Finally! The neurotypical world made more than reasonable accommodations. They made a special effort to include the mobility-challenged into their arena, and I had a blast. Yep. I sat out in a field and painted. No sidewalk for me next to an outbuilding and parking lot — ostracized from other artists.
“How did you get out there with the dragonflies and frogs? With the trees and grasses?” I hear you asking me. I know, I know. Right?
When I first read of the joint venture between the Southwest Michigan Land Conservancy (SMLC) and the Plein Air Artists of West Michigan (PAAWM) to host an Art Walk/Paint Out event at the Wau-Ke-Na Preserve, I thought I wish I could participate. With unusual boldness, I dashed off an email to the president of the PAAWM asking if it would be a barrier-free event all the while expecting the usual reply that the paths would be difficult terrain for a wheelchair. Instead, he said, “Yes, please come.”
“Yes, please come?” Were these words right there on my screen? I couldn’t believe it. I was being included. No, more than that, I was invited – please, come. These words swam before my eyes and a smile spread from cheek to cheek. I was going to participate in an outdoor painting event – really participate – in the fields – with other artists.
The SMLC (who are dedicated to land conservation, duh) had come up with a solution to the barrier problem: drive your vehicle to a site, dump your stuff, drive your vehicle to a designated parking lot. Now, before you start thinking it is incongruous for the preserve to allow a vehicle onto their pristine lands, it was all very carefully planned to keep a minimum impact on the earth.
In the past, I have encountered other land conservation groups who were almost hostile to letting people use the land. Not this group, not this past summer. While being dedicated to protecting nature (a/k/a fields, birds, wildflowers), at the same time, they designed the Preserve to include human nature as part of the natural environment. (After all, what is the point of land conservancy if no one can enjoy it?)
Their balanced approach revealed a respect for God’s creation (which does include us human beings after all). Rather than promulgating a negative attitude about mankind’s relationship with nature and her beauty, the Preserve developed designated lanes, mostly narrow pathways of mown grass, for walkers — which they let me use in a most unique way. These passages are walkable for the able-bodied but dangerous and impassable for a wheelchair.
There I was, smiling all the while as my husband drove me, my wheelchair, and all the paraphernalia associated with plein air painting to a location of my choice. After unloading, my husband moved my mobility van to the parking lot. (Thank you, Dear.)
What a joy! I was just another artist painting in a field. 😀
Once again, I have been invited to participate in the annual Art in Motion Art Show, which raises funds for the Art Therapy and Therapeutic Recreation programs at the Rehabilitation Institute of Chicago.
It is a rare opportunity not only to display my paintings for sale but also to discuss the inspiration behind each piece.
This year’s event will be hosted in the beautiful, newly constructed Shirley Ryan AbilityLab, located at 355 East Erie, from 5:30 p.m.-9:00 p.m.
If you would like to purchase tickets, please visit: Art in Motion Tickets
It was one of those glorious Sunday afternoons. The sun taking no time to make known its ability to enforce the dress code of the day, and I was right there along with the rest of the crowd with my hat, sun screen, and umbrella.
I was at a family gathering. Didn’t matter that it was a baseball game. Yes, I am one of those people who doesn’t really care for baseball. I know, I know, it’s America’s favorite pastime. Or, so I’ve heard all of my life. Nevertheless, even though I am a born and bred American, it is not my favorite. Honestly, it would never even appear on any things-to-do list of mine.
Yet, there I was with the gang watching baseball. And, I wasn’t only sitting there passing time until it was over. Nope. I was yelling and whooping. Yes, I had become a fan in a few short moments. Mimicking the guy behind me, I called out such terms as, “Good eye.” (Huh? Good eye?) What happened? My grandson was playing.
Funny how one’s perspective can change with the slightest alteration in circumstances. It happens all the time. We just don’t notice until something unique comes along – such as my grandson being part of a baseball team. Surely changed my perspective on baseball. (I am even planning on traveling three hours each way just to watch him play in another game tomorrow.)
There is another area where my perspective has changed, also. It is the number of invisible fences that the mobility-challenged face every day, every where.
For example, the playoff park where my grandson was playing, on that beautiful, summer day, was designed with thoughtful consideration of handicapped people. The bleachers had sections carved out for wheelchairs; there was an additional restroom large enough for a wheelchair; plenty of handicap parking spaces; and expansive, concrete sidewalks. All this fabulous planning and accommodation helped make my day more enjoyable.
However, challenges still needed to be faced. Even though the bleacher stands sat on a concrete pad, the sidewalk ended 25 feet short of the stands. In between? A sea of rough, uneven gravel. To make matters worse, on one side were the bleacher stands and on the other side were the restrooms, food stand, and parking lot. Having the wheels of an electric wheelchair (550 pounds unoccupied) spin in gravel is akin to a car stuck in the snow. I can’t even imagine how difficult it would be for someone using a walker.
The clincher (it’s a baseball term, right?) came at the end of the game when the team met for the coach’s pep talk (or whatever it is they say at the end of a game). It is that time when praises are given and awards are handed out. Only, the dugout was another sea of gravel away.
So, there we sat, my grandson’s paternal grandfather and I (his maternal grandmother), watching everyone else gather together as we were left behind another invisible fence.
Recently, I was forced into the noisy and congested world typical of American life. Yep. I had to go shopping.
It all started the moment I tried to squirt a little bit more of the most basic of all oil paints, Titanium White, onto my palette. With a PFFTHHPPPPP the remaining paint plopped out. Reaching for my backup tube, I found. . . nothing. Yep. That tube of Titanium White stuck in the back of the rack? It wasn’t white. It was Ultramarine Blue.
