Resources

Recent Reports from OCOE

Quarterly Newsletter

OCOE Publishes a quarterly newletter about outreach activities, research and our partners. Subscribe


The Office of Community Outreach and Engagement (OCOE) has compiled an extensive list of resources and information on a variety of cancer health disparities topics.

See below to learn more about data, research and findings at a state or national level, as well as by population groups.

Cancer Site Resources

American Cancer Society (ACS)

These regularly updated Facts & Statistics publications present the most current trends in cancer occurrence and survival, as well as information on symptoms, prevention, early detection and treatment.

Visit site

Susan G. Komen

Susan G. Komen addresses breast cancer on multiple fronts such as research, community health, global outreach and public policy initiatives in order to make the biggest impact against this disease. They offer breast cancer educational materials in a variety of languages.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

American Cancer Society (ACS)

These regularly updated Facts & Statistics publications present the most current trends in cancer occurrence and survival, as well as information on symptoms, prevention, early detection and treatment.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

Centers for Disease Control and Prevention (CDC)

CDC works with national cancer organizations, state health agencies and other key groups to develop, implement and promote effective strategies for prevention and controlling cancer. Data/statistics and information on health disparities and survivorship are available.

Visit site

Washington State Resources

Harborview Medical Center's ethnic medicine website contains medical and cultural information about immigrant and refugee groups. Information is specific to groups in the Seattle area, but much of the cultural and health information is applicable in other geographic areas.

Visit site

The Governor’s Interagency Council on Health Disparities is responsible for identifying priorities and creating recommendations for the Governor and Legislature to eliminate health disparities by race/ethnicity and gender in Washington.

Visit site

The Center for Health Statistics provides access to current, high quality health data that covers deaths, births, pregnancy rates, abortion rates and behavioral risk factors. Data are used by policy makers, health professionals, community-based organizations and researchers to understand trends, identify high risk populations and geographic areas, set prevention priorities and plan targeted health promotion strategies. The Center also provides data on the financial performance of Washington hospitals.

Visit site

Cancer incidence and mortality data are available by site and region from 1993–2015. Data requests are welcome, or you may access county and statewide incidence and mortality data online.

Visit site

In 2001, the Washington State Department of Health formed the Comprehensive Cancer Control Partnership. The name changed to Washington CARES About Cancer Partnership, then shortened to Washington Cancer Partnership in 2015. With a better understanding of the common underlying issues related to maintaining health, the Washington Cancer Partnership collapsed 14 state plans, one of which was the Comprehensive Cancer Control Plan, into one Washington State Plan for Healthy Communities. This statewide plan aligns priorities and strategies with national, state and local prevention efforts and serves as a road-map for implementing chronic disease prevention efforts in our communities.

Visit site

National Resources

AHRQ invests in research and evidence to make health care safer and improve quality; their evidence-based tools and resources are used to improve the quality, safety, effectiveness and efficiency of health care in the United States.

Visit site

The ARDA strives to democratize access to the best data on religion. Founded in 1997, the initial archive was targeted at researchers interested in American religion. Both the targeted audience and data collection have greatly expanded, and now include American and international collections and features for educators, journalists, religious congregations and researchers. Data included in the ARDA are submitted by the foremost religion scholars and research centers in the world. There are over 1,000 data files in the collection.

Visit site

The BRFSS is the nation’s premier system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. Established in 1984, BRFSS currently collects data in all 50 states, the District of Columbia, Puerto Rico, the U.S. Virgin Islands and Guam. BRFSS completes more than 400,000 adult interviews each year, making it the largest continuously conducted health survey system in the world.

Visit site

CDC's Division of Cancer Prevention and Control (DCPC) monitors trends in cancer incidence and mortality, and identifies which populations are disproportionately affected by the disease.

Visit site

REACH is a national program administered by the CDC to reduce racial and ethnic health disparities. Through REACH, awardee partners plan and carry out local, culturally appropriate programs to address a wide range of health issues among African Americans, Native Americans, Hispanics/Latinos, Asian Americans, Alaska Natives and Pacific Islanders.

