The Voiceless Minority

   I hope you are having a satisfying Saturday. Although we have made great strides, significant work remains to be done. Yesterday, I posted a blog about Patrice: The Movie . If you haven’t had the chance to read it yet, be sure to click the link at the bottom of this post. On the surface, one may think the movie is just about one disabled couple’s journey to get married, but it is about much more than that. While telling the story of Patrice and Gary, it also highlights the transportation crisis that disabled people face. For most people who have a disability, the inability to access affordable and reliable transportation is a barrier they have to overcome daily. I am lucky to have a support system that can provide me with my vehicle. While I do have to keep up with regular maintenance, I am very lucky because I didn’t have to buy it myself. I am eternally grateful to my parents for their generosity, but I also know what it is like to rely on the paratransit system becau...

Above is an image of a logo from a movie titled Patrice: The Movie. It is yellow and in large print.  Happy, fabulous Friday. Before I get into today’s post, I want to thank everyone for their support and amplification of my articles and the entire Voiceless Minority community recently. Your support and encouragement inspires me and all the other writers who have helped amplify the voice of the voiceless. Several years ago, I wrote a blog, which I will link at the end of this article. It is entitled I Can Write, But It Is Time for You to React. I am happy to report you have taken up that call to action in more ways than I could have imagined, and I am eternally grateful for your support. Okay, enough with inflating your head as you are reading this. Now, down to the fun stuff. Last September, Patrice: The Movie premiered at the Toronto Film Festival. Shortly after, in October, it premiered on HULU. I will link an article written by Amy Kuperinsky for Disability Scoop that outlin...

Above is an image of President Trump signing a bill into law. He is wearing a black suit with a red necktie and is surrounded by people on either side. His pen is poised over legislation, which is on a wooden desk.  What a worrisome Wednesday it is for the disability community. Steps are being taken to erase the work of great disability champions such as Judy Heumann and Ed Roberts, to name a few. As a relative of mine put it a couple of days ago, laws are made, then they are repealed, so advocates must never stop fighting. Although my relative and I sometimes disagree politically, I could not agree more with her words. Indeed, it looks like it is happening yet again. This past January, Donald Trump became the 47 th President of the United States after a four-year hiatus between his first and second term. While I am registered as a Republican, and I agree with most of his platform, I question what he's doing regarding the voiceless minority. Before his election, he stated that h...

Above is a black and white photo of the 504 sit-in from 1977.  Okay, so maybe I’m late to the party. Still, I was recently made aware of a disturbing lawsuit taking place that will effectively erase the strides we have made as disabled people in America over the last several decades. The lawsuit that is slowly gaining traction, Texas vs. Becerra, is an attempt by 17 states to overturn the Rehabilitation Act of 1973 protections for people with disabilities, explicitly aiming to overturn the 504 provision. I will list the 17 states that I believe are harming not only the disability community in America but America as a whole. However, before I do so, I will highlight that my home state of Florida is one of the offenders. The lawsuit is an attempt to not make America great again by using a slogan from our newly elected President. Still, in my opinion, instead, it is an attempt to return to the dark ages of disability in America. Alaska, Alabama, Arkansas, Florida, Georgia, Indiana...

  Image of Against Technoableism: Rethinking Who Needs Improvement, By: Ashley Shew Standing Up On Bookshelf. The Voiceless Minority has gained tremendous traction over the last several months, and it will always be my primary outlet for my advocacy work. We have grown tremendously and had the opportunity to incorporate guest writers, including a permanent contributor, Michelle Zeman. We have also been given an excellent opportunity to present at the largest Disability Expo in the nation this upcoming June. The Expo is known as The Family Café, and we are honored to have the chance to be among some great self-advocates and allies over the three-day event. While all that is something to be celebrated, this blog will discuss my next advocacy adventure and a book that I have recently read. I finished my fellowship with Florida Sands late last year and was unsure what to do next. Luckily, the universe presented my next opportunity rather quickly. I was selected as a 2025 IEEE Spectru...

  In March 2024, the University of Illinois-Chicago opened an inclusive dental clinic designed specifically for people with disabilities. This facility features a desensitization room for patients experiencing anxiety, specialized equipment that allows individuals with physical disabilities to receive care without leaving their wheelchairs, and wider hallways to ensure safe and accessible movement throughout the clinic. Currently, the clinic serves up to 28 patients per day, with future plans to introduce virtual visits for those unable to travel in person. It’s encouraging to see a dental practice committed to creating a safe and accommodating space for people with disabilities. Unfortunately, such inclusive clinics remain rare. Personally, I’ve always disliked going to the dentist—the loud noises, bright lights, needles, and overall invasiveness of the experience make it something I avoid whenever possible. While I can tolerate a visit when necessary, I can’t help but wonder ...

                                              Above is a photo of Marissa Bode from Getty Images Anyone who follows this blog or knows me knows I love theater and film. I even went so far as to get a degree in drama at college. While I love “straight plays,” which are plays without musical numbers, I am obsessed with musicals. I love all the standard ones such as “Rent,” “Avenue Q,” and “Les Mis.” However, I only knew part of the story because I listened to the soundtrack.  That changed this past November when Wicked, the motion picture, hit theaters. I went to see the movie with my girlfriend, Samantha LeBron, who is not as big a musical fan as I am. Because I didn’t know the story well, I was unaware that a character was in a wheelchair. Universe, please forgive me for being late to the party. The movie was great, and the character in a wheelchair was portrayed extr...

  We are one week away from Donald Trump retaking the presidency once again after an overwhelming victory last November. Disability advocates and allies have some concerns regarding a Donald Trump presidency. This article will build on an article published by Disability Scoop late last year. By the end of it, you, the reader, will be more aware of crucial programs like Medicaid and how they affect persons with disabilities. Along with a Trump presidency, the Republicans will maintain a slim majority in both chambers of Congress. This will enable them to reshape public policy and, indeed, policies that affect people with disabilities for years to come. Nothing is known for sure, but it is rumored that the Trump administration aims to cut funding to vital programs such as Medicaid and others. I can understand wanting to provide tax cuts and tax reforms that were promised during his campaign; however, even though I am a supporter of President Trump, in this case, I think he is treat...

 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...

  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...

  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...