Alliance of Dedicated Cancer Centers (ADCC)

ADCC is comprised of 11 nationally recognized comprehensive or clinical cancer centers. The ADCC member cancer centers play a pivotal role in the National Cancer Program, which was enacted by Congress in 1971 to improve the detection, prevention, diagnosis, and treatment

of cancer. The ADCC hospitals are singularly dedicated to deepening the understanding of the causes and cures for cancer; developing new treatments for cancer; and disseminating this knowledge to the provider community at large. The Centers' state-of-the-art therapies and research activities offer the greatest possibility for the successful treatment of cancer patients. Much of the recent progress in understanding cancer's biology and effective treatment is directly attributable to the work of the Centers.

American Association for Cancer Research (AACR)

The AACR is the oldest and largest scientific organization in the world focused on every aspect of high-quality, innovative cancer research. The mission of the AACR is to prevent and cure cancer through research, education, communication, and collaboration. 215.440.9300 or toll free 866.423.3965

American Cancer Society (ACS)

An extensive network of information resources and organizations fighting cancer by providing information, education, support and research funding. 800.ACS.2345 | 800.227.2345

American Society of Clinical Oncology (ASCO)

A non-profit organization, ASCO supports cancer research, especially patient-oriented clinical research. Membership is composed of clinical oncologists from all oncology disciplines and sub-specialties. Patient information: 571.483.1780 | 888.651.3038

Association of Cancer Online Resources (ACOR)

An internet-based public charity dedicated to improve the quality of care provided to patients with cancer and the quality of life of patients, survivors and their caregivers. 212.226.5525

Association of Community Cancer Centers (ACCC)

ACCC helps oncology professionals adapt to the complex challenges of program management, reimbursement restraints, hospital consolidation and mergers, and legislation and regulations that threaten to compromise the delivery of quality cancer care. ACCC works closely with members of Congress, government agencies, and other cancer care advocacy organizations to help assure patient access to quality cancer care. 301.984.9496

Association of Oncology Social Work (AOSW)

AOSW is a non-profit organization dedicated to the enhancement of psychosocial services to people with cancer and their families. AOSW was created in 1984 by social workers interested in oncology and by existing national cancer organizations. AOSW has over 1000 current members who embrace the AOSW Mission “to advance excellence in the psychosocial care of persons with cancer, their families, and caregivers through networking, education, advocacy, research and resource development.” 215.599.6093

Bone and Cancer Foundation

A resource for patients and health professionals concerned with the care and treatment of cancer involving bone. They provide information for cancer patients and family members on the causes and treatment of cancer involving bone. Toll free, 888.862.0999

Breathing Room Foundation

Breathing Room Foundation is dedicated to providing care and support to local families affected by cancer. We recognize that a cancer diagnosis affects every aspect of a family’s life; emotional, physical, spiritual and financial. Breathing Room Foundation strives to provide a family with whatever it is that will allow them a bit of "breathing room" from their daily struggle against cancer. It is our hope that this will allow them to concentrate all of their efforts towards regaining their physical health. 215.277.1006

Cancer and Careers

Cancer and Careers, founded in 2001, is a national nonprofit that empowers and educates people with cancer to thrive in their workplace, by providing expert advice, interactive tools and educational events. The organization reaches more than 325,000 individuals per year online, in print and in person. Its free services include a comprehensive website and library of publications in English and Spanish; legal and insurance information; career coaching; resume review; professional development micro-grants; and national events and workshops for people with cancer and their healthcare providers, coworkers and employers.

CancerCare

Founded in 1944, CancerCare is the leading national organization providing free, professional support services and information to help people manage the emotional, practical and financial challenges of cancer. Our comprehensive services include counseling and support groups over the phone, online and in-person, educational workshops, publications and financial and co-payment assistance. All CancerCare services are provided by oncology social workers and world-leading cancer experts. Headquartered in New York, NY, CancerCare maintains three additional locations in Norwalk, CT, Ridgewood, NJ and Syosset, NY. To learn more, visit www.cancercare.org or call 800.813.HOPE | 800.813.4673.

Cancer Hope Network

Provides free, confidential, one-on-one support to people with cancer and their families. The program is available to all cancer patients and their loved ones from anywhere in the United States at no cost. 800.552.4366

Cancer Insurance Checklist

The Cancer Insurance Checklist is designed to help you when shopping for insurance on your state's Health Insurance Marketplace/Exchange if you have cancer, a history of cancer, or are at risk for cancer.

Cancer Insurance Checklist: Guía de Cobertura Médica para Personas con Cáncer

Si padece cáncer, tiene antecedentes de cáncer o se encuentra en riesgo de padecer cáncer, la Guía de cobertura médica para personas con cáncer puede asistirle con la compra de un seguro en el mercado de seguros médicos de su estado.

Cancer.net

The patient information website of the American Society of Clinical Oncology (ASCO) is designed to help patients and families make informed health care decisions. The site provides information on more than 120 types of cancer and cancer-related syndromes, clinical trials, coping, side effects, a "Find an Oncologist" database, message boards, patient support organizations, and more. (English and Spanish) Patient Helpline: 571.483.1780 or 888.651.3038; for printed materials: 888.273.3508 or 703.519.1430

The Cancer Project

The Cancer Project is a non-profit organization advancing cancer prevention and survival through nutrition education and research. 202.686.2210

Cancer Support Community

Uniting The Wellness Community and Gilda's Club Worldwide, the Cancer Support Community is an international non-profit dedicated to providing support, education and hope to people affected by cancer. 888.793.9355

CURE

Cancer Updates, Research & Education is a unique quarterly magazine bridging the knowledge gap between cancer patients and caregivers. CURE demystifies the science and medicine of cancer and gives readers links to important resources on the web and in the medical community. CURE provides readers the tools they need to take action, such as participating in clinical trials of new drugs that could mean the difference between life and death. 214.367.3500; Toll Free: 800.210.CURE | 800.210.2873

Family Reach

Family Reach is a national non-profit providing financial assistance, education and outreach for families facing a cancer diagnosis. For more information, connect with your social worker or visit familyreach.org.

Good Days

Good Days is a national, independent 501(c)(3) non-profit charitable organization that provides financial assistance to patients so that they do not have to choose between getting the treatment the need and affording the necessities of everyday living.

International Cancer Advocacy Network (ICAN)

ICAN assists patients with cutting-edge information services, patient empowerment, and health information technology tools, as well as research regarding molecular profiling, clinical trials, and compassionate use. 602.618.0183; programservices@askican.org

Lolly's Locks

Lolly's Locks connects high-quality wigs with cancer patients who are suffering hair loss as an effect of chemotherapy, and who are unable to afford them.

National Blood Clot Alliance

NBCA is a patient-led, voluntary health advocacy organization dedicated to advancing the prevention, early diagnosis and successful treatment of life-threatening blood clots such as deep vein thrombosis and pulmonary embolism. NBCA accomplishes its mission through programs that build public awareness, educate patients and healthcare providers.  NBCA works to see a future in which the number of people suffering and dying from blood clots in the United States is reduced significantly.

National Cancer Institute (NCI)

Conducts and supports research, training, health information dissemination, and other programs with respect to the cause, diagnosis, prevention, and treatment of cancer. It also includes information on rehabilitation from cancer, and the continuing care of cancer patients and the families of cancer patients. 800.4.CANCER | 800.422.6237

National Center for Complementary and Alternative Medicine

One of the 27 institutes and centers that make up the National Institutes of Health (NIH). It is dedicated to exploring complementary and alternative healing practices in the context of rigorous science, training complementary and alternative medicine (CAM) researchers, and disseminating authoritative information to the public and professionals. United States: 888.644.6226.

