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Yesterday’s journal drawn in darkness with pencil…..

“I have not loved the world, nor the world me.
I have not flattered its rank breath,
Nor bowed to its idolatries a patient knee.
I stood among them, but not of them,
In a shroud of thoughts which were not their thoughts…

What is the worst of woes-that wait on age?
What stamps the wrinkle deeper on the brow?
To view each loved one blotted from (my) life’s page,
And be alone on Earth as I am now…

There is a pleasure in the pathless woods,
There is a rapture on the lonely shore;
There is society, where none intrudes
By the deep sea, and music in its roar.
I love not man the less, but Nature more.”

Excerpted from writings of Lord Byron (with apologies for my appropriative use and with gratitude)

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Always knew WHO I was; knowing the WHAT was key to making sense of it, and my connections in life. That took longer; blind hookah-smoking doctors kept trying to feed me poisoned mushrooms and I, naively followed their lead, till one day I realized they were blind, and hadn’t a clue what an elephant was, much less a Mer-elephant!! Ha ha!!

After so many blind dates with a parade of Lilliputian medicine men that invariably ended badly, I paused in 2008/9, to consider how long ago I first suspected, and later confirmed, that I was, and have always been, an–if not THE–elephant in the room.

It took me much longer to realize just how many blind Lilliputians, all strangely named “Dr.” (vs THE DOCTOR), there are in the world. THE DOCTOR would have been a much more attractive adventure, to be sure, but mine was replete with spills, granted, but great thrills, as well!! How can I be disappointed about that??

The blind Dr. years were not such great moments in my history by some accounts, but not so for me. They were painful, yes, and some parts don’t work anymore because they couldn’t see what they were doing, but I gained and learned much from them, too, that became part of my strength and tenacity, and resilience, and passion for many great things.

I figured out, among other things, that it is not so bad to be an elephant of any variety, and I have no desire to try to be anything or anyone else ever again, however awkward that may be for the blind, or for “elephantophobes”! Trying to fit into others’ mirrors has never appealed to me, nor worked anyway, and the blind men taught me the folly of that while trying to convince me that elephants were broken by definition!! Try telling that to a free, grown, natural elephant and they’ll laugh loudly whilst they flatten your notions!!

I’ve survived it all, haven’t I? No lessis wonder, as all those naysayers, touting their blind opinions as taunts or whispers from the darkness as their “good times band wagon” pulled away from my house and out into their dark dusty paths, and all th while they just kept riding around in endless circles, so obsessed about an elephant that they forgot where they were trying to go!!.

I’m told that my survival was a miracle many times. Life is a miracle, so I’ll buy that, but there’s more to it, and no doubt more to come! I have gone on so many adventures, and am now an older but a wee bit wiser elephant now!

And not all of those called Dr. proved to be blind Lilliputians, or even men!! So life as an elephant, albeit more often the elephant in the room, is not such a bad thing, even though sometimes others may not quite know how to relate to me, and vice versa, but that’s okay. When necessary enough, and motivation is there, we have found ways to connect and build some kind of common dialogue. If not, it probably was not important enough for both of us to put in the effort, or else it was just not meant to be. Not all species are, after all, compatible.

And there have been great benefits to being an elephant, especially a Mer-elephant, though at times I imagine Mars to be a more hospitable and compatible place to call home vs here, but there’s such good stuff and peeps here and now here and there, and niches where I was welcome and accepted, and there will always be places, in a sense, for most any kind of elephant to be accepted! And there will be benefits and adventures in my future again, for myself and for the world. I am patiently waiting for my next adventure! Ok not always patient, but eager and ready to see what tomorrow has to show me!

After all, since I am, not just an elephant in some room, but a Mer – elephant, I am a very special kind of elephant! I have flowed in many ways in my life, touched many places, many things, and many people, sometimes for the benefit of many, or for a few, or for one, or for myself, or the effort, at least was there, however it played out. Sit gave me great pleasure to give and get benefit from flowing!!

Since being in this cage over the last few years, I’ve learned that I can flow from wherever I am, under the right circumstances! How very delightful!! I hate confinement, but then again, there is no cage yet whose walls could hold back this flow for long–only I, surrendering to what I could not control, chose that as necessity for a while to gather my strength, grow, and prepare to let loose a mighty storm!! I have always been considered a force to be reckoned with, whatever the reckoning might involve. I see no reason to suppress the force, just adjust the flow at times.

So I say, why stop now? Life is ahead! Elephants, and Mer– elephants: go ever forward! All of us! No matter what the blind men may say, we belong in the world, too , and the world needs the elephants!! Remember that!! :-).

