pain with sex

Endometriosis and Endo-Related Sexual Pain

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Endometriosis is a painful, chronic, inflammatory condition that is poorly understood but affects more than 1 in 10 women and an uncounted number of gender diverse people. Previous articles have discussed endometriosis in general and some of the specific symptoms and complications that may arise. Hallmark symptoms include painful periods, painful bowel movements, and painful sex. Fatigue is another major symptom associated with endometriosis, and one which is frequently discounted by physicians due to it being such a challenging symptom to objectively measure. Currently, the gold standard for diagnosis is diagnostic laparoscopy, and the gold standard for treatment is laparoscopic excision.

In this interview, Philippa Bridge-Cook, an international endometriosis advocate, describes how the disease of endometriosis involves tissue that is similar to the lining of the uterus, which grows outside of the uterus. Often this tissue is in the pelvic area, but can also be in other parts of the body completely unrelated to gynecologic structures. These tissue growths are inflammatory and can be hormone-responsive, meaning that often people with endometriosis experience increased pain during menstruation, which can be severe and debilitating. However, endometriosis has much wider-reaching consequences “just” period pain.

Painful bowel movements may occur due to the location of these lesions, either on or within the bowels, or surrounding structures. They may also be related to chronic inflammation in the body. Digestive difficulties may extend beyond pain and include severe bloating, gas, painful cramping, and sensations of fullness, food sensitivities, diarrhea or constipation.

Painful sex can occur and may be related to either the location of these pain-producing lesions (for example, if they are in a place that is directly affected by sexual contact, and therefore directly irritated), or it may be related to pelvic floor dysfunction that arises due to chronic pain. Pain may be experienced during arousal, sexual touch, sexual penetration, orgasm, or after sexual activity.

As a Doctor of Physical Therapy, this specific complication of endometriosis falls squarely into my wheelhouse, and I treat many patients who are suffering from pelvic floor dysfunction related to chronic pain. In this interview, Philippa and I talk about how the pelvic floor muscles (muscles in the area of the groin that control urination, defecation, and contribute to sexual function) can become tense and tender due to the stress of chronic pelvic pain. During sexual activity they may be painful to touch, painful to penetration, or painful when they contract reflexively during orgasm. I discuss physical therapy for sexual pain here (link: Physical Therapy for Female Sexual Pain).

Dr. Bridge-Cook discusses not only the generalities of endometriosis and endo-related sexual pain, but also actionable, specific strategies for charting symptoms, speaking with your physician, and pain management. She reviews different imaging techniques, surgical techniques, and incomplete/inaccurate treatments. She is a true expert in the subject, informed by her years of personal experience as well as her extensive research and advocacy work. She speaks in a way that is easy to understand and provides hope, closing by encouraging women to not give up and to seek help with physicians that are willing to take them seriously.

Endometriosis and Sexual Pain

Share Your Endometriosis Story

Endometriosis affects millions of women but goes largely undiagnosed for years and treatment options are limited. To raise awareness about endometriosis and build the knowledge base, we need your help. Share your experience and your knowledge about living with endometriosis. To learn more, click here and send us a note.

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Thirty Years of Painful Sex Resolved With Pelvic Therapy – An Interview

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In a previous article (Sexual Pain: It wasn’t the ovarian cyst), I presented the clinical case of a woman in her 50s who had experienced painful sex for 30 years. This patient had seen scores of physicians, received multiple diagnosis, and had two surgeries to try to address her pain. Unfortunately, her pain with sex continued.

Over the years she had received diagnoses ranging from endometriosis, to fibroids, to ovarian cysts. She had surgery to remove endometriosis and later on also a hysterectomy. Her pain with sex, known as dyspareunia, continued. She experienced the pain with deep vaginal penetration, that felt like stabbing deep into the right side of her pelvis, her back, and up her right side. Eventually she was experiencing this pain throughout the day, as well as during sex. In addition she experienced digestive difficulties, with no explanation to be found. She says, “Nothing was changing, and I gave up. I pretty much gave up and said to myself ‘this is what I’m dealing with.’”

The mentality of her doctors was, in her words, ‘suck it up, buttercup’. She describes how relationships can start to drift apart when sexual pain is a chronic problem. So, she decided that she would just have to live with it, and lied to her husband about the frequency and intensity of her sexual pain. Eventually, after so many years and so many doctors, she lost hope. Fortunately, though, she never gave up.

With luck and through an indirect path, she was introduced to pelvic floor physical therapy and finally, after a series of treatments, found relief. She explains,

I gave up. I thought I had tried, and I had googled, and I had looked, and all the doctors… And I want to put the onus on other women, the female physicians that I saw! No one talked about physical therapy ever, ever.

In the previous article, I discuss the clinical side of her case. In this interview, she tells about the personal side, her many years of pain, doctors, and finally how it felt to find relief. She gave permission for these articles and interviews because she wants other women to know that it is possible to find relief, even if it’s been many years of pain. She doesn’t want other women to give up hope. She stated it best, saying

Put yourself first, make sure that you’re listening to your body, doing what’s good for your body, making sure that you’re going to the doctor, getting checked out, not taking no for an answer, or not taking that first answer. Look at how many doctors I saw… 8? 10? Who knows how many different OB GYNs or just GYNs that I saw? And none of them gave me that answer that potentially could have avoided surgery. But the goal is to listen to your body and make sure to find the answers. And know that it’s okay to question a physician. It’s okay to question, right? As long as there’s respect there, the physician should be open to you asking questions.

Painful Sex Resolved With Pelvic Therapy

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More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, and like it, please help support it. Contribute now.

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Vaginismus: Inability to Tolerate Vaginal Penetration

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“It’s all in your head.” “Just relax.” “Have a glass of wine before sex.” These are direct quotes, from uneducated and insensitive gynecologists to my patients when they try to open up about the difficulty they are having with sex. Patients leave these visits feeling like they are crazy or defective. Some patients have gone decades in sexless marriages, not knowing that they had a diagnosis for which treatment was available.

