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Stronger Than Ms!

This is for anyone fighting a chronic illness. I wrote this in May 2007 when I first learned I was diagnosed with Multiple Sclerosis. It may feel like the end of the world - but it is not. I hope this gives hope to others with MS or other illnesses.

I accept...

... that Multiple Sclerosis is the name for what is wrong with me
... that my memory may not always be what it used to be
... that if not already, that maybe someday I'll use a wheelchair or cane
... that each day for the rest of my life I'll probably feel some form of pain

I fear...

... Others reactions when they find out what is wrong with me
... the day I wake up no longer to work and support my family
... the day that I don't have insurance and can't afford my meds
... people not understanding that I'm still me despite what's happening in my head

I reject...

... giving up and feeling sorry for me
... succumbing to the depths of depression with this dreaded disease
... the idea of staying down even after a bad spill
... those who tell me I can't, because, dammit, I can and I will!

I hope...

... that people understand most days I feel like crap, although I look just fine
... that others don't get upset when I need more sleep or time
... that friends can accept me for me and not run away or show pity
... and mostly, I hope, that science is able to find the cure for you and me!

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Comments (3)
#1 by  Kim Buck, Nov 3, 2008
Wonderful. I wish you much strength and hope in your fight.
#2 by  Karen Gross, Nov 3, 2008
Very encouraging article. I have Parkinson\'s, so I understand very well. It has been hard for me to give up housework. You would think that would be easy, but clutter and dirt scream at me. I know that I will hurt more tomorrow if I do too much today. I also have to give myself permission to rest. Growing up, I was often told (as many children are, including my own) to stop complaining - you are just fine (which is often tne case - kids will complain about things that grown-ups know are not serious). Now I am always second guessing myself - do I really need to rest, or should I push myself a little harder. It\'s a tough balancing act that we have to do each day, don\'t we.
#3 by jangy metcalf, Nov 7, 2008
Having MS it is a thought provoking comfort! I love K so much and she means much to mysrlf and hubby...keep writing hon!
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