The Voiceless Minority

  The emphasis on science and technology is more critical than ever before. The earlier children are exposed to science and technology, the more likely they are to develop a love for it later in life. However, in my experience, if you are a student with a disability, there is a lot less emphasis placed on these subjects. Late last year, the state of Pennsylvania joined an ongoing effort to bring students with and without disabilities together in a new way. Thanks to Andrew Fee, the vice president of strategic partnerships for Pennsylvania Special Olympics, students in Western PA not only got the chance to build cool robots but also worked together to create a robot with a student with a disability. According to an article published last September by Disability Scoop, which I will link at the bottom of this post, several counties in western Pennsylvania participated in a robotics program developed by Unified Robotics. The program partnered students in science and technology clas...

America is supposedly the land of opportunity. We toute ourselves as being the greatest country in the modern world, and for the most part, I am a proud American, and I tend to agree with this statement; however, did you know that even though we are just beginning 2025, it is still legal to pay people with disabilities less than the federal minimum wage of $7.25 an hour. Let me say that again: it is still legal in the greatest country in the world to pay a group of our citizens less than $7.25 an hour. How is this possible? The rest of this article attempts to answer that question and shed light on the problem of "sub-minimum wage." People with disabilities have been a part of American society from the beginning. However, in this author's opinion, we only began to be seen as human in the late twentieth century. In 1938, there was a provision written into the Fair Labor Standards Act that allowed employers who employed people with disabilities to pay them, and I'm not ...

 Did you know that for the 4th year, law firm Bolt Burdon Kemp announced that entries are being accepted for the Design the Change competition?   It’s true! The firm invites UK students to design a product that helps make the lives of people with spinal cord injuries easier. The winner will receive £5,000, and the runner-up will receive £2,500. Last year’s Design the Change competition winners included Tom Baker, who created a state-of-the-art wheelchair buggy to help parents with spinal cord injuries safely and efficiently transport their children.   I love that this is a competition. I genuinely appreciate the work that Bolt Burdon Kemp is doing to promote innovation and inclusivity. By encouraging young minds to think creatively about solutions for those with spinal cord injuries, they’re making a real difference in people’s lives and showing how important accessibility is in design. This type of initiative raises awareness and inspires a future generation of e...

The National Autistic Society has released a guide to help raise awareness about menopause for people with autism. The guide explains menopause, how it affects people, the latest research, and tips on managing symptoms. One part of menopause is called perimenopause, which happens before menopause begins. During perimenopause, hormone levels change, leading to symptoms like irregular periods, hot flashes, mood swings, and trouble sleeping. It’s important to know that both perimenopause and polycystic ovary syndrome (PCOS) can cause irregular periods, but they are different. Perimenopause is a natural part of aging and comes with symptoms like hot flashes and night sweats. PCOS, on the other hand, is a hormonal condition that can cause extra body hair, acne, and problems with weight or fertility, which you don’t usually see with perimenopause. Understanding these differences is important because it affects how each condition is treated. As a woman with autism, I found the guide v...

  Love on the Spectrum U.S. won two Emmy Awards for outstanding casting and directing of a reality program. The docuseries highlights the dating experiences of individuals with autism, offering a rare look at their unique journeys. While some participants, like Abbey and David, find love, others leave without success or experience relationships that don’t last. So why are we still talking about this two months after the Emmys? Because the challenges faced by people with autism in areas like dating are often misunderstood or ignored. Love on the Spectrum U.S. not only shares the personal stories of its participants but also helps foster empathy and understanding, giving viewers a chance to see the importance of representation and inclusivity in media. Does my own dating journey mirror the experiences shown in Love on the Spectrum U.S. ? Not exactly. I was introduced to the concept of dating in junior high, and at the time, I had a very narrow view: meet someone, fall in love...

This post comes with a note to readers. This may or may not make complete sense. This post comes from a perspective of being stuck in my head. As much as I use this blog to teach and inform, this time, I am using it as a therapy tool as well. When I ask you, the readers, a question, please know that I am questioning you and my own subconscious. Now that I have said all of that, here we go. Initially, I was going to write a post about a movie I recently saw called “Conclave.” On the surface, the film has nothing to do with disability or disability-related issues. Still, if one looks deeper, one can see that the movie is about both self-acceptance and being accepted by others. I will not go into the movie's plot because, like I said, this is not a film review. I only reference it because it got me thinking. For eleven years now, I’ve been an outspoken voice for The Voiceless Minority, of which I am a member. However, I wonder if I have been an adequate advocate for people with disabi...

  Imagine that you are a photographer covering a story. You aren't the story's subject - your only purpose is to zoom in, adjust the settings, and click the button. The subject(s) of the photo are the story - they know what to expect and how to respond given the situation. However, you're not in the picture as the photographer - you're just observing. You aren't asked to be in the photo, let alone be involved in the story, outside of clicking the button. You see the final image, and you publish it online, and when people see it, they comment on the people within the photo and the event that occurred. That is what life is like from my perspective of being on the Autism spectrum - I am on the outside looking into neurotypical life.   Growing up, I didn't have many friends. In elementary school, I went to a Christian school. You would be incorrect if you think a Christian school is different from a public school in terms of how friendships are created. There w...

