As some of you may have heard, or read, Danazol has now been made into a 2nd line defense for endometriosis.
You can only have it prescribed it if you have had all other treatment for endometriosis and they have failed.
Information about Endometriosis, latest news and research.
As some of you may have heard, or read, Danazol has now been made into a 2nd line defense for endometriosis.
You can only have it prescribed it if you have had all other treatment for endometriosis and they have failed.
My own story of Endometriosis is SO different……Please, please read, and let my message give hope.
The content and final outcome of my own story is a stark contrast from that of so many women around the world who suffer from this devastating disease.
The content differs because I did not go through the rounds of drugs, tests, operations, false hopes, mis-guided information, more drugs, more pain, worsening symptoms ….. need I go on; because so many of you know and experience this scenario – year in year out. It is utterly heart breaking.
The outcome of my story was based totally upon my absolute focus and conviction to get well, to get rid of Endometriosis, to banish this disease from my life. And I did. I took the slow, steady, gently, and natural way using alternative therapies and LOTS of positive thinking. And the final outcome …… I did beat Endometriosis, and it never returned. It is nearly 10 years ago that I was given proof that I had beaten endo, by a visual inspection of my internal organs, with a laparoscopy, and the gyne said there was NO active endometriosis and that it had all dried up.
The reason for my second laparoscopy was based purely on a very strong intuitive feeling of the need to be checked internally. I felt something was amiss but I had no idea what, and I had no symptoms. In fact I was fitter than I had been in many years. During the operation one cyst was found on my ovary and treated, but like I said, all the other cysts and signs of Endometriosis had simply dried up.
My homeopath told me that this last cyst was the last physical evidence, the final manifestation of the disease. It was as though all the toxic debris and residue of endo had been moped up into one place, ready for the final treatment. My intuition to get checked internally despite feeling really fit and well, was so strong and would not go away. I tried to ignore it, knowing how fit I felt, but in the end my intuition was screaming at me.
I had worked with my homeopath for 4 years and together we went through ‘layers’ of healing, finally getting to the root causes of my ill health and Endometriosis. The disease was finally laid to rest with the support of homeopathic remedies and many steps I took to help myself. The final cyst on my ovary was the last ‘process’ in my healing, strange as that may sound. This cyst made my intuition kick in, which enabled me to get this last physical evidence cleared up once and for all.
Therefore, it wasn’t simply a case of ‘feeling better’ because my symptoms had subsided, and mine was not a case of simply going into remission, which is the term the medical profession would prefer to call it. I know at a gut level that I was healed. Totally healed.
When I had my first diagnostic laparoscopy, my gyne told me that I had the worst case of Endometriosis she had ever seen – so it is not as though my healing was easier or simpler or quicker because I had a mild case of Endo. No, quite the opposite. I had cysts all over my abdominal cavity and was advised to a have a total hysterectomy.
I have been reading so many desperate stories of women whose lives have been totally devastated by this disease. One woman had actually been omitted into hospital over 100 times. Women are cancelling entire chunks of their lives because of this disease. Many women are opting for a total hysterectomy in a last ditch attempt to gain relief from this disease. Millions of women are in despair of gaining any relief from the pain and agony associated with endo, never mind hoping to be cured or healed.
Which is why I am giving a brief insight into my own story – to give women hope and to spread the word that a ‘cure’, healing, remission, whatever you want to call it, can and does happen. There may be a few successes for women who choose conventional drugs and surgery to treat their endometriosis, but they are few and far between. The best successes are for those women who use natural and alternative treatments.
This is because using natural therapies are natural, and they enable your own body to do the healing by using your immune system to full force. Alternative therapies help you do this by strengthening your immune system. There is not one alternative therapy that does the healing for you – what they all do, without exception, is to help you to heal yourself. Ask any alternative health practitioner, and they will confirm this statement.
It does not matter if you use Homeopathy, Herbalism, Traditional Chinese Medicine, Acupuncture or whatever – they all work to the same basic ‘principle’; that healing comes from within, and any alternative therapy helps the patient to help themselves.
Deciding which alternative therapy to use is down to personal choice with a mixture of finding a practitioner you ‘click with’, combined with a therapy that suits you. For example, if you do not like needles then Acupuncture will not be for you; if you do not like taking strong tasting concoctions, then Herbalism may not be for you. Go for the therapy which ‘feels’ right for you, and it will be right for you.
The other reason why alternative therapies are superior to aid healing is because they are permanent, not temporary, as in the case of drug treatment. As soon as drug treatment is stopped then the symptoms of endo come rushing back with vengeance.
I do read stories of women who have tried different alternative therapies and have felt let down. They have only felt limited benefit from the therapy they have chosen. In every story I have read of women who have ‘tried’ one of the alternative therapies, and have not had total success, the limiting factor has been the time span. These women have not given the therapy a chance to work. They may have only tried a regime of homeopathy or herbalism or whatever, for a few months and then given up because they were not seeing significant improvements.
My own time scale with a homeopath was 4 years – not 4 months. I was committed and determined, and my homeopath forewarned me it could take a long time to get well. But I felt that the ultimate long term benefit of total healing was far better than temporary respite. Therefore, my advice is to see any treatment using alternative therapy for endometrisios as long term (but not permanent).
People are so used to the idea of a quick fix for things in life, especially with modern medicine. We are all so impatient. But if you body has taken years to become dis-eased then it will take a long time to repair the damage and get the body back into equilibrium and balance.
To emphasise my positive message, in my research for my own book and my website, I have started to find stories of other women who have successfully obtained healing from this disease. In almost every case, these women have achieved their healing through different forms of alternative treatment or diet changes or a combination of self help techniques.
This has been more of a positive health and healing story rather then my own personal story of healing. The aim of my communication here is to provide hope that there are other possibilities to gain healing of Endometriosis. Evidence is mounting that it is possible, by the growing numbers of women who have achieved it.
