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“The world is disturbingly comfortable with the fact that women sometimes leave a sexual encounter in tears.” Lili Loofbourow

According to a recent study published in The Journal of Sexual Medicine, about 30 percent of women report feeling pain during vaginal intercourse.

This alarming statistic is only recorded amongst women who are even comfortable speaking to doctors about sex, meaning that a far greater number could be more accurate.

Another hugely concerning fact which the study expressed is that "large proportions" of women don't tell their partners when sex hurts, they simply grin and bear it.

This testifies to the notion that women often sacrifice their pleasure, not to mention their comfort, for male satisfaction. The assumption that “bad sex” simply means the absence of pleasure is a naïve one- for many women, “bad sex” can mean extreme discomfort and even agony.

Debby Herbenick, an academic from the Indiana University School of Public Health and one of those who incentivised the National Survey of Sexual Health and Behaviour, confirmed this suggestion.

"When it comes to 'good sex,'" she commented, "women often mean without pain, men often mean they had orgasms."

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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The satisfaction scale for men and women is clearly imbalanced. Painful sex isn’t the rare outlier that it’s proclaimed to be, in fact, it’s far more widespread than imagined.

For some women, such as those suffering from illnesses such as endometriosis, ectopic pregnancies and vaginismus, it’s part of their reality.

For others, they are in need of more foreplay, lubrication or comfort. Anxiety and tension can have a drastic impact on female sexual pleasure. 

There are dozens of possible reasons why you could be experiencing pain during sex, ranging from the physical to the psychological.

The troubling thing is that so many of these reasons are not well-known, and they are scarcely researched or prioritised in our healthcare systems.

Dyspareunia is the medical term for painful sex, and can be a deeply distressing condition which takes a massive emotional toll on those who experience it.

According to another scientific article on women’s pain:

“Approximately 15% of women have chronic dyspareunia that is poorly understood, infrequently cured, often highly problematic, and distressing.”

The stigma surrounding problems such as the ones mentioned above is part of the reason why women aren’t discussing their sexual pain, especially not with healthcare practitioners.

Even if a woman feels willing and able to discuss her sex life with her doctor, the lack of research into female pain in general as well as in sexual medicine means that even more barriers crop up.

Sexual assault arguably can also contribute towards experiencing pain during future sexual encounters.

Numerous studies support the idea that a mental block is created surrounding sex, which lives with survivors long after their attack.

Without a healthy view of sex and positive sexual experiences, women are not being given the tools to vocalise their pain.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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Other disorders such as vulvodynia, vestibulodynia, interstitial cystitis, vaginitis, vaginal atrophy, fibroids, lichen sclerosus and lichen planus (skin disorders), ovarian cysts and endometriosis have all been grossly under-reported, and awareness of these conditions is extremely limited.

Yeast infections, overly tight pelvic floor muscles, bowel problems and hormonal imbalances can also be major contributors to pain during sex, as well as STI’s.

BBC Three has recently aired a visceral visual essay series, where director Sindha Agha decided to artistically depicted the female experience of painful sex.

The beautiful video uses colourful imagery and imaginative props such as glass, metal nails, sprinkles, knives and fruit to parallel with the emotional narration:

Endometriosis sufferer Rhoda Hierons reads her own words aloud with a gorgeous and vivid backdrop, describing the pain of sex as “glass shattering inside you and embedding itself”.

Sindha Agha emotively explains the meaning behind her video: “I’m trying to create an external language for women’s innermost experiences,” she claims.

“As women, I feel we’ve been led to believe that many of our experiences are indescribable, incommunicable; that even when we can figure out how to talk about what happens inside our bodies and our minds, that we’d better not — that others don’t want to hear it because it’s too gross, too sad, too strange. Above all, that we won’t be understood."

System injustices in healthcare need to change if women ever want to truly understand and gain respect for their own bodies.

Women have never been given the tools to communicate their pain, especially not during sex. Language is not in a woman’s favour, even the medical understanding of the female anatomy is not where it should be.

Without the words, women cannot use language to communicate.

Without language, there is no voice that can even attempt to ask for the help that they desperately need. 

For more information, check out some of these informative websites on pain and female sexual health:

Mayo Clinic – Dyspareunia

https://www.mazewomenshealth.com/painful-sex-vaginal-pain/

Ask Me About My Uterus -New York Times

Centre for Vulvo-Vaginal Disorders

https://Sexual Advice Association UK

https://YouTube- Pelvic Pain

https://rebelliousmagazine.com/guide-reclaiming-pleasurable-sex-dyspareunia-beyond/ 

American College of Obstetrics and Gynaecologists

Vulval Pain Society

Endometriosis Society of Ireland

Feature image: Agnes Cecile/Instagram/@agnes_cecile

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Gender bias in the medical industry is becoming increasingly more prominent as a direct result of women sharing their stories and opening up about their experiences with pain and illness.

