Tag Archives: children

The Conversations We Need to Have

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Open and honest discussions of racism and prejudice matter. The cold, harsh reality in America today is that racism is alive and well. My Facebook newsfeed over the last few months has proven that fact to me and opened my eyes. Not so long ago, when America elected its first African-American president, I believed that our culture had made tremendous progress in overcoming racial discrimination, and in some ways we have. In 2008, I believed racism had been pushed to the fringes, populated only by lunatics and the truly backwards. However, ever since the protests and rioting over Michael Brown’s murder made national news, my eyes have been open to the fact that many, many people still harbor horrific racist views about minorities.

I have long believed that race is merely a mirage. I believed this long before DNA proved it right, and my reasoning was based on observation and experience. I’ve had the good fortune to have lived a rather diverse life among a myriad of people, and what I have learned from my interactions with people of numerous nationalities and religious backgrounds and cultural identities is that people are people no matter where you go. Some would offer you their last bowl of soup if you needed it; others wouldn’t share if their pantry was overflowing and you were dying of starvation before their very eyes; and still others would steal a life-saving meal right out of your hands. And like most everything, there are countless shades in between. The simple reality is you cannot tell who truly falls into which category until you witness their behavior in your moments of weakness.

In college, I discovered the writings of Frederick Douglass and Booker T. Washington and immediately felt a kinship for these former slaves, not because of racial identity but because of the obstacles of poverty that they had overcome. As I studied their works, I began to see that race and bigotry are social constructs used to divide us so that we the populace never learn to cooperate as a unit. Skin color is such an easy divider, and it becomes so easy to say I knew “those people” would behave that way, no matter that you can easily find examples of other skin tones doing the exact same things and no matter what the examples might be. When people, human beings, get upset over circumstances out of their control, a certain element take it upon themselves to destroy other people’s property, usually stuff that belongs to some innocent bystander. Whenever social order breaks down, there will always be an element, irrespective of skin tone, who capitalize on the opportunity to steal material objects. That’s human nature, regardless of “race.”

I always knew that I wanted to write works that would attempt to break down racist thinking, and though I thought progress had been made, I also believed that there was still work to be done to rectify the centuries of slavery and now century and a half of social and economic discrimination. I also knew that as a white man from the hills of East Tennessee, I would have an uphill battle to write about race relations in America. To counter this stereotype (and yes, I live under the yolk of an oppressive stereotype about hillbillies, and no, I’m not making an attempt to draw a comparative analysis of being more or less oppressed than anyone else because that’s counter-productive), I chose to use Fantasy Action-Adventure as my medium for discussing race and discrimination.

The main character in my series is bi-racial and struggles to find his identity between two disparate cultures. Each race carries misconceptions and prejudices about the others, and from those mistaken ideas much of the tension grows. However, through the course of the series, the central characters learn to see each other as individuals, not as part of a “them,” and through this process they learn to work together to defeat their common enemies, those who seek to oppress. I’ve not discussed this facet of the series very often because I had always hoped my audience would find it for themselves. However, as we encounter this new era of racial tension, it is more imperative than ever that we as a society discuss these issues and listen to each other.

So now, I’m going to be something of a capitalist and ask you to buy the first book in my series and share it with the young adults in your life (Because it is fantasy and there is some bloodshed, I do not recommend the series to anyone under ten years old). I’m making this appeal for two reasons. First, we need to have these open and honest discussions about the racial problems that still exist in this country, and I’m a firm believer that fiction can be an excellent bridge to discuss difficult topics. My second reason is that I need to sell more books to be able to afford treatment for this neurological condition that is crippling my body. So if you would like a good work of fiction that examines the racial divide we are facing today and would like to help out a person in need, you can do both by checking out The Brotherhood of Dwarves. As always, thank you for your support.

http://www.amazon.com/dp/B0076OCAKG

Update on My Status

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I just want to thank everyone who has helped out with the GoFundMe that Dave Mattingly started to help me while I deal with this neurological issue. The outpouring of love and generosity has been quite touching.

I got turned down for TennCare, mostly because the state of Tennessee, in its partisan nonsense to go against the president on every possible issue regardless of what that does to its citizens, decided not to accept the Medicaid expansion money. But that’s a different post for a different day. The end result is that in this state there is no safety net for someone like me, so I’m left without a confirmed diagnosis and without medical treatment. Because of that, I’m trying a few different alternative treatments for relief of my symptoms such as acupuncture and herbal supplements. So far, the acupuncture seems to have reduced the spasms somewhat. It’s not much, but at least it is a start.

