Ah HA! So you're the one paris... you're the woman that makes it looks like we can "do it all!" Well, knock it off!
Men, men, men! Don't you all just wish we'd all move to some other planet?
Quote from: dwcrawford on April 14, 2009, 03:21:35 PMMen, men, men! Don't you all just wish we'd all move to some other planet? I use to say that a woman without a man was like a fish without a bicycle.
Hmmmm funny that all the women understand it, eh?
Paris - just know you are not alone. My husband was so clueless when I was doing cancer treatments and if possible - even more clueless through my kidney failure journey. He didn't understand why I was tired ALL the time - "didn't any of those pills help?" He did participate in the heavy lifting of the PD supplies that came every other week. For some reason I find that if a man can't just "fix it" many of them go into a denial thing. I don't know. I just keep trying to explain...... and explain.... and explain......
To my husbands defense, he does care. It is just overwhelming and I think it is easier to not think about. I will always be the caregiver in our family, even though I am the one with kidney disease. I get frustrated some days My role was established years ago and I am having a hard time changing the definition of who I am. The person (me) who did everything, planned all events, cooked every meal, paid bills, cleaned, taught school and now does little of that. And we have been married FOREVER so, maybe his age has something to do with accepting change. Men do become "grumpy old men" at some point Sorry, men, you know we still love you IHD gives me a safe place to complain without upsetting my family----and you guys know how I feel, so you get it.
It makes me sad to hear all these stories about spouses who are uninvolved, unconcerned and, I'm sorry, don't seem to care.I'm on my own, so I don't have that frustration. After reading these stories, I think it would make the whole process that much more difficult.
Hmmm...I always assumed that was "an engineer thing"! my husband's an engineer and so are all of his friends.
To my husbands defense, he does care. It is just overwhelming and I think it is easier to not think about. I will always be the caregiver in our family, even though I am the one with kidney disease.
Quote from: paddbear0000 on April 14, 2009, 10:42:23 PMHmmm...I always assumed that was "an engineer thing"! my husband's an engineer and so are all of his friends. Nope, nope, not an engineer thing. Hubby and I are both engineers. But I am the one who follows most of the details. When he is in the hospital, I had to make a standing rule that if a doctor enters the room and I am not there, he is to call me and put the phone on speaker so I can hear what is said.A typical hospital conversation before the rule:Me - Hey honey, I'm back. Did any doctors come in while I was out?Him - No. Just some nurse.Me - Uh huh. What did this nurse look like?Him - [description]Me - Ok, that was actually the nephrologist. What did he say?Him - Blah blah blah. Nothing, really.[two hours later we'll be chatting]Me - I've been reading about this. I'm really surprised no one has asked about your [symptom].Him - Oh yeah, that nurse guy said something about that.Me - Nephrologist. What did he say?Him - I don't really remember.Me - Well, I wonder why he didn't recommend [medication] for [symptom], I've seen where they've had really good results with that.Him - Oh, yeah, that sounds familiar. I guess he said he was prescribing that for me or something. Maybe. You get the idea.