Just last year, a study carried out by the Heart Association and the National Institutes of Health found that women are less likely to be given CPR. Men were more likely to survive cardiac arrest in a public place by a massive 23%.

This year alone, the CervicalCheck scandal has rightfully caused outrage in Ireland, when it was reported that hundreds of smears were in fact out-of-date, which resulted in the wrongful diagnosis of numerous women who could have survived if they had been given the accurate results in time. Only mere weeks ago, cervical cancer sufferer and campaigner Emma Mhic Mathúna died aged 37, a mother of five.

In tragic and life-altering instances such as these, women deserve compassion and respect in their healthcare journeys, it has since been reported that doctors were told to "use their own judgement" regarding whether or not to tell patients about their misdiagnosis.

The right to information surrounding your own body should be the lowest bar set, it cannot simply be a privilege for the few. Bodily autonomy has never been an equal playing field for men and women.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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Vicky Phelan sued the US laboratory who wrongfully interpreted the results and was awarded €2.5 million in compensation by the High Court, after finding out in September 2017 that her 2011 smear test was a false negative.

In 2016, researchers at University College London found that women with dementia receive worse medical treatment than their male counterparts with the same condition. I could go on.

Statistics and cases such as these may seem like aberrations in the system, yet so many women claim to experience sexism in their GP clinics, local hospitals and consultants offices every day.

Gender, race and poverty are undeniable biases in healthcare- none of these should ever be ignored.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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Sexism has been a major factor in medicine since time began, from Aristotle’s declaration that the female form is naturally inferior, to the connection of the uterus with apparent female “hysteria” in the middle ages, trying to get a doctor to empathise with female pain can be draining and hugely frustrating.

This is not helped by the fact that the majority of consultants and specialists are male, and are rarely trained to spot female symptoms or female illnesses in the same detail as those of the male body.

It may seem absurd in this day and age that the Victorians confined women to asylums, whether they showed any evidence of mental illness or not, but doubt still leaks into clinics and hospitals when it comes to female pain.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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The fact that women have to go through the most difficult time to get a diagnosis of female illnesses such as fibromyalgia and endometriosis speaks volumes into the lack of funding which goes into researching these diseases, which affect thousands of women nationwide.

Fibromyalgia is still suspended in the disbelief of numerous practitioners, despite women pertaining symptoms for years at a time without gaining any appropriate treatment.

Lady Gaga has recently spoken out as a sufferer of this condition, asking for better healthcare to treat this complex disease which causes total body pain.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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Women are portrayed as hysterical hypochondriacs, and men are constantly depicted as the silent stoic types, who refuse to show weakness in the form attending a prostate exam that could save their life.

The Girl Who Cried Pain represents a 2001 study by Anita Tarzian and Diane Hoffman which examined pain management and gender. It showed clearly that women were far less likely to be given pain relief or long-term medication for pain (drugs such as Gabapentin, Lyrica and Amitriptylene), and it also revealed that women are less likely to gain the adequate treatment by healthcare providers.

Ask Me About My Uterus by Abby Norman is another fascinating read which describes her torturous experience of trying to get a diagnosis for her endometriosis, a dangerous illness where uterine tissue grows on organs outside of the womb. Often the only treatment is sedatives, or a hysterectomy. Endometriosis UK has claimed that despite the illness affecting 1 in 10 women, it takes an average of nine years to get a diagnosis.

I had to beg my own consultant for a laparoscopy exam after two relentless years of chronic abdominal pain, and he stopped my GP from prescribing me my vital pain medication after claiming that there was “no reason” for my pain. AKA, he didn’t believe me.

I have since been diagnosed in the US after three years with a congenital pain condition where I was born with a vast excess of nerve endings at the base of my spine, which affects over 13% of women, and yet not a single doctor in Ireland or Britain could offer any treatment or advice.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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When I went to America, the specialist who has thousands of female patients who travel across America to see him told me that he is refused funding daily for his clinical trials and research into female pain, for the reason that all the funding is instead siphoned into drugs aimed at male pleasure, despite there already being several high-quality treatments.

According to PubMed, there are currently over 2,000 trials focusing on erectile dysfunction, and a grand total of 300 on EVERY TYPE of female pain.

If you don’t believe that stigma and sexism is prevalent in healthcare, maybe question why it’s so easy for a man to walk out of a GP clinic with a prescription for Viagra, yet it takes a woman in excruciating pain nine years to get told she has endometriosis, a life-long illness.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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Since 1995, it has been confirmed that women experience stimuli at a more intense level than men.

Women have a proven different experience of pain than men, surely they deserve to be taken as seriously?

Yet society has conditioned women to ignore their pain, to handle it with clenched teeth and no complaints.

If you’re going to focus entirely on male pleasure, don’t ignore female pain, because it won’t be kept silent.

By Kate Brayden

Feature image: Instagram/@kdkatcricket

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