It’s been ten years since my husband had his cardiac arrest at home. Ten years since I resuscitated him and gave him a few more years of life.
Ten years since I committed to looking after him without knowing what I was really doing, that nobody warns you about that caring is really going to suck the life out of you. Ten years since We got the diagnosis of Alzheimer’s. And the everything in between, the nosebleeds, the hernias and the internal bleeds, and the constant warfarin tests. not to mention podiatrist and the dentist, and the caratacts.
Ten years of living my life to accommodate his problems with out a thank you or some sense of appreciation or gratitude…just this is what I need , do it,, not counting the three years before when our marriage selfdestructed with the early signs of dementia.
In other words, I feel I have wasted ten years of my life.. And can’t stand the thought of another year, doing the same. I just can’t reconcile spending another year caring for him when all he thinks about is what goes in his mouth and comes out the other end and his bridge.
,
I understand that I am at burnout but I also realise because he can microwave food and look after his personal hygiene that he is nowhere being considered for care. It’s as simple as the length of time has taken its toll, not all the nonsense and criticisms and paranoia..
I struggle to find the energy to get up and do anything anymore. But he doesn’t understand that. He thinks if he takes the pup for a walk , it will solve everything. He probably couldn’t restrain him anyway and then that becomes one more thing for me to worry about, the pup I mean, not him.
i know that because he is still functioning well even ten years after, that help for me is non existent. His expression of tonights brief discussion was that I was the know it all so there was no discussion to be had was there!
Iam done. I am cooked, I have nowhere to go except where I have already been before.