The Voiceless Minority

 When this blog began 11 years ago, it was fueled by anger and restriction, but it has since morphed into a platform for disability advocacy. I started the voiceless minority because I was denied the opportunity to even attempt to teach because of some people’s short-sightedness and preconceived notions of people with disabilities. Even though that was almost another lifetime ago, the article I read on Thursday has me wondering if I let society cut me out of my dream. They say things happen for a reason, and I am not looking to go backward and redo my life, but the accomplishments of Ana Victoria Espino, a young lady in Mexico with Down Syndrome, make me wonder if I am really doing all I can to advocate for myself and others with disabilities. I will provide a short summary of the article in this post, but I recommend you click the link at the bottom and read the article about this outstanding young woman for yourself. Ana was born with Down syndrome. Down syndrome is caused by an

On Monday, we posted a blog highlighting - Wandercraft, a company with game-changing technology that will hopefully allow many people with disabilities to experience what it would be like to walk or stand on their feet. Since we received such an overwhelmingly positive response, I figured it would make sense to continue the discussion. “Bionic technology continues to evolve rapidly, offering new hope and improved quality of life for people with disabilities. Recent advancements have focused on enhancing sensory feedback, neural control, and the integration of artificial intelligence, making bionic devices more intuitive and functional than ever before.” The above quote is from Bionics for everyone’s official website. It is their mission to raise awareness of the latest bionic technologies for people who have become amputees or lost neurological function in one or more of their limbs. Today’s post will give a basic overview of Bionics and the possibilities that come with them. It wi

I have been in a wheelchair for the majority of my life. I even had one of those cool moms who would decorate my wheelchair and turn it into a rolling Halloween costume. So, in short, I have never known life outside of a wheelchair. Okay, so I may have fibbed a little bit. I used to use a walker and do the gimp shuffle around my elementary school, but for the most part, I have always sat on my ass. While I like the view from my chair, and my feet never hurt, I have always wondered what it would be like to move my feet like everyone else. Well, now there is a company that may one day allow me to experience what walking like a “normal” person is like. A company based in the United Kingdom known as Wandercraft has just received its second U.S. patent for an Exoskeleton that is completely hands-free and allows the user to move with the assistance of a trained companion. When I first learned about Atalante X, I was mindlessly scrolling on Facebook after posting an update on The Voiceless Mi

I am not a homebody. I love to get out and explore the world, but it is a disability. You must consider accessible travel, i.e., how you'll get where you're going and what it will look like when you get there, especially if traveling internationally. However, I recently came across a game-changer for traveling with a disability. Exceptional Vacations aims to “provide high-quality vacation opportunities for individuals with developmental disabilities and special needs.” They provide guided and custom trips for groups and individuals for a slightly higher price. I have linked their website at the bottom of this piece so that you can learn more about this great organization. According to Rebecca Hisamoto, the director of Exceptional Vacations, " Jill and Justin ultimately understood the mental health benefits of being able to travel but saw that there were not many opportunities out there for individuals with intellectual and developmental disabilities to travel independe

Okay, so anyone who has read these past few blogs I've written knows that my brain tends to explode every once in a while. Earlier this month, it was my inner theater kid, and now it is my inner advocate slash nerd. I was checking my email today when I came across Thursday’s Disability Florida Rights podcast (August 8, 2024). This podcast was a gift from the universe because it talked about something I have been dreaming of for a while. It discussed the organization called the Disabled Journalist Association. Cara Reedy founded this kickass organization. As she states in the podcast, she is a light-skinned African American woman and a little person. Throughout the podcast, it is clear that she doesn’t let her disability slow her down even though she says, “…being a dwarf does change the perception in people's head.” She outlines her reasons for starting the disabled journalist association throughout the interview. Ms. Reedy felt that there weren’t enough disabled journalists

  According to Webster's Dictionary, accessibility is easy to obtain or use or easily reached, entered, or used by people with disabilities. To me, this sounds like a bunch of words. What do they mean? I honestly don’t think anyone knows. I have not yet found anything that is " universally accessible.” This is because we are all different. That being said, I have an issue that this blog post will address.   When this blog started eleven years ago, I was twenty-seven. By then, you are supposed to be “maturing,” whatever that means. However, I believe that I am still maturing as I write today. I bring that up because back in 2013, I wrote a blog entitled “But They Said It Was Accessible,” which I have linked at the bottom of this article. The original post discussed accessibility in general and how I believed it wasn’t where it needed to be back then. The rest of the blog will discuss our improvements, if any, since 2013.   In my opinion, we still have much work to do.

