American Cancer Fund (ACF)

Contact: 908-431-9800
Population served: Anyone affected by cancer and needing information
Mission:

ACF™ is dedicated to the education, support and empowerment of those diagnosed with cancer by organizing and clarifying information. Provides information about:

• Living with Cancer
• Clinical Trials
• Complementary and Alternative Medicine
• Nutrition and Exercise
• Oral Health

American Cancer Society (ACS)

Contact: 800-227-2345
Population served: People affected by a cancer internationally; programs and services offered to patients and caregivers residing in the United States
Other language(s): Spanish, Chinese, Korean, Vietnamese
Mission:

In the U.S., ACS is a community-based voluntary health organization dedicated to eliminating cancer as a major health problem.

• Provides educational materials both online and in print about cancer, including blood cancers, as well as related information on topics such as diet, exercise, complementary and alternative medicine, and disease statistics
• Offers support services via online discussion boards and in-person support groups through local chapters
• Cancer Survivors NetworkSM, a global online community, transcends geographic boundaries and builds bonds among cancer survivors and caregivers through shared experiences and feelings
• Road to Recovery, a program offered locally by some chapters, has volunteer drivers who transport patients to and from treatment appointments
• Hope Lodges are temporary housing accommodations for patients traveling far from home for treatment. There are more than 30 lodges
• American Cancer Society’s Wig Bank - Provides free wigs from limited supply to needy patients suffering hair loss due to cancer treatment. Intended for those with insufficient insurance coverage for cranial prostheses (wigs).

American Society for Radiation Oncology (ASTRO)

Contact: 800-962-7876
Population served: Health professionals
Mission:

To improve patient care through education, clinical practice, advancement of science and advocacy.

• Provides members with the continuing medical education, health policy analysis, patient information resources and advocacy that they need to succeed in today’s ever-changing health care delivery system.

Aplastic Anemia & MDS International Foundation

Contact: 800-747-2820 or help@aamds.org
Population served: Patients and families living with Aplastic Anemia, Myelodysplastic Syndromes (MDS), Paroxysmal Nocturnal Hemoglobinuria (PNH), and related bone marrow failure diseases
Mission:

To support, connect and educate patients, caregivers and health professionals on bone marrow failure diseases worldwide

• Free educational materials: Information on research, treatment, and clinical trials
• Online Academy: Live webinars, webcasts, interviews with experts, and interactive learning modules
• Peer Support Network: Patients and caregivers can speak with trained patient volunteers who share treatment experiences and provide emotional support
• Community Connections: Volunteer-led regional support groups connecting patient and families
• Online Community: MarrowCommunity.org is an online community for patients with bone marrow failure and their families. Members can connect with others, share resources, learn about upcoming events and have their questions answered.
• Educational Conferences: Our free conferences in cities around the country offer learning opportunities from leading medical experts, and the ability to connect directly with other patients and caregivers
• Travel Assistance: To ensure that patients can see a specialist to seek the best course of treatment. Financial aid may be available for U.S.-based patients with demonstrated financial need

• Find A Specialist: online search tool.

Cancer Hope Network

Contact: 877-467-3638
Population served: People diagnosed with cancer and their families in the U.S.
Other language(s): Spanish, French, additional translation services available by phone
Mission:

To provide one-on-one support to people undergoing treatment for cancer and their families.

• Provides training to individuals who have recovered from cancer so they can be matched with cancer patients currently undergoing a similar experience.

Cancer Support Community (CSC)

Contact: 888-793-9355
Population served: People affected by cancer in the U.S. and Canada
Other language(s): Spanish
Mission:

To provide support, education and hope to people affected by cancer; to ensure that all people impacted by cancer are empowered by knowledge, strengthened by action, and sustained by community.

• Offers support through a network of more than 52 local affiliates and 175 locations
• Cancer Support Helpline® - offers resources and emotional support via phone or live chat, and is staffed by licensed mental health professionals
• MyLifeLine - create a private, personal webpage to help keep family and friends stay involved and informed
• Frankly Speaking About Cancer® – education series that provides trusted information on a variety of topics important to people affected by cancer; information is available in a variety of formats
• Virtual Home - resources to connect you to education, support, and action opportunities to enhance your health and well-being from the comfort of your computer
• Open to Options – provides general information about clinical trials, helps patients identify important questions about treatment options and decisions based upon personal needs
• CancerSupportSource® - a tool that assesses distress in key areas (such as sleep, nutrition, worry about the future) and provides referral and follow-up care for all patients
• Cancer Experience Registry - a unique online community that brings people impacted by cancer together to make their voices heard, connect with each other, share experiences, learn from and help others
• Cancer Transitions – an evidence-based programs for cancer survivors who have completed their treatment (in partnership with LIVESTRONG)

