3.4 AVERAGE

dimeryrene's profile picture

dimeryrene's review

challenging sad slow-paced

Difficult to give someone's actual life story a review, so I've left that off. This book was difficult and slow and I can't imagine living with Lyme Disease. I didn't know it was so often ignored, overlooked, or misdiagnosed. This book really opened my eyes to more ways in which the health care system fails women. It was a difficult read, but I will recommend it widely. 



Expand filter menu Content Warnings

My takeaway from this chaotic memoir is that Lyme disease is terrfiying (thanks for checking me for ticks at the Cape @cassadycadillac) and the American health system is brutal. My other takeaway is perhaps the jumpy approach is not the right one for a memoir of this kind.
hopeful informative reflective medium-paced
reads2cope's profile picture

reads2cope's review

3.0

A difficult and enlightening memoir. Khakpour writes in loops that made it hard to distinguish one crash from another, but this confusion immersed me in a better understanding of her frustration and agony of being sick and having no cure, no clear cause, and often not even being taken seriously. The gaslighting she received was internalized, and even when she focused on getting better, she questioned if she was practicing self-care or if she was wallowing in depression. Heartbreaking to see how medical ignorance caused so much more pain, so much so that she began to lose her loved one and eventually found almost everyone untrustworthy. 
At the same time, Khakpour seemed to be able to give herself some grace that she was unable to give to her friends. She acknowledges that she abused and was a drug user for a long time, but friends she did drugs with were “junkies” she had no respect for. When she found out another friend was a sex worker, she looked down on her and said their relationship was never the same. 
Khakpour‘s relationship to whiteness was also hard to read. Her terror in moments of heightened xenophobia and Islamophobia were gutting, but at the same time she either missed or didn’t include any moments of solidarity with POC and Muslims in her community. Instead, she gushes about a US-government funded trip to Indonesia (why was the US finding these trips? No reflection on the motives there) and makes sure to mention that she traveled to Israel for a book project (no solidarity with long-running calls for cultural boycotts?) In a taxi with a white driver, she calls her mom but tells the man,  “Just so you know, it’s Farsi. I’m Iranian but not one of the bad people. Please don’t be worried by my language.” As if, were she speaking Arabic, he could have had a legitimate problem, even seeming to suggest that there are Farsi speaking women in New York he should be worried about being near, but she’s one of the good ones. Khakpour acknowledges that she sometimes passed for white, and maybe it was the toll of her incredibly long journey of illness that kept her from interrogating her perspectives on xenophobia, but these stories felt shallow and jarring compared to the depth of her discussions around her sickness. 
Even in those discussions, she sometimes seemed dismissive of other chronic illnesses, particularly ableist in her writings about mental health struggles, and ready to call one alternative health program a cult while completely buying into another. I hope in the time since she wrote this, her perspectives have been widened, especially in the COVID-19 pandemic, and her politics seem to have shifted based on her social medial posts alone, so I would be very interested in a second memoir from her, and hopeful that it would contain more solidarity.

Expand filter menu Content Warnings

by no means an easy read, and not necessarily the relatable story I was hoping for (which tbf isn‘t valid criticism considering it‘s a memoir) but overall I‘m glad I read it

Expand filter menu Content Warnings

"you are reading the middle of a story, I suspect, but I'm not sure where or when it will all end, so one might as well tell it now"

This book wasn't quite what I wanted it to be at the beginning. Khakpour writes more about old lovers than doctors, and hints at family trauma that's never quite unpacked. But her writing is honest and reads easily even when you can tell how hard and scary it was to write. I think some of the hype around this book has led readers to want it to be everything, to point to everything that's wrong with the medical system, especially for a WOC. It's not that, it's just one individual's story, but that story is told really well.

Ugh, why am I so inarticulate every time I want to say how much a book by a disabled or chronically ill writer meant to me? For now, I'll just say I thought this memoir was great, and I hope I'll eventually be able to say why.

Horrifying and fascinating.
slow-paced

Least favorite book of the year. I loved the idea of a chronic illness memoir without a “perfect patient” but this book was clunky and frustrating and seemed weirdly dismissive of other chronic illnesses and also of all of the many many many people who helped her, all of whom felt one-dimensional and most of whom seemingly only existed to try to help but were described in often shockingly negative ways- even those she seems to like. 

vondranarvaez's review

DID NOT FINISH: 0%

Lost interest