Showing posts with label caregivers. Show all posts
Showing posts with label caregivers. Show all posts

Saturday, April 28, 2012

I Never Told You

You came to help me. But I never told you what I needed. I just sat there feeling miserable. I felt sad for your helplessness, too. As you busied yourself tidying things up, cleaning and rearranging my kitchen because that was all you could think to do, I sat silently. What I really needed, what I really yearned for was to put my head in your lap and have you gently stroke my forehead the way my mother used to do. I never told you what I needed. I never got it. You never got the gift of giving it.

Sunday, April 26, 2009

Caregivers

Last week I was at a gathering of people who all shared concerns about the problems of chronic illness. Most of them were the caregiver types. As I listened, I began to wish that I could wave a magic wand and turn the gathering into a Codependents Anonymous meeting! These were wonderful, nice, compassionate and caring people. And sometimes that's the problem.

One after another they mentioned the stress that goes along with being a caregiver. (And yes, caregiving can be stressful.) Most of the people who were on the receiving end of care were hardly invalids. They could do most things for themselves, but the caregivers worried tha the patients did not take care of themselves, didn't take their meds, didn't comply with their treatment plans or (fill in the blank).

I reflected on my own experience with chronic illness adn the reactions of my family when I was at my worst. Caregivers try to fix us. They stress out when they can't do that. The worry that we'll die. (Everyone dies, by the way, even caregivers.) But what they don't realize is that we, the sick ones, pick up on their stress and frustration. Then we get to feel guilty because we are the source of their distress. And there's another part. As long as caregivers do for us what we are capable of doing for ourselves, we are enabled not to take care of ourselves.

Chronic disease brings loss of control. Caregivers "should" on their sick loved ones. The sick folks "should" on themselves. Doctors "should" on patients. "Shoulding" is a way of trying to gain control. Personally, whenever anyone "shoulds" on me, I do just the opposite!

What is there to do? I think there are two starting points. The first is good, honest communication. The second is to walk in the other person's shoes at least mentally. It's a good start!