Tag: Disability Awareness

  • Public Transportation Adventures

    Public Transportation Adventures

    Most people don’t think about public transportation as a national issue For the disability community, this lack of infrastructure is a major barrier to freedom. In the April 15th episode of the Purposely Broken World, Kevin discusses his experiences using public transportation and how some states are better at it than others. Hopefully, this episode will start a conversation around the dinner table that people need to have. As always, all comments are welcome.

  • FDR & Me

    FDR & Me

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  • Content Creation Confessions

    Content Creation Confessions

    Happy Wednesday friends! I hope everything is going well. As you are reading this, I am currently on the way back from the disability policy seminar, and I’m excited to be in our nation’s capital, Washington, DC. I do not consider myself an influencer In this age of digital consumption, it is hard to get people’s attention, let alone keep it for any length of time. I’m just someone who tries to make a small difference in someone’s day. At first, I promised myself I would never charge anything for my creations. It started as a hobby. I don’t expect to have 100,000 followers anytime soon. I have 150 subscribers to the website. Less than a thousand followers on all social media platforms. I started this blog about 4 years ago, and the current version is about 2 years old. The same is true with the podcast. I am proud to say that I have a small but loyal following.

    ‭‭1 Corinthians 12:8 NIV‬ [8] To one there is given through the Spirit a message of wisdom, to another a message of knowledge by means of the same Spirit,

    Here’s something most creators will not admit: it takes a lot of time and energy to produce anything video, audio, or written. For a 20-minute podcast episode, it takes about an hour to record and about 3 hours to edit. My first book took about 10 years to write. My second book, which I hope to have out by the end of September, took about 3 years. Blogs are more fun to write because they’re less time-consuming,are the ones people focus on the least because people don’t like to read. For most people, this would be considered “disposable income” if they charged for their content. For someone like me, this is my income. A few months ago, I decided to start a bonus newsletter for subscribers for a small fee. I have a cash app and PayPal if anyone wants to give me a few dollars. Why does this matter so much to me?

    Since I’m on social security, I can only earn so much. I live below the poverty line. Did you know that the term “handicapped” comes from the 1600s in London, when people with disabilities used to walk around with a cap, playing games and doing tricks for spare change? As a disabled American in 2024. I kind of feel the same way. Don’t get me wrong I love what I do, and I do what I love. It sucks just because I was born a certain way and was never given a shot at a real career or a real job. I love helping others with all my heart, but part of me feels like a very handsome, well-intention Oliver Twist, saying, “Please, sir, may I have some more?”

    Most of my writings are written well in advance. So when I go to Washington, DC, even though I will always advocate for others first, This year I’m going to advocate to raise the asset limit for individuals with disabilities so I can earn a real living without having to stuff money under the mattress like I’m a criminal. Just because I was born a certain way doesn’t mean I should be in a second class. I should have the opportunity to make a living doing what I love. I will never ask for money, but if you’re interested, all the links are above. If you don’t like my content, that’s fine, but I guarantee you that you do follow some other small content creators, so please support them. Thanks for reading this, and I hope to see you guys next week.

  • My Happy Place

    My Happy Place

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  • Disabled Dating Tips

    Disabled Dating Tips

    Hey there, Today, I want to share some advice with you, even though I’m not an expert on anything specific. I thought it might be helpful to talk about something we’ve all experienced at some point: dating. But before we dive in, I want to make a couple of things clear.

    Firstly, some individuals might not fully understand or grasp the concept of relationships due to their disabilities. It’s important to be mindful of this and ensure their protection. This post isn’t aimed at them.

    Secondly, I didn’t start this blog to find dates. My goal is to break down barriers related to disabilities, and dating is a topic that often sparks controversy. Lastly, disabilities affect each person differently, so not everything I say may apply to everyone. With that said, let’s jump into some tips for starting a relationship when one or both partners have a disability.