Vaginismus is a severe, reflexive tightening of the muscles at the vaginal opening (pelvic floor muscles) that prevents penetration. Someone with vaginismus often cannot tolerate the use of a tampon, internal gynecologic exam, or penetrative sex. In my experience, this physical tightening is often coupled with a feeling of upset, avoidance, or what I call the “ick” factor. This is more than just tight pelvic floor muscles- this is a protective spasm that completely prevents penetration. Attempts at penetration are upsetting and painful, and both the patient and their sexual partner are at a loss as to what to do. Physicians performing pelvic exams are often insensitive to the condition, believing that the patients are being overly dramatic, uptight, or difficult. Emotionally this only makes matters worse, at a time when patients are especially vulnerable.

There is value to having a name for something because it makes it possible to have clear conversations about it. “Primary” vaginismus means that the person has never been able to have penetrative sex, and has probably never been able to use a tampon or have an internal gynecologic exam. “Secondary” vaginismus indicates that the person has had normal sexual function in the past, but developed vaginismus as a result of some change in their lives. Vaginismus may be related to a history of trauma, or the patient may have no memory of a traumatizing event. It might be related to a sexually or emotionally repressed background, or not at all. A history of pain, surgery, cancer treatment, or hormonal changes may precede secondary vaginismus.

Pelvic Floor Dysfunction and Vaginismus

To understand the diagnosis it is helpful to have a little background on the muscles in that area. The “pelvic floor” is a group of muscles located in the area of the genitalia- it works to control urination and defecation, to support the organs against gravity, to help with core stability and postural support, and to participate in sexual function. It often works completely reflexively, whether it be to hold in urine when we cough or laugh, to relax to have a bowel movement or to rhythmically contract and relax during orgasm. Just like any other muscle in the body, when it perceives pain or danger it can also go into spasm. With vaginismus, this protective spasm closes off the vaginal opening.

The spasm is completely outside of the person’s control and can be upsetting, painful, and frustrating. It can be inconvenient, in the case of being unable to use a tampon, and can interfere with someone’s ability to receive medical care, in the case of a gynecologic exam. It can prevent women from consummating a marriage or getting pregnant naturally, interfere in intimate relationships, and can cause significant emotional distress.

It takes a great deal of courage to reach out for treatment for vaginismus, and any patient seeking care deserves to be treated with respect and with sensitivity, and after fully informed consent.

In my practice, we treat vaginismus from a multidisciplinary perspective and our patients have great success. Treatment may be a slow process, depending on the individual patient’s situation, but with consistency, it is possible to achieve normal sexual function. We suggest a multimodal approach, which includes one or more of the following: physical therapy, medical review, and potentially medication, counseling (which might include cognitive behavior therapy or EMDR), and sex therapy.  I will discuss the physical therapy side of things and have invited a gynecologist as well as a sex therapist to review their approaches as well.

Physical Therapy for Vaginismus

It is normal for muscles to tighten in response to immediate pain or danger, but with vaginismus, the muscles spasm in the absence of these things. Physical therapy focuses on re-educating the muscles to understand that they don’t need to spasm in response to a non-dangerous situation, such as consensual sex. We accomplish this using dilator training, muscle relaxation techniques (both at the pelvic floor and also in the core, spine, and hips), and lots of education. Let’s talk about each one to understand how PT can help heal vaginismus:

Dilator training is not at all what it sounds like! Rather than trying to “stretch”, it involves progressive desensitization of the vaginal opening. It is simple to do and can be done at home on your own. You would start with a small dilator and simply rest it at the vaginal opening. Over time the area becomes less sensitive to touch and the muscles will relax. You might then insert the dilator just one or two millimeters, until you feel tightness building again. At this point you would stop and wait again, allowing the nerves and the muscles there to become acclimated to the sensation. Throughout the process, you can be doing relaxation techniques given to you by your PT or your counselor. It is very slow, very gentle, and always at your own pace. Consistency is key. Over time you progress through larger dilators until you are able to reach your goals, whether they be tampon use, or sexual penetration.

Muscle relaxation techniques might include breathing exercises, hip and back stretching, biofeedback training, and manual treatment provided by your physical therapist. People with vaginismus often have other muscles that are very tight, such as in the buttocks, abdominals, and inner thighs. By helping to relax these muscles the pelvic floor can also be facilitated to relax.

Lastly, education is incredibly important. Understanding your anatomy and your diagnosis is empowering. You might want your sexual partner to come with you for a session to learn about your diagnosis and even learn to help you with your self-treatments. Communication with your partner is learned and practiced in these sessions. Strategies for progressing to penetrative sex can be discussed, and optimal sexual positioning for your particular needs can be determined. Strategies for engaging with gynecologic exams and physicians can be reviewed. Tips for tampon use or other personal goals can be discussed. Knowledge is power.

While physical therapy can provide self-care training (dilators), muscle relaxation techniques, and education, it works best in conjunction with gynecologic care and psychotherapy.

Gynecological Care

At the very least, every patient needs to be evaluated to determine if there is an underlying condition that needs to be managed, such as infections, skin diseases, or hormonal changes.  These underlying conditions must be treated in order for vaginismus to be successfully resolved. Your physician can also offer medical interventions that may speed your recovery.

