The Audiologist will be sending me 'formal' results- but here's what we know now-
His hearing is good at least in his 'good ear'. (Whatever the crap that means!) He wasn't the most compliant child (imagine that!) in sitting still- so she wasn't able to get 'perfect' pictures of both ears. He was still on antibiotics for an ear infection, which can affect the results.
She said that his Ped needs to keep a close eye on him and we need to push our insurance to cover speech (since he qualifies). Isn't this the story of my life. They are still denying Logen. A 5 y/o NON-VERBAL child that ASPIRATES does NOT qualify for Speech Therapy according to Cigna. Go figure. Thank goodness for Medicaid! Parker has no hope since he doesn't qualify. Don't get me started on the government aspect of helping middle class families! We are to poor to provide medical things for our family, yet according to them- we make to much for help. Makes me love the people that sit on their butts and do nothing all day even more......
For now, I am pretty confident that his speech delay IS NOT hearing related! Yippee.
Wednesday, October 29, 2008
Hearing Test Results
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Tuesday, October 28, 2008
U Know U R A Bit Obsessive Compulsive When
... You are suppose to DRAW one set design from your play, but you actually stay up until 2am building it from cardboard and construction paper. Adam was a terrific help! He did the drawing. 
I'm an amateur. This is *suppose* to be a house and garage. This is my main character (Madelyn) conversing with the "Tire Man" who has brought his tow truck to her home to fix her flat. The name of my play, as you might have guessed it, Fighting With Time.
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10:13 AM
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Hello!
It's a busy week for us!
* Parker did fan-tab-u-lus Friday. I have a picture to share- this deserves a post on its own.
* Logen was seizure free all weekend long!
* Mr Parker has a hearing test this afternoon (FINGERS CROSSED that all goes well!)
* Logen has been *willingly* using his talker more frequently. Last night he carried it to Adam and asked for milk please. :) Go Logen!!!!
* I *think* I did well on yesterday's French exam
* Parker will be 2 Sunday!!! Where does time go?!
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10:07 AM
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Thursday, October 23, 2008
Parker's Going To College!!!! (avec moi!)
Avec moi... with me.
Yes, my littlest Mister has been volunteered to go to my Developmental Psych class tomorrow afternoon for a demonstration. I'm not really sure what they'll do with him- but he's a cute lil mess- so, he's got that going for him :) I asked them to bring a duck. The ONLY think he will do on command is QUACK. Like a duck. It's so stinkin' cute. I only hope he'll perform in a large classroom of about 250 seats (and, who knows how many will show up it varies day to day).
So, wish us luck tomorrow. As we hike together. And, then ride the bus together. And, hike some more before we even get to the building.
I think he's excited about it though. I asked if he was going to school with Mommy and he says, "Yesh". I say- are you going to be good? And, he says "Bubba". I'm assuming that's a no :)
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9:51 PM
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Wednesday, October 22, 2008
Another Call From St Louis
I spoke with the nurse again today. It's almost freaky having a Dr's office call YOU to check on your child.
Here's our most recent plan.
* Blood work- she faxed me the script and we will do this *hopefully* tomorrow afternoon.
* He's up to 75mg AM and 100mg PM on the Zonegran. He cannot go up to much farther on the dose- which mean if he continues to have seizures, we may be switching medications.
* Admission to the St Louis hospital for a 24-48 hour (could be longer, but no shorter) ' videoed seizure watch'. We will begin the paper work for this. She said since he's not having *major* seizures everyday they wouldn't push this to be done now. It will be most likely Decemeber when we get this done.
I asked about a fMRI. The nurse said she would ask Dr Brunstrom and get back to me.
Some of you maybe interested in this. It's a functional MRI.
fMRI is becoming the diagnostic method of choice for learning how a normal, diseased or injured brain is working, as well as for assessing the potential risks of surgery or other invasive treatments of the brain.
Physicians perform fMRI to:
* examine the anatomy of the brain.
* determine precisely which part of the brain is handling critical functions such as thought, speech, movement and sensation, which is called brain mapping.
* help assess the effects of stroke, trauma or degenerative disease (such as Alzheimer's) on brain function.
* monitor the growth and function of brain tumors.
*guide the planning of surgery, radiation therapy, or other surgical treatments for the brain.
*** brain mapping
Mapping the brain's surface using small electrodes to stimulate a nerve so its electrical response can be measured. By determining the role of specific nerves in a patient, this technique helps surgeons avoid damage to sensitive areas while operating on the brain.
