My Nonprofit Reviews

When our son was diagnosed with Celiac Disease at age five, we assumed he would never be able to attend a summer camp as he was so sensitive to gluten. He always felt a little different from his peers, countless class parties he couldn't enjoy, slumber parties that had to be very carefully planned. We found out about Celiac Camp and he attended his first camp in 2016. This camp was life-changing for him. It was the first time he could remember being able to fully participate with his peers, especially around food. All of the kids understood how hard it is to be gluten-free. He came home a changed person. Camp stories fill our house in times of frustration with this annoying disease. He told us camp is the only good thing about being gluten-free. He was a camp counselor last year and now is mentoring younger kids who are dealing with the same struggles. He also has a large, beautiful social network of peers he talks to on a daily basis he met at camp. I'm not sure where we would be without this amazing organization!

CCBs sent our son Oliver a care package when he was in the hospital. The package brightened our day and helped out in the hospital. What a fantastic organization!

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