Dr. Tessa Krantz, a urogynecologist specializing in non-surgical management, explains the variety of medical interventions that are available to patients:

  • Oral medications can be used to manage stress and anxiety associated with an inciting event, such as a benzodiazepine (Xanax, Ativan) for short-term relief of anxiety, or Serotonin Reuptake Inhibitors (SSRI) medications to assist with overall anxiety.
  • Vaginal suppositories containing a variety of medications may provide a more localized treatment directly to the muscles of the pelvic floor. Vaginal diazepam is frequently used to treat pelvic floor tension myalgia and pelvic pain associated with Vaginismus. Vaginal administration of diazepam results in lower peak serum plasma concentration than oral administration.
  • Compounded topical creams may assist with pain management if needed. These creams may include medications for neuropathic pain such as ketamine, gabapentin, clonidine, and lidocaine.
  • Trigger point injections are injections of a local anesthetic to the muscles of the pelvic floor that are tightening and causing pain. Dry needling may also be an option for relieving these trigger points. Injections of this type can be done in the office, in an outpatient setting. After a trigger point injection, a patient may go home and actively use her pelvic floor muscles. These are generally safe and provide significant pain relief within 24 to 72 hours of treatment. Risks are low, the most common is temporary numbness around the injection site and bleeding.
  • Botox is a neuromodulator that relaxes muscles when it is injected- it may be injected into the muscles of the pelvic floor to prevent them from contracting. This may assist to break the cycle of fear/anxiety, muscle tightening, and pain. Injections of this type are typically done in an operating room setting. Results are not permanent and can last from 4 months to a year and may require more botox injections in the future. Side effects may include pain and discomfort at the injection site, swelling at the injection site, and urinary tract infections. However, these risks are low.

Counseling and Sex Therapy

Dr. Sally Valentine, a licensed clinical social worker, and AASECT certified sex therapist explains that the role of sex therapy in clients with vaginismus is to help reduce the psychological components contributing to pelvic muscle spasms, or impacted by the condition, and to work toward a positive and pleasurable sexual template for the client to move forward with. This includes addressing issues that may have developed or co-existed as a result of vaginismus such as anxiety, depression, hypervigilance around sexuality or sex, avoidance of sex, fear of penetration, sexual fear, obvious sexual pain (inherent in the diagnosis), sexual shame, relationship conflicts, sexual relationship decline, fear of intimacy, unprocessed sexual events, such as sexual assault and/or trauma, or even traumas experienced in the process of finding the correct diagnosis.

She describes how she structures treatment around a few key steps, starting with a thorough history taking and using the PLISSIT model, which many sex therapists use to help organize their work:

  • Giving the patient permission to speak about all aspects of her situation and ordeal. This is an opportunity to talk about all her feelings, confusion, pain, hurt, frustration, anger, rage, resignation or hope.
  • Providing information. This starts with understanding what the client already knows, and then filling in the gaps, as well as correcting misunderstandings of myths. This can help demystify the condition, improve sexual communication, and provide resources.
  • Providing specific suggestions, such as breathing exercises, journaling, stress reduction techniques, and sensate focus exercises.
  • Providing intensive therapy as needed. This might include cognitive behavioral therapy to address cognitive distortions, emotional dysregulation, or maladaptive behaviors. It might include EMDR or hypnotherapy, which are modalities that focus on healing from trauma.

Each specialty, physical therapy, gynecologic care, and psychotherapy/sex therapy, has an important role in treating vaginismus. While it can be challenging to find expert care providers, we hope that this overview has given you confidence that you are not alone in your experience, and that there are proven treatment methods available to you. Whatever your goals are, whether it be to participate in penetrative sex, use a tampon, or go to the gynecologist, it is possible to achieve them.

To connect with Dr. Krantz, you can reach out through her website at Women’s Home Health.  To connect with Dr. Valentine you can find her information here. Dr. Wakefield can be reached at Well Springs Health.

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More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, like it, please help support it. Contribute now.

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Sexual Pain: It Wasn’t the Ovarian Cyst

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In previous articles, I have discussed female sexual pain, some common diagnoses, and options for treatment via physical therapy. In this article, I’d like to describe a less common source of sexual pain that I encountered in a patient, and how we successfully treated it. I am describing her case with her permission, and we both hope that it is useful to other women who may be experiencing something similar.

Although it was assumed that her pain with sex was coming from an ovarian cyst, the source of her pain was actually elsewhere, and she is now essentially pain-free. When this woman arrived for treatment, she described a 30-year history of pain with vaginal penetration during sex (pain with penetration during sex is called “dyspareunia”). This pain was on the right side, deep and stabbing, and pierced from her front to her back and all the way up her abdomen. It occurred all the time, but she didn’t let it prevent her from having sex. In fact, she often didn’t tell her husband about the pain, because she knew that it was unavoidable and still wanted to have an intimate physical connection with him. Although some positions were better than others, the pain was always there.

She had made several attempts to evaluate and address the pain. In 1991 she was diagnosed with endometriosis and was told that the only cure would be to have children and then have a hysterectomy. Surgery for endometriosis didn’t improve her dyspareunia. When her doctor found a fibroid on the right side of her uterus, she had a partial hysterectomy (removing the uterus but leaving the cervix and ovaries). Unfortunately, the pain continued. From then on her and her doctors assumed the dyspareunia was related to chronic ovarian cysts. She came in for physical therapy treatment because she knew she had scar tissue from the endometriosis and surgeries. She believed that addressing this scar tissue could benefit her, and would hopefully improve her symptoms.

Pelvic Therapy For Dyspareunia

To understand what we were evaluating and treating, it is helpful to have some background information on what “pelvic health” physical therapy is and what treatment of the “pelvic floor” involves.

The pelvic floor is a group of muscles that are located in the area of the genitalia in both men and women. It functions to support the organs, to coordinate with the other “core” muscles for postural stability, to control urination and defecation, and to contribute to sexual function. Treatment of these muscles and pelvic structures can be done externally, vaginally, or rectally, and should only be done by a practitioner specifically trained in this area, such as a pelvic health physical therapist.

When she arrived for Pelvic Health physical therapy evaluation, this patient did have an ovarian cyst that was being actively monitored by her physician. The lateral location of her sexual pain, how it was triggered by deep penetration during sex, and the diagnosis of ovarian cysts, seemed consistent. I evaluated her with the initial presumption that her diagnosis was correct, and that her painful sex was indeed coming from the ovarian cyst.

