Dehydration and chronic fatigue. That was the diagnosis the doctors at Good Samaritan Hospital gave me when my friend rushed me there in 2011 after insisting I seek medical treatment. This followed several days of insomnia, sensitivity to light, intense headaches and unquenchable thirst. I knew I was tired—hell, I knew I was exhausted. I’d felt this way before —many times. But I didn't realize it had gotten so bad that I was making myself sick.
Still, while lying in the hard, inflexible hospital bed, I wasn’t preoccupied with worry for myself, or even concern for how I was going to get better. I was consumed by guilt. Guilt that, while I was in the hospital, I wasn’t able to be the caregiver I needed to be for my disabled mother.
I shifted my plans to attend graduate school in California and returned home to New York to be my mother’s primary caregiver. I was 22 years old.
My beautiful mother was diagnosed with Progressive Multiple Sclerosis (MS) in 1982, although the first symptoms—numbness and tingling in her fingers; muscle spasms in her lower back; and intermittent spells of blurred vision—appeared as early as 1971. My two younger siblings and I have watched this wretched disease rob our mother of her ability to walk, work and engage in many of the activities that once brought her joy. Walking in the park, writing, and reading her romance novels eventually became things of the past. The first significant progression that impaired her signature graceful gait required her to begin intense physical therapy while I was in college in 1994.
By the time I graduated just two years later, she couldn’t walk without the support of a cane. My siblings were starting college at that time, so, as the eldest, I shifted my plans to attend graduate school in California and returned home to New York to be my mother’s primary caregiver. I was 22 years old. Although I had looked forward to starting my adult life on the West Coast, I was raised in a family—like many other Black families in the U.S.—that took care of one another in every way, regardless of the sacrifice. I was concerned about her health and wanted to be there to take care of her, whatever it took.
Although I had looked forward to starting my adult life on the West Coast, I was raised in a family—like many other Black families in the U.S.—that took care of one another in every way, regardless of the sacrifice.
Related: Download a free caregiving guide from AARP and connect to online resources
As is the case for many caregivers, I began my journey without a handbook or model of how to do it right or how to balance caregiving with self-care. According to a study by the National Alliance for Caregiving and AARP, unpaid family caregivers number 53 million in the United States. Many are thrust into this role without preparation, and Black women—beholden to gender, racial and ethnic conditioning about the role of caregiver—are often expected to carry on legacies of caring for loved ones.
Black women—beholden to gender, racial and ethnic conditioning about the role of caregiver—are often expected to carry on legacies of caring for loved ones.
Navigating the complexities of caregiving while balancing our own professional and social lives can also engender what’s called caregiver guilt. Caregivers experience this distinct type of guilt when we believe we aren’t doing enough for our loved one and we regret taking time to focus on ourselves. This guilt often compounds the existing stress of caregiving and can complicate the relationship with our loved one.
I struggled to balance my burgeoning social work career and my bustling post-college social life when I took on this role. Burnout was inevitable, and I found myself crying to my therapist during those moments when the guilt was too much. At moments I felt like I was trying to give from an empty cup, and eventually I just wanted to give up. My therapist encouraged me to rediscover what experiences, activities, and people brought me joy and commit to engaging in them without guilt or apology. I jumped right in and compiled a list. Travel was at the top of that list.
Navigating the complexities of caregiving while balancing our own professional and social lives can engender what’s called caregiver guilt. Caregivers experience this distinct type of guilt when we believe we aren’t doing enough for our loved one and we regret taking time to focus on ourselves.