Family Network on Disabilities

Family Network on Disabilities Respect,
Independence,
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With Valentine’s Day tomorrow, many children and teens may be thinking about friendships or romance online. Parents shou...
02/13/2026

With Valentine’s Day tomorrow, many children and teens may be thinking about friendships or romance online. Parents should watch for warning signs of romance scams, including relationships moving too fast, requests for money or gift cards, avoiding video chats, or pressure to move conversations off trusted platforms. Open conversations can help protect your child and build safer online habits.

02/12/2026

Taking care of yourself is not a luxury; it's a necessity. Your well-being matters whether you're a family member or a professional caregiver. In "Wellness Tips for Every Caregiver," we share simple and practical ways to manage stress, care for your health, and prevent burnout.

We have lost another giant in the disability community. Patty McGill Smith has passed away. It is hard to overstate Patt...
02/12/2026

We have lost another giant in the disability community. Patty McGill Smith has passed away. It is hard to overstate Patty’s legacy. Her obituary - https://buff.ly/e7jOkEE - touches on many of the highlights of her contributions and achievements. She was among the first family leaders to advocate on the national level. She fostered generations of parent and family disability leaders and advocates. She served on Capitol Hill and brought a strong family-centered voice to national debates as the Executive Director of the National Parent Network on Disabilities (NPND). It was while she was at NPND that she worked with FND’s CEO Emerita, Jan La Belle, who served on the NPND Board for a number of years. Together with many other advocates from across the country, they worked tirelessly to preserve and strengthen IDEA and other cornerstones of disability legislation during the ’90’s and early 2000’s. We are fortunate to be able to build on Patty’s legacy in the work we do today. She will be missed, but her work and words will live on.

Disability focused proms are being held around the world as part of Night to Shine, a global event celebrating individua...
02/12/2026

Disability focused proms are being held around the world as part of Night to Shine, a global event celebrating individuals with disabilities ages 14 and up. With red carpet entrances, dancing, sensory-friendly spaces, and every guest crowned king or queen, these free events are designed to create a memorable evening. Families can find a prom location near them at https://buff.ly/4WbuWxk.

Tomorrow is the deadline! Apply now for the Jan La Belle  , which supports Florida students with disabilities in achievi...
02/11/2026

Tomorrow is the deadline! Apply now for the Jan La Belle , which supports Florida students with disabilities in achieving their educational goals. Learn more and apply via the QR! Or on our website https://buff.ly/JUYmYWI.

Family Network on Disabilities would like to wish everyone a Happy Black History Month!
02/10/2026

Family Network on Disabilities would like to wish everyone a Happy Black History Month!

With Valentine’s Day right around the corner, simple activities can help every child participate and enjoy the celebrati...
02/09/2026

With Valentine’s Day right around the corner, simple activities can help every child participate and enjoy the celebration. From no-cut crafts to hands-on painting and sensory-friendly projects, small adjustments can reduce frustration and create meaningful moments at home or school that do not involve candy. Valentine’s Day can be about connection, not perfection.

In Loving Memory - Joanne ScaturroThe world has lost one of its brightest lights - Joanne Scaturro was one of the most p...
02/09/2026

In Loving Memory - Joanne Scaturro

The world has lost one of its brightest lights - Joanne Scaturro was one of the most positive and uplifting persons I have ever met. She was a force of nature - truly a force of love in this battered world and she will be missed by so many who she helped so selflessly. The power of her love and passion for justice continues to flow through our lives, even though Joanne is now at rest. Near the top of the list of things that I hope I never forget is the sound of Joanne’s laugh. It’s bringing a huge smile to my face as I type these words, even though I am typing through tears. I have been struck by how everyone who knew and loved Joanne (and I think those two things are synonymous), through their grief, rush to tell their favorite stories about the wonderful things she did and the joy she brought to so many. That is a fantastic way to be remembered, in my opinion.