However, during my evaluation, I found that I could reproduce her pain by palpating some of her deep pelvic floor muscles. I could also reproduce the pain by palpating around (but not on) the ovary externally. I found connective tissue restrictions in the area of her ovary, small intestines, and colon. Curious and encouraged, we started treating these areas, albeit very cautiously since she did have an active ovarian cyst that was being monitored. We didn’t want to risk irritating or even rupturing it.

By the end of her series of sessions (12 sessions spread out over 5 months), which were focused on treating the pelvic floor muscles, connective tissue restrictions, and visceral mobility, she had almost no pain with sex. Her ovarian cyst was still there, but she could have sex in almost any position without pain. This was an excellent outcome.

We will never know precisely, but I believe that due to endometriosis, surgeries, and chronic ovarian cysts, she had developed connective tissue restriction that limited her tissue mobility during sex. I believe that she also developed pelvic floor muscle dysfunction related to years of irritation and tension. While I do believe that the ovarian cysts probably contributed to her sexual pain, the major driver turned out to be connective tissue restriction and muscle dysfunction.

This was a good reminder for me as a practitioner to acknowledge the known issues, but also to stay curious and investigate further. This patient had suffered for 30 years, receiving multiple surgeries and even removed an organ (her uterus) to try to resolve her pain. Through specialized physical therapy, she finally found relief and is now able to have a pain-free sex life.

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More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, and like it, please help support it. Contribute now.

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Physical Therapy for Female Sexual Pain

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In a previous article, I discussed some of the many possible causes of female sexual pain. In this follow-up I will discuss how physical therapy can address some sources of pain with sex, give guidance on how to find a therapist, and offer tips to consider when engaging in this specialized type of physical therapy.

A thorough examination by a gynecologist is always the first step in addressing pelvic pain, as not all causes of pain can be treated with physical therapy. Physical therapy works best to address issues including nerve sensitivity, muscle dysfunction, alignment, fascial mobility, and scar tissue.

How Do You Know If Physical Therapy Can Help You?

Your gynecologist may refer you directly to physical therapy for treatment of your pain. Unfortunately, some physicians are not aware that physical therapy can address these issues, or may not know a therapist that they feel confident sending you to.

Here are some signs that specialized pelvic PT may be able to help you:

  1. The gynecologist has not found any medical issues causing your pain. If you have visited your doctor, had a thorough evaluation, and have not had any medical findings, your issues may be musculoskeletal. In that case, evaluation by a pelvic PT is warranted.
  2. Issues with urination or defecation. For example, delayed or incomplete urination, pain with bowel movements or urination, urinary frequency, or urinary leaking may indicate pelvic floor dysfunction.
  3. You have a history of chronic infections, inflammation, or physical trauma. These can cause restriction of the connective tissue in and around the pelvis and pelvic floor. This restriction, over time, builds up and can limit mobility or put strain on pain sensitive structures. Examples might be chronic yeast infections, endometriosis, falls to the tailbone, or sexual trauma.
  4. You have a history of surgeries or scar tissue. Scar tissue restricts the normal mobility of tissues and puts pressure on pain sensitive structures. Abdominal or pelvic scar tissue can cause pain at the site of the visible scar, or in areas that may not seem connected.
  5. You have other issues such as lower back pain, poor posture, or discomfort in sitting. The pelvis is integral to the function of the rest of the body, and dysfunctions here can lead to problems elsewhere.

What Does Pelvic Physical Therapy Entail?

Therapists in this field are specifically trained to treat pelvic structures, both internally (vaginally and rectally) and externally. The most common treatment methods that pelvic health PTs may employ are manual soft tissue work, exercise, biofeedback, and education.

Soft Tissue Work

There are many manual techniques that therapists can use to treat your muscles, joints, connective tissue, and even organs. These each of these techniques requires its’ own specialized training and should not be provided by untrained practitioners. While not a “massage,” these techniques do involve using gentle pressures, applied by hand, to improve function. The most common question I get on this subject is, “will it hurt?” This is an understandable concern – you are going to see the therapist because you have pain, and it can be a scary proposition to have someone touching already painful areas. This is certainly something to discuss with your therapist before treatment so that you are both comfortable with proceeding. In many cases the therapist will need to treat these sensitive areas in order to bring you relief. Because these areas are already irritated you may experience some initial discomfort as the therapist works with them. But the goal of treatment is NEVER to cause pain; in fact this is avoided at all costs. There are strategies that can be used, such as a physician-prescribed lidocaine gel, to make sure you are comfortable.

Exercise

When we think of exercise for pelvic health, most people think of Kegels. However, this is only a small piece of the exercises that can be helpful! Exercises may be prescribed to teach you to relax your pelvic floor, coordinate the pelvic floor with other muscles in your body, or relieve pressure on painful structures by improving posture, stability, or alignment. After evaluating you, your therapist will decide if any exercises are called for in your case. If they are, they will prescribe exercises targeted to improve your specific dysfunctions and will educate you on how to do them safely and effectively.

Biofeedback

Biofeedback is any method of giving you feedback on what your body is doing. In pelvic therapy this is commonly done to bring your awareness to your pelvic floor. Using a sensor, the biofeedback machine will determine how active your muscles are and give you a visual cue to help you learn what “relaxed” and “contracted” feels like. This is extremely useful, as many women who have pain with intercourse have muscles that have forgotten how to “relax.” They may be constantly contracted, tight, and painful. Sensors can be used internally (vaginally or rectally) or externally. There are also tools that you can use at home to continue your training outside of therapy.

Education

The primary job of any physical therapist is to educate, and this will begin on day 1 of treatment, with your evaluation. Your therapist will explain to you what s/he is doing and why, and once your evaluation is complete the results should be explained to you. From there you and your therapist will create a plan for your care. You may be educated sexual positions that might be more comfortable for you, lubricants, better toileting habits, sitting and standing postures to reduce stress on the pelvic floor, home treatments or exercises, relaxation techniques, breathing techniques, common irritants to the pelvic floor, and things to avoid as your treatment progresses. I have found that the more educated and informed my patients are, the better their outcomes tend to be! Your physical therapist can be both therapist and coach to better help you reach your goals.