The medical profession is not the ‘be all, and end all’ of health care for the human body. The medical profession is a relatively new phenomenon in the time scale of human society. Throughout history we have used herbs, healing, and essential oils. The practise of acupuncture goes back centuries; massage combined with oils goes way back in history.
Modern medicine is driven by pharmaceutical companies. There are very few doctors who develop new treatments for any of today’s illnesses and diseases. It is the drugs companies who develop new treatments in the form of new drugs. And guess what, that means more profits! I admit that there have been some wonderful developments in the field of medical surgery with the use of clever, and less invasive surgical techniques, like laser surgery and fibre optics, and many lives have been saved.
But when it comes to treating and healing diseases then modern medicine goes in with a sledge hammer, and does more harm than good. There are the dangers of side effects, some of which are permanent and very damaging to the body.
Your body chemistry is very delicate and the most delicate chemical system is the hormone system. We all know that endometriosis is fed and activated by hormones. In the human body, it takes only microscopic amounts of any given hormone to have a powerful and cascading effect in the body. These hormones are very potent, and yet the very treatment being offered for Endometriosis by modern medicine is synthetic hormonal drugs, which will obviously throw the body into disarray and upset a finely tuned orchestra of natural chemicals in the body.
Please be kind to your body. Healing yourself is simply a matter of being committed. A total commitment to change the way you are doing things. Do not leave it up to others; take control of your own health. I did, because after I heard my treatment options from the gyne, and compared that to the treatment potential using natural therapies, I knew I had no choice.
If you wish to find lots of positive advice about healing of Endometriosis visit my website at http://www.endo-resolved.com/index.html Your feedback about the site is welcome, as I am continuously aiming to improve the site.
I am a 29 year old mom, wife, NICU nurse. I have been living with endo for approx 18 months. I am coming to the breaking point with this disease. I will start from the beginning:
I have had one biological child in 1997. I developed pre-eclampsia at 27 weeks. We held off delivery until 31 weeks. I was on strict hospital bed rest. I am an NICU nurse so my fears were huge. I have since had issues with hypertension. I was scheduled for a tubal ligation one year ago because birth control was not an option for me. The desire for me to have a biological child was not that strong. We have adopted since then. My periods had been becoming increasingly painful. I had spoken with my GYN MD about this. He descided to do exploratory surgery with the tubal.
Well once in surgery my MD found 2 areas of endo inutero and 2 in the pelvic cavity. He hoped with the lap that all of the sites were taken care of for the time being. Well the lap worked for 4 months. By Christmas time of 2002 I was in so much pain that I was vomiting. Tylenol with Codeine was not working. I was not able to work… Which was very difficult for me. I love my job. I could not function as a mother, wife, lover etc….
So my MD wanted me to try Lupron injections. I was willing to try anything by this point. He kept telling me we were not going to do anything drastic (hyst) because of my age also he wanted to be sure we were dealing with the same thing again. I got very frustated with him because here I was in agony effecting my whole life and he is telling me to hold out. I work with this Md on a continuing basis with my job. I trust his judgement but I was beginning to have my doubts. The first month did not show any relief. I tried one more month of injections and proceeded to get a 2nd and 3rd opinion. This was hard for me to do because of the trust and respect I have with him with my job. All the MDs felt the I should see if the injections worked for one more month. Well they did!!! I got injections from January until June. I began to have bone density loss so I had to only do the 6 month cycle. Also my body was becoming “immune” to the injections.
So here I sit….. I am now taking 30mg doses of Provera. I have now been taking this for 3 weeks. As of two days ago the same exact symptoms have started with increased pain. I am back to using the tylenol with codiene when i can. No bleeding, but everything else that acts like a menses of before. I have spoken with my MD at length today. I am going to increase my Provera dosage but he utimately feels the next step is a hyst with ovary removal. And then explore to see were in the pelvic cavity has any sites to burn. I feel this is a tremendous step for him to say.
But I have done alot of research. I have my doubts about this being the next step due to alot of women not getting relief after this. My husband is worried sick. Our love life is next to nothing for the past month. I find it very sad that my 6 year old said to me yesterday :Mom you are not pink anymore. You look like Casper (ghost). Are you sick?
Does anyone else out there have any suggestions? I want to have all the information or paths they have taken that I could try. I don’t want to make a hasty desicion. Also being a nurse, I want as much proof as one can get………
This comment was submitted to us:
Email: poppypub@yahoo.com
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Location: Flagstaff, Arizona
Company: Poppy Publishing
Comments:
I read your story today. You said something about your doc wanting to “burn” if there is anything in the pelvic cavity. Research shows that ablation is the best way to deal with the endo because the tissue is actually cut out, as if to remove the root. Think of it as finding a black spot in a potato. The best way to get rid of it is NOT to use a peeler, and just scrape the layers, but to dig it out, thus making sure that you remove the entire spot. I’m not sure if you are aware of this process, but I would highly suggest you look into this, and see a doc who practices this. Also, please do not worry about hurting your doc’s feeling by seeing a different doc. This is about you and your health. If he can’t accept that you go elsewhere, I would question why I would put my health in his hands. Feel free to contact me. I am involved with the ERC.
This is an update from Nadine.
I had my exploratory laproscopy on Thursday, Aug. 7.
Please do more than just read the results here with interest. I really need input and information from as many people as possible. Quite frankly, I am very confused now.
Despite negative results from a pelvic and abominal CT scan, two ultrasounds and a tagged white blood cell count, I am told that my gyn during laproscopy found 4 cysts on an extremely inflammed left ovary. I was “ate up” with adhesions (hard scar tissue) around my left tube from a tubal ligation I had 17 years ago. Basically, the entire left side of my reproductive system was removed.
There was a hole in my intestinal sac, possibly caused by the scar tissue, and my intestines were pushing through the sac near my belly button. The gastroenterologist that attended the surgery pushed the intestines back in the sac and inserted mesh on both the inside and outside of the hole to strengthen that area. I have a four-inch cut across my belly.
It’s the morning of day two post surgery, it’s the week before the onset of my period and I am in just miserable pain.
