Wednesday, July 8, 2009

The Aftermath And The Fourth

Ahhhh.
The spinal headache ended about a week ago.
I have spent the last seven days attempting to get back all the energy that was drained out of my body during my seven-day-lay-flat-on-your-back-unless-you-want-your-head-to-friggin’-explode period.

As fun as those seven days were, I’m gonna go out on a limb and say that I am SO glad that it is OVER. School ended for me last Thursday and inspired a HUGE sigh of relief. I no longer have to worry about studying and going to class while also trying to recover from tests (ahem… spinal tap) and side effects from medication and my health condition in general.
So. I’ve decided that my doctors have until August 24th to get this all taken care of and straightened out. (August 24th is when I start the fall semester in which I am signed up for 15 no-nonsense-work-your-ass-off credit hours.) I have BIG plans (pharmacy school, anyone?) and have ZERO intention of letting a freaking pseudotumor get in my way. If RSD didn’t knock me out of the game, I’ll be damned if I let a stupid pseudotumor do that job.

I’ve also decided that I really do not like this whole pseudotumor-cerebriraman amplifier situation. The more I read, the more freaked out I become. All I want is information… but the more “information” (aka: internet articles) I come across the more I am freaked out. Now, I haven’t heard this from my doctors yet, but apparently, if the “information” (seriously, can you really trust the internet in matters like this?) is to be believed, if the medication does not work then I am facing having to get surgery to put some sort of shunt in my head to reduce the flow of spinal fluid to my brain. Ummmmm… brain surgery in any capacity? That would be no. No.No.NO. (See how I freak out?) I am trying to just wait until I talk to my doctors again and not flip out until they give me reason to…. sometimes it works, sometimes it doesn’t.

It is absolutely NOT helping that the medication that makes me pee like I’m ten thousand months pregnant doesn’t seem to be working. Oh, I ‘m getting all of the expected side effects (plus the fun unexpected side effect of the stupid medication actually making my RSD WORSE) but the vision in my right eye seems to be worsening, not getting better… Now, I am no doctor, but I’m thinking that this cannot be good. When this whole adventure started, I had a crescent-shaped haze at the very bottom of my vision… think like a quarter-moon kind of shape. Now I have like a HALF-MOON’s worth of haze at the bottom of the vision in my right eye. Umyeah.
If you’re thinking, “Wow. That would probably be sooooo annoying,” you would be dead.on.

Yes. I am all kinds of spooked about my vision worsening. Yes. I am all kinds of pissed off about my RSD getting worse because of this medication. I literally have not slept the night through in about two weeks because I get woken up by the “tingling sensation” in my feet. (Tingling sensation… yeah right. More like someone jabbing small knives into the bottom of my feet sensation.) My RSD foot is usually swollen to some degree now and is usually the color of red kool-aid. Basically, what I’m getting at is that I don’t want to take this medication if it’s not going to work. Because HELLO! My foot is killin’ me (worse than usual) and if it because of this medication that isn’t doing its job anyway… uh…. nothanks.

Monday, July 13th, is the day. The day the eye doctor gives me the verdict on whether or not the swelling in the optic nerve in my right eye has gone down at all. Despite the fact that I am 99.9% sure that my vision has worsened over the last few weeks, I am still hoping that he will tell me that the optic nerve is no longer swollen or no longer as swollen. I really, really want this medication to work… even though it is making my RSD worse. I do NOT want to get a shunt put into my head. That sounds painful, expensive, and like it would take a while to recover from. So. At this point I am just trying to will my optic nerve to calm the heck down and stop being swollen already. (I don’t know if my mind power is strong enough to make my body do what I want it to… but it’s worth a shot, right? RIGHT? ~on the edge of having a panic attack right now~)

Uhhh… Moving on to happier things.
Our fourth of July was fun! (Even though Simon got bit by a mosquito right by his eye and spent much of the fourth nursing his red and swollen eye…)
We started the fourth off by doing nothing for most of the day (which was awesome). Then we took the kids to the driving range for a few hours (family fun for all).
Then we moved on to go and check out the local fireworks scene.
We saw these:

Tried to take some family pictures while watching big fireworks:


But those didn’t really turn out (as usual) so we just watched more of these:


Alright. Nello.Out.
I am busy warding off a headache and the backlight from my laptop is doing me no favors at this point.

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3 Comments »

patti Said:

kelly, holy crap! i’ve had the medical stuff that is scary, so i can sympathize. hang in there girlie. you’re doing great.

Thursday, July 9, 2009 @ 7:52 am
emily Said:

I’m sorry you’re going through all this. What a mess. I’ll keep you in my thoughts – hoping for positive outcomes – the most ppositive we can hope for.

Hang in there. What else can we do, right?

Sunday, July 12, 2009 @ 4:49 pm
shaunee Said:

Give me another update, please?!

Thursday, July 23, 2009 @ 6:47 pm

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