Patient advocacy organizations provide support worldwide.
This association was born from the voluntary work of a handful of people who believed in a project of solidarity and social responsibility. The stories of struggle and courage of our associates fill us with pride and are the main reason that leads us to continue with the project. Many of us when we were diagnosed with the syndrome felt alone. This association was also born with the aim that this does not happen anymore. Sharing adversities, illusions, tricks, all of this is part of this space. Welcome to AFA Lynch.
Advocates for Universal DPD/DPYD Testing’s mission is to advocate for standard of care in US to include DPYD pretreatment testing before 5FU and capecitabine chemotherapy. This will reduce suffering, save lives and save money.
Africa Cancer Foundation launched in 2011 in Nairobi, is a Charitable Trust that works towards preventing cancer and providing holistic solutions for those affected by cancer in Africa. Over the last twelve years (12), ACF has become a trusted institution for breast, cervical and prostate cancer screening and awareness in Kenya. ACF has spearheaded the screening of over 32,000 men and women in 27 counties for the leading cancers in Kenya.
OEKK-AgaliaZO, in its many years of action, always stands by the side of all cancer patients as well as their relatives, trying to offer full support and reinforcement. The purpose of OEKK-AgaliaZO has and always has as its focus the benefit of all those who are faced with the disease of cancer. With oncology patients and their families in mind only, we have shaped our work and strive to achieve our purpose in a context of stability but also continuous development.
We are a non-profit, non-governmental organization of public utility.ASAPRECAN was established in the city of San Salvador, at eleven o'clock on April 3, 2007, with the purpose of fighting cancer in all known modalities or known in the future.It is made up of volunteers, associates and contracted personnel who join efforts to achieve the objectives of the Association. The integrity, professionalism, dedication and responsiveness of all ASAPRECAN members has generated a common culture characterized by teamwork and a great spirit of service.
Sostén is made up of a group of people with the commitment to transform the reality of cancer patients. Since May 2000 we have had the mission of accompanying people with cancer through their treatment, providing support, containment and advice. The work team is made up of professionals trained in different topics of health, management, patient rights, health technology evaluation, communication and institutional development.
We are an association that fights against cancer. We fight to improve patient care and ensure equality and fairness in access to health care and prevention programs. Our actions focus on information, awareness, defense of the rights of cancer patients and screening. We are in several cancer committees and partner of the Ministry of Health for the Algeria cancer plan.
Bhutan Cancer Society is s Civil Society Organization registered with the Civil Society Organization Authority. The Society was established in 2015 under the Royal Patronage of Her Royal Highness Ashi Kesang Wangmo Wangchuck with the primary focus to advocate on the prevention of cancers, provide social support to the affected population and conduct relevant research to deliver evidence-based services. Vision: "Empowering Lives, Easing Journeys: A Cancer-Free Bhutan where Support, Awareness, and Quality Care Converge" Mission: 1. Improve access to quality and timely services. 2. Conduct educational programs/advocacy to reduce incidence of cancer. 3. Improve quality of life of affected population and enable them to lead socially and economically productive lives.
We are confident that strong and functional healthcare will be established in Macedonia, institutions that will fully serve patients, as well as citizens who will be aware of their obligations regarding their own health. Our goal is to actively participate in the creation of a healthy population, aware of the risks and challenges, a country with a significantly reduced number of cancer patients and, of course, a country with a significantly increased number of people cured of cancer. The population in Macedonia has a negative attitude and fear of cancer as a disease. We want to eradicate that fear, educate citizens and raise their awareness, by sending a clear message to everyone that cancer must not be treated as an incurable disease and encourage them to fight to beat cancer.
Bowel Cancer Australia provides practical and emotional support for the growing number of Australians affected by the disease. The 100% community-funded charity offers information, resources, and support to anyone with issues related to bowel cancer.
We may not ever completely eradicate bowel cancer, but through better screening, treatments and support, we can catch it earlier ÔøΩ when itÔøΩs most treatable. ThatÔøΩs why we wonÔøΩt stop until weÔøΩve beaten apathy, beaten embarrassment, beaten the lack of awareness and funding ÔøΩ and above all, beaten bowel cancer.