What? Impossible! Agghh! Okay, don’t panic. Just get some delivered.
Normally I can accomplish this task with a few clicks and, violá, the deed is done. Not this time.
Having pulled out my handy, lightweight laptop computer, I searched for a site that would deliver some paint within a few days. (Another experience of the typical American life.) However, with a click-click here and a click-click there, I discovered that it would take, drum roll – please, two weeks for the paint to arrive.
Oh, phooey, ptooey. I have to go to the store.
So, off I went to one of those big box stores that sell home goods, craft items, and art supplies. I live at least an hour away from any major city. Yet, I only had to travel 15 miles to buy my oil paint. (Another one of those pretty awesome miracles of the ordinary American life.)
As I rolled into the store, my eye noticed a sign for sale, “Be Original, Not Ordinary.” Huh? What’s wrong with ordinary?
Image this: A child who has never had the opportunity to be completely immersed in what would be considered a typical summer activity. Why? Because s/he is confined to a wheelchair or has autism or a brain injury.
I guess you don’t have to imagine it, do it? With all the ADA-compliance modifications that have already been made – and they are wonderful, the world is still largely out of reach for anyone with special needs.
There have been times when I have cried because I was sidelined because of a physical barrier. And, if I cried, I can only imagine how often a child has wept because s/he was relegated to an observer-only status.
Now, image this: A child or adult with special needs has the opportunity to be completely immersed in a typical summer activity. What a fantastic idea!
Well, we don’t have to use our imaginations anymore; someone has finally taken the barriers away: Gordon Hartman, the creator of the world’s first ultra-accessible water park. It is a fantastic idea, and it is a reality!
“Children and adults who have special needs are sometimes left out, not because they want to be but because sometimes things are not always adequate for them to use,” Hartman said.
Today is the opening day for Morgan’s Inspiration Island. A $17 million tropical-themed water park located in San Antonio, Texas. This astonishing park (check out the above link) merges those with and without disabilities into one experience. The greatest part of all is that it includes all special needs people.
There are waterproof wheelchairs that use compressed air instead of batteries (which the University of Pittsburgh helped develop); waterproof wristbands for those who tend to wander, quiet areas for those who get overwhelmed, and a way to quickly change water temperature for those who are sensitive to cold water. There’s more: fast passes for those who have trouble waiting in line, private wheelchair transfer areas, and the riverboat adventure attraction boats rise to meet passengers (instead of wheelchair ramps).
Admission? FREE FOR THOSE WITH DISABILITIES.
Anyone up for a road trip to Texas?
It was one of those mornings, Spring shining through the windows. The promise of warm breezes and light jackets. My favorite way to wake up. Smiling, I lifted myself up. Wait, no. Rather than sitting up, I had remained prone. Okay, I’ll try to push a little harder. Nope. That didn’t work. Time and time again, I tried – and I failed. You’ve heard of frogs turning into princes. Well, I guess I had turned into a turtle on its back.
I happen to be married to one of those sweetheart kind of guys. Knowing that if I quietly called to him, he would wake up and eagerly help me. I guess I could say he loves his turtle. Yet, there was no morning urgency to rise. So, instead of waking him up as I had in similar situations in the past, I decided to let him sleep. This old turtle could wait out the time with prayer. Eventually, he stirred and my prince charming turned me into his princess.
The before Rose – the one who existed before a degenerative neuromuscular disease claimed her body – she would not have been given to wait out any situation. She was always having to do, to go, and to act. There are many disadvantages to living trapped in a body that doesn’t work very well, but there are some advantages, too. This morning’s advantage was to let myself be helpless. Rather than thrashing out against an unmovable force, I chose contentment.
It has not been an easy metamorphosis, and I am not changing from an earthbound, crawling bug into something that can fly in the light. My conversion is taking away freedom of movement, incremental, almost indiscernable pieces of my life – my physical life. In its place, I am finding an upside down turtle. My choices are obvious. Do I pull myself into my shell and hide away? Or, do I lie there vulnerable and patient?
Patience and contentment are choices even when my life is not upside down.
Two weeks ago, I wrote the following: ” Failure is always inevitable for a successful life.”
When I first penned this conviction, I wondered if it would ring true for you. Have you ever felt the same way?
Failure Example #1: When I was about 8 years old, my sisters and I spent the summer at my grandparent’s modest home in Wisconsin. One day, playing at the end of a shallow canal, I noticed crayfish crawling along the muddy bottom. Many times I had watched my older sisters catch these beautiful, rust-colored creatures with their bulging eyes and claws held wide open. On this particular bright, sunny day, I thrust my hand into the cool, still water and made a grab for the largest one. Brave one moment and cowardly the next, I yanked my hand out of the water with a crawfish dangling firmly from the index finger of my left hand. With adrenaline pumping and heart pounding, I shook my hand violently, and the tiny lobster landed on the sandy shore. As it sat there stunned, I seized the empty coffee can next to me and threw it at the terrifying monster. Suddenly, its shell split open and blue blood mixed with yellow slime oozed out. Just as quickly as it had coursed through my veins, my fear transformed into remorse. My pumping heart stopped: I had killed a living creature.
The lesson: Fear is often the catalyst to violence.
Failure Example #2: As a Sophmore in high school, I wrote a science fiction piece for my Creative Writing class. Looking forward to my teacher’s feedback, my jaw dropped open as I read the notation at the top of my paper: “Grade: F. See me after class.”
Waiting for my classmates to slowly filter out of the room, I approached him – paper quivering in my outstretched hand. My brain scrambled to make sense of the words that tumbled out of his mouth. Finally, I heard “plagiarized.” I protested and asked him to tell me what story I had copied.
