On this page, you can learn more about diagnosis, staging, treatment options, statistics, outlooks, cancer type-specific patient support organizations, and more about your cancer type.
What is cancer?
Around 400 BC, Hippocrates believed tumors looked like crabs, with a body and extending legs, so he called them “karkinos,” the Greek word for crab. A few hundred years later, Celsus, a Roman philosopher, translated it to “cancer,” from the Latin word “carcinos” for crab. The word oncology comes from the Greek “onkos,” meaning masses.
Cancer is a group of diseases characterized by uncontrolled cell division and growth, and a proclivity to spread into other tissues (invasion/metastasis). Cancer can also be called a neoplasm or a malignancy.
Cancer cells don’t behave like healthy cells and they do whatever is necessary to continue to grow and spread. Cancer is adaptive and will respond to its environment by changing to ensure survival.
Cancer Cell Origins & Types
The suffix -oma means cancer
What do the little letters in front of my cancer type mean?
Cancers That Immunotherapy Can Treat*
Bladder cancer. Today, there are six FDA-approved options for bladder cancer. They include:
Brain cancer. There are two approved types of targeted antibodies for brain and nervous system cancers. Researchers are testing several others in clinical trials to find out if immunotherapy might work where other treatments have failed.
Breast cancer. At first, doctors thought immunotherapy was a poor option for breast cancer. But newer studies suggest that certain women may benefit from it. They include women who make too much of a protein receptor called HER2. Several types of targeted antibodies take aim at the HER2 pathway. In 2019, the FDA also approved the first checkpoint inhibitor for breast cancer.
Cervical cancer. Doctors use three cancer vaccines to treat cervical cancer. The FDA also approved one checkpoint inhibitor and one monoclonal antibody, a type of targeted therapy.
Colorectal cancer. Several targeted therapies and checkpoint inhibitors are used for this cancer. These may work best for patients with certain genetic traits.
Esophageal cancer. The FDA has approved two targeted therapies and one checkpoint inhibitor for this type of cancer. Researchers are looking at these ways to unleash immunotherapy against esophageal cancer:
Head and neck cancer. Immunotherapy may be especially helpful for people with human papillomavirus (HPV)-related head and neck cancers. It may also help avoid the intense side effects of other types of treatment. The FDA has approved one targeted antibody and two checkpoint inhibitors for these cancers.
Kidney cancer. Researchers are paying a lot of attention to this cancer. The first options used for kidney cancer were targeted therapies and cytokines, which are proteins made by white blood cells that spur your immune system to kill cancer cells. The FDA has also approved a monoclonal antibody and checkpoint inhibitors.
Leukemia. There are several approved immunotherapy options for this blood cancer. These include:
Liver cancer. The hepatitis virus is a major cause of this cancer. The hepatitis B vaccine was the first vaccine developed to prevent cancer. We don’t have a vaccine yet for hepatitis C (HCV). But antiviral drugs that treat HCV may keep liver cancer from starting. Doctors can also use two types of checkpoint inhibitors for this cancer.
Lung cancer. Immunotherapy, used alone or with other types of treatment, has made a big difference for people with cancer in their lungs. Today, targeted therapies and checkpoint inhibitors may even be used ahead of treatments such as chemotherapy.
Lymphoma. Immunotherapy is used to treat this blood cancer for adults and children. This includes:
Melanoma. Checkpoint inhibitors raise survival rates for some people with an advanced form of this skin cancer. Doctors sometimes also use cytokines and oncolytic virus therapy for this type of cancer.
Multiple myeloma. Several monoclonal antibodies are used to treat this blood cancer. Doctors may use them after a stem cell transplant to help keep cancer at bay.
Ovarian cancer. One monoclonal antibody is available now. But many immunotherapy trials are underway for this type of deadly cancer.
Pancreatic cancer. This cancer has few good treatments. Researchers are working hard to explore immunotherapy in trials. In the meantime, doctors may use a checkpoint inhibitor for patients whose cancer cells have certain genetic traits.
Prostate cancer. A cancer vaccine and a checkpoint inhibitor are available to treat some advanced cases of prostate cancer.
Sarcoma. This is a rare kind of cancer that starts in your bones or soft tissue. One type of monoclonal antibody is used to treat sarcoma. As with many cancers, more research is needed to better understand how other immunotherapies might help.
Skin cancer. Early skin cancers often respond well to traditional cancer treatments such as surgery. But advanced cases may benefit from immunotherapy. The FDA has approved several checkpoint inhibitors for skin cancers, including melanoma.
Stomach cancer. This is also called a gastric cancer. A checkpoint inhibitor and two targeted antibodies are approved to treat advanced cases of stomach or gastroesophageal cancer in certain people.
*This list was created by WebMD; published on February 20, 2024.
The Cancer Research Institute also has an Immunotherapy by Cancer Type resource that you can find here.
To view the full list, please visit: https://www.cancer.org/cancer/types/rare-cancers.html
CHILDHOOD CANCER SURVIVORS
Childhood Cancer Survivor Stories: Meet the Patients (Together St. Jude)
https://together.stjude.org/en-us/life-after-cancer/survivor-stories.html
Survivor Stories (American Childhood Cancer Organization)
https://www.acco.org/survivor-stories/
Young People's Cancer Stories (Teenage Cancer Trust)
https://www.teenagecancertrust.org/information-about-cancer/cancer-stories
PANCREATIC CANCER
Stories of Hope (Pancreatic Cancer Action Network)
Survivor Stories (Let's Win Pancreatic Cancer)
https://letswinpc.org/category/survivor-stories/
Survivor Stories (Pancreatic Cancer Action)
https://pancreaticcanceraction.org/news/category/survivor-stories/
Stories of Hope (Lustgarten Foundation Pancreatic Cancer Research)
https://lustgarten.org/living-with-pancreatic-cancer/hope/stories-of-hope/
BRAIN/NEUROLOGICAL CANCER
Stories (National Brain Tumor Society)
https://braintumor.org/brain-tumors/stories/
Stories (Brain Tumour Foundation of Canada)
https://www.braintumour.ca/category/stories/
Rare Brain and Spine Tumor Stories (NCI)
https://www.cancer.gov/rare-brain-spine-tumor/living/stories
Their Stories (Musella Foundation for Brain Tumor Research and Information)
https://virtualtrials.org/survive.cfm
Patient Stories (Glioblastoma Foundation)
https://glioblastomafoundation.org/patients/glioblastoma-patient-stories
Brain Tumor Patient Stories (Johns Hopkins)
https://www.hopkinsmedicine.org/brain-tumor/patient-stories
GASTROINTESTINAL CANCER (COLON, ANAL, STOMACH, RECTAL, ESOPHAGEAL)
Survivor Stories (Colon Cancer Coalition)
https://coloncancercoalition.org/community/stories/survivor-stories/
Stomach Cancer Survivor Stories (Debbie's Dream Foundation)
https://debbiesdream.org/survivor-stories/
Colorectal Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/colorectal-cancer/
Anal Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/anal-cancer/
Esophageal Cancer Stories (Esophageal Cancer Action Network)
https://ecan.org/share-your-ec-story/esophageal-cancer-stories/
Faces of Blue: Stories of Colorectal Cancer (Colon Cancer Coalition)
https://coloncancercoalition.org/faces-of-blue-cancer-stories/
Champion Stories (FIGHT Colorectal Cancer)
https://fightcolorectalcancer.org/champion-stories/
Stories of Colorectal Cancer and Hope (Colorectal Cancer Alliance)
https://colorectalcancer.org/resources-support/community-support/stories-hope
Stomach Cancer Stories (No Stomach for Cancer)
https://nostomachforcancer.org/stomach-cancer-stories/
Stories of Hope (Hope for Stomach Cancer)
https://stocan.org/category/sharing-hope/
LIVER CANCER & CHOLANGIOCARCINOMA
Patient Stories (American Liver Foundation)
https://liverfoundation.org/about-your-liver/patient-stories/
Survivor Stories (Cholangiocarcinoma Foundation)
https://cholangiocarcinoma.org/category/blog-post/survivor-stories/
Patient Stories (Liver Cancer UK)
https://livercanceruk.org/liver-cancer-information/living-with-liver-cancer/patient-stories/
Patient Stories (Columbia Center for Liver Disease and Transplantation)
https://columbiasurgery.org/liver/patient-stories
Jan's Story of Hope (RareDiseases.org)
https://rarediseases.org/jans-story-of-hope/
ENDOMETRIAL/UTERINE CANCER
Endometrial Cancer Survivor Stories (Fight Like A Girl)
https://www.fightlikeagirlclub.com/stories/causes/endometrial-cancer/
Real Stories from Endometrial Cancer Patients (Spot Her)
https://www.spotherforec.com/endometrial-cancer-patient-stories
Uterine Cancer Survivor Stories (CDC)
https://www.cdc.gov/cancer/uterine/stories/index.htm
How I Knew I Had Endometrial Cancer: Six Survivors Share Their Stories (MD Anderson)
OVARIAN CANCER
Empowering Survivorship: Ovarian Cancer Stories (OCRA)
https://ocrahope.org/news/ovarian-cancer-survivor-stories/
Ovarian Cancer Survivor Stories (CDC)
https://www.cdc.gov/cancer/ovarian/stories/index.htm
Your Ovarian Cancer Stories (World Ovarian Cancer Coalition)
https://worldovariancancercoalition.org/about-ovarian-cancer/your-stories/
CERVICAL CANCER
Cervical Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/cervical-cancer/
Cervivor Stories (Cervivor)
Your Stories of Cervical Cancer, Cell Changes, and Cervical Screening (Jo's Cervical Cancer Trust)
https://www.jostrust.org.uk/information/stories
BREAST CANCER
Personal Stories (BreastCancer.org)
https://www.breastcancer.org/personal-stories
Inspiring Stories (African American Breast Cancer Alliance)
https://aabcainc.org/inspiring-stories/
Breast Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/breast-cancer/
Breast Cancer Moments (Komen)
https://www.komen.org/share-your-story/
HEAD & NECK CANCER
Thyroid Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/thyroid-cancer/
Thyroid Cancer Patient Stories (City of Hope)
Patient Stories (Henry Ford Health)
https://www.henryford.com/services/head-neck-cancers/stories
Cancer Survivorship: Interviews with Cancer Survivors (AHNS)
https://www.ahns.info/cancer-survivorship-interviews/
30 Stories from head & Cancer Survivors: 2022 Edition (THANC)
https://thancguide.org/2022/04/the-journey/30-stories-from-head-neck-cancer-survivors-2022-edition/
Survivor Stories: Living with Head & Neck Cancer (Cancer Support Community)
Patient Journey (Throat Cancer Foundation)
https://www.throatcancerfoundation.org/category/patient-journey/
LUNG CANCER
Meet 5 Inspirational Lung Cancer Survivors (Lung Cancer Foundation of America)
https://newsnetwork.mayoclinic.org/category/sharing-mayo-clinic-2/cancer-patient-stories/
Stories of Hope (GO2 for Lung Cancer)
https://go2.org/blog/category/stories-of-hope/
Lung Cancer Journeys (Lung Cancer Research Foundation)
https://www.lungcancerresearchfoundation.org/for-patients/patient-stories/
Lung Cancer Patient Stories (The Patient Story)
https://thepatientstory.com/patient-stories/lung-cancer/
TESTICULAR CANCER
