For many with facial difference, life can be difficult. We meet Canadians who open our heart and eyes to what it’s like to live with a face that looks different.

This episode give us a heartwarming and candid view into the lives of people with Down syndrome, from dating to work and the importance of hugs.

Little people face social stigma and curiosity. In this episode, we meet people from different backgrounds who explain what it is like to live in a world that sees them as disabled.

Through accident, illness or birth, people with limb differences receive a lot of attention. That can be annoying ... and offer an opportunity for raising awareness.

This episode answers questions about what it is like to navigate the world without sight, and the answers are enlightening.  

Often mocked and stigmatized for their disability, Canadians with Tourette syndrome candidly answer questions about what life is like living with what is mistakenly called “the swearing disease.”

We meet Canadians from across the country who reveal what it’s like to be a wheelchair user. They candidly reveal the challenges, frustrations and some surprising benefits.

People on the autism spectrum face stigma and judgment, often because it shows no outward signs. Our panelists discuss what it feels like to be on the spectrum.