or a staff member. The last thing we need is for it to come down to Gavin against a pregnant educator. Then there's the fact that he's constantly influencing the behavior of his classmates with his outbursts and meltdowns. There are a few options that Dr. R wants us to look into. So Rob and I will probably spent the summer researching them. Then we will tour them in the middle to the end of August and make our final decision then.

Overall, I guess it was an okay appointment. Rob left feeling better about it than I did. But it is what it is, I suppose.

That was our lovely week. I'm glad it's over. Although truth be told I don't expect the next week to be much different. Nor the one after that. Or the one after that. After all, it is the last 4 days of school this week. None of them are "education days". They are all fun days. And then it's summer vacation. I hate summer vacation, for a multitude of reasons really. But basically, I reached my saturation point for stress, drama and needless shenanigans a long time ago so I just don't have the patience for any of it anymore.


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The winds of change...

5:17:00 PM Posted In , , , , , , Edit This 1 Comment »

they are a blowing.

Here's in the Cheerio Household that is. (Okay, totally not our real last name but for the sake of some resemblance of privacy and safety work with me here.) Last Monday Rob and I saw Dr. R, Gavin's psychatrist and he feels that Gavin does not have signs of Reactive Attachment Disorder (RAD), which was an idea Rob and I had been kicking around with Patty. He feels that it is much more likely a Conduct Disorder. Now some of you may read the definition of Conduct Disorder, shake your heads and say, "Nope, don't see it." I'm here to tell you that there is so much that most never see. So trust me when I tell you that Conduct Disorder fits. (It's another post entirely for me to explain all the reasons why and I'll try to get to that post ASAP.)

Dr. R said that there is a therapy here in our hometown that is supposed to do wonders with kids with Conduct Disorders. It's called MST. He also stated that children with Conduct Disorders do well in a strictly structured, prison-like environment. Now our lives are structured already. However, if "prison-like" structure is what we need to keep our family afloat then "prison-like" is what we shall have. I'm in the process of putting a plan into action that will create this ultra-structured environment for my family.

I don't do well with structure as a whole. My brain just doesn't seem to work that way. Whenever I attempt to force it to, it just doesn't work out well. However, it is my hope that if it is my plan and implemented by me then I will be okay with it. Believe me when I say this isn't a simple plan by any stretch of the imagination. I'll have to lay it all out for y'all sometime but right now I hear laundry and dishes calling my name.

So the winds of change, they are a blowing. Hopefully they blow us someplace nicer than where we currently are.


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Long time no see...

11:12:00 AM Posted In , , , , , , Edit This 2 Comments »
Ok so my darling Nikky informed me last week via Twitter (I *heart* Twitter!) that it has been roughly 3 weeks since my last post. Yikes! Where has the time gone? Oh, yeah, that's right...life. So as I sit here waiting on about a dozen return phone calls I'm going to try and post the shortest, most informative update I can.

Gavin

Dr. R has placed Gavin on the dreaded Depakote. It is what we call our "Hail Mary" play. We had put it off because it requires pretty frequent blood draws, however, the time has come to bite the bullet. He started out on 250mg BID and then after 5 days my sister and I took him to have his levels checked. That was an experience let me tell you and a post all on it's own. Now he is on 375mg BID. Poor kid is exhausted out of his mind but he flat out refuses to sleep because he's afraid he'll sleep the day away. Overall, he's doing okay I suppose. Well, not really. He's aggressive and violent, distracted and rude. In the past few weeks he's punched, kicked and smacked Elliott Richard across the back with a toy. His imaginary boss is back. He doesn't sleep and stays up all night for days at a time writing songs, writing stories, drawing these intricate plans for things that only make sense to him. Rob and I can see him slipping away again and it kills us.

Elliott Richard

My Tiny Little Twitterbug will be 3 years old this Wednesday. :'( I'm so not ready for this. He's getting so big though, it's just crazy. He still has no interest in potty training. Physically and emotionally he's ready. He still seems to have a mental block about the whole thing though. So we don't push it. I've got a ton of new "Twitterisms" to post. I swear he learns something new to say everyday. He's super excited about his birthday party this weekend. Of course he's been talking about it since Gavin's party in January. lol His 3 year checkup is next week so I'll have more to post about him then.

