FRN’s Support Services provide individuals with disabilities and families of children with disabilities to get the support they need to lead a full and happy life.
FRN’s employment and transition programs support youth and adults with intellectual, developmental, and physical disabilities through mentorship, education, and employment in order to become integrated, productive members of their communities.
FRN’s public health department aims to address the social determinants of health that impact individuals with intellectual and developmental disabilities, physical disabilities, and chronic conditions.
The Family Resource Network provides engaging educational opportunities for professionals, families, and individuals across New Jersey. Our programs are offered both virtually and in person and cover a wide range of topics, including epilepsy, autism, caregiving, transition planning, and IEP development.
How People with Disabilities Won the Right to Choose Their Own Homes.
Most people have never heard of Lois Curtis, but they should.
Lois was a Black woman with developmental and psychiatric disabilities who spent years institutionalized in a Georgia state hospital. Not because she had to be. Doctors had already said she was ready to live in the community. But the system kept her there anyway, because that`s just what happened to people like her.
So Lois did something extraordinary. She fought back.
Her case, Olmstead v. L.C. (1999), went all the way to the U.S. Supreme Court, and she won. The Court ruled that unjustified institutionalization of people with disabilities is a form of discrimination under the Americans with Disabilities Act. The state cannot warehouse people in institutions when they are capable of living in their communities with support.
The ripple effects were massive. The Olmstead decision forced states across the country to shift funding and services so that people with disabilities could live in homes and apartments, not hospitals. It gave millions of Americans a legal right that most of us take for granted: the right to choose where we live.
After winning her freedom, Lois became a celebrated self-taught artist, her work bold, joyful, and full of life. In 2011, she visited the White House and gifted one of her paintings to President Obama.
Lois Curtis passed away in November 2022 at the age of 55. But her legacy lives on in every person with a disability who gets to call a place home on their own terms.
This Black History Month, remember that disability rights are civil rights, and that a Black woman changed the law for millions of Americans by simply refusing to give up.
Rest in power, Lois. ...
Now Enrolling: Pediatric Epilepsy Research Study in New Jersey
Epilepsy Services of New Jersey is inviting parents and children ages 4–12 to participate in a one-time, in-person research visit focused on an investigational seizure-monitoring device.
We are currently enrolling:
- Children diagnosed with Childhood Absence Epilepsy
- Children with no history of seizures
The visit includes seizure education, hands-on use of the Eysz HV Home Recorder, and compensation for time and travel.
By participating, families are helping shape better tools and stronger research for the epilepsy community.
Learn more and review eligibility details at the link in our bio!
#EpilepsyResearch #PediatricEpilepsy #NJFamilies #EpilepsyAwareness ...
Support Coordination that helps New Jersey families move forward.
At Caregivers of New Jersey, our Support Coordinators work alongside individuals with disabilities and their families to make sense of services, uncover options, and plan next steps with clarity. Through individualized, person-centered planning, we help families understand their choices and build paths that reflect their needs, goals, and priorities.
Navigating disability services can feel overwhelming. Having the right person to turn to changes everything.
Connect with a Support Coordinator in New Jersey at njcaregivers.org
Caregivers of New Jersey is a proud affiliate of the Family Resource Network. ...
Every journey looks different, and the right support can make all the difference.
The Family Resource Network offers one-to-one services that are flexible, personalized, and centered on each individual’s goals. From community-based programs and respite opportunities to individualized care at home, we’re here to support individuals and families every step of the way.
For some services, parents or family members may even be hired and paid as the Direct Support Professional (DSP), providing greater continuity, comfort, and peace of mind. Whether you’re seeking a trained professional or exploring a family DSP option, our team will work with you to find the right fit.
Learn more about our services at familyresourcenetwork.org
#FamilyResourceNetwork #DisabilitySupport #RespiteCare #CommunitySupport #DSP #FRN ...
This Valentine’s Day, we’re sharing what we really love.
We ❤️ Seizure Action Plans. They take the guesswork out of seizure response when someone cannot communicate and help the people around them know exactly what to do.
➡️ Share the love. Visit seizureactionplans.org to start or update a plan.
#SAPAW2026 #SeizureActionPlans ...
Sometimes awareness looks like a theme park filled with purple. 💜
Epilepsy Awareness Day at Walt Disney World® brings families, advocates, and individuals from across the country together to show up for the 1 in 26. It’s about visibility, connection, and being surrounded by people who understand the journey.
Epilepsy Services of New Jersey is offering a travel and lodging stipend for up to two New Jersey families who would not otherwise be able to attend.
If you’re a NJ parent, caregiver, or person living with epilepsy, we encourage you to apply. Priority will be given to families who have not attended before.
Learn more and apply at the link in our bio.
Application deadline: February 15, 2026.
#EpilepsyAwareness #WearPurple #1in26 ...
A Seizure Action Plan exists because seizures do not wait for the right moment.
When communication is not possible, clear steps matter. A plan means fewer questions, less panic, and a safer response in a moment that counts.
Families, caregivers, and people with epilepsy share how having a plan helped during real-life emergencies. Your story could help someone else take the first step.
➡️ Learn more or create a plan at seizureactionplans.org. Please share this post.
#SAPAW2026 #SeizureActionPlans ...