I have dyslexia, diagnosed at the age of nine with two separate forms. Reading was incredibly difficult, but I learned to adapt. And I refuse to let it label me as something I'm not.
When people learn that I have dyslexia, it often comes as a bit of surprise. I am a writer and a professional editor, after all. I spend a lot of time behind the computer or with my nose stuck in a book. So, it's not totally out of the realm of possibility that someone would question my career choice when they hear the truth about my history.
There is still a lot of negative stigma surrounding dyslexia, but what people don't realize is that the majority of the people on the planet have one form or another of dyslexia—but they just don't know it.
For most people, their form is so weak that they were able to easily compensate. However, for approximately 15% of American children [1], for 30 to 50% of prisoners around the world [2], the dyslexic forms are severe enough to cause significant issues.
Today, a friend of mine, Beth Beamish, released a book about what it's like to be a parent of a dyslexic child, with practical advice on how parents can help their children through this.
Dyslexia is not a disease. It's just a different way of seeing the world.
To help Beth Beamish spread the word about her book, I thought it might be a good idea to share my own story, highlighting that having dyslexia doesn't stop you from following your dreams, whatever those dreams might be.
