VISUALIZING THE HUMAN EXPERIENCE OF BLINDNESS.


Welcome to the Blind Canvas Project — we’re dedicated to creating new ways to see, understand, and share the human experience of blindness.

PROJECT MADE POSSIBLE BY /

Ora and Blind Can Film Festival Logos.

It all starts with a conversation.

It’s impossible to fully communicate the experience of living with blindness, but perhaps we can help more people gain a better understanding.

Each participant is invited to sit down for an hour-long interview to discuss their condition, their lives, and their perspective on living with blindness.

Using AI image generation software, we then transform key moments within each interview into expressive works of art.

Through the Blind Canvas Project, we hope to spark new conversations, spread awareness, and encourage all to realize that those who are blind are not defined by their blindness.

STORIES

Ben Fox

Founder of the BlindCAN Film Festival, Ben Fox was the diagnosed with Retinitis Pigmentosa at the age of eighteen and has continued making films as an advocate for the blind community.

RETINITIS PIGMENTOSA

Bill McCann profile picture.

Bill McCann

As founder and president of Dancing Dots Braille Music Technology, as well as a gifted trumpet player and composer, Bill McCann has made music his life’s work.

GLAUCOMA

April and Melissa profile picture.

April & Melissa

April LuFriu and Melissa Escobio are sisters and best friends who do just about everything together, including having retinitis pigmentosa (RP).

RETINITIS PIGMENTOSA

Morten Bonde profile picture

Morten Bonde

Morten Bonde is an artist, author, TEDx speaker, and mindfulness instructor who fundamentally transformed his life and career after being declared legally blind due to Retinitis Pigmentosa.

RETINITIS PIGMENTOSA

Marcus Roberts profile picture

Marcus Roberts

Marcus Roberts is a jazz pianist, composer, arranger, bandleader, and teacher. Hailed “the genius of the modern piano”, Marcus is renowned for his remarkable ability to blend jazz and classical works.

GLAUCOMA

Shardasia Hadley profile picture

Shardasia Hadley

As a recent high school graduate and Tallahassee local, Shardasia Hadley has excelled in her early career thanks to her incredible spirit and support of her family.

ASTIGMATISM / COLOBOMA /
MICROPHTHALMIA / CATARACTS

Will Hollimon profile picture

Will Hollimon

For as long as he can remember, Will Hollimon has been driven by his passion for drumming. Over the past decade, he has played in several bands, putting his natural rhythm and impeccable timing to work.

RETINOPATHY PREMATURITY

Wayne Pearcy

Wayne Pearcy is quickly making a name for himself, one trumpet solo at a time. As a graduate student in Jazz trumpet, Wayne’s ear for perfect pitch and his incredible dedication are only outmatched by his joy for life.

ANOPHTHALMIA

Dave Steele

Dave Steele is an award-winning poet, author, speaker, singer and advocate for the blind. Diagnosed with Retinitis Pigmentosa (RP) in 2014, this genetic eye condition left Dave severely sight impaired.

RETINITIS PIGMENTOSA

Craig Ellis

Blindness advocate Craig Ellis has devoted himself to empowering the blind since joining East Texas Lighthouse in 2011, aiming to restore independence and confidence to individuals with visual impairments, serving as a beacon of hope in their lives.

WET MACULAR DEGENERATION

Raquel Alim

Raquel Alim is the Vice President of Foundation Fighting Blindness, San Diego, as well as a dedicated painter and blindness advocate.

RETINITIS PIGMENTOSA

Steven McCoy

As the world’s first blind, deaf, black journalist, Steven McCoy is also an entrepreneur, talk show host, writer, producer, and philanthropist with a goal to inspire the next generation with his story.

USHER’S SYNDROME

Rusty Perez

Rusty Perez is a talented singer, songwriter and musician. Rusty’s original music can be found on all streaming services and some of his music has been used in short films and on TV shows such as The Young & The Restless.

RETINITIS PIGMENTOSA

Ricky Ruzicka

Ricky Ruzicka was diagnosed with Leber’s Hereditary Optic Neuropathy at the age of 23. He has many outlets of joy in his life, including the vision-impairment oriented game of goalball, and most importantly, his loving wife of eight years.

LEBER’S HEREDITARY OPTIC NEUROPATHY

Alayna Lopez

Alayna Lopez, film student at Ohio State University, does not let her retinitis pigmentosa diagnosis interfere with her zest for life.

RETINITIS PIGMENTOSA

PROJECT MADE POSSIBLE BY

Ora Logo and Blind Can Film Festival Lockup

For Ora, this project represents our heart, as our patients are at the center of how we partner with pharmaceutical and medical device companies to bring new therapies to market. Helping them is why we do what we do every day, from our clinical trial execution to working with companies to gain new product approvals. As leaders in clinical research, Ora has a crucial responsibility to understand patient experience, and to bring that understanding to our customers and colleagues.