
This is just perfect!




I’ve spoken about PAIN, I’ve spoken about FATIGUE, now its time to speak about ‘COG FOG‘
“Cog Fog” is a term generally used to describe the confusion, disorientation, general grogginess, and other issues resulting from cognitive dysfunction which commonly occurs with MS.
ability to use and understand language
concentration
thinking
reasoning
problem solving
recognition of people and places
ability to learn and remember new things
ability to plan and execute plans
ability to judge distances
multitasking
prioritizing
Have you ever found yourself in a situation that requires you to use a massive amount of brain power.
Counting… do you save your spare change in a money-box?
Remember those days when we had to count our own coins, before the days of taking it to a machine that counts it for you but only gives you a percentage of what you actually put in!
You want to treat yourself to something really nice but you have to count all those coins yourself before you know if you have enough money!
How about a flat pack piece of furniture that requires assembling, how are you at putting those together? I used to be brilliant!
What ever you find challenges your brain, keep that in mind.
Now imagine you are trying to do that task but you have some very bored children around you that are constantly trying to get your attention, you can’t take your mind off the job in hand but they are so distracting!
Ok, now imagine you’re in a really noisey environment! Lets say a pub & England are playing in the world cup, plus the job your trying to do and the board children that won’t stop nagging.
Someone shouts your name but you can’t stop! You know that as soon as you take your attention away from your task, you’ll forget where you got to & will have to start again!
They keep shouting you, the crowd in the pub are so noisy you can’t hear yourself think. The children are nagging, you start to lose your focus! It won’t stop though! You can’t stop, kids nagging, someone shouting you. You rub your eyes, your heads going fuzzy! England score! What were you doing? Did your head explode!
Now times this by 10 & your half way there to feeling what its like to have MS ‘COG FOG‘ or what I occasionally call a ‘BRAIN FART’
Don’t forget that whilst all the above is happening, you also have that pain I spoke about & the fatigue!
Both of those can make the ‘COG FOG’ worse. So the more pain I am in & the worse my fatigue is then the my ‘COG FOG’ is heightened!
I might forget where I am,
I might forget the way I am going even though I’m in a corridor with only one way out! (Yes that has actually happened)
I might forget your name,
I will probably forget what I am talking about & in so many occasions I actually just stop talking!
You’ll see me just stop talking mid sentence & look at you blankly as though I’m waiting for you to say some something!
This is Cog-Fog!
About half of all people with multiple sclerosis have some degree of problem at some time with aspects of thinking – memory, attention span or concentration. Cognition is the term that covers all aspects of thinking and these symptoms are referred to as cognitive problems.
For most people the symptoms are relatively mild and like other symptoms can fluctuate from day-to-day, worsen during relapse and improve during remission.
As with physical symptoms, not all people with MS will experience all of these problems. Cognitive problems can be made worse by some medications, including those used to treat pain and depression.
Many people may not recognise cognitive symptoms as an aspect of their MS and they can arise early in the course of the condition although the greater the disease duration and severity the more likely problems are to occur.
Whilst frightening, cognitive changes are generally mild and management strategies can provide effective methods of lessening if not eliminating the functional effects.
Many people with MS report that their memory is not as good as previously. Memory difficulties are primarily related to the recall of recent events or information and forgetting to carry out planned actions in the future. Both these situations lend themselves well to using systems to record information and to act as reminders or prompts, eg diaries, notice boards or mobile phones.
This problem is described as experiencing difficulties with being able to follow a series of complex, instructions, especially if the information is given rapidly.
This may arise as the result of an individual being so agitated and anxious about a task, that they are unable to mentally structure their thoughts to instigate a series of separate actions. Consciously breaking down a task into simpler steps or stages can allow progress.
Also called ‘tip of the tongue’ phenomenon, this is a recall problem rather than the loss of memory for that word.
This tends to occur when a lot of information is being delivered to a person at once and only some is relevant, for example where several people are talking at once.
Management of cognitive symptoms often involves finding strategies to minimise the effects of symptoms, and sometimes a retraining approach whereby progressively more challenging exercises are given to strengthen impaired function. Management often involves psychologists, speech and language therapists and occupational therapists.
Constraints of my MS
At the moment I feel I am doing very well with the acceptance of my MS.
Unfortunately this is such an unpredictable disease which I think makes it impossible to say that I have accepted every part of it.
Not many people know a lot about MS, I know I didn’t before I was told I have it.
I’ll explain a little about my MS. I say ‘my’ MS because not one person who has it is the same as another. We are all completely unique with our MS although the symptoms that we all have can be similar.
Now I am going to talk about one certain topic here but for you to understand I will have to go into detail about other symptoms which I will explain briefly with the aid of:
PAIN
Pain is only one of my symptoms!
This is probably one of the biggest things I have had to and still am learning to cope with!
Why do I have pain?
More than half of all people with multiple sclerosis will experience pain symptoms at some stage.
Pain can be defined as unpleasant sensory experiences. In MS this may encompass both ‘painful’ feelings and also altered sensations such as pins and needles, numbness, or crawling, burning feelings (known as dysaesthesia).
No two people will experience pain in the same way; it is very subjective and is best described by the person experiencing it.
There are two broadly recognised types of pain in MS:
Also known as nerve pain, this is thought that this arises as a direct result of the damaged to the covering of nerves interfering with the normal transmission of information to the brain. However, the origin of most nerve pain is not fully understood. Examples of neuropathic pain include trigeminal neuralgia, an intense painful sensations in the face, and Lhermittes sign, sensations like electric shocks in the neck and spine.
Also known as nociceptive pain. Nociceptors are pain receptors found throughout the body that respond to injury and inflammation. They send messages to the brain that are perceived as pain, usually in the joints or muscles. This type of pain is not directly related to MS, but may be worsened by it; for example, musculoskeletal pain can arise as the result of spasms or abnormal pressure on the muscles and joints due to changes in posture, typically in the back or hips.
Yes I take medication for it!
I’ve tried many different types of tablets, I’ve even tried holistic medicine like acupuncture which I find brilliant for relaxation but unfortunately the effect has never lasted long enough for me to use it as a regular way to self-control the pain.
So instead I have opted to continue with my cocktail of medication such as Pregabalin, Nortriptyline & Duloxetine
If you have clicked on the link for Duloxetine you will notice it is taken for depression, that’s a whole different topic which I’m sure I’ll speak about at some point!
So with my lovely cocktail of super strong neuropathic pain meds can you guess what my next biggest problem is with my MS?…..