Showing posts with label Diagnosis. Show all posts
Showing posts with label Diagnosis. Show all posts

Thursday, April 17, 2014

A Demon Inside: A Poem is Inspired by the Dark

A peak into my experiences...


A Demon Inside

Neisha Ulrey

 

Dry cracked lips. 
Swollen. 
Blood stained from the

bite marks.
A driving thirst that can’t be
quenched.
Another moment taken. 
A little more damage

done.
Life half lived

between

each invasion.
Sweat soaked body. 
Shaking from the cold.
Satin sheets

stained.
Ruined.
Another hole to a
shattered heart. 
Hands creeping up. 
Unarmed for 
the attack.
Like a broken clock,

time stands

still. 
Mesmerized by the darkness.
For a moment

all empty sins are washed
away.
Peace settles on a damaged soul.
But

moments are

fleeting. 
And the devil has left
his mark.
Fists unclench. 
Body loosens.
A gulp of

metallic burn.
Wipe away the

blood

and

tears. 
And wait for
his

return.


Friday, March 14, 2014

Me and My Meds: A Love Story

Medication, a necessary evil.
Side Effects, their extra evil twin brother that comes to kill you in your sleep (specifically those found in daytime television Soap Operas).

My doctor prescribed me medication immediately.  As a a woman of child bearing age, I was limited.  If I wanted to save my future kids from having two heads (better than most of the possibilities) then I had a pretty slim choice of medications.

So, I was put on a low dosage of Trileptal (I swore I was on Lamictal but when I reviewed my medical records, or what I could find of them, the paperwork says the other).  I have to admit that I can't remember the dosage (this was October 2005 after all) but it was low, I'm going to assume it was something like 150 mg per day (online says this is the lowest dosage available so I'm going with it).  Either way, it wasn't very much.

Let's talk about how much Trileptal didn't work.  I was tired.  I was, just, off.  I felt different.  Worse than that was how it triggered seizures whenever I missed a dose (I know, I know.  You can't miss a dose, but I was 18/19 and living on my own for the first time, going to school and working...it happens!).  Also, if I took the medicine a little late, hello episode.  Wanna know something even more awesome?  I was still having seizures.  Yay.

My records say I saw my doctor in August 2006 and that I was still on the meds.  So, I spent a year in this endless cycle.  It was shortly after that visit that I chose to go off of the medication.
(Rogue Disclaimer: I'm not saying this was a good idea.  I'm just saying that I did it.)

For three years I made it work.  I knew my symptoms and signs by heart and could predict a seizure coming from a mile away.  I rarely missed school or work.  I hung out with my friends and I successfully hid each and every seizure I had for three years.  People knew I had bad days but, they didn't look at me and see epilepsy scrawled across my face.

It was just me and my demon.  And we managed.  We worked it out.  He got me at night.  On weekends.  At quiet moments, where I could mention a headache and slip away.  My demon held me captive, but he let me continue to live.

Then heartbreak came with more heartbreak scooped on top with heartbreak sauce drizzled all over and heartbreak sprinkles in a heartbreak bowl eaten with a heartbreak spoon leaving me with heartbreak freeze.

I waited.  Where was he?  Where was the fading, the ache, the haze, the panic, the pain?  I waited.  My demon stayed buried, crouching in the shadows.
Where was he damn it?

I got busy being broken.
I got vulnerable.
I got attacked.
I got beat.
Black and blue.
(there is much, much more to this...but for another day)

So, ambulances got involved and emergency rooms and hospital stays and MRI's and new medication was prescribed.

Topamax.
Damn Topamax.
Hi, my name is Topamax and I will consume you in a way that makes your demon seem like a childhood friend.  Have a great day!

In June 2009 my doctor worked me up to dose of 100 mg per day.
Topamax and I did not work well together from the start.  Three months and thirty pounds lighter, I was fading.  I was weak, I was wasted away.  My skin was pale (paler than my usual alabastery shade) and grayish.  Dark circles and all.  My arms, hands, legs and feet would routinely go numb.  Everything I ate tasted like, well nothing.  I didn't want food, I did eat food.  My clothes grew bigger and bigger.  I just wanted to sleep.

And I still had my demon, seizing away.

Eleven months later, it was time to find a new doctor (grrr...more on the old one later).

New year (2010), new doctor.  This time I found a woman and she was better.  Much better.  New doctor talked to me, listened, replied, discussed, seemed to actually care.
But
She kept me on Topamax, raising the dosage.  We topped out at 900 mg per day about three months later.
My mother and I set up an appointment and after some pleading, it was agreed that we should be trying something new.
Next she prescribed Keppra.
Keppra was better, less severe, fewer side effects, all that jazz.  It took us a few years, more breakthrough seizures, a trip to the ER (darn roll-y chairs), and multiple doctor appointments but we got them stopped (for the most part).  All it took was 3500 mg per day.  Yes, 3500.  Anything less wasn't strong enough.

This dose stopped almost everything.  The shaking, the fear, the blackouts, the clenching, the metallic taste, the mumbling.

But, the biting continued from time to time, and certain feelings were there in the background.

He was there.
My demon.  Prickling on the edge of the medication created force field.  Giving it a kick occasionally, just to remind me not to get too comfortable.  That he's there.  That he's mad.  Don't forget.

The meds keep him from taking me over.

But he's there
and sometimes, I miss him.




http://www.rxlist.com/trileptal-drug.htm
http://www.rxlist.com/topamax-drug.htm
http://www.rxlist.com/keppra-drug.htm

Tuesday, January 28, 2014

The Doctor Is In...Well Kinda

So what comes next?  