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9:24 PM
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Tuesday, October 21, 2008
An Incomplete Definition
I found this here. Wish I could have said it that well.
Long before I even met Nick, a friend of mine in Maine learned her beautiful blonde daughter’s developmental delays fell into the category of mental retardation. And though I hate to say it now, I felt sorry for her.
A child with special needs.
What a pity.
I wish I knew then that pity is the last thing us parents need.
(And don’t even think about feeling sorry for our children.)
What does it mean to parent a child with disabilities?
It means the reframing of your worldview.
It means taking nothing for granted and spending more time in the present than in future plans
and dreams.
It means endless appointments and paperwork and the introduction of your child to all kinds of
adults who specialize in understanding his or her needs.
It means missing your own six-month dental check-ups and yearly pap smears.
It means growing comfortable with stares, even if your comfort is in knowing that you won’t be comfortable, but it will happen anyways.
It means knowing how to silence a pesky questioner with a single statement:
“His brain was injured at birth.”
“I have two wombs instead of one.”
“Why do you ask?’
“He has Cerebral Palsy.”
“There’s nothing wrong with him.”
“Well, he’s not looking at you because he’s legally blind.”
“What do you mean by Ok?”
It means redefining the words OK, healthy, and childhood.
It means continually adjusting expectations so you neither expect too little or too much but
rather remain open to wherever your child leads.
It means learning to follow.
It means a redefinition of your social life because either your friends don’t understand or because you find yourself with so much less time to devote to cultivating friendships. You want to extend invitations to dinner, you truly mean to return the favor, but months go by and you still haven’t had an extra second to plan a social evening. It means being so grateful to those friends who do understand.
It means working on learning how to scoop with a spoon instead of learning how to chew with your mouth closed, learning how to walk instead of ballet lessons.
Learning to go slow instead of racing. It means letting go of comparisons and bailing out of the My-Kids-More-Advanced-Than-Your-Kid game.
It means becoming almost fluent in medicalese and actually knowing what the following terms mean: IVH-III, C-PAP, Nystagmus, Strabismus, Hydrocephalus…
It means doling out medications--even if you planned on raising all natural kids.
It means joy in the controlled bend of a knee, a flash of eye contact, sunlight on an orange Lilly, the sound of your young son saying, “No.”
It means befriending therapists, multiple adults that not only love your child but remind you when you most need to hear it that your doing a good job. “You’re a good parent,” they tell you-- and you realize that all parents could benefit from hearing this from interested parties and you think how lucky you are. It means always thinking you could do more.
It means wanting time alone as a family, without appointments, professional judgment, and medical advice.
It means multi-tasking, squared, times three.
It means buckling your son into his car seat to drop him off at daycare and then driving straight to work.It means constant surprise. “Did you see what he just did?!?!”
It means never shaking the specter of death.
It means gulping joy like water.
It means questioning whether you can do this again, whether you can conceive and carry another child.
It means wanting to try.
It means not wanting to try.
It means fear.
It means acceptance.
It means hope.
It means never saying, “I don’t care if it’s a boy or a girl, as long as it’s healthy.”
It means…
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10:43 PM
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Seizure Update
The APN at Logen's Neuro's office called to check in on "Mr Logen" today. Dr Brunstrom was headed to a conference this afternoon and wanted to see how he was before she left. How amazing is that?!?!
She took down some notes (the latest... well, still not a day w/o a seizure. He's having atleast 1 or 2. Lasting 10 seconds to 45s/1 minutes)
She felt like the next step would be a referral to the Epilepsy Center in St Louis. Our fingers are crossed as we think this would be beneficial to Logen!
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10:20 PM
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Monday, October 20, 2008
The Hole
Ya know, you feel like your finally gettin' outta that hole. And you slip. Thats me. I'm there. I peep up over the edge and then miss a step and slip right back down to the bottom. Seriously. It's chaos!!!!
Parker's been on antiobiotics for a bilateral ear infection since Wednesday. Spikes a fever Friday night, lasts all day Saturday, not so much of yesterday, but up last night.
At noon the daycare calls.
DC: "Um, we took his temp .... 101.6 ..."
Me thinks... that sounds like a radio station. la - de - da - de - da - da - daaaaa
Me says: Oh. Well, I'm going to catch the bus and get to my car. It'll be about 45 minutes before I can get there
We go to the Dr. I love co-pays. 20 bucks here, 20 bucks there. I'm rich. What can I say. 20 bucks- no biggie. Not like it takes Adam anytime to make that..... hahahahahaha (got the sarcaism? good)
Dr: That ear looks horrible.
