For a VERY independant person like me, I think the hardest thing to come to terms with is the loss of it. For 4 years after my diagnosis, I could still manage to a sort, on my own, on buses etc. But now, I am having to come to terms with the fact that my life is no longer like that. I can't have a bath, I can't iron my children's clothes for them, I'm not even allowed the pleasure of cooking my kids a roast dinner, as my carer doesn't come out on a sunday, so I have to do them a microwave meal. ( I'm no longer allowed to use a cooker without supervision). I feel like my whole life is run by someone else, but it is part and parcel of my E getting worse. But it's just one more thing to joke about, as it's something that is not going to change in the near future, I have to just accept the way my life is today, and HOPE that it will not be like this forever. Good luck with your sister, but she does sound like a difficult case... I have a feeling that you both need each other in ways that neither of you are willing to admit or accept, she is unwilling to accept that she needs your companionship so she places herself as your 'protector', and you need her practical help, i.e rides to the shops etc, and are maybe unwilling to accept that part of epilepsy? and the fact that you have to accept help from places or people you would rather not, and in an ideal world without epilepsy, you wouldn't have to?