Hey there! So we noticed around 2mo that LO had a flat spot on his head. Pediatrician told us to start trying to reposition his head, talk to him from the other side, etc. We did that until his 4mo checkup at the beginning of June. At that point we were referred to Cranial Technologies in Charlotte for a cranial band. Been working our way thru the process of insurance approval.
Anybody else dealing with plagiocephaly? Just looking for others to help gain some perspective, since I'm a FTM.