“I don’t know, but you could have not come up with this story on your own,” he replied with unfounded certainty.
He went on to tell me in great detail his perception of me. I was quiet and did not participate in class. My previous assignments were uninspired. As a result, he decided that I could not have created the story on my own because the paper I submitted was imaginative and beyond anything I could have written. Thus, he concluded because I had plagiarized, I deserved the failing grade.
Hot tears welling up, I left the room and called my mother. She had been in the kitchen when I had written the piece at the table, and she offered to come to school to give witness. Not wanting to bring any further attention to myself, I refused her help. Failing to pursue the matter with the school office left me with no recourse at the end of the school term: that one undeserved, unfair, prejudicial, failing grade impacted my final grade in the class.
The lesson: Perception is often incorrect. People are capable of more than you think.
Failure Example #3: As I grew older, I became concerned about performance – doing a good job, being a good parent, or having a good appearance. Sadly, my focus on performance was not confined to me, but I applied the same strict benchmark of achievement to others. Even though I cared about people and what they were facing, I secretly sat in judgment of the decisions they made. My previous lesson caused me to swing too far in the other direction. I believed that anyone could do anything if they tried hard enough.
During my clinical rotation as a nursing student, I encountered patients that compromised their health with continuing questionable behaviors. One experience was the time I spent caring for a middle-aged man who had a permanent trachea as the result of throat cancer. The first time I met him, we sat in the Family Room at the end of the corridor. As I reviewed his medical history with him, he enjoyed smoking a cigarette via the trachea opening.
When I went home that night and reviewed my day, I found an unsuppressible anger welling up inside me. My young husband had died just six short months earlier from cancer. How could Mr. Patient X continue to smoke? He had throat cancer, and he continues to smoke! Why doesn’t he just quit?
Because it was easy for me to live a disciplined life, I expected everyone to be able to do the same. I lacked compassion for those who had a difficult time making changes when it came to life-choice decisions. When I decided to quit smoking, I quit. No struggle; no backsliding. As I encountered people who tried but failed to quit smoking, I failed to empathize. I even failed to realize that I failed to empathize.
The lesson: Compassion is more important than perfection.
“I have failed over and over again in my life and that is why I succeed.”
I know that I will continue to fail for it is the way of life. Often, failures are the main theme of our stories. They are the interlocking threads that make up the fabric of our life. In many ways, our failures serve us better than our successes.
Failures are destabilizing, and the resulting disequilibrium demands attention. Maybe that’s the point: We learn from our failures. They teach us valuable lessons. To fear failure is to fear life.
Welcome failures. They are the stepping stones to your destiny.
We don’t seem them much anymore in this era of digital time, sand clocks. As a young woman, I bought one on a whim. It wasn’t one of those big hour clocks that you see in movies. (Remember the one in The Wizard of Oz?) Mine was a minute timer. A simple, tiny, glass and wood device meting out seconds with a stream of white sand. Fascinated, I turned over the timer and would watch the flow. And, even though I knew that it poured at the same speed, it seemed as if time passed more quickly the closer the top portion was nearing the end. Then, I would turn the timer upside down and start the flow all over again. Time was endless.
I feel as if my life has become one of those sand clocks. Time being measured out – with most of my sand now sitting in the bottom half. Each grain representing days spent carelessly without a thought about the stream, about the passing. Sometimes I even wished time would hurry along. Anxious for the future to arrive. It’s different now.
As I lie in bed – those early mornings that are still dark – I wonder if it really is morning or if I have entered some other time continuum. For in those moments, I can feel time standing before me, not still, but shifting. I can hear it pouring out, and I wonder how it happened so quickly. No longer carefree, I caress my clock in my hands and watch time shifting from space to space, moving faster now.
Pushing against gravity, I struggle to sit up and to take hold of what time is left. Each grain is precious. If only I could scoop up some time and put it back in the top half, or turn it over just like I did with the minute timer. Even to have another minute added to my stream. But, I can’t.
There is no stopping the flow. Days slipped into days, months into months, and years into years. Until, finally, each hour stands alone. Time is no longer measured. It is treasured.
Initially, which did you see? How long did it take until you could see both easily and clearly?
Our eyes see more than our brain interprets. Visual cues all around us are being filtered out, and our awareness is limited to our experiences.
When you encounter a set of stairs leading to a building, what do you see? How about a soap dispenser attached to the wall above a sink? What about a store’s double-door entry with no handicap button? The last question gave it away, right?
If you are ambulant, then you probably don’t give much thought when encountering the above situations. Oh, you might have a conscious thought as you grab for the handrail, but you probably don’t even see anything worth noting. For the wheelchair roamer, we see obstacles. In fact, the situation may be so unsolvable (e.g., stairs and no ramp) that we have to change our plans and turn away. And that it how it feels. We are turned away from participating, turned away because we are powerless, turned away because of an oversight.
“(A) public meeting on accessible housing for the disabled in Toronto had to be canceled because the building that was hosting it was not accessible to the disabled. ‘There was an oversight,’ one official conceded.” (The Week, December 23/30, 2016, p 6)
Laying the book down on her lap, she turned her head so that her good ear was aimed toward the sound.
Again, another clunk.
Not knowing what else she could do, she waited with the still patience of a deer in the woods; her heart pounding as if it were the instrument of a mad drummer.
Then, her husband called out, “I’m home. Where are you?”
“Upstairs,” she replied putting her hand to her chest. “In the pink bedroom. You’re home early.”
“Yeah, the meeting ended earlier and traffic was light. I’ll be up in a minute.”