Testicular Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/testicular-cancer/
Testicular Cancer Stories (Prevent Cancer Foundation)
https://www.preventcancer.org/tag/testicular-cancer-stories/
PROSTATE CANCER
Prostate Cancer Patient Stories (The Patient Story)
https://thepatientstory.com/patient-stories/prostate-cancer/
Patient Stories Archive (Prostate Cancer Foundation)
https://www.pcf.org/article-category/patient-stories/
Your Stories (Zero Prostate Cancer)
https://zerocancer.org/your-stories
Stories (Prostatecancer.net)
https://prostatecancer.net/stories
KIDNEY CANCER
Kidney Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/kidney-cancer/
Real Stories (Action Kidney Cancer)
https://actionkidneycancer.org/help-support/real-stories/
Our Stories (KidneyCan)
https://kidneycan.org/our-stories/
Voices of Kidney Cancer Patient Stories (KCCure)
https://kccure.org/category/patient-stories/
BLADDER CANCER
Stories (Bladder Cancer Advocacy Network)
Bladder Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/bladder-cancer/
Real Stories (Fight Bladder Cancer)
https://www.fightbladdercancer.co.uk/real-stories
Stories (BladderCancer.net)
https://bladdercancer.net/stories
SARCOMA
Sarcoma Patient Stories (The Patient Story)
https://thepatientstory.com/patient-stories/sarcoma/
Sarcoma Stories (Rein in Sarcoma)
https://www.reininsarcoma.org/stories/
Stories of Hope (Sarcoma Cancer Foundation of Canada)
http://sarcomacancer.ca/stories-of-hope
SKIN CANCER
Patient & Survivor Stories (Melanoma Research Alliance)
https://www.curemelanoma.org/about-melanoma/melanoma-stories/survivor-stories
Skin Cancer Stories (The Patient Story)
https://thepatientstory.com/patient-stories/skin-cancer/
Personal Stories About Skin Cancer (American Academy of Dermatology Association)
https://www.aad.org/public/public-health/skin-cancer-awareness/personal-stories
#ThisIsSkinCancer Stories (Skin Cancer Foundation)
https://www.skincancer.org/blog/thisisskincancer-if-you-have-skin-you-can-get-skin-cancer/
Non-Melanoma Survivor Stories (SkinCancerCare)
https://skincancerinfo.org/nonmelanoma-survivor-stories/
Stories (SkinCancer.net)
https://skincancer.net/stories
LYMPHOMA
Hodgkin's Lymphoma Stories (The Patient Story)
https://thepatientstory.com/patient-stories/hodgkin-lymphoma/
Non-Hodgkin Lymphoma Stories (The Patient Story)
https://thepatientstory.com/patient-stories/non-hodgkin-lymphoma/
Stories of Hope (Lymphoma Research Foundation)
https://lymphoma.org/waystohelp/soh/
Lymphoma Stories (Lymphoma Out Loud #LOL)
https://lymphomaoutloud.org/lymphoma-stories/
Voices of LLS (Leukemia & Lymphoma Society)
https://www.lls.org/voices-of-lls
Personal Stories (Follicular Lymphoma Foundation)
https://www.theflf.org/your-support-hub/personal-stories/
Lymphoma Stories (Fight Like a Girl)
https://www.fightlikeagirlclub.com/stories/lymphoma-stories/
Inspirational Stories (LLS)
https://tlls.org/someday-is-today/stories
LEUKEMIA
Leukemia Diagnosis Stories from Patients (The Patient Story)
https://thepatientstory.com/patient-stories/leukemia/
Leukemia Patient Stories (Siteman Cancer Center)
https://siteman.wustl.edu/treatment/cancer-types/leukemia/patient-stories/
Voices of LLS (Leukemia & Lymphoma Society)
https://www.lls.org/voices-of-lls
Inspirational Stories (LLS)
https://tlls.org/someday-is-today/stories
MYELOMA
Multiple Myeloma Stories (The Patient Story)
https://thepatientstory.com/patient-stories/multiple-myeloma/
Multiple Myeloma Patient Stories (Multiple Myeloma Research Foundation)
https://themmrf.org/support/multiple-myeloma-patient-stories/
Patient Stories (Institute for Myeloma & Bone Cancer Research)
https://imbcr.org/patient-stories/
Personal Stories of Myeloma (Myeloma Canada)
https://myeloma.ca/recently-diagnosed/personal-stories-of-myeloma/
There is more in the works for this page so stay tuned! In the meantime, take a look at the resource collection at the bottom of the page, each category specific to a cancer type.
You can also download our Diagnosis Details worksheet from the Education Shop to keep the specifics of your cancer all in one place.
If you're recently diagnosed and looking for a thorough overview of the early cancer experience, please visit our Newly Diagnosed page.
We regularly review these resources to make sure that all links work correctly and are of value to our visitors. If you find a link that isn't working, please email coral@oncologyoffense.com. If you would like us to consider adding a resource to our list, please email us with details.
NCI: Cancer Types A to Z
A to Z List of Cancer Types - NCI
National Foundation for Cancer Research: Cancer Types
Cancer Types | National Foundation for Cancer Research (nfcr.org)
American Cancer Society: Find Your Cancer Type
Cancer Types | Find Your Cancer Type | American Cancer Society
Find the NCCN Guidelines for Your Cancer
https://www.nccn.org/patientresources/patient-resources/guidelines-for-patients
UpToDate by Wolters Kluwer: Cancer Basics (by cancer type)
https://www.uptodate.com/contents/table-of-contents/patient-education/cancer
UpToDate by Wolters Kluwer: Cancer Beyond the Basics (by cancer type)
https://www.uptodate.com/contents/table-of-contents/patient-education/cancer
Cancer treatment and survivorship statistics, 2022 (Miller, K. et al., CA: A Cancer Journal for Clinicians, 23 June 2022. https://doi.org/10.3322/caac.21731)
https://acsjournals.onlinelibrary.wiley.com/doi/10.3322/caac.21731
NCI: What is Bladder Cancer?
OncoLink: Bladder Cancer Basics
Bladder Cancer: The Basics | OncoLink
Urology Care Foundation
Home - Urology Care Foundation (urologyhealth.org)
BCAN Bladder Cancer Advocacy Network
Bladder Cancer Advocacy Network (bcan.org)
American Bladder Cancer Society
American Bladder Cancer Society (bladdercancersupport.org)
World Bladder Cancer Patient Coalition
NCI: Bone Cancer
Bone Cancer—Patient Version - NCI
NCI: Soft Tissue Sarcoma
Soft Tissue Sarcoma—Patient Version - NCI (cancer.gov)
NFCR: Sarcoma
Cancer Types | Sarcoma - National Foundation for Cancer Research (nfcr.org)
Sarcoma Alliance
Sarcoma Alliance | Support for your journey with sarcoma
Sarcoma Coalition
The Paula Takacs Foundation for Sarcoma Research
Paula Takacs Foundation For Sarcoma Research
Sarcoma Foundation of America
Patient Resources- What is Sarcoma? Treatments & More. (curesarcoma.org)
Rein in Sarcoma
The Bone Marrow & Cancer Foundation supports patients, their families and caregivers every step of the way during a cancer diagnosis or bone marrow, Hematopoietic Cell Transplantation (HCT) or cord blood transplant. No patient should ever feel alone. The Bone Marrow & Cancer Foundation, founded in 1992, is dedicated to improving the quality of life for cancer and transplant patients and their families by providing vital financial assistance, comprehensive resources, educational information, physician referrals, and emotional support programs.
Financial Assistance for Cancer Patients - Financial Help - Home (bonemarrow.org)
Blood & Marrow Transplant Information Network
Focused Ultrasound Therapy for Bone Metastases (FUS)
Bone Metastases - Focused Ultrasound Foundation (fusfoundation.org)
Myelodysplastic Syndromes (American Cancer Society) Myelodysplastic syndromes (MDS) are conditions that can occur when the blood-forming cells in the bone marrow become abnormal. This leads to low numbers of one or more types of blood cells. MDS is considered a type of cancer.
https://www.cancer.org/cancer/types/myelodysplastic-syndrome.html
Institute for Myeloma & Bone Cancer Research (IMBCR)
Myeloma Link through Leukemia & Lymphoma Society Empowering Black Communities through Free Educational Outreach and Enhanced Access to Care. Black Americans have at least double the incidence of myeloma as any other race or ethnicity, and recent studies show they face additional barriers and lower access to care. As advocates for health equity, The Leukemia & Lymphoma Society (LLS) is determined to erase these disparities. We believe every patient deserves the best care and support possible. Our goal: empower Black myeloma patients, caregivers, survivors, and families by increasing their access to education on and treatments for this disease.
Blood & Marrow Transplant Information Network (BMT InfoNet) is a leading advocacy organization for transplant and CAR T-cell therapy recipients before, during and after treatment. Founded in 1990, BMT InfoNet has pioneered a vast array of services to help transplant patients make critical decisions throughout their transplant journey. BMT InfoNet helps patients and their loved ones navigate the transplant experience with programs that provide the "human touch". One-on-One Peer Support: BMT InfoNet's Caring Connections program links patients who are new to the world of transplantation with trained transplant survivors who can listen to their concerns and offer insights on navigating the transplant experience. This one-on-one peer support is also available to family members of transplant patients. Personal Guidance: BMT InfoNet's staff can be reached by phone (888-597-7674 or 847-433-3313) or email (help@bmtinfonet.org) and can help patients and caregivers think through questions and concerns they have about transplant.
National Bone Marrow Transplant Link (nbmtLINK) Established in 1992, the National Bone Marrow Transplant Link is a 501(c)(3) nonprofit organization dedicated to serving individuals before, during, and after a bone marrow or stem cell transplant. Myra Jacobs founded the nbmtLINK in response to the plight of a woman, Sandy, living in her area. 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.
EHE Foundation We envision a world where Epithelioid Hemangioendothelioma (EHE) is easily diagnosed and treatable. Our mission is to find treatments and a cure for the rare cancer, Epithelioid Hemangioendothelioma (EHE), by advancing research and driving collaboration between patients, researchers, and clinicians. The EHE Foundation, founded in 2015, is a nonprofit 501c3 organization dedicated to pursuing effective treatment for Epithelioid Hemangioendothelioma (EHE) and supporting EHE patients and their families.
Susan G. Komen
Breast Cancer Foundation | Susan G. Komen®
Breast Pathology (American Cancer Society)
Breast Pathology | Understanding Your Pathology Report | American Cancer Society
Contents of a Breast Cancer Pathology Report (Susan G. Komen)
Contents of a Breast Cancer Pathology Report | Susan G. Komen®
NCI: Breast Cancer
Breast Cancer—Patient Version - NCI
BreastCancer.org
Breastcancer.org - Breast Cancer Information and Support
HIS Breast Cancer Our mission is to increase awareness and hence the early detection for all men and to help those who are at high risk due to genetics and other risk factors to gain access to regular screenings. Through our efforts we hope to increase all studies and trials to include men for Diagnostics, Hormonal, Immunotherapy and Genetics, gaining a true understanding of how this disease progresses in men, how it conflicts with that of a woman, and the best course of treatment.
https://www.hisbreastcancer.org/
Living Beyond Breast Cancer
Breast cancer resources, real stories, and support you need | LBBC
National Breast Cancer Foundation, Inc.
Breast Cancer Information, Support & Donations - National Breast Cancer Foundation
Project Life: A membership based virtual wellness house for those living with Metastatic Breast Cancer and their loved ones.