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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.

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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.

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death of a hybridJust a storyline and yes, it’s another self-portrait (I’m the hybrid).  This is more or less a scene in a story, a medical examiner sent to pick up human remains, but finds instead a hybrid, part human, part… something else, they believe.  Ears like a sheep or goat, perceptual abilities that are unimaginable by ordinary human standards, extraordinary intelligence, yet quite vulnerable as extreme sensitive creatures, as well.  What they don’t yet recognize is that these are not hybrids at all, but another human species, highly evolved, but their extremely evolved mental capacities come at the cost of being unable to separate themselves from being severely bombarded by every aspect of their environment beyond human comprehension.  Of course, I’ve given visual form to the sensory sensitivities of hearing by incorporating the large ears, though this was just a 5 minute sketch with 2 cheap colored pencils from a dollar store pack (purple & blue). 

As is so typical of many humans when encountering a new life form or culture or race, the early hybrids faced persecution, even torture, were viewed with fear and treated as monsters because they couldn’t help but be themselves.  Out of fear, the early ones were hunted, eradicated, or locked up in institutions where they were warehoused with the rest of the society’s perceived “freaks.”  And predictably, this store turns on our eventual dependency upon these very creatures for human survival, because they have special gifts, abilities of perception that they can draw upon to find and expose the truth, the reality of situations, to be able to detect every nuance of what adds up to how a system is operating, whether the system is a multinational corporation doing business with other corporations, or the system is a single individual, and their behavior—speech, actions, believes, attitudes, condition, must be correctly understood individually, or when combined with other humans (systems).  To wrap your head around what life is like for these creatures, imagine what it would be actually like to be born able to actually talk to the dead.  Or to all kinds of animals via mental telepathy.  Or to see the future.  And you can’t turn it off, though you might take toxic, noxious substances to try to numb yourself to it sometimes, but that only makes you sick, and it’s worse for you after you get clean again. 

Hybrids, especially “seers” are exquisitely sensitive, and are super perceptive far above the range of human perception in multiple ways.  And while it is possible to find non-hybrid humans who have one sensory perceptiveness close to a hybrid level, you don’t ever find non-hybrids with multiple sensory awareness, much less a global sensitive.  Humans often will reject what they do not understand, and prefer to rely on what they already know and use that to label or categorize hybrids.  When people first became aware of hybrids, not as an isolated freak accident, but when trends in their numbers began to be evident, when the powers of that time got wind of this, what happened next looked like they took a chapter out of Frankenstein, rounding them up like animals and slaughtering them, as they were deemed non-human and needed to be culled before it spread like some infectious plague.

There were survivors, and they pulled away to themselves to avoid capture.  Eventually, though, their gifts were noticed and someone realized that they could be exploited as “seers” or “truthsayers”, and they could investigate any kind of system in the world, build a 3D working model in their heads, tell you what is wrong with the system and how to fix it.  They could “read” systems, provided they had access to information.  Seers were indispensible to world leaders, and they had a constant presence on the court.  But they were not free to come and go as they wished, because of the risk that someone would steal them or harm them thereby disadvantaging the government who relied on them.  So they lived in the most lavish palaces in the world, confined to cage—a gilded cage most of the time, but a cage nonetheless.

And now they have started dying off, and no one seems to know why that is happening.  Even the ancient ones like this one, with no apparent connection to the others, has died.  And that is where this story begins, with a mystery—the death of a seer, specifically MY death.  Not that I am suicidal or anything, but it seemed apt.

The background is done in acrylic, with the scene’s dialogue written in white gel pen in my cheap, $.25 lab notebook from Walmart.  You can do more in these things that I imagined!  Having the pages sewn in, versus perforated is a sturdier option if you abuse these notebooks as much as I do.  This one, started just over 2 months ago, has almost all of the 100 pages filled with journaling now.  My next journal will be an actual sketchbook, and I’ll do the writing as I’ve been doing, but it will be interesting to see how it holds up compared to this option.  My hope is that at least I won’t have the bleeding that sometimes happens when I work with markers in these thin pages, though I’ve managed to work with them and incorporated them into that pages entries.

It might seem morbid to write about one’s death, but death is a part of life, after all, and writing stories that reflect my views and insights about the world and myself, as self-portraits, isn’t at all troubling to me.  It doesn’t make me think of hastening my death, or worrying about death or any such; it is simply part of my story, but told via a fictional character. 

