My Nonprofit Reviews

My son was diagnosed with sagittal craniosynostosis at 4 months of age. It was a very scary time in our lives. First time parents facing a diagnosis we had never heard of. Thankfully I stumbled across a large Facebook community of parents who have had the same or similar experience as my own and they directed me to Cranio Care Bears. Receiving their care package just days before his surgery was so comforting. It was so good to know that there were other people out there who cares and we’re prayinf for our son. We don’t have any capable family near us, so receiving that package was like having a family member watch over us.
Thank you Cranio Care Bears for all you do!