Services and Organizations for Families
An essential part of advocating for services for your child is knowing to whom to reach out. This page lists services and organizations that are relevant to most families who have children with deaf-blindness at some time during their child's life.
State Deaf-Blind Projects – An essential resource for all families of children with deaf-blindness. The types of services offered vary from state to state, but typically include resources, guidance, and annual workshops or other events.
Parent Centers – Although not specific to deaf-blindness, Parent Centers in every state help parents of children with disabilities participate effectively in their children's education and development. Find your Parent Center →
Helen Keller National Center Regional Services – Most relevant to families of transition-age youth and adults, these offices have representatives who connect deaf-blind individuals, their families, and service providers with consultation, advocacy, assessment, training, referrals, and more.
iCanConnect – Provides telecommunications equipment (e.g., smartphones, tablets, computers, screen readers, braille displays) to individuals with combined significant vision and hearing loss who meet federal disability and income guidelines. Find your local contact →
National Family Association for Deaf-Blind – A non-profit membership organization for families with individuals of all ages who are deaf-blind. Professionals are welcome to join, too! Become a member →
DeafBlind Citizens in Action – DBCA's mission is to empower people who are deaf-blind through education, technology, and legislation and ensure they have a strong political voice so they may lead productive lives with equal opportunities.
Etiology-Specific Information and Organizations
There are many organizations that provide information and support to individuals and families with specific conditions (etiologies) often associated with deaf-blindness.