CancerCare

Contact: 800-813-4673
Population served: Individuals, families, caregivers and the bereaved in the U.S. affected by a cancer diagnosis
Other language(s): Spanish
Mission:

To provide free, professional support services to individuals, families, caregivers and the bereaved to help them cope with and manage the emotional and practical challenges of cancer.

• Oncology social workers are available for telephone counseling services to provide support, information and resources to help in coping with cancer
• Offers online support groups and educational publications
• Cancer Out Loud: The CancerCare Podcast features conversations with people living with cancer, caregivers, survivors, loved ones and the bereaved
• Connect Education Workshops in which leading experts in oncology provide up-to-date information in one-hour workshops over the telephone or online
• Financial assistance for transportation, medications, home care, child care, or durable medical equipment may be available for patients in active treatment. Eligibility guidelines vary depending on diagnosis, gender and geographic location. Call for details
• Young Professionals Committee Scholarship Program awards $2,500 grants to young adults who have lost a parent or guardian to cancer in the last two years.  Applicants must be from New York, New Jersey, Connecticut, or Pennsylvania.  Call for details.
• Healing Hearts Family Bereavement Camp - a free retreat for families with children coping with the loss of a loved one to cancer
• Pen Pal Program: Cancer patients age 65 and older can receive letters from a caring volunteer
• Financial assistance for insured cancer patients in treatment in the US to help with co-payments for chemotherapy and targeted treatment medications who meet certain financial, medical and insurance eligibility criteria. Check the website (http://cancercarecopay.org/) or call 866-552-6729 for details.

Caring.com

Contact: 800-973-1540 or Website
Population served: Caregivers
Mission:

To provide information and support for people caring for aging parents, spouses and other loved ones.

• Provides elder care information and support, including information about senior living options and in-home care
• Offers an online section covering a wide variety of relevant caregiving-related topics (e.g. insurance, benefits, coping)
• Offers one-on-one guidance with a Family Advisor at no cost.

Chemocare.com

Contact: 844-268-3901
Population served: Anyone seeking information on chemotherapy or cancer
Other language(s): Spanish and additional languages
Mission:

Chemocare.com® is a website designed to provide the latest information about chemotherapy to patients and their families, caregivers and friends. The site focuses on care during chemotherapy including information about FDA approved chemotherapy medications, nutrition, managing side effects and self-care tips. The content is continually updated and reviewed by oncology specialists.

Chemo Angels

Contact: Website
Population served: Pediatric (age 4 and up) and adult cancer patients undergoing chemotherapy in the US
Mission:

To offer support and encouragement to cancer patients in treatment

• Volunteers send cards and uplifting messages to cancer patients via postal mail
• Website provides links to patient resources.

Eldercare Locator

Contact: 800-677-1116 or Website
Population served: Older adults, caregivers in the U.S.
Other language(s): Spanish
Mission:

To connect older adults and their caregivers with trustworthy support resources.

• Links those who need assistance with state and local agencies on aging as well as community-based organizations that serve older adults and their caregivers
• Provides information on topics such as housing, insurance, transportation, etc.
• Is a public service of the Administration on Aging, an agency of the U.S. Administration for Community Living.

Elephants and Tea

Contact: Website
Population served: Adolescent and young adult cancer patients, survivors, caregivers, and healthcare professionals worldwide
Mission:

To help adolescent and young adult (AYA) patients, survivors, and caregivers know they are not alone in their fight with cancer

• Provides a free quarterly print magazine and online site with stories and experiences written by young adult cancer patients and survivors
• Offers digital programs and events to bring the AYA community together to interact and empower each other
• Collaborates with AYA organizations across the US.

Get Palliative Care

Contact: Website Only
Population served: Patients with life-threatening illness and their caregivers
Mission:

To increase the availability of quality palliative care services for all people living with serious illness. 

• Provides information about palliative care: specialized medical care which provides patients with relief from symptoms, pain and stress
• Explains how palliative care helps people with specific diseases
• Provides a directory of hospitals with palliative care teams
• Offers videos, blog, printed material and other resources including a quiz to help individuals know if palliative care is right for them.