A smile played its own rhythm across her face as she swept her hand through her gray hair. I’m glad he’s home early.
As the minutes passed, the sharp clank of dishes revealed the location of his delay. As she was wondering what could he possibly be doing in the kitchen, he suddenly appeared in the doorway. There he stood looking like a high school suitor with a vase of flowers held out; the wrinkles around his eyes made him all the more charming.
“A gift of lovely flowers for a lovely lady,” he crooned as he placed the vase on her nightstand.
“As I was driving, I found myself getting excited as the miles brought me closer to home. I know you have been having a hard time lately thinking about all the extra work that falls on me because of your disease. The more I thought about it, the more I thought about you. Because of you, I am a better person. Because of you, I wake up every morning with a smile on my face. Because of you, I love being married. I love you, and given the choice, I would marry you again – wheelchair and all. You. . .you are a gift to me.”
I have the unique ability to be invisible. For a while, I thought it was because I am shorter than most adults.
If that is true, I thought, how is it that children are not bulldozed down into the ground? Maybe, I reasoned, that is why kids have such high voices; it is a survival mechanism to alert adults around them that they are “down here.” Eventually, I came suspect that something else is going on – a societal preference. Our mores define children as needing protection and consideration. So, we notice them; we see them. The same is not true for the disAbled; our societal position is muddied and conflicting. As a society, we nod our heads with smug smiles agreeing that the disabled should be treated with respect.
As a wheelchair occupant, I can tell you that society does not often practice what it preaches. I will admit that a small segment of people will notice me and make accommodations. However, navigating the streets, stores, and social situations is a burdensome task. All my plans and movements must – and I do mean must – include me being responsible for everyone in my vicinity because I do not exist. Sounding alarms as I wheel with the foot traffic, I need to watch for cigarettes, purses, bags, and people who swerve in front of me. Without as much as a blush to the cheek, they admit, “Oh, I didn’t see you.”
You might think this is as humiliating as it can get, but no. Worse yet are the times that I am scorned for being invisible.
Recently, my husband and I spent the day in Chicago at Navy Pier. I was sitting out of the major pedestrian traffic path, but still blocking a small walkway. (I have to sit somewhere.) With a quick step and an urgency of importance swirling about her, a woman came straight towards me. She came to a screeching halt (I heard her brakes squeal) as my invisibility faded away. With furrowed brow and lips, she waved her hand as if swatting an annoying insect (speaking is difficult with a frowning mouth) for me to move. Realizing that I had become visible, I turned on my wheelchair. (Let me give you some inside information, electric wheelchairs take about five seconds to charge up before they are operational.) Well, the necessary five seconds was too long for her. Miss I Can’t Wait Because I Have Important Things to Do, huffed and puffed (was she about to blow me away?), told me to move (without wanting to hear that I needed to wait for my wheelchair), stomped about (was she ready to stampede me?), and then turned sharply to her left, took three steps, and walked (or should I say charged?) past me.
With her went my moment of visibility, and I retreated once again to wait for the next moment.
It all started simply enough. Jasper wrote a post (An Amazing Choice) about a young man, Marshall, with cerebral palsy. As typical for him, Jasper piece was insightful and thought-provoking. At the end of the piece, Jasper offered his readers the opportunity to contribute to his post.
As someone who has made certain discoveries and choices with how to live with a chronic illness, much of what Marshall had to say vibrated within me. So, I made the following comment:
“Jasper, thank you for sharing this post. Just recently, I have been formulating a concept that there is the Gift of Suffering. In its most basic form, the idea is that our suffering adds to our spiritual maturity. As we continue to add to our faith, we grow in our relationship with Christ. Once we trust God with our lives (and, we, who are disabled, know the meaning of this), we can move forward in our appreciation of God’s plan for us. One gift: tribulation develops patience; and patience, character (maturity). Another gift of suffering: we can then comfort others with the comfort that we received from Christ.”
Having the opinion that there can exist such a thing as a Gift of Suffering does not dimish the hardship that suffering brings with it. Do not misunderstand me, please. suffering is not a preferred way of life, but it can change us into more compassionate, patient, thoughtful, kind, loving, enthusiast, insightful, creative, and respectful people. There are other ways that these attributes can be added to our lives, but disabilities have a way of hurrying along the process.
Again, do not misunderstand me, please. I am not saying that if you have a chronic illness, you will automatically join the club of those who have found the secret of being content with their situation. It is a choice – always and daily. Jasper made that choice.
In a more recent post, he wrote:
“I was in awe when I realized how my experience and gradual understanding of the suffering surrounding my ABI reflected the comment you made a few months ago. I would reflect on your comment at times and anticipate a blog post in which you had developed your thoughts further. Talk about mutual inspiration and support. . .”
To read more of what Jasper shared, please click on The Gift of Suffering
How many of us are done? Done with the demonstrations, the riots, the “Build the Wall” chants, the Islamaphobia, the cry to dismantle elements of our constitution, and done with hatred in general. I am. Somehow, everything has been turned upside down. It seems as if everyone is getting into the fray. Rather than working towards peace and tolerance, we are witnessing aggression and bigotry. What happened America?
Somehow, everything has been turned upside down. It seems as if everyone is getting into the fray. Rather than working towards peace and tolerance, we are witnessing aggression and bigotry. What happened America?
What happened to: “Give me your tired, your poor, your huddled masses yearning to breathe free, the wretched refuse of your teeming shore. Send these, the homeless, tempest-tossed to me, I lift my lamp beside the golden door!”
