112 Foundation

Bringing comfort to patients and families by providing essentials and enriching lives with fond, lasting memories. We also support community education to increase awareness about the benefits of hospice, funding for special programs and applied research to improve the quality of hospice care. Extending beyond the borders of traditional health care, we treat the whole person and their loved ones in ways that touch the human spirit, adding days to life and life to days.

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