Regular namechanger.
I ask in kind of a professional capacity.
In my job I come across MBS or Congenital Dermal Melanocytosis very regularly.
As I'm not a doctor I cannot diagnose it, so have to refer parents to hospital to have it confirmed. If we don't any mark will be flagged as potential abuse.
I am very, very uncomfortable with the whole pathway. I don't even like saying MBS in front of parents as even the name is awful.
Can I ask of your experiences if your child has MBS?