So how do you go about finding a specialized pelvic therapist who can treat your pain? Your primary care doctor or gynecologist may have someone that they refer patients to on a regular basis.
If they do not, you can Internet search your city with the phrases “pelvic floor therapist,” or “women’s health therapist.” Other key phrases to help you narrow your results include “dyspareunia” (pain with intercourse) and “pelvic pain.”

You can also access directories of practitioners. For example, https://hermanwallace.com/practitioner-directory  and  http://www.womenshealthapta.org/pt-locator/. Therapists listed on these sites have taken continuing education courses in pelvic floor physical therapy. Be aware that not all therapists list themselves on these sites, as some require hefty membership fees to join.

Lastly, here are some helpful tips to consider when beginning pelvic physical therapy:

  1. Research your therapist. Not all therapists who work with the pelvis may have experience working with your particular issue. It’s okay to research the therapist online, or call them to discuss their background and training.
  2. Ask Questions. During your evaluation and subsequent treatment, ask any questions that come to you. When you get home, make a list of any questions or concerns that come up, and bring the list to your next session. The more educated you are on your body and treatment, the more comfortable you will be and the more productive your sessions can be.
  3. Communicate. During treatment please speak up if you are uncomfortable or have pain. We, as therapists, rely upon you for feedback. As I like to say, you are the only person feeling what you are feeling! Please do communicate during and after your sessions so that we can better help you.
  4. You are in charge. You will be asked for your consent to treatment before any treatment is undertaken. You can consent to all treatment, some portions of treatment, or none at all. You can also decline treatment at ANY point in a session, for any reason. Lastly, you can ask to have someone else in the room while you are treated. You are always in control of your treatment session.
  5. Keep a Journal. Keeping a journal of your symptoms may help you to track your progress over time. It can also give valuable information if you have a significant change and we are trying to understand the cause.
  6. Be Proactive. If your therapist gives you a home exercise or self-treatment plan, do your best to work with it. And if they haven’t given you one, it’s okay to ask for it. I find that the more engaged patients are with treatment, the better their outcomes tend to be.

Female sexual pain is more common than most people realize, and in many cases can be treated successfully with physical therapy. Please do not doubt yourself if you are experiencing this- you deserve to have full function, without pain, and it is worth your while to investigate treatment options.

We Need Your Help

More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, like it, please help support it. Contribute now.

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This post was published originally on Hormones Matter on February 18, 2016. 

Vulvodynia: The Silent Pain Syndrome

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I want to talk about a pain syndrome that most women have probably never heard of, but affects nearly 14 million women worldwide. It affects all races and ethnicities with Hispanic women suffering 80% more than other groups. It is a pain syndrome that those affected are reluctant to share with their partners, closest friends, or their doctors. This is because their pain revolves around and within the vaginal area, an area that we women often do not feel comfortable talking about in any company. Making this the “silent pain syndrome” and leaving women everywhere feeling alone and damaged.

This pain syndrome is known by a few names such as Vulvodynia, Vestibulitis, Dysaesthetic vulvar, vestibular adentis and vestibulodynia. It was given several names back in the 1980’s to help doctors refine and come up with treatment plans based on where the pain was located, the condition of the tissues in the vagina, or surrounding areas, as well as what provoked the pain. However, since the 80’s more and more studies have been done on the condition showing that most women who suffer with it have overlapping symptoms from one form to another. This has lead the medical community to start moving away from trying to categorize or compartmentalize it into one of these diagnoses. For the most part nowadays, it is just called vulvodynia.

Vulvodynia was recognized as far back as the 1800’s, when it was treated by surgically removing the vulvar area. Unfortunately, many of these women only got temporary relief. It unfortunately,  was left out of the medical books until the 1980’s when Dr. Edward Friedrich began reporting on it. Since then 80 studies have been done on the condition. It is not clear whether the increase in research is due increased awareness or an increase in the condition itself. The National Vulvodynia Foundation says that the average women suffering with this condition can see upwards of 15 doctors and it can take as long as 12 years to receive a correct diagnosis. This is because so many doctors are still ill informed and poorly educated on vulvodynia. The medical community is lagging in research when it comes to women’s health conditions, especially those that cause chronic pain in our genital areas.

Sadly, most doctors will push their patient’s pain syndrome off as a psychological problem, PMS, stress, lack of love for her partner or even sex in general. Many of these women find no help from the medical community and go on to suffer in pain silently, leading to other co-morbidities such as depression, anxiety, suicidal ideation, irritable bowel syndrome, interstitial cystitis and fibromyalgia. For many women who have been abandoned by the medical community, they will go on to question their own mental and emotional stability. They will often blame themselves for their condition, thinking they have somehow damaged their body physically through picking up an unknown STD or have psychologically thought themselves into this pain syndrome as many of their doctors have suggested. These women often are unable to continue having sexual intimacy, some get so bad that they reach a point of not being able to wear clothes, sit, walk or even tolerate a gynecological exam. Urinating or defecating can bring on horrific stinging pain that leaves many to cry out with the simple act of going to the bathroom, which in turn leaves them drinking less and eating less and holding their urine  or bowels for as long as they can so as to not experience that feeling. Unfortunately, doing some of these things can further the progression and pain from this syndrome as well as to create other dysfunctional conditions. For those women whose conditions continue to progress, they can be left  extremely disabled, unable to work or care for their families, which in turn leads to high divorce rates and financial losses. Couple all of that with a condition that a woman feels she has no one to share it with and it is no wonder that they often go on to suffer with depression, anxiety and suicidal ideation.

What is Vulvodynia?

