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Old 04-04-2008, 03:50 PM #1
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RedPenguins RedPenguins is offline
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Join Date: Jan 2008
Location: Southern California
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15 yr Member
RedPenguins RedPenguins is offline
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Join Date: Jan 2008
Location: Southern California
Posts: 308
15 yr Member
Trig It's been 3 months...

I was diagnosed 3 months ago today. I find myself no longer shaking my head every day wondering if this is really happening to me. I haven't become complacent or accepting of this disease and the fact that I've got it...I just don't find myself waiting to wake up from this nightmare. Or rather, I wake up every morning to know that the nightmare is real and not just some bad dream that will go away the more I pinch myself. Ha, I just realized the irony of that last statement - as I pinch the right side of my face daily to see if any of the feeling has returned!

So, I wrote this last week some time...it is the start of a book that I know I have in me. I've always been told that I should (and would) write a book - but it was always thought that it would be about childhood abuses and whatnot. Just wanted to share it here.....

(the original working title of the book is "Life Sucks: And I Can Prove It" LOL)

It was a Friday afternoon when I hung up the phone. Or rather I hit the “off” button. Then I sat there. Did he just tell me that a UFO landed in my front yard and aliens were heading to my front door? I think he did. I need to call my friend and let her know. But what exactly am I letting her know? Would she believe that aliens were in my driveway? Would she even understand what that meant? I know that I didn’t understand – but more importantly, all I really knew was that I needed someone else to know.

Okay, so he didn’t exactly say that – but he might as well have said that – because what he said was even more distressing, made even less sense, and was more random than aliens.

“You have MS.”
Silence.
“What?”
“Multiple Sclerosis – do you know what that is?”
“Yes.”

The conversation lasted exactly 12 minutes and 37 seconds. I always wondered if the timer/counter on a phone was an important or useful feature – and now I knew that it was. Surely he said more than just those few words – after all, a lot can be said in 12 minutes and 37 seconds. But what did he say? I remember his voice and the matter-of-factness about it. I remember asking two distinct questions (I may have asked and said more, but it escapes me). “Can I still have children?” and “What’s the prognosis?” Of course, I asked these questions but barely heard the answers.

I was sitting on the sofa. At least my body was there as he spoke to me. The rest of me – my mind – was nowhere to be found. (Thinking about it now, this was a state that I was going to have to get used to.)

I had been sitting and waiting for a call from the neurologist. When I had seen him earlier that morning he told me that he believed I had a stroke and that it was affecting my brain stem. He had immediately sent me to have an MRI that instant.

While I laid in the machine for an hour, listening to the loud banging surrounding me, I tried really hard not to think about what was happening. Of course, this was easier said than done, as the facial numbness I was experiencing was rapidly becoming just the tip of the iceberg in terms of my symptoms. Who knew that vertigo and extreme dizziness would feel worse when in the laying down position? That hour seemed like a lifetime....though I was quickly transported back into the moment when the test was done. The imaging facility would not let me leave right away; they wanted to call my doctor first to discuss something. Now I knew I was in trouble.

In the hours I waited for him to review the MRI report I tried to remain calm. I was 31 years old...what did he mean that I had a stroke? Despite being able to access any and all information at my fingertips (sometimes our relationship with the internet and world of knowledge is not only a blessing but a curse), I chose not to spend my time researching strokes and brain stem injury. It was all too surreal. Naturally, as I was struggling with double vision at the time, playing with the computer seemed too difficult without making the other symptoms much worse. What happened to the facial numbness just being from a pinched nerve somewhere in my face? Though the doctor had dismissed that notion hours earlier, I had not let go of that thought. Stroke? What on earth was he talking about? And now he's talking about Multiple Sclerosis? Suddenly stroke didn't sound so scary.

He had never mentioned MS as an option. Stroke was the front-runner, migraines being second at bat. But MS? Surely this was a dream.

~Keri

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