Endocrine Society
Patient Engagement | Endocrine Society
Sharsheret- A Jewish Breast Cancer Organization
Sharsheret - A Jewish Breast Cancer Organization
The Chrysalis Initiative exists to disrupt outcome disparities within breast cancer, so every patient receives the care they deserve. By providing patients with mentoring and resource navigation and equipping Black women (and other disparate groups) with the opportunity and education to assess their breast cancer risk, we are closing the gap one story at a time.
In addition to supporting patients with breast cancer, The Chrysalis Cancer Curriculum Provider Training challenges institutional realities with evidence-based strategies to guide providers as they reshape their paradigms and improve their practices to eradicate treatment disparities.
https://thechrysalisinitiative.org/
Breast Cancer Research Foundation
Breast Cancer Research Foundation | BCRF
Young Survival Coalition: Young Adults Facing Breast Cancer Together
Young Adults Facing Breast Cancer Together | Young Survival Coalition | Home
Triple Negative Breast Cancer Foundation
Home | Triple Negative Breast Cancer Foundation (tnbcfoundation.org)
African American Breast Cancer Alliance
AABCA - African American Breast Cancer Alliance (aabcainc.org)
For the Breast of Us Our mission is to empower women of color affected by breast cancer to make the rest of their lives the best of their lives through education, advocacy and community.
The Donna Foundation: Our mission is to provide financial assistance and support to those living with breast cancer and fund ground breaking breast cancer research.
The DONNA Foundation - Caring for those with Breast Cancer | The DONNA Foundation
The Pink Fund: Breast Cancer Financial Assistance
Pink Fund - Donate Now: Breast Cancer Financial Assistance
National Breast Cancer Coalition
Breast Cancer Advocacy | National Breast Cancer Coalition (stopbreastcancer.org)
METAvivor: Metastatic Breast Cancer Awareness, Research, and Support
METAvivor - Metastatic Breast Cancer Awareness, Research and Support | METAvivor
Metastatic Breast Cancer Network
The Gift of Hope Breast Cancer Foundation (Florida) The Gift of Hope believes that no woman should have to worry about how their bills will be paid. They should only concentrate on getting well.
Social Isolation and Breast Cancer (Journal of Endocrinology, 2023)
Social Isolation and Breast Cancer | Endocrinology | Oxford Academic (oup.com)
Progesterone Receptor Gene Polymorphisms and Breast Cancer Risk (Journal of Endocrinology, 2023)
Bright Pink Our mission is to accelerate, deepen, and expand the impact of life-saving breast and ovarian health interventions.
2for2 Boobs 2for2 Boobs, Inc. is a 501c3 Breast Cancer Awareness-2-Action and African American Survivorship Advocacy Nonprofit. 2for2Boobs is an acronym-a call to action- To take 2 minutes 2 check your 2 (self-breast checks) monthly. We are dedicated towards providing culturally relevant breast cancer education, information and resources to increase knowledge about breast health and the importance of knowing your risks, preventive measures and your family cancer history/genetic history. We also implement engaging survivorship outreach programs that empower, support and connect women/men who have had a breast cancer diagnosis by helping them advocate by giving voice to their powerful breast cancer journey ShadesPink stories that educate, encourage and inspire.
Side-Out Foundation In volleyball, “side-out” means regaining control of the ball. Similarly, The Side-Out Foundation helps people with breast cancer regain control of their lives. After my mother Gloria was diagnosed with stage IV breast cancer, we started the Side-Out Foundation in 2006 to challenge today’s cancer care. We believed if we could extend the lives of those living with the most advanced stage of breast cancer, we could really make a difference for everyone living with breast cancer. We decided to focus on more than just awareness and fundraising; we decided to go ten steps further. My father Bryant hired scientists and formed research teams so we could own, manage, and operate science that actively searches for answers and treatment options for those living with metastatic breast cancer. We don’t just fund research, we do research. Gloria wanted us to impact breast cancer in the most hands-on way possible. She wanted us to stay focused on action. Thanks to Side-Out Foundation supporters and researchers, we’re staying true to that mission.
After Breast Cancer Diagnosis (ABCD): ABCD provides customized, one-to-one emotional support to anyone impacted by a breast cancer diagnosis.
Home - After Breast Cancer Diagnosis (abcdbreastcancersupport.org)
The WISDOM Study: We are a partnership of breast health doctors and researchers, patient advocates, community leaders and women from all neighborhoods who share a common goal: to revolutionize the way breast cancer is detected and risk is reduced.
The WISDOM Study - Join The Movement
Inflammatory Breast Cancer Research Foundation
IBC Research Foundation – Inflammatory Breast Cancer Research Foundation
Reach to Recovery (American Cancer Society) The American Cancer Society Reach To Recovery® is a free program that connects people facing breast cancer - from diagnosis through survivorship - with trained volunteers who are breast cancer survivors. Our volunteers provide one-on-one support to help those facing breast cancer cope with diagnosis, treatment, side effects, talking with friends and family, and more. Volunteers do not provide medical advice.
Unite for Her is a 501(c)3 national nonprofit organization that supports breast cancer and ovarian cancer patients by providing integrative therapies, services, education, resources, and support at no personal cost. We are committed to being a safe space for people of all sexual orientations/gender identities. Through the Unite for HER Wellness Passport Program, you will receive up to $2,000 worth of integrative therapies and services free, without any cost to you. This will allow you to create a personal care plan that speaks to you personally, helping you mitigate unwanted side effects and symptoms. These therapies and treatments, scientifically and research based, are proven to help support empower and restore you physically as well as emotionally, at a time when you are in much need.
ABC Global Alliance Advanced breast cancer knows no boundaries, affecting individuals from diverse backgrounds, all over the world. At ABC Global Alliance, we celebrate the richness of diversity, fostering an inclusive environment where people from different countries and backgrounds can come together, collaborate, and share knowledge and resources to improve the lives of ABC patients worldwide.
https://www.abcglobalalliance.org/
TurningPoint Breast Cancer Rehabilitation TurningPoint was created to address a gap in breast cancer rehabilitation services for both the physical and emotional aspects of recovery. It’s our mission to improve survivors’ quality of life, advocate for evidence-based rehabilitation and minimize various barriers to care. This means that TurningPoint can provide services regardless of a patient’s ability to pay. We’re deeply passionate about helping all breast cancer survivors thrive and get back to doing the things they enjoy. TurningPoint Breast Cancer Rehabilitation is a non-profit, 501(c) (3) organization created to meet these needs and improve the quality of life for patients with breast cancer through specialized and evidence-based rehabilitation, including physical and massage therapy, nutritional counseling, lymphedema screening and management, emotional support and tailored fitness classes. TurningPoint also offers a wide variety of educational programs on topics related to breast cancer survivorship for patients, caregivers and healthcare providers. Since opening our doors in 2003, we have served thousands of women and men going through breast cancer. In-person and virtual services offered to patients in Georgia.
Gloria Gemma Breast Cancer Foundation We are a 501(c)(3) non-profit organization dedicated to providing free services to individuals and families touched by breast cancer in our local communities of Rhode Island, southeastern Massachusetts and eastern Connecticut. We understand the emotions and confusion that occur when you or a loved one is diagnosed with cancer. It can be one of the most stressful and psychologically draining experiences of a person's life. Gloria Gemma is here to provide access to the support and resources you need. Whether you are newly diagnosed, a survivor or you’ve lost a loved one to cancer, our staff and volunteers are here to guide you through your cancer journey with compassion and understanding. We offer a family atmosphere where hugs are plentiful and emotions are never judged, and we are committed to helping you restore your mind, body, and spirit through free holistic programs, education, and support.
Libby's Legacy Breast Cancer Foundation The Mission of Libby’s Legacy Breast Cancer Foundation is to provide comprehensive services to the underserved through education, mammograms, and follow-up diagnostics on the journey from diagnosis to survivorship with the compassion to ensure no one fights alone. Libby’s Legacy also helps stage IV breast cancer patients battling this disease by granting wishes in order to create cherished memories with loved ones through the LIVE BIG program.
MyBCTeam Connect with over 50,000 members who are living with Breast Cancer. MyBCTeam is the social network for women facing breast cancer. Get the emotional support you need from others like you, and gain practical advice and insights on managing treatment or therapies for breast cancer. MyBCTeam is the only social network where you can truly connect, make real friendships, and share daily ups and downs in a judgment-free place.
BezzyBC Bezzy members are excited to meet you, share advice and stories about their experiences living with breast cancer. Join a judgment-free space with a free profile. Bezzy BC is a space for peer support, feel-good stories, and advice. Take a look around and introduce yourself to the Bezzy community. The mission of Bezzy’s Breast Cancer community is to empower those who are living with Breast Cancer to live beyond their diagnosis through compassion, support and knowledge. We work to offer a safe place for our community members to give and receive advice though one-to-one messaging and group discussions, all while offering access to the latest news and research updates. We strive to foster a sense of community through first-person stories and interviews that help members’ feel they are not alone in their journeys.
NCI: Colorectal Cancer
Colorectal Cancer—Patient Version - NCI
NCI: Anal Cancer
Anal Cancer—Patient Version - NCI
NCI: Gastrointestinal Stromal Tumors/Soft Tissue Sarcoma
Soft Tissue Sarcoma—Patient Version - NCI (cancer.gov)
NCI: Gastrointestinal Neuroendocrine Tumors
Gastrointestinal Neuroendocrine Tumors—Patient Version - NCI (cancer.gov)
NCI: Stomach/Gastric Cancer
Colon and Rectal Pathology (American Cancer Society)
Colon and Rectal Pathology | Understanding Your Pathology Report | American Cancer Society
COLONTOWN is an online community of more than 120 “secret” groups on Facebook for colorectal cancer patients, survivors, and care partners. If you or your loved one is facing a colon cancer or rectal cancer diagnosis, you can join groups (we call them “neighborhoods”) based on your stage of disease, specific types of treatment, and special interests – such as colorectal cancer clinical trials, young-onset colorectal cancer patients, and local support groups. Every neighborhood is led by Neighborhood Hosts, themselves living the experience. In addition to our online Facebook community, COLONTOWN offers free educational resources designed for colorectal cancer patients and care partners through Colontown University.
Colontown University: Colorectal cancer education for patients and caregivers, by patients and caregivers.
Fight Colorectal Cancer
Fight Colorectal Cancer | Relentless Champions of Hope
Colorectal Cancer Alliance
GI Cancers Alliance
GI Cancers Alliance – Fight against gastrointestinal cancers
Colon Cancer Coalition
Debbie's Dream Foundation: Curing Stomach Cancer
Stomach Cancer Foundation | Debbie's Dream Foundation (debbiesdream.org)
EC Aware Esophageal Cancer Awareness
Esophageal Cancer Awareness - EC Aware
Esophageal Cancer Education Foundation
ECEF - Esophageal Cancer Education Foundation (fightec.org)
GIST Support International (GSI) is an all-volunteer, non-profit organization that reaches out to GIST patients and their families and friends to provide education and support. GSI promotes and encourages ongoing research in the quest for a cure for Gastrointestinal Stromal Tumor.
Fibrolamellar Cancer Foundation The principal purpose of the Foundation is to encourage, drive and fund research that will substantially improve outcomes for fibrolamellar patients. We envision a world where all people with fibrolamellar carcinoma will be diagnosed early, treated effectively and hopefully cured.