Visit site

The County Health Rankings & Roadmaps program is a collaboration between the Robert Wood Johnson Foundation and the University of Wisconsin Population Health Institute. The annual rankings provide a revealing snapshot of how health is influenced by where we live, learn, work and play. They provide a starting point for change in communities.

Visit site

DiversityDataKids.org is a comprehensive research program to monitor the state of wellbeing, diversity, opportunity and equity of U.S. children.

Visit site

FDA Office of Minority Health and Health Equity (OMHHE) offers many easy-to-use and culturally-appropriate resources on minority health, health disparities, and related topics. These resources are available to view online, print, or share. Some are available in Spanish and other foreign languages.

Visit site

The NCI is the federal government's principal agency for cancer research and training. NCI leads, conducts and supports cancer research across the nation to advance scientific knowledge and help all people live longer, healthier lives.

Visit site

HINTS was created to monitor changes in the rapidly evolving field of health communication. The survey data can be used to understand how adults use different communication channels to obtain health information for themselves and their loved ones, and to create more effective health communication strategies across populations. HINTS data are available for public use.

Visit site

SEER is a premier source for cancer statistics in the United States. The program collects data on cancer cases from various locations and sources throughout the United States. The web site is intended for anyone interested in U.S. cancer statistics or cancer surveillance methods.

Visit site

OMH is dedicated to improving the health of racial and ethnic minority populations through the development of health policies and programs that will help eliminate health disparities.

Visit site

Resources in Other Languages

Cancer Information in Other Languages

The ACS offers information about cancer including prevention, early detection, treatment and managing side effects in 14 languages in addition to English.
Visit site

Health Information Translations

Health Information Translations provides education resources in multiple languages for health professionals to use in their communities. Resources are easy-to-read and culturally appropriate.
Visit site

National Network of Libraries of Medicine

This link contains links to consumer health information and resources in many languages.
Visit site

AHRQ: Español

Information on a variety of health topics from AHRQ in Spanish for patients and consumers.
Visit site

CDC: Español

Links to information from CDC in Spanish.
Visit site

MedlinePlus®: Español

Links to information in Spanish.
Visit site

NCI: Español

Links to information from NCI in Spanish.
Visit site

Resources by Population

ACS: Cancer Facts & Figures for African Americans

These reports estimate the number of new cancer cases and deaths, and provide the most recent statistics on cancer incidence, mortality and five-year relative survival among African Americans. Reports also include sections on cancer risk factors such as tobacco use, physical activity and use of cancer screening examinations.
Visit site

BACPAC Network

The BACPAC network provides connections and resources for Black men who have been impacted by prostate cancer.
Visit site

Susan G. Komen: Know Your History, Know Your Risk

This site includes information and resources on breast cancer prevention, understanding risk, and treatment. The Stand for H.E.R. – A Health Equity Revolution initiative focuses on achieving health equity for the Black community.
Visit site

U.S. DHHS Office of Minority Health: Profile: Blacks/African Americans
Visit site

Urban League of Metropolitan Seattle: Black Health Matters

This site includes a public health equity guide called Black Health Matters: Preventative Care & Screenings to help start conversations for change and empower people to be a health advocate for themselves and for their community.
Visit Site

Asian & Pacific Islander American Health Forum (APIAHF)

The APIAHF influences policy, mobilizes communities and strengthens programs and organizations to improve the health of Asian Americans, Native Hawaiians, and Pacific Islanders.
Visit site

Asian Health & Service Center

This resources in based in Oregon and is a collection of health and service information offered in a variety of Asian languages.
Visit site

APICAT for health

This site hosts a collection of information and advocacy for AANHPI specific community concerns in Washington State. APICAT works to build healthy Asian American, Native Hawaiian, and Pacific Islander (AANHPI) communities through leadership development, education, and advocacy.
Visit site

Asian Pacific Partners for Empowerment, Advocacy and Leadership (APPEAL)

APPEAL is a national health justice organization working to achieve health equity for Asian Americans, Native Hawaiians, Pacific Islanders and other underserved communities. Their website offers valuable information and resources for community members and public health professionals who want to advance equity in tobacco control, healthy eating and active living within their communities.
Visit site

Association of Asian Pacific Community Health Organizations (AAPCHO)

