CP-About Caregiving

Ever had this conversation? “How’s (insert family member’s name here)? You know, that if you ever need anything, anything at

“Can you come here a minute?” I hear that every 30-60 minutes all day long, and you know what? It’s

After years of caregiving, I believe I know Lynn’s body and his emotional and physical needs as well or better

For several months, we’ve seen groups proclaiming their rights for equal treatment under the law and by others. While I

Having just celebrated a great Mother’s Day with my three children and their spouses, I couldn’t help but think that

Each of us filters information through our previous life experiences. We evaluate comments made and inferences perceived through those filters

Since multiple sclerosis often strikes in early adulthood, many times, the family unit includes children who mature into adulthood, watching

I had to make a choice this week about my own care that turned out well but according to the

Often, when I meet someone who has just become a caregiver, they ask me how I do it; “How do

I’ve been thinking a lot lately about respite care. I was asked to participate on a committee to look at

I usually write my blogs on Saturdays because it’s the only time I don’t immediately have another obligation once I’m

Lynn has started a new MS medication–at least new for him. It’s Rebif, an interferon beta-1a therapy that is supposed

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