RESOURCES

Patient Resources

Rx Connect Specialty pharmacy provides direct links to useful resources for patients and healthcare professionals seeking information relative to disease states and organization(s) to which our patients can register. Rx Connect will assist in registering all new patient to organizations that can provide educational resources relative to a particular condition.

Asthma is a long-term lung condition, that cause difficulty in breathing Asthma, we have listed a range of resources and organizations with up-to-date asthma information to help you better understand and manage your asthma, and to help support people living with asthma.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

 

Asthma Canada

Asthma Canada is the only national, volunteer-driven charity, solely devoted to enhancing the quality of life for people living with asthma and respiratory allergies. For more than 40 years, Asthma Canada has proudly served as the national voice for Canadians living with asthma. We empower patients with evidence-based information, education programs and support asthma research in Canada. Our vision at Asthma Canada is a future without asthma.
Website: https://www.asthma.ca/
Contact:acma@asthma.ca

 

The Lung association

BREATHING PASSION AND COMPASSION. Our reason for being can really be summed up in one word: Breathe. It’s what unites us. It’s what inspires us. And it’s what keeps our community of physicians, scientists, clinicians, educators, administrators, volunteers and donors so committed— whether it’s searching for cures to lung diseases, teaching kids about the dangers of tobacco, or fighting for clean air. The Lung Association is the leading organization in Canada working to promote lung health and prevent and manage lung disease. We do this by funding vital research, pushing for improved treatments, smarter policies, or supporting patients in managing their health.
Website: https://www.lung.ca/
Contact:1-888-566-LUNG (5864)

 

CANADIAN ALLERGY, ASTHMA, AND IMMUNOLOGY FOUNDATION

The Canadian Allergy, Asthma, and Immunology Foundation (CAAIF) is a non-profit organization founded in 1995, to improve the quality of lives of Canadians by supporting allergy, asthma and clinical immunology research. Asthma is the third-most common chronic disease in Canada, affecting approximately three million Canadians. It is the most common chronic disease among children and the leading cause of children’s emergency department visits and hospitalizations.
Website: https://www.allergyfoundation.ca/
Contact: info@caaif.ca

Cardiology is concerned with the prevention, investigation, therapy of, and research into, disease involving the cardiovascular system, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with cardiac disease.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Cardiovascular Society

In 1947, it began with three doctors who pondered the idea of creating a group of specialized individuals who could collaborate, learn from each other and talk to each other.

Today, the Canadian Cardiovascular Society™ is over 2000 members strong. We are known nationally and internationally by cardiovascular healthcare professionals for the Canadian Cardiovascular Congress (CCC), the CCS Angina classification system, the pan-Canadian Access to Care Benchmarks for the entire continuum of cardiovascular care, and the development of Canadian recommendations for the diagnosis and treatment of heart failure – just to name a few.


Website: https://www.allergyfoundation.ca/
Contact: info@caaif.ca

Dermatology is the branch of medicine dealing with the skin, nails, hair and its diseases, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with skin conditions.

Note: ) Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Skin Patient Alliance

The CSPA is a national non-profit organization dedicated to advocate, educate and support Canadians living with skin diseases, conditions and traumas.

Our mission is to promote skin health and improve the quality of life of Canadians living with skin conditions*, diseases and traumas. We advocate for best treatment options for all skin patients; we educate on a variety of issues affecting these patients; and we support the members of our Affiliate organizations (www.canadianskin.ca/about-us/affiliates) who work specifically on their disease areas such as acne, scleroderma, melanoma and psoriasis.

Website: www.canadianskin.ca/en/
Contact: info@skinpatientalliance.ca

Canadian Association of Psoriasis Patients (CAPP)

The Canadian Association of Psoriasis Patients was formed to better serve the needs of psoriasis patients across the country. We work in partnership with the Canadian Skin Patient Alliance to improve the quality of life for all Canadian psoriasis patients. The Canadian Association of Psoriasis Patients is run by a dedicated staff and a committed Board of Directors, who are either psoriasis and/or psoriatic arthritic patients themselves, family members of psoriasis patients, or individuals committed to furthering CAPPs Mission.

