Tag: disability blogger

  • The Double Edge Sword of Identity

    The Double Edge Sword of Identity

    What makes a person who they are? Is it their gender? Is it their sexual orientation? Is it their ethnicity? Is it their faith? Is it the legacy they leave behind? Is it the way they’re perceived? Identity politics cannot define a human being As a Christian heterosexual Latino male with a developmental disability, I’m well aware of the labels society has put on me. Can you see me as Kevin?

    Gary Rubin, former SABE representative.

    “Labels are for soup cans, not people.” –Gary Rubin.

    On the back of my business cards is a photo of myself with the quote, “Look at the person, not the disability.”

     This is how most people perceive me. My disability does not define me; however, it is a significant part of my identity that I cannot separate from myself. Likewise, I cannot hide my Puerto Rican heritage or my love for Jesus Christ. A person cannot be defined by just one trait. It is the intersectionality of all these characteristics, combined with their experiences, that shapes who a person is.

    'And why do you look at the speck in your brother’s eye, but do not consider the plank in your own eye? 'Matthew 7:3

    It’s wrong to judge or to have any bias. The fact is we  all judge and have unconscious biases. I am seen as an inspiration or as a token for society. Someone who looks like me should be offered more jobs than just the greeter at Walmart. I’m aware of how blessed I am. I know I was put on this Earth to be the voice for others. We all have gifts and blessings that others desire. 

     The label of “disability” is the one I have to wear to have access to programs such as Medicaid and Medicare. It has never been about a check in the mail, it is my key to life. Without it, I don’t have caregivers to get me out of bed in the morning. In my life, I’ve employed anywhere from 20 to 30 different Direct Support Professionals (DSPs). Supporting individuals with disabilities does contribute to both local and federal economies.“Medicaid dollars”  helped me make notable accommodations to my home so I could live in a community and not be locked away. This will save taxpayers money in the long run. Any cuts or caps to these programs would be a slow death sentence. I have the same right to live as anyone else, but to do so, I have been placed in a societal box.

    The elimination of Diversity, Equity, and Inclusion (DEI) initiatives is extremely damaging to the disability community, which has long been fighting to be seen, heard, and represented. Inclusion is more than just ensuring a certain number of people attend a specific event or hold particular positions; it’s about recognizing the person as a whole. Representation matters, but it must be approached carefully and purposefully to avoid confining ourselves to more boxes.

    I know I’ve said a lot in this post, and I hope this can spark a series of conversations—that’s what I want. People from different ideologies need to start working and talking together. Democrats and Republicans are not evil; they’re human! Don’t categorize people. Don’t judge others before you truly get to know them. Learn to see the whole person, not just certain aspects of what you observe on the surface. Thanks for reading, and I’ll see you next time.

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  • Land of new Opportunities

    Land of new Opportunities

    There is a new day in America, will people living with disabilities be part of it? It’s been less than a month since the new administration has assumed power. America’s voice was heard loud and clear. Congratulations to President Trump, the new Congress, and the new Senate. I look forward to working with all of you. Democracy can only work if the people are equally responsible for holding those in power accountable. The Constitution is more than a piece of paper; it is a contract between the government and its people. As an American, I think we live in an exciting time. I understand and acknowledge that there are lots of scared and anxious feelings. These are valid feelings.

    Democracy is more than voting every two years. To make a difference we have to do more than just make a post on TikTok. We have a new opportunity to educate, collaborate, and advocate for all people regardless of their abilities. We must get to know our elected officials. Instead of complaining, start a conversation with a tangible goal. We must learn to compromise and build off of the success of others. Don’t assume people are against you. You cannot judge those who don’t understand. Get to know the person you’re speaking with and relate to them to find out what’s important to them. Do your research before meeting with them. It’s time for us to show there’s more to us than disability.

    'Blessed are the peacemakers, For they shall be called sons of God.'
    Matthew 5:9

    So often, our community talks to itself and then gets upset when others, don’t understand us. In some ways, our community has become complacent over the last few years. The Americans with Disabilities Act ( ADA) was not meant to be the end of the disability rights movement but the beginning. It is time for us to be seen and heard as decision-makers. We need to organize as a community and decide what the next step is. advocacy organizations from across the country need to stop isolating themselves and work together. We are not just a puff piece at the end of the local news. Bring those in-power solutions instead of problems. Collect data and tell people’s stories. Put a face behind each set of numbers you present.

