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The mission of the American Lung Association® (ALA) is to save lives by improving lung health and preventing lung disease through education, advocacy, and research. Their online Resource Library provides lung cancer patients, and their loved ones, with information on diagnosis and treatment, educational videos, and research. Additional resources include their Lung Helpline and online support communities. Assistance with smoking cessation is available through their Freedom from Smoking programs. Phone and online resources are available in English and Spanish.

Cancer and Careers empowers and educates people with cancer to thrive in the workplace. A variety of programs provide cancer patients and survivors with information needed to navigate the practical and legal challenges that follow a diagnosis. Online resources, available in English and Spanish, include career coaching, information on conducting a job search, resume review services, interviewing tips, free publications, support groups, and educational seminars. There are also resources specific to healthcare providers, employers, and coworkers. Callers may be asked to send an email with questions, or to leave a message.

The Cancer Support Community (CSC) is dedicated to providing emotional support for individuals affected by cancer, including their families and friends. With its online community and global network of 175 locations, the CSC offers a variety of free services, including: support groups, counseling, cancer education, navigating costs, publications, webinars, personal patient websites (MyLifeLine), and healthy lifestyle programs. The CSC also conducts research and advocates for those whose lives have been disrupted by cancer. Select online resources are available in Spanish, Chinese, and other languages.

The Cancer Support Helpline’s licensed counselors provide guidance, resources and support to cancer patients or their loved ones. Counseling is available in over 200 languages. For longer-term support, referrals to local mental health professionals are available.

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.

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.

The International Association of Laryngectomees (IAL) is a nonprofit, voluntary organization composed of member clubs and recognized regional organizations. These clubs are generally known as Lost Chord or New Voice clubs. Club membership ranges from 10 to more than 300 laryngectomees. The purpose of the IAL is to assist these local clubs in their efforts toward the total rehabilitation of the laryngectomee. The IAL exchanges ideas and disseminates information to member clubs and to the public, facilitates the formation of new clubs, fosters improvement in laryngectomee programs, and improves the minimum standards for teachers of post-laryngectomy speech. The IAL Voice Institute trains laryngectomees and prospective instructors of speech in an intensive 5-day course that emphasizes speech restoration as the central component to multidisciplinary total rehabilitation. A directory of laryngectomee-experienced speech instructors in the United States is available on the IAL Web site. Some Spanish materials are also available.

The International Myeloma Foundation (IMF) is dedicated to improving the quality of life of myeloma patients while working toward prevention and a cure. The IMF Hotline answers questions from patients and family members and provides information about medical services, pharmaceutical access, and patient support groups. Free IMF publications include the IMF Multiple Myeloma Patient Handbook; Multiple Myeloma: A Concise Review of the Disease and Treatment Options; and the Understanding Series – treatment specific brochures on new therapies and clinical trials. The Foundation conducts Patients & Family Seminars to educate patients on the latest information about current therapies, research advances, and emerging treatment options. A comprehensive network of support groups from around the world are also available to assist patients and their families. The IMF operates Bank-On-A-Cure®, a unique global gene bank to advance myeloma research. The IMF's research grant program funds research projects around the world for both multiple myeloma and amyloidosis.

The International Waldenstrom's Macroglobulinemia Foundation (IWMF) provides encouragement and support to people with Waldenstrom macroglobulinemia (WM) and offers information and education programs that address patient's concerns, and promotes and supports research leading to a cure. The IWMF offers many patient publications, including a New Patient Information Package (Info Pak). IWMF-Talk is an e-mail talklist for discussion of every aspect of WM (available in English, French, German, Spanish, Nordic Countries, U.K.). Telephone Lifeline Support provides telephone numbers of IWMF volunteers who will answer questions about their first-hand experience with specific treatment for WM. IWMF also provides telephone and e-mail network lists that connect patients and caregivers. IWMF provides funding to researchers studying a treatment or cure for Waldenstrom macrogloblinemia or related blood cancer. Information on the Web site is available in French, Spanish, and German.

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 Mesothelioma Applied Research Foundation (Meso Foundation) is a nonprofit collaboration of patients and families, physicians, advocates, and researchers dedicated to eradicating mesothelioma. The Meso Foundation aims to provide up-to-date information on the disease and its treatment, as well as to connect patients and families with specialists, support resources and community. Mesothelioma experts are available over-the-phone and via email. Patients traveling for an initial consultation and those enrolled in a clinical trial may be eligible for reimbursement of travel-related expenditures.

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 Bone Marrow Transplant Link (nbmtLink) is a nonprofit organization specifically serving stem cell transplant patients, their caregivers, families, and health professionals. The nbmtLink provides information and support services, including a volunteer peer support program, resource referrals for patients and health professionals, and educational guides, videos, and Webcasts. The free nbmtLINK Online Library contains hundreds of journal articles, booklets, and reference materials, as well as comprehensive links to additional online information. Information on how to become a donor is also available.

The National Cervical Cancer Coalition (NCCC) is a nonprofit organization dedicated to serving women with, or at risk for, cervical cancer and HPV disease. Its mission is to promote prevention through education about early vaccination, Pap testing and HPV testing, when recommended. Services include access to online educational materials (publications, videos and webinars), a variety of patient and family support resources, and information on free/low-cost Pap testing. Some resources are available in Spanish.

Sharsheret, Hebrew for “chain”, is a national organization which supports young Jewish woman and families facing breast and ovarian cancer. They offer a peer support network that connects women newly diagnosed or at high risk of developing breast or ovarian cancer with others who share similar diagnoses and experiences. They also provide support and education programs addressing advanced breast cancer, genetics, parenting, cosmetic side effects of treatment as well as programs for caregivers and those facing ovarian cancer. Genetic counselors are available to discuss family history, concerns about cancer risk and the implications of genetic counseling. Sharsheret’s programs are open to all women and men.

The Young Survival Coalition (YSC) focuses on issues unique to young women who are diagnosed with breast cancer. YSC works with survivors, caregivers, and the medical, research, advocacy, and legislative communities to improve the quality of life for breast cancer patients age 40 and younger. YSC can help young survivors find a support group, or match survivors with volunteers who’ve had a similar experience. YSC offers online resources including educational and support materials, discussion boards, and information about conferences and symposia.

Some publications are available in Spanish, and Spanish-speaking volunteers are available to serve as survivor matches in its peer-support program.