Website: www.canadianskin.ca/en/
Contact: info@skinpatientalliance.ca

Canadian Association of Psoriasis Patients (CAPP)

The Canadian Association of Psoriasis Patients was formed to better serve the needs of psoriasis patients across the country. We work in partnership with the Canadian Skin Patient Alliance to improve the quality of life for all Canadian psoriasis patients. The Canadian Association of Psoriasis Patients is run by a dedicated staff and a committed Board of Directors, who are either psoriasis and/or psoriatic arthritic patients themselves, family members of psoriasis patients, or individuals committed to furthering CAPPs Mission.

Website: www.canadianpsoriasis.ca
Contact: info@canadianpsoriasis.ca

Eczema Society of Canada

Improving the lives of Canadians living with eczema is at the core of our mission, and our team of talented and dedicated professionals make that a reality.


Website: www.eczemahelp.ca 

Contact: info@eczemahelp.ca

Lupus Canada

Lupus Canada and local lupus organizations strive to increase public awareness about lupus and provide educational resources to people living with lupus as well as their friends and family. Often known as “the disease of a thousand faces,” Lupus Canada provides the latest information, including strategies to live well with lupus, “ask the experts” section, advocacy resources and tools, and the latest information on lupus research in Canada. To learn more, please contact Lupus Canada.

Website: www.lupuscanada.org
Email: info@lupuscanada.org

Lupus Ontario

Lupus Ontario is the largest provincial voluntary organization dedicated to improving the lives of people living with lupus through advocacy, education, public awareness, support and research. Celebrating 30 years of service in 2008, Lupus Ontario was formed in 2004.

Website: www.lupuscanada.org
Email: info@lupuscanada.org

Save Your Skin Foundation

Save Your Skin Foundation is a Canadian non-profit registered charity, founded by North Vancouver resident and melanoma survivor Kathleen Barnard. In 2003, Kathleen was diagnosed with stage 4 malignant melanoma. By the establishment of Save Your Skin Foundation in 2006, Kathleen’s cancer had spread to her vital organs and her treatment options were limited. Fortunately, one of her sons discovered a trial treatment taking place in Alberta; this trial would save Kathleen’s life. While her cancer treatments have finished, the battle with melanoma is not over for Kathleen. Today, Save Your Skin Foundation works with Canadian government stakeholders to change federal and provincial policy and with skin cancer medical professionals to write patient policy guidelines, while still providing melanoma patients with the one-on-one support Kathleen gave during her own treatments. Save Your Skin Foundation seeks to eliminate melanoma on every level, from prevention to treatment.


Website: www.saveyourskin.ca
Email: info@saveyourskin.ca

The Canadian Dermatology Association

The Canadian Dermatology Association, founded in 1925, represents Canadian dermatologists. The association exists to advance the science and art of medicine and surgery related to the care of the skin, hair and nails; provide continuing professional development for its members; support and advance patient care; provide public education on sun protection and other aspects of skin health; and promote a lifetime of healthier skin, hair and nails.


Website: www.dermatology.ca
Email: info@dermatology.ca

The EASE Program (Eczema Awareness, Support and Education Program)

The EASE Program is a community service provided through an educational grant from LEO Pharma Inc. Canada. EASE is a national, fully bilingual public education program that provides eczema sufferers, families, healthcare professionals and the general public with accurate and comprehensive information on eczema. The goal of the EASE Program is to foster greater understanding and to provide quality educational resources to help better manage this chronic, recurring skin condition.


Website: http://www.eczemacanada.ca/ 

Contact: http://www.eczemacanada.ca/en/Contact-Us

What are orphan Drugs? Orphan Medications are medications intended for diagnosis, prevention or treatment of chronic life-threatening or very serious diseases or disorders that are rare, often referred to as a “Chronic Rare Disease.” We have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with chronic disease.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Organization for Rare Disorders

CORD is Canada’s national network for organizations representing all those with rare disorders. CORD provides a strong common voice to advocate for health policy and a healthcare system that works for those with rare disorders. CORD works with governments, researchers, clinicians and industry to promote research, diagnosis, treatment and services for all rare disorders in Canada.


Website: http://raredisorders.ca/ 

Contact: info@raredisorders.ca

If you are having fertility problems, the great news is that there are options and medical help for many couples experiencing infertility. We have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people with family planning.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Fertility & Andrology Society

The CFAS is a multidisciplinary national non-profit Society that serves as the voice of reproductive specialists, scientists, and allied health professionals working in the field of Assisted Reproduction in Canada. Established in 1954, the mission of the CFAS is to responsibly advance reproductive science and medicine in Canada through leadership, research and guidance. Through its 700 multidisciplinary membership, the CFAS aims to promote excellence in the field of Assisted Reproduction to the benefit of Canadians and children born of this technology.


