For decades in Toledo, Ohio, Lott Industries has excelled at manufacturing small car parts. All 1,200 Lott employees have developmental disabilities, yet the company competes with traditional non-disabled businesses and achieves the highest quality ratings. When the US auto industry crisis hits, however, Lott's market is wiped out and president Joan Browne has 12 months to reinvent or close the doors. For the workers, the stakes are even higher since their jobs are a refuge, not only from the impoverishment that affects the majority of America's disabled, but from social isolation. For employees Kevin, Wanda and T.J., work is more than just a direly needed paycheck, it's a lifeline, a symbol of their dignity, and their dreams made real. The race to find a new business plan drives this engrossing recession economy drama, but it's the humanity the film restores to the balance sheet that makes A Whole Lott More such a rare achievement. Written by Myrocia Watamaniuk
Yu Xiuhua was raised to hope for little from her life in the rural Chinese province of Hubei. At 19, Xiuhua’s mother encouraged her to marry a man nearly twice her age, fearful no one else would accept a wife with Xiuhua’s condition — cerebral palsy. But as her 20th anniversary approaches, Xiuhua’s poetry goes viral, and she becomes the voice of a rising feminist movement throughout China.
Segregation, abandonment, and the meaning of home are discussed by the people that lived in, worked at, and crusaded for one of the largest and oldest Intellectual and Developmental Disability Institutions in the United States. The facility, in its closing, challenged society's perception of those with intellectual disabilities and ultimately fought for better rights.
Faced with a traumatic injury that renders you permanently disabled; how would you reinvent yourself? Full Circle tells the story of Trevor Kennison and Barry Corbet’s shared resiliency and refusal to let their passion for life be limited by Spinal Cord Injury. It is an unblinking examination of the challenges of Spinal Cord Injury, and a celebration of the growth that such tragedy can catalyze.
Sign The Show: Deaf Culture, Access and Entertainment is a feature-length documentary providing insight into Deaf culture and the quest for access to entertainment. It brings together entertainers, the Deaf and Hard of Hearing (HOH) community, and American Sign Language interpreters to discuss accessibility at live performances in a humorous, heartfelt, and insightful way.
Art, activism and disability are the starting point for what unfolds as a funny and intimate portrait of five surprising individuals. Director Bonnie Sherr Klein (Not a Love Story, and Speaking Our Peace) has been a pioneer of women's cinema and an inspiration to a generation of filmmakers around the world. SHAMELESS: the ART of Disability marks Klein's return to a career interrupted by a catastrophic stroke in 1987. Always the activist, she now turns the lens on the world of disability culture, and ultimately, the transformative power of art.
As Daniel Radcliffe's stunt double in the Harry Potter films, David Holmes' work has been seen worldwide by millions of people. Tragically an on-set accident ended what David calls "the best job in the world," leaving him paralyzed. Like the on-screen character he helped bring to life, David is determined to continue seeking adventure and living life to the fullest despite mounting obstacles.
Being alive and having a life are two different things for Ville Jaaranto. Freedom as his dream and equality on his agenda, he sets to travel across Europe by his power wheelchair. While on his journey, he comes to realize that neither he himself nor the world around him are quite ready for it. Crazy dreams are the best cure for a mundane life.
Adam Pearson - who has neurofibromatosis type 1 - is on a mission to explore disability hate crime: to find out why it goes under-reported, under-recorded and under people's radar.
Aging parents of disabled adults, they worry about their child's life after their disappearance. A moving insight into the daily life of a family home in the Vendée region, which offers them the prospect of a peaceful future.
Sima Shimony, age 69, embarks on a mission to find her friends and staff from the "ALYN" Institute for Children with Disabilities, which was situated in the secluded San-Simon monastery in Jerusalem, during the 1960s. Armed with a small camera attached to her wheelchair, she sets off on a journey across the country together with her friend Pini Newirth, also a polio child, to unfold and reclaim the story of the children affected by the Polio epidemic. In a futile attempt to rebuild their bodies so they could walk, the children were subjected to excruciating medical procedures with no parents or family at their side. But growing up together forged a group of remarkable, self-driven women and men with disabilities who eventually launched the Disability Rights movement in Israel.
Doglegs is a cheerfully iconoclastic underground scene where the disabled battle the able-bodied - all in the name of exploding stereotypes. When the disabled champ seeks life and love beyond the ring, his idol, the able-bodied organizer, tries to sabotage his bid for independence. In a battle of the human spirit, can the power of disability win our hero his dreamgirl?
"letters to eleanore" is a poignant feature-length documentary that explores the intertwined journeys of two remarkable girls, Keith from Canto Grande in Lima, Peru, who bravely navigates life with cerebral palsy alongside her devoted mother, and Olivia from Litchfield, Minnesota, whose experiences highlight the stark contrasts in societal attitudes towards disability in their respective countries. As their narratives unfold, they are beautifully interwoven with the legacy of Eleanore and her family, whose life, untimely death, and the impact of her wheelchair ignited a powerful movement of hope for countless children and their families facing similar challenges. This film is not just a story of perseverance and love; it is a testament to the strength of community, brought to life through the collaborative efforts of volunteers, students, and communities across Peru and the United States, embodying a true grassroots style of storytelling that resonates with authenticity and compassion.
A documentary telling the remarkable human story of Stephen Hawking. For the first time, the personal archives and the testimonies of his closest family reveal both the scale of Hawking's triumphs and the real cost of his disability and success.
Martinez's second feature documentary assembles a theatre group of deaf actors in order to portray their lives and at the same time avoid any pedagogic representation of the non-hearing people. Coming from different environments and provinces, la troupe has to overcome various difficulties to put on stage their last play, hoping to attract an audience beyond the Argentine deaf community.
A professional company of actors with disabilities defies expectations by taking center stage in Chicago the musical.
Elite athletes and insiders reflect on the Paralympic Games and examine how they impact a global understanding of disability, diversity and excellence.
As a visibly disabled person, filmmaker Reid Davenport is often either the subject of an unwanted gaze — gawked at by strangers — or paradoxically rendered invisible, ignored or dismissed by society. The arrival of a circus tent just outside his apartment prompts him to consider the history and legacy of the freak show, in which individuals who were deemed atypical were put on display for the amusement and shock of a paying public. Contemplating how this relates to his own filmmaking practice, which explicitly foregrounds disability, Davenport sets out to make a film about how he sees the world from his wheelchair without having to be seen himself.
‘Voices from the Shadows’ shows the brave and sometimes heartrending stories of five ME patients and their carers, along with input from Dr Nigel Speight, Prof Leonard Jason and Prof Malcolm Hooper. These were filmed and edited between 2009 and 2011, by the brother and mother of an ME patient in the UK. It shows the devastating consequences that occur when patients are disbelieved and the illness is misunderstood. Severe and lasting relapse occurs when patients are given inappropriate psychological or behavioural management: management that ignores the severe amplification of symptoms that can be caused by increased physical or mental activity or exposure to stimuli, and by further infections. A belief in behavioural and psychological causes, particularly when ME becomes very severe and chronic, following mismanagement, is still taught to medical students and healthcare professionals in the UK. As a consequence, situations similar to those shown in the film continue to occur.
A documentary on assisted suicide, authored by actor and disability rights activist Liz Carr.