Communal meals, at least in the pre-COVID-19 world, are a big part of the medical profession. We share pastries at morning conferences, bond with colleagues over lunch in the hospital cafeteria and attend an endless series of talks where food is usually provided.
To avoid eating in front of peers and superiors would be to exclude myself from an integral part of my profession’s culture and, some days, entirely miss my opportunity to eat. Instead, I make sure I have a stack of napkins at the ready to wipe my runny nose before anyone notices, and I discretely slip away to blow my nose in the bathroom when I’ve finished eating.
I was born with cleft lip, cleft palate and hemifacial microsomia, a constellation of symptoms that, for me, includes a smaller right jaw and missing right ear. In the past few years, my nasolabial fistula, a commonof cleft lip and palate, has worsened, and there is now a sizable gaping hole connecting my nasal and oral cavities.
Though my fistula is visually imperceptible, food and saliva slowly seep from my nose during meals. While some foods are more problematic than others, and I am selective about what I eat in front of colleagues, it’s an issue I endure at every meal ― and it can only be corrected through an expensive surgical intervention. Depending on who insures me at the time of the procedure, I could be denied insurance coverage for my care, as I have been many times before. This is especially true now that I am an adult.
Insurance companies have done the math and determined it is advantageous to routinely deny coverage and wait for the family or provider to battle that determination, rather than cover what is most certainly medically necessary care.
Although at least 18 states have some type ofrequiring insurers to cover cleft and craniofacial care, families and adult patients living in states with no mandate are left to grapple with denials. Some of the states only extend the mandate to pediatric patients, which ignores the reality of cleft and craniofacial care as a lifelong need. The (ELSA) is a federal bill under consideration in Congress that would mandate insurance coverage of the medically necessary care of adult and pediatric patients with congenital anomalies, thereby putting a definitive end to the coverage denials.
Coverage denials force families to suffer extreme out-of-pocket costs, risk poor outcomes by delaying care while they contest the denial, or forgo care entirely. My mother recalls denials being the norm rather than the exception for my non-surgical care and nearly 20 surgeries. Though my family managed the out-of-pocket costs while we waited for my provider to argue for coverage, not every family has the means to float such large expenses. Once I reached adulthood, coverage was more limited, and a vast portion of the expenses for the reconstructive surgeries I underwent in college was ultimately paid for by my parents rather than our insurer.
Much of the care for individuals with clefts or craniofacial anomalies is functionally critical, ensuring the ability to eat, breathe, speak, sleep and even swim normally. In addition to surgeries, orthodontic appliances and speech-language therapy are vital to achieving good outcomes in these areas. However, it is important to realize that even interventions aimed at normalizing facial appearance are essential to care; they are not merely cosmetic but are medically necessary for complete psychosocial habilitation.
Individuals with facial differences are discriminated against in education and employment and
One would be wrong to assume that, with my law degree or role as a medical student at a respected program, I am immune to such discrimination. In fact, I quit my first law job two weeks after starting because one of the partners of the firm pulled me into her office to tell me, in a longwinded speech, that she was worried judges would not take me seriously because of whatever is going on with my face. This was in the midst of the Great Recession, and I spent the next five months unemployed. If I had stayed, I doubt I would have thrived in an environment where so little was expected of me.
Normalizing one’s appearance is not a mere vanity for people with congenital anomalies.
It is also a commonthat cleft and craniofacial care end at age 18, perhaps reinforced by the fact that patients graduate from craniofacial team care upon reaching adulthood. One’s face continues to change throughout the aging process, and , like my fistula, can emerge. Moreover, technologies change and improve, and adults should be able to avail themselves of those advancements. For example, when I was a pediatric patient, did not exist. I am mostly deaf on my right side, but a surgically implanted BAHA would instantly bestow bilateral hearing, enabling me to better hear patients and colleagues calling out to me in the busy emergency department environment where I dream of one day working.
Incredible innovations are in the pipeline for patients with facial differences; adults should not be excluded from their life-changing benefits on the basis of age, nor anyone denied coverage due to an inaccurate determination that their care is unnecessary.
ELSA, if enacted, would require that medically necessary care of individuals with congenital anomalies be covered by insurers and would eliminate the problem of routine coverage denials. The language of the statute isin that it explicitly mandates coverage for patients of any age, and it defines medically necessary to mean prescribed by a provider or care team, thereby eliminating the potential for future battles to determine necessity. As a federal solution to a national problem, ELSA will provide long-overdue protections to Americans living with congenital anomalies, ensuring lasting smiles for current and future patients alike.
Kristin Pfeifauf is a medical student at Washington University in St. Louis. Prior to medical school, she practiced transactional law. She completed two years of research fellowship with the Cleft & Craniofacial Institute of Washington University. She is also co-founder and director of, a student-run advocacy coalition formed in response to COVID-19. Growing up, she underwent most of her cleft and craniofacial care at St. Louis Children’s Hospital.
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By David Aaron
November 10, 2020