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Theory, practice and insight
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A couple of years ago I sought my 10 visits under a care plan. I attended a psychologist.
At the end of the sessions she told me her thoughts. "You are one of the lucky ones Tony, you have insight into you illnesses, and you know the theory, your challenge is putting it all into practice. You need to put a lid on your emotions and think more before you react."
Back to that in a moment. My wife of 5 years has dyslexia, I've known her 30 years now. When she can't spell a word she asks me. I spell the word without her feeling inadequate. When young she was ridiculed and labelled "dumb". But being dyslexic has little to do with intelligence. She reads books, does our finances, plans holidays and so on. She just has a hard time spelling and with arithmetic.
So the connection I see here is that humans have abilities and inabilities. We have areas where we don't perform to a level we want to be at.
Geniuses can have vision or thoughts well beyond 99.9% of the population but some can't put oil in their car, pump up tyres or test a battery. Churchill defended the world from Hitler but he couldn't shake the " black dog".
So back to "putting theory into practice." I've been trying really hard to ...count to ten before I raise my voice at confronting people, be more patient with others. Seek time out when the bipolar mood arrives etc. But I'm now of the opinion that I have found my limits and therefore found my inabilities, identified both ends of my capabilities and what's important, I've come to terms with this knowledge. I've found peace in this process.
Isnt that significant? Sure is. To me it signals that my incapacity to act on the symptoms of my illnesses actually proved they are indeed serious medical conditions and that means there is darn good reason not to be able to overcome.
Such inability is in my opinion equal to other peoples barriers like dyslexia, socially inept, addicts of many fixes, speech impediment and so on.
The key is giving it your best effort, then accepting that all humans are imperfect. Focussing on what you do well and accepting what you are incapable of doing well as being OK.
The sheer weight on your shoulders of mental illness often leads to low self esteem and withdrawal. Stand proud that you try.
There is no better feeling when at the end if the tunnel that you've accepted who you are.... Worts and all.
Do you have difficulty putting theory into practice? Do you have insight into your illness?
Tony WK
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Great post Tony.
Personally I have never had the patience to count to ten, so what I do is
- completely exhale
- inhale
- speak
I find that completely exhaling first ensures that I have sufficient time to not burst out in flaring red anger. Also, in order to say whatever is on my mind, I need to inhale before I can do so; and that inhalation is more time to think before reacting.
I also agree with your sentiments of: Focusing on what you do well and accepting what you are incapable of doing well as being OK. Its very similar to my version that I preach to my kids: influence change in that which you can, and learn to peacefully tolerate that which you cannot.
For me, peacefully tolerate means that the other person is completely unaware that you totally disagree with their behaviours and are merely tolerating them.
SB
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Your philosophy strikes me as eminently sensible. I think it is only realistic to recognize there are limits to improvements to major long-standing illnesses and that when a certain level is reached the increments, if any, get smaller and smaller (log scale?)
I was first diagnosed with stress-related disorders in the 70’s and declared TPI in the 80’s. From then on things first went down, and since that lowest point have improved, partly by medications, therapies, amazing family support, time and partly by learning to fill my life, accommodate my shortfalls and to avoid triggers. I’ve come to know my limits – mostly. (This reminds me of your other recent thread Fortress…)
It’s not a done deal, I’m still learning and changing, but I’ve accepted I’m not the person who started out. It doesn’t mean I’ve given up all hope of further improvement – for example the meds I’ve been on for the last 2 years have really improved things and came out of the blue - but it does mean accepting.
I now mostly know my strengths, I'm pretty sure I can live though the symptoms, I hopefully know when my judgment is likely to be affected (doesn’t mean I make the right decisions though:(
While not as care-free as before my injury, and with no ‘endless horizons’ ahead of me, life still has much.
My best wishes
Croix
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Hi Criox
Thanks, you are doing a lot of reading.
There was a time I had not accepted my mental illnesses. I could accept my physical ones, DVT, gout, ulcers and the likes. They had visible symptoms or effects.
This is a poem I wrote at that time.
LEGS OF SPOKE
How can I let them know?
When the dark exceeds the glow
When the sun hides behind the clouds
Silence they hear...but I scream so loud.
Some stand beside a 6 foot hole
Shake their heads and see its toll
They ask how he could have dropped
Out of the circle -a forget me knot
Yet they seem to see clear and there is hope
When they sight a person with legs of spoke
A crippled girl pushing her chair
A man be manic- there's no one there.
"Storm in a tea cup" hurts so bad
Like the cyber crow who remains so glad
Keeps flying and in full flight
Achieves his art...in the middle of the night
For some in power see it their way
Even at the side of a 6 foot grave
Shake their head and call out "why"
"Why on earth- he didnt have to die".
So kind some be they reach out so true
Smile away "we want to meet you"
Bring along your vintage car and your smile"
But leave - what's behind your dial.
So we laugh and dine and all's ok
Leave at home come what may
If I be saddled with legs of spoke
They'd lift me around- bloody good bloke.
But as my mind hurts so bad
Cannot hide my feelings- mad?
Can no longer be bloody good bloke
Sometimes I wish.....
I had legs of spoke......
Tony WK
Cont
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So you can see, I was at the same point most of us are in the infancy of diagnosis. Then there was a turn. I began to "fight back". Here was the result and quite a contrast
SOCIETY OF SAND
I’m sitting in a desert
Upon sand of friend and foe
Can’t find a piece of turf
Where I cannot stand on toes
I collect a handful of grain
Then watch as it escapes
Just like some friendships
A barren temporary landscape
I create my own oasis
By weeping on a weed
But the sand around me laughs
Cause it doesn’t have a need
Till lately it be the friends
That helped me walk the land
They holding me up under my feet
-supportive grains of sand
I begin to sink so slowly
As they gather my precious hide
The quick sand laughing so loud
A kind man says goodbye
And as I become one of ‘them’
My heart now granuled and dry
I try to weep to water the weed
But sand has no means to cry
Damn it! I struggle so
Be damned if I be like them
I crawl out of the society of sand
To remain the man I am…
So perhaps it is common for us all to go through the processes from realization of an illness, initial treatment and acceptance. That our journey didn't have in it the intention of such illnesses, the default was we'd go through life without them. Like many things, it happened to others not me.
Tony WK (hope the poetry didn't bore you lol)
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Thank you Tony
C
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Dear Elizabeth CP
Thanks for pointing out we are all works in progress - no matter at what stage and the importance of accepting and dealing with the now.
You example really resonates with me. My wife first blamed herself, then started to respond by doubting my love. Eventually we both came to understand what was happening and things improved immeasurably.
Thank you for that, I hope each day you achieve more and more in the fight I understand so well
Croix