The Life Raft Group Our mission is to enhance survival and quality of life for people living with GIST through patient-powered research, education and empowerment, and global advocacy efforts. The LRG vision is to champion patient-powered science and drastically increase long-term survivorship for all cancer patients.
Hope for Stomach Cancer- Gastric Cancer Patient Advocacy Movement Hope For Stomach Cancer is a 501(c)(3) non-profit organization that provides resources to patients, caregivers and loved ones while promoting early detection and prevention to the general and medical communities. Hope creates and facilitates programs that enable those affected by stomach cancer to take actionable steps to live the best possible life through each phase of the disease. Through research, early detection and prevention we serve the stomach cancer community, helping to save lives and working to find a cure.
Hope For Stomach Cancer - Gastric Cancer Patient Advocacy Movement (stocan.org)
Know Your Biomarker from the Global Colon Cancer Association Know Your Biomarker is an awareness, education, and advocacy campaign offering patient educational materials about colorectal cancer biomarkers and advocacy tools to promote global access to testing.
https://www.knowyourbiomarker.org/
No Stomach For Cancer We Are Here to Provide Support, Guidance, Information, and Resources to Stomach Cancer Patients and Caregivers. No Stomach For Cancer is a non-profit patient advocacy organization that advances awareness and education about stomach cancer. We support research efforts for screening, early detection, treatment, and prevention of stomach cancer.
https://nostomachforcancer.org/
The Farrah Fawcett Foundation We Honor Farrah's Own Fight With Cancer By Passionately Giving To Cutting edge HPV-related cancer research in memory of Farrah’s life and fight to the end; Patient assistance funds for those faced with mounting expenses during treatment; and Prevention programs to help spread the word so the cancer struggle will cease.
https://thefarrahfawcettfoundation.org/
Anal Cancer Foundation The Anal Cancer Foundation is dedicated to empowering anal cancer patients and accelerating prevention and treatment methods that eliminate this disease.
https://www.analcancerfoundation.org/
Global Colon Cancer Association The Global Colon Cancer Association (GCCA) advocates for equitable access to quality colorectal cancer screenings, testing, treatments, and care, because where you live should not determine whether you can prevent or survive colorectal cancer. As both a membership-based umbrella organization and a patient advocacy organization, GCCA works toward this goal by amplifying and supporting the efforts of our member organizations, by developing adaptable advocacy and educational materials for our members, and by conducting our own advocacy, education, and initiatives that ensure patients are at the heart of all policy discussions.
10 Things to Know About Neuroendocrine Tumors (MD Anderson) While the name “neuroendocrine” implies that these tumors involve both nerve cells and hormones, they are mainly thought to come from endocrine cells. The “neuro-” is more of a quirk of history. Neuroendocrine tumors are cancers that can develop anywhere endocrine cells are present. Endocrine cells help regulate various body functions, such as growth, reproduction and metabolism. They are distributed throughout the body, but the most common places for tumors to develop from them are in the lungs, small intestines, and pancreas.
https://www.mdanderson.org/cancerwise/neuroendocrine-tumors--9-things-to-know.h00-159379578.html
Esophageal Cancer Action Network (ECAN)
Appendix Cancer Connection was founded to provide support and information to those newly diagnosed with Appendix Cancer.
Appendix Cancer Pseudomyxoma Peritonei Research Foundation Our organization exists to support and fund promising research that moves us toward a cure for pseudomyxoma peritonei (PMP), appendix cancer, and related peritoneal surface malignancies (PSM). We also endeavor to support the PMP, appendix cancer and PSM community of patients and their caregivers by providing the latest, most accurate information about the best practices in managing their disease.
HPV Cancers Alliance Our mission is to empower individuals with knowledge about the health and lifestyle impact of HPV infection and embolden them to take the necessary action to prevent and treat the virus and eliminate its consequences.
Liver Lovers Legend: Dr. Yuman Fong on Colorectal Cancer Liver Metastasis & Treatments (Colontown, YouTube 2024)
NCI: Uterine Cancer (Endometrial and Uterine Sarcoma)
Uterine Cancer—Patient Version - NCI
NCI: Ovarian, Fallopian Tube, and Primary Peritoneal Cancer
Ovarian, Fallopian Tube, and Primary Peritoneal Cancer—Patient Version - NCI
NCI: Cervical Cancer
What Is Cervical Cancer? - NCI
NCI: Vaginal Cancer
Vaginal Cancer—Patient Version - NCI
NCI: Penile Cancer
Penile Cancer—Patient Version - NCI
NCI: Testicular Cancer
Testicular Cancer—Patient Version - NCI
NCI: Urethral Cancer
Urethral Cancer—Patient Version - NCI
Urethral Cancer (OncoLink)
Urology Care Foundation
Home - Urology Care Foundation (urologyhealth.org)
Endocrine Society
Patient Engagement | Endocrine Society
The Carcinoid Cancer Foundation: The mission of this foundation is to increase awareness and educate the general public and healthcare professionals regarding carcinoid and related neuroendocrine tumors (NETs), to support NET cancer patients and their families, and to serve as patient advocates.
Home - Carcinoid Cancer Foundation
Bladder Cancer Advocacy Network BCAN
Bladder Cancer Advocacy Network (bcan.org)
National Cervical Cancer Coalition
Foundation for Women's Cancer (part of the Society of Gynecologic Oncology)
Home - Foundation For Women's Cancer (foundationforwomenscancer.org)
Cure Cervical Cancer
Cervical Cancer Action for Elimination
Cervical Cancer Action for Elimination
Ovarian Cancer Research Alliance
Ovarian Cancer Research Alliance | OCRA (ocrahope.org)
Endometrial Cancer Foundation/International Society of Gynecologic Cancer
International Society of Gynecologic Cancer (igcs.org)
ECANA Endometrial Cancer Action Network for African-Americans
Endometrial Cancer Action Network for African-Americans | ECANA (ecanawomen.org)
Testicular Cancer Foundation
Donation to the Testicular Cancer Foundation | Support Groups US
Testicular Cancer Awareness Foundation
Testicular Cancer Awareness Foundation
Testicular Cancer Information & Support This site has been developed for the sole purpose of education and support for patients with testicular cancer and their family members. Please take a look at all of our testicular cancer resources and articles. Our site has grown to be more that just information on testicular cancer. The focus of this site is our testicular cancer support forums, where you can share your experience with and/or get answers to your many questions about testicular cancer.
The Testicular Cancer Resource Center is a charitable organization devoted to helping people understand testicular and extragonadal germ cell tumors. Specifically, we provide accurate and timely information about these tumors and their treatment to anyone and everyone interested. We have information for patients, caregivers, family, friends, and physicians. We believe that our information and links are of the highest quality, and we are blessed with the support of some of the finest doctors in the field.
Movember Nuts & Bolts Testicular Cancer Support
Testicular cancer resource center & information (movember.com)
Testicular Cancer Society
Cancer of the Penis: The Urology Foundation
Cancer of the Penis (Penile Cancer) - The Urology Foundation
Steps Through OC: Support for Life with Ovarian Cancer Steps Through OC is a six-month program of The Clearity Foundation consisting of free professional counseling in tandem with education, referrals and other resources for any woman facing ovarian cancer, her family and active caregivers. Our goal is to support physical and emotional health so people feel, function and live well with OC.
Steps Through OC: Support for Life with Ovarian Cancer
SHARE Cancer Support We provide dedicated, experienced support for women facing breast, ovarian, uterine, cervical or metastatic breast cancer.
SHARE | Support for Women's Cancers (sharecancersupport.org)
Cervivor is a global community of patient advocates who inspire and empower those affected by cervical cancer by educating and motivating them to use their voices for creating awareness to end stigma, influence decision and change, and end cervical cancer.
Spot Her® for Endometrial Cancer Too often, women with endometrial cancer (EC) have reported that their symptoms were stigmatized and dismissed. Even though diagnoses and deaths from this type of uterine cancer are on the rise, EC remains under-recognized. Spot Her® is an initiative to help end the silence around EC and empower all people across generations and cultures to speak up, take action, and spot the potential signs at an early stage—when EC may be more treatable. When we rally around a cause, change happens. Join us in our pledge to #SpotHerforEC and raise our voices around this serious cancer—for our friends, our family, and ourselves.
GYNCA Gyn Cancers Alliance provides education, resources and support to local women and caregivers affected by gynecologic cancers. We value our community. We strive to provide as many resources to our survivors as possible and are fortunate to be able to connect with many organizations, businesses, volunteers and donors that help us do just that. GYNCA staff, survivors and volunteers regularly attend community events to spread the word about gynecologic cancer symptoms, diagnosis and support.
Unite for Her is a 501(c)3 national nonprofit organization that supports breast cancer and ovarian cancer patients by providing integrative therapies, services, education, resources, and support at no personal cost. We are committed to being a safe space for people of all sexual orientations/gender identities. Through the Unite for HER Wellness Passport Program, you will receive up to $2,000 worth of integrative therapies and services free, without any cost to you. This will allow you to create a personal care plan that speaks to you personally, helping you mitigate unwanted side effects and symptoms. These therapies and treatments, scientifically and research based, are proven to help support empower and restore you physically as well as emotionally, at a time when you are in much need.
Ovarcome Our mission is to raise global awareness, to fund research in search of a cure, and to provide financial, psycho-social, and informational support to Ovarcomers. Ovarcome is inspired by the simple philosophy of support, love, and celebration of life.
Our dream is a world that is free from the scourge of ovarian cancer.
NormaLeah Ovarian Cancer Initiative In 2016, we changed our name and adopted a new mission that more accurately describes our initiatives and serves as the basis of activities that advance our mission: to enrich lives through early detection education, patient support services and research funding for ovarian cancer — the silent killer of women. Our goal is to empower all women (and those who love them) to recognize the subtle symptoms of ovarian cancer, to assess their personal risk, to explore risk-reduction strategies and to advocate for proper medical attention for the best outcome. Our efforts are contributing to reduced incidence and mortality rates of ovarian cancer. We dream of the day when a screening test is developed and it becomes a routine part of every woman’s annual wellness exam.
Cervical Cancer Resources & Videos (Fight Cancer Global)
https://www.fightcancerglobal.org/info/resources
World Ovarian Cancer Coalition
https://worldovariancancercoalition.org/
International Papillomavirus Society (IPVS)
HPV Cancers Alliance Our mission is to empower individuals with knowledge about the health and lifestyle impact of HPV infection and embolden them to take the necessary action to prevent and treat the virus and eliminate its consequences.
