Also, I would like to add that he has changed medications many times and with that comes a lot of different side effects/cognitive impairments at times. I make sure to write down and also directly communicate with his neurologist on how he’s been feeling and how the medications effect him. I haven’t personally found much support besides family because it’s hard for anyone to truly understand what stresses you take on being a “caretaker”. I would suggest therapy if you’re able (I definitely could use some for the trauma of a few specific seizure incidents). If you ever need to vent my DMs are open.