The Patient Liaison Committee (PLC) serves the needs of MH-susceptible individuals and their family. The members provide educational materials, access to MH expert consultants, and a support network. It functions as an outreach for one-on-one contacts for individuals who would like to talk to someone with similar experience. The committee members are volunteers who either have MH personally or a family member is MH-susceptible, medical professionals, and others interested in MH. Committee members are:
The Patient Liaison Committee sponsors a yearly mini-conference for not only medical professionals, but also family members who want to meet and talk to MH expert medical professionals directly.
The PLC brings a sense of patient ownership to support MHAUS and direct involvement by MH-susceptible patients and their families. The committee focuses on increasing MHAUS memberships as well as volunteers for the PLC.
The goal is to have a committee member in every state and province in North America!
Complete and submit this form to have the PLC contact you.
Faces of MH are stories about people who lives have been changed by Malignant Hyperthermia. Read, and to add your own.
Chapters are charged to help their community, region, or state prepare for MH.