Me: You said that 5 days ago.
Dr: I did? Oh, yes.... Next ear, um not so good either. Well, you know the body can.... he's immune to the antibiotic most likely
Me thinks: give me something else so we can leave
I missed my afternoon class today. I missed all last Wednesday. And Thursday. I have a 6 page critique due tomorrow over a {dumb} play I forced my loving husband to suffer through (Hey, if I had to sit through 3.5 hours of hell-o, shouldn't he?!) And a test. So, I can't really miss that.
I've emailed my teacher to ask if I can bring Parker along. Can you see that? I'm going to do real well on that test. Little turkey trying to escape my lap, disturbing EVERYBODY and their dog to. We shall see. She may so no, no, no do not bring that child with you!
Moral of my post: Venting.... I'm stuck in a hole and I can't get out!!!! Ahhhhhhhh
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5:17 PM
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Saturday, October 18, 2008
I Am Mom!
My little monster Parker has decided to run around saying, "bye bye ess-e-ka!" He started this last night when he squirmed off the bed escaping bedtime. I am pretty sure he's saying, bye bye Jessica in Parkanease. I told him I am his Momma or ma mére, but I am not ess-e-ka to him! Little stinker!!!!!!!
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6:59 PM
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Thursday, October 16, 2008
A 9-1-1 Call
Today has been interesting. Interesting.
At 8:04am my phone rang- I missed the call b/c I was dropping Parker off at daycare. At 8:05am I was in the car heading towards my school and listening through 14 voice mails to get to the one Logen's school had just left me (if that tells you anything, I don't listen to voice mails very often)
The lady had said Logen is in the nurses office and they've called 911. Please call them.
I freak. 1st thing that comes to mind: Seizure. Bad one. Tears, why couldn't this have happened when he was near me?!
I regain composure and call them back. She said he was on the school bus - and had been seizing for about 2 minutes before he even got to school. I can't remember if they had phoned ahead to warn them or not- whoever was there to take him took off running to the nurse's office. The nurse immediately gave him diastat (a form of valium administered rectally). This stopped the seizure. They called 911 and then me.
I headed towards his school. Thankful I was still in town (well, the next town over- but my school is a good 40 minutes *atleast* from Logen's school). I turned on my flashers and drove like any paniced mother would.
When I got there the paramedics asked if I wanted them to transport Logen or if I wanted to. I said them. He was still lethargic and really not even holding his own head up. There were several people in the nurses office with Logen. The nurse was holding him and his teacher was standing next to them. The assistant principle, office ladies, and 2 paramedics were there 2.
We got in the ambulance and headed to the hospital. Logen's teacher drove my van to the hospital so I would have it there. I really thought he would have slept on that drive, but he didn't. He was so out of it. He would have been so excited if he had known he was riding in the back of an ambulance. The paramedic riding back there had been to the school the week before to show the fire truck off and remembered Logen. He said he loved it!
When we got to the hospital Logen was still not totally with it. The Dr there called and spoke with his Neuro at the CP Center in St Louis. They said we did the right thing and decided to up his medicine again. He's up to 75mg of Zonegran/AM and 100mg/PM. He was checked over and besides the fact that he'd just had a severe seizure, he looked good. So he was discharged.
We got home and he slept til about 1:30 this afternoon. He cried when he woke up, he tried to walk but was so wobbly. He ate a little oatmeal and was starting to get his normal color back.
I spoke with the CP Cntr nurse this afternoon and she said she'd call me back in the AM about this. It's alarming to me that his seizures are getting worse. Today's seizure was classified as tonic-clonic. Logen has never had this kind before. Nor has he ever had one lasting over 2 minutes. I'm worried about this. Personally I think if they are getting worse- there must be something we are missing. How is it that seizures just pop up at 4.5 years old and become worse as you increase the preventative medicine? I'll post an update when I get one.
The nurse called this afternoon to check on us. I also spoke to Logen's teacher (everybody wanted an update) She said when the bus got to the school this afternoon, they ladies had tears in there eyes-- they were so so worried about Logen.
I am absolutely AMAZED with his school. So far, in every aspect they've gotten a A+.
I missed class yesterday- Parker has a bilateral ear infection. One he's had for about a week we didn't know about. We got numbing ear drops- they looked horrible. He hadn't had a fever- just wasn't sleeping. He still doesn't have all of his front teeth in, I chalked it up to teething. Guess we won't do that again.
Say a prayer for us, would you? It's kinda stressful here!
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9:01 PM
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