National Coalition for Cancer Survivorship (NCCS)

A non-profit national advocacy organization, NCCS is a nationwide network of independent organizations and individuals working in the areas of cancer support, education, and advocacy. 877.NCCS.YES | 877.622.7937

National Hospice and Palliative Care Organization (NHPCO)

NHPCO is the largest non-profit membership organization representing hospice and palliative care programs and professionals in the United States. The organization is committed to improving end-of-life care and expanding access to hospice care with the goal of profoundly enhancing the quality of life for people dying in America and their loved ones. (Spanish/English) Helpline: 800.658.8898

National Lymphedema Network (NLN)

An internationally recognized non-profit organization providing education and guidance to lymphedema patients, health care professionals and the general public by disseminating information on the prevention and management of primary and secondary lymphedema. The NLN also supports research into the causes of and possible alternative treatments for lymphedema. Hotline: 800.541.3259

National Organization for Rare Diseases (NORD)

A non-profit voluntary health organization dedicated to helping people with rare "orphan" diseases and assisting the organizations that serve them. NORD is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and service. Toll Free: 800.999.NORD | 800.999.6673

National Society of Genetic Counselors

An organization which promotes the genetic counseling profession as a recognized and integral part of health care delivery, education, research and public policy. Genetic Counselors can be searched by State, City, Counselor's Name, Institution or Areas of Practice or Specialization. Cancer genetic counselors are involved with individuals who have cancer or a family history of cancer. 312.321.6834 or nsgc@nsgc.org

North American Thrombosis Forum (NATF)

The North American Thrombosis Forum (NATF) is a nonprofit organization dedicated to improving the lives of those affected by blood clots and related diseases. Through our comprehensive resources and innovative programming, we strive to educate patients and healthcare providers about thrombosis and its complications.

Oncology Nursing Society

The Oncology Nursing Society (ONS) is a professional organization of over 35,000 registered nurses and other healthcare providers dedicated to excellence in patient care, education, research, and administration in oncology nursing. 1.866.257.4667 or 412.859.6100

Ovarcome

We raise global awareness, fund research, and provide financial, psycho-social and informational support to our Ovarcomers (ovarian cancer patients and survivors). Ovarcome is inspired by the simple philosophy of support, love, and celebration of life. Let’s keep Ovarcoming! 

Patient Advocate Foundation

The Patient Advocate Foundation is a national non-profit organization that serves as an active liaison between patients and their insurers, employers and/or creditors to resolve insurance, job discrimination, and/or debt crisis matters related to their diagnosis. It seeks to safeguard patients through effective mediation, assuring access to care, maintenance of employment, and preservation of financial stability. 800.532.5274

Patient Access Network (PAN) Foundation

PAN is an independent non-profit organization that provides assistance to underinsured patients for their out-of-pocket expenses for life-saving medications. PAN supports patients through nearly 60 oncology, chronic, and rare disease funds that cover conditions such as multiple myeloma, metastatic breast cancer, and lung cancer (non-small cell). Since 2004, PAN has provided nearly $400 million in assistance for out-of-pocket expenses through more than 200,000 patient grants. Patients and their advocates can apply for assistance by calling 866.316.7263 or start the application process online at www.PANFoundation.org.

Prevent Cancer Foundation

A national, non-profit health foundation whose mission is the prevention and early detection of cancer through scientific research, education and community outreach. The Foundation focuses its energies and resources on those cancers—including lung, breast, prostate, colorectal, cervical, skin, oral and testicular—that can be prevented through lifestyle changes or detection and treatment in their early stages. 800.227.2732

Triage Cancer

Triage Cancer is a national, nonprofit organization providing information and resources on the full spectrum of cancer survivorship issues to patients, survivors, caregivers, advocates, and healthcare professionals, through a national Speakers Bureau, educational events, and online tools. Triage Cancer also offers an educational blog at www.TriageCancer.org/blog.

Blood and Marrow Transplant

The Be The Match^® Patient Support Center

Provides free support, information and resources for you and your loved ones from diagnosis through recovery. To learn more, call 888.999.6743 or email patientinfo@nmdp.org.

BMT InfoNet

provides information and support services to patients before, during and after a stem cell, bone marrow or cord blood transplant. Our patient handbooks explain in detailed, but easy-to-understand language, what's involved in going through a stem cell transplant. Our annual symposium enables transplant recipients to connect with one another and learn how to manage the joys and challenges of survivorship.

National Bone Marrow Transplant Link

The mission of the National Bone Marrow Transplant Link is 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. 1.800.546.5268

National Marrow Donor Program

A non-profit organization which facilitates unrelated donor stem cell transplants for patients of all racial and socioeconomic backgrounds with life-threatening blood diseases who do not have matching donors in their families. Provides advice, support, and access to resources and information throughout the search process, coordinates research studies, and provides one-on-one advocacy for patients and medical professionals. Donors and other inquiries: 800.MARROW.2 | 800.627.7692; Patients and families: 888.999.6743; International: 612.627.8140

Gallbladder and Bile Duct Cancers

The Cholangiocarcinoma Foundation

Anal Cancer

Anal Cancer Foundation (ACF)

Bladder Cancer

American Bladder Cancer Society

The American Bladder Cancer Society provides a web site with a plethora of information about bladder cancer for patients, survivors, and caregivers. An important feature is an active Forum for sharing experiences and asking questions.

Bladder Cancer Advocacy Network (BCAN)

Since 2005, BCAN is the premier national patient advocacy organization dedicated to advancing bladder cancer research and supporting and educating those impacted by the disease.

Global Resource for Advancing Cancer Education (GRACE)

GRACE provides 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.

Urology Care Foundation

The Urology Care Foundation is the world's leading nonprofit urological health foundation, and the official foundation of the American Urological Association. Partnering with physicians, researchers, healthcare professionals, patients, caregivers, families and the public, the Foundation supports and improves urologic clinical care by funding research, developing patient education and pursuing philanthropic support.

Bone Cancer

National Leiomyosarcoma Foundation (NLMSF)

The NLMSF represents a patient centric advocacy resource for the Leiomyosarcoma Community, offering education, support, advocacy to empower patients and families/caregivers – throughout the diagnosis and treatment journey.  Additionally, our mission is to advance research in order to accelerate treatment options.

Northwest Sarcoma Foundation

We provide hope, education and support to anyone affected by Sarcoma in the Pacific Northwest while investing in Sarcoma research to improve cure rates.   

The Osteosarcoma Institute (OSI)

SARC

Sarcoma Coalition

Collaborative Patient Advocacy throughout the Sarcoma Community to enhance patient care and treatment outcomes and support families and caregivers as well as bridge collaborative support with the Sarcoma Research Community.

Brain Tumor

American Brain Tumor Association

National Brain Tumor Society

Breast Cancer

After Breast Cancer Diagnosis (ABCD)

ABCD provides free, personalized information and one-to-one support to people affected by breast cancer – patients, families and friends. ABCD complements the work of healthcare providers by providing the following breast cancer support services: One-to-One mentoring breast cancer support service, a Breast Cancer Helpline and Resource List, and MORE: Mentor Outreach and Education program. Breast Cancer Helpline: 800.977.4121

Breast Cancer Alliance

Founded in 1996, Breast Cancer Alliance has become one of the most prominent breast cancer organizations in the U.S. Its mission is to improve survival rates and quality of life through better prevention, early detection, treatment and cure. To promote those goals, the Greenwich, Connecticut-based organization provides seed money, scientific venture capital, for leading-edge breast cancer research programs that have not yet qualified for federal grants. It also funds post-graduate fellowships in breast surgery and allocates approximately 20% of its funding annually to support access to breast health care for underserved women.

