Colorectal Cancer Association of Canada (CCAC) is dedicated to increasing awareness of colorectal cancer, supporting patients, and advocating for population-based screening and timely access to effective treatments.

CCAC is a national non-profit organization comprised of volunteers, members, and management led by a board of directors. An expert medical advisory board made up of top health care professionals in the field of colorectal cancer, provides counsel to the CCAC to ensure members are kept up to date on the latest medical advances in the diagnosis and treatment of the disease.

The mandate of the CCAC is threefold: awareness, support, and advocacy. It carries out a wide variety of awareness and education events throughout the year to increase the profile of colorectal cancer in Canada and educate the public.

As a patient-based organization, CCAC recognizes the needs of those diagnosed with colorectal cancer and their families. Compassion, knowledge and understanding are offered through support groups across the country, connecting patients, survivors, and caregivers.

CCAC works to inform key decision-makers of the two biggest concerns for colorectal cancer prevention and care in Canada: nation-wide screening and patient access to effective medical treatment. The CCAC interacts with politicians and remains committed to making sure that patients`rights are heard as issues evolve.

CCAC became UICC full member in March 2008.