After the surgery, the gyn said there was no endometriosis. But the next day, he said he found one spot near my left ovary that may have been endometriosis, but he wasn’t certain. It may have been a speck of blood, he said. Most women who have endometriosis have several lesions, he said, and since there was only that one spot, he suspects it was not endometriosis.
He could not take the spot, because it was on a major blood vessel and if he had nicked the vessel I would have bled to death instantly, he said. He feels certain that my pain was caused by the cysts, inflamation and adhesions. If that spot was endometriosis, however, then the pain will return and we will treat it as endometriosis, he said.
This treatment, he said, would be to start me on Lupron shots and get me scheduled for a hysterectomy.
Supposedly, the vcr was not working, so I don’t have a tape of the procedure. The still camera was malfunctioning, supposedly, as well. I was quickly shown a before and after picture of the “swollen” ovary that did not appear swollen to me. Interestingly enough, they have no photo of the FOUR cysts, the SEVERE adhesions or the possible endometriosis spot.
Please, I need some feedback. My e-mail is nadineparks@webtv.net.
Sincerely,
Nadine
A Review of Endometriosis
© Danny Tucker MRCOG
Women’s Health UK, 2000
www.womens-health.co.uk
Introduction
Endometriosis is a relatively common condition that can cause significant pain and suffering. At the other end of the scale, it can exist without any sign of its presence. Overall, between 3-10% of women aged between 15-45 years have endometriosis. In women who have difficulties conceiving, this rises to about 25-35%.
It used to be believed that the disease is more common in goal-orientated, professional women over the age of 30, but this misconception is now well disproven. It does not usually occur before puberty (though it has been reported), and it can be present for the first time in women who have already had children.
Further information will be found in the sections below:
What is it?
What exactly is endometriosis and what problems can it cause?
Diagnosis
How do I find out if I’ve got endometriosis?
Treatments
An overview of treatment options available.
Drug Treatment
A detailed description of the various drugs used to treat endometriosis.
Surgical Treatment
Laparoscopy and open surgery options, treatment results and recurrence risks…
What is it?
What exactly is endometriosis?
Endometriosis is small deposits of the womb lining that are located outside of the womb cavity. The most common place to find it is on the ovary, the back of the uterus and the ligamentous supports that hold the uterus in its normal position (uterosacral ligaments). It can also be found on the thin lining of the pelvic organs (the peritoneum), on the tubes, between the vagina and rectum (rectovaginal septum), in or on the bladder, in abdominal scars from previous surgery and even as far away from the pelvis as the lung!
Each time that you have a normal period, so this endometriosis does also, and this leads to cyclical swelling, stretching of tissues, inflammation and scarring. Eventually all the scarring and inflammation can lead to symptoms even when you’re not having a period.
It is more common in women whose relatives have endometriosis, in women who have cycles shorter than 28 days and those who typically have a period lasting longer than a week. Many cases occur in women without these associations, of course, and not all women who fit into the above categories necessarily get endometriosis.
What causes endometriosis?
There are several theories behind this, one possible cause is called retrograde menstruation. Normally during a period the menstrual blood comes out of the cervix and into the vagina. In around 75% of women, a small amount of blood flows backwards down the fallopian tubes and into the pelvic cavity. This blood contains tiny seedlings of the lining of the womb – endometrium. It is not known why in some women this might implant and lead to endometriosis, but not in others – it may have something to do with a particular woman’s immune response and ability to fight off & remove these seedlings.
The metaplasia theory suggests that because the uterus, tubes, peritoneum and part of the ovary are all developed from the same area in the fetus, endometriosis might be caused by some cells taking the wrong turn during development.
The vascular theory rests on the fact that endometrial tissue from the lining of the womb can be found in the blood stream. It might be that these small deposits end up in other areas far from the womb and grow from there. This would explain the rare finding of endometriosis in sites such as the lung.
Most likely there is no one simple answer to explain it, and the true cause is a composite of all these.
What problems can it cause?
The most common problems are:
The pelvic pain caused by endometriosis can be very variable. It may be like a dull ache located generally over the lower abdomen, or may be more severe. It can be more localised into the rectum (back passage) or cause urinary symptoms. Sometimes the degree of pain felt by a woman is not related to the extent of disease found when the endometriosis is diagnosed. Some women have very extensive endometriosis, but their pain & discomfort is minimal. Others have only a few spots noted and the pain is very disabling. In general, however, the more endometriosis that is present, the more likely you are to have symptoms.
Painful periods are often the first sign a woman might have that endometriosis is present. The pain usually begins a few days before the period is due and continues throughout the period. It is typically located in the centre of the pelvis, but can be one-sided. It may go into the back or down the legs.
Pain on intercourse is often worse with a particular position and especially with deep penetration. Many women experience an aching in the pelvis after intercourse.
The link between endometriosis and infertility is sometimes difficult to explain. When the disease is so bad that there is much scarring around the tubes, or there are ovarian cysts, it is not surprising that this might interfere with normal fertility. It is less clear how a few small spots of endometriosis might have a detrimental effect on attempts at pregnancy. Nevertheless, studies have found that endometriosis is more common in women who have difficulty conceiving, supporting the link. Also, another major study looking at treatment of mild to moderate endometriosis did find an improved fertility rate in women who received treatment.
Other symptoms
Although the above problems are most common, some women experience other symptoms related to where endometriosis might have implanted:
Diagnosis of endometriosis
Examination findings
A pelvic examination can sometimes suggest the presence of endometriosis. Typical findings depend on the severity of the disease and where it is located. A normal uterus is quite mobile, but the scarring of endometriosis can make it tender and fixed in the pelvis. There may be a swelling felt on one of the ovaries because of an endometriosis cyst. The uterosacral ligaments are one of the supports of the uterus where endometriosis can occur and these can be felt just above the cervix. Tender nodules in this area can suggest its presence.
