Quality of life is a state of well-being that is a composite of two components: (1) the ability to preform everyday activities that reflect physical, psychological, and social well being. (2) patient satisfaction
with a better focus on disease.

My quality of life has changed numerous of times with epilepsy from just having seizure control by one medication and then changing back to the battles of four seizure for seizure control. But after the vns my total feelings changed towards epilepsy.

I still battle the quality if life with epilepsy. What is the real quality of life improvement for people with epilepsy?

We all need to know?