The Thank You List
May 11, 2012 at 3:13 pm | Posted in Megan's Blogs, Our Love Story, Ramblings | 1 CommentTags: daily living, disability and love, disability and marriage, disability and relationships, gratitude, interability marriage, Megan Cutter, vision
We might be a dorky couple, but every night after we get into bed, we cuddle for a few minutes and tell each other our thank you list out loud. Usually we take turns of who goes first- Barton always remembers who went the night before. Many times our thank you list is full of what happened that day, something meaningful, big and sometimes small. We thank God in times of doubt, each other for where we are in our relationship or those who have come to support us on our journey.
There are times when we’ve had a day- you know, the kind of day that smacks you like a truck and you’d rather hide underneath the covers than crawl out of bed to face whatever disaster is going to hit or so overwhelming it’s like you can’t breathe. Or we’ve gotten under each other’s skin, those little irritations puckering up like a blister just waiting to be popped. These are the days when our thank you might be a one-sentence statement.
“I’m thankful to be alive… Your turn.”
And at first, it might seem like a cop out, but this is a powerful, powerful statement.
This week I found out a young man I grew up with, who lived just a couple of doors down from my father’s house passed away after a stroke earlier in the month.
Sunday is Mother’s Day, and I always post a picture in my mother’s memory on Facebook and take time during the day to honor her in my own special way. After her death 10 years ago, I experienced a tangible fear about dying in the middle of the night, and once this experience passed, I found myself walking with personal epiphanies seeping out, about living, and how utterly amazing life is. Our bodies are living, breathing universes.
Being alive is a miracle in the scheme of things. And lying under the covers, wrapping my arms around someone I love is heavenly, even in times of fear or heartache.
No matter what happens during the day- the greatest high or the worst possible day, our thankful list grounds me, it puts brackets on the day. It helps me not to forget all of the minute moments that we so often skip over- that word or phrase that someone says, how a certain experience impacted us, the smell of rain, a dream from the night before.
And this thank you list brings me back to what is so important to me, to us. It’s not about what I got done or didn’t get done- the successes and failures will melt into the background. We are awakened in this reflection, and yet we must lie these moments down to awaken to a new morning, a new time.
What’s on your thank you list?
Wheelchairs are Hazardous to Your Health
March 16, 2012 at 10:30 am | Posted in Around the House, Megan's Blogs, The Nitty-Gritty | 1 CommentTags: daily living, disability, disability and humor, disability and love, disability and marriage, disability and relationships, humor, interability marriage, Megan Cutter, wheelchairs
This week was turned upside down, literally. I don’t know what it was- the time change, movement in other areas of our lives, but it was one strange week. Monday afternoon, I found Barton at his next computer, unable to move his wheelchair out of position.
All of a sudden, there was a flurry of logistics that had to be altered and calls to the computer repair, and a discussion of what now. Luckily, he was able to get a temporary joystick on Tuesday until we are able to purchase another, a $500 replacement. And we thought we were finally treading above water.
Monday night, however, I woke up in the middle of the night, and in my dream-state, ran head on into Barton’s manual chair sitting in the middle of our bedroom. I thought I had only stubbed the skin off my toe, and went back to sleep without another thought.
Yet, in the morning, I felt a horrible pain in the back of my ribs. In running into Barton’s wheelchair, I had crunched my whole body. I was unable to catch my breath, and every movement just plain hurt. I grabbed an ice pack, and we took extra care in getting Barton up, using a back brace to make sure I was stable. The appointment to my dear neighbor and chiropractor Donna Hedgepeth couldn’t come fast enough, and I’m so appreciative how she was able to move things back into place.
All week, I’ve had to take it slow- move slow, work slow, focus on my body and what I am doing, even if I am sitting at my computer. It’s taught me to be more patient with myself. And Barton took more care too- refusing to let me pick him up if I didn’t have the back brace on.
Now, to be honest, this is not the first time I have run into Barton’s wheelchair. It’s just one of those things. One time, when the weather was gorgeous, we were running together. Barton had the dogs and I was behind him- just trying to keep up. We saw two women who waved and said hello. Barton stopped- and I didn’t- it was a full on impact. I wondered how funny it would have looked to the two women who had gapped at our position, as I almost flew over the top of the handlebars.
I admit, too that I have run Barton into people, waiting in line, not paying attention. It’s easy to do- there’s a whole spacial shift that takes place- with a metal frame and foot petals. Many people ask how Barton can train in martial arts with a wheelchair. Believe it or not, a wheelchair provides many hard and sharp angles, hidden places to wedge an opponent’s foot or arm- and that’s when Barton’s in his wheelchair.
It’s an entirely different issue when the wheelchair is empty, and apparently the opponent is me!
The Importance of Our Own Voice
February 29, 2012 at 3:35 pm | Posted in Megan's Blogs, The Nitty-Gritty, Work | Leave a commentTags: communication, creative expression, daily living, disability, disability and love, disability and marriage, disability and relationships, Megan Cutter, vision, writing
While we were out and about this weekend, someone came up to Barton to compliment him on articles in our local newspaper, but then mentioned that it was great that we write them together, implying that I wrote Barton’s articles for/with him. While I’m sure this person didn’t mean to offend, Barton took it as somewhat of an insult, because there was an implication that he wasn’t capable of doing it on his own.
So let’s dispel some myths right away: I am not allowed to touch anything that Barton writes, and if I am transcribing and miss a word, I put brackets around it so Barton can go back to edit what he meant later. In fact, I am not allowed to touch anything we write until the editing phase. It’s really important to me that when our book comes out, that others know Barton’s sections are his own writing.