AAPCHO is dedicated to promoting advocacy, collaboration and leadership that improves the health status and access of Asian Americans, Native Hawaiians and other Pacific Islanders within the United States, its territories, and freely associated states, primarily through their member community health centers.
Visit site

New York University Center for the Study of Asian American Health (CSAAH)

CSAAH is committed to identifying Asian American health priorities and reducing health disparities by integrating and building on the work of researchers and over 55 Asian American community, government, business, and academic/medical partners.
Visit site

U.S. DHHS Office of Minority Health: Profile: Asian Americans
Visit site

Asian Health and Service Center: Asian Cancer Support Resources

Located in Portland, Oregon, AHSC’s Asian Cancer Support program offers a variety of language and culturally specific resources on the topics of cancer prevention, diagnosis, treatment and after-treatment care. Resources are provided in English, Cantonese, Mandarin, Korean and Vietnamese to fill the void of information available in a patient’s native language and help them better understand their diagnosis and treatment options. 
Visit site

ACS Cancer Facts & Figures for Hispanics and Latinos

These reports, available in English and Spanish, provide updated cancer information about Hispanics/Latinos, including statistics on cancer occurrence and risk factors, as well as information about prevention, early detection and treatment.
Visit site

Latino Health Access (LHA)

LHA partners with communities to bring health, equity and sustainable change through education, services, consciousness-raising and civic participation.
Visit site

University of Washington: Latino Center for Health

The Latino Center for Health provides leadership for community-engaged research through capacity building and authentic partnerships with community stakeholders to promote impactful improvements in the health and well-being of Latinx communities in Washington state, regionally and nationally.
Visit site

The Latino Cancer Institute

The Latino Cancer Institute (TLCI) is a nationwide community and research network dedicated to solving the issues and burden of Latino cancer.
Visit site

CDC: Hispanic or Latino People and Cancer

This site provides information on health, research, barriers, and resources for Hispanic or Latino People and cancer.
Visit site

Alaska Native Knowledge Network (ANKN)

The ANKN is designed to serve as a resource for compiling and exchanging information related to Alaska Native knowledge systems and ways of knowing. It has been established to assist Native people, government agencies, educators and the general public in gaining access to the knowledge base that Alaska Natives have acquired through cumulative experience over millennia.
Visit site

American Indian Cancer Foundation

The American Indian Cancer Foundation’s mission is to eliminate the cancer burden on Native American and Alaska Native people through improved access to prevention, early detection, treatment and survivor support. Learn about their projects, check out cancer facts for Native Americans and Alaska Natives, and browse culturally appropriate community-based resources for health and cancer awareness on their website.   
Visit site

Arctic Health

The Arctic Health website is a central source for information on diverse aspects of the Arctic environment and the health of northern peoples. The site gives access to evaluated health information from hundreds of local, state, national, and international agencies, as well as from professional societies and universities.
Visit site

Association of American Indian Physicians

The mission of the AAIP is to pursue excellence in Native American health care by promoting education in the medical disciplines, honoring traditional healing principles and restoring the balance of mind, body, and spirit.
Visit site

Indian Health Service (IHS)

The IHS, an agency within the Department of Health and Human Services, is responsible for providing federal health services to American Indians and Alaska Natives. The provision of health services to members of federally-recognized tribes grew out of the special government-to-government relationship between the federal government and Native American tribes.
Visit site

Native CIRCLE

Native CIRCLE is a resource center providing cancer and non-cancer related materials to healthcare professionals and lay people involved in the education, care and treatment of Native Americans and Alaska Natives.
Visit site

National Indian Council on Aging (NICOA)

The NICOA is a non-profit organization that advocates for improved, comprehensive health, social services, and economic wellbeing for American Indian and Alaska Native Elders.
Visit site

National Indian Health Board (NIHB)

NIHB is an organization providing health care advocacy services, facilitates Tribal budget consolation and provides timely information and other services to all Tribal Governments. Whether Tribes operate their own health care delivery systems or receive health care directly from the Indian Health Services (IHS), NIHB is their advocate. NIHB also conducts research, provides policy analysis, program assessment and development, national and regional meeting planning, training, technical assistance programs and project management. It also serves as conduit to open opportunities for the advancement of Native American and Alaska Native health care with other national and international organizations, foundations and corporations.
Visit site | Indian Health 101 | Tribal Specific Resources

