Dr. Albee discussses endometriosis and some of the medications used during treatment. These include Lupron (Prostap), Synarel, Zoladex and RU-486.
“Fears Over Contraceptive Supply”
This article found on the BBC News site discusses the fact that there is a shortage of Depo-Provera.
“Supplies of a contraceptive that is used by thousands of women across Britain are running out.
Production problems have hit stocks of Depo-Provera, according to manufacturers Pharmacia.”
Depo-Provera Tied to Increased Heart Disease Risk in Small Study
The article found on Ob.Gyn.News states that continued use of depo-provera may have “an adverse effect on cardiovascular health”.
Analysis Confirms Hormone Replacement Dangers
Patricia Reaney’s article from Sept 20, 2002 that starts out by stating “A British study backed US findings on the side-effects of hormone replacement therapy (HRT) on Friday, saying the treatment taken by women to relieve menopause symptoms increases the risk of breast cancer and stroke. ” can be found on MEDLINE Plus.
Dealing with Chronic Pain
Endometriosis symptoms
Endometriosis is a condition that effects about 20% of women. It is a disease that causes chronic pain, emotional torment, and can also lead to infertility. There is no known cause or cure for endometriosis. Treatments are available that can temporarily provide relief, however, none are long term. With such limited resources, all that is left is coping.
When a woman is diagnosed with endo, she may find herself frustrated and angry. She begins to wonder what she did to cause this. The pain continues and she finds herself going through cycles of surgeries and medications. Meanwhile, she is becoming a mental and physical wreck- full of anger, frustration and chronic pain. This cycle keeps repeating and eventually leads to anxiety and depression. The body can only handle so much stress before it wears down the spirit causing depression. The cycle has to be stopped.
There are several ways women cope with endometriosis. You will find that some may work for you while others may not. Experiment and build a “get well” program for yourself.
– Stop feeling like a victim. Realize that you did nothing that caused you to acquire this disease and that you are not responsible for what it has done to your life. It is the endo, not you, causing it.
– Find an outlet to release all of your negative emotions and feelings. Write in a journal, talk to someone, create poetry or art. Find a way to turn bad energy into good.
– Surround yourself with inspirational thoughts. Hang up your favorite poem or quote and read it when you need encouragement.
– Search for support. Find others to talk to that have the same condition. This can be found in a support group, web-site, or official association.
– Learn to focus on you. Treat yourself to a massage, take a bubble bath, meditate- learn to try new things.
– Become an active participant in your health care. You will feel better emotionally when you realize that you are in charge of your health.
– Become an advocate. Educate others about endometriosis. The more awareness about the condition, the better.
– Be optimistic. Visualize good things and do not focus on the bad. Of course you should be realistic, but try reversing the focus of your thoughts.
– It is unhealthy to hold tension in. If you need a good cry, you need a good cry. It is better to let it all out than to allow it to build up.
There is no easy way or a prescription for coping. Each person is different and will deal with chronic pain and emotional distress in their own way. As with any condition, some days will be better than others will. If you start implementing some of the ideas above, you just may find that you are having more good days than bad.
Author’s name omitted by request
Title: Endometriosis symptoms
Description: Endometriosis symptoms:a disease that causes women chronic pain and sometimes infertility. With no cure, women must learn to cope.
ENDO 101
“ENDO 101:”
The Basics
You’re laying in the recovery room after having a laparoscopy and your head is spinning. Your world is a foggy place and all you know is, you hurt. In the midst of this confusion, your doctor pops in and says, “great news! We found the reason for your pain. You’ve got Endometriosis. See you next week at post-op!” When the groggy feeling lifts and you start to regain your strength, you wonder, “what on earth is Endometriosis?!”
The Basics
Endometriosis is a disease affecting an estimated 77 million women and teens worldwide(1). It is a leading cause of infertility, chronic pelvic pain and hysterectomy. With Endometriosis, tissue like the endometrium (the tissue inside the uterus which builds up and is shed each month during menses) is found outside the uterus, in other areas of the body. These implants respond to hormonal commands each month and break down and bleed….
