Hello, Friends and Family! I’m Valerie Cullari, the proud founder of ROCCOSJOURNEY, dedicated to championing autism and neurodiversity inclusion, education, and acceptance.
WE NEED YOU! Every contribution, no matter how small, goes a long way in making a difference. You can read below what every donation goes to. But in short, we give out sensory toys at every monthly "Sensory Sunday" at ChuckE Cheese in addition to holding after school events at the local school district for the special needs students- they don't have anything provided by the school. We like to offer them something to do that makes them feel included! That's the image seen in the event ad. If you’re unable to donate at this moment, we would deeply appreciate it if you could share our campaign far and wide. Let’s spread awareness together!
In addition, allow me to explain what else I had been doing. Sadly a lot of traveling I can no longer do due to my physical condition, however, I will continue Sensory Sundays and the after school events. The kids don't deserve to lose the small bits of inclusion they can find. I refuse to to give up. But we NEED YOU!
I've been visiting police stations and EMS locations with my Emergency Service Presentation. This initiative aims to equip first responders with essential insights on navigating situations with special needs families. It's not formal training—it's an educational experience based on a personal experience. The response has been fantastic and I look forward to continuing this necessary endeavor.
I’ve authored now TWO impactful books on autism and disabilities, with one even winning an international award! It is an honor to be reading my book to 3rd and 4th graders, helping them understand the importance of inclusion and acceptance for all students.
As Ms. Northern NJ International 2026, I'm advocating for profound autism awareness, and I navigate the challenges of being a mother to two wonderful disabled children, one affected very severely.
However, life's not without its battles! I’m also fighting a rare and dangerous chronic illness—superior mesenteric artery syndrome (SMAS).
Currently, our foundation is in urgent need of funds for inclusive and sensory events, which we hold at MINIMUM twice a month. The demand for our services is high, and we’re committed to supporting these incredible children and families. Especially continuing our partnership with ChuckECheese.
Thank you for your kindness and support! Together, we can make this world a more inclusive place for everyone!
We are the difference!!