NCI: Head and Neck Cancer
Head and Neck Cancer—Patient Version - NCI
Head and Neck Cancers (OncoLink)
Head and Neck Cancers | OncoLink
THANC Thyroid, Head and Neck Cancer Foundation
Thyroid, Head and Neck Cancer (THANC) Foundation (thancfoundation.org)
THANC Guide Providing Knowledge, Hope and Support to Thyroid, Head and Neck Cancer Patients
Oral Cancer Foundation
Oral Cancer Foundation | Information and Resources about Oral Head and Neck Cancer
Head & Neck Cancer Alliance (HNCA)
Home - Head and Neck Cancer Alliance
Head & Neck Cancer Alliance Support Community The Head and Neck Cancer Alliance (HNCA) is proud to support a free online community on Inspire for individuals, and their loved ones, who are facing oral, head and neck cancers. This free online community offers peer-to-peer support and a safe environment so you can connect with others experiencing or who have experienced the diagnosis, treatments and outcomes similar to yours. You can start or respond to discussions in the community, upload photos and search for specific topics to find other members who share the same interests.
https://www.headandneck.org/support-community/
NCI: Thyroid Cancer
Thyroid Cancer—Patient Version - NCI
American Thyroid Association
Thyroid Cancer | American Thyroid Association
Endocrine Society
Patient Engagement | Endocrine Society
Hormones and Thyroid Cancer: What You Need to Know (endocrine.org)
hormones_and_thyroid_cancer_what_you_need_to_know.pdf (endocrine.org)
Mechanistic Insights of Thyroid Cancer Progression (Journal of Endocrinology, 2023)
Mechanistic Insights of Thyroid Cancer Progression | Endocrinology | Oxford Academic (oup.com)
Radiation-Related Thyroid Cancer (Endocrine Reviews Journal, 2023)
Radiation-Related Thyroid Cancer | Endocrine Reviews | Oxford Academic (oup.com)
10 Things to Know About Neuroendocrine Tumors(MD Anderson) While the name “neuroendocrine” implies that these tumors involve both nerve cells and hormones, they are mainly thought to come from endocrine cells. The “neuro-” is more of a quirk of history. Neuroendocrine tumors are cancers that can develop anywhere endocrine cells are present. Endocrine cells help regulate various body functions, such as growth, reproduction and metabolism. They are distributed throughout the body, but the most common places for tumors to develop from them are in the lungs, small intestines, and pancreas.
https://www.mdanderson.org/cancerwise/neuroendocrine-tumors--9-things-to-know.h00-159379578.html
Thyroid Cancer: Types, Symptoms, Causes & Treatments (Cleveland Clinic)
https://my.clevelandclinic.org/health/diseases/12210-thyroid-cancer
Types of Thyroid Cancer (City of Hope)
https://www.cancercenter.com/cancer-types/thyroid-cancer/types
Thyroid Cancer Treatment (NCI)
https://www.cancer.gov/types/thyroid/patient/thyroid-treatment-pdq
ThyCa: Thyroid Cancer Survivors' Association
CancerCare: Head & Neck Cancer Information & Resources
Head, Neck, Cancer, Information, Resources (cancercare.org)
SPOHNC Support for People with Oral and Head and Neck Cancer
HNC Living Foundation: Help for Head and Neck Cancer Patients
HNC Living Foundation | Help for Head & Neck Cancer Patients
American Head & Neck Society
AHNS - American Head and Neck Society - Head and Neck Cancer Research & Education
Head and Neck Cancer Support Society A community-based organization of volunteers, working in partnership with researchers, health care professionals, agencies and service providers, to provide peer support to persons diagnosed with and/or recovering from head and neck cancer and their caregivers.
Head and Neck Cancer Support Society | By the patients, for the patients (head-way.org)
Resources for Head & Neck Cancer Survivors (MSKCC) This information includes resources to help people who have survived head and neck cancer manage the side effects of treatment, improve quality of life, and receive emotional support. It includes tips from other survivors, as well as from healthcare providers who treat people with head and neck cancer.
https://www.mskcc.org/cancer-care/patient-education/resources-head-and-neck
The Throat Cancer Foundation (TCF) was founded in 2012 by oropharyngeal cancer survivor Jamie Rae. Following his treatment and recovery, Jamie was concerned by the lack of resources and support available to people facing throat cancers, and established the charity to provide what was missing: information and reassurance for those facing throat cancers. We are dedicated to reducing the impact of throat cancers on individuals and wider society. We are here to offer support, and want to ensure that anyone affected, including the person who has cancer, their friends, and their loved ones, has access to the most up to date information available regarding their illness, the available treatments, and what to expect in recovery. Our work is guided by a team of leading cancer experts and consultants working in research and treatment of the illnesses we aim to fight.
https://www.throatcancerfoundation.org/
Head & Neck Cancer (Cancer Support Community) Head and neck cancers (HNC) include cancers of the oral cavity (including lip cancer and tongue cancer), larynx (laryngeal cancer), pharynx (pharyngeal cancer), hypopharynx (hypopharyngeal cancer), nasal cavity (including nasopharyngeal cancer), salivary glands, and sinuses (paranasal sinus cancer).
https://www.cancersupportcommunity.org/head-neck-cancer
Gromada Head & Neck Cancer Foundation
https://www.gromadacancerfndn.org/
Laryngeal and Hypopharyngeal Cancer (American Cancer Society)
https://www.cancer.org/cancer/types/laryngeal-and-hypopharyngeal-cancer.html
Laryngeal Cancer Treatment Adult PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/laryngeal-treatment-pdq
Hypopharyngeal Cancer Treatment Adult PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/hypopharyngeal-treatment-pdq
Nasopharyngeal Cancer (American Cancer Society)
https://www.cancer.org/cancer/types/nasopharyngeal-cancer.html
Nasopharyngeal Cancer Treatment PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/nasopharyngeal-treatment-pdq
Oral Cavity (Mouth) and Oropharyngeal (Throat) Cancer (American Cancer Society)
https://www.cancer.org/cancer/types/oral-cavity-and-oropharyngeal-cancer.html
Lip and Oral Cavity Cancer Treatment Adult PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/lip-mouth-treatment-pdq
Oropharyngeal Cancer Treatment PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/oropharyngeal-treatment-pdq
Nasal Cavity (Nose) and Paranasal Sinus Cancer (American Cancer Society)
https://www.cancer.org/cancer/types/nasal-cavity-and-paranasal-sinus-cancer.html
Paranasal Sinus and Nasal Cavity Cancer Treatment PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/paranasal-sinus-treatment-pdq
Parotid Gland (Salivary Gland) Cancer (Johns Hopkins Medicine)
https://www.hopkinsmedicine.org/health/conditions-and-diseases/parotid-gland-tumors
Salivary Gland Cancer Treatment PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/salivary-gland-treatment-pdq
Salivary Gland Cancer: 9 Things to Know (MD Anderson)
https://www.mdanderson.org/cancerwise/salivary-gland-cancer--9-things-to-know.h00-159618645.html
Parotid Patient Project is dedicated to improving the total care of patients with parotid tumors. As advocates for the patient, we educate and empower them to make good decisions regarding their care, and we generate funds for research to identify the causes of parotid tumors and to advance the diagnosis, management, and outcomes for parotid gland diseases.
https://parotidpatientproject.org/
Metastatic Squamous Neck Cancer with Occult Primary Treatment PDQ (NCI)
https://www.cancer.gov/types/head-and-neck/patient/adult/metastatic-squamous-neck-treatment-pdq
International Papillomavirus Society (IPVS)
The International Association of Laryngectomees supports, promotes, encourages, and educates individuals with a laryngectomy, along with their caregivers, Speech Language Pathologists, allied health professionals, and support groups around the world. A laryngectomy is the complete surgical removal of the larynx, because of cancer or other reasons, rendering a person speechless, with a different way of breathing and swallowing.
HPV Cancers Alliance Our mission is to empower individuals with knowledge about the health and lifestyle impact of HPV infection and embolden them to take the necessary action to prevent and treat the virus and eliminate its consequences.
NCI: Kidney/Renal Cell Cancer
Kidney (Renal Cell) Cancer—Patient Version - NCI
American Kidney Cancer Association
Home - Kidney Cancer Association
American Kidney Fund
Support Kidney Patients - American Kidney Fund
National Kidney Foundation
Welcome - The National Kidney Foundation
Kidney Cancer Research Alliance/KCCure
KCCure | Kidney Cancer Research | Kidney Cancer Awareness |
Action to Cure Kidney Cancer
ACKC.org | ACTION TO CURE KIDNEY CANCER
Judy Nicholson Kidney Cancer Foundation
Homepage - Judy Nicholson Kidney Cancer Foundation (jnfkidneycancer.org)
KidneyCAN
KidneyCAN | Accelerating Cures for Kidney Cancer
Kidney Cancer Association
Home - Kidney Cancer Association
International Kidney Cancer Coalition
Home - IKCC International Kidney Cancer Coalition
Urology Care Foundation
Home - Urology Care Foundation (urologyhealth.org)
ACC C.U.R.E Crusade Until a Resolution Exists. A Nonprofit Organization For Adrenal Cancer Research
National Adrenal Diseases Foundation NADF
National Adrenal Diseases Foundation - Home (nadf.us)
BHD Foundation BHD (Birt-Hogg-Dubé syndrome) is a rare genetic condition that may cause lung collapses, skin bumps and kidney cancer. At the BHD Foundation, we provide advice on being diagnosed and living with BHD. Find out about the symptoms, hear from other people with BHD and take part in our events. You can also help us raise awareness of BHD. Together we can inform, empower, and connect the BHD community worldwide.
https://www.thebhdfoundation.org/
American Association of Kidney Patients (AAKP)
Action Kidney Cancer
NCI: Leukemia
Leukemia—Patient Version - NCI (cancer.gov)
NCI: Lymphoma
Lymphoma—Patient Version - NCI (cancer.gov)
NCI: Plasma Cell Neoplasms (including Multiple Myeloma)
Plasma Cell Neoplasms (Including Multiple Myeloma)—Patient Version - NCI (cancer.gov)
NCI: Myeloproliferative Neoplasms/Myelodysplastic Syndromes
Myeloproliferative Neoplasms—Patient Version - NCI (cancer.gov)
Leukemia & Lymphoma Society
Leukemia & Lymphoma Society | Blood Cancer Leaders | LLS
Leukemia Research Foundation
Home - Leukemia Research Foundation (leukemiarf.org)
Lymphoma Research Foundation
Lymphoma Research Foundation | Finding Cures Starts Here | LRF
Multiple Myeloma Research Foundation
The MMRF | Multiple Myeloma Research Foundation
Lymphoma Out Loud #LOL We’re a young charity with a rebel spirit, on a mission to disrupt lymphoma. We’re throwing lymphoma the middle finger. Join our campaign and represent your county to give lymphoma the big UP YOURS.
Follicular Lymphoma Foundation Follicular lymphoma (FL) is a type of blood cancer that affects the lymph nodes. Through collaborative efforts with patients and global FL experts, we combine compassion with cutting-edge research to revolutionise treatment and improve outcomes for over one million patients worldwide. On a global mission to cure follicular lymphoma. With patients at the heart of everything we do, we are leading the way in FL research and treatment to ultimately find a cure and fast.
American Society of Hematology
American Society of Hematology - Hematology.org
DKMS We Delete Blood Cancer DKMS is an international nonprofit organization dedicated to the fight against blood cancer and blood disorders – always with the purpose of providing as many patients as possible with a second chance at life.
CLL Society (chronic lymphocytic leukemia and small lymphocytic lymphoma)
CLL Society, the Leading Authority for CLL and SLL Patients
Aplastic Anemia & MDS International Foundation
Learning is Hope | Aplastic Anemia & MDS International Foundation (aamds.org)
MDS Foundation: The Myelodysplastic Syndromes Foundation
MDS Foundation | MDS is a bone marrow failure disorder (mds-foundation.org)
HealthTree Foundation for Multiple Myeloma
Multiple Myeloma News - HealthTree Myeloma
T-Cell Leukemia Lymphoma Foundation
T-Cell Leukemia Lymphoma Foundation | Seattle, WA (tcllfoundation.org)
Blood & Marrow Transplant Information Network
International Waldenstrom's Macroglobulinemia Foundation
National Bone Marrow Transplant Link
National Bone Marrow Transplant LINK (nbmtLINK) | Bone Marrow Transplant
MPN Research Foundation Helping people with an MPN live a better quality of life as we work toward answers to prevention, progression and a cure for polycythemia vera (PV), essential thrombocythemia (ET), and myelofibrosis (MF) – blood cancers collectively known as myeloproliferative neoplasms. Through a combination of MPN cancer research, 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.
