"The Eagle Has Crashed"

Book Review: The Eagle Has Crashed by Ted Lacksonen

I recently had a friend ask me to read his new book, The Eagle Has Crashed, and I quickly said yes!  Ted has been someone who has been helping me to think outside the box when it comes to the plight of America and politics in general.  I respect his opinion deeply and was excited and honored to...

4Walls and AView

Fogged In…

A couple of days ago, I sat here watching the fog roll in.  It waned in and out throughout the day and then returned with a vengeance at night.  I was intrigued to see how at different times during that 24 hour period, the look and feel of the fog changed.  There were times that is was so thick I could not see across the river.  Yet, at other times, I could see slivers of the many buildings downtown, trying their best to peak through.  In the middle of the afternoon, it looked as if a child had taken a huge wad of cotton and dispersed it half-hazardly over the town I love.

The fog reminded me of one of the symptoms I have with the CFIDS.  I have a confession to make.  It is the most difficult of all the symptoms for me.  This symptom cuts to the very core of who I am and it comes and goes like a thief in the night, showing up announced and uninvited.  When it visits, it does its dastardly deed, leaving me reeling and trying to cope.

The symptom is often referred to by most sufferers of these illnesses as ‘brain fog’.  For me this one symptom poses the gravest danger because it affects my ability to remember.  In order to help you understand, I will have to share a little of my history with you.

As a student in grade school and High school, I was what you would call an average student.  Nothing to write home to mom about, if you know what I mean.  On average, I mostly brought home B’s and C’s on my report cards.  I never considered myself smart or intellectual and actually thought I was on the dumb side of the spectrum.

When I got out of the Air Force, I applied to go back to school through Vocational Rehab.  In order to do so, I had to take a test.  I was praying I would pass.  When the test was over, the man in charge pulled me to the side, and I remember thinking,

Oh my gosh!  I must have bombed!

Imagine my surprise when this individual told me I had placed in the top 10 percent of all those tested, ever.  I was like, “What?”  I think I even told him they had mad a mistake.  He assured me they hadn’t and if memory serves me correctly, allowed me to take the test (a different version) a second time.  I scored in the top 10 percent again.  I was flabbergasted!  He told me he had no idea how I had ever come to the conclusion that I was not smart (I won’t go there) but the test proved otherwise.

It took me a little while to come to terms with the idea that I actually had some brains!  I have to say, I was quite excited to start school!  And then my world fell apart.  Within weeks of starting I crashed from what I now know was CFIDS.  I took the semester off to “recover” and then tried to make a go of another semester, only to become so ill, that I was bed bound and at times, wheel chair bound.  I realized that school was no longer an option for me.  That was in 1993.

Now fast-forward to 2000.  I was doing much better and actually thought I was on my way to a full recovery.  So,  I once again applied to return to the program and again had to take the exam.  This time, however, the results floored me.  I barely passed the test in order to be approved to enter the program.  You see…I was having a really bad day when I took the test.

During the next 7 years that it took me to earn my Bachelor’s, I would repeatedly see the havoc of  ‘brain fog’ on my studies.  It was devastating!  One day I would sit in class and know the subject matter cold, especially if it was English or Literature.  The next day, this nasty thing called ‘brain fog’ would show up, and I would have no clue what we were talking about.  In addition, I would forget people’s names, how to spell, or even how to read.  It was embarrassing, humiliating and emotionally devastating.

This past week has been a constant reminder of the difficulties I repeatedly have cognitively.  It is so severe at times that having a conversation can become overwhelming on a difficult day.  Trying to follow multiples lines of thought is almost impossible.

I remember this class I took at church several years ago and a friend of mine had done this incredible presentation.  I went to compliment her on a job well-done, and suddenly discovered I could not remember her name.  Gone!

Another time, I added 2 plus 2 in my checkbook and somehow came up with 800! I think the best ‘brain fog’ day I ever had was when I discovered my shoes in the fridge and my milk in my closet!  :-)

Seriously!  Lately, there doesn’t seem to be a day that passes that I don’t struggle to recall specific words or ideas in a middle of a conversation, or even when trying to write my articles for my blog.

For me this is the most difficult of all my symptoms because my ability to write and think goes to the very core of who I am.  When I get robbed of that, it’s part of me that I am losing.

Thankfully, my schooling and professors taught me some new techniques to get around the obstacles I endure, and thus, have victory from time to time.  Despite that, it never softens the blow to my soul or my psyche when the ‘brain fog’ kicks in and wreaks havoc.

As Ernest Hemingway once said,

The writer must write what he (she) has to say, not speak it.

While the ‘brain fog’ ebbs in and out of my life, it will continue to be a struggle that I must work diligently to overcome.  While I do, however, I am thankful that I have the ability to put pen to paper and share my thoughts with you.  Every time I succeed in doing so, I win.

