Then she suffered what the doctors called a mild stroke. Since then I have become something I wasn't trained for nor had I anticipated....a 24/7 caregiver. Fortunately, I was unemployed at the time and I had the hours needed to wait on her hand and foot.
My daily duties: Fix her meals three times a day, walk her to the portable toilet every 45 minutes, change her bedding when she has urinary or feces accident (GAWD I HATE FECES), Dispense to her several types of medication (2 blood pressure meds, 2 blood thinner meds, 1 nerve.anxiety pill, 1 pain pill and other misc meds; bring her water 12 times a day, buy groceries, pick up her meds at the pharmacy, go to the bank for her, etc, etc.
If the above wasn't stressful enough considering I only get 60-90 minutes of sleep per 24 hour period, I have to listen to her babble of the following:
1. Who are you
2. Where is my son
3. Where are we
4. Whose bed is this
It's heartbreaking for me for my mom not being able to recognize me
Has anyone else gone through this or am I alone?
P.S. There are many days that I feel I am losing my ability to make sound decisions