Feeds:
Posts
Comments

Archive for the ‘personal journal (not art-focused)’ Category

    A Poem for My Children

(A True Story)
by Donna Earley

When I was young, I yearned to be
More like my forest family.
Anchored, bowing toward the creek,
My roots, so strong, would reach so deep.
I asked my trees to show to me
What I could do to be a tree.

“Precious child, we love you so,
You do belong, but you must know
Because your nature is to flow,
You must be free to come and go.
And though so small you still may be,
Someday a river you can be.

Then, when you’ve grown to your full flow,
Into the ocean you may go!
Imagine all that you might see
And how connected you’d then be!
Sometimes, you can return again
When heavens bring you back with rain.

Though anchored here we must remain
The times that you come back again,
Then tell us all that you did see
While you were flowing wild and free!
We’ll feel as if we went along,
And here you’ll always have a home,

Looking back each time, I knew….that what they said was right and true.

But flowing free did have a price,
And many things were sacrificed.
For every time I came back home,
A few more precious trees were gone.
Then one day, I grieved to see,
Apartments where my trees should be!

Now, not a single sapling left,
Tears flooded every place I wept.
Bricks, concrete, and asphalt too
Had taken what I loved and knew.
With grief so great, for years I flowed
Not caring more of where I’d go.

But time did slow me for a while,
And twice gave me a precious child.
While each one carried parts from me,
Each also had some traits of trees.
While little, they did gladly go
Wherever Mother chose to flow.

But each, in turn, declared to me,
“I feel.. I need to be a tree.
Your flowing life, inland or sea
May be what you are meant to be,
But Mother, we are not the same;
At times your flowing gives me pain.

I am part tree, and so I need
A place where roots can grow and breathe.
A forest is where I belong,
Where future saplings can grow strong.
Oh, don’t be sad, and please don’t cry.
My love for you will never die.

Go-be the river that you are,
But just don’t drift away too far.
You’re part of us, as we are you,
There’s still important work for you.
No matter what we choose to be,
Our Mother you will always be.

Just one request we have of you,
If you would try your best to do:
Your flow feeds us in many ways,
But floods can wash the soil away!
A gentle flow would be so kind,
And give us all much peace of mind!”

20120711-102718.jpg

Read Full Post »

20120711-092328.jpg

This is a quick 10 min pencil sketch of me last night.

Then I read this post that our lives are the products of our choices. Partly true but not entirely.

Some days JUST SUCK and there’s not much you can do sometimes to Prevent the sucky part, and you just have to ride it out. Yesterday and the day before I’d like to erase from my calendar, but eventually I won’t feel the same. For now, still in the SUCK zone till I’m done.

Ok I’m responsible for MY choices, including how I feel/what I do within my ability, about others’ choices that affect me, but unless blaming & judgment actually contributes to solution (now or future), that’s the extent of its value for me. But it also depends on the tools that I have to work with and most people don’t l know how to change their toolbox.

Important not to discount perspective about how injustice kept hidden can shape a human being profoundly. The right to articulate one’s perspective about a happening is very important–and more, to be heard. Sometimes that can make a problem a non-problem or prevent getting stuck with hard-wired blame/shame reflexes.

Theoretically, one can CHOOSE, provided their brain is physically hard-wired intuitively to do that; if not, it is possible to rewire, but only with intrinsic motivation and a minimum of ~ 6 months of relentless practice, step by step over and over. Worth it?? For me yes, but I’m not hard-wired to fall back on cognitive distortions as much as other people. Always open to an impressed when I see people develop this who didn’t develop it growing up.

Even then, cog biases as like muscle memory–your brain WANTS to do what it’s used to doing-unless something has tipped the scale that changes the priority, we fall back on defaults and still do when we’re tired and hurting and no resource to focus energy on doing something vastly different. And it’s why I forgive daily other people who do things in ignorance when the red flags and clear facts were in their hands. Eyes can’t see what filters block.

Bottom line: it’s not quite that simple to weather a storm by ordering up a sunny disposition–can’t hurt, and if authentic it helps when you’ve got nothing else. But it just doesn’t show up like fast food; it’s like an acquired taste for a dish that takes a long time to prepare, and skill of a fine Japanese sword maker. Great ideal, though, and the journey for me is worth it however close I get.

Read Full Post »

20120605-145109.jpg
10 years…I truly don’t know how to do this.

20120605-145552.jpg
Why must one’s exquisite grief, so loathsome to me, still have such a powerful and intense beauty? This is not sublime, no. It can’t be. I do not want it, it gives me nothing in the moment that I want, I don’t feel inclined to wear a brave altruistic front or be dignified and put on the appropriate cultural mask, but I guess that’s nothing new to others.

New for me is to see it with and in my eyes, there is something–a terrible beauty–perhaps in the rawness and authenticity of my own agony so dreadful and spontaneous in this moment of feeling that I have not really ever seen from the outside. But I’m not a face gazer, except on pictures.

