I know Alzheimer's is one of the worst things a family can live through, being alone through it all as I care for my mom is so difficult. My dad does nothing. I'm 37 and mom no longer knows who I am, my name or why I'm living in the house. How do I deal with this? The pain is so strong, the anger to. How can she remember my sister (her favorite) so well and on the other hand not remember me at all? Today she was yelling at me I'm not her daughter, and that a stranger can't help her. When I ask her if she knows my name she doesn't. She constantly asks when I'm leaving and who my mom is. She gives me evil looks when I call her mom but I've never called her anything else. It's been almost 2 years now since she "lost me" in her memory. It's like alzheimers has taken every bit of my life from her but my sister is still there. I cry a lot when she talks about my sister her "daughter" and then asks me when I'm going home because I dont live here. The pain is like half my body and soul ripped away and then that leads to anger. If she doesn't know me as a daughter do I have to see her as my mom anymore? All that was my mom is gone. How do I cope with this?
My dad brought his mother, who had Alzheimers, home to live with us when I was younger. She did not know any of her children, not even her baby boy that was living in the home with her, but she knew me. It shocked us all. That is how their brain works. My dad did not take it personal.
You have been ushered into a horrible position without having had the time for yourself to process the devastation of what has become of your family constellation.
Whatever events caused you to regard your sister as “her favorite” are now totally off the table, because your mother no longer has the capacity to deal in anyway with her emotional reactions to EITHER of you. Are you and your sister able to communicate reasonably outside of your home? Are you able to discuss your feelings with her, or someone else, without concern that your own feelings will be criticized?
It MAY be of some help to you at some point to learn some things about the science and dynamics of dementia, but for right now, it seems from what you’ve said that you didn’t have too much control over being designated as her caregiver. Is your father willing to provide time everyday for you to get away from your care giving chores?
Towards that result, you might want to try a couple techniques when you deal directly with your mother. You have already learned that it is rarely successful to challenge the verbalizations of anyone, relative or not, who has been diagnosed with dementia. As you read questions and answers from others who post here, you will find that this simple but often difficult to use technique is basic. If she is insistent, make some neutral comment (“That’s interesting!”) and move on to another topic.
If you refer to her as “Mom” and she reacts negatively, ask quietly “What do you prefer me to call you?”.
Bear in mind, doing this is for your own comfort, not to “help” Mom. When questions hurt you, answer in a non-challenging way- “I’ll go home in a little while“. Sometimes, people turn on caregivers whom they love very much, with no reason. It happened during the tragedy of my grandmother’s illness, lasted for several months, then went away.
Your mother CANNOT reason. She no longer is in possession of that skill. You have the intelligence and wisdom to consider her, and your relationship as her caregiver, in a different way, that can hopefully allow you a more comfortable way to move forward.
If you need changes to be made in your role, please attempt to consider coming up with some ideas that will be safe and comfortable for both your mother and yourself. She is now a victim, suffering from a situation that no one can cure for her. You are in a difficult to manage situation as well, but resources exist that may help you move forward in a more productive way for yourself.
Know that there is understanding and support here for you.
My mom has been gone for almost two years -- the same amount of time my dad's been gone. It's just that she's still here.
I remember about three years ago attending a group meeting for caregivers for the first time. I was so stressed at blame and harshness of treatment you describe that I cried in front of strangers which I didn't expect. Going to support group meetings and hearing others experiences helped me to cope and become educated about what to expect. It's a hard situation.
Understand that with dementia they lose all of their social filters. It is not intentional what they say and do. They cannot control their minds any longer. The worst thing you can do is try to reason or explain to them. You will be fighting a losing battle that will only increase your frustration and mom's agitation.