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  1. What It Means to be Blind During a Pandemic

    People with visual impairments are navigating the Covid 19 pandemic right alongside their sighted friends and family members. At the same time, they’re also faced with some unique challenges of their own. To raise awareness of some of these issues, and to learn how communities can support their blind neighbors and loved ones during this uncertain time, we caught up with Perkins School for the Blind’s Jerry Berrier and Kate Katulak.  Answers have been lightly edited for clarity.  What are some of the challenges you’re facing in day-to-day life as…

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  2. Taking a Humorous Approach – Because Life is Blurry

    For me, life is blurry. One day, while waiting on the Light Rail platform, a man came up to me and proceeded to wave his hand in front of my face. Now, I’m no stranger to men trying to get my attention in obnoxious ways, but I knew the main reason why he was doing this—to see if I am “really blind.” I had my white cane with me, but I had no service dog, and I wasn’t wearing those tell-tale, black sunglasses you often see in movies. I was…

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  3. What It Takes: Four Ways to Become More Independent as a Visually Impaired Young Adult

    Over the years, I have grown into an independent, successful young woman with dreams of helping other blind and visually impaired children grow into successful adults. This wouldn’t have been possible without the help of the Florida School for the Deaf and Blind, my family, Iowa Department for the Blind, Hadley Institute for the Blind and Visually Impaired, National Federation of the Blind and other blind services that have helped me. These services helped me figure out who I was as a visually impaired person, and I’m hoping that what…

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  4. On Me

    There has always music in my life, for as long as I can remember. Mom was a professional singer, and dad was an avid vinyl collector who was always making us mix tapes of his favorite songs. Between the two of them, and the piano and guitars we had at the house, I became a musician without really even being aware of it. I admit though, I never expected to play music professionally when I grew up. I’ve been visually impaired/legally blind since birth, but my parents didn’t realize until…

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  5. #MyBlindStory 2019: An Amazing Year in Review

    Your stories are jhe foundation of the #BlindNewWorld community – and there is no limit to who can join us here. Our 2019 contributors came to us from all over the U.S. – and around the world. They’re stars from Hollywood and hip-hop. Champion athletes. Savvy young adults. Internationally recognized gamers. Eloquent bloggers. Published poets. Accessibility-minded inventors. Talented craftspeople. Passionate artists. Innovative businesspeople. Determined doctors! Staunch advocates and committed allies. And above all, they are change-makers. These are people who are willing to share their voices and their stories to…

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  6. Will You Say Yes to My Blindness?

    I’m excited to publish my first book of poetry this year. As I complete the circuit of local news talking about my poems, I keep coming up against the same question: “Do you think of your blindness as a superpower?” My answer is always, “No, I don’t think of my blindness as a superpower.” Instead of taking me at my word — or even asking, “Why not?” — each host invariably insists, “But it makes you special, offers you nuance, helps you overcome challenges.” These routine objections force me to…

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  7. An Ally – and Innovator – for Accessibility

    This past April, I started my 50th year of working with and for persons with disabilities. With a goal of becoming a teacher out of undergrad, I started out as an O&M instructor at a state rehab center Kentucky, and then went to graduate school to become an O&M Specialist. From there, I moved on to private rehab services in Charlotte, the Veteran’s Administration in Texas, state rehab in NC, then to UNC Chapel Hill. I retired from UNC in 2013 and now consult for the Association on Higher Education…

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  8. Blind & In Technicolor

    Following the loss of my sight, and about five years of total blindness, I developed a gorgeous, technicolor visualization of myself and reality which my neurologists call non-optic sight, or a type of adaptive synesthesia – but let me back up. Even as I progressively lost my retinal vision, my mind was full of light, and my heart was full of music. I embraced non-visual perception, low vision, double vision, and, difficult as it was, the very abstract phase before final retinal loss. This journey has been one, not into…

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  9. Rucking – While Deafblind

    My name is Brian Switzer. I am deafblind as a result of a condition called Usher Syndrome. As a child, I attended a couple schools for the deaf before switching into a public school. I progressively went blind. I was diagnosed with sight loss at age 4, became legally blind at age 16, and now only possess some light sensitivity. I hold a Master’s degree in Public Policy. I am a co-author on a book on living with deafblindness called, “Walk In My Shoes: An Anthology On Usher Syndrome.” And…

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  10. Why I Love My Cane and What It Means to Me

    Imagine having limited side vision – also known as tunnel vision – where you are not able to see what’s on your sides or what’s coming from up-and-down, such as a step off or a dangerous snake on the floor. This is where the white cane comes in handy. Canes are great because they can feel whether something is in front of you or if there is a step off on the sidewalk or stairs. Well, let me tell you about my experience with using a cane and how it’s…

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