Bowel Cancer Support Group UK is a nationwide online peer support group for anyone affected by colorectal cancers.
We're the UK's leading bowel cancer charity. We're determined to save lives and improve the quality of life of everyone affected by bowel cancer. Our vision is a future where nobody dies of the disease.
Since July 2006, CCRAN has been the most trusted colorectal cancer patient and caregiver support, education and advocacy network in Canada. We actively support patient and their caregivers by providing evidence-based information and education in respect of colorectal cancer and we advocate for equal and timely access to effective therapies to improve patient outcomes. Weare dedicated to improving the longevity and quality of life of all colorectal cancer patients in Canada.
CORUM (COLORECTAL CANCER SURVIVORSHIP SOCIETY MALAYSIA) is a nonprofit organization that was first established in 2013 by a group of colorectal cancer patients, cancer survivors, medical and allied health care professionals. The main aim of this society is to guide, support and help improvise the quality of life of those afflicted by colorectal cancer. CORUM engages in public education and stresses on the importance of prevention, early detection and living life after colorectal cancer. Our mission Statement : CORUM is a survivor-volunteer managed group which aims to improve the quality of life of all those affected by colorectal cancer by providing psychosocial support and information to patients, families and care-givers as well as raising awareness and promoting early investigation and treatment of the disease amongst the public.
Our goal is to ensure that credible and reliable information regarding all facets of the disease is readily available and to inform the patient (and the general public) about how to manage their liberties and gain the best results for themselves, creating responsible and proactive healthcare consumers.
Cancer Awareness Foundation of Bangladesh is a government registered non- profit, community based voluntary organization in Bangladesh established in 2016. From the beginning of the journey, Cancer Awareness Foundation of Bangladesh has been working to spread awareness, cancer screening, early detection and ensure proper treatment and rehabilitation for cancer patients and their family. It has fast growing volunteer network composed of people from different age group and socio-economic which is vital for sustained development and success. Mission: *Create awareness * Facilitate early detection *Establish world class comprehensive cancer center *Rehabilitee cancer patient and their family * Facilitate advocacy * Cancer Research *Voluntary chain for cancer prevention & care
Our mission is to provide evidence-based information from a patient advocacy standpoint so that cancer patients can approach treatment based on their own wishes.
Cheeky Charity's mission is to advance colorectal & anal cancer prevention, early detection, and support, focusing on the LGBTQ+ community. Their queer-led organization leverages 'cheeky' tactics for greater awareness, and focuses on: Delivering education Offering support groups for LGBTQ+ individuals facing these cancers Advocating for accessible screenings Supporting research that promises to make earlier detection methods more accessible.
Empower local communities to promote prevention and early detection of colon cancer, and to provide support to those affected.
COLONTOWN is an online peer-to-peer community serving almost 10,000 CRC patients and caregivers in more than 120 unique private neighborhoods for every age, stage, and facet of the colorectal cancer experience. Led by more than 100 trained volunteers, all patients, caregivers and survivors, the COLONTOWN community is the largest online peer-to-peer community for colorectal cancer support. COLONTOWN helps empower patients to take an active role in their own care and treatment, offering psychosocial support, disease education, assistance with second opinions and Clinical Trials, as well as leadership training designed to help improve outcomes and extend lives. COLONTOWN is where Hope meets Science.
To empower a nation of allies who work with us to provide support for patients and families, caregivers, and survivors; to raise awareness of preventive measures; and inspire efforts to fund critical research.
We are dedicated to colorectal cancer awareness and education, support for patients and their caregivers, and advocacy on their behalf. We aspire to reduce the incidence and mortality of colorectal cancer in Canada while improving the quality of life of patients, their families and their caregivers.
We offer information on lifestyles that can reduce your own risk of getting cancer, as well as information on the symptoms of gastrointestinal cancer and the importance of early diagnosis. We offer comprehensible, reliable and up-to-date disease-related information that helps in dealing with the crisis of illness and coping with it. Getting cancer affects many areas of life, so information and support are also needed on a wide scale from different areas of life. We listen to the needs of the target group and strive to meet them. Adequate access to information also has a safeguarding and equality aspect. Peer support complements the field of psychosocial support in a unique way. A peer supporter uses the knowledge gained through his own experience to support and help others. Due to the great value and uniqueness of peer support, Colores cherishes the conditions that enable peer support and appreciates the support people who provide peer support.
