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The American Cancer Society (ACS) is a nationwide, community-based voluntary health organization. In addition to providing a wide variety of services and programs for cancer patients, family, friends, and caregivers, the ACS also supports cancer research, advocacy, and education. The Cancer Helpline, available 24 hours/day, connects callers with trained staff that can help answer general questions about cancer, recent diagnoses and treatment. Cancer Information Specialists can also provide information on support services and assist in finding local and national financial assistance programs.

Information is available in both English and Spanish, with select topics available in 11 other languages.

In response to the COVID-19 pandemic, some services and programs may have been suspended. For up-to-date information on available services, visit the Support Programs and Services web page or contact the ACS at the phone number above.

ACS programs and services include:
Health Insurance Assistance Service: health insurance specialists provide information for those who have lost, or are in danger of losing, their health care coverage
Hope Lodge: lodging for patients and caregivers
I Can Cope: online cancer education classes for patients and loved ones
Online Support Communities
Reach to Recovery: breast cancer support
Road to Recovery: rides to treatment
tlc (Tender Loving Care): catalog and website of hair loss and mastectomy products

CancerCare provides free, professional support services and information to help anyone affected by cancer. Services include individual and group counseling, support groups, educational workshops, publications, practical help and referrals. Limited financial assistance may be available for select cancer-related expenses. Information on current programs is available online or by calling CancerCare directly. Short-term counseling is provided by oncology social workers and is available in-person (at their local offices), online or over the telephone.

Many resources, including counseling, are available in Spanish.

The Leukemia and Lymphoma Society (LLS) is dedicated to funding blood cancer research and providing education and services to patients and caregivers. Support services include local support groups, online chat, an online patient community, and peer-to-peer support that links patients and their families with a trained volunteer who has experienced a similar situation.

Additional resources include educational programs, publications, home-care services, financial assistance, and information tailored to caregivers. Information specialists are available over-the-phone to assist with questions related to diagnosis and treatment, financial and social challenges, and support. Information is available in Spanish, with language interpretation available in 170 languages. LLS has chapter offices located throughout the United States and Canada.

The Multiple Myeloma Research Foundation (MMRF) provides information for patients with multiple myeloma and other types of plasma cell disorders. In addition to resources specific to the disease, including information on signs and symptoms, initial diagnosis, and treatment options, a variety of publications and educational programs are available for patients and their caregivers. The MMRF also provides information on finding a treatment center, support groups, and financial assistance programs. Nurse Patient Navigators offer information and support over-the-phone, via email and through social media. Select publications are available in Spanish.