MPN Research Foundation – Research Foundation funding MPN Research
Patients Against Lymphoma Evidence-based support and information
NCI: What is Liver Cancer?
American Liver Foundation
Liver - American Liver Foundation
Will Rodgers Liver Health Foundation
Will Rodgers Liver Health Foundation
Hepatitis B Foundation: Liver Cancer Connect Program
Welcome to our Liver Cancer Connect Program » Hepatitis B Foundation (hepb.org)
Blue Faery: The Adrienne Wilson Liver Cancer Association
Blue Faery: The Adrienne Wilson Liver Cancer Association
Liver Central/Global Liver Institute: Our values of patient-centeredness, collaboration, integrity, inclusion, and results drive our mission to improve the lives of individuals and families facing liver-related issues.
Liver Central - Reinventing Liver Cancer Education
Focused Ultrasound for Liver Tumors (FUS) In October 2023, the US Food and Drug Administration cleared HistoSonics’ Edison device to noninvasively treat liver tumors using histotripsy.
Liver Tumors - Focused Ultrasound Foundation (fusfoundation.org)
What is Bile Duct Cancer? (Cholangiocarcinoma) (NCI)
https://www.cancer.gov/types/liver/bile-duct-cancer
Bile Duct Cancer Treatment (NCI)
https://www.cancer.gov/types/liver/bile-duct-cancer/treatment
Cholangiocarcinoma Foundation Founded in 2006, the Cholangiocarcinoma Foundation is a global 501(c)(3) non-profit organization and our mission is to find a cure and improve the quality of life for cholangiocarcinoma patients
https://cholangiocarcinoma.org/
Newly Connected Program (Cholangiocarcinoma Foundation) Are you or a loved one navigating a cholangiocarcinoma diagnosis? CCF understands that a diagnosis can leave patients feeling isolated and afraid. Whether you’re newly diagnosed or new to the Foundation, we are here to support you and your loved ones. You are not alone. To help us better guide you, we encourage you to take our Welcome Survey and join our Newly Diagnosed/Newly Connected program. This survey takes 10 minutes to complete and provides quick access to resources such as: A Newly Diagnosed/Newly Connected Care Kit, Navigating a Cholangiocarcinoma Diagnosis: Resource Roadmap Workbook and its related webinar hosted by our Chief Patient Officer and our Newly Connected email series, and a 1:1 meeting with a CCF Patient Advocate. You’ll learn about support groups, CCF’s mentorship program, free books, and more.
https://cholangiocarcinoma.org/newly-diagnosed/
Global Cholangiocarcinoma Alliance The Global Cholangiocarcinoma Alliance (GCA) has united to establish a global voice in cholangiocarcinoma (CCA) through community collaborations. The GCA has a shared vision to raise the awareness of CCA in order to improve prevention, survival and the quality of life of CCA patients globally.
https://www.globalccaalliance.com/
AMMF The Cholangiocarcinoma Charity AMMF is the UK’s only cholangiocarcinoma charity, dedicated to tackling this devastating cancer on all fronts: providing information and support, campaigning to raise awareness, and encouraging and supporting research.
The Bili Project The Bili Project Foundation’s mission is to reduce the incidence and improve the outcome of Hepatobiliary cancers, which are cancers of the liver, gallbladder or bile ducts (Cholangiocarcinoma). We promote research to identify early signs and symptoms as well as treatment options for this silent, fast acting group of cancers.
NCI: Lung Cancer
Lung Cancer—Patient Version - NCI
Types of Lung Cancer (American Lung Association)
https://www.lung.org/lung-health-diseases/lung-disease-lookup/lung-cancer/basics/lung-cancer-types
Types of Lung Cancer (Lungevity)
https://www.lungevity.org/for-patients-caregivers/lung-cancer-101/types-of-lung-cancer
NCI: Malignant Mesothelioma
Malignant Mesothelioma—Patient Version - NCI (cancer.gov)
NCI: Thymoma & Thymic Carcinoma
Thymoma and Thymic Carcinoma—Patient Version - NCI (cancer.gov)
Lung Pathology (American Cancer Society)
Understanding Your Lung Pathology Report | American Cancer Society
LUNGevity
American Lung Association
Home | American Lung Association
GO2 for Lung Cancer
GO2 for Lung Cancer - Support for Patients, Survivors & Caregivers
Lung Cancer Foundation of America
Lung Cancer Foundation of America: Research and Awareness (lcfamerica.org)
Non-Small Cell Lung Cancer (Yale Medicine)
https://www.yalemedicine.org/conditions/non-small-cell-lung-cancer
Lung Cancer Caring Ambassadors Program Our three main methods to fight lung cancer are to Empower patients and providers with access to free educational materials, and resources; to Educate communities about the importance of screening and to share current information with patients and their families; and to Advocate for access to screening and treatment for lung cancer for all communities.
Home | Caring Ambassadors Lung Cancer Program (lungcancercap.org)
Lung Cancer Research Foundation Lung Cancer Support Line 1-844-835-4325 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.
https://www.lungcancerresearchfoundation.org/
LiveLung (and Prosper!) Since 2010, LiveLung has been on a mission to advance lung cancer education, early detection and compassion for people impacted by lung cancer. We do this by hosting a network of monthly community lung cancer patient groups. We also provide gift bags to dozens of cancer centers where nurse navigators give them to newly diagnosed lung cancer patients. We are a 501(c)(3) nonprofit organization that believes we are here to serve the lung cancer community, not the other way around. We understand the financial toxicity that comes with a lung cancer diagnosis. While we gratefully accept donations, we do not solicit donations at our group meetings nor harass patients for donations.
Advancing Small Cell Lung Cancer Research - LiveLung
LiveLung Hope Totes LiveLung provides Hope Totes to dozens of cancer centers where nurse navigators distribute them to newly diagnosed lung cancer patients. Hope Totes are gift bags filled with thoughtful, practical items to help patients on their treatment journey. These gifts are one way we demonstrate compassion for the lung cancer community. In addition to the many helpful items such as a notebook, pocket calendar, “The ABCs of Lung Cancer for Patients and Advocates,” book, and more, Hope Totes include a postcard with contact information and details about a community meeting. So, our Hope Totes are also an outreach tool to connect patients with others in their community. We provide Hope Totes to communities where we host monthly educational patient group meetings. We are also now making it possible for individuals to sponsor a Hope Tote for us to give to cancer centers or send to a patient.
https://livelung.org/hope-totes/
Lung Cancer, Support, Information, Resources (CancerCare)
https://www.cancercare.org/diagnosis/lung_cancer
Comprehensive Biomarker Testing for Lung Cancer (LCRF)
10 Things to Know About Neuroendocrine Tumors (MD Anderson) While the name “neuroendocrine” implies that these tumors involve both nerve cells and hormones, they are mainly thought to come from endocrine cells. The “neuro-” is more of a quirk of history. Neuroendocrine tumors are cancers that can develop anywhere endocrine cells are present. Endocrine cells help regulate various body functions, such as growth, reproduction and metabolism. They are distributed throughout the body, but the most common places for tumors to develop from them are in the lungs, small intestines, and pancreas.
https://www.mdanderson.org/cancerwise/neuroendocrine-tumors--9-things-to-know.h00-159379578.html
Neuroendocrine Cancer Awareness Network (NCAN) is a non-profit organization dedicated to raising awareness of Neuroendocrine Cancer, providing support for caregivers and people with NETs, and funding for NET cancer research. Since 2003, it has been our mission, or as we like to say, our passion, to educate and support the NET community as a whole. That’s our thing.
https://netcancerawareness.org/
Neuroendocrine Tumor Research Foundation The mission of the Neuroendocrine Tumor Research Foundation is to fund research to discover cures and more effective treatments for neuroendocrine cancers. The Neuroendocrine Tumor Research Foundation is committed to improving the lives of patients, families, and caregivers affected by neuroendocrine cancer by providing information and educational resources.
International Neuroendocrine Cancer Alliance (INCA) INCA is the global voice for patients with neuroendocrine cancer and genetic neuroendocrine tumors (NETs) and their carers with a mission to: raise awareness about all types of NETs; push for scientific advancements with a focus on identified unmet needs; and provide a platform for global collaboration to address the many challenges NET patients and the medical community face, in securing a timely diagnosis and accessing optimal treatment, support and care
The Carcinoid Cancer Foundation Serving the Neuroendocrine Tumor (NET) Community for Over 50 Years. The Carcinoid Cancer Foundation began as the Carcinoid Tumor and Serotonin Research Foundation in 1968 when the NIH fund for rare cancers was terminated. The name was changed to the Carcinoid Cancer Foundation in 1995. It is a nonprofit organization chartered by the State of New York for the purpose of encouraging and supporting education and research on carcinoid and related neuroendocrine cancers.
LACNETS Learn. Advocate. Connect. A Neuroendocrine Tumor Society The mission of the Learn Advocate Connect Neuroendocrine Tumor Society (LACNETS) is to provide a community of support and education for patients (those with neuroendocrine cancer) and to advocate for all people impacted by this rare disease by expanding awareness and by voicing the patient’s perspective in collaborative dialogue with healthcare professionals. We aim to improve the quality of life of those with neuroendocrine cancer by offering support and expanded access to information on diagnosis, treatment options, research, and resources. LACNETS makes it possible for patients to share experiences, encouragement, and hope.
A Breath of Hope Lung Foundation fights lung cancer by funding innovative U.S. lung cancer research, raising awareness and supporting lung cancer patients and families.
Free ME from Lung Cancer is a non-profit organization. We are dedicated to raising money for lung cancer research, education, advocacy, and community support. We are committed to making lung cancer a national priority. Our mission is to decrease the suffering caused by a diagnosis of lung cancer by raising much-needed money for lung cancer research, education, and community support.
https://www.freemefromlungcancer.org/
Lung Cancer Registry The Registry was designed so that patients could contribute their individual experiences with lung cancer through survey questions asking about the patient, their medical history and diagnosis, treatment, outcomes, and quality of life. The information provided is completely secure; the user decides who sees the information, how it will be used and if they want to be contacted by Registry staff.
https://lungcancerregistry.org/
The Lung Cancer Action Network (LungCAN®) is a collaborative group of lung cancer advocacy organizations that have come together to raise public awareness about the realities of lung cancer. Our intention is to increase funding for detecting, treating and curing the disease.
Lung Cancer Caring Ambassadors Our Mission is to improve the lives of patients and communities by empowering and educating them to be advocates for their own health.
NCI: Brain Tumors
Brain Tumors—Patient Version - NCI (cancer.gov)
NCI: Neuroblastoma
Neuroblastoma—Patient Version - NCI (cancer.gov)
NCI: Pituitary Tumors
Pituitary Tumors—Patient Version - NCI (cancer.gov)
About Carcinoid Cancer & Neuroendocrine Tumors (CCF)
https://www.carcinoid.org/for-patients/general-information/
Glioblastoma Foundation
Glioblastoma Treatment & Research | Glioblastoma Foundation - Transforming Glioblastoma Therapy
National Brain Tumor Society
National Brain Tumor Society | Community here. Breakthroughs ahead.
