Patient Stories with Grey Genetics

Between Worlds: Usher syndrome type III

03.31.2020 - By Grey GeneticsPlay

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When Rebecca Alexander was 12 years old, she had trouble seeing the blackboard. She made her way from an optometrist to an ophthalmologist and was eventually diagnosed with Retinitis Pigmentosa (RP). Her parents were told that she would be blind by the time she was an adult. Rebecca also had a cookie bite of hearing loss. Through high school, she wore her hearing aids as little and as discreetly as possible. It wasn’t until Rebecca was in college that she experienced extreme tinnitus and saw an otolaryngologist that the diagnosis of Usher syndrome became real.

Today, Rebecca Alexander is an award-winning author, psychotherapist, keynote speaker, group fitness instructor, disability advocate, and extreme athlete. She also has Usher syndrome type III, and is almost completely blind and deaf. Her book, Not Fade Away: A Memoir of Senses Lost and Found is being made into a major motion picture. GAP licensed a mantra from her memoir, “Breathe in Peace, Breathe out Fear,” and launched a campaign on International Women’s Day in March 2020, featuring Rebecca as well as another woman with Usher syndrome. The two t-shirts that GAP created have already sold out, but you can see the campaign video here!

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Rebecca Alexander’s website

Buy Rebecca's book: Not Fade Away: A Memoir of Senses Lost and Found

Connect with Rebecca on Social Media:

Rebecca on Twitter: @Reb_Alexander

Rebecca on Instagram: @reb_alexander

Rebecca on Facebook

Resources related to Usher syndrome

Usher Syndrome Coalition 

Usher Syndrome Society

Ava’s voice (in NJ)

The Foundation Fighting Blindness

The Hellen Keller National Center

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