In order to cope with her blindness, Bobbi Lachance turns to writing novels. Lachance recounts her experiences of domestic violence, and how she found a relationship that became real love.

After being bedridden due to a severe workplace accident, Trieste decided to finally come out as a trans woman. Arielle Zionts profiles Trieste's decision to come out, and dealing with her neuromuscular disorder.

Adjusting to life without her mom, Laura Antranigian has had to get used to caregivers assisting her due to her cerebral palsy. Julie Rawe documents how Antranigian copes without her mother and with her condition.

In July 2013, due to degenerative spinal diseases, Jen Pelletier became unable to work and was forced to rely on others for help. Michelle Mitchell profiles Jenn's experiences and her struggle to reclaim independence.

Growing up with educational challenges and being diagnosed with dyslexia at age 34, Anne Donnell is empowered to help her daughter, Gracie, who also has the disability. Stephanie Strauss documents how Anne is raising her daughter to understand and be proud of her dyslexia.

With little left to live for, Andrew started to think about how his life impacts everything around him. Kelsey Nichols documents how Andrew places himself within the time and space he occupies, applying theory into his recovery.

Born with a rare genetic abnormality, Zev's family is helping him overcome his challenges with walking, talking, and eating. Sylvie Douglis documents Zev's learning disability and the efforts his family goes through to help him.

Thalassa Raasch documents the lives of Randy and Sarah Bellavance, a blind married couple. Raasch highlights how the couple live and see their day-to-day lives.

Bill Àjà never thought he could draw. It took a rapid decline in his vision - and a relocation to an independent living facility - to discover an ability, and a source of joy, that he'd had all along.

In need of advanced medical care, Carmen and Lupita Andrade Solis left their homeland in Veracruz, Mexico to embark on a life in the U.S. Sixteen years later they are still one of few pairs of conjoined twins in the world, and, at the age of eighteen, are beginning to consider how to live independently from their family. The girls dream of going to veterinary school and of returning to Mexico to see their relatives, but face the sobering limitations and instability of their current immigrant status.

After being diagnosed with ALS, Mark Bushey is experiencing first-hand how people connect voice to cognitive function. Morgan Springer documents how people perceive Bushey now that his speaking ability has changed due to his ALS.

Leah Schmalz documents the life of Rosa Tapia, a girl has autism. Schmalz highlights how Tapia's foster parents have opted for a homeopathic alternative for treatment to her their daughter.