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

Our mission is to improve early detection for breast cancer worldwide through creative and empowering education.

Our Mission•to educate the community regarding all end-of-life issues, grief and bereavement.•to support all patients and families facing life-limiting illnesses, grief and bereavement.•to respond with compassion to physical, emotional, social and spiritual needs.•to provide these services without regard to age, religion, race, gender, illness or ability to pay.

To discover new treatments and cures for patients with familial dysautonomia (FD).

Charlotte Gray was born December 5, 2010, filling the hearts of her parents, Kristen and Gordon, with the same joy all parents feel. She developed at the pace of a typical baby and toddler – walking and talking, with an early passion for gymnastics, dancing and swimming. However, after Charlotte’s first full year of preschool, her parents noticed she had hit a plateau developmentally. After countless questions, and seemingly as many tests, Charlotte was diagnosed in March 2015 with Late Infantile NCL Batten Disease CLN6. The diagnosing geneticist explained that this neurodegenerative brain disease was extremely rare and would leave Charlotte blind, immobile, cognitively impaired, and, ultimately, gone…somewhere between the age of 6 and 12. Their world shattered, Kristen and Gordon immediately had their younger daughter Gwenyth tested and she was given the same grim diagnosis. While Charlotte is showing early symptoms of the disease, she remains strong, with her happiness and smile still constant. However, due to the pace at which Batten disease advances, action must be taken immediately to prevent Charlotte’s progression down Batten’s debilitating path and shield Gwen, and all future children impacted by Batten disease, from its painful effects. 

PROVIDE HOSPICE CARE TO INDIGENTS

TO SOLICIT AND ACCEPT GIFTS AND GRANTS FOR THE SOLE PURPOSE OF CONTRIBUTING TO KIDS IN DISTRESS, INC. IN SUPPORT OF ITS MISSION TO PREVENT CHILD ABUSE, PERSERVE THE FAMILY, AND TREAT CHILDREN WHO HAVE BEEN ABUSED OR NEGLECTED.

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.