CP-Emotional Impact

Moment by Moment

I was reading a blog about advice caregivers give to other caregivers, and as I read through the suggestions (all

Caregiving is a very lonely responsibility. If you have ever been a caregiver, you understand what I mean. All caregivers

I try to stay optimistic about the future, but occasionally, an event reminds me of how tenuous life can be.

I keep thinking about how this is a topic none of us talk about, but everyone has to face it

There are a multitude of emotions that play into being a caregiver or being the one with a chronic disease

One of the rarest privileges I have as a caregiver is quiet time. When I’m awake, I am always listening

I think I can do whatever I set my mind and that my body and abilities will fall in line

For the most part, our home life is fairly stable, meaning we have the same things happening daily. We have

As a caregiver, I want to help make my spouse’s life better. I want to help him find answers to

Before Lynn was diagnosed with MS, my experience with the condition was from a distance. I knew of a third

I’m ashamed of how much I complain to Lynn about the things he asks me to do. If he calls

My daughter approached me during our vacation and asked if I would be interested in speeding the day with her