Breast Cancer Research Foundation (BCRF)

An independent 501(c)(3) not-for-profit organization whose mission is to achieve prevention and a cure for breast cancer by providing critical funding for innovative clinical and genetic research at leading medical centers worldwide, and increasing public awareness about good breast health. 646.497.2600 or 866.FIND.A.CURE | 866.346.3228

Breastcancer.org

Breastcancer.org provides reliable, easy-to-understand, and actionable information and support services at no cost to people looking to make the best decisions for their lives. Learn more at www.breastcancer.org and join our community forums to connect with others. 

Brem Foundation

The Brem Foundation maximizes women's chances of finding early, curable breast cancer through education, access, and advocacy.

DiepCjourney Foundation

DiepCjourney Foundation is a non-profit 501(c)3 organization providing education and resources to empower women and men to make an informed decision about options for breast reconstruction after a mastectomy. Resources provided by the Foundation include educating patients about the process of breast reconstruction from exploring options, planning surgery, and support throughout the healing process. We are a global community connecting patients to highly skilled, board certified plastic surgeons via online support and personalized counsel. We provide an educational YouTube channel with a variety of topics and interviews with plastic surgeons, patients, physical therapist, decorative tattoo artists and financial advisement for breast reconstruction.

Facing Our Risk of Cancer Empowered (FORCE)

FORCE improves the lives of the millions of individuals and families facing hereditary breast, ovarian, pancreatic, prostate, colorectal and endometrial cancers. Our community includes people with a personal or family history of cancer, Lynch syndrome, a BRCA1, BRCA2, ATM, PALB2, CHEK2, PTEN or other inherited gene mutation linked to cancer.  We accomplish this through our education, support, advocacy and research efforts.

GPAC Global Patient Advocacy Coalition

GPAC unites patient advocates globally; connecting patients, practitioners, medical societies and regulatory agencies.  GPAC is working to ensure that every patient is given the proper safety information to make an informed and educated decision about their medical procedures.

Inflammatory Breast Cancer Research Foundation

Comprehensive resource for people seeking inflammatory breast cancer information. We provide one on one support/guidance for those with worrisome symptoms or those already diagnosed. Collaborate with the research community to facilitate research through funding and advocate involvement in research projects.

Living Beyond Breast Cancer (LBBC)

Founded in 1991, Living Beyond Breast Cancer is a Charity Navigator 4-star rated nonprofit organization whose mission is to connect people to trusted information and a community of support. LBBC delivers free programs and resources to those diagnosed with breast cancer and their caregivers online, in print, by phone and in person. 855.807.6386. Breast Cancer Helpline: 888.753.LBBC | 888.753.5222

Metastatic Breast Cancer Network (MBCN)

The Metastatic Breast Cancer Network (MBCN) is a national, volunteer, non-profit, patient-led advocacy organization solely dedicated to the unique concerns of women and men living with metastatic breast cancer. MBCN seeks to educate patients, provide information about the disease at its website (mbcn.org) and empower patients and caregivers to use their story and voice to advocate for focused research to lengthen lives. 888.500.0370

National Breast Cancer Coalition

A grassroots advocacy organization consisting of more than 500 organizations and over 60,000 individuals from across the United States, dedicated to fighting breast cancer. Informs, trains, and directs patients and supporters in knowledgeable and effective advocacy efforts. 800.622.2838 or 202.296.7477

Sharsheret

Sharsheret supports young Jewish women and families facing breast cancer at every stage—before, during, and after diagnosis. We help women and families connect to our community in the way that feels most comfortable, taking into consideration their stage of life, diagnosis, or treatment, as well as their connection to Judaism. We also provide educational resources, offer specialized support to those facing ovarian cancer or at high risk of developing cancer, and create programs for women and families to improve their quality of life. We understand that young Jewish women have unique concerns when it comes to breast and ovarian cancer, and we are the only organization that specializes in serving them. Learn more about our services and programs at www.sharsheret.org.

Sisters Network, Inc.

A non-profit African-American breast cancer survivors’ organization. It promotes the importance of breast health through personal empowerment, support, breast education programs, resources, information, and research through its strong affiliate chapter base. 713.781.0255 or 866.781.1808

Susan G. Komen^®

Susan G. Komen is the world’s largest breast cancer organization, funding more breast cancer research than any other nonprofit while providing real-time help to those facing the disease. Since its founding in 1982, Komen has funded more than $889 million in research and provided $1.95 billion in funding to screening, education, treatment and psychosocial support programs serving millions of people in more than 30 countries worldwide. Komen was founded by Nancy G. Brinker, who promised her sister, Susan G. Komen, that she would end the disease that claimed Suzy’s life. Visit komen.org or call 1-877 GO KOMEN (1-877 465-6636). Connect with us on social at  ww5.komen.org/social. 

Unite for HER

Our mission is to enrich the health and well-being of those diagnosed with breast and ovarian cancers – for life – by funding and delivering integrative therapies. OUR VISION is for every person with breast and ovarian cancers to  feel the support of a loving community, and will have access to comprehensive education, services, and tools that enrich their health and well-being. 

Young Survival Coalition (YSC)

The only international, non-profit network of breast cancer survivors and supporters dedicated to the concerns and issues that are unique to young women and breast cancer. Through action, advocacy and awareness, the YSC seeks to educate the medical, research, breast cancer and legislative communities and to persuade them to address breast cancer in women 40 and under. The YSC also serves as a point of contact for young women living with breast cancer. 646.257.3000 or 877. 972.1011

Carcinoid Cancer/Neuroendocrine Tumors

Carcinoid Cancer Foundation, Inc.

Chronic Lymphocytic Leukemia

CLL Society

CLL Society is an inclusive, patient-centric, physician-curated nonprofit organization that addresses the unmet needs of the chronic lymphocytic leukemia and small lymphocytic lymphoma (CLL/SLL) community through patient education, advocacy, support, and research. 

Colon Cancers

Colorectal Cancer Alliance

A non-profit organization of colon and rectal cancer survivors, their families, and the medical community. Dedicated to championing prevention, funding cutting-edge research and providing the highest quality patient support services. Toll free Helpline: 877.422.2030

Fight Colorectal Cancer

Fight Colorectal Cancer (Fight CRC) is a leading national colorectal cancer nonprofit. Through patient education, advocacy, research and awareness, the group demands a cure for the second-leading killer in the United States and envisions victory over colorectal cancer. Fight CRC provides patients with up-to-date, reliable information on how to fight colon and rectal cancer and trains research advocates who get involved in the research process. As the leading colorectal cancer advocacy group, Fight CRC serves as a resource for patients, grassroots advocates, policy makers, medical professionals and health care providers. Learn more at http://www.FightColorectalCancer.org or Facebook.com/FightCRC.