David Omenukor Foundation's mission is to develop a preventive healthcare culture that would drive people to appreciate the benefits of early screening of cancer.
Digestive Cancers Europe (DiCE) is the European umbrella organisation of a large group of national Members representing patients with digestive cancer ÔøΩ colorectal, gastric, liver, oesophageal, pancreatic and rare cancers. Our mission is to contribute to early diagnosis and decreased mortality from digestive cancers and to increase overall survival and quality of life.
It is a non-profit organization, founded with the purpose of contributing to the reduction of mortality from non-communicable diseases, improving their quality of life.To be the First Organization at the national level that provides information, training and support to the Patient, to give them a better quality of life and their families. Inform, educate and guide the population to achieve a timely diagnosis through programs of responsible prevention and control of the disease.
Empowerment for Sustainable Livelihood is a diverse cancer advocacy organization founded in 2007 by William Jacob Ocran and Akua Serwaa. Our mission is to create a positive impact in the lives of cancer patients and survivors by fostering empowerment, promoting sustainable livelihoods, and raising awareness about cancer in all its forms. As a diverse cancer advocate, we believe in inclusivity and aim to support individuals from all walks of life, regardless of their background, ethnicity, or socioeconomic status. Our organization strives to empower cancer patients and survivors by providing them with essential resources, emotional support, and educational opportunities to enhance their quality of life. Furthermore, we focus on promoting sustainable livelihoods for cancer patients and survivors, recognizing the financial challenges they often face due to the cost of treatment and related expenses. Through skill development programs, vocational training, and job placement initiatives, we aim to enable them to regain financial independence and stability, enhancing their long-term well-being. Our efforts extend beyond the individual level, as we actively engage in cancer awareness campaigns, educational workshops, and community outreach programs. By collaborating with healthcare professionals, researchers, and other cancer advocacy groups, we strive to raise awareness about prevention, early detection, and the importance of supportive care for cancer patients. Empowerment for Sustainable Livelihood is committed to making a difference in the lives of those affected by cancer, fostering hope, resilience, and empowerment for a brighter and sustainable future. Together, we believe that through compassion, support, and advocacy, we can bring about positive change in the fight against cancer.
Non-Commercial Partnership on Assistance in Promoting Social Programs in the Healthcare Area "Equal Right to Life is one of the most active and well-known public anticancer organizations in Russia, founded in 2006 by the pioneer in patient advocacy Dmitriy Borisov under auspices of the leading russian oncologists. Equal Right To Life runs activities in more than 100 cities around the country, committed to informing and involving the entire spectrum of the Russian society into developing solutions for prevention, early detection and treatment of cancer. Fostering collaborative efforts of government, scientific community and civil society remains our equally important priority.
The association is open to all patients and relatives of people with colorectal cancer, as well as to all people who want to get involved to promote the objectives of the association.
EuropaColon", founded in 2005, is the leading or umbrella organization for bowel cancer patient organizations throughout Europe. EuropaColon aims to bring together bowel cancer patients, healthcare professionals, policy makers, the media and society at large to fight bowel cancer. The organization is currently represented in 21 European countries, including Latvia.
The EuropaColon Polska Foundation was established in March 2017 as an affiliation of the European organization EuropaColon, which was transformed into Digestive Cancers Europe in 2018. We are its proud member together with over thirty other organizations from all over Europe. The aim of the activities undertaken by the Foundation is primarily to increase the awareness of the general public about cancers of the digestive system. We treat colorectal cancer with special attention because we can prevent this cancer by performing screening tests such as colonoscopy or the FIT test, i.e. the occult blood test.
Digestive Cancers Europe (DiCE) is the European umbrella organisation of a large group of national Members representing patients with digestive cancer ÔøΩ colorectal, gastric, liver, oesophageal, pancreatic and rare cancers. Our mission is to contribute to early diagnosis and decreased mortality from digestive cancers and to increase overall survival and quality of life.
