Showing posts with label Hope. Show all posts
Showing posts with label Hope. Show all posts

Thursday, June 5, 2014

When Your Body Gives You Another Day or Hour of Betrayal

The truth is, I think I have been managing better;  although, my life is not the optimum life I would have expected at 62.  Considering I have several illness, as well as FM and CFS, I guess I am still doing better than some people are.  At least, I do not spend every day in pain that refuses to be shut out.

However, there are moments when the pain or the weird sensations that seem to be part of the FM patient's plight get me down -- way down.  If there was no medicine to take and the pain and weird sensations did not stop, I think they could drive a person mad.  Also, I get deeply tired of the fatigue -- tired of being tired is how I put it earlier this afternoon.

Sometimes, the tears and fog come with the icky tingles and the anxiety.  I start to remember how long I have had this and wonder how I could bear it another second.  But I do.  I have even sometimes asked God why He does not let me die.  However, I know He has a purpose for my life, so I keep on hoping.  I lie down in my bed to try to quiet what is going on, pray, say the 23 Psalm among other scriptures, and I cry.

Then, I usually get up to do something else after that.  Today, I went out on the porch so I could watch the breeze go through the trees and feel the outdoor heat.  I was cold.  Today was a hard to regulate my bodily temperature day, and I have been feeling chilled in air conditioning.

I want you to know you are not alone.  Everybody does not have hunky-dory lives all the time.  Just because someone sounds cheerful does not mean they are not carrying a burden.  Sometimes, I write, and I am afraid you think I can get everything done on my Weekly Schedule.  I don't.  It's a guideline for when I am asking myself what to do next.  I use to say to myself to stop being lazy, but now I realize I am not a lazy person, because I cannot always get things done that I think needs doing.  That is not laziness, it is illness.

I encourage you to hold on to hope.  Look for the good moments, the restful moments, and the memorable moments.  Smell the roses.  And, when those blah days come, remember life is not like this all the time.  This too shall pass.  

Thinking of you often and praying,
Deborah

Monday, December 3, 2012

The First Christmas Supper 2012

Happy Birthday, Jesus!
Tonight is the night of the first Christmas Supper of 2012 for me.  I don't go out much anymore, so I look forward to it, but I also feel a bit of anxiety.  When my husband came home for lunch, I asked him teasingly, "Should I go for beautiful or sick tonight."  Those of you who have Fibromyalgia or/and CFIDS probably know what I was feeling when I said that.  I was thinking about those people who know church services I have missed, etc., and when they see me, I don't look sick.  And I have to say that I don't really want to look sick.  I just get frustrated when I know there are people that probably don't believe it.  I admit -- I am still afraid of being judged.  By the way, I still vote for looking the best I can look.

As much as I know about my illness, there are times I get so frustrated with myself -- I still have moments I have to let putting out energy remind me that life in the Chronic Fatigue Immune Defiency Syndrome realm is never going to be normal, unless a miracle occurs.  I wish someone would tell me why I still feel guilty about something I can't help.  I don't carry that guilt around every moment, but it hits sometimes.

There are things I could probably do if I could afford to have people to do some of the things I have to do at home.  However, I have to make a choice;  and the basic things of life need to be done.  My husband is getting older too.  When I can cook supper, wash clothes, or clean the areas in the house that need to be cleaned, I am helping him.  That is the way I can support his ministry in our church, which still makes it our ministry because I am his helpmate.  I want to sing in the choir, go to every service, play piano, sing solos and do all the things I used to do.  Sometimes, I am so sad I cannot do this, but someday I will be praising my God in Heaven with more energy than I ever had.  I will be able to dance on my toes for Him and leap in the air, and sing too.  So I praise God with all my heart that He just put this picture in my mind to share.


For all you out there that have any chronic illness:  Merry Christmas!  We do not need to fear or grieve, but praise God that in the name of Jesus, we will one day be whole.

P.S.  I won't be writing as much during the Christmas Season, but I always try to remember to post it.  I will also check into a place for you to subscribe.
Love,
Deborah