Tuesday, August 7, 2012

W's Update

We took W to see the neurologist.  He performed an EEG to see if there was any seizure activity in W's brain.

In order to prepare for this test they asked us to keep him up until midnight the night before and then wake him up at 5am.  Then they didn't want him to take a nap before his 1:30pm appointment.  He needed to be sleep deprived for the test so he would fall asleep.  We were also instructed not to let him eat for four hours before the test in case they needed to sedate him.  (Thankfully, they didn't have to)

So, we took an exhausted and hungry 5 year old and headed to the neurologists office.  W fell asleep before they even finished putting all the electrodes on his head!  He slept soundly through the test.

We quickly ate something between his test and the appointment with the doctor.  Our appointment was scheduled at 3pm.  We waited in the room for an hour and fifteen minutes.  1 HOUR AND 15 MINUTES.  That is ridiculous.  Thankfully they had legos and W was feeling better after a nap and some lunch.

When the Dr. came in, he reviewed the CT scan from our ER visit as well as the EEG that was just performed.  He asked us several questions about W's history.  He wanted to know what happened before, during and after the seizure.

In the end, he found no seizure activity in the EEG and no abnormalities in the CT scan.

He felt that the sleep deprivation leading up to the seizure could have played a role. (We had just arrived home from our big 'ol RV trip the night before the seizure).

He suggested that we make sure W gets enough sleep and limit his caffeine intake.  He also suggested that we limit flashy video games.

The only one we need to worry about is the sleep.  We don't have a video game system and we certainly don't give our kids caffeine.  (Momma needs the caffeine, not them)

I find it strange that sleep deprivation can induce a seizure.  After all, wouldn't every mother with a newborn baby be having regular seizures?  I'm just saying.

We are so thankful that the Dr. feels another seizure isn't likely.  He told us we don't need to follow up with him unless another seizure occurs.

We are praising God for the good report and asking for him to show us if there is anything else we need to do.

4 comments:

  1. Been prayimg for all of you. God is good.

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  2. My infant daughter had seizures from birth until age 10 months. They stopped when she had tubes put in her ears (a result of multiple ear infections, nothing at all to do with the seizures). Neither the neurologist nor the ear specialist believe they are related, but I find it incredibly coincidental that they stopped right after the ear tube surgery. Sleep deprivation...needing ear tubes....it's hard to tell many times what our body reacts to, and how it will react. Praying W never experiences one again!

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  3. Just the answer that W prayed for...God punched that seizure right in the face!

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  4. This reminded me of an article I read in Parents magazine not too long ago: http://www.parents.com/toddlers-preschoolers/health/fever/febrile-seizures/

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