Diagnostic laparoscopy
To confirm endometriosis requires a diagnostic laparoscopy. This is where a small telescope is passed through the umbilicus to gain access to the pelvis. A picture of the pelvis is viewed on a TV screen and the presence of endometriosis and its stage assessed. There is an information sheet on the website containing more information on diagnostic laparoscopy. Ultrasound is useful to help diagnose endometriosis cysts of the ovary.
At laparoscopy the appearance of endometriosis is quite variable. It can take one of the following appearances:
In more advanced cases of endometriosis there might be web-like scar tissue, adhesions, sticking the ovary to the side of the pelvis or the tube to the uterus, distorting the normal position of the pelvic organs. Even if the endometriosis is silent, adhesions can cause pain, particularly if they affect the bowel or the ovary. Stretching of the ovary and surrounding adhesions when an egg is developing toward midcycle will cause pain & make it sensitive during intercourse. Similarly the normal movement of the bowel as food passes through can lead to pressure symptoms if it is stuck down in adhesions.
Endometriosis can affect the ovary with the development of benign ovarian cysts called endometriomas. These can be as small as a grape or as large as grapefruit. Bleeding into the cysts leads to collection of old, dark-brown coloured blood and this is why they are sometimes called ‘chocolate cysts’. A woman may suddenly feel pain if there is bleeding into an endometrioma with stretching of the capsule. Similarly if an endometrioma bursts, the blood spilled will cause irritation and can lead to the development of adhesions.
Laparoscopic photographs of endometriosis
The small black spots are endometriosis on the peritoneum
An experienced surgeon should be able to identify this disease in all its various forms and undertake treatment at the time of diagnosis, where appropriate. This is the most effective form of treatment for mild to moderate endometriosis and should be considered the first-line approach. More advanced endometriosis will normally need a separately planned operation where more time is available to sort things out fully.
Laparoscopic view of an endometrioma of the left ovary.
Note the ‘chocolate’ blood coming from where it has burst.
Staging of endometriosis
Endometriosis is staged depending upon the amount present, the areas it involves and the presence of secondary scarring. Staging is graded by the revised American Fertility Society score. Mild disease (rAFS stage I and II) is generally limited to small to medium-sized lesions with variable degrees of penetration. More severe disease (rAFS stage III and IV) suggests the presence of adhesions around the ovaries, tubal disruption and ovarian endometriomas.
Treatments
There are several options for treating endometriosis, and each has its place for different women’s disease. The options are as follows:
If endometriosis is found, for example, at the time of laparoscopic sterilisation and it is only mild, causing no symptoms at all, then it is quite reasonable to leave well alone and avoid any treatment at all. Some surgeons might burn it away at the time of diagnosis even if it isn’t causing symptoms at that time.
Symptom management
Management of the symptoms means using painkillers to make the painful periods more tolerable or for cyclical pain if it is not too bad. Some of the pain is caused by hormones called ‘prostaglandins’ which make the uterus contract. Ibuprofen and mefanamic acid (Ponstan) are anti-inflammatory drugs that reduce levels of prostaglandins and often help with the pain. If there is not prompt response to analgesics, it is sensible to move onto some hormonal treatment, that will actually shrink the endometriosis itself, or to consider one of the surgical approaches.
Assisted conception
If endometriosis is associated with infertility, another way of ‘managing the symptoms’ is to use assisted conception (in-vitro fertilisation or IVF, sometimes called ‘test-tube baby’). This won’t deal with the endometriosis, but the approach might be suitable for a woman with minimal other symptoms, who is older & doesn’t have as much time to undergo prolonged treatments or sit around on a waiting list for surgery. Also, if other treatments have failed and infertility persists, assisted conception is usually the only remaining option.
Medical and surgical treatments
These will be discussed more fully in the next section.
Medical treatment
Treatment of endometriosis with drugs can result in great improvement of symptoms such as painful periods, pain on intercourse and pelvic pain. Three important facts must be understood before choosing a medical treatment:
The aim of medical treatment is to break the cycle of stimulation and bleeding. By stopping the ovary’s usual hormonal cycle and reducing oestrogen levels, the endometriosis deposits shrink down and become inactive. The endometriosis is still there, and will gradually become reactivated when the normal menstrual cycle starts again. Ovarian endometriomas of greater than 3cm diameter are unlikely to respond to medical treatment, and similarly if there is a significant amount of adhesions – these will respond best to laparoscopic breakdown (called adhesiolysis).
It was initially thought that use of the more ‘powerful’ treatments, such as GnRH agonists, was more likely to cure the endometriosis or result in a greater improvement in symptoms. Studies have compared the various options and it is now clear that they are all pretty much the same in terms of improvement of symptoms.
Each drug will be discussed in turn, but continuous use of the combined contraceptive pill or progestogens are usually the best options with the lowest chance of side effects. Medical treatments are typically used for 6-12 months, except for the contraceptive pill, which can be used as long as needed.
Contraceptive pill
The Pill is one of the most commonly used treatments for endometriosis, and is a good choice for young women with mild disease who also require effective contraception. Despite its long-established use, there has been only one study on the use of the Pill for endometriosis. It compared the Pill with GnRH agonists and found an equal improvement with both drugs with regards to pelvic pain, painful periods and painful sex. There was a trend towards the Pill being better at controlling painful periods and GnRH agonists being best for improving painful intercourse.
In the above study the Pill was used cyclically, but many gynaecologists suggest that it is better taken continuously, with no withdrawal bleed in between each packet. This doesn’t do your body any harm and there is no ‘build-up’ of blood as might be expected, since one of the hormones it contains keeps the lining of the womb quite thin.
If used continuously, it should be for 6-12 months, but breakthrough spotting is not uncommon after a few months and you can either have a seven day break at the end of the next packet or your doctor might prescribe some additional oestrogen for a week, which helps to refresh the lining of the womb.
Progestogens
Progestogens are the most commonly used medical treatment and are effective in about 80% of cases. Examples include the drugs medroxyprogesterone acetate (Provera), dydrogesterone and norethisterone. They work by thinning out and shrinking down the endometriosis and also by suppressing the normal cycle of the ovary. They can be used either continuously or in a cyclical way (eg. taken for 3 weeks, with one week off). Depot Provera, the injection form of the drug commonly used 3-monthly for contraception also works, but its use is limited in women wishing pregnancy as it can delay ovulation some time after the last injection (up to 12 months).