  In modern society, whether you are four or forty or somewhere in between, chances are you know someone with a disability. I have been blogging about disability-related issues for over eleven years, and I am just beginning. I have always thought that the earlier and more often people are exposed to disability in some form or another, the better; finally, a TV network agrees.   Okay, I am technically a little late to the party since one season has already aired. Still, I’m excited that the streaming service formerly known as HBO Max, now just MAX, is bringing back a show called “Hop” designed to teach preschoolers about disabilities and differences.   The main character is a frog with only one leg. Along with its friends, Hop aims to teach preschoolers to embrace their own and others’ uniqueness. Recently, I wrote a blog about the need for disabilities to be prevalent in live theater, but this is even more crucial. Even though I don’t know much about the show, from what I have

  My inner theater kid is having a brain explosion. I just learned of a cool new theater project highlighting people on the Autism spectrum. I will link the article I read below and a video from South Florida news media highlighting an upcoming event the Autism Theater Project is putting together.   Before I get into my thoughts on how it is about time that theater and the arts regularly highlight persons with disabilities, let me tell you more about the Autism Theater Project (ATP). (See the links below for those who don’t want to read this blog part.)   The Autism Theater Project was started in 2020 by South Florida resident Gena Sims after a relative of a non-verbal student murdered the student she taught. To learn more about the project, you can visit their website at https://autismtheaterproject.org/   The work Ms. Sims is doing for the Autism community got me thinking: Why aren’t there more theater productions involving people with disabilities in the United States an

As we enter August, we also enter the height of the festival season, whether it be hard rock, country, or my girlfriend’s favorite EDM; if you look hard enough, you are bound to find a festival for whatever you are into somewhere. However, if you're disabled, it is that much more challenging. When you are disabled, you have many things to consider when planning an outing indoors or outdoors. I am not suggesting that disabled people should be homebodies; rather, this piece and the article from Enable Magazine in Scotland will provide ideas so that no matter what kind of disability you may have, you can live your best life regardless of your abilities or disabilities. Anyone who knows me knows I love music festivals. I attended one earlier this summer called ‘Rock the Country.’ You can learn more about ‘Rock the Country’ and plan accordingly for next year at the following website  https://www.rockthecountry.com/ . The information on the 2025 festival is not yet available, but the sit

In America, from an early age, we are conditioned to work and contribute to society; well, at least, most people are.  However, when you have a physical disability like Ms. Samantha Lebron does, you are often not expected to work full-time. Even though Ms. Lebron has a severe case of cerebral palsy and is confined to a wheelchair, she has decided to go against the grain and become a full-time worker. Throughout the rest of this article, we will highlight a recent interview I conducted with Ms. Lebron, in which she discussed what it is like to work full-time with a physical disability. We will gain insight into Ms. Lebron’s everyday routine, and she and I will discuss topics ranging from society's expectations of people with disabilities and her thoughts on whether she thinks it is worth the extraeffort she has to do to work full-time.   J: Hello, Ms. Lebron. Thank you for answering the questions on this important topic of disability and full-time employment. Samantha Lebron: Hello.

  Well, the voice of the voiceless is back. I have taken quite a long break, and during that break, I wondered if the voiceless minority still needed me or if it had learned to develop its voice. While I believe the voiceless minority has made gains on its own, it is clear that it still needs the guidance of its parent and its founder, as illustrated by a series of recent events. Recently, I learned of an individual who was wrongfully treated as if they did not have a brain just because they were in a wheelchair. The rest of this blog is an open letter/memo to my loyal readers and anyone who might stumble across this blog. I hope it serves as a reminder or a sharp kick in the ass to remind people that you can't judge a book by its cover or a person by what you see when you first meet them. I was initially appalled while watching what happened to this individual, but I was not surprised when I thought about it later. Even though it is 2024, and we should be more civilized than w