Search Nonprofits

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 mission of the Noah's Hope – Hope4Bridget Foundation is to raise funds in support of scientific research, and inform the community about Batten Disease. Batten Disease is a rare, fatal autosomal recessive neurodegenerative disorder that begins in childhood.

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.

Summit for Stem Cell Foundation’s mission is to increase awareness, educate and raise funds in support of research working toward a patient-specific neuron replacement therapy for Parkinson’s that will result in a victory over Parkinson’s disease.

The American Hearing Research Foundation serves two vital roles: to fund significant research in hearing and balance disorders, and to help educate the public about hearing loss and balance disorders related to the inner ear.

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.  

The Lupus Research Alliance is the largest nongovernmental, nonprofit funder of lupus research worldwide. The organization aims to transform treatment while advancing toward a cure by funding the most innovative lupus research; fostering diverse scientific talent; stimulating collaborations; and driving discovery toward better diagnostics, improved treatments and, ultimately, a cure for lupus. Because the Lupus Research Alliance’s Board of Directors funds all administrative and fundraising costs, 100% of all donations goes to support lupus research programs. F/K/A Alliance for Lupus Research

The Cystinosis Research Foundation is dedicated to finding better treatments to improve the quality of life for those with cystinosis and to ultimately find a cure for this devastating disease.CRF is committed to finding a cure through an aggressively funded research agenda. CRF issues research grants bi-annually to accelerate the research process and to ensure that there is never a gap in funding new cutting-edge research ideas. We are focused and determined to improve the quality of life for our patients and to find better treatments, including a cure, for our adults and children living with cystinosis

The Children's Medical Research Foundation, Inc. was formed in 1995 for the purpose of raising public awareness and funds to support medical and scientific research into the causes of, and cures for Sanfilippo Syndrome and other neuro-genetic diseases afflicting children.

Since 1991, The Vision of Children Foundation has funded medical research to find cures for hereditary childhood blindness and vision disorders. It also offers programs to improve the quality of life of visually impaired individuals and their families.

1) To provide the LATEST MEDICAL / RESEARCH information and EDUCATION so that they may make wise medical decisions and continue their independence despite their vision. Provide information and research data to the medical and research community so that they may join in our fight against blindness. The AFI International Aniridia Medical Registry and Gene Bank is the main project of our research. 2) To SUPPORT the low vision / blind people born with aniridia and their families who struggle emotionally and financially due to having aniridia. To assist them in accomplishing their dreams and remain independent, self sufficient and a productive member of society. 3) To help fund RESEARCH especially the AFI created program which collects DNA samples, comphrehensive medical questionaires, and clinical photographs to add knowledge to physicians and advance research. Our international faculty of AFI Medical Advisory and Scientific Boards assist us with this program. We also help fund research and patient care services as funds allow and look forward to raising funds to expand our efforts to stop this genetic condition from continuing into future generations.. 4) To further PUBLIC AWARENESS about all the conditions that make up aniridia, and the misconceptions of people who are blind or low vision,

Lyme Warrior is a 501(c)(3) nonprofit organization fighting to bring awareness and support to the sufferers of the silent, debilitating epidemic of Lyme Disease. Proceeds fund Lyme Disease research, awareness campaigns, and impoverished Lyme Warriors.