I’m still not fully comfortable asking for help like this, but my current situation truly feels desperate. I don’t have my medical review for Social Security disability until December, and then who knows how long it will be before a decision is reached? In my current state, I can barely walk and cannot exert myself for more than a few minutes before I am completely exhausted. I’m also in serious pain every waking moment, which gets old. There are so many things I still need to accomplish, but I’m not even up to mowing my yard right now.

If you are able to donate to the GoFundMe, it would help me get through the next couple of months. My place currently has virtually no heat. The only thing I have that still works is one small electric heater that sits by my bed. My preference is to install a wood stove to keep the electric bill down, but it takes money to get everything I need for it. The ceiling also needs a lot more insulation before it gets much colder. A couple of friends have agreed to help me with the labor since I can’t do it myself, but the materials are beyond anything I can afford in my current circumstances. Also, I need money to continue with the acupuncture and to see a nutritionist who may be able to ease off some of the symptoms.

I’ve accepted that I will not get to have my kids for our regular time this winter because of my health and financial conditions, and everyone who knows me knows how much that hurts, but that’s my reality. For now, my goal is to focus on treating these symptoms until I feel well enough to work, and then getting back on my feet so I can see them either late spring or summer. No matter what, I will not give up fighting to get better because I still have too much to accomplish, like being an involved father until they are much older. If you are able to contribute, please help me through this difficult time.

http://www.gofundme.com/brotherhood

Late Night Update

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So, yeah, I haven’t posted an update in quite a while.

I guess the easiest way to do this is just to come out and say it: my neurological stuff is back with a vengeance. It started rather subtly about 9-10 months ago, and I honestly thought it was just the stress and strain of dual enrollment causing a few symptoms to flare up. I was already about 90% committed to resigning my position before the symptoms came back, and as I felt worse and worse, I knew I couldn’t physically handle the teaching load any longer. In the back of my mind, I kept telling myself that as soon as I got out of the stressful environment, I would feel better. All I needed was some time outdoors working in the sun. The semester ended officially on May 11, and for the first few days, I rested and relaxed but didn’t really feel any better. I’ve written before about how much I love working outdoors on the property, so I tried to dive back in and work myself back into football shape, as I like to say.

For the first few attempts, I noticed that my overall strength and endurance had declined quite precipitously, and I figured I had just gotten out of shape because of the harsh winter. I pushed myself a little harder but couldn’t get my body to cooperate. No matter what I did, I felt weak and fatigued, and the neurological symptoms continued to worsen. Also, I kept noticing that I couldn’t focus or concentrate on anything for more than a few minutes at a time. I’ve written five full novels and dozens of short stories; concentration has never been an issue for me before now. All through May and June, I kept telling myself that I just had to get back into good shape and I would start to feel “normal” again. Last summer, I had promised Finn I would build him a fort to play in this summer, so in June I tackled that project. This time last year, I built my home in seven weeks, working mostly alone all day every day. Even though I was tired, I didn’t feel broken down. Just putting together that simple child’s fort, which is in no way elaborate, I felt completely desolated, and my forearms hurt in a way they never have before. Then, at the end of June, I went to get the boys for our summer time. First, the trip to Jacksonville and back nearly wiped me out completely. I’ve made that trip several times, once in a single day. This time, it took me three, and I was absolutely spent when I got back here with the kids. Trying to play with them became more than I could manage. Still, I kept telling myself that I just needed to get back into shape.

My eye-opener came on Independence Day. When the boys are here, I like to do it up right: a big cookout, fireworks, and lots of shenanigans. It’s our thing. I spent seven straight hours that day setting up, grilling, lighting fireworks, and cleaning up after. When I got into bed that evening, I twitched and trembled worse than I ever had before. The next day, my arms and legs literally hurt from the trembling. I don’t mean I had muscle soreness. That’s something with which I’m quite familiar. This pain was something else, and it’s the first time the neurological stuff has been truly painful. That’s when I had to accept that my symptoms haven’t been from the stress of my job or that I was just out of shape. The neurological stuff is back, and this time it’s worse than before.

I saw a neurologist last week, and we’re waiting for authorization for a new MRI before we proceed. At this point, even though a lot of things are up in the air, I’m hopeful that we can find the right diagnosis and get me well. I’ll try to post updates on what we learn and what’s in store. As for now, please, send some positive energy my way.