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The Center for Hope Hospice provides terminally ill patients with the natural, humane care known as hospice and their families or loved ones with physical, emotional, and spiritual support during their time of need. The Center brings to its patients a new, caring quality of life that actively supports the individual's right to live out the remainder of their life with dignity and in comfort, surrounded by the love of family and friends, and eased from the burdens of distress be it physical, emotional, spiritual, financial or social.​ The Center provides family and loved ones with the opportunity to discover and embrace the gift of life as they journey through loss. The Center welcomes all terminally ill patients, their families and loved ones without concern for race, ethnicity, religious affiliation or ability to pay.

The VNA provides compassionate, innovative care of the highest quality, setting the standard for patients and caregivers needing home health, hospice and community health services, regardless of a patient’s ability to pay. The VNA works to provide innovative access to care for the community through home health, hospice and community health & education programs. The VNA's wellness programs encompass the community education and outreach aspect of our mission, promoting health throughout the counties we serve.

International Esperanza Project strengthens communities in Latin America from the inside, out, partnering to create impact through lasting improvements to homes, healthcare, and education -- so everyone can realize the future they hope for.

debra of America supports people with Epidermolysis Bullosa (EB) by funding research toward better treatments and a cure, while also delivering direct services and education to patients and families (including wound‑care distribution, nurse support, advocacy, and community programs). This work combines patient services, advocacy, and research funding to improve quality of life for people affected by EB.

LymeDisease.org seeks to make the patient voice stronger, to support patient-centered research, and to create a future where Lyme patients can receive the treatments they need to get well. Its focus is on large scale science-based advocacy, communications and big data research. Founded in 1989, it is one of the oldest, largest, and most trusted sources of patient information on Lyme disease, drawing millions of unique website visitors a year. Its MyLymeData patient registry and research platform has enrolled over 14,000 patients and is among the top 5% of patient-led registries in the nation. Its communications network distributes resources and educates the public about the science of tick-borne diseases via website content, blogs, social media, and an online journal, the Lyme Times

ESTABLISHED IN 1978, THE CENTER FOR HOSPICE CARE (CHC) IS AN INDEPENDENT, COMMUNITY BASED, NOT-FOR-PROFIT ORGANIZATION, IMPROVING THE QUALITY OF LIVING THROUGH HOSPICE, HOME HEALTH, GRIEF COUNSELING, AND COMMUNITY EDUCATION WITH OFFICES IN SOUTH BEND, PLYMOUTH, ELKHART, LA PORTE AND MISHAWAKA. CHC SERVES A NINE-COUNTY AREA IN NORTHERN INDIANA, INCLUDING ELKHART, FULTON, KOSCIUSKO, LAGRANGE, LA PORTE, MARSHALL, ST. JOSEPH, STARKE, AND PORTER COUNTIES. CHC'S MISSION IS TO IMPROVE THE QUALITY OF LIVING THROUGHOUT NORTHERN INDIANA, AND OUR VISION IS TO BE THE PREMIERE HOSPICE AND PALLIATIVE CARE ORGANIZATION FOR ALL END-OF-LIFE ISSUES. OUR CORE VALUES INCLUDE COMPASSION, DIGNITY, INTEGRITY, INNOVATION, QUALITY, SERVICE, AND STEWARDSHIP.

Halo House Foundation helps to save the lives of blood cancer patients by providing affordable and fully furnished housing so they can receive treatment at the Texas Medical Center.

Northeast Ohio Hospice promotes the hospice concept of caring and encourages and aids in the development of quality hospice programs for terminally ill patients and their families. We educate the public about hospice care and respond to the needs of the local community with hospice services that are consistent with the medical-moral teachings of the Roman Catholic Church

RESEARCHING CURES AND TREATMENTS FOR CTNNB1

The Autoimmune Association leads the fight against autoimmune disease by collaborating to improve healthcare, advance research, and support the community through every step of the journey.

The White Ribbon Project works to change public perceptions about lung cancer and reduce stigma by producing and distributing large white ribbons, building community, and promoting awareness, early detection, research, and support for people affected by lung cancer.

We help heal the hurt for boys and girls in need.