The thing about life changing moments is that you don't always see them
coming.
Whether it's a happy life changer, like winning the lotto, or a sad one like
the death of a loved one, the common thread is... you didn't necessarily
see it coming.
So was my diagnoses of Multiple Sclerosis.
I was 23 when my life was basically forever changed.
How I make my decisions, who I allow in my life, and how I see the future
all changed the day my doctor called and said "Naomi, you have MS"
I was hysterical and in tears of course. 1000000 questions flooded my mind.
First of which, strangely enough was "who will marry me now???"
Months of tests culminated in a diagnoses I never expected. I was now
afflicted with a disease I knew very little about.
MS??? Didn't it leave you blind? Didn't it put you in a wheel chair?
Weren't you in need of constant care? wasn't there endless pain?
My arm was numb and "heavy" for 6 months after that day. I found myself
in a deep depression. I don't know whether it was the diagnoses or the
disease itself which made me depressed, but I wanted to end my life
on a daily basis. My heart felt as numb as my limbs.
I did all I could to learn about MS and what it meant to me. I was
comforted and terrified all at once. I knew that medicine would slow
down the progression of the disease, but I knew that slowing it down
didn't mean it wasn't still marching on. It was leaving scars in my brain
and lesions in my spinal cord. I saw my future in a different light, and for a
while doubted whether my dream of motherhood would ever come true.
Everyone around me changed as well.
At moments I was heralded as strong Christian who was facing her
Affiliation with bravery, faith and courage
Other moments treated as a frail paper doll who could break at any moment.
I was ordered not to lift, or carry things if other could do it for me
Told to say home and rest...even if I felt perfectly fine
Or others deeply looked into my eyes with sorrow, as if I was given a
death sentence.
Mostly though, I was given blank stares as people sheepishly admitted
they knew nothing of the disease, although they donated money for a walk
one time.
Well since then, I've become very educated about MS.
I no longer fear the same things, at least not to the same degree.
While the course of my life has been altered by MS, I am not
defined by my MS.
I continue to dream about being a mom, owning a home, and working
for as long as I choose. These are dreams I wont give up on, and MS
can't steal... at least not with out a fight :)