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Given the lack of understanding of the causes of and treatments for neuropathic facial pain, FPRF is established to foster and support effective translational medical research (i.e., from fundamental discovery to clinical application). In pursuit of that Mission, FPRF is to establish a well funded translational research continuum that is dedicated to identifying the mechanisms underlying neuropathic facial pain and to developing ground-breaking therapeutic strategies that will permanently stop the pain of TN and related neuropathic pain syndromes.

To connect, support, and inform the Coffin Siris Syndrome community and to promote related research.

Support and fund the development of life-saving treatment for patients with pyruvate dehydrogenase complex deficiency and related genetic diseases.

Agape Hospice Care's mission is to provide the very best care for our patients.

To increase awareness and prevention of Sudden Cardiac Arrest (SCA) within families, communities, schools and Student-Athletes through education, healthcare screenings as well as donating automatic electronic defibrillators to schools that cannot afford them.

Dedicated to raising awareness for 22q11.2 Deletion Syndrome while connecting, supporting and offering accurate information for families affected by 22q.

Our main focus is Cystic Fibrosis (CF) awareness and to raise funds through the selling of our global crafts which include handmade Soy Candles, Jewelry, Crocheting, Pottery and much, much more. Our Story: Our daughter Hannah was born with Cystic Fibrosis, a genetic life-threatening disease. Our family’s and friends mission in life has been to make a difference by raising awareness through volunteering and fundraising for Cystic Fibrosis. Our lives drastically changed on July 22nd, 2012 when our only other child, our son, SPC Brenden N. Salazar-Nelson was killed in the line of duty in Afghanistan, decorated with the Bronze Star and Purple Heart. I created Angel’s Life in 2003, I chose this name because it is the symbol of peace and salvation. Now this name means that more than ever. Together with my friends and family, we create soy-based candles and sell them to help draw awareness for Cystic Fibrosis.

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

OMRF was founded with the mission of helping Oklahomans and people everywhere live longer, healthier lives. That mission has remained our organization's compass, guiding our scientists not only to perform groundbreaking scientific research but to research that helps mankind in the battle against human disease. Our goal, quite simply, is to make discoveries that make a difference.

In the fight for a DIPG/DMG cure, we help patients and families by funding game-changing research and providing navigation throughout their journey.

Corazon de Vida (CDV) is a 20+ year US 501c3 non-profit organization providing life-changing support for orphaned and abandoned children in Baja, Mexico by funding local orphanages, providing quality of life improvement services and investing in the children’s future by funding higher education.

Thanks to incredible community support, the new Alberta Children's Hospital is the most state-of-the-art children’s hospital in North America. Caring for 76 thousand kids and families each year, the Alberta Children’s Hospital is the provincial referral centre for Bone Marrow Transplantation and is establishing itself as a national leader in pediatric Neuroscience, family centred care and child health research. The Alberta Children's Hospital is home to the largest pediatric vision clinic in western Canada and is the only hospital in Canada that performs vision-saving laser eye surgery on children.