June 7-9, 2019
Presented by the Kids and Dreams Foundation
Hosted by Covenant Cedars Bible Camp Hordville, NE
June 7-9, 2019
Presented by the Kids and Dreams Foundation
Hosted by Covenant Cedars Bible Camp Hordville, NE
OPERATION SHINE CAMP is a two-day camp for kids ages 7-12 experiencing Autism Spectrum Disorders and related conditions. The camp is held at the Covenant Cedars Bible Camp near Hordville, NE. The days will include arts/crafts, swimming, fishing, archery, crate stacking, sensory activities and more!
Each Camper has at least one "1-on-1" Dream Big Camper
All Staff & Volunteers have received training in the specific disorders that will be present at camp.
There is nursing staff on-site 24/7.
All cabins have handicap accessible full bathroom facilities
Volunteer registration is now open for 2019!! We are very excited to offer online registration this year!
Click the red button below and you will be directed to our third party site, CampDoc, for registering.
No amount is too small. From helping cover the cost of online registration fees, t-shirts for volunteers, snacks, training materials, and the food & lodging at camp, all these things factor in when supporting a volunteer or little camper’s life-changing experience of camp! We appreciate your generosity!!
We are currently full for 2019 and have a waiting list for new campers. If you are interested in having your child attend camp next year, click the button below and your child will be added to next year’s waiting list. We collect this information throughout the year, and when registration opens for new campers (in February), an email will be sent with the registration details.
“I believe that the Operation Shine Camp run by the Kids & Dreams Foundation is important because it gets kids out doing things like zip-lining, boating, swimming, and arts & crafts that they otherwise would not. As a result, these kids show their parents, teachers and themselves that they are capable of doing great things and exceeding any perceived limitations and expectations.”
The Kids & Dreams Foundation was founded in November 2013.
The foundation will introduce you to...
My wife, Kerri, and I have adopted five children. Trae, our middle child, has autism. He was developmentally delayed and did not walk or talk until he was 2 ½. At the age of three, he was diagnosed as being on the Autism Spectrum. Over the next couple years, Trae began a variety of therapies to help him progress and develop. It was during this time, Trae began having intense meltdowns and pulling his hair out, which was very out of character from his laid back personality. His pediatrician at the time told us Trae was the way he was, and that he would not change. Well, that was not good enough for us! After researching, we decided to remove dairy products from his diet. One day later, Trae was a completely different child. We were concerned about what he would eat because he was very picky. Dairy was the majority of what he ate; however, this dramatic change gave us the incentive to continue. He is still dairy free at 10 years of age. A couple years later, we attended a seminar about autism and nutrition. This was very timely for us because we were considering removing gluten from his diet as well. This seminar also educated us on the biomedical approach to treating autism. We were able to find a doctor that had several hundred autistic patients. We made the appointment and decided on a variety of biomedical tests, which would show allergies and food intolerances, allow the doctor to determine what vitamins and supplements his body needed, and to monitor his intestinal tract and treat accordingly. Since we began this journey, Trae has made leaps and bounds! He is now in the fifth grade and doing excellent academically, interacting better socially, and sees the world in a refreshingly different way. The combination of therapy services, diet, and biomedical treatment has helped Trae blossom into the kid he is today!
My son, Peyton, was nine years old before he was diagnosed as being autistic. At age five and prior to the diagnosis, I drove him to therapy weekly (two hours round trip), so he could receive hippotherapy, occupational, and physical therapy to address his sensory needs. These services were not covered through insurance. I was a single mother at the time, and due to lack of funds, they only lasted one summer. Since preschool, Peyton had been receiving physical and occupational therapy. Our family moved when he was in 2nd grade, and the new school would no longer provide these services to my son. Even after the diagnosis of autism, he was not able to receive the services because he did not qualify. As Peyton entered the fourth grade, he began to report being bullied at school. This was discussed with staff and administration, and they seemed to be trying to help take care of the situation. When the administration changed at the school, the bullying worsened in fifth grade after his diagnosis of high-functioning autism. Peyton entered middle school where the bullying only increased. He had chronic stomach aches, did not want to attend school, and withdrew even more. The school responded to the bullying by having him be bused home early each day. We have since moved to a new town. Peyton is now 15 and in the ninth grade, where he is thriving and doing very well. He now receives physical therapy each week and is improving. He enjoys school and is no longer bullied. The school is receptive to his needs and does everything they can to ensure Peyton is safe and ready to learn.
