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Karen Lynn Vidra, The Texas Tornado

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     Eddie struggles to write in her journal, writing about her latest troubling symptom with her MS, which continues to raise its ugly head.

Image (C) 2008, Karla Dorman.

Eddie Garcia here. 

This won't be long, not like my past entries; y'see, I am continuing to have trouble with my darn MS acting up.  Between my spasms in my face, arms, and legs, the discoloration of my legs from time to time, the weakness or tiredness, the pains in my back, and whatnot, I'm afraid to see what the MS will dish out next.

Now, on top of all that, my vision has blurred.  It's almost like looking through a thick curtain of fog, making it difficult to see.  My mama is here, helping out; she's acting as my eyes as I try to navigate around my place.  I have been sitting in my wheelchair; mama won't let me walk, in case I run into something again.  Lately, I have been nothing but a big klutz!

I have the bumps and bruises to back that claim.  It looks like someone beat the holy crapola out of me!

I am still trying to get my stupid SSDI.  Got a letter from them last week.  Denied.  Not disabled enough.  This makes the fourth time; now I am going to have to get that lawyer!  I am so frustrated with the government I could just scream!!  Why do I need a stupid attourney to prove that I am disabled while those who intentionally use (or abuse) the system seemingly get it without little difficulty?  It doesn't make any sense whatsoever!!

Ever since I got diagnosed with my MS, I haven't been able to work.  My mom or other family members have had to come over to help me, especially on my bad days where I am flaring!  Seems that lately my life has been nothing but one huge, continuous MS flare!!

God, I hate having this damn MS!!!!

Tomorrow is Easter; who knows what I will be dealing with next??  I pray I will get to be able to get out and go to church:  church is having some special Easter music, and it's always so crowded; we have to get there early in order to find a good seat.  I usually end up coming in halfway during the worship service, and then I end up leaving early because I pissed myself again or some other stupid MS symptom is acting up!  It's nothing short of embarrassing!!

I pray I can get through the Easter service tomorrow without Miss MS rearing her ugly head!  This is when I wish I didn't have to live with it; I wouldn't wish MS on my worst enemy!  (Okay, okay, maybe on the terrorists of the world, but that's another story altogether!  LOLOL)

Well, it's hard for me to see to write this, so I am going to go now.  My vision is more akin to dancing, writhing, wiggling worms:  that's what the scene looks like before me, and it's making me terribly dizzy (not to mention, extremely queasy).  I will write in here again when my eyes decide to behave themselves. Until then, this is Eddie signing off; take care, and try to have a happy Easter Sunday!

~Love, your friend, Edwina (Eddie) Garcia.  :(

 

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Reviewed by Mary Coe 4/11/2009
A very interesting and well written story. Thanks for sharing.
Reviewed by Michelle Kidwell Power In The Pen 4/11/2009
A very real account of a frightening condition, they believed at one time I had MS, that was ruled out though and MD was the diagnosis as you know, keep it up and be blessed
In Christs Love
Michelle~
Reviewed by J'nia Fowler 4/11/2009
Such a realist account of some of the issues one encounters when you have MS. My previous husband had MS and suffered so much from the time he was 30 and experiences numbness and blurry vision until he passed away 2 years ago, unable to speak, eat or move. He worked til he was about 37, fell out of his wheel chair at the office, brought his work home for me to do and finally went on disability. Very painful time for both of us. Excellent write my friend, Hugs, J'nia
Reviewed by Cynthia Buhain-Baello 4/11/2009
How sad and terrible to have been denied those benefits, I think and appeal could help. Very moving story, Karen.
Reviewed by Georg Mateos 4/11/2009
Eddie, hang in there, everyday they get a step nearer to do something out of this world with their search for the MS cure, or slow it down or use stem-cells to get rid of it. Just hang in there, hope is one of the tools to surviving.

Georg

Reviewed by Paul Berube 4/11/2009
MS can be a terrible struggle. Well written Karen. God bless.
Reviewed by Karla Dorman, The StormSpinner 4/11/2009
The daily tasks of trying to get through puzzling symptoms clearly deliniated here, Karen. Well done.

(((HUGS))) and love, Karla.

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