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  1. My Vision for a Better Boston

    When I was really young, I knew I was going to grow up to be the next great Boston sports athlete. I was thinking Mo Vaughn or Drew Bledsoe. Mind you, this was back when we loved our teams but they never won anything. My dreams changed when I was eight years old and I began to lose my vision. It started in my left eye, then moved to my right. By the time I reached middle school, my dream of playing professional sports came to a sharp end. For…

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  2. Breaking Down Barriers to Become a Blind Scientist

    I have always been so curious about how the world works. I remember I had a keen mind for deduction even when I was a young kid, listening to audiobooks of Sherlock Holmes. The detective said he could tell the height of a person by listening to his or her footsteps. I became more inspired and more interested in science by watching The Magic School Bus and Bill Nye the Science Guy and then by the work of Marie Curie and my mentors throughout my journeys. I loved all I…

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  3. Attention and Action: My Campaign to #EndAbleism

    My name is Olivia, and I’m the founder of Attention and Action, an international movement to raise awareness around the barriers and inequalities people with disabilities face in society. This week, from January 11th to the 16th, we are running a campaign called #EndAbleism to raise awareness about how ableism affects people with disabilities, spark discussion and put an end to it. #EndAbleism is open to all ages – we want to get people talking about ableism and to work toward collective action to end it. We’re asking participants to…

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  4. #MyBlindStory 2020: Reflecting on this year in the #BlindNewWorld

    What a year, huh? The good news is that, even with everything that’s happening out there in the real world, we have a strong, supportive community to help us keep it together and keep going here in the #BlindNewWorld. As always, we wanted to take an opportunity to reflect on and highlight all of the incredible stories that have been shared with us this year. 2020 brought us personal insight from artists, musicians, athletes, innovators, actors, scientists, content creators, professionals, bright young adults, chefs, rock-star parents – as well as…

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  5. We’re Bad Blind Moms and We Know It!

    I’m Stacy Cervenka – and I’m a Bad Blind Mom. From the moment I found out I was pregnant with my first child, I’ve pretty much been a hot mess. Between three complicated pregnancies, several years of 2 a.m. feedings, dragging the kids around on public transportation to endless school and community activities – all while working full-time – I don’t think I’ve had a decent night’s sleep in eight years. Also, the fact that my husband and I are both blind has not exactly made the journey more convenient….

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  6. A Lifelong Love of Sports Leads to Building Beautiful Lives

    My name is Bryce Weiler. I was born almost four months premature, and shortly after my birth – due too much light or oxygen in the hospital – I developed an eye condition called retinopathy of prematurity, which caused me to become blind. Today, I’m the cofounder of The Beautiful Lives Project, a nonprofit that helps people with disabilities across the United States live their dreams in sports, performing arts, visual arts, nature and more. A Lifelong Love of Sports… During my time at the University of Evansville from 2010 through…

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  7. Why Braille Books Matter – for Blind Kids and Sighted Kids

    My name is Jared. I was born blind with no useful vision. Today, I am employed full-time as a Senior Software Engineer – a job I couldn’t do if I hadn’t learned braille. I am also married and a father to two young children, both of whom are sighted. Because I can read braille, I am able to read them bedtime stories and pass along to them my love for the written word. My parents and teachers deserve much of the credit for my being braille-literate today. They insisted that…

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  8. Becoming a Bad Blind Mom (and Why it’s a Good Thing)

    When I was 22, my senses narrowed to four; and really, my sense of smell has never been that great, so, it became more like three senses. And crikey, what’s a girl to do? Several infections slammed my body simultaneously. I was expected to die, but as all my independent ladies can attest to, we tend to be survivors. Sitting among family and friends, I became a brave soul and was often eulogized. With raised brows, I said, “Sure,” and sauntered towards my future. The future was unclear, a bit…

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  9. Aniridia, Acceptance and Building the Live Accessible Community

    As a young, shy girl with a visual impairment, I felt isolated and alone in crowded school hallways. I questioned my worth and was surrounded by self-doubt. There are so many stories of blind people not only succeeding at life, but thriving – yet I felt ostracized, incapable, unaccepted and lost. I grew up with aniridia syndrome alongside my sister, father and grandmother – all of whom also had this hereditary condition. My brother was totally deaf, though fully sighted. My mom was the only one without a disability. I…

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  10. Blind, But Not Beaten

    At the age of around 18 months, my parents rushed me to the doctor after I fell down a flight of 30 steps. I was diagnosed as being blind as the result of a rapidly growing brain tumor. I had surgery and the tumor was successfully removed—I would live, but I didn’t escape unscathed. Besides being blind, I had no sense of smell, and no endocrine system, which meant that I had no thyroid, no adrenal function and the list goes on. It could have been much worse. It was…

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