Somewhere along the way, a seething, acrid rage began to smolder in our country’s belly. Hidden behind the smiles and proclamations of acceptance, we ate the poisoned fruit of jealousy and hatred. Until, finally, with glad relief, we spewed the foul bile from our hearts. And, what happened then? Did we look upon our vomit and hastened to sweep it into the trash? No, instead we declared it good.
“Look!” we cried. “Finally, my passions of greed, jealousy, lust, pride are unbridled, and I am ecstatic.”
Honestly, how many of us can follow our roots to the indigenous people of this land? We are an immigrant-founded country. Yet, we want to close our borders to the “alien,” the “illegal,” and the “refugees.”
We blame others for our failures. Our appetites are insatiable. Just like children, we dream of the good life – which has yet to be achieved because it is unachievable. Our bellies grow as we lust after more.
It is time to grow up, America. Look in the mirror, and ask yourself In what ways am I responsible for my life? Am I willing to change? What can I do be positive? In what ways do I take offense? How often does bigotry play a part in my actions and thoughts?
There seems to be a prevailing consensus that life should be good. Period. No ups and downs. No struggles and successes. No failures. We want things the way they were – as if our memories are accurate storytellers.
Life doesn’t always have to be good. In fact, life is pretty darn hard most of the time. Many of us face financial troubles, relationship dilemmas, or health issues. Yet, we find ways to cope. When I look around me, I see potential. Everyone I encounter has the ability to do good. No matter what you are experiencing, you have the option to think well of people or to complain and find fault.
Life doesn’t always have to be good for you to be good, to do good, and to think good.
Time for something besides politics? How about reading a book?
Reblogged on WordPress.com
Source: Meet the Author – M J Smith
An essential concept in design theory is the use of negative space: the area around and in between the subject matter. Basically, the idea is that what you leave out is as important as what you put in. For example, if I decided to paint a landscape, the spaces of sky and the deep shadows help support the shape of the trees. Even though the object (the positive space) is what people tend to notice, the negative space is what keeps the eye moving through and around the painting. The cooperation between the positive and negative spaces make the painting continually engaging.
The same can be said of the mind.
This past month, I found myself on an unexpected journey of fascinating concepts about the fundamentals of my beliefs. As I struggled to examine my mindset about God, love, humility, relationships and suffering, I become acutely aware that I needed to challenge my every thought. My mind moved through negative space where I struggled to write for I could not articulate the inner quest. What I held as foundational was as important as what I did not hold as foundational. The question What is left out? kept my mind engaged. As I transitioned from being the object to being the space around the object, I found myself on the precipice of reorientation of assumptions and beliefs.
Those negative spaces in my mind helped to form positive thoughts:
Let us begin to experience the world through our neighbor’s eyes; let their sorrows be our sorrows and their joys our joys.
I am. I am guilty. We don’t use the word anymore, do we? The only time that we hear the word guilty is when it’s applied to someone who’s committed a crime. Nevertheless, I will use the word guilty because it applies to me.
I am guilty of having a genetic disease. I carry a debilitating, muscle-wasting criminal in my DNA. The sentence handed down? The rest of my life spent in prison – barred without walls. The worst part? This genetic-code criminal is capable of dwelling in my child’s DNA.
How many people with genetic diseases feel guilty, I wonder? Who do we tell? We know that we can’t apply social justice standards. No crime committed. Still, we feel responsible.
For what you might ask? For the extra load that our partner has to carry, for not being able to participate fully in the lives of our loved ones, or for having to excuse ourselves from functions, for a myriad of reasons. Still, others may feel, as I do, responsible for our genetic makeup. What can we do?
Not everything is worth saying, much less repeating. In fact, we should probably spend a lot more time thinking before we let words tumble from our tongue.
A few days ago, I read another FaceBook rant. Yes, I confess, I try to read everyone’s post. It is a character flaw of mine. Somewhere along the way, I developed the belief that if it is worth putting down on paper, then it must have some value, some weight. After all, it takes initiative to articulate concepts. Big mistake on my part.
At one point, there was an effort to writing. Grammar, sentence structure, word choice, spelling – all the old rules of written communication. While I will acknowledge that there are new ways of communicating and that rules do morph to reflect current trends, I still am stuck on the idea that giving life to words should mean something – something of value.
Instead, we have devolved into a multicultural, international mess of inarticulate, hotheaded, screaming mass. In this tumultuous time of insanity, an eruption of control grabbing is spewing acidic hate around the globe. Chants of peace and love have been married to war and hate. Oh, and yes, we (whomever that might be), we are right.
What does all of this have to do with me, a handicapped woman trying to thrive in her Midwestern town? Everything. There are people struggling each day to “cope” with pain, disease, and despair. All the while, physically healthy people are wasting their time – and mine – finding ways to bash or belittle another person.
So, before, you write another rant about some topic that happened to fall into your mind, take a moment to think.
Wha’d ya say that was worth my time?
Finally, brothers and sisters, whatever is true, whatever is noble, whatever is right, whatever is pure, whatever is lovely, whatever is admirable—if anything is excellent or praiseworthy—think about such things. Phil. 4:8
Autism is misunderstood. The following post gives us a moment behind the curtain.
“I feel like I’m living for the weekend at the moment. Its been a busy week. Dylan had a monthly educational workshop at the beginning of the week so we’re chasing our tails trying to ca…
Have you ever tried your high-beam headlights when driving in a dense fog? Scary, isn’t it? The greater the illumination, the less that you see.
Sometimes, medical personnel used their “high-beam headlights” when caring for the chronically ill; they are so intensely focused on their area of expertise that they cannot see the person before them. Scary, isn’t it?