Love Your Buns

Esophageal Cancer

Esophageal Cancer Action Network (ECAN)

Esophageal Cancer Awareness Association (ECAA)

Esophageal Cancer Education Foundation

Gynecologic Cancers

Endometrial Cancer Action Network for African-Americans (ECANA)

Facing Our Risk of Cancer Empowered (FORCE)

Foundation for Women's Cancer

National Cervical Cancer Coalition

National Ovarian Cancer Coalition

Ovarian Cancer Research Alliance (OCRA)

Ovarian Cancer Research Alliance is committed to curing ovarian cancer, advocating for patients, and supporting survivors. OCRA is the largest ovarian cancer charity with over $110 million invested in research. Committed to the gynecologic cancer community, OCRA offers a range of advocacy, support and educational initiatives ensuring the those impacted by a gynecologic cancer are heard and cared for. Our national conference, webinars, and website offer the most up to date information on diagnosis, treatment and living with ovarian and gynecologic cancers. Our support programs include our Patient Support line, peer mentor program, Staying Connected support series and online community. OCRA builds community through advocacy, research, collaboration, and support.

Patient Access Network (PAN) Foundation

Sharsheret

Society of Gynecologic Oncology

Unite for HER

Our mission is to enrich the health and well-being of those diagnosed with breast and ovarian cancers – for life – by funding and delivering integrative therapies.

Head and Neck Cancer

Global Resource for Advancing Cancer Education (GRACE)

GRACE provides 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.

Head and Neck Cancer Alliance

The Head and Neck Cancer Alliance is a patient advocacy nonprofit organization working to advance prevention, detection, treatment, and rehabilitation of oral, head and neck cancer through public awareness, research, advocacy, and survivorship.

Head and Neck Cancer Fund

The HNC Fund facilitates comprehensive financial support for the well-being of one Head and Neck Cancer patient a year.

Oral Cancer Foundation

OCF provides online and phone support to patients and survivors. It sponsors research in the head and neck world, advocates in government agencies for issues impacting patients, and provides a website rich with information about this cancer. 

Support for People with Oral and Head and Neck Cancer (SPOHNC)

A non-profit organization involved in the development of programs of support. As such it can have an enormous positive impact on meeting the psychosocial needs of patients as well as preserving, restoring and promoting physical and emotional health. SPOHNC is dedicated to raising awareness and meeting the needs of oral and head and neck cancer patients through its resources and publications. Visit SPOHNC at spohnc.org to become empowered with the essential programs and resources. Together We Heal!

THANC (Thyroid, Head and Neck Cancer) Foundation

The THANC (Thyroid, Head and Neck Cancer) Foundation supports research and education in the early detection and treatment of thyroid, head and neck cancer; advances new therapeutic approaches and works to alleviate the suffering and functional impairment of patients who undergo treatment. This mission is accomplished through the THANC Guide (https://www.thancguide.org) - an online resource for patients and caregivers as well as TIRO (Thyroid International Recommendations Online (https://tiro.expert).

Kidney Cancer

Kidney Cancer Association (KCA)

KCA is a national non-profit membership organization made up of patients, family members, physicians, researchers, and other health professionals which offers a broad range of services, including advocacy on behalf of patients, support of both public and private research, information, and education. 800.850.9132

KidneyCAN

KidneyCAN is a nonprofit patient advocacy organization with the mission of accelerating cures for kidney cancer. KidneyCAN provides patient support and education, engages in legislative advocacy for research funding, and propels collaboration amongst researchers.

Urology Care Foundation

Leukemia and Lymphoma

Aplastic Anemia and MDS International Foundation (AAMDSIF)

The Aplastic Anemia and MDS International Foundation supports, connects and educates patients, caregivers and health professionals on bone marrow failure diseases worldwide. It promotes and invests in collaborative clinical research to accelerate the discovery of better treatments and cures for aplastic anemia, MDS, PNH and related bone marrow failure diseases. Patient Information: 301.279.7202 or toll free 800.747.2820.

Be the Match

We're here to help you and your loved ones from diagnosis through survivorship. Our navigators can help you learn about blood or marrow transplant (BMT), cope with uncertainty, access financial grants, find clinical trials, and connect with people who've been through BMT. All our programs and resources are free.

International Waldenstrom's Macroglobulinemia Foundation

The International Waldenstrom's Macroglobulinemia Foundation (IWMF) is a patient-founded and volunteer-led nonprofit organization that is dedicated to a simple but compelling vision: Support everyone affected by Waldenstrom's macroglobulinemia (WM) while advancing the search for a cure. To accomplish this vision, the IWMF offers Information from our website, www.iwmf.com, and our publications written in a patient-friendly way to promote understanding of our rare disease: Education at our annual Educational Forum to help patients and caregivers learn about our disease from WM researchers and clinicians; On-going updates about WM and the IWMF sent through our quarterly Torch newsletter and our NEWS releases; Peer support from others who've been where you are; Information for medical professionals who may have limited experience with our rare disease; and Research directed to better treatments while we search for a cure. Visit www.iwmf.com for more information.

The Leukemia & Lymphoma Society (LLS)

The Leukemia & Lymphoma Society (LLS) is dedicated to developing better outcomes for blood cancer patients and their families through research, education, support and advocacy and is happy to have this comprehensive resource available to patients. www.LLS.org/Patient-Support.

Lymphoma Research Foundation

LRF creates, promotes, and supports lymphoma research and provides comprehensive educational and supportive programs for lymphoma patients and their families. 800.500.9976

MPN Cancer Connection

MPN Cancer Connection provides patient education, self-advocacy resources and support services for people with MPNs.

MPN Education Foundation

The MPN Education Foundation is the only all-volunteer, charitable organization that has been devoted to education of myeloproliferative neoplasm patients for 20 years. Access our archives, and join 3,000 fellow patients with the MPN-NET link on this page: mpninfo.org

MPN Research Foundation

The mission of the MPN Research Foundation is to stimulate original research in pursuit of new treatments -- and eventually a cure -- for the blood cancers polycythemia vera, essential thrombocythemia and myelofibrosis, known collectively as myeloproliferative neoplasms (MPN). Through a combination of research funding, advocacy and education, we bring together patients, researchers and clinicians around the common goal of realizing new treatment options and ultimately, a cure for MPNs. In 2017 MPNRF launched myMPN, a registry for people living with PV, ET and MF. This is a tool that allows patients to record information about their diagnosis, symptoms, demographics, disease change and more in real time and allow that information be used for research purposes. We are committed to the MPNs for the long haul.

Patient Access Network (PAN) Foundation

PAN is an independent non-profit organization that provides assistance to underinsured patients for their out-of-pocket expenses for life-saving medications. PAN supports patients through nearly 60 oncology, chronic, and rare disease funds that cover conditions such as multiple myeloma, metastatic breast cancer, and lung cancer (non-small cell). Since 2004, PAN has provided nearly $400 million in assistance for out-of-pocket expenses through more than 200,000 patient grants. Patients and their advocates can apply for assistance by calling 866.316.7263 or start the application process online at www.PANFoundation.org.

Liver Cancer

Blue Faery: The Adrienne Wilson Liver Cancer Association

Global Liver Institute

American Liver Foundation

The Bili Project Foundation

Lung Cancer

ALK Positive

ALK Positive is the largest online support group for patients, caregivers, family and friends of those diagnosed with ALK-positive lung cancer; representing over 40 countries. Our commitment is to provide hope and help those diagnosed obtain information, support and empathy. We believe that facing this disease as a community improves patient outcomes. Most importantly, we are determined to be active participants in helping medical science improve treatment options, advance research and raise awareness for ALK-positive lung cancer. Visit http://www.alkpositive.org for more information.

