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  1. 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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  2. 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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  3. 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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  4. 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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  5. 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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  6. 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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  7. Marvelous Adventures with Marly and Aerie

    My name is Juliet Cody. I am an immigrant from Colombia. When I was a child, to stay in touch with our strong ties to the tropical beaches of the Caribbean, my parents moved our family to the beautiful beaches of Southern California, where I still reside. I have a daughter, and taught pre-kindergarten until blindness struck. Despite this unexpected life event, I chose not to sit in the dark. Instead, I turned on the light of independence – I became involved in the blind community and returned to school…

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  8. Raising My Blind Daughter in India

    My daughter is blind. She is also funny, cuddly, silly, a lover of music, and has the cutest laugh. Her blindness isn’t the first thing I think about when I am asked about her. It is a part of her, but not something that defines her. We live in India and tend to stand out wherever we go; the white woman dressed in Indian clothing with the brown 4-year old holding a cane. It frustrates me when people wait until I look to the side, and then rush to snap…

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  9. An Early Arrival

    It is amazing when you hear a miraculous story over and over again how ordinary it becomes. It is like a song that is played repetitively on the radio – you can’t wait to hear it, but then it is requested constantly so it doesn’t seem quite as special anymore. I cannot count the number of times I have heard about my birth. It was told to me so many times that I almost believe I was there to experience the whole thing as an observer! I was born premature,…

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  10. Inclusion

    I’m a mother to my 17-year-old daughter. She lost her sight 3 ½ years ago to a brain tumor. I have watched her work hard to gain the physical skills necessary to function independently in a sighted world. I have watched her learn and practice the reading and technological skills necessary to participate in school and future professions. The hardest thing to watch is her social struggles. She can do her part, but it requires another willing participant to have a conversion, let alone a relationship. I saw BlindNewWorld and…

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