Have you ever heard the joke: What’s the difference between God and a doctor? God knows he’s not a doctor.
Joking aside, I have a benevolent attitude regarding people, even doctors. However, it is true that some medical care providers have trouble listening. Still, doctors do their best with what tools they have available to them. And, that is the problem: their tools. Every doctor approaches their patients with a complete set of lights (beliefs) that they carry around with them.
Those of us within the chronic illness community have more doctor appointments than the average person; consequently, we begin to understand our doctors’ weaknesses and strengths. In addition, we develop a greater understanding of our body’s messages. We know when something is wrong, and often we know the likely culprit. Yet, it is difficult to convince our doctors to see us through the fog of symptoms.
For example: Because my lung muscles are inadequate, my blood oxygen levels drop during the night. Consequently, I need a CPAP machine. Essentially, it has two cycles: one which blows air into my lungs and another that stops blowing to allow air to be pushed out of my lungs. Since my muscles are getting weaker, the pressure necessary to blow air into my lungs is continually being increased by my pulmonologist. This is where it gets sticky for me. The complicating factor is that my lung muscles are too weak to push the air out. The result: a build-up of carbon dioxide in my bloodstream. Not good.
How does the above work as an example? Testing for carbon dioxide levels in the bloodstream is very expensive. (In my case, this would be a low-beam headlight.) Consequently, the relatively easy and cheap measurement of oxygen levels is used to measure lung function. (The high-beam light.) So, even though the results of the tests are indicating that I am getting adequate oxygenation at night (thanks to my CPAP), the test does not measure carbon dioxide levels – which are being elevated as a result. The medical community is shining their bright light on the problem of oxygenation; however, the problem of carbon dioxide levels is hidden in the fog.
It is not only doctors who carry around a satchel of lights (attitudes and beliefs) that often blind us. How I now approach a solution to the conundrum of oxygen/carbon dioxide all depends on what light I choose. The reality may be that I cannot resolve the problem on my own. I may have to battle the medical community (and insurance company) to take another look at the problem. Or, there may be no solution available. No matter what, my perception will affect what I see.
All this to say the following:
Every person around us is facing difficulties. Are we being blinded by our prejudices? Can we see the person, or do we see our own light reflected back on us?
If you think you don’t pre-judge people, let me say two words: Trump, Clinton.
My daughter called me the other day. It was one of those “just to say, ‘Hi,'” phone calls. Nothing important, no purpose – a lunchtime catch-up. Although it was a sweet moment, this isn’t what made me cry.
We talked about her job and a recent promotion. I am very proud of her work ethic and her accomplishments. I am delighted when others see in her the beauty of her mind and her soul. My love for her flows to those around her. She has worked hard to gain the respect she deserves, but this isn’t what made me cry.
Recently, in a moment of high energy, I took a moment to do a little, silly “dance.” It all started as I was leaving the sanctuary and I noticed a friend enjoying the closing song. Most of the congregation had left, but a few of us remained. Rising out of my wheelchair, I grabbed my friend’s hand. Together, as we sang and swayed to the music, another friend joined us. (My husband caught the moment on his phone and had sent the video to my daughter.) My daughter and I laughed about the joy of the moment. As I related the story behind the video, we talked about spontaneous physicality and about how few of these opportunities were available to me. The energy required to stand and sway is not often possible. Usually, my heart wants my body to participate, but my disease refuses to comply. However, this isn’t what made me cry.
She turned the conversation around to me. “How are you doing?” she asked. I told her that I was taking a painting class at the local art museum, again. This time around, the art instructor had demonstrated a technique that had broken a creative barrier for me. I was elated with the new style and eager to generate some new pieces. (Maybe even a Christmas gift or two.) This isn’t what made me cry.
My refusal to give in to my disease keeps me busy (with lots of naps). Once a month, I attend a writing group. They are a great group of people, and I told her about the inspiration and constructive insights I have gained from their critiques. We meet in the late evenings, and I need to take a long nap before I head over to our meetings. The energy cost is high and the next day is spent in bed. Nevertheless, this isn’t what made me cry.
Finally, the conversation turned to the progress of my disease. I told her that I have had more incidents of the falling/slipping out of bed. My husband springs out of bed and rushes to me as I quietly call out in the middle of the night, “Dennis, help me. I am falling.” In addition, I am starting to have trouble sitting up in bed in the morning. My brain tells my body it is time to wake up; my body refuses to comply. I cannot sit up or roll over. I just lie there: observing the war between mind and body. Again, I need to ask my husband for help. “Dennis, I can’t sit up. Will you please come help me?” As always, my husband responds quickly. Telling her about this isn’t what made me cry.
When I finished telling my daughter about the physical problems I am having, I said, “I don’t know what I do would if something happened to Dennis.”
Immediately She said, “Mom, you would come to live with us. Not in our current home. We would get a different place that would accommodate your needs.” You guessed it. This is what made me cry.
(Photo courtesy of DeviantArt.com)
I was standing at the very edge of a pool – the kind used in ancient days – a healing pool. Suddenly, children were walking toward me. Each one reaching out a hand for me to pull them out of the water. They ranged in age from 2 years to 18 years old. As I grabbed them, they stepped aside and stood behind me. No one spoke – not even me.
With the last one lifted out of the water, her hand in mine, I turned to survey the sea of children. The older ones held little ones in their arms.
We all understood that each one was responsible for the other. But, I knew that ultimately I was to care for all of them. Somehow, I needed to find a safe haven. They needed food and clothes and a place to stay. How can I feed all of them? I wondered. There must be at least a hundred children.
