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Brain Research Foundation supports neuroscience research that leads to advanced understanding of brain function in children and adults. This Foundation is committed to advance discoveries that will lead to novel treatments and prevention of all neurological diseases. We deliver this commitment through both research grant programs, which provide initial funding for innovative research projects, as well as educational programs for researchers and the general public.

paws4people foundation trains and places customized Assistance Dogs for two general populations: children and adolescents with physical, neurological, psychiatric or emotional disabilities; and Veterans and active-duty Service Members with Chronic/Complex Post-Traumatic Stress Disorder (C-PTSD), Traumatic Brain Injuries (TBI), and Military Sexual Trauma. p4p Volunteers perform thousands of hours of Social Therapy and Educational Assistance work with their p4p certified Assistance Dogs.

NEADS World Class Service Dogs was founded in 1976 to train and place assistance dogs to help people who have disabilities and children who have autism. NEADS has trained over 1,800 Assistance Dog partners (person and dog) now living and working together across the USA, including assistance dogs to help veterans of our wars with physical disabilities and with PTSD. NEADS is the oldest continuing Hearing Dog program in the country and the first program on the East Coast to train a Service Dog.

The California School-Based Health Alliance (formerly the California School Health Centers Association) improves the health and academic success of children and youth by advancing health services in schools.  We envision a day when all of California's children and youth are healthy and achieving at their full potential. Since hiring our first paid staff in 2003, the Alliance has successfully grown to have an annual budget of more than $1,500,000 and thirteen staff.  We conduct policy work, promote the school based health center (SBHC) model, and assist SBHCs with program development to expand and strengthen school health services.  Our large network of collaborating partners includes 231 SBHCs, numerous school districts, federally qualified health centers and other providers, dozens of state and local policy organizations, and an e-communications network of more than 3,200 individuals. Our goal is to make school health centers an integral and sustainable part of the health care and educational systems. By putting health care where kids are – in schools – school health centers increase access to care and take health problems out of the classroom so that teachers can teach and students can learn.

The mission of the Sophia Sunshine Foundation is to bring joy and connectivity into the universe through various acts of kindness that empower children experiencing adversity, especially those battling pediatric cancer. Sophia’s love for horses, dogs, dance, music, art, books, golf and tennis brought her a tremendous amount of joy and laughter, even during her most challenging weeks. Through the Sophia Sunshine Foundation, we want to help others experience that joy and heart-mind well-being through activities such as equine therapy, service dog sponsorship and literacy outreach. We also support pediatric cancer research towards a cure for DIPG.

To provide support to parents of children born with rare chromosome disorders, gather together and share information, and to promote research and a positive community understanding of these disorders. CDO envisions a time in the not too distant future when doctors will have a great deal of information available on each and every chromosome disorder. They will be able to tell parents symptoms associated with a particular deletion, duplication or other disorder as well as what not to worry about. It is also our hope that appropriate therapies or other treatments will be recommended specific to particular disorders and that affected individuals will have a much greater chance of a fuller life. This is already beginning to happen and it is CDO's goal to further support this research in any way possible.

AshaUSA's m​ission is to provide culturally specific programs to the South Asian community t​​o foster health and harmony in their lives. Formed in July, 2014 in Minnesota, AshaUSA (Asha means hope) is a non-profit organization focused on engaging and empowering South Asian women, men, and children through culturally specific programs and services. Over 3.4 million South Asians (originally from India, Pakistan, Bhutan, Nepal, Bangladesh and Sri Lanka) live in the United States out of which about 44,000 live in Minnesota (2010 census). 75% of South Asian Minnesotans are first generation immigrants. The South Asian population in Minnesota has more than doubled since 2000. With the increase in population, challenges associated with acculturation in terms of health, youth development, and family relationships have become more distinct. There is a need for culturally specific programs that proactively address acculturation challenges for the South Asian community in Minnesota. ​

Our Mission is to work so that no one is isolated because of Parkinson’s disease. Parkinson’s Resource Organization (PRO) is dedicated to improving quality of life for families and individuals affected by Parkinson’s disease through education, support, and practical resources. PRO was established in 1990 by caregivers who were overwhelmed and struggling to find the support network they needed. So they decided to create one. What started as Children of Parkinson's morphed into Parkinson's Resource Organization and today we continue to maximize quality of life for people with Parkinson's, their families, and caregivers through education, resources, and person-to-person support. PRO works to improve quality of life for everyone impacted by Parkinson’s. We do this through emotional and practical resources, support groups, educational materials, and access to a network of professionals who can provide guidance and assistance. Additionally, we advocate for the needs and rights of caregivers and patients, ensuring they receive the necessary care and resources. Caregivers play a crucial role in the management and support of Parkinson's patients. PRO acknowledges their efforts and aims to equip them with the tools and knowledge required to provide effective care. Through continuous outreach and dedicated services, we strives to create a supportive community where caregivers and patients can find the help and companionship they need.