    ‭Ephesians 6:12 NIV‬ [12] For our struggle is not against flesh and blood, but against the rulers, against the authorities, against the powers of this dark world and against the spiritual forces of evil in the heavenly realms. 
    • Communication is key. Make sure to talk openly and honestly with each other. Taking care of each other goes beyond just the physical aspects.
    • Don’t Fear the Disability: It might seem daunting at first, but understanding how the disability affects your partner is crucial. Don’t let fear hold you back from building a strong relationship.
    • Ask Questions and Learn Together: Don’t hesitate to ask questions and learn from each other. Assuming things can create distance between you two.
    • Encourage Self-Independence: It’s important for both partners to maintain their independence. Constantly challenge each other to grow and become more self-aware.
    • Be Prepared for Society’s Reaction: Sadly, not everyone is accepting of relationships involving people with disabilities. Stay patient and educate those willing to learn.
    • Stay open-minded: People with disabilities often have unique perspectives. Keep an open mind and embrace different ways of seeing the world.
    • Find Joy in Laughter: Life with a disability can be stressful, so don’t forget to laugh together. Enjoy the good times and support each other through the tough ones.
    • Love the Person, Not the Disability: If you’re in love with someone with a disability, love them for who they are, not their disability. It’s an important part of them, but it doesn’t define them.
    • Seek support from the disability community. Remember, you’re not alone. There’s a whole community out there ready to offer support, resources, and understanding.
    • Sex Can Work: Yes, sex can be a part of your relationship. Just communicate openly and find what works best for both of you in a safe and consensual manner.
    • Remember, people with disabilities are just that—people. Treat them with the same respect and consideration you would anyone else. Take care, and feel free to leave any comments or questions below!
  • “The Normal Life” Episode 1 Part 2

    “The Normal Life” Episode 1 Part 2

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  • The Disability Love Paradox

    The Disability Love Paradox

    Hello friends,

    Happy Wednesday to you all! Thank you once again for spending a little time with me. There’s been something on my mind lately, and I want to share it with you guys. This is going to be a bit of a controversial blog. A lot of people will not agree with this. Some people will call me an ableist. Ableism is defined as

    “discrimination in favor of able-bodied people.“discrimination in favor of able-bodied people”.

    Last week, I wrote a blog entitled The Disability Paradox. This is a very complicated sequel. There’s no nice way to say this; romantic relationships are complicated. Having a disability is also complicated. Mixing those two things is not easy. I need to say from the outset that there are individuals with such complex needs that they are not able to have a romantic relationship. That does not mean that they’re not allowed to feel their feelings and try to process them the best way they can. Remember that no two individuals living with a disability are the same, despite whatever the diagnosis says.

    Reality television has done a much better job of including individuals with disabilities in its programming. There was a man on the spectrum who won a season of Big Brother. Years later, there was another female who won the Favorite House Guest award on another season of Big Brother without disclosing her autism diagnosis until the very end of the season. In addition, there was a deaf contestant on the competition series The Circle.

    There is another reality show called Love on the Spectrum that features individuals trying to date with various intellectual disabilities. These are very real people with real feelings I don’t know if it’s the production and editing of the show, but the show comes across as very “inspirational and safe.” They want the individuals to be seen as happy and overcome all kinds of obstacles in their way. Yes, people with disabilities need more support, but the show does not focus on the long-term issues of the relationship, and how they handle those is scarcely shown. This show is designed to make the viewer feel happy. This show doesn’t feel real.

    ‭‭1 Corinthians 13:4-5 NIV‬‬ [4] Love is patient, love is kind. It does not envy, it does not boast, it is not proud. [5] It does not dishonor others, it is not self-seeking, it is not easily angered, it keeps no record of wrongs.

    As a person with a physical disability, I feel left out. There is another show I want to focus on called Love is Blind. For those of you unfamiliar with this show, able-bodied folks meet without seeing each other; they date for a few weeks before deciding to get married. This is appealing to me because this is the only scenario where someone would get to know me and not see me as someone in a wheelchair first. I cannot hide, nor do I want to be part of myself. I just want people to learn to look past the disability first.

    I want to have a real conversation about faith, finances, long-term goals with a partner, sex, etc. Why are people with disabilities always segregated amongst ourselves? Everyone on Love is Blind is physically fit and has solid careers. The casting department was able to cover all ethnic backgrounds, but they forgot about the largest minority in the United States. It is important to show that individuals with disabilities should have romantic relationships. However, they are insinuating that they can only date others with disabilities This is not an example of inclusion but rather of exclusion. We are all part of the same human race, and we will have obstacles to overcome, regardless of ability. Real love should be what’s on the inside, not the outside. I know this is the beginning of a much deeper conversation Hopefully, someone will continue around the dinner table tonight.

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  • Chosen Last

    Chosen Last

    In the March 15th episode of the Purposely Broken World, Kevin delivers a very short testimony on the benefits of being chosen last by this world. In the real kingdom, the weak are the strong, and the strong are the weak. Don’t give up; pray first, and pray last. All comments are welcome.

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  • The Diisability Paradox

    The Diisability Paradox

    Hey everyone! How are you doing today? I have something to share with you: I wasn’t always into advocacy. When I was growing up, I thought advocacy was just something my parents did to make sure I had what I needed from my school. To me, people who did advocacy seemed like they were just loud and not really helpful. My parents did a great job treating me like any other kid. They celebrated when I did well and corrected me when I made mistakes. They made sure everything at home and everywhere else was set up so I could do things on my own, like having a low bed I could easily get in and out of.