American Lung Association

The American Lung Association provides comprehensive Lung Cancer patient education and awareness programs in screening, biomarker testing, targeted therapy, and many supplemental pieces. We also gather and disseminate patient stories, as well as provide online support communities, and peer-to-peer mentoring.

Bonnie J. Addario Lung Cancer Foundation

The Bonnie J. Addario Lung Cancer Foundation (ALCF) is the largest global patient-founded, patient-focused, and patient-driven non-profit devoted exclusively to eradicating Lung Cancer. Through funding innovative research, patient education, and awareness the Foundation's goal is to turn lung cancer into a chronically managed disease by 2023. The Foundation works with a diverse group of physicians, organizations, industry partners, individuals, patients, survivors, and their families to identify solutions and make timely and meaningful changes. The ALCF was established on March 1, 2006 as a 501c(3) non-profit organization and has raised nearly $30 million for lung cancer research and related programs.

Caring Ambassadors

LungCancerCAP.org is our primary community outreach and education tool. We provide all our educational materials free of charge. Lung Cancer Choices, 5th Edition is a decision-aid and comprehensive resource book providing information about lung cancer for patients and their loved ones.

Clifton F. Mountain Foundation for Education and Research in Lung Cancer

The Clifton F. Mountain Foundation for Education and Research in Lung Cancer was created approximately 30 years ago by Clifton F. Mountain, MD, who developed the International System for the Staging of Lung Cancer while at M.D. Anderson Cancer Center in Houston, Texas. The Foundation’s primary function has been to educate physicians about application of the Staging System to lung cancer patients, and to emphasize that early detection of lung cancer is key to the best outcomes possible. The Foundation has created and distributed (worldwide) handbooks for physicians’ pockets, as a practical aid to proper staging. The Foundation has a current interest in educating primary care providers to keep lung cancer in their differential diagnoses. As President, Merel Mountain Nissenberg participates as the Advocate for the M.D. Anderson Lung Cancer SPORE; serves on the Lung Cancer Collaborative Group of the Early Detection Network of NCI; and is a participant in LungCAN. 

Dusty Joy Foundation

With patients' best interest at heart, NCCN defines the standard of care for patients and physicians through proven scientific methods and expectations for new discoveries leading to improved patient outcomes. As a lung cancer advocacy nonprofit, our organization wholeheartedly supports NCCN Guidelines for Patients.

Free ME from Lung Cancer

Free ME from Lung Cancer provides early lung cancer screening for uninsured patients, help single family low income home owners get access to radon air abatement systems and fund research.

Global Resource for Advancing Cancer Education (GRACE)

GRACE provides 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.

Lung Cancer Alliance

Lung Cancer Alliance is the leading nonprofit organization solely dedicated to saving lives and advancing research by empowering those living with and at risk for lung cancer. We provide live, professional support, referral and information services free of charge for patients and their loved ones to improve outcomes; conduct national awareness campaigns to reduce stigma, and educate about the disease, risk and life-saving early detection; advocate for multiple millions in federal research funding to increase treatment options leading to cures; and improve access to care for all those impacted. 800.298.2436 (U.S. only); 202.463.2080

Lung Cancer Circle of Hope

Lung Cancer Circle of Hope (LCCH) is an educational nonprofit committed to providing comprehensive, state of the art information about lung cancer. With early detection and increased therapeutic options, it is our goal to reduce the current statistics associated with this cancer. POB 7092, Rochelle Park, NJ 07662

Lung Cancer Initiative of NC

As the state's leading non-profit organization supporting lung cancer research and education, Lung Cancer Initiative of North Carolina specializes in connecting patients, survivors and loved ones with the medical and research community. Our mission is to save lives and provide support to those affected by lung cancer through research, awareness, education and access programs across North Carolina.

Lung Cancer Online

A website, maintained by the Lung Cancer Alliance, devoted to education and support of lung cancer patients and their families.

Lung Cancer Research Foundation

The mission of the Lung Cancer Research Foundation (LCRF) is to improve lung cancer outcomes by funding research for the prevention, diagnosis, treatment and cure of lung cancer. LCRF provides free educational materials that are available for print and digital order, and a Lung Cancer Support Line that is equipped with extensive and up-to-date resource guides to help you navigate the various uncertainties that come with living with lung cancer. Additionally, LCRF hosts webinars and in-person programs to bring the lung cancer community together to discuss topics important to them. All these resources can be found on our website at: LCRF.org/resources.

LUNGevity Foundation

LUNGevity provides an active community for patients and survivors—and those who help them live longer and better lives. Comprehensive resources include a medically vetted and patient-centric website, a toll-free HELPLine for support, the International Lung Cancer Survivorship Conference, and an easy-to-use Clinical Trial Finder, among other tools. All of these programs are to achieve our vision—a world where no one dies of lung cancer.

Melanoma/Skin Cancer

AIM at Melanoma

AIM at Melanoma Foundation strives to provide patients and their families— both the newly diagnosed as well as those looking to gain a greater understanding of their disease—with a full suite of tools to guide them along their treatment journey. Our website provides reliable, relevant, and current information about all aspects of melanoma. 

American Academy of Dermatology

A professional organization representative of all dermatologic associations. With a membership of more than 13,700, it represents virtually all practicing dermatologists in the United States. Includes resource pages for various skin diseases including melanoma. 847.330.0230

Melanoma International Foundation (MIF)

MIF develops personalized strategies with patients so they may live longer, better lives. Their Vision is a future where top-notch melanoma treatment is accessible to all patients globally. Toll-free Helpline: 866-463-6663; Global: 610-942-3434. Moderated forum: www.melanomaforum.org

Melanoma Network of Canada

The Melanoma Network of Canada (MNC) was founded in 2009, to respond to the needs of melanoma and skin cancer patients in Canada. MNC is a National organization dedicated to coordinating education and prevention efforts, raising awareness, providing a strong voice for advocacy, and support services and programs for melanoma and non-melanoma skin cancer patients and caregivers. MNC works tirelessly to develop and implement programs, and offer services to meet the needs of melanoma and skin cancer patients and their caregivers from initial diagnosis, through treatment and recovery, and in case of recurrence.

Melanoma Research Alliance

The mission of the Melanoma Research Alliance is to end suffering and death due to melanoma by collaborating with all stakeholders to accelerate powerful research, advance cures for all patients, and prevent more melanomas.

Melanoma Research Foundation (MRF)

MRF supports medical research for finding effective treatments and eventually a cure for melanoma. It educates patients and physicians about the prevention, diagnosis and treatment of melanoma and acts as an advocate for the melanoma community to raise the awareness of this disease and the need for a cure. Patient Helpline: 877.MRF.6460 | 877.673.6460 | 800.673.1290

Merkel Cell Carcinoma Seattle Support Group

Located in Seattle, WA, this flexible, open discussion group is for anyone touched by MCC (patients, spouses, family and friends) from the Seattle area and out of state. This is an informal opportunity to meet others coping with MCC, share stories and information, answer questions and provide support. We have first-hand knowledge and experience to share about treatments, clinical research trials and coping with MCC.

Patient Access Network (PAN) Foundation

PAN is an independent non-profit organization that provides assistance to underinsured patients for their out-of-pocket expenses for life-saving medications. PAN supports patients through nearly 60 oncology, chronic, and rare disease funds that cover conditions such as multiple myeloma, metastatic breast cancer, and lung cancer (non-small cell). Since 2004, PAN has provided nearly $400 million in assistance for out-of-pocket expenses through more than 200,000 patient grants. Patients and their advocates can apply for assistance by calling 866.316.7263 or start the application process online at www.PANFoundation.org.

