We have had a shift in another routine, though. The
little pot of pills that mom would take in the morning and evening have now got
to be put in her mouth directly so that she can chew them and swallow them
without losing them. (FYI: swallowing is one of those things that is impacted by
Alzehimer’s. It becomes harder and harder to swallow until even liquids can be
difficult. I think thick liquids like applesauce are actually easier for her to
swallow than liquids or solids, like her pills. Hence, the chewing of her
pills.)
Mom has begun playing some fun games with her pills. She will take them out of the cup and line them up on her dinner tray. Or she will use her fork or spoon to scoop them out of the pill tub. Either way many of them end up on the floor and I have to scramble around under the chair to find them. This is apparently quite funny to watch… To Watch. Humph! ;)
Another favorite play of late is to take whatever she is
eating and pile it into the pill cup. I’m really not sure where that comes
from? Maybe it’s because they are applesauce cups, originally, and she thinks
that she should be eating out of them? But never the less, the pills begin to
break down when the moist, warm food hits them, so I begin a rapid feeding
process to get the food and pills into her before they breakdown and melt into
the cup. Again, the problem with swallowing comes into consideration and so we
try to balance slow chew and swallow with the rapidly dissolving pills. Not as
funny to watch apparently, but that’s when the feeding games begin and mom
starts playfully pretending she won’t open her mouth for food until I cajole
her into it or laugh at her joke then tell her I’ll send her to bed without
dessert. Hey… It worked on me when I was the kid!
So now, I just pop the pills in her mouth for her and we
avoid all the fun for her and all the games for me! I know… I’m just no fun anymore!
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