Showing posts with label visual expression. Show all posts
Showing posts with label visual expression. Show all posts

Monday, August 6, 2012

What I Know That I Didn't Know Before

Is it really August? Six months out from my brain surgery and I sometimes have no idea how to look at my life. I have to say the overarching theme is acceptance, and the undertow is over-doing, but maybe those are just on the surface, maybe underneath those obvious things something else is happening. Am I really different than I was before I was diagnosed with a benign meningioma last October? Yes, I am. No, I am not.



If you’ve been reading this blog or following me on Facebook, you know that I’ve been very prolific in expressing myself through working with oil pastels since March. My interest in doing that goes back before the brain surgery, but then something blocked my ability to accept that my drawing was acceptable. Much of my pre-surgery work is muddied with a question mark about whether or not I’m good at it or whether I should spend so much time playing with it when there are other more important things to accomplish. I would say that after the brain surgery I misplaced the filter that didn’t allow experiment or even a development of concepts and practice time. That filter disappeared nearly completely, though now I am conscious that I must choose to ignore it when it returns, and it does, until hopefully someday it will just be an archived file of used-to-be.

Falling in love with visual art again has opened new doors for me about how I view my future, how my family sees my time and efforts and how I connect with my friends and acquaintances. This is something I’ve been seeking for years! The enjoyment I get from simply sharing my work and seeing how it strikes people’s fancy is immeasurable. Just fills my heart with joy.

Dare I be honest? Of course, honesty, as undoing as it is, is the mission of Kosmic Egg Projects, myself by a company name. Nearly a decade ago I had already reached the end of my love affair with being a “hack” as my father might define me -- a copywriter, a content provider, a writer-for-hire, a copy editor and yet I continued to pursue the work for the pure reason of supporting my family and having some “freedom” to raise my children. More recently, after 20 years as a word-based communicator, I was already having trouble keeping even an ember of interest lit for a business focused on selling things and ideas with words. Before I was diagnosed, I was deeply depressed about losing my way off the creative path that I *really wanted* to be upon even though I enjoyed teaching creative screenwriting more than just about anything else I made myself do for a living. Still, I felt it was fraudulent, since I could no longer make myself write three scenes myself. I could not appreciate that I had anything valuable to share except what I had failed to stick to myself and achieve even though I knew what needed to be done. This obsession leaked into every part of my life before I was diagnosed. Who knows? It may have fed the tumor to begin with, or, perhaps, the tumor was the crime.

Diagnosis of having a brain tumor just exactly on the part of my brain that should be getting things done, that should be writing well was a huge relief. It was like a “get-out-of-jail” card. It opened the possibility that I didn’t have to write anymore. Can you believe someone who has spent thirty years now studying, practicing, working, and teaching writing was so elated to even think, “I may never do it again,” as a good thing? It is true, as much as I wrung my hands over it here. It is true. There was a little elation.

So I have watched this part of my life and wondered, “Am I really allowed to stop?” I mean we have discovered, together, that I can still write. It has nothing to do with the brain or lack thereof, if I choose not to write anymore. Accepting this possibility into my thoughts throws me into a fit, an internal argument about who I am down to my core. I have been a writer. I may not have achieved what I expected to achieve, but that is what I have been for so long that I cannot think of myself without that definition attached like a talking bubble that follows me everywhere. To claim it as my own without disrespecting my effort was the argument before diagnosis, but the idea of stopping and cutting it free, is unbelievably shocking. Almost like the thought of losing a parent or child, it is that close to the heart. Do these things happen? I feel like I must go to the edge of this abyss and decide finally whether I’m going to walk back away from it, or finally jump in with all my heart.

What does that mean? Wait. I am an artist. I draw pictures. There is a future there that makes sense to begin. What is this writing thing? It’s just an old, beat up stone that’s hanging off a cliff now, and I could cut the chain.

Six months out from surgery, I’m recovering. The left side of my face is feeling heat now for the first time in that long. I am taking tango lessons again and re-learning how to walk in my body, to be flexible, to glide, to feel sexy again. I am drawing better and better, and learning about how a picture can be a thousand words. Still, those words...they keep on pulling me until I decide.

The great thing I know now, that I did not know before this brain adventure, is that there is no way to predict the outcome of my decision. I could do everything right and be exactly where I stand today. I could "catch the thread of luminescence" as Oriah Mountain Dreamer calls "The Call" and have a glorious adventure. I only have to decide whether I am curious about what might happen if...



Thursday, June 28, 2012

Word. Words?

The Cave
The most difficult thing is to communicate, to explain anything as I am recovering from the removal of my benign meningioma (the brain tumor that was diagnosed in October of 2011). While I may seem to be myself, I really do not feel myself yet...over four months out from surgery. I enjoy being alive and I am experiencing a creative surge that my productivity can barely keep up with, and most of all I am grateful surgery went well and I can still be available to my kids and my husband in the most important and general ways. Yet, there are disconnections and missteps and losses that pop up into my day-to-day existence that cause me to ponder how to really get to recovery that feels 100% beyond the general and that is specifically me, the person I know myself to be.
Moonsight

Writing from the heart is, perhaps, my greatest challenge. I write something over and over again now, that, before this adventure, may have seemed acceptable after one or two tries. My heart feels disconnected from words mostly. I do not know currently if it is because I was blinded to the confusion in my structure and connection before, or whether it is because I will run into a word that I have an idea for but cannot locate in reality, and this is part of recovering. I’m quick to replace those words but often my replacements lead me down another road than I’d intended. This happens in conversation as well, a constant reaching for words that match my ideas and thoughts. I used to have a vocabulary.

Further developing this word replacement in a “benign” way, a way that is constantly entertaining to my kids, my brain seems to work a lot like a smartphone type screen - in that it offers a slew of words that are somewhat similar in spelling and often chooses that word arbitrarily. Spelling or phonetic choice having a higher priority than meaning everytime. I try to catch these words and replace them correctly as soon as I can, but, if you’ve used a smartphone at all, you know that it is a frequent problem to have commented in a way you never intended. Bring that to a conversation. Add another person to the conversation, or a roomful of conversations, or a radio or a television in the background and imagine the brain reaches out and grabs any number of words and spews them into the conversation you’re having with complete disregard to what you’re actually talking about. Yes. I’m a lot of fun. My daughter says with an awesome smile on her face, “Mom, you said that with so much confidence!”



I’m wondering if I’m writing any of this in a way that you can understand, but I’m going ahead and posting it just to see what the response is because maybe I’m the only one that is frustrated. Because this is the other thing, when I try to read this stuff, it is difficult to decipher. It is difficult to decipher an article, a chapter, anything longer than 144 characters. I feel like I should hold my hand and get serious about sitting for an hour reading, but after 10 minutes, I’m lost sometimes. Not always, but sometimes I am simply unable to read. Sometimes a person hands me a business card or an appointment card and I look at it as if it is a picture, waiting for comprehension.
Nature's Balance

All of this word stuff would be driving me even more crazy except for the fact that I feel free, in a way, of the obligation to know everything for once. I have become aware of the weight of my expectations around words. I would like to skip the know-it-all need sometimes. Sometimes I would like to turn my back on the old way, and accept that I’m now primarily a visual person, someone who communicates with icons and symbols. Sometimes.

Then I have an idea for a story, or a letter, a good conversation or a speech and I’m revived in the battle to win my brain back.



2012 (c) Amanda Morris Johnson