Vision, Voice, Vibes: Laisha Gonzalez on Vision Loss

Posted by The Newsette

After moving from the Dominican Republic to New York, Laisha Gonzalez faced a new language, a new country, and the realities of vision loss due to lupus. With help from Lighthouse Guild and Educational Vision Services, she gained the tools and confidence to thrive. Now a recent grad, artist, and mentor, Laisha shares how embracing her identity and a strong support system helped her find her voice on and off the stage.

Can you tell us a bit about your journey with vision loss?
I’m originally from the Dominican Republic, and at first, we didn’t know my vision loss was caused by lupus. We just thought I needed glasses. When I moved to the U.S. and was properly diagnosed, the term “legally blind” was hard to accept. I didn’t want to be labeled that way. But starting school here and working with an amazing team, including my mom and local vision support services, helped me find confidence in my identity.

What was the transition like, moving to New York?
It was a big shift… new language, new school, new diagnosis. But I’m grateful to have access to resources here. In the DR, I don’t think I’d have been able to achieve what I have now.

How did Lighthouse Guild and Educational Vision Services help you adjust?
Lighthouse Guild was recommended by my high school team. They helped me prepare for college with mobility training, digital tools, and even cooking lessons. I also received counseling, which really helped after COVID. Most recently, I joined Lighthouse Guild’s Tech Pals program, where I taught seniors with vision loss how to use phones and screen readers. I learned just as much from them as they did from me. The organization has truly shaped who I am today.

Was there a skill that helped you feel most independent?
Definitely assistive technology—screen readers, specifically. I use VoiceOver on my phone and computer constantly. It’s such a vital part of how I live day to day.
You recently graduated from Bronx Community College. What inspired your path in performing arts? In the DR, being an artist didn’t seem like a viable option. But once I moved to New York, I met people, like my theater club teacher, a Juilliard grad, who showed me it was possible. I’ve always loved performing, and when I stepped on stage for the first time here, it just felt right.

What advice would you share with others navigating vision loss?
Don’t be hard on yourself. Give yourself grace. The world isn’t built for people with disabilities, so every step takes effort. It’s okay to feel overwhelmed, but know that you’re not alone. Some people’ve got your back, even if you don’t feel it yet.

What’s next for you?
I have two concerts coming up, and I’m also working as a social media coordinator for the theater company I perform with. I want to keep growing, learning, and doing what I love—on stage and off.