 

Well there was a doctor, a neurologist.  He was local, from the hospital that we used.  He was on our insurance.  He was the one who was supposed to fix me.  He was my exorcist.  

The first appointment was amazing.

Nothing was really answered in definite terms.  But as my mom and I sat in the little room, I read the posters on the wall.  

 

Do you ever experience …

1. feelings of Déjà vu

Check

2. loss of vision or blurring

Check

3. tingling feelings

Check

4. profuse sweating

Check

5. dizziness

Check

6. racing heartbeat

Check

7. lightheadedness

Check

8. blackouts

Check

9. severe headaches

Check

10. an overwhelming fear

Check

If you answered yes to one or all of these you may be experiencing epileptic seizures.

Please see a doctor immediately.

Check, well kinda.

 

I was so excited!  

Mom! Mom!  Every one of those, that’s what I feel.  That’s what it is.  I have seizures; we are in the right place.  We’ve got it!  I felt like I had found the buried treasure, this was medical.  Doctors fix stuff, I’d be fine.  My demon would be gone in no time.  See ya later sucker.  

And, the doctor seemed to agree…well kinda.  He believed what I “say” I experienced sounded like seizure activity.  He could not say for sure due to no actual proof.  

You see, I didn’t mention the fact that the ER nurses never actually got me hooked up to anything, at all, ever during my multiple seizures that night in the ER.  They watched them happen, though I don’t think there was ever a detailed report given to anyone, certainly not to me.  

 

So, we would do tests.  Find out for sure, see what was going on.

The doctor gave us some details.  Seizure disorders are more common then I realized, that there were medications that could control the episodes, that most people get their medication set and only come back to the doctor for a yearly check up, that many people just grow out of them.  

This didn’t sound bad, barely even an issue.

All I had to do was get through the tests and then I’d know why.  I’d know what.  I’d know if it was a tumor crushing my skull or a scar in my brain, or whatever else caused this weird brain activity.  

Tests.

Then I’d know the facts.

 

I was naïve and positive, or maybe just hopeful.  Desperate is probably the best word.  I was desperate.

 

So we did the tests.  I laid therestill in claustrophobic tunnels.  I stared at flashing lights.  I slept.  I didn’t sleep.  I had nasty goop in my hair.  Electrodes stuck across my head, my chest.  I was tested.  

My parents and their insurance companies paid a lot of money for a lot of big beeping machines to test me.  For nurses to hook me up, and aids to monitor.  For doctors to read and diagnose.

 

I passed!  Or, as I saw it, I failed.

 

The tests were all clear.  Clean.  Nothing.  Nada.  

 

Which in epilepsy terms apparently meant I was just likethat vast majority of people that have seizures.  No body knows a damn reason why my brain went nuts.  

I didn’t even get to officially have seizures.  I had presumed seizures.  

Which pissed me off.  

Presumed.  Like maybe I was lying.  Like maybe I acted like a crazy person for fun. Like maybe the little demon who consumed my body was my imaginary friend.    

 

Okay, as a grown up I do know that presumed is more of a legal term and was never meant to offend (though occasionally I do think these doctors mean to offend…more on that later).  

 

But it did feel like a kick in the gut.  It felt like my demon chuckled, can’t catch me.

 

The plus side?  They still treat you for presumed seizuredisorders.  So it was medication time.  Yay, well maybe.  

In my case, not yay.  

But that is for another day.  

 

Below I have a list compiled from Epilepsy.com.  I’m posting it because I think it helps to actually read a list like this.  It is broken down into categories (beginning, middle, and end seizure activity) which I will explain more later.  

I’ll place a star by the ones on the list I typically experience with my episodes…never mind.  I literally just started almost every single one.  The few that I didn’t star I’m not sure about since someone else would have had to observe me to tell me what I was doing, since almost all of my seizures have occurred in private I don’t know everything that I do or have done during an episode.

 

Early seizure symptoms (warnings)

Sensory/Thought:

Deja vu
Smell
Sound
Taste
Visual loss or blurring
Racing thoughts
Stomach feelings
Strange feelings
Tingling feeling

Emotional:

Fear/Panic
Pleasant feeling

Physical:

Dizziness
Headache
Lightheadedness
Nausea
Numbness

No warning:

Sometimes seizures come with no warning

Seizure symptoms

Sensory/Thought:

Black out
Confusion
Deafness/Sounds
Electric Shock Feeling
Loss of consciousness
Smell
Spacing out
Out of body experience
Visual loss or blurring

Emotional:

Fear/Panic

Physical:

Chewing movements
Convulsion
Difficulty talking
Drooling
Eyelid fluttering
Eyes rolling up
Falling down
Foot stomping
Hand waving
Inability to move
Incontinence
Lip smacking
Making sounds
Shaking
Staring
Stiffening
Swallowing
Sweating
Teeth clenching/grinding
Tongue biting
Tremors
Twitching movements
Breathing difficulty
Heart racing

After-seizure symptoms (post-ictal)

Thought:

Memory loss
Writing difficulty

Emotional:

Confusion
Depression and sadness
Fear
Frustration
Shame/Embarrassment

Physical:

Bruising
Difficulty talking
Injuries
Sleeping
Exhaustion
Headache
Nausea
Pain
Thirst
Weakness
Urge to urinate/defecate

 

Source: https://www.epilepsy.com/101/ep101_symptom