Showing posts with label seizures in autism. Show all posts
Showing posts with label seizures in autism. Show all posts

Friday, July 18, 2014

EEG update; To be or not to be... it's up to us.


Ok.

So according to the neuro #2+++ "idiopathic staring spells" are common in severe autism and the prolonged episode we experienced after his EEG was not a seizure but rather my Boy's brain shutting down from over-stimulation. Which is the OPPOSITE of a seizure. Okthen.

He felt that Boy's "autistic spells" are mild enough in nature as they occur in daily life that they can be accommodated (rather than medicated) and that it is up to us whether we want the 24 hr EEG. Yeah-NO.

Because of the severity of my boy's autism** (
**Cue Boy hiding under exam table and growling) he said that if we decide to do that he would like us to go to the epilepsy center, but again, because they are short and mild in nature, they would likely choose NOT to treat medically, even if the diagnosis were epilepsy. Which they can't be sure it is. And can't be sure it isn't. Got that? Good.

So that's a pretty firm yes/no/I dunno accompanied by a very adamant "move forward with life as you're doing it".

Additionally, (because there's always more and it's always an after thought) previous Drs who were unable to elicit post-rotary nystagmus and patellar reflexes may or may not have been incompetent. I didn't share this diagnostic opinion with our pediatrician (who rotated under neuro #2) when we updated him yesterday. I'm thoughtful like that.

So.... odd reflexes that come and go? Who knows. Epileptic? Who knows. Idiopathic staring spells are 'best guess' by a highly revered Neuro? Um... ok.

On with the show.


 

+++Neuro #1 said that despite his obvious Challenges (cue Boy licking my shirt and rubbing his teeth on my arm) we are doing an amazing job and to keep up his therapies.

Monday, June 30, 2014

12.5 Seconds

Breakfast was good.

We've weaned off of YouTube (YouTube; simultaneously the salvation and bane of ASD Mom existence) so now during meals he wiggles, wriggles, skips, hops and basically does everything except sit down to eat, but the food gets in him and I can see his eyeballs so it's progress.

I was watching his little YouTube-free eyeballs.

And I saw it.

After a weekend that was mostly filled with denial, punctuated with a couple dozen (okay, a hundred) YouTube videos I had convinced myself that he does not, in fact, have seizures. Petit mal/absence or otherwise.

But I saw it.

Staring at his plate. "Hey Buddy. Can you hear me?"

"Yeaaaahhh...."

Then nothing.

Nothing. 

Nobody home.

"Hey, Boy. Can you hear me?"

Nothing.

"Gee gee goo goo."

Nothing

1, 1 thousand.
2, 1 thousand.
...
...
...
12 1 thou....

Blink.

Hey Buddy.

Blink.

Shakes head.

Blink.

"You okay?"

Blink.

"Momma, you give me too much sugar
And sugar is a headache."

"I just gave you a banana, sweetie."

Wiggle. Wriggle. Skip and hop off the bench.

That did it.

One super-routine EEG coming right up.

"Bring an iPad or something with movies or games to keep him busy."

I can do that. Exceptions to the YouTube ban can be managed if the excuse is good enough and being strapped to a cot with electrodes sticking out of your little AutoBot head is certainly up there with "a good excuse" in my book.

Momma needs some chocolate.
YouTube eyes.