"Reaching Out When MS Strikes"
by Debbie Wells, aka TXdebbieNew2MS
Here is a poem I wrote last night about MSWorld chat... (submitted 3/27/08)
The hands that so steadily painted canvas lines Now the trembling causes ice cubes to clatter In the crystal as it shines.
The lesions are growing, inside my head The brain so complex yet now Making divisions of my speech, so the doctor said.
The abdomen that once before carried babies Feels heavy and twists like a towel in a wringer Doctors say it’s probably the MS, well maybe.
The back is all crumbling but what did it matter They needed a spinal tap, he missed three times And finally they got the spinal cord matter.
Six weeks the headache was intolerable to stand I laid in the bed isolated from family But as long as we got the tap, that was the plan.
First it was a cane, embarrassing to admit That I could not stand steady Or get up when I sit.
Then came the walker, because I fell I am not an old person, But they say I needed it to get well.
My legs that walked the hospital floors Working many hours taking care of others As a vibrant nurse, were no more.
Sometimes, I now forget people’s names or event And then next day my mind is sharp as can be And then I find myself looking at the bills unsent.
So how did I get this ugly disease? Multiple Sclerosis, it's labeled MS That robbed my sight, I just want it to flee.
It rattles my spirit, and the pain is unbearable My family is silent just trying to handle. My friends all avoid me saying my diagnosis is terrible.
The doctor said reach out to groups of my kind. Search the internet he said and click on a link. Do I want to hear others, sick, just talk and whine?
I clicked to the link and found the sight Of people with hope of a life with MS With similar symptoms but they had a light.
They said MS is a disease; that I am able With meds and treatments I can live and work and keep food on the table?
No one allowed me to give myself pity. They let me vent and sometimes cry, And some make me laugh, they are so very witty.
Why did I avoid this group for so long? I thought I was different, I could deal myself I tried it alone….but I was so wrong.
I have MS and have a choice each day To grumble and groan and feel sorry for myself Or live with the disease and pray and pray.
I can thank the Lord for each moment today To use each second to do His will To serve Him with zeal until HE clears the way For me to meet Him in Heaven Oh, that will be a Glorious day! All materials published in LivingMS™ are protected by copyright laws.
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