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VicMac This title should not appear as a general description of all my entries . For some reason I can't change it. It should really be titled "Vicki's Stash"! Also, entry titles number more than what are visible here. Click on "Read my Diary" at the bottom, and you will see the other entries at the end of the scroll down list!


The War

Mar 31 2012

I haven't really journaled much about how I feel about having Lyme and coinfections even though I have SO MUCH I can say about it!

 For one thing, the shock of realizing that my life has been radically altered by an invader that I could tell from the very start - was here to stay - has worn off to some extent.

I guess what I mean is that to some extent, I have become used to having this illness. But I will never forget the deep depression I felt for many months after first becoming infected - knowing that I would never again be the same. Lyme disease isn't like the luxury of having a fleeting cold or a flu.

 And I remember how the antidepressants only made me look even less sick on the outside. So I felt even less believed.

  18 years later, I have also given up so many things in life anyway, that not being able to have them because of illness doesn't bother as much as it might someone else.

  I have forgotten how it feels to feel "normal". And I can't imagine what it would feel like to be completely free of fighting this battle every day. Like a soldier at the front lines who is told that the war is finally over, I suspect.

I guess I dont have much faith, because the only time I anticipate that happening, is after I have died and gone to meet God. To imagine that there will ever come a day while I am alive on earth, when I will be completely healed, seems completely impossible to me.

Every day I feel as though I am fighting at the front line of a battle. The enemy is always just inches away from  overtaking me. I use every bit of weaponry that I have to hold it back, but can never seem to defeat it.

 I am exhausted with fighting. I absolutely depend on my stomach, liver, and kidneys to hold up under all the stuff I have to take every day. But can this go on forever? I have to keep adding more and more things to my arsenal and trying new strategies.

I wish I could put my full energy elsewhere. Where I know it is more useful. I try all the time to do that. To be useful to God the way I think he wants me to. And the enemy disease keeps trying to destroy me in the mean time.

The good thing out of all this, is just that - that I keep fighting the battle so I can do what I think I am supposed to be doing every day. If I didn't have a purpose, I probably would not have the strength to keep fighting, and probably wouldn't have the desire.

 I think that if I did not have a purpose, I would look high and low for one, so that I could see the purpose for fighting the battle. I feel for anyone with this disease who does not know their purpose in life.   



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