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  1. 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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  2. 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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  3. 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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  4. Setting my Sights on Medicine – Insight from a Deafblind Medic

    It has always been the case where, if someone told me I couldn’t do something, I would go out of my way to prove that I, in fact, could. Despite going to a residential school geared toward supporting students with visual impairments, nearly all the teachers discouraged me from following my dreams of studying medicine at university, saying that it simply wasn’t possible for visually impaired people like myself to do.  So when I dismissed this advice, and finally got accepted into medical school following my interview, I was elated….

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  5. Don’t Be the Bird in the Box

    Let’s face it, the world will end someday. Zombies and nuclear energy compete for the top method of human demise – but Netflix’s Bird Box has other ideas. In a world overrun by creatures that cause insanity upon first glimpse, it’s only natural that whoever hasn’t seen these beings would attempt to survive by using their vision as little as possible. The story follows one woman as she survives against all odds in order to get herself and her children to safety, training the kids to listen for danger and…

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  6. Surfing and Finding Serenity: What We Can Do When We Have Faith

    I have always been close with my father. I may make fun of his big belly now, but we are best friends. He’s my hero and he has always encouraged me to do anything. Before I was even born, my father had dreams of me becoming a pro surfer. He even named me after champion surfer Derek Ho. However, I was born blind due to congenital glaucoma. It goes with out saying that surfing is a dangerous sport. In split seconds, a crashing wave can slam a surfer against the…

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  7. A Look Back at 2018: These Are the Stories of the #BlindNewWorld

    2018 has been another incredible year in the BlindNewWorld. We love hearing – and sharing – your stories of adventure, triumph, love, family, learning and so much more. These stories are what keep us going – and what keep our community strong. And we don’t want you to miss a single one of them. So to close out the year, we’re bringing together the full collection of 2018 #MyBlindStory posts. Get to know each and every one of the people who have shared their stories with us this year. And…

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  8. You Don’t Need Sight to Have Vision

    Hello, my name is Holly. I’m a disability and lifestyle blogger from the UK. My story is nothing unique – I went through mainstream education, graduated university, I love all things beauty, fashion, concerts, and all the usual girly stuff. Oh, and I’m blind. I get up every day, go to work, see friends and do blogging/film content for my YouTube channel. I’m blind, but I live a pretty normal and independent life. I have things that I want to achieve. I have goals and aspirations – and I think…

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  9. Coffee, Community and Overcoming Challenges

    I have been legally blind since birth with my most recent diagnosis being photoreceptor disorder. From my understanding, this is a catch-all, because they cannot determine a specific disease. The number one question I am most often asked is what I can see. This is a very difficult question since I have always seen this way. I can see extremely vague details within five to ten feet. This means I can usually tell where people are, but I cannot pick up on facial expressions or other nonverbal communications. Beyond ten…

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  10. Suddenly Sightless

    When you lose your sight, it can make you feel incredibly lonely. The feeling of isolation, the snatch of your independence and the knock of your confidence with everyday life is a massive impact. The overwhelming feeling of grief is awful. You yearn for what you have lost, unknown whether it will return or not. At least that’s how we felt. I’m Laura. My first noticeable decline was February 2016 – the cause of which is still unknown. As time went on, I eventually lost my career as a lab…

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