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The Bone Marrow Foundation, founded in 1992, is dedicated to improving the quality of life for bone marrow, stem cell and cord blood transplant patients and their families by providing vital financial assistance, educational information, and emotional support programs. Transplants treat over 70 life-threatening diseases including cancers and genetic disorders. The Foundation works with transplant centers nationwide and is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. All of The Foundation’s services are offered free to patients and their families. Patient Programs Lifeline Fund provides funding to help cover the costs of transplant-related expenses. In addition, the program leverages social media to enable patients to reach out to their family, friends and social networks for additional financial support. One-to-One Funds assist patients and their families with fundraising efforts by creating a personal fund at The Foundation. Medical & Educational Handbooks provide comprehensive patient education and resources to assist patients and family members in obtaining information regarding all aspects of transplantation. Ask the Expert enables individuals to pose questions concerning transplantation and to have them answered by healthcare professionals. SupportLine provides support services to transplant patients and their families by linking them with volunteers who have gone through the transplant experience. Survivorship Program provides support and information to post-transplant patients, their families, and caregivers as they continue to navigate their transplant journey. Survivor Telephone Support Group staffed by oncology social workers, provides bone marrow, stem cell and cord blood transplant survivors with a weekly scheduled telephone conference support group to share experiences and draw support from others. For patients one year or more post-transplant.  

The Progeria Research Foundation's (PRF) mission is to find treatments and the cure for Progeria and its aging-related disorders, including heart disease. Progeria is a fatal, 'rapid aging' disease that afflicts children, who die of heart disease at an average age of 14 years. PRF was founded in 1999 in response to the complete lack of resources and research on Progeria, and is the only organization in the world solely dedicated to discovering treatments and the cure for this devastating condition.

The Mission of The Miles Hall Foundation is support families by educating communities about mental illness and protect those impacted with mental illness from excessive use of force by law enforcement. We do this life-saving work to honor the life and legacy of Miles Hall, who was killed by the Walnut Creek police in June of 2019 during a mental health crisis. Our work falls into three categories, prevention, education, and advocacy.

Unicorn Children's Foundation is dedicated to creating cradle to career pathways for kids and young adults with developmental or learning challenges and helping their families navigate the complex journey. Neurodiversity encompasses a range of neurologically-based disorders such as autism, Asperger’s, ADHD, bipolar, dyslexia, and other learning disorders. We have chosen to view these disorders from a different perspective by seeing each child as uniquely capable and talented with specific strengths and interests that should be cultivated. In essence, every individual, regardless of his/her “disability”, deserves an opportunity to lead a fulfilled and productive life.

We assist families with children 3-18 who are wheelchair bound, purchase wheelchair accessible vehicles. Through the foundation and its board of directors, SFF focuses its activities in the Portland and SW Washington area. Through special events like the annual “Boo Who?” a family focused Halloween event held every October, SFF raises funding to support families touched by various disabilities focusing mostly on Cerebral Palsy and Autism. Transportation, scholarships, respite care, caregiver support activities are just a few of the ways SFF gives back.

Established in 1998, The Eye Cancer Foundation is an educational and supportive resource for eye cancer patients, their families, and physicians. Our mission is two-fold: one part focused on multi-center research of new diagnostic treatments for eye cancer research, the other focused on providing much needed, world-wide patient support services. Our mission is to create a world-class resource for patients and their families diagnosed with ocular tumors, radiation macular degeneration, and related ophthalmic conditions. We want to help you, your children and families around the world. ECF Specific Goals: 1) Find cures for patients with ocular tumors and related eye diseases. 2) Provide eye cancer specialists for unserved and underserved countries. 3) Coordinate international cooperative evaluations of new methods of diagnosis and treatment. 4) Support family and patient support programs to ease emotional stress and real-life adjustment issues related to eye cancer. 5) Promote transparency related to doctors and patient outcomes. 6) Promote quality assurance and education for eye cancer specialiatly centers. 7) Empower patients to find the resources to improve their lives.

Sponsor and support research, education and treatment of cancer for the benefit of the general public.

Our national mission is to educate the American public as to the growing seriousness of Alzheimer's, Dementia and Traumatic Brain Injuries (TBI) in the American population by raising the necessary donations through strategic research initiatives and heightened public awareness to accomplish our objectives.   We are also dedicated to helping fund the necessary research to find a cure for both Alzheimer's and Dementia while promoting awareness, education, and research funding in the area of improved safety standards to prevent TBI (traumatic brain injury), potential precursors to Alzheimer's and Dementia.  

Goshen Valley provides hope and healing to foster youth and vulnerable families through relational, trauma-responsive services to cultivate personal healing and generational change.

Beyond the Orphanage works with government, community groups and other not-for-profit organisations to meet these children’s urgent needs. We are working to protect them and give each child the chance to build a stronger, brighter future. Help us celebrate our 10-year anniversary by donating.

For nearly five decades, Fort Hudson Health System has provided the very best in care and services for the seniors of our region. They are the region’s first choice in senior care, filling a critical role in the health care system. They are the place and the people that families turn to when experience, expertise and excellence mean the most.

The Village Network is an experienced, multi-discipline behavioral health nonprofit organization helping youth and families become resilient, healthy and have brighter futures.