Flowing together, I lead the river of lives as we streamed down the crowded streets. Even now, we made no sound. Not knowing where to go, I wandered – each step with the weight of a hundred souls. As if it were the line from a psalm, the words How can I feed them? kept cycling in my mind.
Winding our way through unknown streets, I became disoriented, but the children continued to follow me unheeded. Where will these children be safe? I can’t take care of them. Look at how the older ones care for the younger ones. What am I going to do?
We came to a clearing – a piazza akin to the kind in Rome. At the far end stood a Cathedral. I headed there. Certainly, they will help me. As I drew closer, the lines across my brow disappeared, and I smiled at the children nearest me. I nodded my head in the direction in which we were headed, for an orphanage stood 300 yards away.
Nuns dressed in the traditional habits worn in the 1960s or earlier stood in the courtyard of the orphanage. Brushing dirt from her skirt as if the swiping action of her hand could remove the stains from a garment that had been worn beyond its useful years, one of the nuns approached me. Her clear, brown eyes scanned the children and came to rest on me.
“Good afternoon,” she said with a voice as pure and clear as her eyes.
“Hello,” I replied – hoping that my panic was not too evident to the children. “It seems as if I need some help. We need food and a place to stay. Actually, the children need food and a place to stay. I am not asking that you care for me, also.”
Tears flooded her eyes. “We have no food, and we are at full capacity – beyond full. There is no room for more.”
“I understand.” As I reached out my hand in farewell, she closed the short distance between us and hugged me. The embrace felt natural as if she were my sister, and I hugged her in return. Then, I pulled back and looked once more into her eyes. She understood, also. No words were necessary.
Turning away from the orphanage, I noticed the faces of the children. They calmly stood before me, waiting to follow. They understood, too. They always had.
“We have not found home, yet. Let’s continue onward,” I called out to them.
They said nothing in return. Their silence was a comfort to me. It was at that moment that I knew that my search was over. There was no other place for them; they were my children. Hadn’t I pulled them out of the healing pool?
9/22/2016 “As I walked out the door toward the gate that would lead to my freedom, I knew if I didn’t leave my bitterness and hatred behind, I’d still be in prison.” – Nelson Mandela
The above photo and quote are reblogged from the Eyes & Words blog site.
In 1962, Nelson Mandela, an anti-apartheid activist in South Africa, was sentenced to life for conspiring to overthrow the state. Due to international pressure and fear of a racial civil war, he was released after serving 27 years in prison.
Even though he had justifiable reasons to be angry and to encourage his supporters to seek retribution, he chose the path less traveled. His decision to forgive and forge forward is helped him to be a great leader. We all could stand to learn from his example.
Often, we imprison ourselves by our perceptions, attitudes, and thoughts. We react to situations rather than respond. Whatever situation you are facing right now, the choice is yours.
Do you choose bitterness or freedom?
For more of Eyes + Words blog posts, click here
I don’t know if you have heard of, or if you have ever considered having your medications delivered to you in blister packs. It had been suggested to us by Laurie my social worker when we tol…
Source: How a good idea, goes bad
Recently, I read an article wherein the author, who has lived with a chronic illness his entire life, was lamenting how he felt pressured to “put on a happy face.” His main complaint focused on the inability of the people in his life who were reluctant to address the depression and dark moments that the chronically ill face, especially death. The author was angry that he had no outlet to express his feelings. Due to his chronic illness, he has spent long periods of time in hospitals. As a result, he has met and lost friends. Death is a strong, real presence in his world. Now, he is facing a serious deterioration in his condition, and death cannot be ignored any longer. In fact, I got the feeling that he doesn’t want to ignore the topic of dying. He is angry, frustrated, and depressed. Inasmuch as he is in a troubled state of mind, he extrapolated his feelings to include all chronically ill who are facing death. He believes that anyone who chronically ill and at peace with death must be “faking it.”
Due to his chronic illness, he has spent long periods of time in hospitals. As a result, he has met and lost friends. Death is a strong, real presence in his world. Now, he is facing a serious deterioration in his condition, and death cannot be ignored any longer. In fact, I got the feeling that he doesn’t want to ignore the topic of dying. He is angry, frustrated, and depressed. Inasmuch as he is in a troubled state of mind, he extrapolated his feelings to include all chronically ill who are facing death. He believes that anyone who is chronically ill and at peace with death must be “faking it.”
While I acknowledge that dark moments are part of the human psyche (chronically ill or not), not everyone fears death. Personally, I know of three people who were at peace with the inevitability of their death: my first husband, my niece, and a friend. However, I have also watched others who faced death with anger, fear, and resentment.
There are at least two issues underlying the ranter’s anger: (1) The perceived pressure to “put on a happy face” when the author would rather have talked about his impending death, and (2) the author’s assumption that everyone fears death. In fact, the author went so far as to say that if the dying person was content with the situation, then they were faking it. He said he hated those fakers.
I feel sorry for the author. He is facing the end of his life, he is angry, and he can only see the world from his point of view. To be at the end stage of your life and only see bleakness is a horrible way to spend your remaining days. I am also sorry that he does not have the support that he needs. (I wonder if the support is missing or if the support is not what he wants to hear.) Many people do not want to talk about death and they do not want to be around angry people. He might be in a Catch-22 situation. No matter what the specifics of his situation, I wish there was something that could be done to help him.
My chronic illness puts me at risk for a stroke or sudden cardiac death. Rather than churning my insides into a rancid soup of anger and hatred, I made the decision to be happy and do as much as I could for as long as I can. One of my new mantras is Don’t Give Up – Ever. I fear that the author has given up – on themselves and on others. Hence, the Great Divide and why he can’t understand how people can choose a different approach.
