All About Adoption, Medical

When the Adrenaline Crashes

When the Adrenaline Crashes

When the Adrenaline Crashes…reality sets in.  I feel the heaviness on my chest like a herd of elephants.  The emotions flood over me and I yield to the pain of what I have experienced.  Yet, my pain is nothing compared to the fear and pain of my child.

I can’t even articulate what he is feeling right now.  We try and work on communication, but lets face it, communication with a teenage boy is like licking a porcupine.  It doesn’t really work well.  Within 3 days, he has had 3 Tonic-Clonic Seizures.  He has been to the ED twice, in which we waited for hours, for nothing.  Nothing.  Just nothing.

Total Random Finding

Let’s all just realize that we accidentally found out he had Juvenile Myoclonic Epilepsy about 4 weeks ago.  He had gone through a year of testing to determine his sleep issues.  We had to rule out sleep apnea, adenoids, snoring, getting good sleep at night, etc.  All that was good.

Next we moved to an EEG…which was fine.  Just because it is fun, we did have Jude do a 2-4 day MLST.  We were told things were fine and that he didn’t hit REM cycle during his naps.  That ruled out cataplexy.  He was diagnosed with Idiopathic Hypersomnia.

Then we got a strange phone call from the nurse at the neuro office.  She said “did the pharmacy call you to tell you they denied the medication for seizures?”  I’m like, no…Jude doesn’t have epilepsy, he has narcolepsy and to my knowledge he was prescribed anything.

Jokes on me.

She said, oh, he has seizures.  It showed on his EEG and his MLST and the Dr. needs to get him started on medication.  I sat there for about 5 minutes and said something to the effect of “he doesn’t have that.  That’s not what we were testing him for.  Are you talking about him having epilepsy?  What are you talking about?”  Then she realized no one cued me in on the verdict.

That was super special.

We got into the dr and he could tell I was miffed.  I asked why he thought it was so important for a pharmacist to inform me that my son had Epilepsy.  Why he didn’t make the call and what was he going to do to help my son.  He half way listened and then he referred me to his colleague.  Apparently, he works more with epilepsy and the current neuro did more of the sleep stuff.

I said well, then, when are you helping with the sleep stuff?  The answer was not what we wanted to hear.  It was more of when the epilepsy gets under control.  Alrighty then.  Well 3 triggers for his Juvenile Myoclonic Epilepsy is lack of food, stress, and sleep deprivation.  He is never hungry, our house has a decent amount of stress, and he has FREAKING NARCOLEPSY.  So it would seem that you would need to treat the narcolepsy in tandem with the JME to prevent breakthrough seizures.

Apparently, I am stupid.

The ED dr was an idiot the first time around.  She said he was fine and didn’t have anything.  We left AMA.  The second time we went, we had a friend there and a great doctor who was very thorough and helped us transitin his meds.  The fourth dr finally walked in after about 3 hrs.  Normal.  It is normal to not breathe during a seizure.  Yep, that’s when I lost it.

So they got us into the neuro and he and I had lots of words.  He said that not breathing was rare, that it isn’t worth alarming parents for something so rare.  I told him I would rather be alarmed then finding my son dead in his bed because of SUDEP.  I asked how he would feel if this were his son.

If a dr didn’t disclose all the things and that his son would stop breathing for 10-15 seconds and you couldn’t get him breathing.  If you were the one that waiting for about 30 minutes because of the ambulance.  Then, when they got there, they couldn’t even transport him due to rules of another county.

Changing Meds

Instructions are to wean him off one epilepsy medication (the one that makes him mean) and slowly add in the new med.  I have told the other neuro that we need to move forward with some narcolepsy help.  If his sleep issues make his seizures worse, seems like it would be wise to get that under control so that he can have some idea of what it feels like to be normal.

But…what do I know?  I’m just the mom and my adrenaline is crashing.

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