# The Gender Gap in Pain

**URL:** https://forum.livingwithnarcolepsy.org/t/the-gender-gap-in-pain/44
**Category:** General
**Created:** [March 21, 2013, 8:46am UTC](https://forum.livingwithnarcolepsy.org/t/the-gender-gap-in-pain/44 "2013-03-21T08:46:13Z")
**Posts on this page:** 2
**Page:** 1

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### Author: ![Ben\_Munoz](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithnarcolepsy.org/ben_munoz/32/1_2.png) [@Ben\_Munoz](https://forum.livingwithnarcolepsy.org/u/Ben_Munoz)
#### Post date: [March 21, 2013, 8:46am UTC](https://forum.livingwithnarcolepsy.org/t/the-gender-gap-in-pain/44/1 "2013-03-21T08:46:13Z")

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The New York Times Sunday Review - The Opinion Page  
 By LAURIE EDWARDS  
Published: March 16, 2013  
  
Source: [http://www.nytimes.com/2013/03/17/opinion/sunday/women-and-the-treatment-of-pain.html](http://www.nytimes.com/2013/03/17/opinion/sunday/women-and-the-treatment-of-pain.html)  
TO the list of differences between men and women, we can add one more:  
the drug-dose gender gap. Doctors and researchers increasingly  
understand that there can be striking variations in the way men and  
women respond to drugs, many of which are tested almost exclusively on  
males. Early this year, for instance, the Food and Drug Administration  
announced that it was cutting in half the prescribed dose of Ambien  
for women, who remained drowsy for longer than men after taking the  
drug.  
  
Women have hormonal cycles, smaller organs, higher body fat  
composition — all of which are thought to play a role in how drugs  
affect our bodies. We also have basic differences in gene expression,  
which can make differences in the way we metabolize drugs. For  
example, men metabolize caffeine more quickly, while women metabolize  
certain antibiotics and anxiety medications more quickly. In some  
cases, drugs work less effectively depending on sex; women are less  
responsive to anesthesia and ibuprofen for instance. In other cases,  
women are at more risk for adverse — even lethal — side effects.  
  
These differences are particularly important for the millions of women  
living with chronic pain. An estimated 25 percent of Americans  
experience chronic pain, and a disproportionate number of them are  
women. A review published in the Journal of Pain in 2009 found that  
women faced a substantially greater risk of developing pain  
conditions. They are twice as likely to have multiple sclerosis, two  
to three times more likely to develop rheumatoid arthritis and four  
times more likely to have chronic fatigue syndrome than men. As a  
whole, autoimmune diseases, which often include debilitating pain,  
strike women three times more frequently than men.  
  
While hormonal, genetic and even environmental factors might influence  
the manifestation and progression of autoimmune diseases, we don’t yet  
know the reason for this high prevalence in women.  
  
Pain conditions are a particularly good example of the interplay  
between sex (our biological and chromosomal differences) and gender  
(the cultural roles and expectations attributed to a person). In 2011,  
the Institute of Medicine published a report on the public health  
impact of chronic pain, called “Relieving Pain in America.” It found  
that not only did women appear to suffer more from pain, but that  
women’s reports of pain were more likely to be dismissed.  
  
This is a serious problem, because pain is subjective and  
self-reported, and diagnosis and treatment depend on the assumption  
that the person reporting symptoms is beyond doubt.  
  
The oft-cited study “The Girl Who Cried Pain: A Bias Against Women in  
the Treatment of Pain” found that women were less likely to receive  
aggressive treatment when diagnosed, and were more likely to have  
their pain characterized as “emotional,” “psychogenic” and therefore  
“not real.”  
  
Instead of appropriate care for physical pain, this can lead to  
treatment for mental health issues that might not even exist. The  
situation is further complicated by the fact that antidepressants are  
absorbed differently in women and vary in effectiveness, depending on  
hormonal cycles.  
  
