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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

GO2 Foundation for Lung Cancer (formerly the Lung Cancer Alliance) is dedicated to improving the lives of those living with or at risk of lung cancer. Through the Lung Cancer Helpline, callers can access free one-on-one support, educational materials, guidance on screening, treatment and clinical trials, referrals and a variety of other resources. Programs include peer-to-peer support, support groups and online patient communities, clinical trial matching, webinars, and monthly presentations. Most resources, including their Helpline, are available in English only.

HIS Breast Cancer Awareness educates and supports those at risk of or diagnosed with male breast cancer. They provide information packets, how to perform a self-breast exam (as a man), hereditary cancer risk factors and support groups. Their website is designed to help educate, provide resources and support with our expert medical advisors, genetic counselors and programs. Support services and resources are available in English and Spanish.

The Lobular Breast Cancer Alliance’s (LBCA) mission is to make all who are touched by invasive lobular carcinoma (ILC) aware of its unique characteristics and the critical need for more ILC research; to be the go-to source for information on ILC studies, clinical trials and educational tools; to foster partnerships among patients, scientists, clinicians, and breast cancer organizations to increase dialogue about ILC and research advocacy; and to fund vital ILC research.

LBCA provides comprehensive, scientifically vetted and downloadable patient information in 16+ languages on our website, links to clinical trials accepting patients with lobular breast cancer and links to other patient supports and resources. Our primary audience is individuals who have or have had lobular breast cancer and their family and friends. We have an international scientific advisory board and an international following and individuals who receive our monthly newsletter. Resources are available in English and Spanish.

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.

The National Lymphedema Network (NLN) provides education and guidance to lymphedema patients, health care professionals, and the general public by providing information on the prevention and management of primary and secondary lymphedema. The NLN provides referrals to lymphedema treatment centers, health care professionals, training programs, and support groups. Lymphedema garments are also available for patients who meet eligibility criteria. Limited information is available in Spanish.

Information is available on the website or via the toll-free number. If you call the toll-free number, you may need to leave a voicemail message.

The Sarcoma Alliance strives to extend and improve the lives of sarcoma patients through accurate diagnosis, improved access to care, education, and support. The Alliance offers financial assistance (grant maximum: $500) for expenses related to second opinion consultations. Support is available through their Peer-to-Peer Network which matches individuals affected by sarcoma with members who have had a similar experience. The Alliance also maintains a list of medical centers and hospitals specializing in sarcoma.