National Network of Libraries of Medicine

Native American/Alaska Native Resources
Visit site | Cancer Project | Native Boost

U.S. Census Bureau: Intergovernmental Affairs: Tribal Affairs

This site highlights the Census Bureau’s relationship with tribal governments and provides important American Indian and Alaska Native (AIAN) and tribal resources. The Census Bureau collects data for the AIAN population and publishes specific counts, estimates and statistics.
Visit site

U.S. DHHS Office of Minority Health: Profile: American Indian/Alaska Native
Visit site

Urban Indian Health Institute

In July 2000, the Urban Indian Health Institute was established as a division within the Seattle Indian Health Board, a community health center targeting urban American Indians and Alaska Natives (AI/AN). The UIHI is one of 12 tribal epidemiology centers funded by the IHS. The UIHI focuses on the nationwide urban AI/AN population.
Visit site

Governor’s Office of Indian Affairs: Washington Treaties

This is a resource for addressing health equity for American Indian and Alaska Native peoples includes understanding, recognizing, and honoring Tribal Sovereignty and the rights of Tribal communities.
Visit site

Asian & Pacific Islander American Health Forum (APIAHF)

The APIAHF influences policy, mobilizes communities and strengthens programs and organizations to improve the health of Asian Americans, Native Hawaiians and Pacific Islanders.
Visit site

Asian Pacific Partners for Empowerment, Advocacy and Leadership (APPEAL)

APPEAL is a national health justice organization working to achieve health equity for Asian Americans, Native Hawaiians, Pacific Islanders and other underserved communities. Their website offers valuable information and resources for community members and public health professionals who want to advance equity in tobacco control, healthy eating and active living within their communities.
Visit site

Association of Asian Pacific Community Health Organizations (AAPCHO)

AAPCHO is dedicated to promoting advocacy, collaboration and leadership that improves the health status and access of Asian Americans, Native Hawaiians and other Pacific Islanders within the United States, its territories and freely associated states, primarily through our member community health centers.
Visit site

‘Imi Hale Native Hawaiian Cancer Network

‘Imi Hale Native Hawaiian Cancer Network is a program of Papa Ola Lōkahi. ‘Imi Hale collaborates with key local, state, national and international partners to reduce cancer incidence and mortality among Native Hawaiians and Pacific Islanders. Browse culturally tailored cancer education materials on their website.
Visit site

U.S. Census Bureau: Native Hawaiian and Other Pacific Islander:  American Community Survey Reports
Visit site

U.S. DHHS Office of Minority Health: Profile: Native Hawaiians/Pacific Islanders
Visit site

Weaving An Islander Network for Cancer Awareness, Research & Training (WINCART)

WINCART's mission is to promote healthy Pacific Islander communities. WINCART addresses cancer health disparities among Southern California's Pacific Islander populations through increasing cancer awareness, collaborative research programs and providing valuable leadership and training opportunities. Learn about Native Hawaiian and Pacific Islander communities and browse culturally tailored cancer education materials on their website.
Visit site

CDC: Lesbian, Gay, Bisexual and Transgender Health

Provides information on a variety of lesbian, gay, bisexual, transgender health topics.
Visit site

Healthy People: Lesbian, Gay, Bisexual, and Transgender Health

Healthy People 2020 includes goals and objectives to improve the health, safety and well-being of LGBT individuals.
Visit site

Human Rights Campaign (HRC)

HRC is the largest civil rights organization working to achieve equality for LGBTQ Americans. HRC strives to end discrimination against LGBTQ people and realize a world that achieves fundamental fairness and equality for all. Browse resources on a number of topics on their website.
Visit site

LGBT HealthLink

LGBT HealthLink is a community-driven network of experts and professionals enhancing LGBT health by reducing tobacco, cancer and other health disparities within their communities. They are one of eight CDC-funded cancer and tobacco disparity networks. They link people and information to promote adoption of best practices in health departments and community organization to reduce LGBT cancer and tobacco disparities.
Visit site