American Brain Tumor Association
Home - American Brain Tumor Association (abta.org)
Oligo Nation: Uniting for a Cure
Brain Cancer Research - Oligo Nation
Keep Punching Let's knock brain cancer out for the count. Keep Punching, Inc., supports patients, healthcare providers, and researchers in their fight to prevent and eradicate brain cancer and minimize treatment-related side effects that may impact function and comfort.
Funds raised assist individuals with brain cancer and their families; providers who are pursuing integrative approaches to healing; and researchers who are investigating traditional and complementary cancer-related therapies.
The Carcinoid Cancer Foundation is the oldest nonprofit carcinoid/and related neuroendocrine tumor organization in the United States, founded in 1968. The mission of this foundation is to increase awareness and educate the general public and healthcare professionals regarding carcinoid and related neuroendocrine tumors (NETs), to support NET cancer patients and their families, and to serve as patient advocates.
Brain Tumor Network: Our mission is to provide free, individualized navigation to help patients and loved ones manage a primary brain tumor diagnosis, overcome treatment obstacles, and facilitate access to quality healthcare.
Meningioma Mommas Our mission is to provide support and valuable resources to all those affected meningioma brain tumors. Meningioma Mommas is a 501 (c) (3) not-for-profit organization, which provides support and valuable resources to all those affected by meningioma brain tumors. We are dedicated to raising meningioma awareness and funding for meningioma specific research.
https://www.meningiomamommas.org/
Brain Tumor Foundation: BTF raises awareness among medical professionals and the public about the need for the early detection of brain tumors while continuing to offer support groups, medical referrals, and informational events. The Foundation’s expertise, compassion and resources ensure that brain tumor patients have a powerful ally in their fight against this disease.
End Brain Cancer
Ivy Foundation: We fund cutting-edge research that will improve diagnostics and treatment options for patients with brain cancer.
The Broach Foundation for Brain Cancer Research
Musella Foundation for Brain Tumor Research & Information
Brain Tumor Treatments and Information (virtualtrials.org)
Acoustic Neuroma Association (ANA) was founded in Carlisle, PA in 1981 by Virginia Fickel Ehr. After having surgery for the removal of an acoustic neuroma in 1977, she resolved that future acoustic neuroma patients should have easy-to-read medical materials about their condition, as well as support and comfort from other patients. The ANA is a 501(c)(3) nonprofit organization (Tax ID 23-2170836) that serves over 3,000 members including acoustic neuroma patients, family members, friends, and healthcare professionals.
Brains for the Cure Advocacy, Education, and Connection For the Brain Tumor Community. Advice, stories, and resources, in collaboration with doctors, patients, and caregivers for every step of the brain tumor journey.
Chordoma Foundation In 2007, a handful of families affected by chordoma came together with the conviction that the options available to us weren’t acceptable. We realized that by teaming up, we’d have a chance of creating a better future for those of us affected by this disease then and everyone who came next. Despite long odds, the chordoma community has fueled progress that's virtually unprecedented for a rare cancer. And we'll keep pressing forward until everyone facing chordoma has the treatments we need.
https://www.chordomafoundation.org/
Mission4Maureen provides financial assistance to families burdened by the staggering cost of brain cancer treatment. Mortgages, utilities, and car repair expenses need to be met, and many brain cancer patients simply do not have the wherewithal to meet those obligations. Mission4Maureen provides financial assistance to families who are burdened by the staggering cost of brain cancer treatment.
Tug McGraw Foundation Improving quality of life for those affected by brain-related military trauma and glioblastoma brain tumors through education, resources and brain wellness programs.
NCI: Pancreatic Cancer
Pancreatic Cancer—Patient Version - NCI
Let's Win Pancreatic Cancer
Pancreatic Cancer Action Network
Pancreatic Cancer Action Network – Research, Patient Support, Resources (pancan.org)
Lustgarten Foundation Pancreatic Cancer Research
Home - Lustgarten Foundation: Pancreatic Cancer Research
National Pancreatic Cancer Foundation
Home - National Pancreatic Cancer Foundation (npcf.us)
Hirshberg Foundation for Pancreatic Cancer Research
Home - Hirshberg Foundation for Pancreatic Cancer Research
Pancreatic Cancer Action
Pancreatic Cancer Action | Saving lives through early diagnosis
Project Purple: A World Without Pancreatic Cancer
Home | Project Purple | A World Without Pancreatic Cancer
National Pancreas Foundation
Home - National Pancreas Foundation
Seena Magowitz Foundation
Seena Magowitz Foundation - We Fund Pancreatic Cancer Clinical Trials
Pancreatica
Confronting Pancreatic Cancer: Symptoms, Signs, Causes, Treatment (pancreatica.org)
10 Things to Know About Neuroendocrine Tumors (MD Anderson) While the name “neuroendocrine” implies that these tumors involve both nerve cells and hormones, they are mainly thought to come from endocrine cells. The “neuro-” is more of a quirk of history. Neuroendocrine tumors are cancers that can develop anywhere endocrine cells are present. Endocrine cells help regulate various body functions, such as growth, reproduction and metabolism. They are distributed throughout the body, but the most common places for tumors to develop from them are in the lungs, small intestines, and pancreas.
https://www.mdanderson.org/cancerwise/neuroendocrine-tumors--9-things-to-know.h00-159379578.html
Pancreatic Neuroendocrine Tumors (Islet Cell Tumors) Treatment (PDQ®)–Patient Version (NCI) Key Points: Pancreatic neuroendocrine tumors form in hormone-making cells (islet cells) of the pancreas. Pancreatic NETs may or may not cause signs or symptoms. There are different kinds of functional pancreatic NETs. Having certain syndromes can increase the risk of pancreatic NETs. Different types of pancreatic NETs have different signs and symptoms. Lab tests and imaging tests are used to diagnose pancreatic NETs. Other kinds of lab tests are used to check for the specific type of pancreatic NETs. Certain factors affect prognosis (chance of recovery) and treatment options.
https://www.cancer.gov/types/pancreatic/patient/pnet-treatment-pdq
Neuroendocrine Tumor Research Foundation The mission of the Neuroendocrine Tumor Research Foundation is to fund research to discover cures and more effective treatments for neuroendocrine cancers. The Neuroendocrine Tumor Research Foundation is committed to improving the lives of patients, families, and caregivers affected by neuroendocrine cancer by providing information and educational resources.
Neuroendocrine Cancer Awareness Network (NCAN) is a non-profit organization dedicated to raising awareness of Neuroendocrine Cancer, providing support for caregivers and people with NETs, and funding for NET cancer research. Since 2003, it has been our mission, or as we like to say, our passion, to educate and support the NET community as a whole. That’s our thing.
https://netcancerawareness.org/
International Neuroendocrine Cancer Alliance (INCA) INCA is the global voice for patients with neuroendocrine cancer and genetic neuroendocrine tumors (NETs) and their carers with a mission to: raise awareness about all types of NETs; push for scientific advancements with a focus on identified unmet needs; and provide a platform for global collaboration to address the many challenges NET patients and the medical community face, in securing a timely diagnosis and accessing optimal treatment, support and care
The Carcinoid Cancer Foundation Serving the Neuroendocrine Tumor (NET) Community for Over 50 Years. The Carcinoid Cancer Foundation began as the Carcinoid Tumor and Serotonin Research Foundation in 1968 when the NIH fund for rare cancers was terminated. The name was changed to the Carcinoid Cancer Foundation in 1995. It is a nonprofit organization chartered by the State of New York for the purpose of encouraging and supporting education and research on carcinoid and related neuroendocrine cancers.
LACNETS Learn. Advocate. Connect. A Neuroendocrine Tumor Society The mission of the Learn Advocate Connect Neuroendocrine Tumor Society (LACNETS) is to provide a community of support and education for patients (those with neuroendocrine cancer) and to advocate for all people impacted by this rare disease by expanding awareness and by voicing the patient’s perspective in collaborative dialogue with healthcare professionals. We aim to improve the quality of life of those with neuroendocrine cancer by offering support and expanded access to information on diagnosis, treatment options, research, and resources. LACNETS makes it possible for patients to share experiences, encouragement, and hope.
NPF Pancreatic Cancer Centers of Excellence (National Pancreas Foundation) NPF Centers of Excellence are premier healthcare facilities that focus on the multidisciplinary treatment of pancreas disease, treating the “whole patient” with a focus on the best possible outcomes and improved quality of life. There are currently over 170 NPF Centers of Excellence throughout the United States.
https://pancreasfoundation.org/patient-resources/npf-centers-of-excellence/
HIPEC Surgery: What You Need to Know (Johns Hopkins Medicine)
Hyperthermic intraoperative intraperitoneal chemotherapy (HIPEC) as an adjuvant to pancreatic cancer resection (2021)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100705/
Cytoreduction with Hyperthermic Intraperitoneal Chemoperfusion for Pancreatic Cancer with Low-Volume Peritoneal Metastasis: Results from a Prospective Pilot Study (2023)
https://pubmed.ncbi.nlm.nih.gov/35972667/
Intraperitoneal chemotherapy in the management of pancreatic adenocarcinoma: A systematic review and meta-analysis (2022)
https://www.sciencedirect.com/science/article/abs/pii/S0748798322004802
Endurance Athlete Enduring Pancreatic Cancer Treatment (Let's Win Pancreatic Cancer)
https://letswinpc.org/survivor-stories/cytoreductive-surgery-pancreatic-cancer-treatment/
A 4-drug chemotherapy regimen improves survival in stage 4 pancreas cancer (UCLA Health 2023)
https://www.uclahealth.org/news/release/4-drug-chemotherapy-regimen-improves-survival-stage-4
NCCN Patient Treatment Guidelines for Pancreatic Cancer
https://www.nccn.org/patients/guidelines/content/PDF/pancreatic-patient.pdf
Pancreatic Cancer Surgery Types
https://pancan.org/facing-pancreatic-cancer/treatment/treatment-types/surgery/
Radiation Therapy for Pancreatic Cancer
https://pancan.org/facing-pancreatic-cancer/treatment/treatment-types/radiation-therapy/
Pancreatic Cancer (City of Hope)
https://www.cityofhope.org/clinical-program/pancreatic-cancer
An mRNA vaccine to treat pancreatic cancer (NIH, 2023) An NIH-funded research team led by Dr. Vinod Balachandran from Memorial Sloan Kettering Cancer Center (MSKCC) have been developing a personalized mRNA cancer-treatment vaccine approach. It is designed to help immune cells recognize specific neoantigens on patients’ pancreatic cancer cells. Results from a small clinical trial of their experimental treatment were published on May 10, 2023, in Nature.
https://www.nih.gov/news-events/nih-research-matters/mrna-vaccine-treat-pancreatic-cancer
Advancements in medical treatment for pancreatic neuroendocrine tumors: A beacon of hope. (Giri, Somdatta, and Jayaprakash Sahoo. World journal of gastroenterology vol. 30,12 (2024): 1670-1675. doi:10.3748/wjg.v30.i12.1670) This editorial highlights the remarkable advancements in medical treatment strategies for pancreatic neuroendocrine tumors (pan-NETs), emphasizing tailored approaches for specific subtypes. Cytoreductive surgery and somatostatin analogs (SSAs) play pivotal roles in managing tumors, while palliative options such as molecular targeted therapy, peptide receptor radionuclide therapy, and chemotherapy are reserved for SSA-refractory patients. Gastrinomas, insulinomas, glucagonomas, carcinoid tumors and VIPomas necessitate distinct therapeutic strategies. Understanding the genetic basis of pan-NETs and exploring immunotherapies could lead to promising avenues for future research.