Emmett John

Mr. Emmett John is now 8 months old, 7 months adjusted. He's been able to roll over from his back to his tummy for months but really didn't seem to see the need. Now that he can get from his tummy to his back, it's a whole different ballgame. Back to tummy. Tummy to back. Back and forth. Over and over and over again. :) lol He's babbling with "ba-ba-ba" now as well. He's also starting giving what Rob and I call "kisses", which is basically just Emmett John attacking your jawline with his one tooth. lol Yes, that's right....he has his first tooth and is working tirelessly on his second!

And speaking of Emmett John he's hungry (still nursing on demand) and tired so I'll have to leave this long overdue update here. I'll try and be back later to update on me, Rob, life with a big sister, Maggie and everything else.

Stay tuned!

The Party to End All Parties

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Literally.

Saturday, January 24th at 4:00pm we all gathered together to celebrate the life of my beautiful, special little man. In hindsight, perhaps this was not the best idea.

So despite my best efforts to prepare and be ready long before the day of the party arrived, Saturday was a crazy day. I had tried to get the cleaning done and the shopping done long before the party. Yeah, that didn't happen. So of course while we are all running around like chickens with our heads cut off, Rob bent down and picked up an empty duffel bag. He didn't move in a funky way. It wasn't heavy. But that's all it took and his back was G-O-N-E...gone!

There I was with a house to clean, shopping to do, children to care for, and a party to set-up and my partner in crime was down for the count. (Oy!) I admit it, I was freaking out. Luckily, I had already called Mom G. and begged her to come and help. I was waiting for her to call me so I could pick her up. Even with Rob's Mom coming, I was still freaking out and feeling the day spinning wildly out of control. Enter "Super Sister"! (duh tu da da) I called my big sister, Trisha, near tears because I had no idea how I was going to get everything done. True to form, Trisha saved the day. She was everything a big sister should be, in my opinion.

Mom G. called me at about 10am to say that she was ready. Mr. Emmett John and I went to pick her up. Then while we were out I did my running around. We hit the Dollar Store for cups, silverware, napkins, table cloth and some other odds and ends that weren't really on my list but I bought them anyway. :D (lol) Then we hit Giant Eagle so I could pickup the ice cream and pop. I completely forgot the chips and candy that I had also intended to pick up. Eh well. We swung through McDonald's for 2 ice teas and then headed home.

All of that build up, now for the party. ;)

The party was scheduled to start at 4pm. Trisha arrived at 12noon, shortly after Mom G. and I returned from our running around. And by running around, I mean Mom G. was kind enough to hang out in the car with a sleeping Emmett John. We ate lunch and then tackled the house. Mom G. took on the dishes, which then morphed into her cleaning the kitchen. Trisha and I tackled the laundry that needed folding and the bathroom. She was also kind enough to get Elliott Richard dressed, which is no easy feat. He made her offer every single shirt he owns. Only to choose the shirt she offered him first in the end. (lol) Between Mom G., Trisha and myself we managed to knock out the cleaning, shopping and general party-prep by 3pm! :) (Woo who!)

People started to arrive around 4pm, right on time. (I love punctuality.) All told, the guest list was pretty long. :) We had:

Grammy (Great Grandma C.)
Great-Aunt Sharon
Aunt Trisha
Grandma G.
Pa-Pa G.
Grandma W.
Grandpa W.
Uncle Brian
Uncle Jon
Aunt Teri
Aunt Kate
Uncle Tim
Jenna (Uncle Tim's girlfriend)
Aunt Jenny
Matt (Aunt Jenny's boyfriend)
Michelle ("Mo-Mo", our neighbor)

The party itself was a huge success! We had pop and cake and ice cream. I had baked some cupcakes. My parents picked up a 1/4 sheet cake from Giant Eagle. We talked, laughed and mingled. Gavin bounced off the walls until it was time for cake and ice cream. We sang "Happy Birthday" to him and he blew out his candles. Then Elliott Richard got ready to blow out his candle (my method for keeping him from blowing out Gavin's candles) but he refused to blow it out without us singing "Happy Birthday" to him. (lol) While we mingled and ate cake, Gavin continued to bounce off the walls. (Perhaps this should have been a clue as to what lie ahead.) Before long my Grammy and Aunt Sharon said they needed to get going, plus Gavin was getting more and more hyper as time went on so we opted to move right along to the presents.

