Two people with rare medical conditions meet and spend a week together to share their experiences, hardships and triumphs in this series, which begins with two boys who have a painful muscular disorder called Schwartz Jampel syndrome.
Two women with a skeletal disorder called Jarcho-Levin Syndrome, which is characterized by malformations in the spine, ribs and thorax, share their experiences and hardships.
Kids with a facial deformity called Goldenhar Syndrome share stories of being bullied for their appearance and their feelings of isolation from their peers.
Two adults with a skin condition known as Lamellar Ichthyosis, typified by dark, plate-like scales covering most of their bodies, begin a life-changing friendship.
Three children, including 7-year-old twins, with Ectodermal Dysplasia, a group of conditions that can affect the development of the skin, hair, nails, teeth or sweat glands, share their experiences and hardships.
Two women with a genetic bone disorder called Osteogenesis Imperfecta, or brittle bone disease, share their experiences and go on a seemingly impossible trip.