    The power of the country lies in more than who sits in the Oval Office. The power is with its people. I understand we can not all run for Congress. However, we can go to our local town council meetings. if a position on the school board opens up and run for that. We must speak when we are given the floor. Disability needs are more than curve cuts and elevators. However, people don’t know that. Remind your neighbors that disability is part of the human experience. Some folks with disabilities cannot stand up but maybe we were born that way to stand out!

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  • Playing Games

    Playing Games

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  • All  Dressed Up

    All Dressed Up

    Today, let’s chat about clothes—not from a fashion standpoint, but how they make us feel. Most people feel comfortable working from home in socks, shorts, and T-shirts. I imagine some of you might feel slightly envious when I say that’s my usual work attire. Working from home truly is a blessing, especially for accessibility. It’s a gift I never take for granted.

    If I worked a typical job, I’d have to navigate public transportation and spend extra time getting dressed. Yet, here’s my paradox: I love getting dressed up! There’s something about wearing a freshly ironed shirt and a tie that makes me feel invincible like I’m donning a suit of armor. It might sound a bit vain, but looking sharp boosts my confidence. When people think of disabilities, they often picture someone disheveled or in poor health. Dressing up helps counter that stereotype, and people stare a little less.

    Ephesians 6:11 NIV [11] Put on the full armor of God, so that you can take your stand against the devil’s schemes.

    I’m not ashamed of my disability, but dressing well feels like the closest thing I have to a day off from the assumptions people make. It may sound odd, but it makes perfect sense to me. I love showing people that those with disabilities can lead successful, goal-oriented lives.

    There’s an old saying: “Dress to impress.” If you want people to see you differently, sometimes you need to show them a different side of you. Some people need to see the miracle before they believe it. I’m not claiming to be a miracle, but I see the miracle in the people who help me get ready, making sure I look my best. That’s the real magic!

    I know only a handful of you read this blog It comes out, but I hope when you get dressed for work tomorrow, you’ll take a little extra time to make yourself look different. Maybe it’s a new bow in your hair or a tie you don’t usually wear. Do the small things that make you feel good. When you look good, you feel good, and when you feel good, you look good. It takes extra effort for me to look good, so when I do, I feel exceptionally great.

    As always thanks for reading. I am always looking for new blog ideas, let me know what topics you want me to cover next.

  • Coming Soon

    Coming Soon

    Greeting All Readers:

    Proverbs 11:25 NIV [25] A generous person will prosper; whoever refreshes others will be refreshed.

    Greetings and warmest regards. I’m back with book number two! My name is Kevin G. Núñez, a 36-year-old male living with a developmental disability known as Cerebral Palsy. (CP) I use a wheelchair daily to help me ambulate throughout the day – in other words, no wheelchair, no legs. Additionally, I can’t get out of bed on my own or get dressed without the help of others. Things you take for granted are things I long for in life: driving, hugging someone, and even cleaning my backside.

    A quick disclaimer before I get rolling. I’m currently the vice-chairman of the New Jersey Council on Developmental Disabilities (NJCDD), and this work does not reflect them or any other advocacy organization that I have been a part of. No one has endorsed this, and I have not received any money upfront to write it. Bragging about my accolades is not the purpose of this writing. I’m going to do the exact opposite.

    Photo by picjumbo.com on Pexels.com

    I should have felt a sense of completion and joy when I clicked the “publish” button on Amazon’s Kindle Direct Publishing (KDP) for my first book, Confessions from Disability Limbo. Yet, something felt out of balance, and without balance, we have nothing. I promise that I’m not writing this out of vanity. You see, I did not start out planning to write a book. I had a few successful blog posts to help grow my website. Then, I wanted to write some letters of appreciation to my family and friends for helping me get to where I am today.

    Up to that point, I mainly wrote about my life for my reflection. But I wrote my book for others. I wrote Confessions as if it were my first kiss: I didn’t know what I was doing, but I knew I had to share what was in my heart. As a result, I love my first book, and I stand by it, but I’m not too fond of the finished product. Confessions was and is beautiful. It holds a special place in my heart, but – to be honest – it’s wild and disjointed.

  • An Almost Experience

    An Almost Experience

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  • My Voting Experience

    My Voting Experience

    Yesterday was election day in the United States of America. I love this country and am so proud to be American. This blog is not going to focus on any other election day results but rather on my personal experience as a disabled voter. It was amazing!

    I’m almost 40 years old, so I have been voting since the 2012 general election. Usually, it’s very quiet and subdued at my polling place. I acknowledge that being a coworker is not easy. If I’m honest, previously, I’ve had limited interaction with them. They don’t usually say much after you sign your name before stepping into the voting booth. There are roughly about 32,000 people in my town. Before yesterday there was little turnout in my district. I never kept track but I feel there’s never been more than 10 or so people in line to vote when I’m gone. I’m not saying people in my township don’t vote I’m saying you don’t see them. I was expecting more of the same this year.

