19-year-old Gabe Adams was born with Hanhart syndrome, a rare medical condition characterised by underdeveloped limbs, mouth and jaw. In Gabes case, none of his limbs grew at all. At school Gabe tried out for the dance team as a way of making friends discovering he could use his limbless body to his advantage in the art of break dancing. After graduating from high school he has continued to prove his independence, moving out of the family home and embarking on a career as a motivational speaker. From a young age Gabe started using a wheelchair but his parents were determined that their son would be as independent as possible. At school Gabe would wedge a pencil or pen between his shoulder and cheek to write in class. The day of the dance tryouts they called us all in a line and they said, okay dancer remember to full out extensions and point your toes. What am I gonna point? My nose!? I am just standing there in front of the judges and then I see girls do the spins and I am like, I can do that, so I do the spins. The next day at school and I hear two girls talking behind me and they say: They are only gonna put him on the stage because he is handicappedand that crushed me. I ran to the dance coach and I said please do not put me on the team because you feel sorry for me, and she said: I would not put you or anybody else on the team because I felt sorry for them, you get a spot on this team because you deserved it. And that was just a huge opening moment for me.