Let me just say this, he made out like a bandit! And boy can my boy open gifts! Michelle commented on the fact that she's never seen a kid open gifts that fast before. (lol)

He was thrilled beyond words with his new Kinex Ferris wheel. After he had torn the wrapping off all the gifts, he grabbed the box and made a bee-line for his room. Throughout the night Brian went upstairs and helped Gavin put it all together and get it sorted out. Thank God for Brian! Rob and I are horrible with complicated sets like that. While I'm confident that Gavin would have eventually had the whole thing built, it happened just that much faster with Brian's help. :)

People slowly trickled out after Gavin opened his gifts. In the end, it was Rob, me, Trisha, Jenn, and Matt. Elliott Richard went to bed between 8 and 9pm. We let Gavin stay up until 10-ish since it was his birthday party and all. At around 9:30pm the adults decided we were starving and we ordered Pizza Hut. (My first Pizza Hut pizza in about 6 months! That's another post that's coming.) It was a really awesome way to end the evening. Sitting around and eating pizza with some of my favorite people in the world. Overall, it was a good day.

That was then. Sunday was a whole different story.

At the time when I planned the party, I wanted to celebrate Gavin. I wanted to make his birthday big and bright and special. I wanted him to be able to look around and see just how much we all love him. In that respect, I accomplished my goal. What I failed to take into account were the side effects. I failed to think past Saturday into Sunday and the next week. That was my fault.

We spent Sunday and the week following trying to...adjust. Sunday night we couldn't get Gavin to give up on his Ferris wheel and go to bed. The insanity that ensued over the next week...I can't really find words to describe it. It wasn't any single behavior. It was more a general feeling running through the household, controlled by Gavin. Much like the under-tow of the ocean is controlled by the moon and God. It's nothing that can be seen by an outsider. However, it is certainly something that can be felt by the swimmers in the ocean.

Because of this feeling, this current, Rob and I have made the decision that this year's birthday party was quite honestly the party to end all parties, at least as far as Gavin is concerned. That's not to say that we won't celebrate his birthday every year, because we most certainly will. Nor will we prohibit others from celebrating. It will just have to be celebrated in little, tiny bursts either over the course of a week or possibly in a single day (scheduled in a fashion similar to doctor's appointments). Either way we won't attempt to overwhelm him with that many people again. Even when it comes to Elliott Richard and Emmett John's birthdays, we will likely make arrangements with my parents to leave early and take Gavin with them. That way we are not forced into avoiding birthday parties for them as well.

So the party itself was a smashing success, in my opinion. The aftermath, fallout and next 7 days...yeah, not so much. You live. You learn, I suppose.

9 years old and Growing Stronger Everyday

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Tomorrow is Gavin Alexander's 9th birthday. I can't believe that 9 years have gone by already. Likewise, I can't believe all that we have survived and endured over the past 9 years. Wow.

If you follow me on Twitter, you may have read about Thursday's 9 year well-child check-up. If you don't, hold on tight because it was a bumpy ride!

First things first, the stats:

Height: 54.3in/4ft 5.3in (75%)
Weight: 63lb 2oz (51%)
BP: 80/62
Vision: 20/25

My darling bottomless pit has only gained 2oz in the past few months. Dr. H doesn't seem worried. In fact, he said he's very happy with Gavin's height and weight because he's consistantly gaining and growing. I guess, in the end, that's all that truly matters. Although between you and me, I wouldn't mind if some weight stuck to him because it's getting next to impossible to find pants that are both long enough and slim enough to fit him. (lol)

He hasn't really grown any either. I mean he's grown like 0.3in but that doesn't seem like much. As long as Dr. H is happy though, I'm good.

Gavin had taken his "Funfolio" with him to the appointment to help keep him distracted. (That think is amazing!) So while Rob and I talked to Dr. H, Gavin sat and drew pictures and played. We discussed the fact that Gavin was due for a chickenpox booster. Dr. H said that we could do a blood test to see if the booster was necessary but that would mean the possibility of having to bring Gavin back in at another time for the booster shot anyway. We opted out of that. Then we discussed the fact that Gavin has never had bloodwork. No liver panel. Or kidney functions. Or CBC. Or even a lead level. While none of us relished the fact that the bloodwork was obviously necessary, we did agree that it had to be done. Dr. H even schmoozed the Lab Ladies into sending a Lab Tech up to do the bloodwork while we had him held down for the booster shot. Apparently because of Gavin's PICA we need to do lead levels on him more frequently than usual to make sure that he isn't slowly poisoning himself. (Yippee.) After we talked and caught Dr. H up (this was his first time seeing Gavin for a well-child appointment), he did his exam. Everything was perfect.