I don’t pose for the camera. Not my way. And I must not hide from facing dark and perplexing feelings, but how strange and complex and I have no idea what to do with them but watch them going through me and me through them. Is this my face? Was that his? How dark can the corners of a grieving soul become? I can’t say; I can only seek and face the dreadful darkness until I finish with what is there for me to learn and to process,, and whatever emerges with or from it. Still, I’d rather hide…

Read Full Post »

List in journal entry 090210 for medicaid appln

I’ve posted some of my drawings and paintings, in some cases showing stages and process, and I’ve posted before about having disabilities preventing me from being able to draw, and having terrible handwriting and so on, but I rarely show you just how bad it is, when performed at a natural pace in  routine setting.  What you see above is a scan of a list of items that I was writing down as it was dictated to me by my case worker, just last week.  In order to make it legible, I have to slow it wayyyyy down, often write it first in pencil so I can correct it (many times), and then write over that in pen.  It is a severe strain for me physically, both to be able to see the marks to control them (my eyes don’t see together—binocular vision, when present, is fuzzy, and I can’t hold visual lines still when I look at them, to track the lines or bring them together, like with circles.  I can’t  make my hand follow a circle around and connect it without error—making the points complete the circle.  The effort causes a lot of strain on my hand and grip, because it’s difficult for me to grip things consistently with fine motor control, and my hand starts to tremor, then I get pain or numbness or both in my hand, and my shoulder hurt more and more and become immobile over time—frozen.  I end up with nerve impingement chronically from the effort.

This and other problems that I have, such as being extraordinarily clumsy, falling constantly, injuring myself, spilling, dropping, breaking, losing things, tripping over my own feet, in fact, they are all features of dyspraxia, also known as developmental coordination disorder.  It also affects my ability to regulate volume, pitch and rate of speech, as well as other things.  It is one of 4 developmental disorders that I have, the others being chronic toxic poisoning during infancy, Asperger or high functioning autism, and sequelae of chronic traumatic brain injury at age 5 yrs 0 months.

VR provided me with typing classes starting when I was about 13, for 8th, 9th, and 10th grades, to give me a tool for written communication, if I could develop proficiency with a keyboard.  The interesting thing about that is that it worked in ways that I did not anticipate or understand until very recently, and certainly the VR folks wouldn’t have known.  At first, it took me a really long time to remember the keyboard to be able to type pretty automatically without thinking about where each key was.  But once I was touch typing, it was easier for me in many ways, as my memory retention/recall is stronger with the tactile aspect, and I am able to process more of interactions spontaneously if my fingers are active with something, like a keyboard, or something else.  Without it, I am weak and straining to process information and remember anything that was said.

Before I went to college, the note taking problem wasn’t a problem in class so much, because I had a photographic memory and it was easy to hold the details in y head and work with them mentally.  I missed a lot of the lectures, but made up for it by consuming information voraciously.  But in colllege, there was no way to keep up with it, especially since I utterly lacked organizational or study skills.    In some cases, using a laptop helps me to offset other functional issues, such as problems with spontaneous social interactions, as the clicking of the keys are almost like stimming for me (also called stereotypy), and can be soothing when I am feeling sensory overloaded or stressed in other ways.

It wouldn’t bother me quite as much to have these functional challenges, perhaps, if I didn’t also have a special kind of brain that processes information via images.  It is natural for me to think this way, and words are quite *unnatural*.  and I not only have many of the classic problems of trying to communicate and have reciprocal relationships with others not like myself (I call them human—what I am in their categories doesn’t fit), they have tremendous difficulty reconciling what sort of creature I am and what things mean because I don’t fit into their buckets, hence why I refer to most humans as “bucket people”.  One of my old rough sketches of bucket people:

bucket people across the world But I have to basically double translate, first into language as fits my thought processes, then into language that is accessible to humans.  It is exhausting.  Someone once asked me if I dream in English when I have been living abroad or in one of my adopted languages.  The answer is “no” I really don’t think in words, unless I am having discussions with someone in my dream.  I know this very well, because until recently, I lived my sleep like another aspect of being awake, or semi-lucid, and would wake up with extensive knowledge of my dreaming the night before, usually working on solving some sort of problems.

So I am face-to-the-world, a picture thinker, in possession of a vast vocabulary, having studied and/or practiced in many languages and in many alphabets, and I’m being questioned about something, interrogated, examined, and my attempts to respond through words can quickly become a trip around the world.  That would be great fun if we both had unlimited time, no pressure or judgment about me, and we were talking about something fun for me.  But that’s not the way it works.  It’s actually excruciating for me to explain something complex to someone who doesn’t think like me and comes into it cold with no understanding of the information in advance or of me, and they quickly become more distracted by my strange behavior and the message is lost to the ethers. 

