To wrap up Multiple Sclerosis Awareness Month, I thought I’d do something a little different and hand the floor off to someone who is very much aware of the effects that MS can have on a person and their relationships: my husband. Caregivers are often overlooked and need just as much support (if not more) as we do. These silent warriors stand beside us, stealing and forging spoons so that we can just simply get through the day.
So! Handsome and fearless caregiver, take it away! Continue reading “Through the Eyes of a Caregiver”
This summer really flew by, didn’t it? This year’s heat and humidity seemed to make a pretty noticeable difference in my day-to-day–more so than the last few summers. Or maybe it seems that way because it’s still so fresh in my mind.
I went in for a routine visit with Dr. Brain last week and, while my fancy sobriety test-esque exam went well, he told me precisely what I didn’t want to hear.
Something popped up in my Facebook Memories app today that I thought might be kind of nice to share, especially in the wake of Father’s Day.
Continue reading “I Hope The Apple Doesn’t Fall Far From the Tree!”