CP-About Caregiving
Following the get-together last Saturday with my family, Christmas was fast upon us two days later. On Christmas Eve, our
Yesterday, we celebrated Christmas with my side of the family. Several traveled about five hours to be together. We had
When I tell friends, family, acquaintances, etc. what I’m up to these days (i.e., being a full-time caregiver for
Today was Lynn’s six-month visit with his dentist. Tonight, after his shower, was time to cut his fingernails and file
For most people, deciding to go somewhere is simply a matter of making the decision to go and then going.
Have you ever thought about how many choices you make in a day? Mine start before I open my eyes
In the early days of my journey as an MS Caregiver, Lynn would fall, or we would get into
Are you the type of person who keeps a calendar and checks their watch several times daily? I am. Since
I’ve been thinking a lot lately about respite care. I was asked to participate on a committee to look at
Do you remember when the person you care for was first diagnosed with MS? You might not have been around
Out of the blue today, Lynn asked me to write about advocacy. He said, “Please stress to your readers the
Lynn has started a new MS medication–at least new for him. It’s Rebif, an interferon beta-1a therapy that is supposed