The routine attribution of abdominal pain from conditions like  
appendicitis or gastrointestinal disease to gynecological problems can  
also delay or complicate the diagnostic process. A 2008 study  
published in the journal Academic Emergency Medicine, designed to  
gauge gender disparities among emergency room patients complaining of  
abdominal pain, found that even after adjusting for race, class and  
triage assessment, women were still 13 to 25 percent less likely than  
men to receive high-strength “opioid” pain medication. Those who did  
get opioid pain relievers waited an average of 16 minutes longer to  
receive them.  
  
Conditions like fibromyalgia or chronic fatigue syndrome, for which  
definitive causes have not been identified and concrete diagnostic  
tests are not available, illustrate the problems associated with the  
perceived reliability of the female patient as narrator of her pain.  
Women are more likely to receive diagnoses of many of these more  
nebulous conditions — fibromyalgia, which affects about six million  
patients in the United States, is nine times more likely to be  
diagnosed in women than in men — and this discrepancy surely  
contributes to the widespread skepticism that still exists over the  
legitimacy of these disorders.  
  
I AM a sufferer of pain and chronic disease. Like many, I’ve had  
physical symptoms (in my case, respiratory problems and infections)  
explained away as emotional. My freshman year in college, I was in the  
emergency room, flanked by machines and struggling to breathe while  
doctors lobbed questions at me: Why wasn’t I responding to the  
medication the way they expected I would? Was I just too anxious?  
Could I not handle stress, and was that making me sick?  
  
I was 23 before I was given a correct diagnosis of a rare genetic lung  
disease called primary ciliary dyskinesia. I’d been sick since birth,  
but long diagnostic journeys are occupational hazards of living with  
conditions doctors don’t often see. Still, my journey was  
unnecessarily protracted by my doctors’ dismissal of my symptoms as  
those of a neurotic young woman.  
  
For all the medical advances of the past few decades, we still know  
shockingly little about pain and how to control it. Sex-based research  
is a crucial part of understanding not just the underlying mechanisms  
of pain, but the most effective ways to treat it for men and women  
alike. The Institute of Medicine report found gaps in research,  
particularly in terms of effective treatments, as well as in the  
oversight of pain research. The report recommended that these problems  
be addressed and that strategies to resolve them be implemented by  
2015.  
  
Among those improvements must be a renewed focus on discovering why  
women respond differently to some drugs and diseases, as well as an  
emphasis on training physicians to better diagnose and manage women’s  
pain. A report by the Campaign to End Chronic Pain in Women found that  
inadequate physician training in diagnosing and treating just six pain  
disorders that affect women either exclusively or predominantly,  
including fibromyalgia and chronic fatigue syndrome, added as much as  
$80 billion a year to America’s health care bills.  
  
Part of the reason the diagnosis and treatment of women’s pain lag so  
much is simply the pace of medical research itself, which is slow to  
move from publication to clinical practice. Unfortunately, if  
anything, changes in assumptions about gender evolve even more slowly.  
  
Laurie Edwards is the author of the forthcoming book “In the Kingdom  
of the Sick: A Social History of Chronic Illness in America” and a  
writing teacher at Northeastern University.

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### Author: ![pwntek](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithnarcolepsy.org/pwntek/32/79_2.png) [@pwntek](https://forum.livingwithnarcolepsy.org/u/pwntek)
#### Post date: [June 13, 2013, 9:28pm UTC](https://forum.livingwithnarcolepsy.org/t/the-gender-gap-in-pain/44/2 "2013-06-13T21:28:18Z")

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i have narcolepsy/cataplexy \*and\* severe, unrelenting, intractable pain. i have indeed been told my pain is not 'real'. it is my hope that the attached file will help our physicians understand.

if this [unfortunately] applies to you, please share it with your doctor[s]!

p.s.: below is the link to the original pubmed.gov abstract:

[http://www.ncbi.nlm.nih.gov/pubmed/21570344](http://www.ncbi.nlm.nih.gov/pubmed/21570344)

[139-Highpainfrequencyinnarcolepsywithcataplexy12.SleepMed.2011PubMedNCBI.pdf](https://us1.discourse-cdn.com/flex019/uploads/ben_narcolepsy/original/1X/169ad097bbc6f849ffa8bff7431a0e98aaa70cdf.pdf) (75.6 KB)
