The only way is via the diagnosis.

For myself my mom would talk to my about my seizures. He or she would tell my mom what seizure type I was having.
My seizures types haven’t change much. Although I haven’t had cluster seizures since my DBS was put in.

You can just ask your neurologist and they’ll tell you what type of seizures you have

Mine called the same. Was 6 yrs old. Now have clonic tonic. Convulsions… Longest I’ve been out is 5 hours.

People need to see a Neurologist or Epileptologist, and go through a lot of tests to learn what is happening. I was diagnosed at 7. Back then they were called Petit Mal. From what I read today, they would call them Absence Seizures (now Partial Awareness).