The Voiceless Minority

    I have been giving a voice to the “Voiceless Minority” for over 12 years. I have been blessed by both my loyal readers and by my amazing colleagues and friends. I have been able to use this platform not only to document my advocacy journey, but I have also been able to highlight fellow disability champions. Today, I would like to highlight 1 of those fellow champions. Gordon Hartman of Texas is a former home builder in San Antonio, Texas, who has a daughter with multiple disabilities. In 2010, he founded Morgan’s Wonderland, the first fully inclusive amusement park in the United States. I hope to visit the park sometime next year, not just as a journalist, but as a fellow member of the Voiceless Minority. The park is only one part of Morgan Enterprises. Since it opened in 2010, the organization has added a camp and other offerings. You may be asking yourself, Why is this news in 2025? The answer is quite simple. The next chapter in Morgan Enterprises is here. Morgan’s Hote...

  Happy Monday, everyone. We hope you enjoyed our post from Friday. Today, we will discuss a rather disturbing trend. Last October, Disability Sco T op published an article entitled How School Shooting Fears Led to A 10-Year-old Boy with Autism Being Handcuffed. Due to the publication's limited number of free views per month, I will summarize the article below before I comment on the issues it raises. In 2023, after saying to a teacher that he should bring a gun to school so that kids would listen to him, it would come out later that the student wasn't referring to using a firearm in the typical way. Instead, he wanted to ride it like a horse so that kids could laugh with him. While this does not make sense to most people, we must understand that people with Autism have a different way of thinking about things sometimes, and they may not understand the impact of their words. Especially given the context in which they say certain things. America has always been on edge, and righ...

  The picture above shows a little boy being examined by a doctor. The boy is pale and wears a striped shirt, blue shorts, and socks. The clinician is shown talking to the little boy.  In a world where artificial intelligence is more prevalent now than ever, it is crucial to understand the technology and its possible impact on the disability community. Most of us are familiar with applications such as Chat GPT. Chat GPT allows a user to provide a prompt and then has artificial intelligence write a document based on the prompt for those unfamiliar. Numerous other applications are similar to Chat GPT, and AI is slowly taking over the world. Soon, we will live in the Matrix, but not all AI will necessarily be bad. In an article published by Disability Scoop last August, which I will link below, a new and exciting use for AI was discussed. Researchers at the Karolinska Institute in Sweden have developed an app that has the potential to diagnose Autism early in childhood. The model...

Happy Taco Tuesday everyone! Thank you for the continued support you have shown over the past few weeks. Today will be the third in a series about parenting with a disability. I did not intend for this topic to be a series of blogs but the topic keeps finding relevance in my life and I hope to continue to impact others as well.  I began writing about parenting with a disability a decade ago. The first blog was entitled "Who Says We Can't Have A Family".  Who Says We Can't Have A Family   Two years later I wrote a second blog entitled “Parenthood & Me”.  Parenthood & Me   If you read both blogs, you may be a little confused. I sound like a rolling contradiction (: Both of these blogs were written while I was single as a pringle. In the first blog, I had a positive outlook on having a biological child. In the second blog, I said something to the effect of after thinking about it I would be doing a disservice to a young child, and I stated that I thought it...

Almost two years ago, I wrote a blog about disability parenthood called "Who Says We Can't Have A Family?"  http://thevoicelssminority.blogspot.com/2013/07/who-says-we-cant-have-family.html  In it, I discuss several issues about being a parent and having a disability. When I wrote the blog, I had just turned 27 and had a different view on life. As I am approaching my 29 th  birthday, my perspective on the world is somewhat the same, but on the disability and parenting issue, I don't know if I still hold the same belief.             In that first blog, I laid out the following arguments: It is natural to want to pass genes to offspring, considering human life is just a blip in the cosmic makeup of things, and all we have are the legacies we leave behind. While I still agree with that argument, I find myself internally struggling with the question. Although I believe disabled people as a group have the right to b...

  So, it's been about a week or so since I last posted.  Since then, I've gotten older.  I had my 27 th  birthday, which was a quiet one this year.  One of the more unexpected gifts that I got was a  Voiceless Minority  T-shirt. It looks pretty awesome.  I will soon post pictures, thanks to my family for getting it for me.  Speaking of family, it due to recent conversations that family and disability will be the subject of this post.              I am not a psychologist, even though I took a few classes here and there.  However, I do believe it is human nature to want offspring. Our lives are only a blip on the cosmic radar.  It is through offspring that one leaves impressions and legacies behind.  This blog will not discuss how there is an overwhelming number of disabled children in America that need to be adopted, even ...