As of mid-2005 AZ has 19 registered PF members. This is a little misleading because registration for the forum and the foundation registry are two seperate registrations. The forum is open to all: patient, family and friends. The PF Registry is open to all who have personally had pe and its related disorders.
I encourage all AZ pe patients on the forum to add their names to the foundation registry at: https://www.preeclampsia.org/RegPC/startToNewReg.do
When you mention handouts, do you mean the brochures? For questions about the brochures, I encourage you to e-mail Carol Hamilton at firstname.lastname@example.org. Does this help? Please let me know if I can clear anything up.