The Fight: Science Against Cancer

How far have scientists advanced toward solving the riddle of cancer, and what are the key problems now facing them? To explain the enormous complexity of the problem, the film traces briefly the growth and multiplication of a single fertilized cell into an adult man, and asks why some outlaw cells begin persistent growth after the whole body has reached maturity. Research scientists are shown following up clues with test tube, microscope, controlled diets and other aids that may guide them to the eventual solution. Methods of treatment being used meanwhile for different types of cancer are briefly described. As each new aspect of the disease is revealed, the secret of cancer is seen to be as complex as the universe itself, and the quest for its solution one of the greatest adventures on which a scientist can embark.

This short film offers a thorough account of science's battle against cancer. Animated sequences depict the growth and multiplication of cells in both healthy and cancerous developments. Live-action dramatizations follow a patient with a cancerous growth as he seeks treatment in a medical research facility. Dominant issues and actions in cancer research and treatment are covered in detail.

This documentary introduces us to Stephen Jenkinson, once the leader of a palliative care counselling team at Toronto's Mount Sinai Hospital. Through his daytime job, he has been at the deathbed of well over 1,000 people. What he sees over and over, he says, is "a wretched anxiety and an existential terror" even when there is no pain. Indicting the practice of palliative care itself, he has made it his life's mission to change the way we die - to turn the act of dying from denial and resistance into an essential part of life.

This documentary is about Edmonton filmmaker Joe Viszmeg and his battle with cancer. In 1991, Viszmeg was diagnosed with adrenal cancer and told he wouldn’t live through the year. Four years later, he made In My Own Time—Diary of a Cancer Patient. In My Healing Journey: Seven Years with Cancer, he tells the story of how he survived the roller coaster of a deadly disease. He died in 1999.

In a moving conversation with Dr. Balfour M. Mount, friend, colleague and treating physician, cancer victim Jean Cameron, a one-time volunteer social worker in the Palliative Care Unit of Montréal's Royal Victoria hospital, discusses how she has come to terms with her own illness and the perspective it has given her on the meaning of life. What she has to say is relevant to all. The depth of her insight and the grace of her being leave viewers moved and open to thinking more carefully about the meaning of their own lives.

This feature documentary is a portrait of Robert Coley-Donohue a man living with ALS or Lou Gehrig's disease, a fatal degenerative neuro-muscular disease that strikes two in 100,000 people. The film follows Robert over the last 3 years of his life. His experience is arduous, but also filled with hope and healing. If, like Robert, we can face death with grace and the comfort of family and friends, then death will hold less fear.

This documentary tells the story of Joseph Viszmeg, an Edmonton filmmaker who was diagnosed with a rare form of adrenal cancer in 1991. Doctors gave him a year to live, but 4 years later Viszmeg is very much alive. This is his personal account of living with this disease.

Sometimes Paul Oliver has to laugh to keep from crying. He's placed his mother, Jean, in a nursing home that cares for Alzheimer's patients. With bewildered fellow residents constantly interrupting and Jean's own erratic behaviour, Paul finds it hard to have a quiet moment with his mother. Yet he knows that his company and attention are vital to her.

Like all of the heroes in the Caregivers series, Paul is doing his best. Although he works full-time and lives an hour away, he still visits twice a week. Jean does not like the nursing home and she is often depressed. Her anger is vented on anyone near, including Paul. At other times Jean can be lucid and make Paul laugh with her sharp comments about fellow residents.

Produced with the help of individual caregivers and community agencies, this is a 'how-to' series with soul. Shot over the course of a year, these five episodes immerse you in the joys and sorrows of providing care. The caregivers featured in the series are honest and open about their feelings--and their eloquent insights offer an assessment of our health-care system's strengths and weaknesses.

What Paul finds most difficult is his mother's increasing memory loss. He's aware that, in time, she won't remember him at all, and he's determined to make the most of his visits. As Paul says, 'I try to make her laugh. I try to make whatever length of time she has left enjoyable.'

When she was a student nurse, Pat Tucker received training in bedside care. Today, she puts those skills to good use in caring for her mother. Molly, 95, is confined to her bed for most of the day and requires round-the-clock attention. Like all of the heroes in the Caregivers series, Pat offers loving and conscientious care. Despite her nursing experience, she nevertheless feels exhausted by the incredible demands of looking after Molly.

Pat acknowledges the support of her family--especially her husband; she knows that without their help, she would be hard-pressed to carry on. At Molly's 95th birthday party, we see just how important this charming "wee soul" is to all the people who love her. Even if she's too frail to blow out the candles, Molly is still the link that keeps this family together.

Produced with the help of individual caregivers and community agencies across Canada, this is a "how-to" series with soul. Shot over the course of a year, these five episodes immerse you in the joys and sorrows of providing care. The caregivers featured in the series are honest and open about their feelings--and their eloquent insights offer an assessment of our health-care system's strengths and weaknesses.

When Molly eventually dies, Pat is devastated. But through her tears she is clear about one thing: she would do it all over again. "Memories," she says, "last longer than dreams."

The strain of caring for his mother shows in the face of Kurt Weitz. He's alone, with no family available to help him provide the constant supervision she requires. Elizabeth, 88, suffers from a variety of illnesses, including Alzheimer's. Her dementia drains Kurt of all his energy. Even ordinary housework seems overwhelming.

However, like all of the heroes in the Caregivers series, Kurt carries on. Just before Kurt's father died, he left his son simple instructions: "Take care of mum." For eight years, Kurt has been doing his best to respect his father's whishes--but as Elizabeth only gets worse, he clearly needs some relief.

Produced with the help of individual caregivers and community agencies, this is a "how-to" series with soul. Shot over the course of a year, these five episodes immerse you in the joys and sorrows of providing care. The caregivers featured in the series are honest and open about their feelings--and their eloquent insights offer an assessment of our health-care system's strengths and weaknesses.

Elizabeth cared for Kurt most of his life, and this son's love for his mother is obvious. Yet when Elizabeth dies, he admits to a strong sense of freedom. Kurt's mixed feelings are in fact common to everyone who faces the emotional challenges of caregiving. As he says, "I hate to say it, but the relief off my shoulders is just tremendous."

This short documentary journeys into the spiritual world of traditional Indigenous medicine, a world inhabited by Dr. Mary Louie (a spiritual leader of the Syilx or Okanagan Nation), and her husband Ed Louie. With a lifetime of experience in the ways of spirituality, they are committed to practices that keep them accountable to the spirit world, their people, and Mother Earth. When one of the crew members get sick while shooting, his subsequent care is recorded for the purposes of this film.