Search Nonprofits

The United MSD Foundation was established to enhance the quality of life for MSD (Multiple Sulfatase Deficiency) patients by facilitating the development of treatments, funding research, providing resources and building a network of MSD patients and families.

The Propionic Acidemia Foundation is a 501(c)3 non-profit organization dedicated to finding improved treatments and a cure for Propionic Acidemia by funding research and providing information and support to families and medical professionals.

The International FoxG1 Foundation’s Mission is to raise awareness and educate others about this rare genetic condition, to facilitate relationships within the FOXG1 community, and to raise funds to directly benefit families impacted by FOXG1.

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives. It will support pediatric leukodystrophy research as well as assist and care for children and families affected by one of the leukodystrophies and/or other disabling conditions.

The Kabuki Syndrome Foundation (KSF) is the only US based 501c3 nonprofit organization dedicated to advocating for the advancement of Kabuki syndrome research. Since its inception in 2017, the Kabuki Syndrome Foundation has strived to promote activities that support, enable, and accelerate research efforts that will advance therapeutic treatments for those affected by Kabuki Syndrome (KS). Our mission is to drive research efforts that show promise to treat, prevent or cure Kabuki Syndrome through fundraising, knowledge-sharing and collaborating with researchers around the world.

The Sturge-Weber Foundation’s (the SWF) international mission is to improve the quality of life and care for people with Sturge-Weber syndrome and associated Port Wine Birthmark conditions through collaborative education, advocacy, research and friendly support.

The Boomer Esiason Foundation is a dynamic partnership of leaders in the medical and business communities joining with a committed core of volunteers to heighten awareness, education and quality of life for those affected by cystic fibrosis, while providing financial support to research aimed at finding a cure.

The KAT6 Foundation supports people and their families who are living with KAT6A and KAT6B syndromes around the world. We advance scientific research aimed at developing treatments and spread awareness of KAT6 syndromes so they can be more easily identified, treated and studied.

The Team Drea Foundation funds and supports bold, innovative research to find a cure or effective treatment for ALS. We see raising awareness about this devastating disease as an opportunity to inspire people to live bravely, love joyfully, and appreciate the gift of life.

Westminster Canterbury Foundation inspires generosity at Westminster Canterbury Richmond. Growing from our roots in faith, we nurture the spirit of generosity of Westminster Canterbury Richmond to ensure the best life possible for our residents and to cultivate leadership in senior services. Our founding mission emphasized our Fellowship Program, which helps provide life care – guaranteed access to long-term assisted living or healthcare if needed – as well as necessities such as housing, food and medical expenses for seniors-in-need. A newly established Fellowship Outreach effort is in response to Westminster Canterbury Foundation’s Community Needs Study assessing the barriers to healthy aging in greater Richmond. Westminster Canterbury Foundation also supports areas of excellence including healthcare, memory therapies and spiritual support, chaplaincy programs and internships, wellness and fitness programs, enhancements and scholarships for the Child Development Center, workforce development, and thriving creative programs that include studio and performing arts. Innovation and leadership in senior services are made possible every year.

The Fetal Hope Foundation's mission is to provide support, provide information, fund research, increase awareness and be an outlet for leading medical information pertaining to fetal syndromes. We are all about arming families and healthcare providers with information and helping to save babies' lives.

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.