You Don't Have to Be A Standout to Be Somebody

Thanks to Facebook I was invited to the 30 year reunion for the class I went to school with, but didn’t graduate with.  Midway through 11^th grade my family moved.  That didn’t matter to those who planned the reunion.  It was about the shared experience of growing up here.

There were over 400 who graduated from FHS in 1982.  I wasn’t involved in any activities, wasn’t athletic, or a standout by any definition of the word.  I doubted many people would even remember me.  In addition to that, the big hairstyle of that era has been replaced by a crewcut and mostly relocated to my face in the form of a beard.

That tiny insecure voice inside told me to be ready for someone to tap me on the shoulder and say, “You didn’t actually graduate with us, so you have to leave.”

It also told me to be ready in case someone copped an attitude with me, like a high school student would.  Health issues (some potentially fatal), life in some big cities, vision loss, life in a couple of large cities with vision loss have all created a much less easily intimidated version of me than the one people might remember in high school.  I’ve had to learn to stand up for myself over the years.

Then a different tiny voice told me that time and maturity hasn’t ignored all those people.  It told me to just expect a good time.  Never mind the high odds of me being the only legally blind one there.  Or the only one with a couple of transplanted organs.  I might not be the most enviable one there, but I was pretty sure I had the most atypical life.

Three weeks before the reunion, I had my gall bladder removed along with a hernia repair.  I was down 15 pounds, which would have been a blessing for some, but not in my case.  In just a few weeks I went from being in the best shape of my life to the same scrawny body I had in high school.  It was a chore to find clothes that didn’t hang off me.  Everybody wants to look at these things, whether it’s been 10 years or 70. 

Yes, I was a little self-conscious beforehand about being the only visually-impaired one there.  But, that's almost always the case and I'm finally coming to terms with it.  Besides, most of the others have to use reading glasses these days.  I guess that makes me a trendsetter.

I had a good time.  People walked up and spoke to me, so it didn’t matter that I couldn’t see across the room.  I said, “You actually remember me?” about a dozen times.  The usual response was, “Of course I do.”

When I said that to Ziva, followed by, “I was such a nobody,” she looked me in the eye and said, “Everybody is somebody.”  This from one of the cool, tall, pretty chicks back in high school who I didn’t really know back then.  I had approached her wanting to connect with a fellow writer.

The next thing I knew, I was having a great time with her, Jinger, and Lisa (more cool, pretty girls who were at the reunion) on Dickson Street.  I expected to see old friends that night, but never expected to make new ones of people I hadn’t known back then.

Since then, I’ve done a little revising on the history book in my head.  I already knew that sometime since 1982, I had become somebody.  It turns out you don’t have to be a standout to be somebody and more people notice you than you think.

Now I stand out without really trying and not for the reasons I would have chosen.  Now I’m somebody because of that.  But it turns out I was somebody all along.   

My L.A. Odyssey Part 7: Diagnosis and Time Warp

Friday, my parents and I get up before dawn and drive to Oklahoma City.  For the first time ever, I hope I’m having a rejection episode.  If that’s the case, I’ll be put in the hospital and given strong anti-rejection drugs that virtually take my immunity to zero.  But, my pancreas may start working again.  If it’s not rejection, it means the pancreas is just worn out.

We're at OU Med Center, where it all began in 1998 with a new kidney and pancreas.  I want to go back in time to when I was full of optimism, full of excitement and wonder about what my body was about to experience.

My battered veins don’t want to cooperate and it takes several tries before they can draw blood.  The result: it’s not rejection.  Aside from high blood sugar, all the other numbers are normal.  I'm diabetic again. 

Then I get more bad news.  I have t be cancer-free 2-5 years before I can list for another one.  That means I’m looking at another year or more before I can be put on the waiting list.  I will have to wait before I can wait.

Now I have my answer.  It’s a long, quiet drive back to my parents’ house.  Everyone is very tired.

That evening I was feeling restless and sat on the covered patio behind my parents’ house.  In the distance I heard cheering every few seconds and remembered Greenwood High School was holding graduation at the football field not far away.  I walked to the front and stood on the driveway, caught up in the swirling memories of the past couple of weeks and a graduation ceremony on that same football gield thirty years ago.  How can it be thirty years already?  But the past week made me feel every minute my age and then some.  The images of my high school graduation flicker by me, but none take form.

I’m a middle-aged man standing on a driveway listening to a man’s voice on a loudspeaker.  I can’t make out what he says but I can tell he’s reading names.  Applause and cheers follow each one.  A few lots behind me, little kids play in a yard.  They’re really little—much too young to imagine high school, much less have trouble remembering it. 

The hot breeze whips around my face and I am in a time warp.  In only a few days I’ve been drawn backwards from racing toward my future at an amazing conference in fast-paced L.A. to high school graduation in 1982.  I’ve just been diagnosed with diabetes again, like when I was twelve.  Except I’m not back there.  These are just pale watercolor shades of the past being brushed onto the modern version of me.

The task ahead of me is to blend the new ambitions, plans for the future, and a newfound self-confidence and identity with a disease I had through my teens, twenties, and early thirties—a disease that damaged me, a disease that I hated and felt I had conquered 14 years ago when I got the new pancreas.  It will be a struggle to keep from being sucked into the diabetc time machine pulling me back there.