NCI: Prostate Cancer
Prostate Cancer—Patient Version - NCI
Prostate Pathology (American Cancer Society)
Prostate Pathology | Understanding Your Pathology Report | American Cancer Society
ZERO Prostate Cancer: ZERO is the primary destination for all impacted by the disease to convene, get support and education, and come together as one united voice to create a better future for the prostate cancer community.
ZERO Prostate Cancer Connects People to Lifesaving Support | ZERO Prostate Cancer (zerocancer.org)
Prostate Cancer Foundation
PCF-Curing Together | PCF | Prostate Cancer Foundation | Prostate Cancer Symptoms
Prostate Cancer Research Institute
Prostate Cancer Research InstituteThe Prostate Cancer Research Institute (pcri.org)
Prostate Cancer Impact Alliance
Prostate Cancer Impact Alliance - Urology Care Foundation (urologyhealth.org)
Movember: Prostate Cancer True North
Movember - Men's Health - Prostate Cancer
American Prostate Cancer Foundation
American Prostate Cancer Foundation – A Non-Profit 501c3 Foundation (amprostatecancerfdn.com)
Fans for the Cure: Prostate Cancer Awareness and Education
Prostate Cancer Awareness and Education | Fans for the Cure
Male Care Men Fighting Prostate Cancer Together
malecare.org – Men Fighting Prostate Cancer, Together.
National Alliance of State Prostate Cancer Coalitions
National Alliance of State Prostate Cancer Coalitions - Home (naspcc.org)
Focused Ultrasound Treatment for the Prostate (FUS)
Prostate Cancer - Focused Ultrasound Foundation (fusfoundation.org)
Prostate Health Education Network (PHEN) PHEN's mission is to eliminate the African American prostate cancer disparity, and to increase the overall support and resources for a war on prostate cancer that will lead to a cure for the disease for the benefit of all men.
NCI: Skin Cancers (including Melanoma)
Skin Cancer (Including Melanoma)—Patient Version - NCI
NCI: Soft Tissue Sarcoma
Soft Tissue Sarcoma—Patient Version - NCI (cancer.gov)
Sarcoma Coalition
The Skin Cancer Foundation
The Skin Cancer Foundation Official Website - The Skin Cancer Foundation
American Academy of Dermatology
Skin Cancer Resource Center (aad.org)
SkinCancer.net
Skin Cancer Health Information & Community
National Council on Skin Cancer Prevention
National Council on Skin Cancer Prevention
Prevent Cancer Foundation: Skin Cancer
Skin Cancer – Prevent Cancer Foundation
The Skin Cancer Education & Research Foundation
Skin Cancer Consortium for Advocacy, Research & Education (Skin Cancer C.A.R.E.)
AIM at Melanoma Foundation
AIM at Melanoma - Reshaping the Future Together - AIM at Melanoma Foundation
Melanoma Research Foundation
Home - Melanoma Research Foundation
Melanoma Research Alliance
Melanoma Prevention, Treatment, Research & Resources - Melanoma Research Alliance (curemelanoma.org)
American Melanoma Foundation
The American Melanoma Foundation
Melanoma Action Coalition (MAC) The Melanoma Action Coalition was established in 2014 by leaders of seven community-based foundations focused on increasing awareness about melanoma, providing education about sun safety, and raising money for melanoma research. Originally based in the mid-Atlantic region of the United States, we have since grown to include organizations and individuals from throughout the United States and Canada. We continue to welcome new members. Organizations across the country are working every day to tackle melanoma, the most deadly of all skin cancers. Many of these organizations are grass-roots foundations established and led by those who have been touched personally by this disease. The Melanoma Action Coalition accelerates the end of melanoma by bringing together these organizations, who are at the forefront of this fight, and providing the support they need to amplify their effectiveness and impact. MAC also welcomes individual melanoma advocates and fundraisers.
Home (melanomaactioncoalition.org)
Merkel Cell Carcinoma (MCC) (Cleveland Clinic) Merkel cell carcinoma is a rare but aggressive type of skin cancer that can be life-threatening. The cancer affects your skin’s outer layer, or epidermis. It often spreads to lymph nodes and organs. UV light exposure, a weak immune system, age and viral infection may cause this cancer. Healthcare providers surgically remove the tumor, but the cancer often comes back.
https://my.clevelandclinic.org/health/diseases/17971-merkel-cell-carcinoma
Merkel Cell Carcinoma Treatment PDQ (NCI)
https://www.cancer.gov/types/skin/patient/merkel-cell-treatment-pdq
Merkel Cell Carcinoma Overview (Skin Cancer Foundation)
https://www.skincancer.org/skin-cancer-information/merkel-cell-carcinoma/
Jimmy Buffet's Death Puts Merkel Cell Carcinoma (MCC) in the Spotlight (Skin Cancer Foundation) Merkel cell carcinoma is a rare and aggressive type of skin cancer that affects the top layer of skin, known as the epidermis. MCC is about three to five times more likely to be deadly than melanoma, and is 40 times rarer than melanoma, with about 3,000 new cases diagnosed in the U.S. every year. The disease has a high risk of metastasizing (spreading) within two to three years after initial diagnosis. Once MCC has spread, treatment becomes increasingly difficult. Fortunately, MCC survival rates are improving due to advances in the field of immunotherapy.
https://www.skincancer.org/blog/jimmy-buffetts-death-puts-merkel-cell-carcinoma-in-the-spotlight/
NCI: Carcinoma of Unknown Primary (CUP)
Carcinoma of Unknown Primary—Patient Version - NCI (cancer.gov)
Cancer of Unknown Primary Foundation-Jo's Friends (CUP Foundation) Our mission is to ‘Make the Unknown, Known’ by: Providing information and support to CUP patients and those who care for them; Raising awareness of CUP,; Promoting improved diagnosis and treatment; and Undertaking, encouraging and supporting CUP research with the ultimate goal of seeing the end of CUP.
Rare Cancers, Cancer Subtypes, and Pre-Cancers (ACS) Long list of rare cancers
https://www.cancer.org/cancer/types/rare-cancers.html
Global Genes: Allies in Rare Disease Global Genes is committed to providing information, resources and connections to all communities affected by rare diseases.
Fibrolamellar Cancer Foundation: FLC is a rare liver cancer that primarily occurs in adolescents and young adults who have no history of liver disease.
Fibrolamellar Cancer Foundation Home - Fibrolamellar Cancer Foundation (fibrofoundation.org)
The EHE Foundation: Epithelioid Hemagioendothelioma (EHE) Our mission is to find treatments and a cure for this rare cancer by advancing research and driving collaboration between patients, researchers, and clinicians.
The EHE Foundation - Epithelioid Hemangioendothelioma (fightehe.org)
Acinic Cell Carcinoma of Parotid Gland (Quyen, Huynh-Thi Do et al. Radiology case reports vol. 18,6 2194-2198. 11 Apr. 2023, doi:10.1016/j.radcr.2023.03.017)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123319/
DDFRA DIPG/DMG Research Funding Alliance: WE ARE FIFTY + SEPARATE NON-PROFITS & FUNDS which make grants together for research, trial access and data integration or utilization. We are passionate about providing funds to develop an understanding of Diffuse Midline Gliomas, including Diffuse Intrinsic Pontine Gliomas.
Cholangiocarcinoma Foundation (bile duct cancer) Founded in 2006, the Cholangiocarcinoma Foundation is a global 501(c)(3) non-profit organization and our mission is to find a cure and improve the quality of life for cholangiocarcinoma patients
https://cholangiocarcinoma.org/
National Leiomyosarcoma Foundation Providing education, advocacy, support, and research for the LMS Community as we move forward in the quest for the cure. Leiomyosarcoma is a rare cancer that originates in smooth tissue and can occur anywhere in the body. Our mission is to advance research in order to accelerate treatment options and offer supportive resource assistance to patients and caregivers throughout the diagnosis and treatment journey.
EHE Foundation We envision a world where Epithelioid Hemangioendothelioma (EHE) is easily diagnosed and treatable. Our mission is to find treatments and a cure for the rare cancer, Epithelioid Hemangioendothelioma (EHE), by advancing research and driving collaboration between patients, researchers, and clinicians. The EHE Foundation, founded in 2015, is a nonprofit 501c3 organization dedicated to pursuing effective treatment for Epithelioid Hemangioendothelioma (EHE) and supporting EHE patients and their families.
LeioMyoSarcoma Support & Direct Research Foundation (LMSDR) is run by volunteers dedicated to find better treatments for leiomyosarcoma and support patients and those who love them. All of us have been involved with leiomyosarcoma, either as patients, caregivers, medical providers or researchers.
National Organization for Rare Disorders (NORD) Since 1983, NORD has been a national steward and a steadfast partner helping those who battle and care for rare disease feel seen, heard, supported and connected. We’re a full-service, mission-driven nonprofit reimagining a future where every person with a rare disease, and their families live their best lives.
Rare Diseases Report: Cancers (NORD, June 2023) This edition highlights the latest breakthroughs and remaining unmet needs in the management of rare cancers. In addition to celebrating the great progress that has been made in recent years, we also discuss new challenges, such as how the healthcare system can prepare to manage the growing number of rare cancer survivors who are living longer due to improvements in disease management.
https://rarediseases.org/wp-content/uploads/2023/08/Hem_Onc_NORD_Supp_0623_All_no-Ads_LR.pdf
Rare Cancer Alliance RCA's primary purpose is to disseminate information and provide support to all pediatric (childhood) and adult rare cancer patients. RCA's secondary purpose is to offer a consolidated venue to raise awareness and funding for rare cancer research, which seldom benefits from donations made to general cancer research organizations.
VHL Alliance VHL (von Hippel Lindau disease) is a genetic disease that can cause tumors (benign or malignant) to develop in up to 10 different organs throughout a patient’s life. The VHL Alliance is a 501c3 non-profit focused on supporting patients, families, and caregivers affected by VHL. Founded in 1993, the VHL Alliance is the preeminent resource for patients, caregivers, researchers, and the medical community.
International Waldenstrom’s Macroglobulinemia Foundation Waldenstrom’s macroglobulinemia (WM) is a rare, slow-growing cancer of the lymphatic system. Cancers of the lymphatic system are called lymphomas. WM is a type of lymphoma called non-Hodgkin lymphoma. Non-Hodgkin lymphoma is not a single disease; it refers to a group of different lymphomas that start in the lymphocytes (white blood cells). WM affects a specific type of white blood cell, called a B-lymphocyte or B-cell for short.
TargetCancer Foundation Rare Cancer research & Support. At TargetCancer Foundation, we believe everyone diagnosed with a rare cancer should have effective treatments and a chance to live, and works to advance the development of more effective and personalized treatments for people with rare cancers.
Deadliest Cancers Coalition
https://www.deadliestcancers.org/
Rare As One Project Rare disease is anything but rare. More than 7,000 rare diseases affect over 300 million people globally. The vast majority are not well understood, and less than 5 percent have approved treatments. Yet worldwide, patients are meeting these challenges head-on. The Rare As One project is committed to uniting these communities in their quest for cures. We support patient-led organizations working to improve the lives of people affected by rare disease. We aim to lift up rare disease communities, providing them with resources and tools to be more effective advocates for—and partners in—research.
https://chanzuckerberg.com/science/programs-resources/rare-as-one/
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