Website: https://cfas.ca/ 

Contact: info@cfas.ca

Canadian Fertility Support Services and Resources

Fertility Matters Canada (FMC) is the national organization that empowers Canadians to help reach their reproductive health goals by providing support, awareness, information and education; and promoting equal access to fertility treatments. We are Canada’s fertility resource.

FMC grew out of a volunteer group in Ottawa called the Infertility Self Support Group (ISSG), which began in 1983. Today, FMC is a national charitable organization, providing educational material, support and assistance to individuals and couples who are experiencing the anguish of infertility, the reproductive health disease that affects over half a million Canadian men and women.

Website: http://fertilitymatters.ca/
Contact: info@fertilitymatters.ca

Gastroenterology is the branch of medicine focused on the digestive system and its disorders, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with digestive disorders.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Website: https://www.catie.ca/
Contact: info@catie.ca

Canadian Association of Gastroenterology

The Canadian Association of Gastroenterology (CAG) was founded in 1962 with a mandate of:

  • Supporting and engaging in the study of the organs of the digestive tract in health and disease,
  • Promoting the advancement of the science and art of gastroenterology by providing leadership in patient care, research, teaching and continuing professional development (CPD), and
  • Promoting and maintaining the highest ethical standards.

Over 1100 members including gastroenterologists, surgeons, pediatricians, basic scientists and nurses comprise the Association. The CAG provides professional gastroenterological education and funding opportunities for gastrointestinal health and disease research, and more recently, has advocated for improved timeliness and quality of digestive health care for Canadians.

The CAG/Canadian Institutes of Health Research (CIHR)/Industry Research Program is an exceptional research opportunity in which the federal government matches 1:1 all money raised from industry partners in support of gastrointestinal research. Funding is available for all levels of training including for clinicians, gastroenterology residents, postdoctoral fellows, and graduate and summer students. The Program has been a successful and highly sought-after funding avenue for over fifteen years; in the first ten years 87 researchers were funded to a total of over $8.7 million, in support of the highest quality research in gastroenterology in Canada (Canadian Journal of Gastroenterology 2003;17(7):437-9). Many of these researchers have gone on to secure clinical and/or academic appointments within Canadian institutions and CIHR funding, as well as becoming the mentors for the next generation of scientists.

The Canadian Association of Gastroenterology remains dedicated to research, professional education, and patient care in all areas of digestive health and disease, in support of the economic and social health of all Canadians.

Website: https://www.cag-acg.org/
Contact: info@cag-acg.org

Canadian Digestive Health Foundation

The Canadian Digestive Health Foundation (www.CDHF.ca) aims to improve quality of life by providing trusted, accessible, and accurate information about digestive health and disease. We are here to help you recognize symptoms, understand a disease you’ve been diagnosed with, connect with others who have similar experiences, and find effective ways to manage your digestive health.

As the Foundation of the Canadian Association of Gastroenterology, we are directly connected to Canada's leading digestive health experts, physicians, scientists and other health care professionals. In addition to developing practical, respected and unbiased education resources, the CDHF also funds research and advocacy initiatives.

Website: http://www.cdhf.ca/
Contact: info@cdhf.ca

Canadian Celiac Association / L’Association

The Canadian Celiac Association / L’Association canadienne de la maladie coeliaque is a volunteer-based, federally registered charitable organization with its national office in Mississauga, Ontario. It was founded in 1972 with financial assistance from the Kaufman Foundation. The association was started by two women from Kitchener, Ontario, who, from personal experience with celiac disease, recognized vital needs of people suffering from the disease.

The CCA is governed by an elected national board of directors with regional representation across Canada. The Board develops policies and strategies for the association and provides leadership and guidance to chapters. Chapters are charitable organizations each of which is governed by an elected executive committee. The national office is staffed by two full-time and two part-time people

Website: http://www.celiac.ca/
Contact: info@cdhf.ca

Crohn’s and Colitis Canada

Crohn’s and Colitis Canada is the only national, volunteer-based charity focused on finding the cures for Crohn’s disease and ulcerative colitis and improving the lives of children and adults affected by these diseases.

