Speaking of Understanding

Recently, one of our Facebook friends asked us a fabulous question about our public speaking and how we navigate Barton’s thick accent from Cerebral Palsy. We felt our response deserved more than a simple reply and thought her question would be an excellent topic to explore deeper.


 

 

First of all, I love this question, so I really want to thank our friend for asking it! There are a whole plethora of layers that I want to dive into here. So, bear with me, it may take a while.

As some of you may know, Megan and I have been speaking or teaching publically for most of our marriage in some fashion or another, and over the years, the way we do this has evolved through several iterations. There are times when I can be hard to understand, particularly, if it’s the first time we meet, or if I’m excited. For a long time, before Megan and I met, I worked extremely hard to find ways to make myself more understandable. I used a lot of relaxation exercises and breathing techniques to calm myself so that the muscles in my mouth and throat could function better.

I also became very comfortable and enthusiastic about encouraging others to ask me to repeat myself. I am still happy to say something a hundred times if it allows someone to understand what I’m saying. Of course, when we speak publically, however, this isn’t a realistic option.

For the first several years, I asked Megan to repeat every word I said, and as someone with a deep love for the specificity of language, I wanted her to interpret my word choice verbatim. Of course, when I get on a roll, I tend to go so fast and so far that there was no possible way for her to keep pace, never mind get every word exact. No matter how much I tried to slow down for her benefit, I would inevitably speed up as the conversation went on.

After a while, Megan and I began to explore other ways to facilitate my voice being heard. The first step for me was letting go of my need for precision and allowing her instead to interpret the concept that I was trying to convey in her own words.  This worked fairly well to a point.

Over time, we began to notice that those that we were addressing automatically began to look to her for understanding rather than even attempt direct communication. To us, this eventually caused a shift in energy as the line of communication was forced to pass through Megan rather than going directly from me to another person.

We began to explore this and ways to correct that flow so that it once again became direct and equally meaningful. One of the most important points and feedback that we continually receive is how expressive my face and body are, regardless of how understandable the words are. This gave us an idea. We asked ourselves what would happen if we invited others to listen to our talk from a different place. Rather than trying to grasp every word, we ask people to see if they can pick up on my intent and underlying meaning regardless of how understandable my words were to their minds.

Here’s what happened this first time we did this.

We also played with having a printed script, but found the magic of our speaking happens in the spontaneity of the moment. Now that we are reading from Ink in the Wheels: Stories to Make Love Roll, we will have copies of our passages available to audience members, but we will still speak off the cuff, playing off of each other, to keep the magic alive.

For the most part, this has served us well, and seems to have a lasting impact on our audiences. Sure, there are still times when I ask Megan to repeat for me, particularly in certain situations when I’m trying to get something very particular across or if it is clear to both of us that the audience is totally lost. But by and large, when we look into the eyes of our audience members, we are usually met with sparkling eyes that glow of understanding.

Stay tuned for Megan’s perspective…

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Team Cutter- National Mobility Awareness Campaign: Packin’ It In with Week 3

When we travel, we typically have bags, tools for workshops, BOOKS!, wheelchair (or more than one), ramps, and sometimes Bear rides in Barton’s lap!

We’ve survived week 3 of the National Mobility Awareness Campaign coming up just shy of 3,500 votes! You can vote here!

We think we’re hanging on to the 5% by the skin of our teeth! What we’ve found is there are many people with a handful of votes & a number of others with a boatload of votes (5-9,000).

So what have we been up to this last week? Well, we wanted to show how we go on the road- Barton and Megan style, of course.

There are times when Megan just can’t fit it all in!

We travel- a lot! It’s part of our vision to help other families and individuals, with and without disabilities become more independent, overcome obstacles and find joy and passion in their lives. So inevitably, we spend a lot of time on the road.

This last week, Megan drove 4+ hours every day, in the broken down Honda, praying that it would keep running. We were also so thankful that our local Van Products sponsored travel to a workshop “Staying Safe in Your Community” to youth in Charlotte this week!

Our hope is to expand our speaking throughout the US (and we hope even beyond), over the next two years. Having an accessible van is a vital tool in this goal as it will allow Barton access to increase independence and the ability to speak, teach and lad with more freedom and flexibility.

Hang in there with us and keep voting- we have just over one more month to go, and the more votes we have, the higher our chances are of continuing to the next round.

~Megan and Barton

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Team Cutter- National Mobility Awareness Campaign Week 2

A whole lot of fun!

We began to show our true colors, with matching, well almost matching. It’s safe to safe to say you’re in a bit of a treat to see what we’ll be able to come up with next, since Barton is a bit of a nut and Megan, well, she’s the perfect one. ;o)

For both of us, asking for help isn’t easy. In fact, when Megan was asked by one of her mentors what it was like asking for help, she said she would rather die. Pretty harsh words, right?

The perfect pair.

But for two stubborn people (who have blasted through many preconceived notions saying they can’t), asking for help takes a bit of work… trust, letting go, faith.

“No wheelchair, no baggage, just a dork hitchin’ a ride…” Transportation is one of our biggest hurdles to independence.

Yet, there’s something very freeing about asking for help. We can’t do it on our own, any of us. We all have had people who have challenged us to go further than we ever thought we could, cheered for us from the sidelines, carried us when we haven’t been able to walk. AND, we have also been in positions to help others, to extend a hand to someone we see struggling, needing a cheerleader to boost them from the sidelines or to be the hands who have carried someone else for a time. There is an unspoken dialogue and flow in this act of asking and giving help.

