When the ER doctor called just as I was heading out the door for a holiday weekend away, I didn’t think about what life lessons I might be learning by putting the needs of others before my own. When my dad greeted me by rattling his water glass at me for a refill before I even walked through the door, my heart didn’t fill with gratitude. That Labor Day I spent moving my mothers’ belongings to a new apartment so she could have a fresh start after another summer spent in rehab? Well, let’s just agree my actions should speak louder than my words.
In the ten years I spent helping my parents (that is, caregiving), I was dedicated, for sure -- but I was also occasionally disgruntled. I advocated for my parents through a dozen or more hospitalizations, each of which was stressful and ill-timed. I supervised four moves, each preceded by an urgent round of research and frenzied cost analysis. I made countless appointments and grocery runs and phone calls on their behalf. Over time and at their request, I took over the management of, well, “everything”: their household, health, financial, legal, and property matters. At times, I put their needs before my own, and sometimes I thought helping them with their lives would swallow my own.
For ten years, I administered their life in addition to managing my own. And now, I don’t. Earlier this year, I held my mother’s hand as she died, just as I had held my dad’s five years ago in his final moments.
I admit I didn’t love every minute of caregiving but I did do every minute out of love. Everyone talks about the burden and challenge of caregiving but I've found there were some “gains”, too. I learned new skills, yes. But I also made new realizations that have changed the way I live.
Here are a few of the lessons I’ve learned:
YEARS, NOT MONTHS
If I’d known I’d be caregiving for years, not months, I might not have tried to superhero my way through those first few months after the initial crisis. If I hadn’t tried to fill every gap that appeared after my parents’ diagnoses, I might not have burnt out before setting boundaries and making backup plans so I could get a break. According to the Family Caregiver Alliance, theaverage duration of a caregiver’s role is four years(and only 30% of caregivers have a role that lasts less than a year.) At first, I made the mistake of thinking of caregiving as a short-term “project”, something with a beginning, a middle, and an end in sight. Caregiving is not a project, though. I learned that for me andso many others, it’s a phase of life. I never got the work-life balance right. I only survived by learning to integrate caregiving into my life.
WORRYING WON’T HELP
The night my parents told me of my father’s cancer diagnosis, I stayed up until 2 a.m. interrogating Google. When my mother had a stroke, I punished the search engine with query after query about her prognosis. Each CT, MRI, angiogram, another worry. I worried about what my life would be like without them and I worried that pressure from all the competing demands would crush me. I worried about keeping my job through so many days off and distractions and I worried my parents would hurt themselves when they wouldn’t accept more care at home. And never once did worrying change the outcome. Worry was stealing my time, robbing me of the only time in which I could truly make a difference: the present moment. Over time, I learned to “release the worry”, a phrase I first heard fromcaregiving expert Denise Brown. Once I learned to do what I could and truly let go of the rest, I was able to stay calmer in emergencies, focus better at work, and enjoy my family more.
There are additional lessons Karen shares that are deeply valuable. If you want to read more of this story, please continue reading at Life in Motion Guide.com