Caleb’s Dream Beach Trip

This summer, Caleb, who lives with Common Variable Immunodeficiency, and his family experienced a much-needed escape to the beautiful North Carolina Outer Banks – a trip filled with sunshine, laughter, and unforgettable memories. 

Family Thank You

“Caleb had an amazing trip to the Outer Banks of North Carolina thanks to the Sunshine Foundation! We enjoyed being able to spend time as a family doing things we all loved. Caleb went fishing, swam in the pool and the ocean, caught some crabs, and enjoyed sightseeing. He says he can’t wait to go back one day. Caleb has a primary immune deficiency, so sometimes vacation can be challenging, working around appointments and medication schedules. We are so incredibly thankful we were able to take this trip and can’t thank everyone enough!” – Caleb’s mom, Lauren

Caleb’s Diagnosis

Caleb is diagnosed with Common Variable Immunodeficiency (CVID), a genetic condition that causes low levels of antibodies in your body. This weakens your immune system, which usually helps your body fight off germs and prevent infections.

People with CVID are more likely to get repeated infections, such as ear, sinus, or lung infections. They also have a higher risk for more serious conditions, such as gut problems, blood and autoimmune disorders, and cancer.

Sponsors

We are grateful to Neshaminy High School‘s Interact Club, Sam’s Club Langhorne, Feasterville Business Association, Gannon Insurance, and Adopt a Dream donors

Our Mission

Sunshine Foundation answers the dreams of children, ages three through eighteen, who have severe or profound physical/developmental/intellectual challenges or trauma from physical/sexual abuse, and whose families have limited income. Since 1976, Sunshine Foundation has spread Sunshine into the lives of more than 43,280 children.