What an amazing journey it has been to feel our community support us in this way- so we thank you!!

Now, about this contest thing: it’s all about the numbers. When we first entered the contest, there were 200 applicants, that means 5% was only 10 people. Now, there are 535 applicants, so 26 people will go to the independent panel to be considered to win an accessible van.

With so many applicants, it’s hard to go onto everyone’s page to see our exact standings. But from what we can tell, we are about #19 or #20 down on the list. So we still have a great shot at this!

We know it’s a long time for a voting contest, but if we can ask you to keep continue voting, and to spread the word to any family, professional or social groups you think would get a kick out of helping us out.

I'm thankful for you!

What will we dream up next?

On tap for week three… the beginning of a comical story (we’re writers, what do you expect??) that well, we hope will get you laughing, and a reminder to vote here!!

Thanks everyone!

~Barton & Megan

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National Mobility Awareness Month: Wild and Wacky Stunts for a Van

The timing couldn’t be more detrimental, or more perfect. You’ve read about the week of our book launch, our car began to fall apart and how we’ve entered the National Mobility Awareness Month contest to win a new van!

A 9-week voting contest is a looong time, especially by social media standards. We know that after a while, all of our friends are going to be sick of hearing for our pleas to vote over FB and Twitter. One morning I was brainstorming, what could we do to show why we need a van and make it more fun? A wheelchair, a ramp, a car, and us. Hmmm.

“Friends don’t let friends ride in the trunk” commented Sloan Meek, friends of Barton & Megan Cutter!

Wild Wednesdays, Terrible Tuesdays- originally we were going to do just a few pictures a week, just to be cute. What’s began as a silly doodle on a scratch piece of paper has turned into a hilarious photo op.

 

Need we say more?

Now, I will say that before I met Barton, I never laughed. Not like I do now anyway. I was always so serious (and sometimes still can be). But, there’s something contagious about Barton’s smile. You can’t help but crack a smile when you look at Barton, even on a bad day. And Barton’s ability to jump wherever we need to go, full throddle, no holding back is something I am still learning. And so it is with this contest- we see it as a first step. And if it doesn’t work, we’ll move on. But what if?? What if it actually worked? And we could take our book on the road, and reach hundreds of other families by sharing our story.

“Somehow, i don’t think that’s going to work, but don’t let me stop you…”

And so we have found ourselves jumping into the middle of a wild & wacky ride. Won’t you join us??

If you like what you see and it makes you smile, you can vote once a day & support us here! The highest contenders are receiving 500-800 votes (a day). So, feel free to forward on to the groups or social circles you are involved with!!

~Megan

Megan: “How’s the air back there??”
Barton: “It was fun ’till she hit the breaks.”
We’re on the cusp of being in the 5%. Help us move ahead!!

Greatest Quote of the week: from Elizabeth Galecke
“Please vote for Barton Cutter- he is an amazing person-and they could really use this accessible vehicle- the day they went to Elizabeth’s studio for their photo shoot(photo below), he drove in his wheelchair to the studio and then back to their home (in rush hour traffic and they are not close). There was a concern he might not have enough battery power to make it back home, but he did AND arrived home to Megan with wine and flowers that he stopped to purchase on the way back! So sweet!
It really makes us realize how much we take for granted every day.
An accessible vehicle that fits this chair would have made their day less stressful and make many, many days easier for him! I really hope he wins, if anyone deserves it, he does!!!!”

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One Way Around the Van in the Middle of the Road

On our last post, we talked about Megan’s car breaking down, and how we hoped to transform this challenge into an opportunity to propel us forward in both professional goals- to get Ink in the Wheels: Stories to Make Love Roll a national success, and personally to create the freedom of mobility that Barton needs for his family.

While we’re looking for a long-term strategy and permanent solution, we could use your help. The National Mobility Equipment Dealers Association is giving away 3 vans for their annual Mobility Awareness Monthcampaign. Vote for us! It is a social competition, and the top 5% of voters will then be judged by an independent panel.

You can vote here: http://www.mobilityawarenessmonth.com/entrant/barton-cutter-raleigh-nc/ The great thing is you can VOTE ONCE A DAY from your ip address. (we are going to use Outlook Reminders to remind us to vote everyday between now and May!) AND they give you a question for an EXTRA POINT!

Our goal professionally with the book is to positively impact individuals and families with and without disabilities, and we couldn’t be more excited that we are reaching that goal. But the book can’t stay in Raleigh.

We need to get it out into the world! And we need an accessible van to help us do that! http://www.mobilityawarenessmonth.com/entrant/barton-cutter-raleigh-nc/

We’ve never done a “voting contest” before, so we thought we would make it fun. We’ll be posting funny photos on our social media. Follow us here: http://www.facebook.com/inkinthewheels 

Since we don’t know what the chances of winning a social + judged competition will be (last year there were 1700 entries & top entries received thousands of votes), we’re looking for long-term strategies. We’re looking for out-of-the-box ideas, foundations, agencies, or philanthropists who would be willing to help us.

If you know of anyone who would love to spread our message of independence, overcoming challenges and finding love, please let us know!

~Barton and Megan

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