My family and I were diagonased with metacillin sensitive and metacillin resistant staphylococcus aureus Panton-Valentine Leukocidin several years ago. I’ve only known one other person with it who was diagnosed a while after me. Despite several years since diagnosis, there is very little new information that is relevant to families and children. Our decolonisations haven’t worked due to various incompetences.
Is there any one else out there?