We are one of the top two health charity funders of Crohn’s and colitis research in the world, investing $115 million in research since 1974, leading to important breakthroughs in genetics, gut microbes, inflammation and cell repair as well as laying the groundwork for new and better treatments.

We are transforming the lives of people affected by Crohn’s and colitis (the two main forms of inflammatory bowel disease) through research, patient programs, advocacy, and awareness.

Our Crohn’s & Colitis – Make it stop. For life. Campaign has already achieved $57 million (or 57%) of its goal, and funds raised are already advancing our mission.

Website: http://www.crohnsandcolitis.ca/
Contact: info@crohnsandcolitis.ca

Canadian Society of Intestinal Research

In 1976, the Canadian Society of Intestinal Research (CSIR) arose as the first registered charity in Canada to enhance public awareness by providing patient and professional information and funding medical research on a wide array of gastrointestinal diseases and disorders.

When CSIR first formed in 1976, it was intended to serve British Columbia only. So, an unalterable clause was inserted into the constitution that required all research funding granted by the Society to be designated to research at the University of British Columbia and its teaching hospitals. This has caused a number of difficulties, as the gastrointestinal ‘community’ has grown and changed substantially since CSIR was originally registered. Even though the CSIR constitution allows us to operate coast-to-coast-to-coast in the area of patient education (lectures, newsletters, pamphlets) and demand for the Society’s patient information resources is strong, the unalterable clause has held us back from fully servicing all of the Canadian gastrointestinal medical community. In 2008, we created the Gastrointestinal Society (GI Society) to provide Canadians with a broader range of resources in this sorely neglected health area. By incorporating a federally registered charity, without these limitations, a new national granting system is under development.

With quality and integrity, we continue to be the leading provider of evidence-based, free patient information in the GI health field. We work to dispel myths about GI conditions. Although gastrointestinal diseases and disorders are rarely a subject of public discussion, they are highly prevalent in the Canadian population and are the second most frequent reason for employee absenteeism, surpassed only by the common cold.

Website: https://www.badgut.org
Contact: info@badgut.org

Hepatitis is a disease characterized by inflammation of the liver, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with liver disease.

Note:The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Action Hepatitis Canada

Action Hepatitis Canada (AHC) is a national coalition of organizations responding to hepatitis B and C. Our work engages government, policy makers, and civil society across Canada to promote hepatitis B and C prevention, improve access to care and treatment, increase knowledge and innovation, create public health awareness, build health-professional capacity, and support community-based groups and initiatives.

Website: http://www.actionhepatitiscanada.ca/
Contact: info@actionhepatitiscanada.ca

Canadian Liver Foundation

In 1969 the Canadian Liver Foundation was born out of the passion and concern of a committed group of business leaders and doctors who believed that liver disease needed a champion. With the help of volunteers, patients and families, researchers, doctors, donors and corporate supporters who share our vision of a world without liver disease, we are bringing liver research to life.

Website: https://www.liver.ca
Contact: clf@liver.ca

Canadian Network on Hepatitis C

CanHepC is a collaborative research network funded by the Canadian Institutes of Health Research (CIHR) and the Public Health Agency of Canada (PHAC) dedicated to translational research linking over 100 researchers, trainees, knowledge-users (community members, community-based organizations, policy and decision makers) in the field of Hepatitis C (HCV) from across Canada as well as international partners.

Our overarching goal is to conduct innovative and interdisciplinary research, build research capacity, and translate evidence for uptake into practice and policy, to improve HCV prevention and health outcomes of Canadians and contribute to the global effort to reduce HCV burden worldwide, by focusing on the following themes:

Website: http://www.canhepc.ca/
Contact: info@canhepc.ca

HIV stands for human immunodeficiency virus, It is the virus that can lead to acquired immunodeficiency syndrome (AIDS), we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with AIDS or HIV.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure

Canada's source for HIV and hepatitis C information

CATIE strengthens Canada’s response to HIV and hepatitis C by bridging research and practice. We connect healthcare and community-based service providers with the latest science, and promote good practices for prevention and treatment programs.

As Canada’s official knowledge broker for HIV and hepatitis C, you can count on us for up-to-date, accurate and unbiased information.