Side effects of progestogens can include: irregular bleeding or breakthrough spotting – which affects around one third of users, weight gain, breast tenderness, water retention and rarely depression. This list of side effects is just what is possible, many people don’t have any ill-effects at all and it would be unlikely that all would be experienced at once! Once again, breakthrough bleeding can be managed with a short course of oestrogen tablets.
It has long been known that progestogens can alter the blood lipids (fats) in an unfavourable way, which might theoretically lead to an increased risk of blood clots (thrombosis). Two recent studies have provided more evidence that this could be the case. Although they looked at progestogens used for period problems, the doses used are similar as would be for endometriosis, and the risk of thrombosis was around 5-fold higher than expected. Whilst this is an acceptable risk for women not already at risk for thrombosis, if you have other risk factors (eg. a previous clot or a strong family history) then an alternative treatment might be preferable.
GnRH agonists
GnRH stands for Gonadotrophin Releasing Hormone and an agonist is a drug that acts the same way as the body’s own hormone. The body normally makes GnRH in a small gland in the brain (the pituitary) and it is this hormone that stimulates the ovary to develop eggs and produce oestrogen, leading to the normal menstrual cycle. If you give GnRH agonists, this floods the system and confuses the delicately controlled balance, leading to a complete block of egg development, oestrogen production and menstrual cycle. It effectively makes you ‘menopausal’ for the short time that you use the treatment and without the oestrogen stimulation, endometriosis shrinks down and becomes inactive.
Examples of GnRH agonists include: goserelin (Zoladex), nafarelin (Synarel), Buserelin (Suprecur) and leuprorelin (Prostap). They are all either given by injection or nasal spray – tablet forms are unfortunately not available.
GnRH agonists are effective in relieving symptoms in 80-90% of patients and the best affect is in small areas of endometriosis. Although ovarian endometriomas will shrink down by around 20%, surgery remains the optimum treatment for the more severe disease. Studies looking at the effectiveness of GnRH agonists have found that the benefit is comparable with the other forms of medical treatment.
GnRH agonists work by lowering oestrogen levels and the main side effects of the treatment are due to this: hot flushes, reduced sex drive, vaginal dryness, emotional symptoms, depression and headaches. It really is like going through the menopause for a short time. The other main problem limiting longer courses than 6 months is that bone thinning is a side effect, with around 5-6% reduction in bone density in the spine. This is completely reversed by 9 months after stopping treatment.
There is now good evidence that the use of add-back hormone replacement therapy (HRT) is effective in preventing the bone thinning and the unpleasant side effects of GnRH treatment. The HRT used can be a normal cyclical oestrogen/progestogen one, a continuous ‘no bleed’ preparation or a newer type such as tibolone (Livial). It can be started at the same time as the GnRH agonist and does not diminish the effect of the treatment. It might seem surprising that using oestrogen replacement doesn’t undo the effect of the GnRH, but there appears to be a threshold level of oestrogen where endometriosis will be stimulated, and HRT doesn’t reach that level, but is enough to prevent the side effects.
Danazol
Danazol is a drug that was once used as first-line medical treatment for endometriosis and it is effective in 80-90% of cases. Fortunately, there is now good evidence demonstrating other drugs as equally effective, as Danazol can have some quite unpleasant side effects. It works by preventing ovulation and reducing oestrogen levels as well as having a directly suppressive effect on the endometriosis itself.
It has some properties that are similar to the male hormone testosterone and possible side effects include: weight gain, water retention, tiredness, decreased breast size, hot flushes, acne, oily skin, growth of facial hair and emotional symptoms. Although some side effects are experienced by about 80% of users, they are only troublesome enough to make women stop treatment in 10% of cases. It can irreversibly deepen the voice. It is also important to use an effective contraceptive, as accidental use in early pregnancy can masculinise a female fetus.
Gestrinone
Gestrinone is a treatment used more commonly in Europe. It works in much the same way as danazol with similar, but milder, side effects. It is taken twice weekly and around 85% of women do not have any periods at all when on treatment.
Reference list (hyperlinked on website)
Moore J, Kennedy S, Prentice A. Modern combined oral contraceptives for the treatment of painful symptoms associated with endometriosis (Cochrane Review). In The Cochrane Library 1999, Issue 3. Oxford:Update Software.
Vercellini P, Trespidi L, Colombo A, Vendola N, Marchini M, Crosignani PG. A gonadotropin-releasing hormone agonist versus a low-dose oral contraceptive for pelvic pain associated with endometriosis. Fertil.Steril. 1993; 60:75-79.
Vercellini P, Cortesi I, Crosignani PG. Progestins for symptomatic endometriosis: a critical analysis of the evidence. Fertil.Steril. 1997; 68:393-401.
Prentice A, Deary AJ, Goldbeck-Wood S, Farquhar C, Smith SK. Gonadotrophin-releasing hormone analogues for pain associated with endometriosis (Cochrane Review). In The Cochrane Library 1999 Issue 3. Oxford:Update Software.
Vercellini P, De Giorgi O, Pesole A et al. (1998) ‘Endometriosis drugs and adjuvant therapy’ in: A Templeton, ID Cooke, PMS O’Brian (Eds) Evidence based fertility treatment, p225-245. London: RCOG press
Poulter NR, Chang CL, Farley TMM et al. Risk of cardiovascular diseases associated with oral progestagen preparations with therapeutic indications. Lancet 1999; 354: 6 November. (link requires Lancet website registration, which is free)
Vasilakis C, Jick H & del Mar Melero-Montes M. Risk of idiopathic venous thromboembolism in users of progestagens alone. Lancet 1999; 354: 6 November. (link requires Lancet website registration, which is free)
British Medical Association & Royal Pharmaceutical Society of Great Britain. (1999) British National Formulary. Oxon: The Pharmaceutical Press
Surgical treatment
Surgical treatment for endometriosis is usually carried out in one of the following situations:
Surgery can either be conservative or radical. The aim of conservative surgery is to return the appearance of the pelvis to as normal as possible. This means destroying any endometriotic deposits, removing ovarian cysts, dividing adhesions and removing as little healthy tissue as possible.
