Celiac Canada is a national charity dedicated to supporting individuals in Canada living with celiac disease and gluten-related disorders through advocacy, education, and community engagement.

Cystic Fibrosis Canada is the national charity dedicated to improving the health and well-being of Canadians living with cystic fibrosis by advocating for access to medicine, funding research, and providing community support.

Canadian Hearing Services provides trusted solutions and support for Deaf and hard of hearing Canadians, including hearing tests, interpreting services, and free support programs.

The Canadian Hemochromatosis Society provides information, support, and community for individuals and families affected by hereditary hemochromatosis, promoting awareness and early diagnosis of this genetic disorder.

The Canadian Hemophilia Society advocates for individuals with hemophilia and other inherited bleeding disorders, providing education, support, and resources to improve their quality of life.

Immunodeficiency Canada Network is a community-driven organization dedicated to supporting individuals and families affected by primary immunodeficiency disorders through advocacy, education, and resource sharing.

Liver Canada is dedicated to improving liver health through research funding, education, and support for those affected by liver disease.

The Canadian Organization for Rare Disorders advocates for health policy and a healthcare system that supports individuals and families affected by rare disorders in Canada.

The PBC Society Canada supports individuals affected by Primary Biliary Cholangitis (PBC) by providing resources, information, and community engagement opportunities to help manage the disease.

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The Canadian MPS Society supports individuals affected by Mucopolysaccharidoses (MPS) and related diseases by providing information, resources, and advocacy for better health outcomes.

The Canadian Stuttering Association supports individuals who stutter by promoting awareness, providing resources, and fostering a community for advocacy and support.

The Canavan Foundation focuses on preventing childhood genetic diseases, specifically Canavan disease, through education, screening, and support for affected families.

The Canavan Research Foundation funds and supports research to cure Canavan Disease and aims to develop therapies for other genetic brain diseases.

Canavan Research Illinois is a nonprofit organization dedicated to supporting medical research for Canavan disease, a rare genetic neurological disorder, and provides networking opportunities for affected families.

Cancer Care provides support, counseling, education, and financial assistance to individuals affected by cancer, helping them navigate the emotional, physical, and financial challenges of a cancer diagnosis.

Cancer Commons is a nonprofit organization that provides personalized action plans and expert guidance for metastatic cancer patients, helping them navigate treatment options and access clinical trials.

Cancer Hope Network provides personalized support and connections for individuals facing cancer by matching them with trained Peer Mentors who have similar experiences.

Cancer Research UK is dedicated to funding research and providing support for individuals affected by cancer, offering resources such as information on symptoms, screening, and a moderated forum for sharing experiences.

Canine Companions provides highly trained service dogs to children, adults, and veterans with disabilities, including those with insulin-dependent diabetes, to help them live with greater independence.