I was born with severe prenatal brain damage at the term of the 2nd trimester preventing development of corpus callosum. To my understanding, I suffer extreme nocturnal myoclonus, daytime myoclonus, possinbly essential myoclonus and absence seizures. I also suffer essential and intention tremor. I experience extreme pain more than anything else. I have very little knowledge of when and how I seize but my daughter tells me I have several occasions during waking hours of the week.
You have better chance of determining your seizures by doing an EEG.
I started with grand mal and I never had any indication it was about to hit. The last couple of years it changed to nocturnal seizures. These cause more injury and pain than the grand mal and I have had numerous in the pasture with cows, caught in barb wire...
We think mine started as nocturnal seizures, because I used to be a "wild sleeper"; kicking friends during sleepovers, wriggling around on the couch during naps, etc. The kicking stopped when I started my Epilepsy meds, after the Grand Mal that got me diagnosed.
The best way to find out is to talk to a neurologist, and perhaps get an EEG done.
The best thing to do is talk to a neurologist or Epileptologist and ask them for an EEG appt. they then can determine what type of Epilepsy you have and what kinds of seizures your having.
I have simple partial, complex partial & Absence. The absence have dramatically decreased from at least 4 daily to where I now have 3 at the most in a month. Some of your descriptions fit several seizures. So theres no way too know without a video EEG, CT scan or even MRI along with a nuerologists diagnosis.