Website: https://www.catie.ca/
Contact: info@catie.ca

Canadian AIDS Society

Created in 1986, the Canadian AIDS Society (CAS) is a national voice for people living with HIV/AIDS and represents our members at the national level. We are a movement built at the grassroots level and we are proud of those roots. We are devoted to the idea of people working together with a certain knowledge that the stakes have never been higher and the humble notion that we can work together to dramatically change the outcomes of HIV in Canada.

Website: https://www.cdnaids.ca/
Contact: casinfo@cdnaids.ca

Canadian Association for HIV Research (CAHR)

CAHR is the organizing body for the Annual Canadian Conference on HIV/AIDS Research (CAHR Conference). CAHR encourages Canadian researchers to be leaders in knowledge translation and to effectively respond both to the Canadian and global HIV/AIDS epidemics.

Since its founding in 1991, CAHR has promoted excellence in HIV research, including mentorship and career development of investigators entering the field. CAHR fosters collaboration and co-operation among HIV research communities, including basic, clinical and social sciences, epidemiology and public health. CAHR also engages people living with HIV/AIDS and AIDS service organizations in ongoing dialogue and information exchange to ensure that HIV/AIDS research remains responsive to the epidemic and its stakeholders. CAHR is a registered charity.

Website: https://www.cahr-acrv.ca/
Contact: info@cahr-acrv.ca

The Canadian Foundation for AIDS Research

CANFAR is dedicated to funding all aspects of HIV research – from increased prevention efforts, increased opportunities for testing, improved health outcomes for people living with HIV in Canada, and reduced stigma.

Through funding innovative research, national awareness programs, and strengthened advocacy efforts, CANFAR remains a trailblazer in its mission to end HIV in Canada.

Website: https://canfar.com/about-us/
Contact: info@CANFAR.com

Multiple sclerosis is a chronic illness of the central nervous system, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with Multiple Sclerosis.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Multiple Sclerosis Society of Canada

The MS Society provides services to people with multiple sclerosis and their families and funds research to find the cause and cure for this disease. We have a membership of 17,000 and are the only national voluntary organization in Canada that supports both MS research and services. Since our founding in 1948, the core support of the MS Society has been from tens of thousands of dedicated individuals, companies and foundations in communities across Canada. The Society receives almost no funding from government.

The MS Society is governed by a board of directors comprised of 14 volunteer members who are elected annually. There are seven regional divisions and more than 90 chapters that engage in many community-based activities.

Some 1,500 volunteers serve on MS Society national, division and chapter boards and committees. An estimated 13,500 women and men are volunteers for service programs, fundraising events, public awareness campaigns and social action activities.

The head office of the MS Society is located in Toronto, Ontario. Division offices are located in Dartmouth, Montreal, Toronto, Winnipeg, Regina, Edmonton, and Vancouver.

Website: https://mssociety.ca/
Contact: info@mssociety.ca

National Multiple Sclerosis Society

The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS. Everything we do is focused so that people affected by MS can live their best lives as we stop MS in its tracks, restore what has been lost and end MS forever.

We are more than an organization. We are a movement. United in our collective power to do something about MS now and end this disease forever. The gathering place for people with MS, their family and loved ones, healthcare providers, volunteers, donors, fundraisers, advocates, community leaders and all those that seek a world free of MS. A place to connect and take action. In order to change the world, we mobilize all possible human and financial resources to achieve results.

Website: https://mssociety.ca/
Contact: info@mssociety.ca

Cancer never takes a break, and for that reason, neither does the fight to conquer cancer, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with cancer.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Association of Medical Oncologists

The Canadian Association of Medical Oncologists, a national specialty society of the Royal College of Physicians and Surgeons of Canada, will contribute to cancer control, through research, education, and clinical practice in prevention, screening, diagnosis, treatment, supportive care, palliative care and rehabilitation.

The Association is committed to achieving and maintaining, among its members, excellence in clinical and scholarly activity, within a culture of compassion and respect for human dignity.

Website: https://camo-acom.ca/
Contact: info@camo-acom.ca

Canadian Association of Nurses in Oncology/Association

Established in 1985, the Canadian Association of Nurses in Oncology/Association canadienne des infirmières en oncologie (CANO/ACIO) is a national organization with a mission to advance oncology nursing excellence through practice, education, research, and leadership for the benefit of all Canadians, and a vision of being an international nursing leader in cancer control. We are a member-run association that takes direction from its membership in formulating activities and initiatives.