Then we discussed the fact that Gavin has dextracardia. Dr. H seemed a little...excited by the fact that Gavin has dextrocardia. (lol) He said that he had learned about it in medical school but had never actually seen a case before so he wanted to do some research and get back to me about it. He said depending on what he learns in his research he may want to schedule some tests to see the extent of the dextrocardia's effect on Gavin. Dextrocardia is incredibly rare. The rarest form is when the heart is flipped and lies on the right side of the chest and nothing else is effected. There are other forms where all the organs in the body are flipped and on the opposite side, which is the most common form of dextrocardia. There can also be lung and other issues tied to the dextrocardia. So we are waiting to hear back from Dr. H about what he would like us to do on that.

After the exam and all of the grown-up talk, Dr. H left to see another patient while the nurses gathered and the Lab Tech made her way up to our room. The point of no return had arrived.

Dr. H had wanted to be in the room to help us during the shot and bloodwork but once Gavin figured out what was about to go down, well the anxiety was too much for him so we opted to get started without him. It took 2 nurses, 1 Lab Tech, Rob and myself to hold Gavin down for his booster shot. We opted to lay him on the exam table so that we could just transition from the shot to the bloodwork. When Rob picked Gavin up to lay him on the table Gavin flung his legs out trying to hook his feet under the exam table and a chair to keep us from laying him down. Let me tell you, he may look little but my boy is a scrapper! He fought hard! Luckily I had the presence of mind to tell Rob to leave Gavin's shoes off otherwise things would have been pretty painful on my end. Dr. H's nurse that always treats Emmett John, Christine, was the one giving the booster. God bless her. I've never seen anyone give a shot so quick in my life!

Not only is Gavin strong but he has a set of lungs on him! He screamed. He begged. He pleaded. It was horrible and heart-breaking for me as his mother (and Rob as his father) to hear him. He was desperate and begging us to stop it and "don't let them do this to me". At one point I could do little else besides hide in the corner and shake. Well, during all of the hullabaloo Dr. H was in the neighboring exam room and he began to BEAT on the wall. He hit it so hard you could see the wall shaking! It was crazy. Just after we got the booster in, while Gavin was catching his breath and before he had figured out the Lab Tech's role Dr. H came rushing into the room. He walked over to Gavin's side and began helped to hold him still. All the while telling Gavin, "It's okay buddy. I'm here. It's almost over but we have to do it." It was so nice to see how much he cared about my special little boy. Well, Gavin wasn't having any of it. He looked Dr. H in the eye and screamed as loudly as he could, "I.Don't.Like.You.Anymore!" Dr. H just took it in stride and told Gavin, "I know you don't but it has to be done buddy. I'm sorry." In the end, the Lab Tech took 6 vials of blood so that they could run all of the necessary tests. Gavin was hysterical during the whole thing. The Tech was awesome. Gavin has never had bloodwork done before, unless you count the bloodwork he had done 9 years ago in the hospital. I'm really curious what it will show.

Overall, the day was one of our more stressful with Gavin. At least more stressful and unrelated to court or Gavin's meltdowns for anger-based-reasons. I'm so glad to have it over and done with though. On the bright side, Gavin doesn't have to get any more shots - booster or otherwise - until he's like 15 years old. Woo who! In the end, he played the drama card for a little while after the appointment but he made a full recovery by Friday. Plus, as a bonus for...surviving...he got to spend the night at Grandma W's house! Then Grandpa W asked if he could spend Friday night there as well. Woo who! So Gavin got a cool reward for having survived the day. And Mommy and Daddy got some time to recover. (lol)

The Story of Gavin

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Ah, yes, the Story of Gavin. Definitely not your "fairy tale princess" story, that's for sure. But it's part of our story and it's the beginning of his story, nonetheless. So it must be told. Besides I know you're all simply dying to know where it all began with my ex. ;)

Before (Coming Soon!)

The Pregnancy (Coming Soon!)

Labor & Delivery (Coming Soon!)

Birth to 6 months (Coming Soon!)

6 months to 1 year (Coming Soon!)

Gavin's 7 Rules

Our Support Teams

What is Autism?

What is Aspergers?

What is Bi-Polar?

What is ADHD?

What is OCD?

What is PICA?

What is Sensory Integration Disorder?

What is a Conduct Disorder?



