The Voiceless Minority

 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...

Hello again, yes it’s me your friendly neighborhood super advocate. A warm welcome to all of my new readers who are checking out the blog for the first time. I want to welcome you to a friendly, engaging, informative, and sometimes funny look at anything and everything that has to do with disabilities and the disability community. To all my returning readers, welcome back. No matter which group you fall into, you’ve stumbled upon the Voiceless Minority on a very special day. Yes, it has finally happened after a decade of writing this blog - today marks the 100th post for the Voiceless Minority. I could not have done it without you. I started this blog as an outlet for my anger and the hurt I was feeling after being denied the opportunity to follow what I truly believed at the time was my passion. When I started this blog, I thought I wanted to be a high school history teacher and teach theater after school. I apparently didn’t know myself as well as I thought. They say that “things hap...

So, I was talking to a couple friends tonight and I realized that I missed another episode of Speechless. For those who don’t know, Speechless is a show about a young boy named JJ with Cerebral Palsy. JJ cannot speak and has a wonderful mom as a disability advocate. The cool thing about this show is that as a few shows in the past, they actually use an individual with a disability to play the disabled character. I wrote a blog early on in the history of this blog that was relevant to tonight’s episode. Tonight’s episode dealt with the idea of “inspiration porn”. I will not go into detail about the episode as I have not watched it fully yet. Towards the end of this blog, I will link the above-mentioned post. Why am I writing about it now? I am writing because it is amazing that a major network like ABC is finally paying attention to disability issues and portraying them fairly. Perhaps if this show gets picked up for more seasons the perception of people with disabilities in societ...

So, this weekend I attended my first Florida SAND conference. At first, I wasn't sure what to expect; I had never been to an event like this. I had heard mixed reviews from those who have attended in the past. It started slow; there were a bit of technical and arrival glitches with myself and my PCA. However, once we got there, it quickly became apparent that this would not be anything like I had heard. Friday night was a chill night; I met some pretty amazing people and lost Uno's rather exciting game of No official conference business that took place that night. Although my PCA won a bag of espresso beans for some strange reason, I was hoping we would win the autographed football but still pretty awesome. Saturday was the heart of the conference, right away Saturday morning, I realized that something was different. My college brain had kicked in again, and I was in learning mode. I have tried two other academic endeavors since I graduated with my Masters, one in real esta...

It has been nearly eight months since there has been anything new posted on this blog. A lot has happened in eight months hiatus. I have finished my master's degree program in Teacher Education. However, due to the trials and struggles that have occurred during that process, which can be read about in earlier entries, my focus has drifted away from teaching and advocacy for persons with disabilities. Most of this blog has been dedicated to advocacy and discussing various issues that people with disabilities encounter. However, the point of view of the author, me, has changed. A lot of the writing in earlier entries came in a time of my life when I was unhappy with the circumstances faced with. I have since re-evaluated The Voiceless Minority. There was a time where I thought about abandoning the project altogether if I'm honest. However, I decided I would resurrect the blog at this time and take it in a slightly new direction. It will still address social issues, but I will als...

What is it to be disabled? Disability is a label that society puts on you, but this label has preconceived notions that come with it. This label often causes others to view the one with a disability as something less than human. However, there is more to disability than just a label. A recent situation that has come up regarding my disability has inspired me to write this blog.             As many of you know, I have Cerebral Palsy. Due to the Cerebral Palsy, I require aide care. In a book that I am in the process of publishing, I describe my journey through grad school and the aide care system. However, the aide care system needs a wake-up call. Recently, I have switched to an agency model of care. I am aware that this is a different type of care system, in that I do not hire my employees anymore. However, lately, I feel like a pawn in the aide care system chess game.        ...

            What a disgrace! These are the first three words that came to mind when I read an article on the social media giant known as Facebook recently. The report detailed how KFC, a chicken place famous in the U.S. A turned a little girl away because Pit bulls had recently mauled her. According to the article, "She has turned out because other patrons may be scared by her face and injuries. The link to the full report can be found at the end of this post.             When I first read this, I couldn't believe that it could be true. However, since I read the article in the day and a half, I have read other people's posts about the incident, which leaves me to believe that it is true. Not only do I feel bad for the little girl who is most likely going to have psychological damage for a long time, but I feel bad for society.           ...

It's been a long time since I have written, but I recently watched a video that got me thinking. The video is linked below. I have shared it tons of times since I have watched it. In it, the speaker Stella Young brings up an idea of something called inspiration porn.             She says that the lie that has been perpetrated is more social than physical. I could not agree with her more when I posted the following status "No, I am Not an inspiration for getting my Master's degree and having a disability. No, I am Not an inspiration for getting out of bed every day. Having a disability doesn't make me inspiration, just food for thought." I got a mix back of responses. Some did not understand my point for posting the status, my point being that the inspirational things that I have done should have nothing to do with my disability. My achievements should be based strictly on their merit. They should not have an aster...

             It’s funny what you find on the Internet. It’s been a while since I’ve written anything because I’ve been busy reading and writing a book, but today I came across something noteworthy. As many of you know, I recently graduated with my masters who have followed this blog. You may not know that I have been planning to move from my Pennsylvania home to a home in Florida.             The home is currently being built, so as far as a physical structure, I will have an accessible place to live, but moving is never simple when you are non-disabled, much less when you are disabled. Because I require so much physical care, I use at home health services to provide that care. I use these services to avoid going into a group home or a nursing home. These services fall under what is known as home and community-based services.         ...