My L.A. Odyssey Part II: Exactly Where God Wanted Me to Be

Thursday morning, the conference starts.  There are a whole lot of people.  I sit next to a spirited, outgoing woman in her 50s who is a bit of a mother hen to me.  In light of the huge crowd, extra drinking water at a distance, and speech at which the information comes at us, I accept her doting gladly. 

James is a dynamic speaker and right away, my brain is cooking, coming up with ways to implement his advice to my own situation.  I’m having ideas like never before.  Just as I suspected, a clearer picture of my future starts to gel.  Not only are all the parts taking shape, but I’m getting the sequence it should come together.  By the end of the first day, I feel like I’ve learned a week’s worth.

During the breaks, people spot my cane and offer to help me get around.  They’re interested in my life story and my plans for sharing it.  For the first time, I realize my visual limitations make me more interesting, not less so, like I believed for years.  Here and there, I get bits of advice, which breed even new ideas.  I’m totally in my element.  This was one of the most sublime times of my life.  Why?

Because I knew I was exactly where I was meant to be, doing exactly what I was put here to do.

Telling my story, telling the stories of others, giving hope, and really making a difference in the lives of thousands--it’s was God has chosen for me to do and when I’m doing it on a larger scale, the feeling is like nothing else I’ve ever experienced.

Finally, I was getting usable advice about how to market myself, how to think on a much larger scale than I have before.  It was an up-close look at a future that is both easier and more successful.

On the second day, Cuba Gooding Jr. speaks about having a mission.  It was a good talk but I’ve already had mine in mind for a while.  I donate 10 percent of the What Makes Us Stronger line to charities and organizations helping people recovery from a life crisis.

Later, Steadman Graham speaks on the importance of defining our unique self.  This resonates with me.  I’ve only recently come to terms with my extremely unique life and how I don’t fit into any category.  Not long before flying out to L.A. I realized there’s more freedom than isolation in that because I get to define what a middle-aged legally blind ex-diabetic writer with a kidney/pancreas transplant looks like.  Me.  I own it.  I define it.

At the conference, I have a light-hearted self-acceptance I haven’t felt since college.  The notion finally hits home that, even legally blind, middle-aged, with two transplanted organs to take care of, I can still have off-the-wall kind of fun I hadn't had since I was younger and I had better eyesight.  It turns out a long-lost side of myself was hiding at the LAX Westin.

Streadman Graham gives me plenty of things to write down.  This would be the high point of the Boot Camp.  How ironic that my sitiation would take a huge plunge.

Next: Seismic Jolt 

Why I Talk About It

This coming weekend, I’ll be competing in a speech competition.  I’ve given this particular speech twice already, with some refinement between the first and second time.  The topic: organ donation—from the viewpoint of someone who was lucky enough to receive one.

Actually, I received two.  Maybe I should have titled this post Why I Talk about Them.  But "it" is my personal experience of being a transplant recipient.

One of the main reasons I started writing my memoir was to raise awareness about diabetes, visual impairment, and organ donation in general and pancreas transplants in particular.  Most people still don’t know one can be transplanted.  Some of them are diabetics who could possibly benefit from one.

While reading a book about how to write a non-fiction book proposal for a publisher or agent, I ran across an interesting bit of advice for building a platform—that all-important built-in audience of potential buyers.  It suggested doing speaking engagements.  That made sense.  It went on to suggest joining Toastmasters to improve your speaking skills so you don’t fall flat on your face at those speaking engagements. 

An organization that could teach me how to be a more dynamic speaker?  That sounded like a good idea.  I joined and started getting comfortable talking about myself for a few minutes at a time in front of a room full of people.

It’s a surreal experience, standing up and speaking in front of a bunch of people with normal vision when you can’t see their faces clearly.  They say public speaking is one of the most common fears people have.  I don’t think they polled legally blind ex-diabetic organ recipient cancer survivors.  After all that, it doesn’t frighten me.  Few things do anymore.  But, like so many things I experience, it’s surreal. 

Fast forward a couple of years to last month, when I spoke about what it’s like to go from being diabetic and doing dialysis to suddenly being free from both.  Later, a few people commented that they were going to have the “talk” with their family to let them know they wanted to be a donor if something happened to them.

My first taste of success in this new realm. 

I had given other speeches about interesting or funny things I’ve experienced.  The one about being a legally blind substitute teacher got plenty of laughs.  The objective was vocal variety, which any substitute (or regular) teacher knows something about.

One speech objective was to use my body.  I talked about the day George H.W. Bush flew into our little airport in 1988 to campaign for president.  I worked at Drake Field at the time and ended up being the one to flag in the last plane before he landed—the one that would be parked closest to his.  It had to be just right.  Airport employees were allowed to be closer to where he was than the general public.  We also got to board Air Force II for a quick look while he was out campaigning.

Then I was ready for my speech about organ donation.  The objective was persuasion.  Not surprisingly, it’s a topic I feel very strongly about.  This was my chance to inspire and motivate.  It brought me full circle to when I first started writing my story.

It’s hard to describe the feeling of fulfilling your purpose in life.  It’s sort of a heady, tingly, warm sensation with a sense of powerful intuition—the kind you know in your gut.  It’s being swept up and carried aloft by it without having to struggle.

I already knew my story was meant to be told in writing.  Talking about it and putting some emotion in my words and voice is a different level of intensity.  This rounds out the picture.  It gives a face—a healthy one—to something still shrouded in mystery by most Americans. 

It will be a larger audience this weekend.  Some of them will be competing against me.  I’m going to do my best, but even if I don’t win the contest, I will have won anyway.