    Mark 12:31 NIV [31] The second is this: ‘Love your neighbor as yourself.’ There is no commandment greater than these.”

    After a medical appointment and running some errands, I arrived with my family around 6:30 p.m. There were easily over 250 people in line. We went to the back of the line and began to wait. For those of you who don’t know, I have a twin brother who also uses a wheelchair. One of the poll workers saw us and asked if we needed assistance voting. We informed her that we didn’t mind waiting we knew it was part of the process. I never knew there was a different entrance for the elderly and disabled at this polling place. It was nice to be recognized and accommodated. There was still a line but this one was accessible. It was not overwhelming. Fortunately, I don’t have sensory issues, but if I did, this would have been much safer. A shorter line is not about convenience.

    My identification was verified along with my address to make sure I was in the right polling place. My brother could not reach the tablet to sign his name because the court would not stretch that far. Our father had to sign on his behalf. He had to document himself as our assistant. To sum this might seem like a hassle but it was nice to know my vote was safe and secure. My brother does not have the best communication skills so it was good for him to have my father as an assistant instead of having to communicate with someone else. Our father has always assisted us during the voting process, but it was never documented before. These extra steps matter. They assure equity and equality.

    As an individual, I know my voice as a US citizen was heard. Regardless of who is living at 1600 Pennsylvania Avenue come January. I’m still going to live with disability I’m still going to have to fight for my rights. I know I did my part in the Democratic process and I did my civic duty. This country does not ask much of me. I was happy to cast my balance! Thank you for reading and may God bless America!

  • False Expectation

    False Expectation

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  • Awakening the Disability Workforce

    Awakening the Disability Workforce

    Awakening the Disability Workforce

    By Jesse Schwartzman

    This National Disability Employment Awareness Month, Celebrate how far we have come! The Disability Employment rate has never been higher! The labor participation rate for people with disabilities in 2018 was 37.8 percent; in 2024, it is now 40.0. Tremendous strides have been made! It is also important to acknowledge that more can be done and how we get there.

    How do we get there? Two things need to happen, Everyone needs to support each other and know that getting a job could take some time, especially a job with health care and a living wage. I enjoy what I do and most importantly I enjoy helping people. It makes me happy. My happiest moment last year was hearing that a former client heard back from her dream job and received a job offer. She has been working there ever since. I have yet to help anyone land their dream job this year, but the year is still not over. My inspiration for this opinion article is to inspire business owners, human resource officers, and the public at large to hire more people with disabilities. People with disabilities, stay at jobs longer and are great workers. If they need an accommodation it will not cost much money the average accommodation is $300. I would also like to say that if you are a person with a disability you should advocate for yourself. It is also important to advocate for others because there is strength in numbers. Every human rights moment was moved forward with a large number of people and yes disability rights are human rights.

    This passion for helping people with disabilities is very personal to me. I came out of college with an internship at a Senator’s office, multiple student leadership and work experiences as well as nearly graduating with honors. I thought I would have multiple full-time offers coming out of college boy was I wrong? I would have an easy time getting an interview based on my resume but when it came to going on the interview I would be so self-conscious as a person who stutters and born with missing fingers on my right arm. I would not get hired because I did not show that I could do the job and I do not bring the confidence or passion either. Through hard work, going back to school, and networking I finally got a full-time job three and a half years after I graduated college. I did not get a permanent full-time job in health care for 12 years after I graduated college. I never gave up but it took time. I saved up money to get driving lessons, and then a car so I could drive myself to speech therapy. I continued and to this current day continue to work on myself. Working gave me the ability to do these things and more. Work gives me purpose and the ability to better myself and maybe one day start my own family. I want every person in the disability community to be able to work if they want to work.

    I call on leaders in the disability field, elected leaders, people with disabilities, and the general public to not accept the status quo on disability employment. We need more mentors, more willingness to move forward on ideas, and most importantly more opportunities in society. The time is now to not just say these things but to truly implement them in real time. If you would like to join me and help advocate for more employment opportunities for the disability community here’s my email jesseschwartzman00@gmail.com I await your message.

    i

    Jesse Schwartzman is a disability advocate who has worked in the legal, political, and advocacy fields. He currently works as an outreach and advocacy worker in the disability field. Jesse enjoys helping people and watching sports and movies. He can be reached at jesseschwartzman00@gmail.com.

  • Blind Love

    Blind Love

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