The jingle about Jello Instant Pudding® is running through my head right now, but honestly this is a serious post about a serious question. The other night, Burt, in the midst of his confusion, was lamenting how “sick” he feels. My response was to tell him that whatever was bothering him, hurting him and upsettingContinue reading “It’s never too late”
Tag Archives: #caregiving
Figuring it out
Okay, this is a bit weird. One of my fears is that by the time I get the hang of caring for Burt, it will be too late. It’s a huge learning curve, at least for me. So many things to consider and do. I want him comfortable, safe, and secure. I want to love himContinue reading “Figuring it out”
A question of time
Recently, a kindred caregiving spouse wondered how many hours of care she should consider for her husband. She had been going it alone, and with all her heart and love. Anyone who’s been there knows how intensely draining and lonely this can be. There comes a time on this journey when caregivers need relief. ForContinue reading “A question of time”
It’s the money, honey
Caring for a family member with dementia can be heartbreaking and difficult in so many ways. One of the hardest tasks may be protecting them from ruining their finances as their condition deteriorates. Research shows that those with dementia often show signs of financial trouble years before diagnosis. Left unchecked, their unpaid bills, gratuitous spendingContinue reading “It’s the money, honey”
Caring while under…
Yesterday, it appears, the combo of an RSV shot on Monday and a Covid booster on Friday made me feel crappie. My body ached, and my temp was slightly elevated. Of course, both my arms hurt at the injection sites. Mildly unwell as I was, I was hard pressed to show patience; I skimped on preppingContinue reading “Caring while under…”