One of the most important missions of the Association is to provide all patients with the best possible treatment and complete care before and after treatment, as well as to ensure that they understand all proposed treatment methods as well as possible, that they are included in clinical research and that they can exercise the right to a second opinion .
europa colon slovensko is an independent patient non-profit organization that fights against colorectal cancer - cancer of the colon and rectum. It was established in Slovakia on May 22, 2007, as part of a pan-European association connecting patient groups from various European countries. Our goal is to inform about this insidious diagnosis, bring real facts about its seriousness, effectively fight against it - teach the general public to recognize the first symptoms of the disease, know how to prevent it and thus prevent senseless death due to colon and rectal cancer. We support patients and their relatives, we help them - we provide an info service through a continuous free info line and electronic online advice. We educate the general public, patients, and hold seminars. We unite patients, doctors, politicians, the media and the general public in the fight against this insidious disease.
Our mission at FLAT is to support the health and quality of life of Japanese residents in the United States. The current situation in the U.S. is that there are few medical professionals who speak Japanese, and there are challenges in understanding the medical disparities that people experience while living in the U.S., as well as the complex medical system that people encounter when they become ill or suffer an injury. Aiming to alleviate these everyday problems that Japanese people experience in the U.S., Japanese-speaking medical professionals, patient advocates, and other specialists gather to share their skills, maintain a relationship without hierarchical relationships, and provide a forum for everyone to participate.
Fomento de Desarrollo Teresa de Jesús I.A.P. (FUTEJE). FUTEJE is a non-profit organization established in 1991, whose primary interest is focused in the implementation of prevention programs, timely detection, as well as comprehensive treatment and support to patients with limited resources who suffer from Colorectal and Gastric Cancer, in addition to promote a culture of prevention and timely detection of these types of diseases through specific programs.
We fight to cure colorectal cancer and serve as relentless champions of hope for all affected by this disease through informed patient support, impactful policy change, and breakthrough research endeavors.
The ARCA.D Foundation, Aid and Research in Digestive Cancer, created on the initiative of Professor Aimery de Gramont, was recognized as being of public utility by decree of the Council of State on December 22, 2006. The ARCA.D Foundation is the only research foundation recognized as being of public utility in France dedicated exclusively to the fight against digestive cancers: esophagus, stomach, pancreas, liver, colon, rectum, etc.
Friends of Cancer Patients is a non-profit organization, founded in 1999 under the directives and patronage of Her Highness Sheikha Jawaher bint Mohammed Al Qasimi, Wife of the Ruler of Sharjah, Founder and Patron of the Friends of Cancer Patients, International Ambassador of the World Cancer Declaration for Union for International Cancer Control (UICC), International Ambassador for Childhood Cancer for UICC and Patron of the Global NCD Alliance Forum. Since 1999, we have successfully helped cancer patients and their families overcome a multitude of challenges, bringing hope in the most difficult circumstances. We plan to keep our steadfast commitment to the community by upholding excellence, continuously improving, and looking for opportunities to provide much-needed support.
To increase proactive gastrointestinal health and early detection.
The GI Cancers Alliance works to raise awareness, provide education and advocate to prevent, treat and cure gastrointestinal cancers through a collaboration between advocacy groups, industry and institutional partners.
We are a non-profit foundation, an active community, whose mission is to improve the quality of life of people with gastrointestinal cancers and their families and companions.
HENARAN is a cancer patient advocacy organization and its mission is to actively participate in the fight against cancer in Armenia, as well as promote and raise public awareness about oncological diseases and their possible prevention. The main objectives of HENARAN Foundation are: 1. Arrange material, psychological, social, legal, and rehabilitative assistance for its beneficiaries, ensure patient education and patient empowerment. 2. Emphasize the importance of cancer screening programs and early detection of cancer by promoting the introduction and further development of pilot and/or nation-wide screening programs through partnership with government agencies of healthcare sector, as well as other national and international organizations. 3. Raise the level of public awareness about oncological diseases in Armenia. 4. Contribute to development and publication of educational and public awareness materials on oncological diseases, design and/or translation and publication of clinical guidelines, dissemination and exchange of other relevant information. 5. Enhance the institutional and professional capacity of cancer care institutions through organization of training sessions, seminars, symposia, and conferences.