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Let's wrap it up

6:53:00 PM Posted In , , , Edit This 1 Comment »
So we left Dr. H's office and went into the basement of the building to their Radiology department. Mom G hung out with Mr. Emmett John. We waited for maybe 5-10 minutes before the pager (like they use at popular restaurants) went off. I went back with him but then the Radiology tech kicked me out of the room. Gavin said he was okay with me leaving the room, so I went. Before I left I explained to him what was going to happen. He took one look at all the big tubes and whatnot coming from and going to the x-ray machine and asked if we were going to suck his stomach out of his body to take it's picture. (God love him.) I then explained again what would happen and tried my best to assure him that we were not going to suck his stomach out to take it's picture. I was an absolute nervous wreck while they were in there but Gavin did beautifully. He told me later that he was still a little scared about the whole stomach sucking thing but after the first x-ray (they took 2) he was okay. :)

Now we wait. As I said before, Dr. H said he will call me tomorrow and give me the results. If there is something there, we will formulate a plan of attack. If the x-ray is clean, we will just keep an eye on Gavin. If he gets worse, we will obviously call Dr. H back. So now we play the waiting game. Fun. Fun.

I just want to say that I am so incredibly proud of Gavin. Dr. H had about a half dozen newborn patients come in while we waited which threw his schedule off in a big way so we ended up waiting for like an hour in the waiting room. Gavin almost lost it a few times but for the most part he held it together. When we saw Dr. H he answered his questions to the best of his ability and he held it together. The x-rays went far better than I had even dared to hope for. It felt as if I had a hybrid of Gavin-before-Autism and Gavin-with-Autism. His answers and many behaviors were very Autistic. But the manner in which he handled the day was very unlike Gavin with Autism. It was nice and I am so proud of him.

Does this xray make me look fat?

12:34:00 PM Posted In , , Edit This 0 Comments »
Dr. H came in with a med student. We talked. He cracked jokes about how my kids are on "very short list" of super difficult cases. (lol) He said hi to Mr. Emmett John. Then he checked out Gavin. Dr. H said his tummy felt fine. He sent us downstairs for the x-ray. If the x-ray doesn't show anything, then we'll keep an eye on him and report back if there's any change (ie. Vomitting, stomach ache, potty issues etc). If the x-ray does show something, well then the ride will get a whole lot bumpier and grumpier. Dr. H said we would form a plan of attack then if need be. So x-ray today. Phone call from Dr. H with the results tomorrow.

Hopefully Gavin does okay in the x-ray. I'll be sure to let y'all know.

Hanging in the Office

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We sat in the waiting room for about 45 mins. Now we're in the exam room. Today seems to be the day for newborns...teenie, tiny, sleepy newborns. I can hear them all screaming. Emmett John is content for now. Mom G is with me to help with Emmett John. Thank God for her. And the wait continues...I'll update when I have something new to report.

*vigorously waves the white flag*

6:03:00 PM Posted In , , , , Edit This 0 Comments »
Didn't God see my white flag? Doesn't he understand that I can't possibly carry anymore? Can't he see how much pain I'm in? Hasn't he noticed how I'm buckling under the weight of all I carry now? Can't he see how much I'm struggling? How little sanity I have left? My patience is gone, too. Can't he tell I feel utterly alone? That I feel as if everything I touch falls to pieces. Can't he hear me screaming for him? Why doesn't he answer?

All I've ever wanted, ever since I can remember, was a family. The stereotypical American dream...a house, a husband, a cat and a dog, 2.5 kids. Granted I have .5 more kids and I traded the dog for 2 more cats than the stereotypical American dream but you get the point. Now that I have want I wanted, I don't know if I was up for the challenge.

I've read the poems about being a parent to a child with "something more". I've heard the euphemisms. It's all crap. Complete and utter crap. I didn't plan a trip to Italy and end up in Holland. I am the mother of a child with special needs. Technically, if there is something more complicated than special needs, that would probably fit better. So far Gavin's laundry list of diagnoses are:

Asperger's/Autism
PTSD
ADHD
Bi-Polar
OCD
Sensory Integration Disorder

And now it has come to our attention that Gavin may also have Pica. Apparently he has been eating toilet paper and the stitching on his comforter. Last night he came downstairs and asked us if his gums were bleeding. I told him no and asked why they would be bleeding. He cheerfully informed me that he sometimes cuts his gums when he's eating his blanket. So we had the food vs non-food conversation. During which I asked him why he would eat toilet paper and his blanket. He said because it tastes good and we don't feed him enough so he eats these things.

