Iolta Fund

The Waterfront Project Inc., founded in 2013, is a non-profit legal clinic and HUD-Certified Counseling Agency dedicated to preventing homelessness and preserving affordable housing in Hudson, Union, and Bergen Counties. Committed to the belief that housing is a fundamental right, the organization offers free comprehensive services to individuals and families at risk of losing their homes. Through its legal and housing services, The Waterfront Project empowers clients to navigate complex legal systems, halting evictions and preventing foreclosures while providing vital support and guidance. The organization has made a significant impact in the community, helping countless families maintain their homes and advocating for neighborhood stability one family at a time. Generated from the website

United Cerebral Palsy of New York City is part of a network dedicated to empowering individuals with disabilities. For over 75 years, they have championed a world where people with disabilities can lead lives without boundaries. Through advocacy, research, education, and an array of resources and programs, they strive to foster inclusion, independence, and opportunities for all. As an affiliate network, UCP offers crucial support and aid to those who are differently abled. With a focus on unity, they connect individuals to services and resources, helping them navigate challenges and access vital assistance. Their commitment is evident in the 155,000 individuals served annually, the 56 affiliates, and the over $4.5 million invested in assistive technology over the past decade. Generated from the website content

Dysautonomia Foundation, IncDysautonomia Foundation 57 years of care, treatment, research and advocacy for the FD populationThe Dysautonomia Foundation is a nonprofit organization supporting the best possible medical care and scientific research for the benefit of people afflicted with FD. The Foundation also conducts social service and public awareness programs for the benefit of the FD community and for those in the general population who may be at risk for FD.The Dysautonomia Foundation supports research studies into FD and the FD gene. Basic scientific research and clinical medical research regarding FD is currently being supported at a number of prestigious hospitals and universities.The Dysautonomia Foundation provides a continual flow of information to families, the medical community and other lay and professional persons who request medical, educational or promotional material concerning FD.Advocating for the FD Population The Dysautonomia Foundation works with the medical community and works with the government to further the concerns of people with FD. We work with the medical community to educate doctors about FD, to let them know that they can call on our experts for assistance in treating FD patients, and to encourage medical governing bodies to recognize the need to require doctors to inform patients about the existence and risk of FD ( in 2004, due in part to our efforts, the American College of OB-GYNs, ACOG, published an opinion telling doctors to inform Ashkenazi Jewish patients about the risk of FD and the need to get tested for FD ). We also advocate on the government level to try to get states to recognize FD as a developmental disability so that FD patients can more easily obtain benefits / assistance for FD treatment, and to require insurance companies to provide coverage for the cost of genetic testing.Chicago. Buffalo Buffalo Grove. IL Dysautonomia Society of Great Britain Bernie Hattenbach. Norwalk. CT