Website: https://www.cano-acio.ca/
Contact: cano@malachite-mgmt.com

Canadian Association of Pharmacy in Oncology

At the Canadian Association of Pharmacy in Oncology (CAPhO), you will be able to meet colleagues, exchange views, post professional papers, find oncology pharmacy resources, complete continuing education courses, locate contacts in other provinces, and much more. Website: https://www.capho.org/
Contact: info@capho.org

Canadian Association of Psychosocial Oncology

The Canadian Association of Psychosocial Oncology (CAPO) is an organization of professionals, clinicians, researchers, educators, and others dedicated to the understanding, treatment and study of the social, psychological, emotional, spiritual and quality-of-life aspects of cancer.

CAPO leads nationally and globally in promoting capacity for, and excellence in psychosocial oncology services to enhance the wellness of individuals and families.

The purpose of the CAPO is to foster and encourage interdisciplinary excellence in psychosocial research education and clinical practice in oncology. Website: http://www.capo.ca/
Contact: capo@funnel.ca

Canadian Cancer Society

The Canadian Cancer Society is a national, community-based organization of volunteers whose mission is the eradication of cancer and the enhancement of the quality of life of people living with cancer.

At the Canadian Cancer Society, we are committed to improving and saving lives. That’s why we are always looking for new ways to prevent cancer, find it early and treat it more successfully. It’s why we’re always ready to give people with cancer the help and support they need to lead more fulfilling lives. We set ourselves apart from other cancer charities by taking a comprehensive approach against cancer. We are also the only national charity that supports all Canadians living with all cancers across the country. Website: http://www.cancer.ca
Contact: connect@cancer.ca

Ophthalmology deals with the anatomy, physiology and diseases of the eyeball and orbit, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with eye conditions.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

Canadian Ophthalmological Society

The Canadian Ophthalmological Society (COS) is the national, recognized authority on eye and vision care in Canada. As eye physicians and surgeons, we are committed to assuring the provision of optimal medical and surgical eye care for all Canadians by promoting excellence in ophthalmology and by providing services to support our members in practice. Our membership includes over 900 ophthalmologists and 200 ophthalmology residents. We work collaboratively with government, other national and international specialty societies, our academic communities (ACUPO), our provincial partners and affiliates and other eye care professionals and patient groups to advocate for health policy in Canada in the area of eye and vision health. COS is an accredited, award-winning provider of Continuing Professional Development (CPD) through the Royal College of Physicians and Surgeons of Canada (RCPSC) and is an affiliate of the Canadian Medical Association (CMA). Website: http://www.cos-sco.ca/
Contact: cos@cos-sco.ca

International Council of Ophthalmology

The International Council of Ophthalmology (ICO) represents and serves professional associations of ophthalmologists throughout the world.

The International Council of Ophthalmology works with ophthalmologic societies and others to enhance ophthalmic education and improve access to the highest quality eye care in order to preserve and restore vision for the people of the world.

The ICO is working to build a “World Alliance for Sight” by leading, stimulating, and supporting the efforts of ophthalmologic societies, eye departments, and related organizations worldwide to enhance ophthalmic education and eye care.

Through this collaboration, the ICO focuses on three main program categories:

  • Eye care delivery
  • Leadership and society development
  • Education

Website: http://www.icoph.org/
Contact: info@icoph.org

Rheumatology is a branch of medicine devoted to the diagnosis and therapy of inflammatory arthritis and rheumatic diseases affecting muscles, bones and joints, we have listed a range of resources and organizations with up-to-date information to help you better understand and manage your condition, and to help support people living with rheumatic conditions.

Note: The resources listed below and elsewhere on this website is for general information only. It is designed to be educational and is not intended to be and is not a comprehensive or definitive statement on any area of medical practice or procedure.

About Kids Health?

About Kids Health is a health education resource for children, youth and caregivers that is approved by health-care providers at The Hospital for Sick Children. About Kids Health empowers families to become a partner in their own health care by equipping them with reliable, evidence-based health information. It makes complex health information easy to understand for families, and makes it immediately available whenever and wherever they have questions about child health regardless of where they are in Canada or the world. Website: https://www.aboutkidshealth.ca/
Contact: info@aboutkidshealth.ca

Alberta Rheumatology

In 2010, we launched EdmontonRheumatology.com as a resource for patients, medical students, residents and physicians on all aspects related to rheumatology in Edmonton.