Vulvodynia is known as a neuropathic or inflammatory pain condition to the genital area in women. As of yet it is caused by an unknown etiology. It is thought to be from the same family and act much like “phantom limb syndrome”. Vulvodynia causes a myriad of symptoms such as inflammation, redness around the vestibule (opening to the vagina), the vulva itself (outside vaginal lips also known as the labia major) and to the inner or small lips (also known as labia minor), as well as the vagina itself (the inside tissues). It can effect specific spots in or around the vagina, like the perineum, rectum, thighs, pubic bone or pubic hair, clitoris and the urethra. For some women it can affect all of these areas making their situation life  altering, disabling and agonizing. Women who have this condition experience stinging, burning, itching and razor cutting like sensations with the slightest of touch, making intercourse, tampon insertion, wiping or washing the area and the wearing of clothes painful to impossible.

Some women also complain of feeling as if they are dried up down there, while others feel as if their insides are falling out of them. Often when the clitoris is involved, it can cause agonizing pain that shoots up into the abdomen. In many of these cases, the women’s abdomen can become inflamed and reddened as well, leading to irritable bowel syndrome symptoms. For many the pain is so agonizing that they are left unable to wear clothes, walk or even sit. For some the pain can extend into the urethra or even the bladder setting off another pain syndrome known as interstitial cystitis. This condition can leave them in severe burning pain during and after urination.

Vulvodynia is unique to each woman with some having it constantly while others have it intermittently. Some will only suffer from specific areas of pain while others have it everywhere. Some will only have pain with intercourse while others have it with anything entering or touching  the vagina. Some will suffer with only hypersensation while others will suffer with all of them. For some the pain will be manageable while others it will be life altering. Each women’s pain level and frequency is different making this illness hard to understand and even harder to treat.

What Causes Vulvodynia?

Well that is a good question, and unfortunately, no one in the medical community has yet been able to answer. However, there are several theories about what increases the risk for developing vulvodynia.

Compressed Pudendal Nerve

We know that some women have a damaged, compressed or pinched off pudendal nerve. The pudendal nerve is a nerve that comes off the spine and innervates the pelvic floor region. It is what allows you to control urine flow or bowel movements. It is also, what activates your glands when aroused to produce the moisture in the vagina and allows you to have an orgasm. It has many important and enjoyable functions, but if it becomes damaged it can also create a lot of pain, dysfunction, and grief. Damage to this nerve can happen by a fall to the back or butt. It can be injured during labor. It can become inflamed or compressed by an arthritic condition or by a cyst or tumor. Some of these conditions can be fixed with surgery or nerve blocks, which in some instances may relieve the vulvodynia. Unfortunately, compressed nerve affects only a small number of vulvodynia sufferers.

Infections

It has also been shown in studies that 54% of all women with vulvodynia also test positive for HPV, however scientists has not been able to say with certainty that this specific viral infection is the cause for these women. Instead of it being the cause, it may just be the women’s own immune response to the infection. Researchers have also studied other viral infections that are known to cause neuralgic pain syndromes like this, such as cytomeglavirus and the herpes viral family, but have not found any evidence of these infections.

Researchers have looked at candidiasis infections as well; this is because so many women with vulvodynia have a long history with chronic fungal infections with many using repeated “azole” therapy to treat it. Yet again, they have not been able to find a link or correlation with any species of fungi. Although there is a question as to whether the use of any of the “azole” drugs could have possibly caused this condition or whether it is just associated with it because so many patients with vulvodynia are misdiagnosed with yeast infections. Due to this, the medical community warns women to be careful when using the OTC “azole” drugs and to follow the manufacturer’s recommendations. Additionally, if the yeast infection is not cleared with the usual course of treatment or a second infection develops, you should not use the cream again without first seeing your doctor.

Studies have also looked at bacterial infections as the cause, here they found that 17% of sufferers had an infection with what is known as ureaplasma, which is often seen infecting the Bartholin glands. For these women treating the infection often times cleared the vulvodyina. They also found a small number of women with the Streptococcus B infection and again in many of these cases, treating the infection cleared the vulvodynia. None of these studies have been able to state with certainty that any particular infection is the cause, but they do show that if you suffer with a long standing, chronic or hard to treat infection of any kind (viral, fungal or bacterial) you could be at a higher risk of developing vulvodynia.

Childbirth and Episiotomy

For other women there was no clear accounting of an infection but they could relate the start of it back to the birth of a child or the episiotomy. Here again we are looking at damage to the nerve or the soft tissues.

Hormonal Birth Control, Cancer Medications and Other Steroids

Other studies have implicated oral contraceptives and early childhood intercourse as a cause, both of these may be linked to hormonal imbalances. Some drugs have been implicated as the cause of it too, such as cancer drugs and both oral and topical steroids. Even though the topical steroids are used to help with the inflammation and itching in this condition, they are known to cause thinning of the tissues and sloughing. They tend to lower the immune system allowing for other infections to pop up making the situation worse.

Comorbid Fibromyalgia and Chronic Pain

Fibromyalgia has also been implicated in vulvodynia, mainly because so many women who suffer with fibromyalgia also suffer with vulvodynia. However, it is believed that fibromyalgia is due to an unknown muscular etiology and as if often seen alongside chronic fatigue. Both of which are thought to be caused by an abnormally high level of a neurotransmitter involved in pain sensation, so having this pain syndrome alongside of these would stand to make sense and put you at a higher risk for vulvodynia.

Oxalates

Older studies have suggested high oxalates in urine may be responsible for the pain. Oxalates are like little sharp slivers of glass made up of calcium that are excreted through our urine, but as of recently this theory is no longer being considered. This is because so many women have not tested positive for excessive oxalate output. Those who have gone on low oxalate diets have had some to no response, leading the scientific community to suggest that the oxalates themselves are not the problem but instead the fragile irritated tissues that the oxalates cross are more the issue. Now even though this may not be the cause, going on a low oxalate diet may be worth a try to lessen the pain. Another study suggests pH imbalances may be involved, but again cannot be confirmed as of yet and does not hold true for every women.

Inflammatory and Allergic Reactions

Recent studies have shown a correlation with inflammatory allergic reactions, like those seen in people with mast cell reactions. This is also seen and been implicated in interstitial cystitis too. However, we are still in the beginning phases of understanding not only this correlation but also Mast Cell Disease. If you suffer from this, you may be at a higher risk of developing vulvodynia as well.