    My family accepted my disability because it was all they knew about me. I even played baseball with other kids who had disabilities. But my family also knew that the world wouldn’t always make things easy for me. They enrolled me in regular classes at a public school. That’s when I learned about what I call “the Disability Paradox.”

    Advocacy is about teaching people and changing their minds about things they’re not used to. Even though we have laws like the Americans with Disabilities Act (ADA), it doesn’t mean everyone with a disability is treated equally. Think about it: When a mom is expecting a baby, she hopes the baby will be “healthy.” But what does that mean? Why should having a disability be seen as a bad thing?

    Did you know that Franklin D. Roosevelt used a wheelchair because he had polio? He hid it by using special braces on his legs, even though it was really painful. But even now, many people with disabilities still feel like they have to hide who they are. People have done amazing things like going to the moon and building tall buildings, but there are still a lot of people with disabilities who don’t get the help they need.

    We talk about big issues like climate change, but sometimes the solutions don’t work for everyone. Imagine not being able to drink a lemonade on a hot day because of a ban on plastic straws. This is something that could’ve been avoided if people with disabilities were included in the decision-making process.

    We’re not just here to inspire or be pitied. We’re part of society just like everyone else. But why don’t we see more people with disabilities in positions of power? We’re more than just a feel-good story during prom season.

    Lots of people have disabilities, but society often sees us as broken and needing to be fixed. But we’re not broken. We just need the same chances as everyone else.

    This is just the beginning of many conversations we need to have. It’s okay if you don’t understand at first. Just listen and learn. Once we all know better, we can all do better.

  • A Disabled Father

    A Disabled Father

    Happy Wednesday Good people I hope everyone is having a wonderful week. This week I was planning to do a whole blog about the new rules the Department of Transportation (DOT) is hoping to implement to help disabled travelers when they are traveling on airplanes. I read a few articles and even drafted a few lines, but I wasn’t feeling it. It was written without love. So I went back and rewrote something I wrote back in 2020. All these years later, it’s still one of my favorite pieces of writing. You can find the original version in my first publication, Confessions from DisabilityLimbo. I hope you enjoy it. See you next week!

    ‭‭Exodus 20:12 NIV‬‬ [12] “Honor your father and your mother, so that you may live long in the land the Lord your God is giving you.

    Hi there, I’m Kevin Nuñez, and I’m all about standing up for people with disabilities in New Jersey. I’ve got Cerebral Palsy, but that hasn’t stopped me from joining state committees to make life better for folks like me and our families. Now, I get it—when you saw the title of this blog, you probably laughed or rolled your eyes. “How could a guy like me be a dad? Can I even handle changing diapers or holding a baby without dropping them?” Sound familiar? You might’ve even thought, “This is too far-fetched. Let’s talk about something else.”

    Let’s clear the air. I don’t have all the answers. I’m what you call a “realistic optimist.” That means I know how tough life can be, but I’m always on the lookout for the good stuff. I’m 33 years old, and it’s been forever since I went on a real date. So yeah, the chances of me becoming a dad anytime soon are pretty slim. But here’s the thing: life isn’t just about having all the answers. It’s about the journey, about keeping hope alive even when the odds are stacked against you.

    I know not everyone with a disability can have kids. It’s complicated, and I get that. This blog might not resonate with everyone, and that’s okay. All I want is to start a conversation—maybe even one you’ll have at your next family dinner.

    Hey, William Christopher,

    I’ve been holding onto this until you turned 18 because I want you to know how much you mean to me. I wrote this back in 2020, when everyone was thinking about their lives. It was before I met your mom, back when I had all this love in my heart but no one to share it with. So even though I might not be the perfect dad, I want you to know that I’ve always loved you.

    I can’t wait to be there for all your big moments—teaching you to ride a bike, helping you up when you fall. I’m not sure how we’ll figure it all out, but we will. And hey, you’re going to be bilingual—English and Spanish. Trust me, it’ll come in handy someday when you’re filling out job applications.

    It’s not going to be easy when people stare at us in public, but you’ve always handled it like a champ. I’m looking forward to watching baseball games with you and having fun wrestling matches, even if you know it’s all staged. Just remember to balance the fun stuff with hard work, and always treat everyone with kindness and respect.

    Happy 18th birthday, buddy. Make it a good one.

    Lots of love,

    Dad Kevin

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