Now I don't owe anyone an explanation on this matter, however, I will offer one. First of all, we do feed Gavin enough. In reality he eats more than me, the nursing 28 year old grown woman. Also because of his Autism and various mental disabilities he does not possess the ability to self-regulate so we have to limit his access to food. We have tried in the past to allow Gavin to eat until he feels he is full. What ends up happening is he eats until he vomits. Then after he vomits, he tries to go back and eat some more. So we cannot allow him to attempt to self-regulate during meal times. We make sure that he at least gets all of the suggested values on the food pyramid everyday. So please, rest assured that Gavin is getting plenty to eat.

I checked his comforter last night to see which part of it and how much is missing. All of the "decorative" stitching that holds the center of the comforter together, is gone. He's eaten it. The fact that he's eating the toilet paper actually solves a mystery Rob and I have been pondering for a while, where does all of our toilet paper go. Now Gavin believes he's been eating his comforter for 2 years, however, I know that the last time I washed it (maybe a week or so ago) all of the stitching was there. Just to give you an idea of Gavin's mindset about this whole situation, while I was checking his comforter last night Gavin asked me if I would be replacing it. I told him no. Then I aksed, "Why would I?" His response, "Because this one is almost gone." Yup, he expects us to help him continue this behavior. (Oy vay.)

Obviously it's not a good thing that Gavin is eating non-food items. This is new territory for both Rob and myself so the first thing I did was call Patty. She said that contrary to what Gavin is claiming, she does not believe that we are not feeding him enough. She has seen his inability to self-regulate and as such trusts that we are feeding him plenty. She said that us not feeding him enough is an excuse. She doesn't have a lot of experience with Pica so she suggested I call Dr. R and Dr. H and ask them for their thoughts. So I called both of them and left messages with their nurses. Dr. R said Pica is more of a physical, developmental disorder and we should call Dr. H. Then Dr. H's nurse called back. He wants to see Gavin tomorrow (Tuesday) morning and then he will likely refer us for an x-ray. Dr. H wants to make sure that the string Gavin has eaten hasn't formed a solid ball in his stomach because if it has and it tries to make it's way through his system in one piece it will likely cause a bowel obstruction. And so that is where we are now. (By the way, it's 8:30am on Tuesday now because I had to take a break last night when my laptop died.)

In 2 and 1/2 hours I will pack up Gavin and Emmett John. We will pick up Grandma G and head to Dr. H's office. While we are there I will change Gavin's name! (Yay!) Then our morning of ultra-fun, super cool doctor's appointments and tests will begin. (That was sarcasm by the way.) I will update from my phone on Twitter while we are gone and if I get a chance I'll post updates to the blog as well.

Prayers and positive thoughts would be much appreciated.

A Super LONG and Long Overdue Post

8:14:00 AM Posted In , , , , , , , , , , , , Edit This 2 Comments »
Okay, Emmett John is fussy so this is going to be the fastest update I can manage. (Yeah, right. lol) Please forgive me if this seems jumbled and disconnected, Emmett John and Elliott Richard aren't big on sleep at the moment.

I'm sorry I haven't posted in nearly forever. I simply haven't been in the mood, which stinks because I was hoping to partake in NaBloPoMo (National Blog Posting Month) but I can only do so much. I do apologize though if my being MIA has made any of you worry.

Gavin

About a month ago Gavin was started on a new bi-polar medication, 150mg Trileptal BID. Everything was fine. It seemed to be working. His moods were gradually evening out. Then the bottom fell out. His moods took a nose dive. He began rapid cycling again. So we called Dr. R and he decided to double Gavin's dose to 300mg BID, which he had planned to do anyway. So two weeks ago, we double the Trileptal. We give Gavin his meds and proceed with getting ready for Gavin and Elliott Richard's flu shot appointments. On our way to Dr. H's office for flu shots, Gavin broke out in a serious rash. Dr. H wasn't in the office but one of the other peds saw him and confirmed that it was a reaction to the Trileptal. She said that there wasn't anything we could do for the itching (apparently Benedryl doesn't work on drug reaction rashes), so that was fun. We were told to keep an eye on his breathing etc but told he should be fine. (Ever try explaining to an Autistic 8 year old that he can't scratch and you can't help the itch? Yeah, I don't recommend it.) Since the ped wasn't worried, we sent Gavin to my Mom's as planned. At like midnight or 1am our phone rings. Gavin now has a fever, the chills etc. His breathing was fine so Mom gave him Tylenol for the fever and we all went back to sleep. He was fine in the morning so it appeared that the worst had passed. Until he got home. The chills, fever etc had returned. He was now running a 104 degree fever! So Rob is calling Dr. R and Dr. H's offices trying to figure out what to do. I'm trying to get Gavin comfortable and giving him Tylenol etc. Dr. R's office decides he has the flu and not a drug reaction at all. Dr. H's office said to keep a very close eye on him, if anything changed or the fever hit 105 we were told to call back ASAP. To give a general idea of how Gavin was feeling, he went to bed at 5pm and slept through the night until 8am the next day!!!!!! (This is a big deal because I don't think he's slept that much since he was Emmett John's age!) On the bright side, he recovered really quick. On the not-so-bright side, I'm definitely not going to win "Mother of the Year" this year. When Gavin went back to school, I accidentally gave him the 150mg dose of Trileptal. Luckily, he survived and we now know for 100% certain that Dr. H was right (it was a drug reaction) and Dr. R was wrong (it was NOT the flu). So while he broke out in a rash again, he handled it like a champ and it was gone within a day or two. So since this whole drama went down Gavin has been unmedicated for his bi-polar, which at the very least is making things interesting. Rob and I see Dr. R today to figure out what the next step is.

