Partner Camps

CPATH is a Central Texas-based non-profit organization created to support individuals with cerebral palsy. Camp Cpals is a weekend family camp for Texas families living with cerebral palsy.

Our Purpose- To create happiness in the lives of children and families battling cancer. Our programs provide children battling cancer a chance to have a fun and "normal" camp experience that they may not be able to have at a traditional residential camp, while also fostering new skills, individual growth, and personal development. Our family programs allow the entire family to enjoy a releaxing weekend of fun camp activities, as well as opportunities to connect with other families who have shared a similar cancer journey with their child.

Camp Heroes is a grief camp for children/teens who have experienced a death loss of a family member or friend. During Camp Heroes, campers will participate in grief-related activities that allow individuals to process their grief feelings, learn coping skills, and honor their person who died. In addition to grief activities, campers will also be given a chance to engage in some fun camp activities of their choosing!

Eva's Heroes is dedicated to enriching the lives of individuals with intellectual special needs by providing an inclusive setting built on four tenets: Interact, Grow, Learn and Love. We provide opportunities for participants ages 14 and older to enjoy unique recreation and socialization experiences in our community. Their involvement with Eva's Heroes enriches their lives and allows them to become a more active member of our community.

Epilepsy Camp offers a safe and fun residential camping experience for teens living with epilepsy. Through generous donations, Epilepsy Foundation Texas provides this unique opportunity at no cost to the families of the campers with epilepsy.

Moran Camp Xtreme is a wheelchair sports camp for kids and young adults with physical disabilities. MCX provides 4 camp opportunities throughout the year- Spring Break Camp (Sibling Camp), Adult Camp (21 years and older), and Family Camp.

Our camp is geared for children who live with any type of chronic pain condition. This week is an opportunity for the entire family of the pediatric pain warrior to experience camp together.

A safe and secure place for kids with Prader-Willi Syndrome. A time for PWS kids 8 and up to be able to interact with other kids just like them. We offer one on one counselors. Different activities for all of our PWS kids to do. We follow a low calorie diet for our Prader-Willi kids. We have a nurse on staff at camp. We have been having camp for 10 plus years.

The Siegel Rare Neuroimmune Association (SRNA) is an international, not-for-profit organization dedicated to the support of children and their families living with rare neuroimmune disorders, including Acute Disseminated Encephalomyelitis (ADEM), Acute Flaccid Myelitis (AFM), MOG Antibody-Associated Disease (MOGAD), Neuromyelitis Optica Spectrum Disorder (NMOSD), Optic Neuritis (ON), and Transverse Myelitis (TM). Our Annual Quality of Life Family Camp is open to family applicants (parent/guardian, child diagnosed, and siblings) who are members of SRNA. Membership with SRNA is completely free of charge. We bring together families from around the world impacted by these rare disorders together for a time of connection, learning, understanding, and tremendous amounts of fun!

The Chromosome 18 Registry & Research Society is an advocacy organization composed primarily of the parents of individuals with a chromosome 18 abnormality. We consist of three separate organizations located in the United States, Australia, and Europe, all with a common mission: To help people with chromosome 18 abnormalities overcome the obstacles they face so they may lead happy, healthy, and productive lives. We are proud to count among our members those who are affected by a chromosome 18 abnormality, extended family members, and professionals. Membership is free and open to any interested person. We are a 501(c)(3) non-profit, tax-exempt public charity.

The TBRS Summit is a scientific and family conference. Our goal is to support people affected by Tatton Brown Rahman Syndrome, and to advance research toward interventions. Families, researchers, and clinicians are all welcome to attend.

The HUB Houston brings around 20 of their high school students to Morgan's Wonderland Camp for 3 days and 2 nights.