My Nonprofit Reviews

Our son, Heath, was born with a very rare form of craniosynostosis, his was frontosphenoidal. After doing some research on craniosynostosis, we found Cranio Care Bears and what a blessing it was. Summer, one of the founders of the organization, her son had the same type of craniosynostosis. I emailed her our story and the next day I received an email back with encouraging words. A few days before Heath's surgery we received his care package. In the midst of fear, this package of goodies made our hearts happy. Heath will always have his prayer chain to look back on, and pictures of him in his handmade hat they provided, as well as all the other items they had that was so helpful for his hospital stay. We can not thank Cranio Care Bears enough for the support they provided in the most fearful time in our lives. Thank you, thank you, thank you!