The Voiceless Minority

On Monday, we posted a blog highlighting - Wandercraft, a company with game-changing technology that will hopefully allow many people with disabilities to experience what it would be like to walk or stand on their feet. Since we received such an overwhelmingly positive response, I figured it would make sense to continue the discussion. “Bionic technology continues to evolve rapidly, offering new hope and improved quality of life for people with disabilities. Recent advancements have focused on enhancing sensory feedback, neural control, and the integration of artificial intelligence, making bionic devices more intuitive and functional than ever before.” The above quote is from Bionics for everyone’s official website. It is their mission to raise awareness of the latest bionic technologies for people who have become amputees or lost neurological function in one or more of their limbs. Today’s post will give a basic overview of Bionics and the possibilities that come with them. It wi...

As humans, we crave interaction with others. Indeed. when we don’t have social interaction with other people, feelings of despair and loneliness can overwhelm us. However, in the age of social media have we gone too far? Every aspect of most people’s lives is available for consumption by others now. This may be a new concept to the majority of the world but for one segment of the population, I argue that a lack of privacy is not a new concept. Indeed, it may even be a bigger problem for people with disabilities than their able-bodied counterparts.  Frequent readers of this blog know that I have a disability known as Cerebral Palsy. Cerebral Palsy, for my new readers, is a congenital disability that occurs at birth. It usually occurs during the delivery process; it is not genetic or at least there is no evidence that it is as of yet. There are many forms of Cerebral Palsy and it can affect people in a variety of ways. Some people with Cerebral Palsy have a slight limp when walking, ...

In Tuesday’s blog post, I talked about a speech I heard this past weekend from a young man by the name of Matthew Walzer. His speech came at a perfect time in my life. As I said in the blog Tuesday, until this past weekend I had been lost and in a sort of never-ending fog. Since Matthew’s story impacted me so much, I thought I would share it and its similarity to a point my dad has been trying to get both me and my sister to appreciate for years. By the end of this piece, you will not only understand the great wisdom of my dad but also you will hopefully appreciate the tenacity Matthew showed in his effort to redefine sneakers for people with disabilities. In short, by the end of this piece, you will understand why I believe in the saying, “Attitude is altitude”.  Every good story must start with a problem that the protagonist must face. Only this time, Matthew Walzer wasn’t writing fiction. Matthew was born with Cerebral Palsy. While some with Cerebral Palsy are wheelchair bound l...

So, it's been nearly a week since the last time I posted here.  This is not to say that there haven't been things bubbling around in my mind, just that I've been a little busy.  Since the last time I wrote, I've been busy promoting the blog by creating a Facebook page.  You can now show your support for the blog and disability advocacy in general by visiting  The Voiceless Minority  on Facebook.  I've also been busy continuing to write my first full-length screenplay.  Now, however, it is time to get back to the meat of things.         I've written extensively about several different issues, including how disabled people desire to be treated equally but still use the "Disney World" principle, as I like to call it, cut lines, etc.  While I've said that, in most cases, disabled people do want equality and strive for it legitimately, it does not mean that they are always support...

First off, I must thank you guys for the continued support of this blog. It means the world to me. Second off, I’m writing this blog because several people have asked me that they are curious about the issue. There are multiple types of disabilities but they can be categorized in two ways: disabilities developed at birth or disabilities encountered later in life. My one friend who works with the disabled population indicated to me that this is a hot topic for debate and also got me thinking. I have a family member who is going through similar issues at this point in their life. I myself was born with a disability. I have Cerebral Palsy and it is a neuromuscular disability. It is basically like I have the ability to do everything but my brain does not know how to send the signals to the appropriate muscle groups. Due to my circumstance, I have had a long while to adapt to challenges and I have never known what it’s like to walk, even without the assistance of a walker or another perso...