National Coalition for LGBT Health

The Coalition is committed to improving the health and well-being of lesbian, gay, bisexual and transgender individuals through federal and local advocacy, education and research. The Coalition strives to address the entire LGBT community, including individuals of every sexual orientation, gender, gender identity, race, ethnicity and age, regardless of disability, income, education and geography.
Visit site

National LGBT Cancer Network

The National LGBT Cancer Network works to improve the lives of LGBT cancer survivors and those at risk by educating the LGBT community about increased cancer risks and the importance of screening and early detection; training health care providers to offer more culturally-competent, safe and welcoming care; and advocating for LGBT survivors in mainstream cancer organizations, media and research.
Visit site

National LGBTQ Task Force

The National LGBTQ Task Force advances full freedom, justice and equality for LGBTQ people.
Visit site

HIV/AIDS Network Coordination (HANC)

HANC shares resources covering various aspects of community engagement in clinical research, including transgender resources.
Visit site

UTOPIA Washington

United Territories of Pacific Islanders Alliance Washington (UTOPIA Washington) is a queer and trans people of color-led, grassroots organization born out of the struggles, challenges, strength, and resilience of the Queer and Trans Pacific Islander (QTPI – “Q-T-pie”) community in South King County.
Visit site

CDC: People with Disabilities
Visit site

Healthy People: Disability and Health

Healthy People 2020 includes goals and objectives to maximize health and improve quality of life among individuals with disabilities of all ages.
Visit site

U.S. Census Bureau: Disability

The Census Bureau collects data on disability primarily through the American Community Survey and the Survey of Income and Program Participation.
Visit site

CDC: Alzheimer's Disease and Healthy Aging Program

The Alzheimer’s Disease and Healthy Aging Program (AD+HAP) develops evidence-based, scientific information to educate, inform, and assist in translating its research into public health practice. Located within CDC’s National Center for Chronic Disease Prevention and Health Promotion, the Program focuses primarily on adults age 50 or older. Access health information on a variety of topics for older adults.
Visit site

MedlinePlus®: Older Adult Health
Visit site

National Council on Aging (NCOA)

The NCOA is a respected national leader and trusted partner to help people aged 60+ meet the challenges of aging. They partner with nonprofit organizations, government and businesses to provide innovative community programs and services, online help and advocacy.
Visit site

The Commonwealth Fund: Medicare

Explore this portal of the Commonwealth Fund related to improving the efficiency and quality of Medicare and the health care system as a whole.
Visit site

U.S. Census Bureau: Older Population and Aging

Detailed information and statistics on population aging and the older population.
Visit site

National Rural Health Association

The National Rural Health Association is a national membership organization with more than 21,000 members. The Association’s mission is to provide leadership on rural issues through advocacy, communications, education and research.
Visit site

Rural Health Information Hub (RHIHub)

The RHIHub, formerly the Rural Assistance Center, is funded by the Federal Office of Rural Health Policy to be a national clearinghouse on rural health issues. They are committed to supporting healthcare and population health in rural communities. RHIhub is your guide to improving health for rural residents. They provide access to current and reliable resources and tools to help you learn about rural health needs and work to address them.
Visit site

Build Healthy Places Network: Rural Resources

This page is a collection of resources curated for organizations interested in creating cross-sector health partnerships and increasing community investment in rural areas and small towns to create the conditions that support improved community health.
Visit site

Rural Resources Community Action

This page contains information on rural community building in NE Washington.
Visit site    

Educational Resources

Cancer Health Equity NOW! Podcast

Our Cancer Health Equity NOW podcast amplifies health equity work being done by community organizations, OCOE Community Health Educators, and researchers. Join us for conversations about cancer inequities and transformational change, new ideas and resources, and the incredible people working toward health equity in Washington State. 

physician talking with a patient


Patient Education

Our patient and family education team works with experts at Fred Hutch to create resources that are clear, accurate and useful. We rely on trusted cancer organizations to provide valuable information, including handouts on a variety of topics and links to resources. Our educational resources include videos  explaining common side effects of cancer treatment and how to manage these side effects.