Hi .My dad also has LBD.He had rivastigmine patches and quetiapine, both of which helped in the early stages.After bouts of aggression , these were both increased. He’s in hospital with a chest infection at the moment and they have sedated him with lorazepam (after hitting a nurse and having 2 security guards hold him down)Everything is magnified when an infection is involved.His hallucinations are horrid and frightening for him as well as others. I agree it’s hard to explain to people what LBD is.We can’t find what triggers dads outbursts.When it happens it’s like he’s not seeing what we are.Its like a switch is turned on and he’s in another world.So quick to start and then afterwards he can be aware of what he’s done which really upsets him .Untill this dreadful disease, I was like most people, thought dementia was just forgetting things.How wrong was I. I want to wish you all well and please , please get help .Dont struggle on especially if aggression is involved. Dad had to go into a carehome as I struggled and had carers breakdown.There is only so much we can do and then others who don’t care 24/7 ,need to take the strain. Virtual hugs to all ,going through this horrible illness.