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  1. An Iron Will Makes An IRONMAN

    A little bit about me: I am an 18-year-old high-school senior from St. Paul, Minnesota. I have Stargardt Disease and I’m significantly visually impaired. A couple of years ago I started a non-profit called Louie’s Vision that works to help kids with visual impairments find adventure. About a year ago, I approached my parents and told them I wanted to do the Ironman, a one-day race that consists of a 2.4-mile swim, a 112-mile bike ride, and a full 26.2-mile marathon. I was just 17 years old, had no experience…

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  2. When It Comes to Demanding Access, Take the Big Swing

    I am a 14 year old blind skier, horseback rider, cross-country runner, Challenger Little League baseball player, singer, musician, voiceover artist, radio personality, advocate, student lobsterman and geek supreme from a small fishing village named Beals Island, Maine. Oh, and one more thing you should know, I’m a huge Boston Red Sox fan! I was born totally blind from a rare genetic condition known as Leber’s congenital amaurosis (LCA); because of this, I’ve been thrown lots of curveballs in my life. I’ve been bullied in school to the point of…

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  3. Our Nystagmus Story

    When my baby daughter was 6 weeks old, somebody wearing a white coat told me she was blind. She wasn’t blind. I knew that. But I also knew there was something wrong with her eyes. It turned out to be nystagmus. I’d never heard of it before. From that day on, our nystagmus journey began. Nystagmus is characterized by uncontrolled eye movements, which make focusing very difficult. It is a lifelong condition and cannot be corrected with glasses or contact lenses. Most people with this condition have impaired depth and…

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  4. Renegades

    “Long live the pioneers Rebels and mutineers Go forth and have no fear… It’s our time to make a move It’s our time to make amends It’s our time to break the rules Let’s begin” –X Ambassadors, Renegades   Earlier this month, I was at the X Ambassadors concert here in Minneapolis. I have been a fan since I first heard them. I went with my family, friends and a few people from the Louie’s Vision Board of Directors. The show was above and beyond what I could have expected….

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  5. Why I Learned to SEE: Set Extraordinary Expectations

    My three children, two sons and a daughter, are typical teenage kiddos. They go to public school. They play sports. They have friends. They often stay up too late, keep their rooms quite messy, and talk back to me every now and again. Yep, pretty typical. But my kiddos also each have a certain, not-so-typical aspect that makes them, well, them. Many people describe my children as extraordinary. But I don’t. High achievers? Yes. Resilient? You bet. But extraordinary? No. However, it is my expectations for them and their expectations…

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  6. Trail Blazing the World of Blind Skimboarding

    My name is Kai Owens, and I have an aggressive form of Retinitis Pigmentosa (RP). RP is a form of vision loss that causes night blindness, blind spots known as scotomas, and loss of central acuity and peripheral vision. After being diagnosed in the third grade, I began learning braille, typing, and screen reading computer software – and I decided that no matter what happened, I wasn’t going to let it stop me from doing what I wanted to do. Ever since I was a young kid I have been…

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  7. Learning Through Love

    Vicky is our four-year-old girl and she is losing her sight due to a rare genetic condition called Leber Congenital Amaurosis. And I would like to take a moment to thank her. I have redrafted this post many times, writing and rewriting all the little things I thank Vicky for. No words seem to capture all emotions and feelings. The truth is simple: I want to thank Vicky for what she’s teaching us. When you hug me strongly and tell me “Mummy, I love you sooooooo much,” you are teaching…

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  8. Living My Normal, Blind Life to the Fullest

    My story is probably pretty boring to some. I am a husband, father and content creator who just happens to be visually impaired. I spend my days at home, making sure my kids are taken care of, making podcasts and videos, preparing dinner and so forth. It’s not the most exciting life, but it is my life. And, I think it displays what being a VIP is all about. It’s more than trying to do “amazing” things as a blind person. It is about getting up every day and living…

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  9. We Can All Be Exactly Who We Were Made to Be

    We all have those definitive moments, those HUGE moments, in life when you just know things will forever be divided into before and after. Meeting our daughter Primrose was one of those moments. Our family of four became a family of five through international adoption in January 2016. We saw a photo and description of our daughter on a Facebook adoption advocacy group and instantly fell in love. The photo showed her as an infant, her eyes the most piercing silver/blue – and the description included her diagnosis, blindness from…

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  10. BlindNewWorld’s 2017 Holiday Gift Guide

    The holiday season is here – and BlindNewWorld wants to help you figure out the coolest and most accessible gifts for your blind and visually impaired friends and family. From apparel to toys to tech, we’ve compiled eight of our favorite gifts for everyone on your list!         Two Blind Brothers Apparel This clothing company – created by Bradford and Bryan Manning, brothers who were both diagnosed with a retinal disease – pays special attention to the details in each of their garments. Their original collection is uniquely identified with a small metal…

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