My mom is the primary caregiver for my father. He has Parkinson’s Disease which is a result of being in contact with Agent Orange when he was in Vietnam. He also has other illnesses and diseases that have developed after Parkinson’s. Imagine you retire and you develop a disease that DRASTICALLY changes your outward appearance and your mental and emotional well being.
My dad has always been this strong guy with muscles. I remember him lifting weights and hanging from his biceps. I remember the big round weights that go on the weight bench. I remember the children in the neighborhood racing against him and they would lose. So, if it’s hard for me to see all of that, his mobility, his muscles, his strength disappear, it must be incredibly hard for him to deal with. He’s stubborn, but I think by now he realizes he needs help or assistance. Yet, he fights to keep most of his independence because he doesn’t like anyone doing anything for them. Especially, if they make it known they really mind doing it for him or that it’s a problem. I get that and the stubbornness from him. My dad has always had a sharp mind. He still has it. He is like a walking history buff and Bible. He is still pastoring and this is his last year as his health has really declined. Last week when he was in the hospital for rehab, we talked about poetry and just when I thought I knew it all about poetry he throws out poets I never heard of. He recites some lines. This is my dad.
This week my mom was out of town on church business and I was “hired” to take care of my dad. Even though my mom is the primary caregiver, all six of us children are there to do our jobs. We all chip in. Some more than others because some work full time and others have illnesses of their own (like me). We seem to take on our roles and fill in when needed of roles of the others. It just worked out that way. I took care of Dad this week and I got to see him in a different way. I got to see the struggles in a different way. I heard the yelling as he napped. It was something about war. I got to see the depression that he sometimes denies. I got to experience the moodiness and irritability that we rarely see. But, I also got to see the determination to wash his own clothes, put his dishes away, wash up, and put his clothes without my assistance a few days. I saw the sweat pouring down his face and the tiredness that followed those simple tasks.
My favorite part of the experience was getting him out of the house to sit on the porch as he likes to do and we listened to a famous sermon on YouTube by Reverend C.L. Franklin (Aretha Franklin’s father). He was unsure he could get out of the house or go anywhere with his new fancy walker (which he calls the Cadillac). I had to encourage him and he made it to the barber shop with his new walker.
Even though it was really hard work taking care of him all week from 7 am to 7 pm it was time well spent. The pain and exhaustion that I felt daily, the pain meds I had to take, the willing myself to get up, the swelling and the joint inflammation, the mental battle, reminded me of why I had such a hard time working my last full time job. By the time you recover, it’s time to work again and creates an endless cycle that worsens your health. However, all that I experience this week was worth the quality time spent with my dad. Care giving is a job. It’s a job for the one doing it all the time and the ones who do their parts regularly and the ones that have to fit it in. However, it’s rewarding knowing that you helping someone you love and it has it’s moments that will someday become memories.
3 thoughts on “Sunday Morning Coffee Musing: Time Well Spent”
This brings back alot of memories of my mum selflessly taking care of my brother who had health issues for many years before eventually passing on.
That quality time with your dad is priceless and he needs it I believe.
I wish you love and light❤️
Thank you Kui
I miss my mom and dad a great deal. Cherish them while you have them.