For our patients, it was an opportunity to provide accurate & trustworthy information, as well as a resource to answer those simple but at times frustrating questions: Where do I find my rheumatologist’s office? What should I do at my first appointment?

For our students, it was an opportunity to provide a one stop resource for teaching rheumatology, with salient up to date links to papers, videos, and rotation information. For ourselves, it became a place to keep forms and links to data we need to ensure we provide the best and most efficient care to our patients. Website: https://albertarheumatology.com/
Contact: info@albertarheumatology.com

Arthritis Society

The Arthritis Society is a national health charity, fueled by donors and volunteers, with a vision to live in a world where people can be free from the devastating effects that arthritis can have on lives.

The Arthritis Society began nearly 70 years ago with one very clear goal; to alleviate the suffering of people crippled by arthritis. Founded in 1948 by Dr. Wallace Graham and his medical peers from across the country, it was Mary Pack, a fiercely driven community advocate who worked tirelessly to put people's needs truly into the spotlight. Today we bring that passion to communities across Canada.

We are proud to have the trust and support of donors and sponsors who provide the funding capacity to invest in cutting-edge research, proactive advocacy and innovative solutions that will deliver better health outcomes and an improved quality of life for people affected by arthritis. That support has resulted in broad educational outreach to people living with arthritis and over $200M invested, the largest source of charitable arthritis research funding.

We benefit from the advice of subject matter experts on our National Board, our Division Advisory Boards and Medical, Scientific and Patient-centric committees along with countless committed volunteers. Website: https://www.arthritis.ca
Contact: info@arthritis.ca

Canadian Arthritis Patient Alliance

The Canadian Arthritis Patient Alliance (CAPA) is a grass-root, patient-driven, independent, national advocacy organization with members across Canada and supporters both Canadian and International.

CAPA believes the first expert on arthritis is the individual who has the disease, theirs is a unique perspective. We assist members to become advocates not only for themselves but all people with arthritis.

CAPA facilitates links between Canadians with arthritis and their support systems through collaboration and partnerships with other organizations, representatives from all levels of government, researchers, and other individuals to help achieve CAPA's strategic priorities. The organization communicates the latest news on health policy issues, research, technology and emerging issues relevant to members through its website and Facebook pages.

CAPA welcomes all Canadians with arthritis and those who support CAPA's goals to become members Website: http://arthritispatient.ca/
Contact: contact@arthritispatient.ca

Canadian Rheumatology Association

The Canadian Rheumatology Association (CRA) is the national professional association for Canadian rheumatologists. In 1936, when Canada was emerging from the depression and war clouds were gathering in Europe an organization named the Canadian Rheumatic Disease Association (CRDA) was founded.

The mission of the Canadian Rheumatology Association is to represent Canadian rheumatologists and promote the pursuit of excellence in arthritis and rheumatic disease care, education and research.

Today, the CRA comprises over 500 members throughout all 10 provinces and territories as well as some international members. Since its inception, the CRA has promoted and advanced the field of rheumatology by organizing networking, training and education opportunities for clinicians, students, allied health professionals and researchers. More recently the CRA has become involved in the promotion and coordination of funding for important rheumatology research (CIORA).

The CRA carries out its mission through a multifaceted network of activities and investments. A cornerstone activity of the CRA is the annual scientific meeting, whose purpose is to showcase the various clinical and research endeavors of CRA members and other arthritis health professionals. The meeting also serves to foster professional collaboration and an exchange of ideas in the rheumatology community.

As a nationally and internationally respected organization, the CRA continues to serve as a national voice for practicing rheumatologists and researchers with an interest in rheumatic diseases. Website: https://rheum.ca/
Contact: info@rheum.ca

Rheum Info

RheumInfo.com was developed in 2003 to serve a need of providing accurate and reliable arthritis information for patients and healthcare providers. Through simple “word of mouth” the site has grown to become respected internationally for the value and creativity of the content.

Audience: Our audience consists of rheumatologists and allied health practitioners (physiotherapists, occupational therapists, nurses, social workers, psychologists etc.). Patients with arthritis and musculoskeletal disorders may also freely access the website. Membership is free of charge. Website: https://rheuminfo.com/
Contact: info@rheuminfo.com