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 As a relative of mine put it a couple of days ago, laws are made, then they are repealed, so advocates must never stop fighting.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...

  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 ...

  My name is Gizelle Koontz, and I am a woman in my fifties currently residing in Belleview, Florida, a small town outside of Ocala. I was born in Canada and moved to Florida as a child. I graduated high school in Florida and eventually became an American citizen. I have worked in healthcare for a few decades, mainly as a Phlebotomist and Laboratory Technician. However, I have also worked as a Medical Assistant and have had employment outside of the medical field, such as working for the post office as a mail carrier. I am currently studying medical billing and coding and working in home healthcare, which is how I met my current client (and friend) Jason, for whom I am honored to write this article. Many of Jason’s blogs discuss the physical side of disability; however, this piece will discuss a hidden disability. I am an individual who has struggled with depression and anxiety for as long as I can remember. When I first started experiencing depression, I was a teenager. Needless t...

                                              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...

  Today, we welcome a new guest writer to The Voiceless Minority community. Thank you for joining the fight, Sally. Sally  Ouimet  Waters , MA CCC-SLP, received her undergraduate and graduate degrees from the University of Florida. She completed her Clinical Fellowship at the Malcom Randall VA Hospital in Gainesville and has over ten years of clinical experience in the Ocala area, specializing in adult dysphagia and neurogenic cognitive-communication disorders.  Sally  utilizes current evidenced-based practice to inform her treatment programs for individuals who have experienced CVA, Traumatic Brain Injury, Voice Disorders, Parkinson’s Disease, and ALS to improve communication and swallow function according to the patient’s objectives.  She specializes in the evaluation and treatment of individuals who have experienced Head and Neck Cancer, including those with tracheostomy, laryngectomy, and post-radiation dysphagia. She advocates for the oncology team t...

  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...

  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...