Typing answers is far easier, but still exhausting for me, as words are not natural for me—sort of like if every language that you spoke, including your birth language, was forever spoken as a foreign language.  You have to think of the words carefully, and edit many times to get to the point where it has some semblance of what I want to convey, but is not as good as what is in my head….EVER.

I tried to tackle this problem (not knowing what the problem was), by reading voraciously, learning everything I could about language use, critical writing, analysis, and even acquiring multiple other languages, hoping to find a comfort zone with others.  That’s what super systemizers do when tackling problems—they have to figure out the system, find the connections, build the detailed model in their head, make it operational, and work off of it to know what to do.  When something goes wrong, they refer back to the system they build in their head, and analyze the data and problem against their conceptual working system.  It’s an ongoing dynamic process that continues for me day and night, never stops until I sleep, and I’m sure continues in my sleep as well.  It’s how I process everything that I experience—nothing is intuitive except the process of systematizing itself.  This is likely my strongest savant ability, and also the harshest aspect of how I’m different from pretty much everyone else in the world, both physically and socially.

I think that ultimately it does help to write, but no matter how much language and knowledge I acquire, using it will never feel natural to me.  It’s like walking with crutches on a tightrope….I might be forced to gain proficiency, but never speed or comfort with the process.  Notwithstanding that, I have written a lot of stuff over the years, in magazines, a great honors’ thesis, unique contractual terms in my former job that were brilliant sometimes for the purpose, good other times, and sometimes unintelligible, even with  keyboard.  But i keep plugging away with this inadequate tool.

I hope to develop greater proficiency with drawing, and trying to come closer to producing how my mind thinks in visual ways.  I’d like to take classes or get training that would help me with that, and therapy to help mitigate the physical problems of the effort in my arm and shoulder.  That might enable me to feel less “disabled”.  Getting help with the strain from the sensory disorganization and dyspraxia would be really nice, if I had a wish list, though I was told by the audiologist at UNC that there are no longer programs for that in my area, particularly in working with adults who never had services as a child.  But hope springs eternal, and I will keep looking for solutions, as I always have.  In the meantime, I will keep working with what I have and do my best.

Read Full Post »

IMG000069

Doctor’s appt today to circle back on how I’m doing.  I’m both looking forward to this and dreading it, all at the same time.  So much to review about options.  If they ask me what’s my number, I must NOT blow up at them!  Argh….pet peeve when you have a chronic illness!  Okay, find my quiet place…calm…..waited so long since the last review.  I was so patient,especially for me!  I’ve come a long way; I can do this! My other doc appts went well, and hopefully I can get this guy on board with making sense of how to better manage all these comorbid conditions and not fry my brain in the process!  He listened to me last time and earned my respect; I need to trust that it will be easier for him this time with more information.  I’m bringing comparison images for him, in case he’s forgotten how I looked last time.  But I’ve lost so much weight since then, and so much muscle!  <sigh>  I can tell that the steroids are starting to lose their effectiveness, though symptoms are still not as bad as without them, assuming I don’t use any of my joints.  How much longer till I can get this in remission?  Hope springs eternal (stubbornly so with me, thank goodness!)

BE BRAVE!!  YOU ARE BRAVE!!  IT WILL BE OK!! 

Sheesh, my heart is racing!  Why do I get so anxious about these meetings?????  Nothing else has triggered anxiety for me in quite a while, now I’m having this completely unhelpful reaction.  Gotta jet, and take a little calming time before my appt. 

Well, I’m bringing some doodling with me, and that always helps.  Working up some new pattern sheets for some of my abstract zen kinda stuff that I use for pain management and stress reduction.  Will post them as I finish them.  There are 12 pattern squares to a page, and developing new designs takes a little longer than putting down patterns that I’ve already worked with.  Still, it’s very calming and opens up flow.

 

Read Full Post »

« Newer Posts

Tasha Miller Griffith

Sustainability and Belonging through Textiles

The Baggage Handler

I made the impossible easy in both worlds!

prophetbrahmarishi

Just another WordPress.com site

Love. Life.

It's simple, yet powerful.

Life is but a dream!

Wisdom from all around the world.

Bucket List Publications

Indulge- Travel, Adventure, & New Experiences

Abandoned Kansai

All abandoned: Chernobyl / Pripyat, Nara Dreamland, Anti-Zombie Fortress, Japanese Sex Museum - and many, many more! Plus: North Korea Special - 2 trips, 16 days / 14 nights! As seen on CNN...

Break Room Stories

Service Industry Stories and More Since 2012

Sumthin' Creative

Just another WordPress.com weblog

LornaPhone

Visual essays for a digital world

My Life Disconnected

adventures in a disturbed mind

Kay Solo

I suck at writing taglines.

MesAyah

Melodic hiphop meets deep reflections about life and death

Window to the Diamond

A Blog by Betty Rogers

C.B. Wentworth

Just following my muse . . .

The Rag Tree

poems, essays, encouragement