I usually write these anniversary posts on the actual anniversary of the first post on this page.(August 4th, 2013). I missed that for whatever reason.I can quite remember what I was doing on that day, but it is what it is. You know what they say, better late than never, right? I still find it difficult at times to believe that I have been maintaining this blog for five years. This blog admittedly was a cop out from writing a book my mother had been nagging me to write for years. I convinced myself that if I kept up with this blog, then I wouldn’t have to write a book. The funny thing about this life is, God has a way of really pushing us toward his will through others. People would be so impressed with the quality of writing on this blog that they would throw the book idea around. Everywhere I went, people would suggest that I write a book. My mother would also continue to nag me, time and time again. It wasn’t until last year that I would finally cave, and start going to town. I’m almost 200 pages in, so you can expect quite the epic. Continue reading
No, I’m afraid this blog post isn’t about President “Not Everybody’s President” Donald “Mine is Bigger” Trump. I don’t care to waste a blog post ranting about this guy at the moment, so instead we’re going to talk about something else that is probably more relevant to my life as well as the lives of others on the spectrum. Executive functions are a subject we as humans don’t broach, because often times a neurotypical never has to worry about this; They work without you having to do much about it. The executive functions are a set of processes that all have to do with managing oneself and one’s resources in order to achieve a goal. It is an umbrella term for the neurologically-based skills involving mental control and self-regulation. To break it down, executive functions fall into several key categories, Continue reading
I had dreams of fucking an R&B bitch!
Okay good I got your attention. Welcome back to one of few reliable sources for all things Autism and, life in general. Today we’re gonna broach a subject that I don’t talk about much. Show of hands, how many of you like to daydream? Everyone? I thought so. Those who know me well know that I am a chronic daydreamer and no, none of those day dreams consist of fucking R&B bitches; Biggie dreams of fucking R&B bitches. My daydreams always depended on my mood and, what was going on in my life. Growing up, I daydreamed as much as I breathed. In school I wasn’t challenged as much as I should, especially in math. Math was super easy for me so, It was very hard to keep my attention. When something didn’t interest me, I’d often retreat into my head and start to dwell on what preoccupied my mind. Most of the time it was what ever video game I was playing at the time. I would constantly think about a solution to a dungeon I was stuck in or, plan on how I was going to beat a tough boss. Other times, I would be thinking about ideas I had for video games I wanted to create. I would conceptualize characters, worlds and, music. It was always a great escape, nothing could stop me, not even the,
“Flemmings!!!!!!!!!! ARE YOU DAY DREAMING AGAIN?” my fourth grade teacher would yell. Continue reading
Hello world! It’s been a while since I’ve been on here. Life has been pretty hectic but, those events are for another blog. Today I will be touching on something I realize I’ve never really talked about on here much to my surprise. Tonight were gonna talk about the dreaded three letter acronym, an acronym that strikes fear in parents of children with special needs yearly or however many times a year you have to deal with it. Parents who read this blog already know what rabbit hole we’re gonna jump in today or, you’re probably impatient and jumped to the second paragraph of this blog post. Gosh people, y’all gotta rush through shit and not take time to appreciate it. You’re the type of people who skimmed through books in English class and didn’t take time to take in the symbolism. Then again, I also skimmed through books and didn’t take the time to take in the symbolism which I’m pretty sure our English teachers made up because let’s be real, I don’t think that bowl full of fruit or those blue curtains were ever meant to serve any other purpose except to exist in the scenery. You have to wonder if English teachers did that shit intentionally to justify making homework assignments, quizzes and, essays for a book in the first place. Anyways, before I get carried away let’s just get on with it shall we? You have to wonder if these first paragraphs are as unwarranted as the small talk nurses make when they’re about to stick you with some needle or other sharp medical instrument. Like, we already know you’re gonna inflict some form of pain on me for the longest 2-3 seconds of my life so can we just get on with this shit already. Without further adieu, let’s just get on with this shit shall we? Continue reading
So two weeks ago I had the chance to watch Finding Dory and, once again Pixar has delivered another masterpiece and most importantly, something blog worthy. So without spoiling anything, Finding Dory center’s around Nemo’s friend Dory who is very scatter brained and is notorious for short term memory issues. The movie takes a look back at her childhood and how she got separated from her family in the first place. A series of events causes Dory to remember her family thus begins yet another journey that makes for an epic Pixar film. Their adventure brings them to an aquarium that specializes in rehabilitating injured aquatic animals. Now, where the film truly succeeds is how it tackles living with a disability. A lot of this movie’s important characters including Dory all have some sort of disability that has an adverse affect on how they live their lives. From a visually impaired whale shark named Destiny to a Dolphin named Bailey who is unable to use his echo location abilities, a cognitively impaired loon named Becky and of course Dory, this film stresses not only how people live and function in this world with disabilities but, it also explores the topic of ableism which can be a huge problem for those of us with disabilities. Continue reading
Another year, another dollar. Gosh is this blog really two years old? It feels like yesterday when I decided to start spilling my feelings and opinions on all things Autism on the internet. It’s been a pretty crazy year of blogging and antics. From dragging Autism Speak’s name through the mud to dragging the names of really shitty parents of children on the spectrum through the mud to voicing my opinion on all things Autism, this year has been a thriller. I’m thankful to have so many loyal readers, a decent amount of which live across the pond. I never thought this blog would get all of the positive buzz that’s been getting over these years and for that I am truly thankful. It’s people like you that give me the energy to continue writing. Get ready, because this coming year will be huge as far as this blog goes. Now I had a long synopsis of these two years planned for this post but I just couldn’t come up with anything so I will leave you with a picture since those things are apparently worth a 1000 words.
Stay classy folks
Okay, there’s been a hot button topic within the Autism community that I have yet to discuss but lately has gotten pretty heated on some forums so I feel I need to offer some of my insight on the issue. Within the community there seems to be a stigma around “self diagnosis” which is exactly what it implies, it’s someone diagnosing themselves as being on the spectrum without any medical proof or evaluation from a psychologist. Now you may remember back in the fall of last year when Jerry Seinfeld stated in an interview that he may be Autistic. Within moments of that interview there was a shitstorm of backlash from parents of children on the spectrum who saw this as simply a publicity stunt. To them it was nothing more than a celebrity attempting to capitalize on a struggle that affects many families. Their worse fear was that their struggle would be overshadowed by a celebrity who doesn’t look like they should ever be the face of Autism. Now while I feel for the families with children on the spectrum and those on the spectrum who feel that people are hopping on the bandwagon because they think it’s cool or hip, there’s something you need to understand about the world’s perception of Autism. Continue reading