Save Your Skin Foundation (SYSF)

Save Your Skin Foundation (SYSF) is a patient-led organization dedicated to the fight against non-melanoma skin cancers, melanoma, and ocular melanoma through education, advocacy, and awareness initiatives across Canada. SYSF provides a community of oncology patient and caregiver support throughout the entire continuum of care, from prevention and diagnosis to survivorship.

Skin Cancer Education & Research Foundation

The goal of the Skin Cancer Education and Research Foundation is to educate and support people concerned about or diagnosed with skin cancer and those who care for them through education, community-building, advocacy, and research to achieve the best care and outcomes possible.

Skin Cancer Foundation

The Skin Cancer Foundation is an education organization offering information about skin cancer, its prevention by means of sun protection, the need for early detection and prompt, effective treatment.

Mesothelioma

Mesothelioma Applied Research Foundation

• Funding the highest quality and most promising mesothelioma research projects from around the world through our rigorous peer-reviewed process;
• Helping mesothelioma patients connect with national mesothelioma experts and obtain the most up-to-date information on treatment options;
• Advocating in Washington D.C. for government mesothelioma research funding to stop this national tragedy.

To date, the Foundation has funded over $9.4 million in mesothelioma research. To contact, visit www.curemeso.org or call 877.End.Meso | 877.363.6376.

Myelodysplastic Syndromes

Aplastic Anemia and MDS International Foundation (AAMDSIF)

The MDS Foundation

Myeloma

Global Resource for Advancing Cancer Education (GRACE)

GRACE provides 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.

Multiple Myeloma Research Foundation (MMRF)

The Multiple Myeloma Research Foundation (MMRF) drives discoveries for new treatments, accelerates groundbreaking clinical trials and fuels the most robust data-driven initiatives in cancer research. Our goal is to find a cure for each and every patient diagnosed with multiple myeloma.

Myeloproliferative Neoplasms

The Leukemia & Lymphoma Society

MPN Cancer Connection

MPN Education Foundation

MPN Research Foundation

Neuroendocrine Tumors

Neuroendocrine Cancer Awareness Network (NCAN)

Our passion pays off! Thanks to the community of NET patients and caregivers that we serve, NCAN has once again been awarded top rated nonprofit organization status by greatnonprofits.org. It's an award bestowed upon us by the community, and we're proud to say that we've been honored with this award every year since 2011. This status helps bring even more credibility to our organization, which in turn helps donors and volunteers feel more confident in their choice to support us.

In addition to the NET hotline and the thousands of information packets that have been sent to patients and caregivers, the NCAN organization has produced over 60 conferences around the country.

866.850.9555; info@netcancerawareness.org.

Neuroendocrine Tumor Research Foundation (NETRF)

• Regional patient and caregiver educational conferences
• NET doctor database
• Regional NET support group listings
• Info on different types of NETs
• Online library of videos explaining NET treatment options
• NET research updates
• Self-care and survivorship tips

NETRF is committed to improving the lives of patients and families affected by this uncommon and often overlooked disease. 617.946.1780

NorCal CarciNET Community

The Carcinoid Cancer Foundation, Inc.

The Healing NET Foundation

Ovarian Cancers

Facing Our Risk of Cancer Empowered (FORCE)

A national nonprofit providing support, education and awareness to help those facing hereditary breast, ovarian and related cancers—such as uterine, prostate and pancreatic—know their healthcare options and make informed decisions. The organization is the de facto leader in guiding critical research and policy issues that impact the hereditary cancer community. 866.288.RISK | 866.288.7475

Foundation for Women's Cancer

The Foundation for Women's Cancer raises public awareness of ways to prevent, detect and optimally treat gynecologic cancers; provides education about gynecologic cancers and the importance of seeking care first from a gynecologic oncologist if a gynecologic cancer is suspected or diagnosed; and supports promising, innovative gynecologic cancer research.

Mucinous Ovarian Cancer Coalition (MOCC)

MOCC provides support to women with mucinous ovarian cancer, as well as funding to researchers around the world.  Our resource-rich website has a learning center where women can find GYN oncologists who offer second opinions, and guides and articles on the disease.

National Ovarian Cancer Coalition

For more than 25 years, the National Ovarian Cancer Coalition^® has been committed to raising awareness of ovarian cancer in communities across the country and to providing education, support and hope for women with ovarian cancer and for their families. For more information or to find a support chapter near you, please visit www.ovarian.org, call 888.OVARIAN | 888.682.7426, or connect with us on social media.

NormaLeah Ovarian Cancer Initiative

Women with ovarian cancer have very special needs. As the nation’s largest volunteer-led organization providing patient education and support, NormaLeah Ovarian Cancer Initiative relies heavily on the NCCN Guidelines for Patients®: Ovarian Cancer. This guide should be used by all women who have been told “you have ovarian cancer”. It is a resource that empowers women to partner with their healthcare providers and helps patients advocate for proper care for better health outcomes.

Ovarcome

We raise global awareness, fund research, and provide financial, psycho-social and informational support to our Ovarcomers (ovarian cancer patients and survivors). Ovarcome is inspired by the simple philosophy of support, love, and celebration of life. Let’s keep Ovarcoming!

Ovarian Cancer Research Alliance (OCRA)

Ovarian Cancer Research Alliance is committed to curing ovarian cancer, advocating for patients, and supporting survivors. OCRA is the largest ovarian cancer charity with over $110 million invested in research. Committed to the gynecologic cancer community, OCRA offers a range of advocacy, support and educational initiatives ensuring the those impacted by a gynecologic cancer are heard and cared for. Our national conference, webinars, and website offer the most up to date information on diagnosis, treatment and living with ovarian and gynecologic cancers. Our support programs include our Patient Support line, peer mentor program, Staying Connected support series and online community. OCRA builds community through advocacy, research, collaboration, and support.

Patient Access Network (PAN) Foundation

PAN is an independent non-profit organization that provides assistance to underinsured patients for their out-of-pocket expenses for life-saving medications. PAN supports patients through nearly 60 oncology, chronic, and rare disease funds that cover conditions such as multiple myeloma, metastatic breast cancer, and lung cancer (non-small cell). Since 2004, PAN has provided nearly $400 million in assistance for out-of-pocket expenses through more than 200,000 patient grants. Patients and their advocates can apply for assistance by calling 866.316.7263 or start the application process online at www.PANFoundation.org.

Sharsheret

Sharsheret supports young Jewish women and families facing breast cancer at every stage—before, during, and after diagnosis. We help women and families connect to our community in the way that feels most comfortable, taking into consideration their stage of life, diagnosis, or treatment, as well as their connection to Judaism. We also provide educational resources, offer specialized support to those facing ovarian cancer or at high risk of developing cancer, and create programs for women and families to improve their quality of life. We understand that young Jewish women have unique concerns when it comes to breast and ovarian cancer, and we are the only organization that specializes in serving them. Learn more about our services and programs at www.sharsheret.org.

Society of Gynecologic Oncology

The Society of Gynecologic Oncology (SGO) is the premier medical specialty society for health care professionals trained in the comprehensive management of gynecologic cancers. SGO promotes excellence in the care of women at risk for or affected by gynecologic cancer through advocacy, education, research and inter-disciplinary collaboration.