Give an Hour

Contact: Website only
Population served: U.S. troops and families affected by the wars in Afghanistan and Iraq and other post-9/11 conflicts
Mission:

Give an Hour™ asks mental health professionals nationwide to literally donate an hour of their time each week to provide free mental health services to military personnel and their families. Individuals who receive services will be given the opportunity to give an hour back in their own community.

• In addition to direct counseling services, the providers are working to reduce the stigma associated with mental health by participating in and leading education, training, and outreach efforts in schools and communities and around military bases.

Global Resource for Advancing Cancer Education (GRACE)

Contact: 1-888-501-1025 or info@cancerGRACE.org
Population served: People with blood cancer (and lung or head & neck cancer), caregivers, health professionals
Mission:

To provide expert-mediated information on current and emerging cancer management options in order to empower patients, caregivers, and health professionals to become direct partners in cancer care.

• Offers cancer information and video library, podcasts, email newsletter and online discussion forums.

HelpPRO

Contact: 800-652-0155 or website
Population served: Anyone seeking mental health clinicians in the U.S.
Mission:

To improve the public's access to the services of mental health clinicians and organizations. Our vision is that every person in America can readily find mental health services to meet their needs.

• Therapist Finder carefully identifies users’ needs and interests and matches these with our therapists’ capabilities. Matching process increases the likelihood that users and therapists will make positive, lasting connections from their very first meeting. Database contains detailed information on thousands of mental health professionals, their services and their organizations across the country.

Imerman Angels

Contact: 877-274-5529
Population served: Anyone with cancer
Mission:

To provide personalized connections that enable one-on-one support among cancer fighters, survivors and caregivers.

• Provides a unique matching program in which a “Mentor Angel” is partnered with an individual seeking cancer support. These one–on–one relationships inspire hope and offer support from someone who is uniquely familiar with the experience.

International Myeloma Foundation (IMF)

Contact: 800-452-2873 (US & Canada) or 818-487-7455 (Worldwide)
Population served: Anyone needing information on myeloma, including patients, caregivers and health professionals
Mission:

To improve the quality of life of myeloma patients and their families while working toward prevention and a cure through four founding principles: research, education, support, and advocacy.

• Offers disease and treatment information via toll free number and publications in multiple languages
• Makes referrals to support groups and hosts an on-line support group
• Offers seminars, workshops and webcasts
• Provides Veterans Against Myeloma (VAM), a resource for patients who have served in the military and developed myeloma through their service
• IMF Advocacy group helps guide individuals to advocate for critical health issues that affect the myeloma community
• Supports research initiatives.

Lacuna Loft

Contact: Website
Population served: Young adult cancer patients, survivors, and caregivers, ages 18 to 45
Mission:

To encourage, empower and connect young adult cancer survivors and caregivers

• Provides online support programs
• Lifestyle information and resources
• Creative workshops, writing group, Speaker Series, and more.

LIVESTRONG Foundation

Contact: 855-220-7777
Population served: Cancer patients and survivors in the U.S.
Other language(s): Spanish
Mission:

To inspire and empower people affected by cancer; to provide support to guide people through the cancer experience, bring them together to fight cancer—and work for a world in which their fight is no longer necessary.

• Provides information on topics that influence the “physical, emotional and practical” effects of cancer
• Provides free, confidential, one-on-one support to anyone affected by cancer, not just patients, through education, referrals and counseling services
• Planet Cancer connects young adults and helps them access support, advocacy and resources.
• LIVESTRONG Fertility - Dedicated to providing reproductive information, support and hope to cancer patients and survivors whose medical treatments present the risk of infertility.
• Maintains a list of LIVESTRONG Survivorship Centers of Excellence, which is comprised of National Cancer Institute(NCI) Comprehensive Cancer Centers
• Offers The LIVESTRONG Guidebook to help cancer patients and survivors as they navigate the health care system.

MPN Advocacy and Education International

Contact: 517-899-6889
Population served: Patients with myeloproliferative neoplasms (Essential Thrombocythemia, Idiopathic Myelofibrosis, Polycythemia Vera), caregivers, professionals worldwide
Other language(s): All European, Spanish, Arabic, Japanese, Urdu
Mission:

To make a difference in the lives of those affected by myeloproliferative neoplasms.