To create awareness that cancer is preventable and curable To facilitate early detection of cancer To offer emotional support and medical aid to cancer patients To establish and encourage cancer survivorship programmes To reintegrate cancer survivors back into society To facilitate advocacy and research for cancer
We are a non-profit association that assists people diagnosed with cancer, their families and caregivers. We serve people with any type of cancer, regardless of gender, socioeconomic status or stage of treatment. Our mission is to promote assistance and social reintegration of people with cancer, by strengthening their self-esteem and autonomy. We believe that cancer can be a life sentence!
Strengthen, encourage and guide people living with cancer to get through this challenge in the best possible way.
We work to influence policy, legislation and national budgets so that patients are at the heart of cancer services and cancer care. We push Government to take action to improve the quality of life for patients and to make decisions that will help to reduce the number of people getting cancer and improve survival rates.
Jahandad Society For Community Development aims to bring about positive change in spheres of health, education, environment and socio-economic status of the underprivileged and marginalized population of Pakistan with particular emphasis on women and children.
KRAS Kickers is an online global patient empowerment group. We connect people with any KRAS cancer biomarker to kick cancer's KRAS using: KRAS Knowledge + Research + Advocacy = Survivorship
To create a social structure with high public awareness of cancer, strong individual knowledge and resistance, and a patient-oriented treatment system.
Kenyatta National Hospital Patient Navigation Program offers patient centered heath care services to optimize patient experience through innovative, evidence-based specialized healthcare; facilitate training and research, and participate in national health policy formulation. The patient navigation program is a patient centered model of care which was set up in Kenyatta National Hospital (Kenya) to assist patients diagnosed with cancer to overcome barriers which they face as they access care. We organize support groups for specific cancers which includes one for colorectal cancer. we encourage care givers to attend such support groups together with their patients. We also organize for awareness activities for selected cancers.
Kilimanjaro Clinical Research Institute's (KCRI)vision is to be an internationally distinguished center of excellence in health research and mission is to conduct and coordinate high quality biomedical research which will provide evidence for medical interventions in national and global health policies development. KCRI has grown as an academic center for evidence based health interventions in which investigators initiate and conduct medical research to develop evidence for interventions in improving health outcomes and provide research training and necessary research infrastructures and logistics to students, collaborators and partners. KCRI offers a diversified and flexible exposure to both clinical and biomedical research areas in a typical tropical setting.
NORD (National Organization for Rare Disorders), a 501(c)(3) organization, is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services.
Ensure for the public benefit, families affected by Lynch Syndrome are provided with information, support and access to screening. Increase public awareness of the syndrome, educate members of the general public plus health care professionals and provide support for Lynch syndrome research projects. Enable prevention of cancer developing and early diagnosis.
Man Up to Cancer inspires men to connect and avoid isolation during their cancer journeys. As North America’s leading support community for men impacted by cancer, we offer these free services and programs that are all geared toward improving the quality of life of our members. PEER-TO-PEER SUPPORT THROUGH OUR PRIVATE HOWLING PLACE FACEBOOK GROUP ANNUAL RETREAT - THE GATHERING OF WOLVES CHEMO BACKPACK PROGRAM MORE THAN 30 LOCAL CHAPTERS When faced with cancer, women tend to “reach out,” and men tend to “check out.” This leads men down the path toward mental health problems, strained relationships, and poor medical outcomes. It’s time for a new path. We are changing what it means to “Man Up” in the face of cancer. It’s not just about being tough. It means having the courage to accept help, and knowing we are smarter and stronger as a pack than we are as lone wolves.
Mbakuran Vaakaa Cancer (MVC) Foundation is a non-governmental organization that was founded out of passion when Mbakuran Vaakaa died of cancer (Colorectal). Her children saw a need to establish a foundation in her name that will educate, increase awareness and sensitize the general public on Cancer and other dreadful illnesses such as Tuberculosis, HIV/AIDS, Malaria etc and cater for the wellbeing of the infected persons hence most of those infected die as a result of knowledge gap/care. MVC Foundation envision a future where dreadful diseases that escalate death will be mitigated and people living with these illnesses will not be preyed with fear of death or discrimination. While our mission is to improve the living condition of the people infected/affected with dreadful diseases and the general public through proper sensitization, treatment, care and capacity building aim at reducing their morbidly and mortality rate.
