47 pages • 1 hour read
Susannah CahalanA modern alternative to SparkNotes and CliffsNotes, SuperSummary offers high-quality Study Guides with detailed chapter summaries and analysis of major themes, characters, and more.
A plethora of tests is run on Cahalan. All the results say she is normal. Dr. Siegel is no longer on her team of doctors. His replacement is Dr. Najjar. Najjar wants to try a form of immunotherapy that is experimental. Other doctors on her team are giving up on Cahalan. They are not stopping by or following up and are asking for help from other doctors to replace them.
Cahalan says that, “[o]n April 2, the nurses started [her] first round of five intravenous immunoglobulin (IVIG) infusions” (116). It is too early to tell whether the treatment is working or not. Cahalan’s health is slightly worse than before, but not dangerously so. Everyone is concerned about the presentation of a new symptom, catatonia, which is characterized by rigidity, disinterest in eating, staring, quietness, and mimicking other people’s words automatically.
Cahalan’s father and Stephen bond over their commitment to fight for her, whereas before, they were not on good terms. This chapter includes further presentation of immunology-related science.
Cahalan’s test results continue to return as normal. The experimental therapy is not working. Her team of doctors is giving up, and, in some instances, do not show up for appointments. Cahalan is again showing signs of psychosis, which everyone fears.
Cahalan’s family is exhausted from a lack of answers or insight into Cahalan’s illness. The results from the Cahalan’s spinal tap reveals inflammation in her brain.
Dr. Najjar proves to be the hero of the Cahalan family. He shows up to speak with all of them. He performs the longest intake process of all the doctors. The scope of his intake is the broadest, encompasses the most people, and goes the farthest back in time. He treats Cahalan and her family as if they were people and friends. His tests yield a drawing produced by Cahalan that is the missing piece to her illness. He asks her to draw a clock, and Cahalan puts all the numbers on the right-hand side. From this drawing, Dr. Najjar is able to diagnose her. He coins the expression “brain on fire,” the book’s title. She has anti-NMDA-receptor autoimmune encephalitis, an autoimmune disorder in which her own body attacks itself, causing brain inflammation.
Cahalan’s parents describe Dr. Najjar as being like the protagonist, House, from the show, House M.D. Najjar orders a brain biopsy, which frightens Cahalan’s family. Cahalan, in an altered state, begins to tell visitors and well-wishers with strange ease that she is having a brain biopsy. She does not understand the severity of the procedure until she experiences her friends’ reactions to the news. The surgery goes well, although Cahalan awakes and believes she has lost feeling in her legs (she has not). Her post-op MRI shows that everything is ok.
The dangerous surgical procedure of the brain biopsy proves to be worthwhile for Cahalan: “The results of the brain biopsy confirmed what the team had expected: my brain was inflamed” (143). Cahalan begins a steroid treatment, as prescribed by Dr. Najjar. Some of her symptoms are exacerbated. Her cousin, Hannah, visits and is deeply moved by the changes Cahalan has undergone. Cahalan is moved back to the epilepsy floor, where her roommate is an alcoholic suffering from seizures brought on by substance abuse.
Dr. Najjar contacts Dr. Dalmau, the senior author on a study about patients like Cahalan, Dr. Dalmau’s research and now-streamlined procedure for treatment are what truly saves Cahalan’s life, giving her a chance at recovery.
This point in the book marks the beginning of Cahalan’s recovery. She begins a long series of post-op assessments. She has to see many doctors. She is weak, unable to speak, and unable to write. She is, though, mentally alert, and showing signs of frustration in regard to how much she cannot do. She is trying her hardest to consciously improve, yet at this point, doctors believe her condition to remain precarious.
Cahalan now has an accurate diagnosis. Her prognosis is hopeful, but she still has a long way to go before she has fully recovered. She has to receive chemotherapy at this stage of treatment. Doctors are still testing to see if she has teratomas—cysts that can grow hair, eyes, and teeth. While present for tests at NYU, she is treated as if she is an exhibit at a zoo or carnival:
Now that we had a diagnosis that had never before been seen at NYU, young MDs, hardly a day older than me, stared at me as if I were a caged animal in a zoo[.] […]The young man leading the group of nascent MDs introduced my case as if I weren’t in the room (159).
Cahalan’s father, appalled at this kind of disregard for Cahalan’s humanity, shouts until all medical staff have left her room.
Dr. Najjar proposes the next stage in her treatment, which is an aggressive, three-pronged attack. Cahalan is receiving outpatient treatment and living with her family after spending a month in the hospital. Her family has shaky hopes regarding the long-term treatment plan that is now in place. Whether or not Cahalan will fully recover remains unknown.
This group of chapters covers some of the most painful and brutal aspects of Cahalan’s illness. While this section may be one of the more heart-wrenching ones in the book, this section’s contents ultimately become the beautiful inspiration for Cahalan to change her life and share her story. In this section of chapters, doctors subject Cahalan to numerous tests. Also, in this section of chapters, Cahalan’s family outwardly express their emotions. Sometimes they are crying, sometimes they are yelling, and sometimes they are feeling lost. They experience a range of intense emotions, including fear, hope, anxiety, anger, and relief. Further, in this group of chapters, Cahalan’s doctors try several treatments to counter the effects of her illness, and many of them do not help her condition.
This section also marks the time when Cahalan receives the healthcare she needs to live. It took a number of doctors, prescriptions, examinations, and diagnoses before Cahalan met Dr. Najjar. Luckily, Dr. Siegel was one of the rare doctors who realized he was far out of his depth with Cahalan’s case and reached out to a more qualified colleague to increase the chances that Cahalan’s life would be saved. Interestingly, Cahalan later rooms with an alcoholic in the epilepsy ward, which becomes a nod to one of her first, completely inaccurate diagnoses.
Cahalan’s points out that her journey has always been dehumanizing; her doctors frequently ignored her and her family, she was passed from ward to ward when she became too difficult, and she physically could not function well as a human (walking, talking, eating) when her condition worsened. Now that she actually has a diagnosis, she faces even more dehumanization; rather than relief from her symptoms or remorse from the medical community, they treat her as a specimen.
In addition to recognizing that her friends and family are fellow victims of her illness, Cahalan also sees the positive outcomes of the people she loves working toward a common goal. Her father and mother, once divorced and estranged, team up to help their daughter in her recovery, and her father and Stephen also become close, setting aside their previous issues.