• Offers disease, treatment and clinical trial information
• Website lists online and in-person support groups worldwide
• Offers an email digest, educational events and webcasts
• Provides outreach to the entire MPN community to grow awareness, understanding, and a better quality of life for MPN patients

• Engages legislators and governmental bodies on behalf of their constituents to ensure the MPN Community is represented.

MPN Cancer Connection

Contact: Website
Population served: Patients diagnosed with Myeloproliferative Neoplasms (MPNs), caregivers, professionals
Mission:

To empower patients to better understand their disease and treatment options; to improve patient care

• Provides information about the MPNs such as Essential Thrombocythemia, Polycythemia Vera and Myelofibrosis
• Provides links to recent news, articles, Facebook groups and resources

MPN Community Support

Contact: Website only
Population served: Patients diagnosed with Myeloproliferative Neoplasms (MPNs), caregivers, professionals
Mission:

To provide a directory of resources for people living with MPNs (Essential Thrombocythemia, Polycythemia Vera and Myelofibrosis)

• Curated by MPN patients and advocates
• Provides links to reputable MPN-related resources, such as for support services, financial assistance, clinical trials, transplant information, etc.

Myeloma Crowd

Contact: Website
Population served: Patients with myeloma and caregivers
Mission:

To empower patients each step of their disease journey – from diagnosis, through education, care and on to a cure.

• Myeloma Crowd is a division of The HealthTree Foundation, a patient-driven nonprofit organization.  It provides online disease, treatment, clinical trial and research information, educational programs, articles, monthly meet-ups, myeloma ‘coaches’ and more.  The website lists financial resources and myeloma specialists

National Bone Marrow Transplant Link (nbmtLINK)

Contact: 800-546-5268 or 248-358-1886
Population served: Patients, caregivers who have had or will have a bone marrow/stem cell transplant in the U.S.
Other language(s): Spanish, French
Mission:

To help patients, caregivers, and families cope with the social and emotional challenges of bone marrow/stem cell transplant from diagnosis through survivorship by providing vital information and personalized support services.

• Offers educational publications, webcasts, online library
• Provides an extensive volunteer peer support program
• Offers Telephone Education and Support Group for Bone Marrow/Stem Cell Transplant Survivors: Coping with Chronic Graft versus Host Disease (4 week program).

National Coalition for Cancer Survivorship (NCCS)

Contact: 877-622-7937
Population served: People touched by cancer in the U.S.
Other language(s): Spanish
Mission:

To advocate for quality cancer care for all people touched by cancer.

• Advocates for changes in how the nation researches, regulates, finances and delivers quality cancer care
• Empowers cancer survivors through its publications and programs, which provide tools for self-advocacy
• Convenes other cancer organizations to address nationwide public policy issues affecting cancer survivors
• Cancer Survival Toolbox is a free, self-learning audio program to help people develop important skills to better meet and understand the challenges of their illness.

National LGBT Cancer Network

Contact: 212-675-2633 or Website
Population served: Cancer patients, survivors, caregivers, healthcare professionals in the US
Mission:

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, the media and research.

• Resource library contains up-to-date research articles, webinars, videos, fact sheets, etc.
• Maintains directories of LGBT-welcoming cancer screening facilities and cancer treatment facilities in the US
• Provides LGBT cultural competency trainings for health and human service providers.

Nikolas Ritschel Foundation

Contact: Website only
Population served: Young adult cancer patients ages 18-24 in the US
Mission:

To provide enrichment opportunities and encouragement to young adult cancer patients

• Apply online to request a wish for respite, travel, technology or other needs.

Patient Resource Cancer Guides

Contact: (913) 725-1600
Population served: Patients and caregivers
Other language(s): Spanish
Mission:

To empower people who are suffering with life-altering diseases by giving them the most comprehensive and up-to-date guides to treatment and facilities for their disease free of charge.

• Provides free educational materials, written for ease of understanding, in print and online.

Patients Into People

Contact: info@patientsintopeople.com
Population served: Anyone affected by cancer in the U.S.
Mission:

To brighten the day of a cancer patient with a gift of a cheerful, new hospital gown.

• Provides gowns in a variety of sizes to men and women battling cancer 

PREPARE for your care

Contact: Website or info@prepareforyourcare.org
Population served: Patients, caregivers, survivors, healthcare professionals worldwide
Other language(s): Spanish
Mission:

To ensure all people are prepared and able to make informed medical decisions for themselves and their loved ones and to have a voice in their health care.

