Okay get ready...I am gonna talk about Multiple Sclerosis here.Â
Today I experienced feeling as thick as molasses and just as slow. My body was not only affected but my mind was as well. And I must say that I did not like it one bit! This is probably one of the most frightening aspects of this disease to me. I knew that my motor movements could become impaired. But my mind? Please don't take my mind!
My brain may not be the best brain in the world but it has gotten me to this point in life thus far. I have survived many challenges in my life due to keeping my wits about me. I owe my brain a lot! My survival depends upon my grey matter. And now here I am wondering how I can keep my mental abilities intact.
What does it feel like?
Some people with MS describe this cognitive phenomena as being in a brain fog: "More specifically, 'brain fog' refers to a type of clouded thinking where the mind itself, the part which is used to accomplish tasks, becomes clouded, as if there is a type of 'mental cataract' obscuring 'internal' vision." For more details go to this web site.
This seems a pretty good description to me. It was as though all my thoughts were vastly slowed down to a point where coordinating them with things needing to be done proved quite a challenge. I have never felt anything like this before as usually my thoughts are racing out of the gate. I am used to multi-tasking, being alert, and responsive to my environment. It was as though there were a haze to cut through before I could access my thoughts. It isn't quite like being drunk but close enough to it. I understand now why some people with MS are mistaken for being intoxicated during an episode.
Basically you feel as though something is just not right. When you aren't used to this brain fog it can be quite frightening. It feels like yet another loss of control.
Yes it sucks.
But the good news is...is there good news? Yes there is. In an article by Anne Frederickson entitled, Multiple Sclerosis and the Self, she points out:
"At a time when they are losing control of their body, they do not also need the extra burden of believing that they are also losing control of their mind. However, Britell acknowledges that a failure to remember or concentrate is not a sign of a decline in intellect. In fact, a decline in intellect is one of the rarest cognitive dysfunctions. She notes that people with MS retain their abilities with regard to intelligence tests. They are able to reason and solve problems. Just because they are slow to respond to a question does not mean that they do not know the answer. It is rather a sign of other problems. They may not be able to connect the thought with appropriate words or may be having problems concentrating on the question. Slowness is a failure of speed rather a failure of ability."
I am not losing my intellect. I am just sometimes a little slow is all.
Anyways...I have always liked Molasses.
by
Synchronicity W.
Member since:
July 29, 2006 Slow as Molasses
August 30, 2007 06:34 PM UTC
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comments: 23
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Comments: 23
While in most cases, deep grief DOES go away, MS only goes into hibernation sometimes....I think it would be the most difficult to cope with.
My darling high school sweetheart married a woman who has MS...I have another friend whose husband was a fighter pilot. He had MS and had to get out of the Air Force and stop flying...while I don't know first-hand what you are experiencing...I do know that I care deeply about what happens to you.
I also thought, as I read your excellent article, that maybe someone newly diagnosed might read your piece and it would give them a measure of comfort to know they are not alone. I hope you sent your article to "All" on Gather...you may touch lives in ways you would have never expected.
I know you put MY life in persepctive.
For that, I thank you. I will keep you in my prayers and in a special pocket of my heart!
I had a day of major brain fog a few days ago....was so bad I was about ready to chuck the whole idea of graduate school! It passed .....thank God...it is NOT a nice feeling
Most excellent profile in courage, my dear.
On the other hand, this used to occur long before my MS diagnosis, and I have been asked if I am ADD because of it, as well as other things. I used to be embarrassed not to have an excuse for it. At least I do have one now.
I don't think anyone who reads your articles will ever mistake you for unintelligent, either. You write with such clarity...
Keep the faith, Sync, you're a valued piece of this Gather puzzle.
Thanks for giving words to my frustration and fear as well.
Thank you for an encouraging article. God bless you.
be PROUD of your efforts to cope Syn...
L.
We are going to get you through this. There is no more can't. There will be clarity and precision in everything you undertake. I know this disease. I know it
can be beaten. Check your diet to see if you are getting enough beta caratine, and take a yoga class. Oh my GODDESS I can't believe this is going to try to get in my WAY again. However I am armed with knowledge of QUANTUM TOUCH , REIKI , and NUTRITION. You will BEAT THIS. I KNOW it.
Robert Scott
Thank you for writing such a touching article.
I came to Gather tonight with tears of frustration... 19yrs with this MS dis-ease is getting on my nerves :) Your words expressed what I have not been able to, and you did it with honesty, compassion, and charm!
Feel Well!
Fuzzyballerina :)