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Wednesday, November 22, 2017

Live Outside The Box


Hello once again fine people,

I hope everybody studied their Pantera lyrics, along with the subject matter of the last article because there will be a test! Haha.

For this quarter’s article, I have chosen to strategically dismember the stereotype of what you shouldn’t, and should be, or what you’re supposed to do with your life, if you have a medical diagnosis such as cerebral palsy, or anything else. That’s why this quarter’s musical stylings are Alice in Chains’ “Man in the Box.” It’s the ultimate song about censorship, especially for people like me, who aren’t allowed to be who they are, without hearing the phrase, “Don’t you know you have, (insert your medical diagnosis here), and how are you going to do that?” at every turn.

Yes I know I have it, but I don’t care like I said in the first article. I’ve learned to make it work, make the best of what I have, and adapt so that I can be as productive of a member of society as everybody else, even though I may go about it in a different way physically. I use the internet to compensate a lot for not being able to walk under my own power, but I can with assistance. That’s how I submit my creative material to various places, and people. I love it when people question if I’m depressed because I’m thinking, when do I have time to be depressed, especially for those of you that have read my previous articles? On top of that I have to keep up with the daily grind that is football. Hehe. While other people see just looking at the computer all day, my body and brain feel like I’ve worked 12- hour days per week for seven days a week.

I’m here to tell you that I’ve been living outside the box my whole life, and I am unapologetically proud of it. I don’t do things because other people expect them of me, and I don’t do things because that’s what society told me I should be, and furthermore, I certainly don’t do things that I’m not 100% comfortable with. I study the subjects I want, listen to the music I like, and attempt to date the women I like, even though they are perceived to be out of my league etc. It all comes down to one thing. I’m only interested in being the first Brad Freeman at all times. I’m not able to explain it. It’s just my natural personality, and part of my uniqueness.

Life is too short. You can’t be afraid to make your mark on the world when the opportunity arises by being the most authentic version of yourself that you can be. You can’t live your life in fear of what other people think. You have to live it for you. You can’t be what others want you to be, and when they want you to be it. The only person you have to worry about pleasing ultimately, when you go to bed at night, is yourself. When teachers, parents, friends, random people, and even significant others that you’re in romantic relationships with doubt you, and tell you, “you can’t, you won’t, and you’re never going to, and you’re taking too long for my lack of patience, so just quit!” You have to be stubborn enough to believe in yourself, your ability, and what you’re doing with your life to the point where nothing, and no one once so ever will stop you. In the face of everything, you have to feel like everything you do, and everything you are as a person, is undoubtedly going to be a success. In other words, achieve greatness and become the very personification of excellence from the moment you roll out of bed in the morning until you lay your head down on the pillow at night! It can’t just merely be a state of mind. It has to be a way of life. This is how you become a winner at life!

Whatever your goals are in life, NEVER, and I mean NEVER EVER give up your hopes and dreams because others told you to, especially those who are perceived to have authority, and power over what you do because they feel that whatever you have medically, makes you less of a person in their eyes. Don’t ever be embarrassed, or ashamed for being your own unique individual. There’s only one version of you. Stop worrying about being someone else, and be the first version of you.

I really do speak from personal experience. I’ve heard it all. It started when I was a child. He can’t go to regular public school. He has to go to a specialty school for other kids with “disabilities”. Then as a teenager, he wants to go to college? No, he needs to go to a group home because he won’t study what we want him to. When I couldn’t be swayed, these authority figures called my mom.  My mom responded, “I don’t tell Bradley what to do, say, think, or feel. Have you ever heard the boy talk?” I’ve heard similar things during college, and after college. Whenever people in power or authority can’t get me to change my mind, they accuse me of not having a mind of my own, and not being aware enough to know what is best for me. Only they seem to know what’s best for me, even though I live it every day. To this day, mom and I have no idea why people do that. I realize that they are taught a one size fits all application of people with “disabilities,” and as many of you have come to figure out, Brad Freeman isn’t the stereotype. I don’t want to make it sound like all people of importance are like that. The people out there reading this must learn that we’re individuals, just like they are. We all don’t meet the clinical definition of “disability.” I assure you. Look at me as your proof.

So in closing, let me ask everybody this. Why is it that when you have some sort of medical diagnosis such as cerebral palsy, why do certain people, think they know better than you what’s best for you, and then try to put you in a box of what you’re supposed to be, like you need to be saved from yourself? In my case, with my cerebral palsy, it all depends on the level of severity. The palsy, or paralysis, was brought on by a lack of oxygen, which caused my brain to be underdeveloped along the cerebral cortex. Some of us are able to walk, and talk, while some of us are not able to walk, and/or talk. Some of us are able to write, such as myself, but others are not. As it applies to me, I’m able to handwrite, and type, but it takes me a long time physically, and becomes tiring like working out. This is why I use voice-activated software to compensate. I speak and think faster than I write obviously.

I’ve always found the box to be quite limiting personally. Live outside the box because I don’t know if you realize this, but you don’t have to be in the mold that everybody else lives by, instead you should always try to be the person that broke the mold, when you were born.

I’ve been breaking the mold since the day I was born. If I did it, why can’t you?

Friday, July 7, 2017

The New Denial


Hello fine people,

Like a Ric Flair wrestling promo, get ready for a ride. WOOOOOO! I also encourage everyone to listen to Pantera's "Walk", while reading this because it fits my natural personality, and that's why this article has a rhythm to it.

It's once again time for me, Brad Freeman, to break some stereotypes. This time I would like to discuss how in this day and age, being the non-stereotype is apparently the new denial. That's right. If you can believe it, being ultra positive, and not ate up about the fact you have cerebral palsy throughout your lifetime, is seen as a negative by A LOT OF PEOPLE!