Radical surgery means doing a hysterectomy with removal of both ovaries and is reserved for women with very severe symptoms, who have not responded to medical treatment or conservative operations. Sometimes, if there are other reasons to carry out a hysterectomy it is done earlier than this.
Treatment at the time of diagnosis
This approach is rapidly becoming standard practice in the management of endometriosis. It is typically carried out where the endometriosis discovered is mild to moderate and the extra time required to do the surgery will be able to be accommodated within the operating list planned. A further key-hole into the abdomen is often needed.
Laparoscopic management of endometriosis
Mild to moderate disease
The endometriosis spots are destroyed by diathermy, where an electric current is passed down a fine probe burning the lesion. Some surgeons use laser to evaporate the endometriosis.
Fine adhesions can be cut using small scissors. Bleeding is usually minimal and having avoided an open operation means that the risk of subsequent adhesion development is reduced. Laparoscopic managment also has the advantage of needing a minimal hospital stay, it is usually possible to go home the same or following day.
Improvement in pain symptoms following this type of surgery can be expected in 70% of cases, moreso if the location of adhesions divided corresponds to the area of maximum pain.
There has been only one good quality study of the effect of surgical treatment of mild to moderate endometriosis on subfertility. It found that laparoscopic destruction of lesions resulted in a 13% increase in pregnancy rate – equivalent to, on average, a benefit for one out of every eight women receiving treatment.
Moderate to severe disease
Where endometriosis is more than a few spots, and in particular where there is more severe scarring or an ovarian endometrioma, there is still the option of laparoscopic treatment in some hospitals. In the UK, it is usually only an option in the larger, central hosptials or where a local Gynaecologist has a special interest in laparoscopy. The aim of laparoscopy, as usual, is to restore things back to normal. For endometriomas this will mean shelling out and removing the cyst from the underlying normal ovary tissue. An alternative is to make a hole in the cyst wall, empty out the ‘chocolate’ collection of blood and diathermise the cyst base so all endometriotic deposits are destroyed.
Removal of endometriomas and division of scar tissue can be expected to improve the pain symptoms of endometriosis. The success of surgery in improving subfertility is related to the severity of endometriosis in the first place. It is difficult to give exact estimations, but women with moderate disease can expect pregnancy success rates of around 60%, whereas the comparable figure with more severe disease is around 35%. If a pregnancy does not occur within 2 years of surgery for endometriosis, the chances of success are poor, and referral for in-vitro fertilisation should be made.
Open surgery
This is the usual method of approaching the more severe degrees of endometriosis, particularly where endometriomas are large and there is more extensive scarring involving the bowel and bladder.
Hysterectomy is an end-stage treatment for women who have completed their family and where endometriosis is severe. It is usual to suggest removal of the ovaries, particularly in a woman who is over the age of 40 or where the disease is particularly severe. Hormone replacement therapy will protect the bones and avoid the menopausal symptoms.
Using drugs with surgery
Overall the evidence to support drug treatment before surgery is not good. 3-6 months of drugs prior to surgery may make endometriomas smaller and therefore more accessible by laparoscopy, helping avoid the need for an open operation. There is nothing to suggest that it improves fertility rates or pain after the operation, however.
The use of drugs after conservative surgery in women wanting pregnancy does not improve pregnancy rates, but just adds delay. For women who have pain there is some evidence that pain is improved with a course of drug treatment following surgery, but it may just be limited to the period whilst the drugs are taken (as would be expected given the results of studies on long-term effect of medical treatment alone). This may be useful if it helps reduce pain whilst recovering from surgery – indeed it will take 2-3 months in any case for the true benefit from surgery to become apparent, as things gradually heal.
Recurrence of endometriosis after surgery
Recurrence rate for endometriosis has been estimated to be 10% per year by one author, another study found it to recur in 40% of women within 5 years after conservative surgery.
There is a 6 times higher risk of recurrence after hysterectomy if the ovaries are not removed. Even in women who have the ovaries removed, there is a small (0.01%) risk of further recurrence, usually involving the bowel.
Risks of laparoscopy
Keyhole surgery is generally very safe, especially in experienced hands, but it is important to be understand that any laparoscopy carries with it some degree of risk, as do all operations. When placing the laparoscope into the abdomen, there is a small risk of accidental injury to bowel, the bladder or blood vessels leading to haemorrhage – this risk is inherent in the procedure. It is greater if the surgery is more advanced involving dividing of adhesions, diathermy of endometriosis, removal of cysts, etc.
Large studies have found that complications might affect around 1/370 diagnostic laparoscopies and 1/50-100 where more prolonged and difficult operation is necessary. Not all of these complications will have serious implications, but it might mean an unexpected open operation and a longer hospital stay. Complications are more common where there has been multiple previous open surgeries.
Reference list (hyperlinked on website)
Jensen FW, Kapiteyn K, Trimbos-Kemper T et al. Complications of laparoscopy: a prospective multicentre observational study. Br J Obstet Gynaecol 1997; 104: 595-600
Harkki-Siren P, Kurki T. A nationwide analysis of laparoscopic complications. Obstet Gynecol 1997; 89: 108-12
Sutton C (1990) Advances in the surgical management of endometriosis. In: Shaw RW (ed) Endometriosis. Parthenon, Camforth, pp209-226
Marcoux S, Maheux R, Berube S and the Canadian Collaborative Group on Endometriosis. Laparoscopic surgery in infertile women with minimal and mild endometriosis. New Engl J Med 1997; 97: 212-22
Olive DL & Lee KL. Analysis of sequential treatment protocols for endometriosis-associated infertility. Am J Obstet Gynecol. 1986; 154: 613
Wheeler JM & Malinak LR. Recurrent endometriosis: incidence, management and prognosis. Am J Obstet Gynecol. 1983; 146: 247
I am 24 years old. I have had 2 laps and one full year of Lupron shots. I have been close to symptom free for 3 yrs, with only a low dose B.C. Last month I went to the doctor because of a lower back ache. I was give 3 rounds of 5 different antibiotics for a suspected bladder and uterine infection. My last visit to the doctor was exactly what I expected and dreaded…It’s back, again! The problem now is I have new insurance and this is a “previous condition,” nothing to do with endo will be covered. I work full time, attend college full time, and support myself. I can’t afford to pay for these upcoming treatments, however, I can’t afford this much pain. I need advise and quick!
