The Voiceless Minority

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...