If we were to meet one another on happenstance, I wonder how the author would react to my words? Would he believe me that not everyone fears death? The range of feelings surrounding death are as varied as there are people. It is not a simple matter. In truth, the way we feel about death has a lot to do with the way we feel about life.
The three people I mentioned at the beginning of this post (who were ready to face death) were Christians. Whether or not you believe in God is not the point. My point is that Christianity gives the believer hope about the future and strength to face the present.
Please don’t misunderstand what I am saying. All three people had to deal with pain, a slowly deteriorating body, and dark moments. Still, spending time with them was a rewarding, enriching encounter. The more that they released themselves to the passing, the more serene they were in spirit. They had hope and a vision.
On the other hand, I have known people who did not have faith in God. As they faced death, the angrier they became. They spent their last days spewing hatred. Their beliefs had a deep impact on their feelings and psyche. Before you jump all over me, I know that there are people who do not believe in God but have passed away in peace. Still, there is a Great Divide about facing death.
Is death an end or the beginning?
You just might be wrong.
Because you believe something doesn’t make it true. Your perception is a reality, not the reality.
Take my uncle for example. Diagnosed with myotonic dystrophy in his 40s, he was scuttled off to live with his 82-year-old mother. As soon as he heard the news, he was done. It was his free ticket to sit all day, watching television, while his mother did all the work. He did nothing – not one thing.
For four years she waited on him. By the time my grandmother was 86, she needed help herself. So, we made room, and they came to live with my family and me. Four adults and two children in a three-bedroom ranch. The roles were modified. Now, my grandmother and uncle both sat and watched television from morning to night. They did not
participate in any family events. They did not want to do anything. They did nothing – not one thing. I did all the work. It was okay with me. I did it because it needed to be done. No expectations and no rewards.
So, what was my motivation? My grandmother and uncle needed help. Neither one had ever been kind to me. It was a fact. I didn’t care. The relationships were determined the moment I was born. (Probably before I was born.)
What does this have to do with truth and perception? My uncle was a skeptic. He would tell me I had an ulterior motive. “What motive could I have?” I would ask. “You have nothing. Grandma has nothing. I am taking care of you because you need a caregiver.” He never answered the question. He refused to believe that I took them in because they needed help. He would not (could not?) understand that their lack of grace towards me did not determine my actions towards them. He could only see life as a reflection of himself.
Grandma’s point of view? I don’t know. She would tell me stories of her life. In all of them, she was the sad victim. I would wipe her tears. Unhappy and dissatisfied, she looked at life through a glass streaked and stained with misery.
Today, I live with myotonic dystrophy. I do not sit all day watching television. I write, read, and paint. In addition, I visit people and invite people into my home. I attend church, a writer’s group, and a painting class. What do I see? Hope and love. Why? Because my belief is based on a faith in God.
For the last three months, I have been working on a portrait. It is still in process; an unfinished, challenging, ongoing, all-encompassing activity. In fact, it is a series of problem-solving steps. Every brush stroke is a considered motion. Ahead of that, there is the choice of hue, value, and type of brush for each stroke.
Yet, before I even contemplated the paint colors, I needed to have a vision of what I wanted to paint. After some time spent looking through photographs (life model was not available), I made my decision. Finally, I knew what I wanted to paint, who I wanted to paint, and what I wanted the painting to look like when I finished.
This brings me to today. Just as with any creative process, there is labor. Oil painting is something I love to do; nevertheless, there is frustration and aggravation. When I am not painting, my mind often wanders back to the canvas. In fact, I take several photos so that I can examine the current state of my painting. What can I do better? Where are the problems? How can I improve the image?
I have probably wiped down and scraped off more paint than is currently on the canvas. In fact, I am positive of it. Some of what I rubbed off was good. Indeed, one image was beautiful. Nevertheless, it did not reflect my plan. A portrait is more than capturing the likeness of the person; it is an attempt to capture the character of the individual.
We have all see portraits of dignitaries or famous people. Have you ever noticed the tilt of the head, what they are holding in their hands, what type of clothing they are wearing? All of it is designed to convey an important fact. The intention of the artist and individual is for you to know an answer to a “who” question. That big consuming question for so many of us.
All of this got me to thinking: our lives are canvases. We began life with an image already imprinted before any paint was applied. Upon birth, our parents started to add the paint with their brushes. They took a beautiful plan and added to it. Some of what they applied was solid and worth keeping. Much of it needed to be wiped off – maybe, it needed to be scraped off.
As you matured, you also began to add to your image. Eventually, at some point, you took the brush out of the master’s hand. Formulating a plan in your head, you changed the image. You might even have painted something beautiful – probably not. After awhile, your portrait started to have problems. You started to ask yourself What can I do better? Where are the problems? How can I improve?
At this point in your life, you might be struggling with a disability or some other difficulty. They are wayward strokes. Unlike other times when you could wipe down or scrape off unwanted “paint,” these strokes are permanent changes. It could be that the problems have helped you to focus on what needs to be changed. Maybe, you are finding that your troubles are developing your character. As we examine our lives, we are afforded the opportunity to stand back and unearth the original vision. The discovery process, the hard work and frustration, is answering the “who” question.
It may not be a neurotypical life; it may not be what you or I envisioned for our lives. Nevertheless, the portrait is not to be trashed. Your character will shine through. There is still a beautiful portrait sitting there – unfinished.
“What you see and what you hear depends a great deal on where you are standing. It also depends on what sort of person you are.” ~ C.S. Lewis (1898-1963)
Found this quote on The English Lit Geek blog site. C.S. Lewis’ words ring true today. What do you see and hear?