Michael's Mission is focused on improving the quality of life and treatment options for those suffering from colorectal cancer through education, research and patient support. Michael's Mission is a registered 501 (c)(3) nonprofit organization. Funds raised go to patient care and support and research initiatives led by a medical advisory board comprised of leading physicians.
The Movement is partnering with the state and public health authorities to increase public awareness about the programs of clinical examination and mass screening for early detection of cancer .MichaelÔøΩs Mission is a registered 501 (c)(3) nonprofit organization. Funds raised go to patient care and support and research initiatives led by a medical advisory board comprised of leading physicians.
Nest of Hope was founded out of experience and passion by a cancer survivor as an advocacy and support group. The organization aims among other things to advocate for patients, raise awareness about the cancer burden. We are dedicated to ensuring that all people impacted by cancer are empowered by knowledge, strengthened by action and sustained by the community.
The Nigerian League for the Fight Against Cancer is interested in all cancers in General. Its specific objectives are: cancer prevention, facilitating access to medical care, training, research and palliative care.
To ensure Nigerians from age 40years be screened for Colorectal Cancer, this can be achieved by having minimum of two Screening centers in each state which will be equipped with Stool-based screening service ; Guaiac-Based Fecal Occult Blood Test (FOBT) and Fecal immunochemical test (FIT) including Colonoscopy unit by the year 2030 so has to have a free colorectal cancer patients in Nigeria and Africa at large. The screening Centers will facilitate early detection of the disease, accurate assessment and allow appropriate management before the disease becomes life threatening. _
Our mission is to raise the awareness of the general and specialist public about oncological diseases, their prevention, early diagnosis and treatment options. The goal is an informed and proactive public. We strive to reduce the incidence and mortality of oncological diseases not only through interactive educational experiences within the Gut Tour and Healthy Lungs roadshows. The domain of the roadshow is an inflatable model of the colon and lungs, which helps to understand the risks and causes of various diseases.
Project PINK BLUE is a cancer organization engaged in cancer awareness, free cancer screenings, support to people battling with cancer, patient navigation, advocacy, fundraising for cancer patients, cancer research, oncology training and psychological support.
AWARENESS Increase awareness about CRC and CRC screening. Improve detection through decreasing barriers to participation in CRC screening. Involve doctors and general practitioners in advising patients about the necessity of early screening starting at the age of 45. ADVOCACY Advocate with stakeholders to establish an organized CRC screening program in Lebanon while assuring access to high quality screening.
SPKS is a foundation of and for people who have (had) stomach or esophageal cancer. Based on experience and additional expertise, SPKS supports fellow sufferers and loved ones in the various phases of the disease. SPKS aims to ensure that all people with stomach or esophageal cancer receive the best possible care while maintaining the highest possible quality of life.
Saving Pennies 4 A Cure is, 501(c)(3) nonprofit organization, dedicated to improving the lives of breast cancer patients by providing custom care packages for those undergoing chemotherapy. These packages provide helpful information on the adverse effects that accompany this treatment, easeing patient anxieties. We also provide resources that emphasize the importance of self-care and self advovacy. Our goals are to educate, advocate, public awareness and give back to the Cancer community.ÔøΩ
To improve the lives of anyone affected by cancers of the liver through information, resources, and support; deliveringng hope and ensuring no one makes the journey alone.
The Association of Colon and Liver Cancer Patients is dedicated to the fight against colon cancer, with an emphasis on early detection, improving the quality of life of patients, the availability of modern therapy and providing assistance to those who need it.
Contribute to the reduction of the incidence, mortality and morbidity of cancer through education, research and early diagnosis to create collective awareness of the dimension of cancer in Venezuela and promote prevention among the healthy population.
AMS Laborator Genetic constantly brings to the Romanian market innovative oncogenetic tests, capable of having a real benefit in the medical approach and the personalized treatment of patients with various oncological pathologies. Along with the provision of genetic test results, AMS Laborator Genetic provides patients, through its specialists, genetic counseling and results interpretation services.
To assist in breaking the myths and misconceptions surrounding cancer. To Provide emotional, financial ,support materials and to help cancer patients build confidence in themselves. To offer education, counseling and promote awareness of cancer treatment and screening options to the general public.