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journal page 080610 So much has been happening, and I’ve been happening to so much, as well!   Change and transition and uncertainty and obstacles/threats, and both anger and fear, triggered by the present, but often with fuel from the past, leaves me somedays feeling positively beaten about the head and neck!  But it passes.  That’s the cool thing, and also the not cool thing.  It’s cool, because I know that even in the throes of pain, confusion, anxiety, depression at times, not knowing what exactly to do/how to cope, I also know that I am experiencing this pain right NOW, and the time of suffering will pass, the fog will clear, the mood will lift, and I will emerge from those moments with something more than I had before—more insight, more relief, more control over the experience (not so much restrictive, as experiencing it intentionally, mindfully, as the process unfolds).  I am keenly aware, as I never have been before, of how I have been shaped by experiences that I didn’t even remember, that telling the story of what I learn along the way, including detailed scrutiny of processes at work, both passive and active/proactively, is itself a multitude of lessons.  It gives me insight into how my own thought processes work—very differently from most of the world, I might add, and why it’s always been so difficult for me to fully connect with others effectively. 

The image is of me, approximately in my 20’s, but connected to me is this elephant.  The elephant represents the fact, unbekownst to myself or my family, that I was, since birth, the “elephant-in-the-room” born autistic (Aspergers), with all the cognitive, functional, and medical potential that Aspies are shaped by, even before they are born.  And this little Aspie “elephant” spent the better part of the first two years of her life, being forcefed toxic pollutants while living next door to a coal burning power plant, years before the Clean Air Act even existed, and decades before they managed to effectively enforce restrictions on coal-fueled electricity.  The damage was already done to this autistic girl who already had a compromised immune system to begin with.

I was constantly sick, and had even been hospitalized once in 1963 with severe dehydration.  I got every virus that came my way, and, as my father later reported to a pediatric neurologist in 1971, “allergic to everything.” 

The third major developmental “insult” occurred when I fell from the upper floor fire landing of a local gymnasium, head first onto solid concrete. It was a very bad head injury, 3” skull fracture, intracranial hypertension and secondary brain injury, also referred to as “diffuse axonal injury.”  The secondary injury, caused by swelling and increased pressures on the brain, caused a lot of the connections between nerves to “shear” or tear apart, while at the same time the brain has trying to heal itself and keep me alive.  This went on for so long, that how it healed, and the rewiring to do it, took the hard wiring in my brain another huge step further away from “normal”.  From the outside, one could observe that the swelling and bruising finally went down, I did not die, and about 9 months after I came home, I was able to sit up in bed without head pressure problems. 

But there was not only no understanding whatsoever of Aspergers Syndrome back then, but also doctors had no idea what such an injury might do to a brain that survived such a fall.  No therapies or medications were administered, no tests for functional damage was done, and I, being only 5 years old at the time, had no idea that I had even less in common with neurotypical humans in how I would interact with my world going forward.  I had a strong sense that I was different from other children as early as 3 years old, but I had no idea why, nor any ability to understand the minds of others. 

Bridging the communication gap has been a lifelong struggle for me, both to understand and to be understood.   I want to be able to relate to other people, to connect with them in ways that are valuable and mutually beneficial.   It’s been agonizingly difficult, cumbersome, time consuming, and exhausting for all parties when I am trying to explain, to clarify my thoughts, feelings, overall perspective on a thing, yet know that I have failed, based on the reaction of those on the receiving end.  I fail for a number of reasons. I have gotten quite expert at being able to profile others, to analyze their behaviors, provided that I am not interacting with them at the time, or at least interacting where I have to be concerned about their perception of me.  This became a huge strength for me in my former job, and as it turns out, is a manifestation of one of many savant abilties.  The way that I journal now helps me really give glimpses into my own mind.  While I do my journaling totally for myself (as I do all of my art these days), I’m open to sharing parts that may be  of interest or benefit to others, or where it illuminates where my head and heart were, on some past event that may have gone totally awry. 

It’s interesting to me how varied my self-portraits are—the images are relative to time, heavily symbolic, even iconic at times.  This was done in my cheap standard lined lab-type notebook, in whic the pages are stitched into a cheap cardboard cover, typically imprinted with some sort of marbled effect, in various covers.  My thoughts that day are about my present situation, but the connections to past events…looking back and experiencing the connections more than the details, how I am represented depends upon what I am experiencing as the most important aspects of the connections in that moment.  Here, I am in my early 20’s.  The elephant part of me, has existed and endured the onslaught of many “insults” that have altered my brain to render me something almost other-humanly in how I think and process input from the world.  With the exception of autism, which I was born with, most of it was caused by the decisions by others act or fail to act—some were family, others including teachers, judges, police, school official, and it developed its own momentum after a while, with the blind following the blind, being slapped with labels/definitions that came to be accepted because the path was well worn, and, neuro-typical humans of all ages, and socioeconomic backgrounds, being naturally susceptible to their own attributional and cognitive biases, unique creatures like myself more often will not be able to sustain acceptance when I come up against those biases.  They used to think people like me were schizophrenic, and often spent their whole lives in institutions.  I was kept in one as a child for 2.5 years, records show that I was orderly, compliant, a good student, and remained there only because there was no stable place for me to live who would accept me.  No one.

