Cristina Fntnlli Fundation Inc

The VII Association, Inc is a dynamic organization based in New York, NY that specializes in providing innovative solutions for a variety of industries. With a focus on collaboration and creativity, they offer a range of services to help businesses thrive in today's competitive market. Through their unique approach and dedication to excellence, The VII Association, Inc has established a reputation for delivering high-quality results that exceed client expectations. Their commitment to integrity and professionalism sets them apart as a trusted partner for companies seeking strategic growth and success. Generated from their business information

Stage Directors and Choreographers Society (SDC) is a theatrical union based in New York City that unites, empowers, and protects professional stage directors and choreographers across the United States. Their mission is to foster a national community of directors and choreographers by advocating for their rights, negotiating employment agreements, facilitating the exchange of ideas and opportunities, and educating current and future generations about the vital role of these artists in leading the field. SDC is dedicated to ensuring the rights, health, and livelihoods of its members, while also promoting the importance of directors and choreographers in the theater industry. Through their extensive network and expertise, SDC plays a crucial role in supporting and advancing the careers of professional stage directors and choreographers nationwide.Generated from the website

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