St. Cyril Cancer Treatment Foundation Mission is to increase the number of treatment facilities available and provide quality holistic care to cancer patients in Africa.
ÔøΩSharing knowledge saves livesÔøΩ is the leitmotif of this action group which became a non-profit organization in 2012 . This pursues the objective of informing and sensitizing the entire population around a simple message: early detection of polyps and colon cancer drastically reduces mortality. Thanks to various communication channels, among which the internet and social networks play an important role, the association organizes actions to inform about colon cancer. Indeed, the general public's knowledge of this silent killer is far from satisfactory.
Strive for Five was set up in 2017 as there was so little positive news about stage 4 cancer. Strive for Five's aims are: -Give hope to people with stage 4 cancer -Raise awareness of bowel cancer -Advocate to improve careÔøΩ
Late SUMITA BHATTACHERJEE, wife of Mr. MADAN KUMAR BHATTACHARJEE,had been undergoing treatment of the dreadly OVARIAN CANCER since October 2006 . Ultimately she passed away on 13th September 2008 leaving the beautiful world. With her sole inspiration behind this philanthropic effort, Mr. Bhattacharjee finally came to the decision to set up the society with a motto to fight against the deadly disease cancer through it.
My foundation was set up in honour of my wife susan who died from bowel cancer aged 35 in 2021.My mission is too spread awareness and educate people about bowel cancer.Also my mission is too lower bowel screening in ireland which currently is 60-69
We are committed to a single goal; helping the fight against colorectal cancer. The Blue Hat Foundation is a colorectal cancer organization whose mission is to educate, raise awareness, and provide resources to free screenings for minority and medically underserved communities. We work hard to take care of the neediest members of our community and provide them with unconditional support.
Our mission is to raise awareness, educate, and help those with colorectal cancer, particularly those diagnosed under age 45, along with their community of support.
ÔøΩWeÔøΩre on a mission to free the world from cancer. We claim quality of services and the right to life for people with cancer and their familiesÔøΩ.
We do not want one more family to be affected by this disease. To that end, we are tireless advocates for colon cancer education, outreach and patient empowerment. Through meaningful collaborations with professional societies, outreach and advocacy organizations we are making a dramatic difference and saving lives around the globe. Through early detection and prevention strategies, we are confident that an end to colon cancer is in sight. Our vision is crystal clear - we can see it, can you?
Triage CancerÔøΩ is a national, nonprofit organization that provides free education on legal and practical issues that may impact individuals diagnosed with cancer and their caregivers, through events, materials, and resources. The Legal & Financial Navigation Program offers one-on-one help with issues such as work, health and disability insurance, finances, and estate planning. CancerFinances.org is an online toolkit to help people manage finances after a cancer diagnosis.
To bridge the gap between underserved cancer patients and their healthcare providers; and to encourage inclusive clinical trials and other cancer reasearch. This will be achived through advocacy, education, and support for the breast cancer community.
The mission of the Tulasi Maya Memorial Cancer Relief Foundation Nepal is to beat cancer. The goal is to prevent cancer, bring about early diagnosis, and develop treatments. Every cancer patient is supported in his or her recovery and to live a full life regardless of the disease or its aftermath. GOAL To help to reduce the incidence of cancer the Himalayas and Nepal while contributing in the well- being of the people living with cancer.
UOAA promotes quality of life for people with ostomies and continent diversions through information, support, advocacy and collaboration.
WOCACA mission is to contribute towards cancer prevention and control through advocacy, campaigns, awareness, education, training, networking, counseling, screening, timely treatment and patient support among rural women and girls.
Empowering patients to positively impact the healthcare system in the best possible way
Our mission is to be the global voice of patients working toward patient empowerment and engagement, improved access to safe innovative treatment and patient centered healthcare throughout the world.
The association works by raising public awareness of the risks of the disease and the importance of prevention by performing tests for early detection. At the same time, the association constitutes a 'home' for SMG patients and their families by sharing the medical-professional knowledge that exists today and organizing professional lectures on topics important to them. The "Restraining Order" campaign is led by the "Shamir" health insurance company, which provides medical information for the benefit of the public