However, unlike the endometrium, these tissue deposits have no way of leaving the body. The result is internal bleeding, degeneration of blood and tissue shed from the growths, inflammation of the surrounding areas, expression of irritating enzymes and formation of scar tissue. In addition, depending on the location of the growths, interference with the bowel, bladder, intestines and other areas of the pelvic cavity can occur. Endometriosis has even been found lodged in the skin and at other extrapelvic locations like the arm, leg and even brain.
The presence of disease can only be confirmed through surgery like the laparoscopy, but it can be suspected based on symptoms, physical findings and diagnostic tests.
Often, younger women and teens who present to their healthcare providers with symptoms are dismissed and told they have PID or that they are too young to have Endometriosis. This is not the case. Endometriosis has been found in autopsies of infants(2) and in menopausal women. Endometriosis has even been found in men!(3)
Contrary to common misconceptions about the disease, there is no cure. There are, however, several methods of treatment which may alleviate some of the pain and symptoms.
Symptoms include: chronic or intermittent pelvic pain
dysmenorrhea (painful menstruation is not normal!)
infertility/ miscarriage(s) / ectopic (tubal) pregnancy
dyspareunia (pain during intercourse) / pain after intercourse
backache
leg pain
painful intercourse
nausea / vomiting
abdominal cramping
diarrhea
rectal pain
constipation
painful bowel movements
blood in stool
rectal bleeding
sharp gas pains
bloating
tailbone pain
blood in urine
tenderness around the kidneys
painful or burning urination
flank pain radiating toward the groin
urinary frequency, retention, or urgency
hypertension
coughing up of blood or bloody sputum, particularly coinciding with menses
accumulation of air or gas in the chest cavity
constricting chest pain and/or shoulder pain
shoulder pain associated with menses
shortness of breath
collection of blood and/or pulmonary nodule in chest cavity
deep chest pain
pain in the leg and/or hip which radiates down the leg
painful nodules, often visible to the naked eye, at the skin’s surface…can bleed during menses and/or appear blue upon inspection
fatigue, chronic pain, allergies and other immune system-related problems are also commonly reported complaints of women who have Endo. Remember, it is quite possible to have some, all, or none of these symptoms with Endometriosis.
Because Endo symptoms are so inconsistent and non-specific, it can easily masquerade as several other conditions. These include:
adenomyosis (“Endometriosis Interna”)
appendicitis
ovarian cysts
bowel obstructions
colon cancer
diverticulitis
ectopic pregnancy
fibroid tumors
gonorrhea
inflammatory bowel disease
irritable bowel syndrome
ovarian cancer
PID (pelvic inflammatory disease)
What does it look like?
Endometriosis can present in almost any color, shape, size and location. This includes clear, microscopic papules that can lodge themselves on the underside of organs or beneath the skin. Unfortunately, physicians who are less trained to recognize all manifestations often miss diseased areas, instead searching for visible, common “powder-burn” type lesions on the reproductive organs. In reality, the lesions can be black, red, blue, brown, clear, and raspberry colored, and microscopic in size. The lesions can be spread throughout the entire abdominal region, bowels, bladder, and other areas, and may not be visible without proper magnifying equipment.
Is it Fatal?
The disease itself is classified as “benign.” However, recent studies indicate that women with Endometriosis may have a slightly greater risk of developing cancer of the breast or ovaries and a greater risk of cancers of the blood and lymph systems, including non-Hodgkin’s lymphoma. Researchers caution that the cause of the relationship is unclear. The association may be due to drugs or surgery used to treat the condition rather than Endometriosis itself, and only women with the most severe form of the disease may have the excess risk, according to a report in the American Journal of Obstetrics and Gynecology(4) .