The Autism Research Institute's mission is to meet the needs of the global autism community through research, networking, education, and support for families and people of all ages on the autism spectrum.
Provides information, education, supporting research, programs, and services for the autism community. More than 50,000 members and supporters are connected through a working network of nearly 200 chapters nationwide.
Stimmi is the only Caregiver website designed to support individuals with disabilities or complex needs. Stimmi lets you create a cloud based, person centered Care Plan custom tailored for an individual that connects the whole care team.
This independent site is for education and information about digestive enzymes. There is a large need to provide practical and general information on enzyme therapy for a wide range of uses.
Provides support for those experiencing cerebral palsy. Our mission is to provide helpful cerebral palsy resources
The Gluten Free Casein Free (GFCF) Diet is one of the very first recommendations for children diagnosed with autism. This is because many of the children lack the [dpp4] enzyme that allows them to break down gluten (proteins in wheat) and casein (proteins in dairy). This can cause poor attention, odd behavior, a deficit in socialization skills and poor speech. Consequently, when gluten- and casein-based foods are removed improved behavior, better attention, at times improved speech and an increase in socialization skills can follow.
Inspired by the late Bernard Rimland, PhD., a leader in the biomedical movement, MAPS embodies his vision and direction of physician education and development in the field of ASD care.
Special Eats to assist others on the healthy path toward embracing gluten and dairy free living. The site is designed to help educate and enable people to find delicious recipes.
The Autism Hope Alliance embodies hope for families facing the diagnosis of Autism through education, financial support and volunteerism. It is the first non-profit foundation for Autism to emerge from the natural foods industry.
Beginning in 2000, TACA began providing support services to Californians. In 2007, TACA expanded its services throughout the United States. 95% of what TACA offers to families affected by autism is free.
EEG Biofeedback is a learning strategy that enables persons to alter their brain waves. When information about a person’s own brain wave characteristics is made available to him, he can learn to change them. You can think of it as exercise for the brain.
Pediatric Therapy Center was started by two occupational therapists with a passion for helping children with special needs gain confidence and autonomy through physical, occupational, aquatic, and speech and language therapy. Candice Mullendore and Stephanie Adam drew on their vast experience in outpatient, inpatient, and school-based services to help children with special needs, developmental delays, and a variety of other diagnoses including Asperger’s Syndrome, autism, Down syndrome, ADD, and ADHD reach their fullest potential. After years of practice, they saw a great need for a pediatric based therapy center in Omaha that specialized in the unique needs of children. Their vision became a reality in 2008 when Mullendore and Adam opened Pediatric Therapy Center, one convenient location offering occupational, physical, and speech therapy.
Bullying is unwanted, aggressive behavior among school aged children that involves a real or perceived power imbalance. The behavior is repeated, or has the potential to be repeated, over time. Both kids who are bullied and who bully others may have serious, lasting problems.
No Bully’s mission is to bring innovative, sustainable solutions to bullying and harassment in schools. No Bully® is a 501(c)(3) nonprofit organization. It began in San Francisco in 2003 as a collaboration of educators, psychologists and lawyers committed to preventing the current generation of students from enduring the bullying that they experienced when they were in school. Today, No Bully is helping schools in California and across the nation - from Hawaii to Delaware - stop bullying and transform into learning communities which are inclusive of everybody.
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Children’s Rehab Center is committed to providing outstanding care for children in combination with their primary care providers, daycare, school and community services. We are a medically based facility offering 2 locations in Grand Island and Hastings, NE. The Children’s Rehab Center offers Physical, Occupational and Speech Therapy to children on an intensive one-on-one basis. The therapy sessions are designed to allow children to play and have fun while working on developing functional abilities. At Children’s Rehab Center, we believe that children are sensory motor individuals needing complete body involvement and concrete interaction with their environment to maximize learning and mastery of skills. We are designed to assist individuals with developmental disabilities become more independent with mobility, self-help skills, fine motor, communication, vocational tasks and community skills.
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You can help sponsor a camper through our "Michael Houghton Scholarship Fund". Click on the image below to be directed to our scholarship funding website. If you have questions or need assistance please feel free to contact us for assistance.