Pancreatic Cancer

Hirshberg Foundation for Pancreatic Cancer Research

The Hirshberg Foundation for Pancreatic Cancer Research is focused on finding a cure for pancreatic cancer, and empowering the patients and families whose lives are touched by this disease. Founded in 1997, the foundation funds groundbreaking scientific research, provides patient education and support, and sustains hope that this cancer will be eradicated once and for all.

Lustgarten Foundation

The Lustgarten Foundation drives bold, innovative research to transform pancreatic cancer into a curable disease.  To date, we have funded more than $250 million in research grants and have been a leading force in every major advancement in pancreatic cancer research.

Pancreatica.org

Pancreatic Cancer Action Network (PanCAN)

Prostate Cancer

California Prostate Cancer Coalition

CPCC networks all of the prostate cancer support groups in the State of California, provides Support Group Leaders’ Workshops; and holds an annual CPCC/UCSF Patient Conference on Prostate Cancer.

Malecare Cancer Support

Malecare is America's leading prostate cancer support and information network. Online and in-person groups help thousands of Americans fight prostate cancer, every day. Download the Cancergraph app (iTunes &Android) to track your symptoms and stay in touch with your doctor.

National Alliance of State Prostate Cancer Coalitions (NASPCC)

NASPCC provides educational resources such as PROSTATEPEDIA (Magazine and weekly DIGEST); the Annual Meeting; Laminates; and Webinars, to improve shared decision-making in prostate cancer.

PCaAware

The National Prostate Cancer Awareness Foundation Inc. (PCaAWARE) is the only national non-profit corporation whose single mission is to educate men and the women in their lives on the critical need for men to be pro-active when it comes to the need for an annual prostate cancer screening. At its core, the Foundation is a speaker's bureau. Our presenters are prostate cancer survivors and medical professionals who are personally involved with the disease. To that end we offer professional level speakers for community and corporate events, workshops, and employer wellness events. 860.651.9611

Prostate Cancer Foundation

A non-profit public charity dedicated to finding cures and controls for prostate cancer and the world's largest private source of prostate cancer research funding. 800.757.CURE |800.757.2873

Prostate Cancer International

Prostate Cancer International works to transform global understanding of the risks associated with prostate cancer and the strategies to manage those risks until prevention is possible and a cure can be found.

Prostate Conditions Education Council

PCEC saves lives through awareness and the education of men, the women in their lives as well as the medical community about cutting edge prostate cancer biomarkers and genomic testing, treatment options for all stages of the disease, and current information on treatment overlay and sequencing based on the input of the world leaders in the field. PCEC also coordinates national free men’s health checks including a multitude of blood tests for prostate cancer and other diseases. www.ProstateConditions.org 1.866.4PROST8 | 1.866.477.6788

The Prostate Health Education Network, Inc.

PHEN is a non-profit 501(c)(3) organization founded in 2003 to eliminate the African American prostate cancer disparity. In the United States, Black men have the highest prostate cancer incidence and mortality rates. PHEN's mission also includes advocacy efforts to increase the overall support and resources to find a cure for the disease for the benefit of all men. Key activities include Survivors Networks, annual Father’s Day rally and a Virtual Walk to Raise Prostate Cancer Awareness. 617.481.4020

Urology Care Foundation

The Urology Care Foundation is the world's leading nonprofit urological health foundation, and the official foundation of the American Urological Association. Partnering with physicians, researchers, healthcare professionals, patients, caregivers, families and the public, the Foundation supports and improves urologic clinical care by funding research, developing patient education and pursuing philanthropic support.

US-TOO! International, Inc.

An independent network of support group chapters for men with prostate cancer and their families. Offers fellowship, peer counseling, education about treatment options, discussion of medical alternatives without bias and increases public awareness of prostate disease. 800.80.USTOO | 800.808.7866

Veterans Prostate Cancer Awareness

VPCa provides educational resources and raises awareness of prostate cancer in the Veterans and Active Duty military populations.  Our educational resources include information on navigating the resources available at the VHA system as well as through the Community Care Network outside of the VHA.  We also provide support group functions specifically educating Veterans and their caregivers about “Life on ADT” and how to mitigate the side effects.

ZERO Prostate Cancer

ZERO is the leading national nonprofit with the mission to end prostate cancer and help all who are impacted.  ZERO advances research, provides support, and creates solutions to achieve health equity to meet the most critical needs of our community.

Rectal Cancer

Fight Colorectal Cancer

Sarcomas/GIST

The Alan B. Slifka Foundation

Founded in 1965, the Alan B. Slifka Foundation is a private family foundation dedicated to the pursuit of inclusion, diversity, peace and healing. The Foundation seeks to combat cancer, especially childhood cancer, through the support of innovative biomedical research. Among the Foundation’s top priorities is funding research into less toxic, more effective and potentially curative therapies for a variety of cancers, but especially for connective tissue cancers, known as sarcomas, that disproportionately impact children and young adults. The Alan B. Slifka Foundation is particularly interested in supporting bench-to-bedside research that results in targeted therapies, and also research that enhances our understanding of the metastatic process. 

The EHE Foundation

The EHE Foundation’s mission is to seek treatments and a cure for Epithelioid Hemangioendothelioma (EHE) by increasing awareness, pursuing scientific research, advocating for and supporting EHE patients, and bridging information between researchers, providers and patients. 906.280.6432 

Clear Cell Sarcoma Foundation

The goal of the Clear Cell Sarcoma Foundation is to advocate for patients and to fund Clear Cell Sarcoma research and drug development to fast track a cure for Clear Cell Sarcoma.  We give these young warriors fighting this rare cancer hope and a voice.

GIST Support International (GSI)

Friends of TJ Foundation

The Friends of T.J. Foundation was founded to increase sarcoma research, improve treatment, and aid in the goal of finding a cure. 

Leiomyosarcoma Support & Direct Research Foundation

LMSDR provides information and support to patients and funds promising LMS research.

The Life Raft Group (LRG)

A leader in GIST research and patient advocacy, The Life Raft Group (LRG) isa recognized source of information for patients and caregivers and the medical community through our online content, publications, webinars, educational materials, regional meetings and personal consultations. The mission of the Life Raft Group is to enhance survival and quality of life for people living with GIST (Gastrointestinal Stromal Tumor) through patient-powered research, education and empowerment and global advocacy efforts. 973.837.9092

National Leiomyosarcoma Foundation (NLMSF)

The NLMSF represents a patient centric advocacy resource for the Leiomyosarcoma Community, offering education, support, advocacy to empower patients and families/caregivers – throughout the diagnosis and treatment journey.  Additionally, our mission is to advance research in order to accelerate treatment options.

Northwest Sarcoma Foundation

We provide hope, education and support to anyone affected by Sarcoma in the Pacific Northwest while investing in Sarcoma research to improve cure rates.   

The Paula Takacs Foundation for Sarcoma Research

The Paula Takacs Foundation funds local, innovative sarcoma research of all types, helping patients gain access to new treatments and accelerating progress in discovering cures. The Foundation’s very supportive and active sarcoma community also works to amplify awareness to help save more lives.  

QuadW Foundation (What Would Willie Want)

The QuadW Foundation provides financial support to people and organizations pursuing innovative ideas and opportunities in the areas of higher education, sarcoma research, personally transforming mission experiences and general philanthropy. Our accomplishments will reflect the light-hearted but whole-hearted spirit that Willie embodied. 