I've had millions of friends of every color, creed, religion, sexual orientation, and gender. For all those millions of friends, I've had a gazillion more people of all backgrounds, tell me I was in denial throughout elementary school, middle school, high school, college, and even though it's hard to believe, post college. Others have wondered why I don't join Facebook groups as well. It's for the same reason. Unfortunately, there are people of all shapes, sizes, and colors with "disabilities" that feed in to the woe is me classic stereotype of a person with a "disability." The people they grew up with also foster that behavior. The people that think this way usually feel like everyone with a "disability" thinks this way, and somehow because I don't, there is something wrong with me. They're the types you see in the movies, and on TV. You know, I'm just a poor mentally deficient, and physically incapable, failure of a person, who can't do anything. So let me numb myself because I don't like myself, and don't think much of myself. And if I don't think much of myself, others probably don't either. The other thing I find disheartening, and insulting in movies/TV is when a character does have something such as cerebral palsy, they are either overly sensitive, or they are killed off when they find some form of normalcy, or success, so to speak. Supposedly these film directors, and producers are supposed to be more sensitive, and inclusive, but they only perpetuate negative stereotypes unfortunately. That's why I write my own stuff, so that I can act in it, and dismantle these offensive and just utterly wrong portrayals. How's it going to help me to be stereotypically ate up about my cerebral palsy? Isn't that just going to make people feel more sorry for us, than they already do? How will that help us, and me personally, when trying to strategically dismember these bogus perceptions? It won't. It will just continue to perpetuate them.

On that same hand, the fact that I take issue with the words, "disability", and/or "disabled" usually rubs people the wrong way also. It's the politically correct term I know, but as someone who studies history on a regular basis, people who live inside the lines don't make history! They're just doomed to repeat it. I don't use any form of that word because it makes it sound like we're defective pieces of equipment, and have no value at all, like I said in the previous article. Don't you want history to remember you for hundreds, and thousands of years, and speak of your great deeds for generations to come, instead of being remembered for feeling sorry for yourself? I know I do. I feel like I've been destined for greatness from a very young age. What are you destined for? Feeling sorry for yourself is going backwards in life, when you should be thinking of ways to move the world forward, and benefiting society light years from now.

So with that, I leave it up to those reading this to decide. Will you just wallow in mediocrity, or will you dare to be great? No one can make up your mind for you. I'll leave that decision up to you. But as a person who speaks from experience, the stereotype is kind of insulting. Be much more. Being a rebel isn't always easy, but it's way more fun, and satisfying!

RE-SPECT! WALK! You talking to me!? :)

Friday, April 7, 2017

I Am The Non-Stereotype


Hello everyone. My name is Brad Freeman. I'm 32 years old. I graduated from Park Hill South high school in May 2003. I'm sending this mass email out to let everybody know that I've been busy doing stuff since I graduated college in May 2009.

Since I was about 10 years old, I've had 4 to 5 career paths planned out for myself. 1. Entertainment career (actor/writer/musician/artist) since about 10 years old. 2. Football coach since about six years old. 3. Martial arts historian since 11. President of the United States since 18, and just recently I've been told I should become a motivational speaker. Although, every time I do a speaking presentation for a family member at their schools', I'm told I should be a motivational speaker.

Not trying to make anybody feel inferior by any means, but as a lot of you know by being around me at some point, or will come to learn, if you're ever around me. I expect and demand a lot of myself. My own expectation bar is always set much higher than everybody else's. I would have sent this stuff out sooner, but being that my Cerebral Palsy causes things to go a little slower than most; I wanted to make sure my work was good, and not just mediocre.

I'm sending out the first seven theater stage plays of my creative portfolio. They have been copy written already. I finished number eight, but it needs to be edited and copy written, and then I will submit it to the Dramatist Guild of America. After that I will send it to everyone. I have four other plays that are half way done. I have artwork that goes with a couple of the plays, as well as clothing, but clothing falls under the patent and trademark office, and their fees are much steeper than the copyright office, so everyone is going to have to wait on those. Sorry.

On the football front, I went to my first football clinic February 3rd through the 5th. It was in Kansas City. For those of you that aren't aware, it's basically like football school. I've been self-taught for 26 years. I made great contacts with a few coaches, including the Assistant Linebackers’ Coach of the Kansas City Chiefs. If you doubt my football knowledge, I can send you the hundreds of pages of research I have.

As far as the historian and motivational speaker pursuits, I'm just now really looking into those more closely. I speak history like I lived it. I'm such the history whiz that I know the different names that different cultures called certain modern places, and which language a modern country speaks by which country either founded/colonized it. As of right now, I have a large list of famous books from history broken down by country and time period from all around the world. I plan to read those at some point in time. As far as the speaker part, I guess I'm starting that right now with this.

As far as the POTUS, I can't run until at least 35 years old. I have my general stances written out, but I have to research them more thoroughly and I'll get back to you. Plus, I'm not going to tell everyone what they are because 1. I don't want to get blackballed by half of you, who may not agree with me. 2. While I know generally what I believe, I need to be able to articulate certain stances better. 3. I don't want anyone stealing my ideas to improve the country. Haha.

So with that, anyone reading this can clearly see I've just been sitting around twiddling my thumbs. Hehe. No. In all seriousness, if any parents or kids with a "disability" are reading this, know that just because you have a "disability" doesn't mean your life is over. I'm picture proof. And just so everyone understands, I'm not in denial. I know I have it. I just don't care. Therefore, I don't like to use the word "disability" because it makes it sound like we are defective pieces of equipment that can't do anything, and have no value. And again, I'm the non-stereotype, and proud of it! My Cerebral Palsy is part of my uniqueness.