The research on pelvic pain and specifically on sexual dysfunction has focused on heterosexual women, leaving a large gap in the clinically-based evidence. A study published last year in the Journal of Sex & Marital Therapy aimed to narrow this gap by studying the characteristics of vulvar pain in women in a variety of relationships. The associations between qualities such as love and communication were evaluated in relation to the participants' perceptions of how pain influenced their relationships. Within the research report, the authors establish that pelvic pain commonly causes pain and limitation with sexual function, and that queer women (defined in their work as women who identify as something other than heterosexual) also experience pain with sexual function.

The women in the study provided information about demographics, experiences of genital pain and pain characteristics. They completed surveys including the Dyadic Trust Scale (measures trust in a close relationship), the Rubin Love Scale (assesses level of romantic love), and the Communication Subscale of Evaluation and Nurturing Relationship Issues, Communication and Happiness Marital Satisfaction Scale (measures level of communication). Participants' average age was 25, and of the 77% who were in a relationship, most (60%) were in a mixed-sex relationship. Average length of relationships was 3 years, with nearly 84% of the women being white with some level of higher education.

Of the 839 women, 31% reported genital pain, with 12% of the women with genital pain in a same-sex relationship, 67% in a mixed-sex relationship, and 21% being single. Of the 260 women reporting genital pain, 39% identified as heterosexual, 15% identified as lesbian, and 46% identified as bisexual. The most common pain locations reported were inside the vagina (48%), in the pelvis or abdomen (45%), at the vaginal opening (39%), and 21% of the women reported global vulvar pain. From the data, the authors also report that women in same-sex relationships were likely to report that tampon insertion was painful.

The authors point out that challenges to healing for women who identify outside of heterosexual are many, and can include:

- homonegativity and heterosexism at a medical provider's office
- failure to disclose sexual identity due to fear of negative interaction
- fear that a symptom is linked to a sexual practice
- being in an unsupportive relationship or having poor adjustment within relationship

The limited research on sexual pain in women in same sex relationships has highlighted strengths within the relationships as well. Women in same sex relationships have been noted to have more effective communications skills, which may in turn foster better understanding of conditions such as pelvic pain. The authors concluded that while the characteristics of vulvar pain were similar across groups, there was a difference in the perception of pain impact on relationships. Better communication for same-sex couples and more love for mixed-sex couples was positively associated with impact on relationship. Of the women reporting pain, nearly half of the participants indicated that the pain negatively impacted their relationship in general, and 64% reported that the pain interfered with sexual health.

This type of research provides insight for pelvic rehabilitation clinicians and adds to our data base of considerations when working with women. The truth is that most of us were not provided adequate training in how to evaluate and manage issues of sexual health, nor were we provided with the means to value our own sexuality as a normal and healthy part of being. This lack requires education to fill in our own gaps, so that we can be of best service to our patients. If we are able to be present and nonjudgmental, our patients can in turn share openly and provide information that can direct best care. Holly Herman, co-founder of the Pelvic Rehabilitation Institute, offers a 2-day course in Sexual Medicine, so that providers can learn more about healthy sexuality as well as how to dialog with our patients.

The following comes to us from Herman & Wallace faculty member Michelle Lyons. Michelle travels the world spreading the word about pelvic rehabilitation and the powerful benefits it can have on a patient's everyday life. Michelle will be teaching her newest course, "Oncology and the Female Pelvic Floor: Female Reproductive and Gynecologic Cancers" in White Plains, NY this August 14 - 15. Join her to learn more about evaluating and treating oncology patients.

According to the Scientific Network of Female Sexual Health and Cancer, ‘Sexuality is an experience that really is at the intersection of mind, body and relationship, and cancer treatment can impact all three of those elements”. Dr Sharon Bober of Dana Farber says ‘Part of the problem is that doctors are so focused on saving a cancer patient's life that they forget to discuss issues of sexual health. My sense is that it's not about physicians or health care providers not caring about your sexual health or thinking that it's unimportant, but that cancer is the emergency, and everything else seems to fall by the wayside".

If you harness the power of Google to look up female sexual dysfunction after gynaecologic cancer, you may see phrases like ‘Possible sexual side effects…’ or ‘Cancer treatment can cause physical changes that make having sex more difficult’ or even ‘cancer treatments may make intercourse painful’. To call these descriptions ‘understatements’ does not really do them justice.

For many women post-gynaecological cancer, resuming sexual function can be a multi-faceted problem. Issues can range from dealing with Cancer Related Fatigue and nausea, vomiting or diarrhea to physical changes in the size and shape of the vaginal canal. Cancer treatments can also cause hormone imbalances and tissue damage. Add to this issues with post-surgical/radiation adhesions, a disruption to the ability to produce lubrication, challenges to the musculo-skeletal systems within the hips and the pelvis as well as the onset of medically induced menopause….well you get the picture.

In a 2009 paper, ‘Interventions for sexuality after pelvic radiation therapy and gynaecological cancer’, Katz talks about the fact that ‘…very little attention has been paid to the sexual difficulties women experience after radiation to the sexual organs. There are a limited number of interventions for the woman who has been treated for gynaecological cancer with radiation. These focus on the provision of information and some specific suggestions related to treating vaginal dryness, the need for vaginal dilatation after radiation therapy, and management of fatigue. In ‘A systematic review of sexual concerns reported by gynaecological cancer survivors’ (Abbot Anderson 2012), the author points out that common concerns in the physical dimension were dyspareunia, changes in the vagina, and decreased sexual activity.

In the psychological dimension, common concerns were decreased libido, alterations in body image, and anxiety related to sexual performance. And in the social dimension, common concerns were difficulty maintaining previous sexual roles, emotional distancing from the partner, and perceived change in the partner's level of sexual interest.

The good news is that you can return to a normal sex life after surviving gynaecological cancer – particularly with the help of a skilled pelvic rehab provider.

In part 2 of this blog series, I will look at specific interventions in sexual rehab for the gynaecological cancer survivor. Interested in learning more about pelvic rehab and oncology? Join me in White Plains in August!

A US study published in the International Society for Sexual Medicine last year reports on the available evidence linking cycling to female sexual dysfunction. In the article, some of the study results are summarized in the left column of the chart below. On the right side of the column, we can consider ideas about how to potentially address these issues.

Because women tend to be more comfortable in an upright position, the authors recommend that a recreational (more upright) versus a competitive (more aerodynamic and forward leaning) position may be helpful for women when appropriate. Although saddles with nose cut-outs and other adaptations such as gel padding in seats are discussed in the article, the authors caution against making any distinct recommendations due to the paucity of literature that is available. The paper concludes that more research is needed, and particularly for considering the varied populations of riders ranging from recreational to racing.

Within a pelvic rehabilitation setting, applying all orthopedic and specific pelvic rehabilitation skills is necessary for women cyclists who present with pelvic dysfunction. Because injury to the perineal area including the pudendal nerve can have negative impact on function such as bowel, bladder, or sexual health, skills in helping a patient heal from compressive or traumatic cycling injuries is very valuable. To learn more about pudendal nerve health and dysfunction, the Institute offers a 2-day course titled Pudendal Neuralgia Assessment, Treatment and Differentials: A Brain/Pain Approach. This course is offered next in Salt Lake City in April, so sign up soon!