SARC - Sarcoma Alliance for Research through Collaboration

SARC works closely with the greater sarcoma advocacy community, which includes many groups spanning a broad spectrum of sarcomas as well as subtype-specific groups. Together, we are working to build awareness about sarcoma, resources available to help patients and their families, and opportunities to support sarcoma research and clinical trial participation.  

Sarcoma Alliance

An advocacy organization that provides support, education, and guidance for patients/family members with sarcoma. Also provides patient materials, web links, support group locations, and other resources. 415.381.7236 

Sarcoma Coalition

Collaborative Patient Advocacy throughout the Sarcoma Community to enhance patient care and treatment outcomes and support families and caregivers as well as bridge collaborative support with the Sarcoma Research Community. 

Sarcoma Foundation of America

SFA provides support for patients and families affected by sarcoma through clinical trial resources and matching services, as well as education and awareness building efforts.

Summer's Way Foundation

The Summer's Way Foundation aims to further Summer Hammond’s legacy through advancing childhood cancer and Rhabdo research, recognizing through scholarships, graduating high school students in the community who have faced adversity, and connecting families dealing with Rhabdomyosarcoma and childhood cancer through webinars and support groups. 

Stomach Cancer (Gastric Cancer)

Debbie's Dream Foundation

Debbie's Dream Foundation: Curing Stomach Cancer (DDF) is a 501(c)(3) non-profit organization dedicated to raising awareness about stomach cancer, advancing funding for research, and providing education and support internationally to patients, families, and caregivers. DDF seeks as its ultimate goal to make the cure for stomach cancer a reality. DDF provides information about stomach cancer including risk factors, symptoms, screening, early detection, diagnosis, staging, choosing a treatment facility, treatment options, molecular testing, clinical trials, and more through educational symposia, webinars and on our comprehensive, self-service website. Our website is translatable into more than 60 languages. DDF offers grants for basic, translational, and clinical research in stomach cancer to scientists and clinicians at various career levels. To date, DDF has funded grants to young researchers and early career professionals totaling $1,000,000.

Hope for Stomach Cancer

Hope For Stomach Cancer is a 501(c)(3) nonprofit organization that provides support, resources, and awareness to those affected by stomach cancer. Hope creates and facilitates programs through collaboration with other organizations that enable those affected by stomach cancer to take actionable steps to live the best possible life through each phase of the disease. We focus on serving the stomach cancer community, starting with the patient and their granular immediate needs.

No Stomach For Cancer

No Stomach For Cancer is a 501(c)(3) nonprofit organization whose mission is to support research and unite the caring power of people worldwide affected by stomach cancer. NSFC advances awareness and education about stomach cancer, including Hereditary Diffuse Gastric Cancer (HDGC), provides a support network for affected families, and funds important research for screening, early detection, treatment, and prevention of stomach cancer. Headquartered in Madison Wisconsin, and serving individuals across the globe, No Stomach For Cancer is a worldwide thought leader in stomach cancer awareness and education. For more information about No Stomach For Cancer, or to support their global mission, please visit www.NoStomachForCancer.org.

Thyroid Cancer

American Thyroid Association

The ATA is the leading organization devoted to thyroid biology and to the prevention and treatment of thyroid disease through excellence in research, clinical care, education, and public health.

Head and Neck Cancer Alliance

The Head and Neck Cancer Alliance is a patient advocacy nonprofit organization working to advance prevention, detection, treatment and rehabilitation of oral, head and neck cancer through public awareness, research, advocacy and survivorship.

THANC (Thyroid, Head and Neck Cancer) Foundation

The THANC (Thyroid, Head and Neck Cancer) Foundation supports research and education in the early detection and treatment of thyroid, head and neck cancer; advances new therapeutic approaches and works to alleviate the suffering and functional impairment of patients who undergo treatment. This mission is accomplished through the THANC Guide (https://www.thancguide.org) - an online resource for patients and caregivers as well as TIRO (Thyroid International Recommendations Online (https://tiro.expert).

ThyCa: Thyroid Cancer Survivors' Association, Inc.

ThyCa (www.thyca.org) is an international nonprofit organization founded in 1995 and advised by thyroid cancer specialists, educates and supports patients and families worldwide through its comprehensive web site, in-person and online support groups for all types of thyroid cancer, one-to-one support matched by diagnosis, free patients’ handbooks, free newsletters, free downloadable Low-Iodine Cookbook, seminars, workshops, and conferences. ThyCa provides free materials for patients, caregivers, and physicians and sponsors Thyroid Cancer Awareness Month as well as year-round awareness campaigns, plus thyroid cancer research fundraising and research grants awarded every year starting in 2003.

Waldenström's Macroglobulinemia

International Waldenstrom's Macroglobulinemia Foundation

Cancer and Careers

The Leukemia and Lymphoma Society Clinical Trial Support Center (CTSC)

Finding a clinical trial can be overwhelming. Patients are often left to search on their own, leaving them with more questions than answers. Fortunately, The Leukemia & Lymphoma Society provides a free service to take this burden of patients and families. Work one-on-one with an LLS Clinical Trial Nurse Navigator who will personally assist you throughout the entire clinical trial process.

Massive Bio

Massive Bio empowers cancer patients to find their best treatment options, providing convenient access and enrollment services for oncology clinical trials worldwide, powered by advanced artificial intelligence. Founded on the belief that all people should have equal access to leading-edge therapies, Massive Bio combines its best-in-class AI platform with expertise in genomics, engineering, and data analytics to remove the many barriers to cancer patient enrollment and participation in clinical trials. Headquartered in New York City, Massive Bio is a privately held company that operates in 12 countries.

Trialjectory

Trialjectory uses an artificial intelligence (AI)-powered digital health decision support platform to empower cancer patients to find advanced treatment options. Get matched with clinical trials that fit your exact cancer diagnosis in minutes. 100% FREE. trialjectory.com

American Psychosocial Oncology Society (APOS)

APOS is the only multidisciplinary organization in the United States dedicated to researching and treating the psychosocial aspects of cancer. For more information go to www.apos-society.org.

Association of Oncology Social Work (AOSW)

AOSW is a non-profit organization dedicated to the enhancement of psychosocial services to people with cancer and their families. AOSW was created in 1984 by social workers interested in oncology and by existing national cancer organizations. AOSW has over 1000 current members who embrace the AOSW Mission "to advance excellence in the psychosocial care of persons with cancer, their families, and caregivers through networking, education, advocacy, research and resource development." (215) 599-6093

Good Days

Good Days is a national, independent 501(c)(3) non-profit charitable organization that provides financial assistance to patients so that they do not have to choose between getting the treatment the need and affording the necessities of everyday living.

Ovarcome

OvarCare is Ovarcome’s financial, psycho-social, and informational support program for ovarian cancer patients and OVARCOMERS in active treatment.

Fertile Hope

Hope for Two the Pregnant with Cancer Network

MyOncofertility.org

Family Reach

Family Reach is a national non-profit providing financial assistance, education and outreach for families facing a cancer diagnosis. For more information, connect with your social worker or visit familyreach.org.

Good Days

Good Days is a national, independent 501(c)(3) non-profit charitable organization that provides financial assistance to patients so that they do not have to choose between getting the treatment the need and affording the necessities of everyday living.

Ovarcome

OvarCare is Ovarcome’s financial, psycho-social, and informational support program for ovarian cancer patients and OVARCOMERS in active treatment.