Digging a bit deeper below this particular misconception can hit on an even more profound concept for those with and without disabilities. My work as a writer and coach for others- adults and young adults alike, is to provide the avenue for each person to find their own voice, whatever that voice may sound or feel like.
It’s easy to dismiss the communicative arts. I’ll get comments like, “My daughter can’t write.” Creative expression may be in a look of the eye, a cry or sound, a green scribble or a body movement. We can build these relationships and communications over time. Who am I or you to say what it should look like? One of my best successes is one of my students who told me there were no adjectives to describe love. We can build goals around learning our own voice or expression, to tell someone how we feel for example or to navigate within our community.
Recently, an episode of Switched at Birth looked at the determination and challenges of a young man learning to speak with a hearing impairment. In many ways, his learning to speak verbally was a direct reflection of his identity, wanting to relate, be a part of and connect within a hearing world.
When do you feel like you may not have a voice? It could be during a discussion of a particular issue, wanting to keep a job, in the midst of a health crisis or illness. It could be when you feel that no one else could possibly understand where you are. There are many times throughout our lives when we feel like we don’t have a voice.
For me, it was when, as a child, I would write stories under the covers of my bed or hide notebooks in my school locker because family, teachers or professionals thought my writing stories was somehow interfering with other aspects of my life. Years later I was still questioning if I had all of my childhood notebooks, still trying to claim my voice.
The vitality of owning our own sounds, words, non-verbal communication, language is an essential piece of who we are. Claim it, own it and value others who have their own voice, no matter how it may manifest itself.
Honey, We Have a Problem
December 12, 2011 at 9:53 pm | Posted in Megan's Blogs, Ramblings, The Nitty-Gritty | Leave a commentTags: daily living, disability, disability and humor, disability and love, disability and marriage, disability and relationships, humor, interability marriage, Megan Cutter, technology, Work, writing
Barton and I had spent the morning making revisions and changes to the memoir we are writing, and we returned home to implement these revisions into our working document, and I also had planned an afternoon of catching up on work. I turned on the computer, opened all files, and a few seconds later- it all froze. Frozen- completely.
I pressed the power button, and the computer booted up with a purple and green striped screen, which looked like Christmas wrapping paper, with an error message to reboot, in more than one language. I did try, with the same result- in which case you know not to try anymore otherwise you will hit a high level of frustration just from producing an identical result.
Barton was on the deck with the dogs, and I made a face through the windows. “Honey, we have a problem.”
I turned the computer around so he could see the ‘70’s tv color stripes on the screen. I was determined not to freak out.
The afternoon ensued with preparation in case I had lost all data, and a trip to Apple amongst several hundred Christmas shoppers, to thankfully discover it was a graphic card failure, known to fail, and the repairs would be at no cost. As chaotic as the store was, I was still impressed with their customer service.
Barton mentioned more than once that he was proud of my reaction- a far cry from a few years ago. And when I needed a minute so that I could keep my composure and not get lost in the fear of computer crashes, Barton was gracious enough to give me the space I needed.
Several years ago, with a PC, I was working on an article for the News and Observer North Raleigh News, and interview contacts were in an email by the editor who had sent them just as he was going out of town. I don’t know why, but I had this nightmare that my computer wouldn’t turn on, and well, I must have been on that weird wavelength because I woke up early to find the computer would not power up. 7:00am, and poor Barton woke up to my blood curling scream and hyperventilation. Several trips to Best Buy, $100 data recovery plus repair costs to the power strip- all in early December, and it just happened to be the day the Wii was making its debut. What a nightmare it was.
Even with a calmer response, for a writer, any technical glitch can be frustrating and set one back on their deadlines. More than once I tried to get up “to check my computer,” sitting back down to realize there was nothing to check. I sat with my Tension Tamer tea in hand, realizing that whatever work I thought I was going to get done just went out the window.
I breathed in a mixture of peppermint and chamomile, and pulled out a notebook and pen.
Slow is Smooth and Smooth is Fast
October 24, 2011 at 8:30 pm | Posted in Around the House, Megan's Blogs, Ramblings, The Nitty-Gritty | Leave a commentTags: daily living, disability and love, disability and marriage, disability and relationships, household chores, interability marriage, love, Megan Cutter, time together, vision
One of my mentors talked to me about how as creative peoples, we have a tendency to go until we drop, especially when we get inspired. It happens to me when I get on a writing kick- I’ll wake up at 2am, writing before a full day of work, and find myself crashing the next day at six or seven in the evening or I get so wound up I can’t go to sleep. I feel that if I don’t get it down on paper at that moment, it’s gone.
And I mentioned about how- no matter how early I get up, ten minutes before I leave the house, I tear through every room finding keys, papers, notebooks, lesson plans, phone, books. There may be times when I am working on two lists- what I need for the day and what Barton needs for the day.
I was reminded to slow down, on a couple of fronts. To prepare for the next day, not just in logistics, but also in projects. I noticed a huge shift when I found myself ten minutes late, and I was not freaking out at all. I moved from one place to another, and I found myself actually on time for the event.
I’ve also felt like I’ve planned projects out better, giving myself enough time to complete them, and while nothing seems to go as I fully expect, I’m able to adapt to necessary changes in flow or needs.
Yet, I’ve completely resisted the notion of slowing down that I know will smooth the day out even more. During this time of planning multiple events, creating new brochures and working on the best ways to reach new youth and families, I’ve been itching to get to the to-do list. It all seems to go too slowly for my racing mind.
On the days when Barton & I have worked together, we’ve been focused and while we may have only gotten one item off of the long list, we know that we’ve done it well, and that has been a great feeling.
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