Well, after last night's conversation DH made dinner tonight, cleaned up the kitchen and went to the hardware store to replace the burned out lightbulb over the stove. I also noticed he already took out the recycling for tomorrow. Not saying he's out of the doghouse yet, but at least there is a little improvement,
Biilybags - instead of coming back as man next time - ask God to give your hubby the experiece of kidney failure and birth - and see how he likes it. Grumpy
I'm coming back as a man next time.
I don't mean to be contentscious here, but caregiver for PD? this seems to be a term that has crept in since NxStage which does require a giver. unless someone is old, frail or hasoncapacities that prevent them doing their own care, PD does not need a caregiver. my husband knew absolutely nothing about PD and never provided care. we weren't trained to expect care, and I certainly didn't get it.actually even now, doing NxStage, caregiver is a nominal term since I do everything myself except for hanging bags, and once I get on Pureflow, I anticipate doing the whole kaboole myself.
Amanda, I'm talking about NxStage. I agree, with pureflow, I do everything related to the treatments on my own. But I feel like since I am doing all the treatment related stuff, it would be the least that DH could do to take care of chores and laundry while I am dialyzing instead of just sitting on his behind.
do you have any mutual male friends that you could talk to about this, and the ask them to talk to him? if another guy points out to him that this behaviour and lack of help is selfish, he may just get the message. if you decide to kick him out, why does your dialysis unit need to know? after all, he doesn't do anything anyway?
Cattlekid, my comment was not directed at you since I know that you are on NxStage. Billybags mentioned about having a caregiver for PD, ad have people on other threads. LMunchkin, I am not exceptional. I first did PD twenty years in the UK. my husband was not trained to be my caregiver, and I never had any expectation that he would be. when I did it again starting nine years ago, Again, I had no expectation of needing a caregiver. anything that he does around the house has got nothing to do with the fact that I am on dialysis, just the fact that these are shared things that we do because we share the same house.
I do count my self as a care giver. My husband has been on PD for 3 years, he does manage with my help to set his machine up, he can not lift the heavy bags or empty the fluid in a morning. He has had two heart attacks in the last two years which has left him with a badly damaged heart. He can not walk very far, only down the hall. He can not breath properly because his lung keeps filling up with fluid. YES, I DO CLASS MY SELF AS A CARE GIVER. With out me he could not manage every day things.