Determined to continue forward,

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About Dominique

Dominique is a part-time writer and blogger. She currently writes about the challenges of living with Myalgic Encephalomyelitis (ME) and Fibromyalgia (FMS) which she has now lived with since December 1992. She also has her own column, which is published in Life Skills Magazine (LSM) in England. In Feb. 2011, she founded, Becoming VISIBLE 4ME, an organization designed to help raise awareness about the reality of living with ME – 1Story@aTime. Dominique has a BS in Drama with a minor in English Lit. ***When not writing, she spends time working on a variety of creative projects, playing scrabble, reading audio books, and looking forward to spending time with her daughter and grand-daughter as often as possible.
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Comments
  • LD Jackson January 19, 2010 at 5:30 am

    I can not imagine a world where I could not think my way through my problem, but I can easily see where you are coming from. Because of my wife’s illness, I have watched her go through days when she was hardly aware of where she was or what she was doing. It has been so bad at times that our youngest daughter has had to drive her home.

    Keep writing and telling us how you do it, Dominique. You are an inspiration to all who come and read what you have written.
    .-= LD Jackson´s last blog ..Earthquake in Haiti =-.

    • Dominique January 19, 2010 at 9:22 am

      Larry, I had no idea that she was struggling cognitively as well. I guess, now that I think of it, I should have given all the other symptoms. I would put chronic, (unknown) illnesses on my worst enemy. This is a most difficult way to live. I’m glad for the technology that allows us, however, to share and encourage each other. You have been a great source of inspiration to me and for me.!

      • Dominique January 19, 2010 at 10:54 am

        BTW – I sent you an email that may offer some hope!

  • Sue Jackson January 19, 2010 at 5:58 pm

    What a touching story. I know I am very, very fortunate to have only minimal cognitive dysfunction, mainly with word-finding (bad enough for a writer!). I couldn’t write without the thesaurus in Word – not to think of better words, just to figure out what word I’m trying to think of!

    By the way, I forgot to mention when I discovered your blog yesterday that you write beautifully. One would never know that you struggle with brain fog – you express your thoughts and experiences so well.

    For me, the worst symptom of CFIDS is the exercise intolerance. Like you mentioned in an earlier blog entry, I used to love to be physically fit and strong – had lifted weights since I was 16. Not being able to even take a walk most days is just torture for me. I’m trying to start small (not my usual style!) and bring my stamina back up a bit. These last 6 months have been tough.

    Congratulations on completing your Bachelor’s degree with CFIDS – that’s quite an accomplishment and you should be proud!

    Sue
    .-= Sue Jackson´s last blog ..The End of the Marathon =-.

    • Dominique January 19, 2010 at 8:53 pm

      Sue – Thank you for the wonderful comment about my writing. I do enjoy doing it even when I have to write with the awful brain fog! I, too, struggle with the exercise thing. I have gained almost 100 pounds as a result of not being able to exercise anymore. I try to get out every day and do at least five minutes to 20 minutes on a really good day but it is hard. Having to pugs helps because I have to take them potty but even that can be a struggle.

      I’m sorry these past 6 months have been tough. I do understand. I have entered phase 3 (Only Dr. Cheney seems to talk about the different phases) and I now find that I really struggle to function outside my four walls. Within the four walls I don’t do too bad but the minute I’m in public, I get easily overwhelmed on bad days.

      Take it really easy on the exercise. I have found it much hard to find balance in exercising with the CFIDS versus the FMS. Sometimes, I find just being outside is enough. Just to have that fresh air, see the clouds, feel the grass. Lovely.

      Thank you. I never want to repeat college again. That was the hardest thing I have ever done. I think I am still paying for it physically.

      I’m glad you came back. I will visit your blog tomorrow. I was focused on the Massachusetts election today so writing kind got put off to the side.

      Dominique

  • Kathie January 27, 2010 at 4:32 pm

    Dominique,

    I am new to your blog and happy I found it. I too have huge problem with memory, word finding, and anything out of my small world.

    It’s been about 3yrs since I was able to drive. Being able to take a road trip whenever, wherever I wanted is no longer in my scope of things I can do.

    I’ve also gained about 100 pounds. I was always very fit and loved to exercise. I used to walk 4 miles a day. Now it’s counted in minutes. Maybe on a good day I can walk 5 minutes. Some days I really force myself to try, but always pay the price by having to stay in bed for days.

    I am very fortunate to have a very caring husband of 40 years. He retired early to help care for me. We recently downsized from a 3000 square foot house to a motor home. So just the two of us with our 2 boys (poodles).

    Keep up your wonderful writing. It’s a pleasure to read.

    Regards, Kathie

    • Dominique January 27, 2010 at 7:54 pm

      Kathie, Thank you so much for “finding me!” Some of your story could have been taken right out of mine! It is amazing how out lives really do overlap.

      You are lucky to have a wonderful husband. That is a blessing.

      Thank you for your gracious compliments and I intend to do just that…keep writing.

      Please be sure to comment often and let me know what you think and how things are with you!

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