Other than that whole mess, things with Gavin have been fairly....typical for Gavin. He's rapid cycling. We're struggling to keep up with him. The whole situation is just exhausting. Of course that could have something to do with the fact that he hasn't adjusted to the time change at all. He puts himself to bed at 6pm every night and asks for him meals an hour early. We've tried to explain it to him but he doesn't get it. Poor thing. Hopefully he'll adjust soon.

On a positive note, a few days after the adoption was finalized (we should have the paperwork any day now - woo who!) the school had an Awards Assembly for the students. Gavin received awards for Perfect Attendance (which was blown for this grading period with the drug reaction), an award for meeting his reading goals with his Title 1 tutor, and another one I can't remember. (Hey, I already told you I wasn't winning Mother of the Year.) The school even went and changed his name on all of his awards so that they read Gavin G. :)

Elliott Richard

Well, unofficially potty training has begun. We've started buying Elliott Richard Lightning McQueen Pull-Ups. It took a little bit of convincing to get him to wear them but now he's in love. He's now changing his own diapers, well, he's taking his wet (and dirty - unfortunately) diapers off and then running around the house buck naked screaming "New biper!" He also tells us (sometimes before and sometimes after the diaper removal) that he's peed or pooped. He will sit on the potty, sometimes for nearly an hour. Then he gets up, puts on a Pull-Up and pees. Oy. So progress is slow and basically non-existent at some points but we are getting there.

During Gavin's whole Trileptal reaction, Elliott Richard received his flu shot. I expected a lot of tears and screaming. Daddy said that he was fine with the shot. (I was meeting with the ped about Gavin.) It was having his legs held down that ticked him off. Once they let him go, he was fine. lol I swear he never ceases to amaze me.

Other than that stuff, there's really not much to report in the land of Elliott Richard. He's still completely obsessed with Emmett John and helping me as much as possible. Which usually means that whatever I'm doing is taking twice as long as it would normally but whatever. He's growing like a weed. Eating us out of house and home or not eating at all. (I just love the terrible two's!) And as his hair grows back from his first hair cut, I'm thrilled to say that it is still wavy/curly! :)

Emmett John

I think I probably have the most to update on when it comes to Mr. Emmett John.

I'm thrilled to report that Emmett John is now the new and improved wireless version. We saw Dr. K and our nurse Vick at the Apnea Clinic last month (yes, I'm really that behind). The only concern they had was one Apneic episode that wasn't a full-fledged episode. His breathing slowed way down and then seconds after his breathing picked up again his heart rate dropped. Since they didn't happen simultaneously, it doesn't count as a true Apneic Episode and he was cleared for release. :)

Since then, he's gained a few pounds and grew a few inches. He now weighs 17lb 3oz and is 26.75 inches long!!!! That's the 80th and 90th percentiles respectively!! Craziness I tell ya.

