The Voiceless Minority

On April 6, 2025, the U.S. Autism Show occurred in Honolulu, Hawaii. Speakers Michelle Zeman (L) and Martin Slyngstad (R) are standing with Daniel Zimmerman (M) to show off the Proclamation that Slyngstad and Zimmerman received in honor of April being Autism Acceptance Month in Honolulu A couple of weeks ago, I shared that I would travel to Honolulu, Hawaii, to speak at the first U.S. Autism Show. Now that the event has wrapped, I wanted to reflect on the experience and share what that was like.   I was honored to be one of only eight presenters at this event. Standing at the podium and sharing my story was profoundly personal and empowering. It was a chance to speak openly about my journey – through diagnosis, therapy, professional growth, and advocacy – and connect with others through shared experiences.   If you couldn't attend the talk, I shared my journey through several key areas of my life. I started by talking about my experiences before receiving a diagnosis—what life...

Image description: Voting stations against a wall. On March 25th, President Trump issued an Executive Order (EO) titled "Preserving and Protecting the Integrity of American Elections." This EO proposes many changes to how our elections work, including voter eligibility, maintaining voter registration lists, vote-by-mail processes, which voting machines can be used, and who is responsible for managing elections. American Association of People with Disabilities (AAPD) is highly concerned that if any aspects of this EO go into effect, voters with disabilities and other marginalized communities will be disproportionately harmed. Already, disabled voters face increased challenges in accessing their right to vote because of policies and practices that make voting difficult. The policies in the Executive Order are voter suppression tactics – policies that make it harder for many Americans to vote. This order comes at a time when Congress is actively considering similar voter sup...

   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 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...

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 ...

 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...

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 ...

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: H...

  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...