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Our status as a division of the National Federation of the Blind, the largest and most influential organization of blind people in the world, provides many benefits. Our members are well informed about the technological, legislative, and societal issues that affect blind people. We also enjoy the resources, support, and expertise of 50,000 blind people who can serve as mentors and role models for our children. And finally, as our children grow up, they, too, have the Federation to belong to. The purpose of the NOPBC is to: create a climate of opportunity for blind children in home and society. provide information and support to parents of blind children. facilitate the sharing of experience and concerns among parents of blind children. develop and expand resources available to parents and their children. help parents of blind children gain understanding and perspective through partnership and contact with blind adults. function as an integral part of the National Federation of the Blind in its ongoing effort to achieve equality and opportunity for all blind persons.

Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

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.

Our mission is to return a sense of self, confidence and normalcy to children suffering from hair loss by utilizing donated ponytails to provide the highest quality hair prosthetics to financially disadvantaged children free of charge.

Our mission is to provide safe long-term residential programs to help homeless pregnant and current parents heal, find stability, and start building a better path forward.

Our mission is to provide comfort care at the end of life. We believe that a life fully lived, no matter how long, should include an end-of-life experience of comfort, dignity, and peace. Our goal is to keep each patient as comfortable and independent as possible, while supporting the emotional and spiritual needs of our patients and their loved ones. We were the first non-profit Hospice in the area and one of the first 100 Hospices in the nation. Our founders were a group of dedicated doctors, nurses and community volunteers that began providing care to the dying on their own time. Our organization began in 1979 before there was insurance reimbursement for Hospice care and this dedication to our patients remains our culture to this day. Ionia Area Hospice approached Hospice of Lansing joined forces and a formal partnership was formed in 1984. Should the time come when it is no longer possible for a patient to remain at home, Stoneleigh Residence is a unique, comfortable, peaceful, and home-like alternative. Surrounded by gardens, a cascading pond, trees and wildlife, the Residence is designed to take full advantage of the natural beauty of its wooded 20-acre site. We are a true community-based Hospice, created out of necessity and driven by our mission to serve all by bringing kindness, respect and quality to the end-of-life. Hospice of Lansing, Stoneleigh Residence and Ionia Area Hospice provide pain management and personal care, respite care, emotional and spiritual support for patients, volunteer support and grief support for family members after the loss.

Establishing homes. Investing in lives. SMILE of Hopatcong is working to meet the housing needs of the developmentally disabled in Morris & Sussex Counties.

Their mission is to provide high quality, compassionate care at the end of life.

NEUROHOPE STRIVES TO MAKE LONG-TERM REHABILITATION AND WELLNESS AN AFFORDABLE REALITY FOR PEOPLE RECOVERING FROM NEUROLOGIC INJURY.