 We are less than two weeks away from the 2024 presidential election. Both campaigns are making their final pushes for votes because they are aware that this election may come down to just a few thousand votes. However, there is one group of people that both former President Donald Trump and Vice President Kamala Harris have not paid much attention to people with disabilities.   In this instance, people with disabilities are without a voice. In an article written for Disability Scoop written by Michelle Diament earlier this month, she notes that there are      40,200,000. People with disabilities who are eligible to vote. She also pointed out that if people were counted based on disability, the number of eligible voters would outnumber the combined total number of eligible black and Hispanic voters. The article also points out that disability organizations have not received responses to their questionnaires. As noted in the article, Lisa Schur, th...

  This past September, an article was published in a disability magazine known as Disability Scoop. Michelle Diament wrote the article. It highlighted an incident where former President Trump equated having a mental disability to poor job performance. He did so when he attacked Kamala Harris and Joe Biden at back-to-back political rallies. I will attach the original article to the bottom of this piece. The rest of this piece will not discuss that particular incident but use it as a jumping-off point to analyze the former president and his behaviors as a whole. I am political, but I am nowhere near a politician. In my 38 years on this planet, I would like to think that I have seen quite a lot and know a little something about a lot of things and a lot about a few things. Unfortunately, having a disability in today’s world means you encounter a lot of misunderstanding, ignorance, and discrimination. A recent incident with former President Trump highlights an overall problem that st...

This post is from Jason's literary corner. It discusses a book I recently read about disability and what it means to have one. I hope you enjoy it.  Thank You, Alice: How Year of the Tiger Reignites a T-Rex's Passion   I recently finished the book “Year of the Tiger,” written by Alice Wong.  I thought I would be reading another disability memoir, but I was wrong. Alice’s book was not a memoir. It was what I like to call an anti-memoir. Her book made me rethink the direction that my advocacy is meant to take. The rest of this piece will highlight key concepts of the book that I believe will improve how I advocate for people with disabilities.  Finally, it will serve as my version of a thank you letter to Alice for her tremendous honesty and bluntness. Her book is divided into seven sections. Each section follows a theme and comprises several essays embodying that theme. For example, all the essays in Origins describe how Alice’s activism began. Two essays in this...

Times are crazy here at The Voiceless Minority. Over the last month and a half, we have had overwhelming support from both the disabled and the able-bodied community, and today, we continue that momentum.   Today is the beginning of a new era here at The Voiceless Minority. Today, we welcome our newest voice for the voiceless, Michelle Zeman. Michelle is an Autistic Board-Certified Behavior Analyst (BCBA) living in Winter Springs, FL. She discovered the value of self-advocacy and activism through her career in behavior analysis and her time in Partners in Policymaking (PIP). She's a 2023 PIP Graduate, a FL SAND Fellow, and an advisor to FL SAND's MAGICAL self-advocacy group serving greater Orlando. Michelle is passionate about policy change in behavioral health services and disability training for all community workers. Below is Michelle’s first contribution to the blog. The content has not been altered. It has only been edited for clarity purposes. Thank you for joining the te...

 The movie-going experience has been part of American life for decades now. At the same time, being disabled has also been a part of the human experience since the beginning of time. This piece will address the idea that although we are thirty-four years into the ADA era, movie theaters in Ocala, Florida, demonstrate how little respect people with disabilities have earned in thirty-four years. Over the weekend, I was treating my friend/caregiver, who I will call Jane, on a trip to the movies for her 24 th birthday. She was nice enough to not only drive my van for only the 10 th time since she started working with me but also because my power wheelchair broke several weeks ago and there was a delay in the delivery process of my new chair; she was willing to push me around. The first of many problems we encountered that day occurred when we got to the front door. It was only then we noticed that even though disabled people do go to places by themselves without caregivers or atten...

 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...

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...

  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 t...

  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...

Whether this blog goes “viral” or even gets read by anyone else is not why I am writing it. Usually, I write to inform or to educate and maybe I will do both with this piece as well, but this time I am writing out of disgust anger, and fear. If anyone asks, I am not shy about giving my opinion about something, and most of my opinions on almost every issue tend to gravitate towards the middle or the left of the political spectrum, but for this issue, I am sure I will piss off some of my regular allies when I say, “what the hell America?” There is a difference between being accepting of others and sanitizing language to erase History and an entire culture’s identity.  When I originally heard about the change of the name of the agency that runs the program that provides my support services from “the agency for persons with disabilities”, to “the agency for persons with unique abilities” I was angry just like many of my colleagues within the disability community are. That has not chang...

People with disabilities are often infantilized even by those closest to them.  I am 37 years old but sometimes I feel like I’m twelve. I am currently reading a book with my girlfriend Samantha who I affectionately refer to as my “little alien.” The book is entitled The Woman In Me by Britney Spears. Spears’ memoir talks about her early life as a performer and how much she enjoyed it but it also talks about the conservatorship she was under for thirteen years. During the conservatorship, every aspect of her life was controlled by others. My situation is not as severe as Ms. Spears's, but I can sort of relate to her on some level.  For those who are new readers of this blog, you may not know that I have a disability known as Cerebral Palsy or CP, or as I like to call it, T-Rex syndrome. I know some people in the disability community will read this and not like the self-deprecating language I use to describe how cerebral palsy affects me physically. Notice how I didn’t say how m...