He's been babbling and laughing (whenever he isn't screaming in pain from the reflux) for a while now but he's recently added the squealing to his list of tricks. He seems to have a very select sense of humor though. Only certain silly noises, scaring/startling him and whatever it is Daddy does seems to amuse him. Although there are times now when he will laugh when he hears someone else laugh, which is super cute! He gets super excited when he sees Mommy, Daddy or Elliott Richard. (Gavin hasn't shown much interest in him so Emmett John doesn't see him hardly ever.) He's rolled over but didn't seem terribly impressed with the accomplishment and hasn't done it in a while. He can't decide between his thumb, his Nuk binkie (he'll take other binkies but strongly prefers the Nuks), and this little blanket I actually bought for Gavin like 7 years ago. He had his first bowl of cereal on Wednesday. In keeping with his tradition of being polar opposite of everything I know from raising Gavin and Elliott Richard, Emmett loves his cereal. I couldn't shovel it in fast enough. lol He holds on to toys that we hand him for a moment or two but gets the biggest kick out of reaching/batting at his hanging toys on his bouncy seat. Speaking of which, he loves that bouncy seat. He'd sit there and kick (making it bounce) all day long if it weren't for little annoyances like hunger and diaper changes. lol

We are keeping a close eye on his reflux because he is on 15mg of Prevacid once a day and he developed a hoarse voice about two weeks ago that isn't really going away. It hasn't gotten any worse, which is something I suppose, but it's not really improving either. We saw Dr. H yesterday for his 4 month checkup and 3 of the 5 vaccines he was due for. Dr. H said to give it until the middle/end of next week, if it hasn't gone away by then I'm supposed to call back and he'll send Emmett to a ENT to have his vocal cords checked out. Other than the hoarseness, Mr. Emmett John is practically perfect in every way. And quite possibly the cutest 4.5 month old in the house. ;)

The Adoption & Legal Issues

Not a whole lot to report on this front. The paperwork for the adoption has been filed. We are just waiting on the judge to sign and date them and get them back to my attorney. At that point I can drive around town and change Gavin's last name with everyone. The school is almost as excited about this as we are. ;)

As for the fact that Gavin will never see them again, well Rob is currently out having "Guy Time" with Gavin to discuss that very fact. Per the suggestion of Dr. R. So I will be sure to update you on how that went when I know more.

There is still the small matter of the contempt motion that Pam filed against me. I filed an objection on September 4th and we just learned that the courts are requesting transcripts from the court date on July 31st. (You know, the court date I didn't attend because I felt it wasn't in Emmett John's best interest?) John, my attorney, emailed Pam's attorney handling the matter and informed him of the adoption and the circumstances surrounding the adoption and the only response he's received so far was "I'll have to get back to you." This lead me to believe that Pam and/or Nick hadn't informed him that Nick no longer has any rights to Gavin. That was probably an interesting conversation. The way John has explained it to me, Pam can drop the whole case but since I didn't do what I was court ordered to do the magistrate can still try and force the jail time issue if he really has a bee in his bonnet over me. This remains to be seen, however, I'll be sure to let you know as soon as I do.

Life in General

Life in general is...well, it's life. I'm exhausted. Emmett John gets up at 4am every morning. Elliott Richard usually isn't too far behind - getting up at 5 or 6am. I'm up so I usually just bring Elliott downstairs with me so that Rob can sleep. That way if we have a few empty hours during the day I can grab a nap. I've started seeing my therapist, Nina, again. I love her. She also has a massage therapist, Kim, whom I also love. She does wonders for my fibro, which is currently kicking my butt. So overall, things are...trying to find a new sort of norm.

Okay, I started this at like 8am this morning. It's now 4pm. Emmett John is screaming because he's tired and starving. I have a raging migraine. We are going to lay down. (Woo whoo!) As soon as Daddy mows up the leaves. (Stupid lawn. Stupid trees. Stupid fall.)

Falling apart at the seams

3:00:00 PM Posted In , , , , Edit This 3 Comments »
So much of our lives for the past 8 years has been wrapped up in Gavin. Now he is coming unraveled and taking our family down with him. I have called everyone I know to call. I'm waiting to hear back. I'm at a complete loss. I don't know what to do. I, me personally, need to break-down. I need some help. I'm not likely to get any. I think Emmett's fussy period is because I'm so stressed out. I'm worried that if I can't get a break, get some help, or something then my milk supply is going to suffer. That may seem like a silly thing to worry about given everything else that we have going on but it's important to me. Breastfeeding is important to Emmett and important to me to be able to give him that advantage.

This blog does absolutely nothing to convey exactly how lost I feel. I'm sitting here watching everything fall apart and there's nothing I can do to stop it. I love being a wife and mother more than anything else and I know I'm completely useless in both regards lately. My patience is gone. I'm falling short on keeping up with stuff. My marriage is suffering. We are about to be faced with some very difficult decisions and I'm so worried that they will tear my marriage apart.

I honestly don't know what to do...I am completely and utterly lost.

Ah...true love...

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