According to lead study author, Dr. Louise Brinton of the Cancer Epidemiology and Genetics Division of the National Cancer Institute in Bethesda, Maryland, the results are “provocative in suggesting that women with Endometriosis may experience elevated risk of certain cancers.” In the study of 20,686 Swedish women hospitalized for Endometriosis, the women had a 20% greater risk of developing cancer overall, particularly of the breast, ovaries and the blood and lymph cells, during an 11-year period. The women actually had a lower risk of cancer of the cervix. “The Endometriotic tissue and its surroundings will be enriched in growth factors and cytokines that might have a deleterious effect on the growth regulation of other cells, some of which may be in distant organs – for example, breast tissue,” Brinton wrote. The growth factors might act as carcinogens, thus promoting cancer.(5)
There are other possible explanations as well. Women with Endometriosis are also more likely take certain drugs, such as Progestagens and are more likely to have had their ovaries or uterus removed, another factor that influences hormone levels, and possibly cancer risk. It is also possible that women with Endometriosis may be screened more often for breast cancer and therefore be more likely to be diagnosed with the disease. Endometriosis has also been linked to a lack of physical activity and to exposure to the environmental contaminant, dioxin. These two factors might be to blame for the cancer risk, rather than Endometriosis.
Findings of one of the largest surveys conducted of over 4,000 Endometriosis patients in the United States and Canada(6) have indicated possible links to other serious medical conditions, including a 9.8% incidence of melanoma, compared with 0.01% in the general population, a 26.9% incidence of breast cancer, compared with 0.1% in the general population; and an 8.5% incidence of ovarian cancer, compared with 0.04% in the general population. Women with Endometriosis who participated in the survey also had a greater incidence of auto immune conditions and Meniere’s disease.
What are “Stages?”
Your surgeon determines the extent and severity of your disease once confirmation of diagnosis is made through both sight of the lesions as well as biopsy results(7). Staging has been defined by the American Society for Reproductive Medicine (formerly the American Fertility Society), with criteria based on the location of the disease, amount, depth and size. These factors are all graded on a point system and classification is thus determined. The first classification scheme was developed in 1973, but since then it has been revised and refined 3 times for a more precise method of documentation. As of 1985, the stages are classified as 1 though 4; minimal, mild, moderate, and severe. Stage of the disease is not indicative of level of pain, infertility or symptoms. A woman in Stage 4 can be asymptomatic, while a Stage 1 patient might be in debilitating pain.
How is it Treated?
Endo can be treated in many different ways, both surgically and medically. Most commonly, surgery will be performed during which the disease will be excised, ablated, fulgarated, cauterized or otherwise removed, and adhesions will also be freed. When adhesions are present, a women’s organs are literally bound together.
It is extremely important that a woman with Endo obtain treatment from a highly trained Endo treatment provider. There are many inexperienced physicians out there, sadly enough, who will a.) miss the disease altogether and not perform biopsies on tissue samples to confirm the diagnosis; b.) will confirm the presence of disease but make no attempt to remove it during surgery; or c.) will make the diagnosis, but will remove it in an incomplete or ineffective manner (such as ablation, which has been shown to be relatively ineffective on deep lesions). Doing so will unfortunately (as has been my experience and that of other survivors of the disease) allow the disease to flare again in a relatively short time. This vicious cycle only requires more surgery thereafter to once again lyse adhesions and treat the disease. Starting disease management with an Endo expert in the beginning of treatment can prevent repeat surgeries and ineffective treatment measures.
Surgeries include but are certainly not limited to: the laparoscopy; the laparotomy; presacral and uterosacral neurectomies – primarily done to lessen pain associated with Endo, where the nerves transporting sensation to the uterus are cut; and various levels of hysterectomies, where some or all of the reproductive organs are removed. It should be stressed that this method will only relieve the symptoms associated with growths on the reproductive organs, not the bowels or kidneys and related areas where Endo can be present.
There are several drugs utilized either alone or in combination with surgery. These include contraceptives, GnRH agonists, and/or synthetic hormones. GnRH agonists are commonly used on women in all stages of the disease and may sometimes have serious side affects. Be sure to inform yourself about all aspects of any drug before undergoing therapy with it.