Joanne was a founder of FND and she played a crucial role in helping us survive as a young organization and then continue to thrive through the years. She was always a source of wisdom and sage counsel, whether it was dealing with governmental bureaucracy or internal politics in the Board of Directors. My wife, Janis (who Joanne encouraged to apply for the position of Executive Director of FND back in 1995), and Joanne worked together closely and often traveled throughout the state together, reaching out to families and delivering workshops. As they traveled and helped families across the state, they accumulated enough hilarious stories about their journeys to fill a Netflix comedy special.

For our own family, Joanne was there for us through many of our own “firsts” - some good, some not so great - of our journey into the disability community. She shared with us diagnoses, evaluations, first days of school, referrals, IEP meetings, testing - and more testing, and our anxiety and stress of how to be certain that what we were doing for our children was the right path to follow. Joanne was there for Janis and me through it all. If Janis and I disagreed about a particular course to follow, Joanne’s opinion was the deciding factor. She was never wrong and we are so grateful to have had her in our lives at this extremely challenging time when we didn’t know which way to turn.

She loved her family deeply and constantly talked about her parents, her siblings, and their children. After Joanne moved to North Carolina, she stayed in contact, both personally and professionally, and we were fortunate to host her on a number of occasions for more trainings during the day and evenings filled with laughter. I know she made a huge impact in NC, too - many, many times, speaking to colleagues in NC, Joanne would be mentioned at some point - she was like a treasure or secret weapon that our states were so fortunate to share.

FND is proud to have named an award in Joanne’s honor. I’ve attached a photo of her with one of the first award winners, Nelson Perez, from 2023 (photo attached). The formal title of the award is the “Joanne Scaturro Professional Leadership Award”, presented to professionals working in the disability community. The stated purpose of the award is to recognize and celebrate “the contributions of a professional partner who has worked tirelessly to create meaningful, systemic change”. We feel that this encapsulates what Joanne was always doing.

Joanne did not have biological children of her own, but she can count thousands of children across the country as her children. Many literally would not have survived without her and would certainly not have thrived in the way they were able to after their families met Joanne. The number of lives that she touched - and changed for the better - is literally beyond knowing.

A memorial is being planned by her family for May and I understand it will be open to all who wish to attend, in person or virtually. Here is a beautiful tribute put together by her sister, Margaret (https://obituaries.nationalcremation.com/obituaries/raleigh-nc/joanne-scaturro-12727426). Please pause a moment a give thanks that Joanne was sent into the world and that we were fortunate to be here with her. There will never be another like her.

A grandmother’s love sparked an innovative idea: inspired by her grandson Coen, who lives with autism and cerebral palsy...
02/06/2026

A grandmother’s love sparked an innovative idea: inspired by her grandson Coen, who lives with autism and cerebral palsy, Linda Beedle created Sockietalkies, adaptive socks designed to make dressing easier and more independent. With simple pull holes and uplifting messages, these socks are a powerful reminder that small design changes can create a big impact for people with disabilities.

02/05/2026

Strong collaboration with your child’s healthcare providers can make a meaningful difference in care and outcomes. This short video shares practical strategies to help families communicate effectively, ask the right questions, and speak up for their child’s needs.

February is Low Vision Awareness Month, a time to recognize the millions of people in the U.S. living with visual impair...
02/05/2026

February is Low Vision Awareness Month, a time to recognize the millions of people in the U.S. living with visual impairments that cannot be corrected with glasses, contacts, medicine, or surgery. Vision rehabilitation services can help people build skills and access supports to keep doing everyday activities and the things they love.

PBS Kids’ Daniel Tiger’s Neighborhood recently aired an episode told from the perspective of Max, a recurring character ...
02/05/2026

PBS Kids’ Daniel Tiger’s Neighborhood recently aired an episode told from the perspective of Max, a recurring character with autism. The story highlights an important message for children and families: everyone is more than one thing, and our identities are made up of many strengths, interests, and experiences. To watch, you can visit PBSKids.org.

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Family Network on Disabilities

Family Network on Disabilities (FND) was founded in 1985 by a group of parents of children with disabilities who came together for mutual support and information-sharing. FND is a grassroots organization for persons with disabilities and their families that is family-centered and family-driven.