• Offers free easy-to-read advance directives for all 50 states in both English and Spanish
• Information is available in a step-by-step program with video stories
• Provides pamphlets, question guide, and movie with toolkit for group events
• Offers a newsletter and links to related research topics

Stupid Cancer

Contact: 877-735-4673
Population served: Young adult cancer patients and survivors, caregivers
Mission:

To empower, support, and improve health outcomes for the young adult cancer community

• Offers CancerCon - an annual 4-day gathering which includes informational workshops, educational breakout sessions, group discussions, networking opportunities, and social activities
• Organizes meet-ups - volunteer-hosted social gatherings of local groups of survivors
• Hosts the Stupid Cancer Show - a YouTube Channel featuring interviews with survivors, informational episodes, and radio show content
• Offers an online community including regional Facebook groups, online forums, blogs, and social media
• Stupid Cancer Summit: free, one-time events hosted at cancer centers to share information, provide resources, and bring together the local young adult survivor community
• Lists other organizations that provide financial, legal, reproductive, and other assistance.

The Bone Marrow & Cancer Foundation

Contact: 212-838-3029 or 800-365-1336
Population served: Transplant patients and families, caregivers, survivors in the US
Mission:

To improve the quality of life for cancer and transplant patients and their families by providing vital financial assistance, comprehensive resources, educational information, physician referrals, and emotional support programs.

• Patient Navigators provide guidance and support to anyone faced with a cancer diagnosis or needing a bone marrow or hematopoietic cell transplant
• Lifeline Fund provides financial support to help cover the costs of donor searches, medications, home and child care services, medical equipment, transportation, cord blood banking, housing costs and other expenses associated with transplant​
• Carelines provides social media tools for crowdfunding, journaling and a volunteer task calendar for anyone with a cancer diagnosis or receiving a bone marrow, stem cell or cord blood transplant 
• Scholarship Grants help make educational aspirations a reality for bone marrow, stem cell or cord blood transplant survivors
• Clinical Care Counseling provides confidential individual and family supportive counseling, financial guidance and resource referrals for cancer, transplant patients, and family members
• Ask the Expert enables individuals to anonymously pose questions concerning transplantation and to have them answered by transplant specialists
• SupportLine links transplant patients and their families with volunteers who have gone through the transplant experience
• Support Groups provide patients, families and caregivers the opportunity to share experiences and draw support from one another
• Medical and Educational Handbooks provide comprehensive transplant information and resources

The Feather Foundation - Hope for Parents with Cancer

Contact: (862) 702-9559 or Website
Population served: Parents with cancer in the US
Mission:

To provide emotional and practical support to parents who have cancer. 

• Provides emotional support through online groups, guidance and tips on parenting with cancer and self-care
• Offers resource list of other assistance available for parents with cancer
• Parents with cancer who reside in New York or New Jersey may have a social worker or health professional inquire about possible one-time financial help toward childcare-related costs.

The Patient Story

Contact: Website
Population served: Patients with various types of cancer (including Hodgkin and Non-Hodgkin Lymphoma), caregivers and interested individuals
Mission:

To humanize every cancer diagnosis; to help improve quality of life and health outcomes

• Gives cancer patients and caregivers a sense of calm and control by showing them what their lives may look like post-diagnosis with FAQ-type answers and simple yet detailed visuals like timelines
• Provides cancer survivors a chance to share their stories with those who need that help the most, empowering them to help turn their experiences into something positive.

WidowedParent.org

Contact: Website only
Population served: Widowed mothers and fathers with children in the home, professionals
Mission:

To support widowed mothers and fathers with children in the home.

• Hosted by the UNC Lineberger Comprehensive Cancer Center, the website offers information for parents and children about dealing with grief plus an online list of resources and supports.

Women Survivors Alliance

Contact: 615-719-0741
Population served: All women cancer survivors
Mission:

The Women Survivors Alliance has undertaken a national call to action to address the burdens of survivorship issues on women, their families, and by extension, society as a whole.

• Hosts an annual National Women Survivors Convention
• Develops a comprehensive resource with an online magazine format, its dynamic content will include nutrition, exercise, the latest in survivor news, a marketplace, a blog, a directory of cancer organizations across the internet, and more.
• One day educational events held in cities across the country, the first one scheduled for 2014. These events will be hosted in partnership with Triage Cancer.