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To improve the health and quality of life of women living with or at risk of heart disease, and to advocate for their benefit.

The National Coalition for Latinxs with Disabilities (CNLD: Coalición Nacional para Latinxs con Discapacidades by it’s Spanish acronym) was established in 2017 as a volunteer national organization made up of disabled Latinxs and allies who work towards a seamless society in which the human rights of Latinxs with Disabilities are upheld and all their intersecting identities are embraced. CNLD works in solidarity to affirm, celebrate, and collectively uplift Latinxs with Disabilities through community building, advocacy, protection of rights, resources, research, and education around all issues disabled Latinxs experience. This includes collaborating with allies, organizations and leaders in the disability community who support our vision and mission. 

​​"Our mission is to reduce the prevalence of Lyme Disease through Education, Prevention, and Research. Working together with other groups and organizations, as well as government entities, sharing in resources, to enhance and extend service to the community."

The mission of the National Coalition for the Homeless is to prevent and end homelessness while ensuring the immediate needs of those experiencing homelessness are met and their civil rights protected.

The organization raises awareness, advocates, and fundraises in the United States to support the global work of UN Women — promoting gender equality, advancing women’s rights, reducing violence against women, and mobilizing resources for UN Women’s programs.

Prevent Heart Disease: In the past this fund has donated to national organizations involved in heart health, like the Hope Heart Institute.

Our mission is to recover our communities through educating, enhancing, empowering, strengthening, and improving women and families personally, professionally, and socially. We are passionate about helping women recognize their needs and potential to be restored as successes in society through study, workshops, seminars, and conferences.

The Paget's Association is the only national charity dedicated to helping people with this chronic bone disorder. It works to provide information, education and support to members of the public and health professionals and supports research into all aspects of Paget's disease.

The National Organization for Women Foundation (“NOW Foundation”) is a 501(c) (3) organization devoted to achieving full equality for women through education and litigation.The Foundation focuses on a broad range of women’s rights issues, including economic justice, pay equity, racial discrimination, women’s health and body image, women with disabilities, reproductive rights and justice, family law, marriage and family formation rights of same-sex couples, representation of women in the media, and global feminist issues.The NOW Foundation is affiliated with the National Organization for Women, the largest feminist grassroots organization in the U.S., with hundreds of chapters in all 50 states and the District of Columbia and hundreds of thousands of contributing members and supporters

Our mission is to secure an active, long-lasting, and unified support to children with cancer in Bosnia and Herzegovina. Our vision that every child in Bosnia and Herzegovina has an equal and secure upbringing. We are a non-profit organization that offers services to children with cancer. The Association Heart for Kids with Cancer was founded in 2003 with a mission of creating best practices and opportunities in treating and supporting pediatric cancer patients and cancer survivors, as well as providing professional and financial help to children with cancer and their parents in Bosnia and Herzegovina. To this day, our ultimate focus has remained the same: providing help and support to pediatric cancer patients, survivors and their families. Our organization has been steadily developing ever since its inception. In 2016 we have built The Parents' House, a modern residential building with 10 apartments located on the premises of the Clinical Center of the University in Sarajevo, which provides housing for children undergoing therapy and their families. The Parents' House functions as a separate and independent project of our Association, and is financed solely through our fundraising activities. This has solved a major problem in our field of work, as the Clinical Center of the University in Sarajevo does not have means of accommodating parents of children undergoing therapy, most of which come from areas outside of Sarajevo. We document and closely monitor all our activities. As we are in a constant and direct contact with our clients, their feedback provides a valuable source of information for us. We use questionnaires, evaluation forms and pre/post interviews to derive quantitative and qualitative indicators in order to measure a relative success of our initiatives. All our activities are meticulously planned in advance, and monitored and evaluated along the way and retroactively. We rely extensively on short term and long term strategic planning to set the goals and objectives, and to determine the best way we use resources to tackle problems or exploit opportunities. Since all our operations are funded through fundraising activities and institutional and individual donations, we have put a special emphasis on transparency. We conduct external financial audits and employ independent consultants for all issues of any degree of sensitivity. We are proud to boldly claim that, on account of our dedication, achievements, and our meticulous approach to work, we enjoy a complete and unreserved trust of our clients, governmental institutions and the general public in Bosnia and Herzegovina.

𝐀𝐛𝐨𝐮𝐭 𝐂𝐨𝐧𝐠𝐞𝐧𝐢𝐭𝐚𝐥 𝐇𝐞𝐚𝐫𝐭 𝐃𝐢𝐬𝐞𝐚𝐬𝐞: 1 in every 100 newborns are born with congenital heart disease, making it the most common birth defect. That means every 15 minutes a new CHD story begins, altering the course of a family’s life in unpredictable ways for a lifetime. 𝐎𝐮𝐫 𝐌𝐢𝐬𝐬𝐢𝐨𝐧: At Conquering CHD, we exist to conquer the most common birth defect. We engage, listen, learn, and act. We create visibility and empower all impacted by congenital heart disease. We accomplish this through awareness, knowledge, community, and research.

We exist to conquer the most common birth defect. We engage, listen, learn, and act. We create visibility and empower all impacted by CHD. We accomplish this through awareness, knowledge, community, and research.