My name is Nadine. Here I sit in my tiny apartment in a narcotic stupor. Tylenol 3 with Codiene, one every four hours around the clock. Aleve doesn’t work any more. A nightgown is my constant wardrobe now. My left side and abdomen hurts too much for pants. Besides, the gown makes it easier for the frequent runs to the ladies room (bladder pressure).
I am a newspaper reporter, but I haven’t been able to work for weeks. Thank God my publishing company has a generous, short-term disability plan. It will pay 100% of my salary for six months while I’m out of work. I only have six months to find out what’s wrong with me and get better. I am frightened that I will lose my job. It’s a 10-year career at stake. My gynecologist suspects endmetriosis and has scheduled an exploratory laparoscopy and hysteroscopy for Aug. 7, 2003. A second surgeon will attend to repair my belly button, which herniated or popped out a few weeks ago. They suspect that there may be a section of colon adhered to the belly button. They plan to place a piece of mesh behind my belly button for support when the surgery is complete. This started about three months ago with mild lower back pain and a swollen abdomen. My white blood cell count was elevated to about 15 and lab tests revealed traces of blood in my urine. We checked my records for the past several years and I have never had blood in my urine. I couldn’t get comfortable in any position except standing. Then my left side started hurting and I developed a small lump just under my left rib on the abdomen. It went away for about a week, came back then went away. When it came back again, it was much worse and the pain eventually grew to an excrutiating level and I had to stop working. I’ve had both a vaginal and abdominal CT scan, vaginal ultrasound, colonoscopy and IVP, all were clear. We didn’t make the potential endometriosis link until my general practitioner said this was acting like an infection or cyst in my fallopian tube or ovary and she asked about my periods. About a year ago I had two episodes of vaginal breakthrough bleeding inbetween periods. Since then, my periods have become very painful the week before menstruation and the first couple of days of menstruation. They have become very heavy as well. When I am menstruating, every time I sit on the toilet blood and large clots drip into the bowl. I used to have my period about every 28 days like clockwork. Now they are coming every 23 to 26 days and last for five to seven days, where they used to be a short three to five days. Sex has been painful for at least six months now and after sex I have what feels like menstrual cramps. When I visited my gyn about a year ago about this he said I was getting older, the body changes as you get older and I may even be beginning early menopause. It was nothing to be concerned about, he assured me. When I saw him three months ago about the lump and the pain on my side and abdomen, he said the pain was up too high and sent me to a gastroenterologist. That specialist found no problems with my colon. After my general practioner mentioned my periods, I went back to my gyn and he said we needed to “get in there and see what’s going on.” If I understand correctly, he will check my uterus area with a scope (hysteroscopy). For the laparoscopy, he will expand my abdominal cavity with a gas, make three small incisions in my belly, insert a scope and search for any endometriosis spots and for any cysts or tumours, etc. If he finds any he will cut and remove them, unless they are attached to critical areas, such as the colon or bladder. He has warned me that laparoscopy may not get all the lesions, if there are any, and that many women ultimately require a hysterectomy, which he said has a high cure success rate. I’m 41. Both of my children are grown and I do not wan’t any more children. I had a tubal ligation 16 years ago. I asked him if he found endemetriosis if he could just go ahead and perform a hysterectomy. I want to knock this thing out and get back to work. He said he could but that insurance companies generally won’t pay for it unless laparoscopy and medications don’t work. I’m a little frightened about the surgery next week. The doctor said the pain should not be intolerable and I should recover in a few days. Still, it is surgery, there will be pain. I’m sure it will be complicated by the herniated belly button repair as well. My poor boyfriend. We live together. He has had to go without sex for so long. I thank God he sent me an understanding man. He’s been great, done all the cooking and cleaning, the grocery shopping, everything. At my son’s graduation ceremony, I could not walk from the car to the auditorium. I cried through the ceremony and everybody thought I was being sentimental, but I was crying because I was in pain. I didn’t want to spoil the event as we had family come in from all around the country. My mother had a pacemaker put in last month and I went to Georgia to try to help her with her recuperation. But I had to leave the day after her surgery because my period started and I was hurting too much to help her. I really feel quite useless right now. But I am praying that the surgery leads to a diagnosis and, ultimately, an end to this pain. I plan to update this after the laparoscopy to let you know the outcome. I may not have endometriosis. But I think it is important for all women to know that painful sex and debilitating menstruation is not normal and should be reported to a physician.
Re: SCHEDULED FOR LAPAROSCOPY
by Ariadm
Hi Nadine,
I read your story with interest and I apologise if my response sounds blunt.
First of all – a hyst is in no way a cure for endo – many women who have adeno no longer have problems after a hyst, but for women who have endo at least 90% of them continue to have problems. Endo doesn’t need the ovaries to produce food – it makes it own. If you have a hyst, but you have endo on the bowel, bladder, ureter, etc. the endo doesn’t go away – it stays there and can cause a lot of problems.
Second – it’s very possible to remove endo from the bowel, bladder, ureter etc etc as I’ve had that done by a top endo specialist in August 2001 and I’ve been pain free since.
Make sure you rest a lot after your operation – whether it’s a hyst or a lap. Why is your doctor not going to remove endo he finds on the bowel or bladder? Could he not work with someone who can do this for you?
