Tuesday, September 25, 2012

Dear all the forces that be,

Dear God, Karma, and Universe,
I would just like to say "Thanks" for this opportunity to open up for me and advance so smoothly. It's like you saw my charitable donations, positivity, and heart and decided to open up my world. I've worked hard these past two years on myself in order to ready myself for this opportunity. I'm often asked how I stay positive, but the truth is, I work at it and I don't see any other choice of being. However, I would also like to thank you, God, for not labeling me as "negative" when I ran out of energy and could not put forth any positivity.  Thank you for rewarding me for working so hard to be a good person. I understand that as a person with a disability the trials I face are not  the worst ever, I realize that children suffer with illness, veterans suffer with injury, and many parts of the Earth struggle with Violence, yet you, God, understood that it was not perspective that I needed but change of circumstance to work to my optimal ability.
This is the beginning of great things.

Thursday, September 20, 2012

I can't sit still

I can't sit still
I'm ready, waiting to break free
I know I'll be missed
I need to do this
I will be more independent with assistance than ever before
Free of thinking "How will I do it?"
 Thinking "When?"
Not having to try so hard to live with passion
just living not waiting
 Becoming who I am supposed to be

Wednesday, September 5, 2012

For World CP day


On How I got Here
By Melissa Taylor

Ideally, every person would accept their challenges in life and find a way around these.  A strict schedule of grief and acceptance, including the how-to manual would be included in a kit, and everyone with challenges and disabilities would know that “Everyone feels like this!” and “Everyone has challenges!” and magically, everything would be ok.
      However, no typical chart exists. Or if one exists, I have never been on the chart. Although I  draw inspiration from article, persons I meet with challenges, and segments on television, nothing ever resonates  as away of being.
       Every person owns their journey in life with disability. Some may visualize it as a mountain, others deep valley, others still a swimming in a crashing ocean. A Segway, a walker, a wheelchair, or crutches may be used to transport him or herself through the terrain, and the representation of acceptance or success different for each individual. For some it may be walking independently, for others, adapted sports. Until about age 23, I was gung-ho about life; an avid student, I worked part time, and I fulfilled every commitment ever promised.  I never thought I’d feel “stoppable.” As I got older, I had less energy for positivity. I didn’t walk by myself as much, I’d endured a frustrating internship at an inner-city school, a successful internship at a school in town. My heart makes up for whatever I cannot do.  I realize now that I compensated with soul for not only cerebral palsy, but my organizational deficits caused by learning disabilities. This compensation takes energy, and  suddenly, my reserves depleted. Usually a go-to for positivity, happiness, and love for my students, fatigue paralyzed me. After deciding to end student teaching, I was lost. Ever since, well-meaning acquaintances have asked me “What do you want to do with your life?” I am  First, what I wanted in life was for people to stop asking me questions. I focused on getting a ride to work, and staying positive, which took energy. Finding my path in life required stamina not available to me. Trying harder with teaching proved impossible, and returning to school not feasible. These factors caused me to give up on myself, the saddest part of my journey. I stopped dreaming when discovering  neurological and personal aspects caused me to cross out opportunities, feeling infinitely disabled. All I thought of were impossibilities.  I’ve always known that my path to success would be defined differently than a non-disabled person. However, I refuse to have lower expectations for myself, as  I know myself best. With with the right job, self-support  is a reality. This right job will not appear as a position as a neurosurgeon,  a mathematician, but a job that holds passion and promise. Cashiering is respectable, but there’s a “happiness  ceiling”,; a limit to which I can be happy having other interests, expending much energy for little money, at a location I have been working since high school.  No longer can I look on the bright side to a job with no promise of professional growth. I never intended to be tethered indefinitely to the income limits of social security or the intellectual limits of cashiering. I came to the realization that as hard as it s that doctors and psychologists box me in with a label, it is even more disturbing when I box myself in with the labels assigned to me.

Sunday, September 2, 2012

Knowing

Knowing how much I have, how lucky I am, and how much I can do, it surprises me that I get down on myself still.  This knowledge does not render my life perfect or mean that I am always happy, even if (and here's the big part) I pressure myself to be.  The problem isn't that I'm a negative person, I'm just like everyone else. As much as having a disability, my number of siblings, and life experiences have shaped me, I am bound to get frustrated, because people do.  It may seem that I blow up over little things, in reality, I can keep it in control for a long time. I brush it off because I get that people are going to become impatient (being human and all). Usually it's the ninth time in the day, or even the week that someone said I was sitting down on the job, or that I look tired, or tries to get by my walker and I can't and I was doing something while the customer behind me wanted to get by and I lost concentration I can feel the need to let off steam. The steam I feel isn't even about the person asking me to move, or my not being able to move as quickly. It's because I need the walker at all, and I used to not use one at work. (although I seem to forget the fact of the painful feet and walking when I didn't have a seat readily available.)