I am currently doing an sociological research project for an undergraduate course, and one of the focuses for my research is the effect involvement in support communities can have on an EBV sufferer’s quality of life. I am interested in this topic because I, along with a number of my loved ones, suffer from EBV, but I do not personally know anyone who is regularly involved in a formal support community or group such as this one.
How have you been affected by your involvement in this or other support communities? For instance, have you learned helpful tips or gained comfort by hear other’s stories?