I really wish you all the best and I hope the surgery does work for you. Please keep us updated, and you’re welcome to post any questions you may have on the forums.
*HUGS*
Arianna
Re: SCHEDULED FOR LAPAROSCOPY (Score: 1)
by nadineparks
Arianna, thank you so much for your response. It is very comforting to know that I am not alone at a time like this. It is very difficult to talk to friends and family because they dont really understand what I am going through. So to have an caring and empathetic ear is very comforting. I guess we’ll have to see what the laparascopy reveals. If I do have endometriosis, I plan to find an endometriosis speciliast. I am in Charleston, S.C. Can anyone recommend a reliable, compassionate specialist in my area please?
Re: SCHEDULED FOR LAPAROSCOPY (Score: 1)
by EvaAnn
I have just found this website and read a few comments – Yours peaked my interest. I have lived with endometriosis for 8 years and it has been progressivley worse. The medications dont work anymore – either to minimize endo or to treat the pain. The laporoscopy didnt do anything. The specialist wants me to consider a hysterectomy – we are not having more children. I am hoping to find success rates for a hysterectomy as treatment for endo. What can you share with me as far as the likelihood of symptoms after surgery?
Thanks
Re: SCHEDULED FOR LAPAROSCOPY
by JenBison
Wow. First off, I wish you all the best. 2nd, I’m still new to this endo thing and didn’t realize the bladder thing was part of my symptoms. I’ve been going a lot more frequently lately. Also my periods: I, too, used to be every 28 days like clockwork. Then I started with the pain and the gyn put me on the pill. And then my period got messed up. I thought it was something to do with the pill. Anyway, I’m also having a lap. I was supposed to have on 7/28. I got all the way down to the Surgery Center and was told the laser was not working. The repair guy was coming later that afternoon, but didn’t know if he could even fix it that day. So I called the Dr’s office and the lady who schedules surgery was quite pissed at the surgery center. The upshot of all this is my surgery got rescheduled for 8/11, which is today! I’m very nervous.
But anyway, thanks for letting me know some of these symptoms are normal, and not just me. And I hope everything works out for you. 🙂
Source: Human Reproduction 2003; 18: 985–9
Human leukocyte antigen (HLA) systems may be involved in the etiology of endometriosis, indicates research conducted in Japan.
HLA genes have already been implicated in insulin-dependent diabetes mellitus, systemic lupus erythematosus, and pre-eclampsia, and women
with endometriosis have higher rates of autoimmune and other chronic diseases than do women in the general population.
To investigate the possibility of an autoimmune contribution to endometriosis, Keisuke Ishii (Niigata University School of Medicine, Japan) and co-workers genotyped 83 women with a laparoscopic diagnosis of the condition, looking specifically for the HLA-DQB1 and HLA-DBP1 alleles.
Ishii et al report that the prevalence of HLA-DQB1*0301 was 16.3 percent among patients versus 8.3 percent among 222 healthy male and female controls. This difference reached borderline statistical significance (odds ratio, 2.13).
In contrast, the prevalence of the HLA-DBP1 alleles was similar between patients and controls.
In 2002, Ishii’s group reported that HLA-DQB1*1403 was significantly more prevalent among patients with endometriosis than in controls, and this
is the first study to demonstrate a significant association between the two.
“Further investigations by increasing sample size and by replication in both Japanese and other populations are needed to fully understand the
association between HLA genes and this disease,” the team concludes.
Today is the 29th May and yesterday I found out that i had endometriosis. I cried to start of with then went numb I havent felt a lot since. I am getting married in a year, and had planned kids soon after that so this has come as quite a shock. I had a laporoscomy to see what years of painful periods erregular bleeding and pain during sex was infact endo or not. The gyno didnt speculate but told me i shouldnt worry that it might not be anything, but i will never forget the look on his face when he came to tell me. I think the person it has hit the most was my mother we are very close and she broke down in tears and went to tlk to the gyno without me. It turns out I only have 4 spots and he burnt then, though i apparently have a 60% chance of them growing back and having slight problems falling pregnant. I would just like to see if anyone can help me though this initial denial stage and if anyone eles is going though it or went though it themselfs and can give me some pointers on what to expect next!
Tristelle
Women who have endometriosis appear to have a higher risk of developing several different kinds of cancer, say researchers.. The BBC have posted the following story… URL BBC Story
Endometriosis is a condition in which the type of tissue that lines the inside of the womb is found elsewhere in the pelvis.
Since the natural menstrual cycle of a woman involves the swift growth, then shedding of the womb lining during her period, this is not beneficial.
Typical symptoms include pelvic pain, heavy menstrual bleeding, bloating and fatigue.
It has also been linked with difficulty conceiving.
Researchers from Huddinge University Hospital in Stockholm, Sweden, looked at whether there was a link between having endometriosis and cancer risk.
They found a woman’s risk of developing ovarian cancer increased by just under half, for endocrine tumours by a third, for non-Hodgkin’s lymphoma approximately a quarter and for brain tumours just over a fifth.
However, the risk of cervical cancer fell by roughly a third.
No panic
The author of the study, presented at the annual meeting of the European Society for Human Reproduction and Embryology in Madrid, said that as these were relatively uncommon cancers, even apparently large increases in lifetime risk were not necessarily anything to be concerned about.
Dr Anna-Sofia Berglund said: “It is very important to keep these findings in perspective.
“The overall risk of cancer does not increase after endometriosis, and where there are slightly increased risks, they are in some of the less common cancers.
“For instance, in Sweden just under 20 women in every 100,000 develop ovarian cancer each year.
“My study shows that for women with endometriosis, another eight women in 100,000 could develop it – and it may be even fewer than that.”
The study found that women who had a hysterectomy before or at the time that endometriosis was diagnosed did not show this increased risk of ovarian cancer – suggesting a preventive effect.
Dr Berglund said the study did not prove endometriosis caused cancer – but that it was possible that whatever led to endometriosis might increase the risk.
Material Source BBC News 2003
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