Lynne Tillman Breaks the Rules

What spurred Lynne Tillman to write Mothercare, her first work of memoir, is in many ways a mystery. In a long and prolific career of writing fiction, criticism, and essays, she has avoided personal writing and does not seem to feel liberated by it now. “I have strong reservations about doing it,” she writes, “and now I am doing it.” The book is Tillman’s account of her mother’s decline from normal pressure hydrocephalus, a form of dementia caused by excess cerebrospinal fluid accumulating in the brain. Mothercare chronicles the experience, recounting it through surgeries, doctors’ appointments, the hiring and firing of live-in caregivers. Obtaining a proper diagnosis and care proved difficult in the 1990s, because normal pressure hydrocephalus was not widely understood at the time and was frequently misdiagnosed as Alzheimer’s, which, unlike NPH, is not reversible. Once the illness was identified and a treatment found—a shunt to drain the fluid—the difficulties continued: The shunt backed up repeatedly, like rickety plumbing, causing seizures and other debilitating neurological problems. Tillman’s mother was incapacitated for the rest of her life: 11 years of illness and dependence.

Mothercare is billed as an odyssey through our “unnavigable medical world,” but though the book largely takes place in the medical world, it’s not about that. Instead it skates on the surface, directing blame at individual caregivers: the aide who was a “lunatic,” the hospital interns who were “lame,” the neurologist who was too “arrogant” to reconsider an initial diagnosis. Geriatric medicine, Tillman argues at one point, is not of the caliber it should be because doctors are scared of how “the elderly represent mortality.” She mentions money only once, to say:

Without Medicare, it would have been impossible to give Mother the care we did. Her savings, which could have lasted for her lifetime, would’ve been savaged, my sisters’ and my finances decimated. Medicare paid for her operations; and, with co-pays, also her doctor visits. All of Mother’s doctors took Medicare assignments. Still, be prepared: Medicare statements and bills are confusing. What has been paid, what hasn’t, is hard to figure out. Luckily, we were helped by a family friend who did that work professionally.

That “Still, be prepared” gestures toward a desire to be helpful to others that runs through this book, but it never goes further than this. Even when Tillman addresses the political currents of a situation, she does not fully confront the implications. On hiring aides—often women of color—Tillman writes:

My privilege lived through the after-effects of colonialism and imperialism. The terms and effects were not abstract, they were personal, embodied in the women we were able to hire to care for Mother. I was conscious of it, but didn’t forsake my privilege.

Later she admits, “Sometimes overwhelmed, I lost time and capacity to think clearly, if at all, about the ethical questions raised by her needs and our finances.”

Tillman approaches her mother, and her sisters, with a similar reluctance, to fascinating effect. To provide backstory, she turns not to memories or stories of her mother but to old photographs: “Sophie Merrill is always fashionably dressed, often wears a cloche hat, or lets her long dark hair flow freely down her back.” When she writes about her mother’s aging body, she does so with clinical remoteness: “She lost her bowels on the living room floor” is how a seizure is described. This lack of tenderness is deliberate. Early on in the book, Tillman writes, “My possibilities and fantasies were being stolen by Mother, whom I didn’t love.” It’s exhilarating to hear this said point-blank: a delicious taboo that is as seldom admitted as it is frequently thought. With it, Tillman pushes back on the sentimental idea that in moments of crisis, our emotions rise up to carry us through. “To care” is both an action and an emotion, and Tillman reminds us that they are distinct.


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