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Displaying 101–110 of 160
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Oct 15, 2020
Maeva’s Independence With Her White Cane
We’re celebrating White Cane Awareness Day with spirited 5-year-old Maeva, who is an independent explorer thanks to her white cane.
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Oct 5, 2020
The Dutterers Aren't Afraid to Share Their Story
Steve and Dot Dutterer have kind and approachable personalities that captivate everyone they meet. With their expansive network, and a lot of hard work and dedication over the past 19 years, Steve and Dot have raised more than $743,000 for the Foundation through the Baltimore VisionWalk.
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Jul 6, 2020
Tracy was the fourth generation of his family to receive the diagnosis of retinitis pigmentosa, but he never let that stop him from dreaming big. Tracy has worked at NASA’s Johnson Space Center for over 36 years, making significant contributions over the many years.
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Jun 15, 2020
Jumping into an Uncharted Arena
Thirty-one-year-old Wren Blae Zimmerman always loved horses. But it wasn’t until a few years ago that Wren finally learned to ride. Now her life revolves around this equestrian dream, and she’s given herself the title of the “Blind Show Jumper.”
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May 27, 2020
Lulie Gund: Beloved Philanthropist, Role Model and Confidant
Llura Gund, often referred to as Lulie, was known for her infectious kind smile and love of life.
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May 26, 2020
How To Qualify For Social Security Disability Benefits With Vision Loss
A guide to receiving Social Security Disability Benefits if you have vision loss or are legally blind.
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May 18, 2020
Allen has always wanted to be known as an artist, first and foremost. His photography hints at the ever-changing nature of people’s lives and their environment, much like his own progression with retinitis pigmentosa (RP).
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Apr 20, 2020
Coping with COVID-19: Welcome to the “New Normal”
We checked in with a few of the Foundation’s volunteers to get their perspective on these unprecedented times.
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Apr 13, 2020
Sue Lives Life to the Fullest and Wants to Help Others Do the Same
Meet Sue Sanger. Sue was diagnosed with retinitis pigmentosa (RP) at the age of 29 but has continued to travel, advance in her legal and political career, and more. In the following story, Sue explains, in her own words, all she has accomplished since learning she has RP and why she’s a supporter and member of the Foundation Fighting Blindness Legacy Society.
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Apr 6, 2020
Carolyn is a business professional and beauty industry leader in Raleigh, North Carolina. In spite of her diagnosis with retinitis pigmentosa, Carolyn pursues exactly what she wants and knows what she is purposed to do in her life.