Researchers at John Hopkins in Baltimore looked for two cytokines (immune stimulating cells) associated with inflammation. They found significantly higher levels of interleukin 1 beta and alpha necrosis tumor factors in test subjects. This would suggest that there is an inflammatory process going on, possibly due to an autoimmune problem. Then pathologists out of Rotterdam in the Netherlands found through biopsies chronic inflammatory infiltrates in all the patients and none in the control group. The infiltrate was composed of T-Lymphocytes as well as a small number of B cells, plasma cells, mast cells and monocytes. An immunoglobulin important in antibody reactions, IgG was found in plasma cells of 75% of the patients. This again suggests that there is an inflammatory process caused by an autoimmune reaction going on, however, they are not ready to confirm or deny this yet.

Finally, the University of Iowa has found impaired natural killer lymphocyte activity in the women effected as compared to a control group. Natural killer cells are needed to defend the body against certain cancers, so this finding may explain why some women with vulvodynia also suffer with dysplasia, despite having not contracted the aggressive cancer producing HPV strains. This finding may bring us back to implicating the HPV virus. However, this is all new information and nothing has been confirmed yet.

Diagnosing Vulvodynia

There is no specific test for this condition. It is diagnosed by ruling out other conditions and diseases. Physicians may want to test and treat for any infections first and see if that relieves the pain. If not, then it may be vulvodynia. Vulvodynia is frequently misdiagnosed as a chronic vaginal infection from fungi or bacteria. However, if your cultures are negative for an infection you may want to consider vulvodynia.

Treating Vulvodynia

This is the million-dollar question that both women and vulvar pain specialists are asking. Unfortunately, we really do not know what causes it. This means that without an identifiable factor, we are guessing at how to treat it. We also know that every woman experiences vulvodynia differently, making a “one size pill” that treats everyone impossible. Each woman will go through a trial and error with treatment modalities. This can often make the journey long and tedious, as well as, quite discouraging and even painful, especially when something heightens the pain instead of lowering it. This is why it is very important to get involved with a vulvar pain specialist, not just a pain clinic or pain doctor, but one that has been truly trained in treating this condition. Here are some of the many modalities in the arsenal to treat vulvodynia.

  1. Trigger point injections. This will numb the area for a few hours to days, giving some relief with the hopes that they will be able to shut off the nerve or reprogram it. Lidocaine is usually used for this. However, this procedure can be quite painful and risks damaging the nerves and tissues further, so for many women this is not an option. Now some doctors will also prescribe lidocaine jelly or even xylocaine jelly to be smeared on the painful areas. These can topically numb the tissues and nerves, giving some minor relief for a few hours. Although once again, for some women just putting this gel on can be too painful and does not last long enough to make it worth it.
  2. Topical steroids. These are often prescribed to help with the itching and inflammation, even though research has repeatedly shown them to be ineffective.
  3. Baking soda douches. If the vagina is too acidic, some doctors will recommend baking soda douches, which is non-toxic and in a few cases, it can help.
  4. Interferon. Several studies have tried treating women with interferon. This has shown some success, but the relapse rate is very high and one study showed that using interferon on women who do NOT have HPV actually worked better.
  5. Topical estrogen creams, progesterone and/or testosterone. Early research was promising. However, it may be painful for those women who cannot tolerate any kind of a cream placed around or in the vagina. It is important to note that estrogen cream can activate Mast Cell Syndrome.
  6. Prophyllin compresses. Some women find compresses made of prophyllin ( a prescription powder) to be soothing to the area.
  7. Low oxalate diet. Oxalates are in nearly everything we eat, but you can avoid the high oxilate foods. Doctors who prescribe this diet often times prescribe calcium citrate to go along with it. The calcium citrate helps to neutralize the oxalates in the urine. The Vulvar Pain Foundation reports the two most consistently helpful regimes for their members are the estrogen creams and low oxalate diet with calcium citrate. Another thing that sufferers report helping them is, drinking lots of water. Water dilutes the oxalates in the urine which decreases irritation.
  8. Anti-depressants and anti-convulsants. Fibromyalgia researchers have suggested that certain anti-depressant drugs may be useful in women also suffering with FMS.  Vulvar pain researchers have not done studies, however, clinical experience; they suggest that the SSRI’s are not effective in treating this condition. There is no research on the anticonvulsants.
  9. Capsaicin (an extract of the red pepper). Capsaicin has been used successfully in other neuralgic pain conditions like, diabetes, HIV, herpes infection and even in interstitial cystitis. An ongoing study of topical application suggests it may relieve pain, however, because Capsaicin produces significant burning when applied it may not be appropriate for those suffering with vulvodynia due to inflammation. It may not even be appropriate for those women with skin break down or seriously sensitized tissues.
  10. Opiates and other pain relievers. These may be effective in the short term, but long term they are problematic.
  11. Physical therapy. Specialized pelvic floor therapy has helped some women suffering with vulvodynia, especially those who also have FMS. Dr. Glazier, a psychologist from New York, states that biofeedback along with physical therapy to the pelvic floor can help to strengthen and relax the muscles in women with vulvodynia. This therapy is often also used in people with interstitial cystitis and irritable bowel syndrome too.
  12. Surgery. There are multiple surgical options but none appear to reduce the pain and many increase it.
  13. Cannabis oil. Cannabis oil applied topically has become all the rage, but as of yet, there are no studies to evaluate its effectiveness. Vulvodynia sufferers, however, report significant relief .

What is the Prognosis with Vuvlodynia?

I wish I had better news to report here and maybe one day I will have it, but for now this is not known as a curable condition. Do not be discouraged. We have many diseases that we are not able to cure but have the ability to effectively control. The first step is getting properly diagnosed and ruling out any other conditions or infections. The second step is finding a vulvar pain specialist or a vuvlar pain clinic to start the treatment process. Both of which can be found through your doctor or through the National Vulvar Pain Foundation. Once you reach this point, your journey to getting better will begin.

