Do you make yourself a priority?
The past few days have been ones of self-reflection. I had my annual physical last week. Blood work was fine, yet my cholesterol is still elevated (like last year). We chatted for a few minutes about increased caregiver responsibilities for my aging parents and hubby. My physician strongly cautioned about making myself a priority if I want to continue to be an active, healthy early retiree. Ouch!
He’s right, you know. I’ve made sure hubs has had what he’s needed for the past 5 years of his cancer journey. He’s currently stable (best possible outcome with his particular type of cancer) and well-matched in a volunteer opportunity that keeps him active and involved. We kept expenses in check during our gap period and my job navigating the maze to my official teacher retirement is done. At this point, I can focus on myself for a change.
Today, I had lunch with a good friend. We spent 2-1/2 hours catching up. It was good for my soul. He gave me an update on his brother, who is currently battling brain tumors and asked me for some tips on being a caregiver. I explained that the role changes over time. I shared that our journey has been one where I was more of a “nursing” caregiver after his surgery and recovery to more of a facilitator today.
My best caregiver advice:
- Don’t take anything the patient says personally. Mood swings are a reality. No-so-nice comments made by patients are generally directed at the current situation/circumstances – not at you. Remember this always: it’s not your fault.
- Abide by the patient’s wishes when it comes to the treatment plan – even if you disagree.
- Ask for help if you need it.
- Make yourself a priority. Keep up with your own medical check-ups. Eat right, drink water, get a good night’s sleep, take a walk, pray, meditate, read, journal, wear make-up and pretty, but comfortable clothes or whatever makes you feel good.
- Assemble a support group you can lean on when times get tough. I have two friends who went through something similar I can reach out to at anytime. They have kept me sane the past five years.
- Keep up with your own hobbies and interests as much as you can. It’s too easy to become isolated when you are in a high-maintenance caregiving stage. My friends check-in on me when it’s been radio silence on my end for an extended period of time. If you are unable to get out to be with friends, keep a small hand project nearby – knitting, crochet, cross-stitch, embroidery, EPP, calligraphy, adult coloring book, sketch book and pencils, etc. It does help.
This caregiver phase of life will eventually end. My husband and I tend to be rather pragmatic about things. We had some difficult conversations when he was first diagnosed. Quality of life, not quantity of life was his stated goal and I’m 100% onboard with this. Is it easy? Not by a long shot. We take it one day at a time and try to live our lives doing what makes us happy and fulfilled. Whatever happens, we have peace of mind knowing the other person will be okay afterwards. It will be hard, but life will go on.
So, if you are a caregiver of any sort, remember to make yourself a priority.



