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The Spencer Foundation is a Chicago-based organization that focuses on investing in education research to promote learning and transform lives. Established in 1962 by Lyle M. Spencer, the foundation supports innovative research on education in various forms, including research grants, training grants, fellowships, and field building programs. With a commitment to diversity, equity, and inclusion, the foundation aims to improve education systems for greater equity and opportunity. The Spencer Foundation offers funding opportunities for high-quality research projects that address educational issues from a broad perspective. Through their grant programs, they support research on topics such as racial equity, education reform, and collaborative partnerships for educational change. The foundation also provides resources and tools for applicants and grantees, as well as publishes white papers and news updates to share insights and findings from their research initiatives.Generated from the website

About STS Society Mission The mission of the Society is to enhance the ability of cardiothoracic surgeons to provide the highest quality patient care through education, research, and advocacy. Founded in 1964, the Society of Thoracic Surgeons is a not-for-profit organization representing more than 6, 200 surgeons, researchers and allied health care professionals worldwide who are dedicated to ensuring the best possible outcomes for surgeries of the heart, lung, and esophagus, as well as other surgical procedures within the chest.

The Pulmonary Fibrosis Foundation, based in Chicago, IL, is dedicated to advancing care for patients with pulmonary fibrosis (PF) and providing support and education resources for patients, caregivers, and healthcare providers. The foundation aims to accelerate the development of new treatments and ultimately find a cure for PF. It is the largest non-profit organization funding research and advocating for the PF community. Through various programs and services, the Pulmonary Fibrosis Foundation offers valuable resources such as the PFF Help Center, support groups, and opportunities to participate in research studies and clinical trials. Patients can access educational materials, connect with healthcare professionals, and find support in navigating their PF journey. The foundation strives to empower individuals affected by PF by offering free programs and services, including online resources, webinars, and fundraising events. By supporting research, education, and advocacy efforts, the Pulmonary Fibrosis Foundation plays a crucial role in improving the lives of those impacted by PF. Generated from the website content