Sunday, January 22, 2012

Where are we now?

So where we left off on the old blog, Dr. Rockstar in Detroit said that C~Monkey wasn't a surgical candidate and prescribed Phenobarbital and sent us packing on our sad way. He told us that if his EEG pattern ever changed and if we ever saw a focus to his seizures to contact him. We soon saw C~monkey's regular Dr. neuro, and we agreed that was a good plan. Time went by & we reviewed what other meds we haven't tried, which aren't many, and prayed for the best. We never did go with anything new. What was the point? I knew in my heart that meds were never going to help him. We had already tried over 10, and the research shows that with each failed med you have less and less chances of finding one that works. So eventually we agreed that the best next option was a Vagus Nerve Stimulator. The neurosurgeon at the hospital that Dr. Neuro is at did the surgery the Wednesday before Thanksgiving 2010. We went home on Thanksgiving, thankful there was an option for once and praying that this would work for our sweet lil' guy. It is the most horrible feeling as a parent to feel helpless in ways to help your child live their best life.
The recovery period went great and we made frequent trips to see Dr. Neuro to adjust the settings on the VNS. We were seeing some benefit from it, and C~monkey's seizures seemed to be lowering in number and intensity. It is a complete pain in the tush to keep up with the magnets, and I think someone is eating them (the seizure monster maybe?), but atleast it was "something".

Then this past Summer, the seizure monster sensed we were getting too comfortable and maybe even too happy? We started noticing C~monkey have these strange episodes of hysterical laughter. Except they were happening when things weren't funny and completely out of the blue. This wasn't normal laughter either. We are talking scary, manic, demon possesed laughter. I knew it had to be a seizure. I had never heard of someone doing this before though? I was at the Dr. with my Mom, who was having her own scary health problems at the same time, and while waiting for the Dr to mosey on in I decided to Google "laughing seizures" on my phone. Well, this is what I found out: they are called "gelastic seizures". This is the exact article I found in the Dr's office that day. Sounds fun right? I wanted to cry right there. Something else. We never seem to catch a break. The seizure monster seems intent of ruining our lives.

We had an appointment with Dr. Neuro so we wanted to try and catch this pesky monster on video. We had to do this because to hear it described and to see it are two different things. We knew he always has them in the morning after waking. We knew that was our time. So I made sure the flip cam was ready and I sat and I waited. It took no time at all.

I've been hesitant to show this video to anyone. I can't really explain why. Maybe to keep people from knowing what was really going on? To avoid the pity? To keep it from sounding like it was this bad? Fear of admitting this was really happening? I don't know.... Only a handful of people have seen it. Over half of them have cried after seeing it. When I started this blog, I knew I was going to keep it real. None of this fake "we are fine." crap. I have to show this video. I have to put it out there to help other Moms and Dads that are desperate to save their kids. To put awareness out there. To explain why I'm a raging B!@#h some days because I start every. single. day. of my life like this. Some days I'm okay and can deal with it. Other days I want to punch random strangers in the throat because I want them to hurt  like we hurt deep in our hearts. Because I'm angry that innocent kids have to start their day like this. Because I'm sad that I can't take it away from him. So here, gleam whatever you may from this:

(ignore the hideous sofa cover, we thought we could stop him from stimming on the pattern on the sofa by putting that on there. it didn't help so we yanked it off)

Pretty crazy right?

Dr. Neuro seemed pretty amazed by it too. He was also stumped. He admitted C~monkey to the hospital a couple of weeks later for a video EEG to see if we finally had something we could do something about. Come to find...we may have.

Stay tuned for the next post where we will talk about what we've found out and where we go from here....

2 comments:

  1. There is something SO vulnerable about sharing videos of our kids. Especially seizure videos. I think it must be because it hits our hearts so profoundly, that when someone else feels it differently...it hurts. Or frustrates, maybe. IDK.

    When we were on Banzel, Trevy would have a bizarre laughing/smiling seizure right in the middle of his clusters. It was scary as H-E-double hockey stix! To me. When other people saw it, they thought he was happy!?

    Anyway...

    I'm glad you're opening your heart up again...and letting us in.

    Love you!

    ...danielle

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  2. Drake has had the laughing seizure thing weekly for a couple years! We have yet to catch it on any crappy EEG, but there is no doubt he is in another place when the laughing begins!

    As with Happy Mommy's comment above, strangers and still, some family think he's so cute and laughing... just easier to smile and say "he sure is". That's what they want to hear anyways!!!

    Glad to see you blogging again.

    Trish

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