Please know that it may take quite a while to reach a point of lessened or no pain. It may also take several attempts at different or mixed modalities including medications, creams, diet, physical therapy and trigger point injections to find what works best for your condition. If you are also suffering with depression, anxiety or suicidal thoughts then you also need to find a psychologist to help you work through all of this as well. Please know that these mental and emotional conditions are very common in women with vulvodynia. This is due to many factors such as constant pain, loss of intimacy and all that goes along in a relationship because of it, including, a loss of self-sexual beauty and feeling damaged. Suffering in silence also causes distress. So, please if you take nothing else away from this article, just know you are NOT ALONE!

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Love Hurts – Sex with Endometriosis

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 “Bolts of electricity shoot around my abdomen and pelvis and down my leg as I lie on the pillow-topped hotel mattress, attempting in vain to remain silent. My husband’s arm, heavy from sleep, is draped over my aching body. I turn to look at him as he snores softly, blissfully unaware. No one told me the wedding night the night I dreamed about, would end with unbearable pain. Is this normal? Should it have felt like shards of glass stabbing me while moved inside me? I try not to let him hear me crying as I close my eyes and try to ignore the sharp electric-like currents terrorizing my body…

There is no one to speak to. I am the sole occupant of a vast and desolate island on which my innermost secrets cannot be shared, not even with my husband. Who to speak to? What to say? What to do when the event that should bring pulsating all-encompassing passion brings only excruciating pain instead? Who to tell when the one act that should create ecstasy and bliss causes pure agony?  I should adore the sense of unity I feel with my husband when we are together, treasure each second that my body fuses with his. But, instead, all I feel is the white-hot sear of pain when he enters me, the blackness of despair when I know that I cannot share my pain with him and the blushing red of embarrassment when he knows I am not being honest…

How can I share the feelings of torture that overwhelm my body when he is inside of me? How can I let him know that he, my beloved husband, is the cause of my misery? How can I share with him that his body alone creates immense wretchedness in mine. I will never do that to him. I will never make him aware that he is the source of the agony that rocks my body through and through. Instead, I will live with this agonizing, heart-wrenching secret of mine. This secret that isolates me, that creates a fissure so large between me and my husband that I wonder if we will survive as one. And I will continue to allow my body to be exposed to the beatings and abuse that are, in reality, tender loving touch.” 

Sound familiar anyone? Can you relate? Do you know what this girl means when she describes the pure agony that consumes her as she tries to have sex with her partner? Or the emotional turmoil she experiences as she tries to hide the pain from her partner? Well my friends, that girl is me, writing in my journal for the first year of my marriage.

You see, for many women with endometriosis, myself included, sex is not the erotic, passionate and pleasurable experience that we all wish it to be. In fact, according to a recent study in Italy, more than half of women with endometriosis experience dyspareunia, or genital pain associated with sex. Two types of dyspareunia exist. The first type, called superficial dyspareunia, is when the pain is felt at the opening of the vagina, and the lower part of the vagina. This pain is usually felt during the act of penetration and can easily be diminished by ceasing penetration. The second type, called deep dyspareunia, is felt deeper in the pelvis and thighs and can last for hours or even days. Women who have endometriosis, specifically recto-vaginal endometriosis and endometriosis on the cul-de-sac experience this type. There are many medical causes for dyspareunia other than endometriosis, such as vulvodynia, vulvar vestibulitis and interstitial cystitis. While this condition has historically been defined as a psychological issue, more recent treatment approaches lean towards the theory that dyspareunia is a combination of both physical and psychological causes. (More on dyspareunia theories).

In women with endometriosis, physical pain during sex is due to the presence of lesions found all over our insides, specifically behind the vagina and in the lower parts of the uterus. Having anything inside of us pushing or stretching those growths causes sheer agony, also described as burning, stabbing or deeply aching pain. It is intolerable, enough to make us scream, cry, or even throw up. This pain can start as early as the beginning of penetration and last up to 24-48 hours later. Women with endometriosis who have had a hysterectomy or who are going through hormonal treatments may experience pain due to vaginal dryness as well.

Dyspareunia has also been connected with more negative emotional attitudes towards sexuality as a whole. Studies have found that complaints of pain with sex are associated with low physical and emotional satisfaction, as well as decreased general happiness. Depression and anxiety were found more often in women with dyspareunia than control subjects.

Experiencing dyspareunia causes a loneliness inside of us that is worse than the most agonizing pain. Aside from simply not being able to connect sexually with people that we care about, we often feel compelled to hide our feelings from our loved ones so as not to hurt them. We would rather harm ourselves than tell our partners that they are hurting us. Keeping that a secret from them isolates us terribly, and fills us with a guilt that eats at our hearts. We are also consumed with incredibly strong guilt stemming from our inability to allow our partners the pleasure we know they deserve.

Fear of rejection is also a large part of the emotional pain associated with sex. We worry that our pain will cause our partners to reject us, whether because they have sexual needs that are lacking, or because they don’t want to cause us any harm. Ironically, many of us have experienced the strange situation in which we find ourselves begging our partners to have sex with us even though we know we will suffer.  Aside from the pain experienced by those of us actually suffering with this disease, it is also important to mention the emotional anguish that our partners who don’t have endometriosis go through. They too have feelings of rejection when we refuse to have sex, and can sometimes feel insecure about the relationship. Unfortunately, their need to be loved and love another is sometimes inadvertently ignored.

Due to endometriosis-associated dyspareunia, sex is often a dreaded nightmare fraught with worry. We worry that we’ll have unbearable pain if we choose to have sex and that we will offend our partners if we choose not to have sex. We worry that when we do want to have sex our partners will refuse for fear of hurting us. Instead of bringing us closer to our partners, sex puts a strain on the relationship that is hard to overcome.

This post was published previously on Hormones Matter in January 2013.