The filters are a kind of lazy rule-based system that assumes that I should think and act in a certain way because I look like I belong to a certain group, and when I violate the social rules—spoken and unspoken, the belief is that I knew, or should have known about the rule, and that the violated social rule is something that I can and should conform to, without question.   What

I don’t feel invested in the “blame and shame” game, at least when it comes to my own family’s roles in that damage.  I am less forgiving of societal institutions that participated or turned a blind eye, when they could have taken some simple steps to help.  I understand the things that motivated their choices, their biases at the time as society existed.  That does not mean that I am prepared to forgive.  I still feel that I am owed a debt, at a minimum for the many intentional harms (ie., rapes), looking the other way when abuse was staring them in the face and I was complaining of being molested and raped (which they chose not to even report), noticing, documenting irregularities provided them in reports that they never questioned, never investigated, and never told me about, and leaving it for this brain-damaged woman who happened to have certain gifts, to discover from their own records, piece together the connections, and discover the truth, and even then, only after becoming totally disabled by the ravages of all the mistakes and abuses that had accumulated.  No one is willing to take responsibility.  That is wrong.  I am accustomed to that, but that doesn’t mean that it is right to just accept that nothing should be done to right the wrongs that can be righted, and at least recognize these human-made perfect storms. 

Is it any wonder that I feel safer far away from civilization?  Disasters happen in nature, as well, but nature operates by rules, at least, and they may have undesirable outcomes, but at least they make sense.  That is something I can live with.  I can accept death by tsunami, however tragic.  I’m not yet prepared to accept “that’s just the way things are” when the way things are is entirely constructed by humans motivated by personal agendae, that may or may not have anything to do with justice or even equity.  That is my issue.  And if it can happen to me then, and still happens to me now (except that I fight back), it can happen to others, so it’s not just in the past.  I feel a deep sense of personal responsibility to do something before I die to prevent similar harm from befalling others.  I need to become an advocate.

But first, I need to become an effective advocate for myself, and that means going through this right now.  My art enables me to communicate with others, and to get them to be more open through the way I approach presenting the principles, getting acceptance of possible situations like mine, and only then, telling them my story.  It is becoming easier to have dialogues that are more receptive to understanding my perspective, suspending disbelief long enough to consider the reality, and build bridges of understanding. 

I think in pictures, not words.  I learned many languages, trying to discover the key to communicate with others, but it was woefully inadequate.  Now that I can draw, can do art (since almost one year ago for the first time), I am finding ways to bridge the gaps and find opportunities to improve things.  I hope I can live long enough to do something with it that will help others.  Then it will have been worthwhile.

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Ok, I’m way behind in getting some images uploaded…long story, will update this over the weekend, but here’s the last image I was working on yesterday.  I’ve been drawing, but had to modify to cope with lots of stuff going on.  This one has lots of meaning for me, but will revise this post with that later this week/weekend.  Here’s an image.  Direction in drawing has become very integrated into medical treatment now, and I’ll explain that, too.  I may yet tweak this one a little bit more, but this one was done in pen & ink, watercolor, and colored pencil.  The book is actually just a retail catalog that someone had discarded that was on fairly heavy paper and the size seemed suitable for my purposes (app 7.5” square).  On some pages, like this one, I have glued some cheap manilla-colored children’s drawing paper over the catalog pages to give it some thickness.  I use this book for random doodling like this.  Odd how I often do some of my favorite drawings in recycled books like this. I have a smaller one that I’ve been working in, that I’m going to have to rebind, as the painted pages have torn away from the stitching somewhat. 

For the most part these drawings at least start and progress for quite a while as automatic drawing, and later compositions arise out of them as the image begins to take form.  If I had to plan this picture, I probably couldn’t have done anything that I would enjoy nearly so much or that would mean as much to me.  That process of not planning that seems to have been consistently successful in my drawing apparently still holds true, although I did set an intention to use a limited pallet, primarily blue(without regard to what the actual image might become). 

 

Small Worlds, Big Potential 012810

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