Molly Watt born without hearing and later diagnosed with Usher syndrome resulting her being registered deafblind explores the notion of whether you are ever fully seen by society. Company Director and co-founder of Molly Watt Trust charity and now international Ambassador/ Advocate she shares her drive of living with her diagnosis, embracing technology to find her place in the world around her.
Those excluded understand inclusion, like no other
My name is Molly Watt, 22 years old. I was once written off by society! However, today I am a tech/web, accessibility and usability consultant, a motivational speaker, author, illustrator, blogger, International Ambassador/Advocate. Company Director, co-founder of Molly Watt Trust charity. Oh did I mention I’m deafblind.
