The Voiceless Minority

 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...

  Luke Jackson (pictured above) has been working with Disability Advice and Welfare Network (DAWN) and Suffolk Law Centre on the Autism Education Leavers Passport. On October 14 th , lawmakers in Canada approved an educational passport, thanks to a University of Winchester graduate. The passport is geared toward helping young neurodivergent people transition from education to work. The 25-year-old, who graduated with a degree in Computer Aided Design in 2023, contributed to the content and design of the 35-page booklet. Luke drew from his experiences as a job seeker and the skills he learned at university. “I enjoyed what I learned at Winchester and the one-to-one tutoring I received,” said Luke, a volunteer with DAWN, where he is a website administrator. The booklet comes in response to the findings from the Office of National Statistics, which showed that almost 80% of autistic adults are not working and that they are the least likely disabled group to be in any employ...

 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...

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 t...

  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, fr...

  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 t...

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...