Anyone who wants to learn more about Pfeiffer syndrome, please don't hesitate to reach out. I'm no expert, but I'm more than willing to share what I am learning. If you're a parent with a new craniosynostosis diagnosis or an old one, PLEASE connect with me. Talking to each other will only make us better advocates for our children! I am also here if youu need a shoulder to cry on like others have been there for me.