GnRH (gonadotropin releasing hormone) analogues are classified into 2 groups: agonists and antagonists. Agonists are commonly used in the treatment of Endo by suppressing the manufacture of FSH and LH, common hormones required in ovulation. When they are not secreted, the body will go into “pseudo-menopause,” stalling the growth of more implants. However, these are again only stop-gap measures that can be utilized only for short term intervals, and the key word here is suppression. Once the body returns to it’s normal state, the Endo will again begin to implant itself.
Commonly Prescribed medications include: Leuprolide Depot – “Lupron” (Leuprolide Acetate) – administered as subcutaneous injection
Synarel (naferalin acetate) – administered as a nasal spray
Zoladex (goserelin acetate) – a subcutaneous implant placed into the abdominal wall
Suprefact (buserelin acetate) – also administered as a nasal spray
Danazol, a synthetic male hormone commonly marketed as Danocrine or Cyclomen
Depo-Provera (medroxyprogesterone acetate)-injectable form of progestins
Provera (same as above; administered in pill form)
Any combination estrogen/progesterone oral contraceptive recommended by your doctor
For treatment updates, please see “Endometriosis 2000 & Beyond: the Future of Research & Treatment.”
Living with a Chronic Illness:
While it cannot currently be cured, it is important to understand that Endometriosis is a disease that can be managed. It does not have to own you. Finding the right surgeon and choosing the right approach to treat your disease is crucial. Whether it be excision surgery, medical therapy or alternative healing that appeals to you and works to relieve your symptoms, the answers are out there. And remember…you are not alone.
For more information and support, please visit the Endometriosis Research Center on the web or call the ERC toll free at 800/239-7280.
Copyright (c) by Heather C. Guidone. All Rights Reserved. Do not Reproduce Without Express Permission From Author.
Endometriosis Treatment Danger
Drug Commonly Used to Treat Endometriosis Linked to Ovarian Cancer
By Liza Jane Maltin
March 19, 2002 — A drug used to combat endometriosis may increase a woman’s risk of developing ovarian cancer. Researchers have found that women taking danazol are three times more likely to get the disease than if they take an alternate drug.
The team from the University of Pittsburgh Graduate School of Public Health presented their findings March 17 at a gynecologic oncologists meeting in Miami.
Endometriosis is a painful condition in which pieces of the uterine lining — the endometrium — migrate outside the uterus and grow abnormally.
Roberta B. Ness, MD, MPH, associate professor of epidemiology, and colleagues reviewed pooled data from two studies including more than 1,300 women with ovarian cancer and nearly 2,000 similarly aged healthy women. They looked at the relationship between endometriosis, endometriosis treatments, and ovarian cancer.
In all, 195 of the women with cancer and 195 of the healthy women had been treated for endometriosis. Women with endometriosis were one and a half times more likely than those without endometriosis to have ovarian cancer.
The researchers found that women with endometriosis who’d taken danazol were nearly three times more likely than were women who’d taken another drug to have ovarian cancer. This link held even after taking into account various factors known to influence the risk of getting ovarian cancer including having been on the pill, having had a baby, and having a family history of the disease.
“Our previous studies have found that women with endometriosis are already at a 50% increased risk for ovarian cancer, and treating them with danazol appears to further increase their risk. This new result, even though it is preliminary, may factor into the equation when [doctors] and their patients with endometriosis are deciding on the best treatment,” says Ness in a news release.
© 2002 WebMD Inc. All rights reserved.
More Information on Lupron
Lupron Depot interrupts normal menstruation and the production of estrogen.
The absence of estrogen reduces the growth of endometrial tissue. In some cases, Lupron can shrink the implants and provide significant relief from pain.
This medication creates a pseudo-menopause. Even though most women stop having periods during treatment, occasional spotting can occur. If you continue to have regular menstruation after your second injection, you should notify your physician. You could also experience hot flashes, headaches and vaginal dryness, which are menopausal symptoms.
A reduction in estrogen might also cause a reduction in bone mineral density. Once treatment is stopped, this is partially or completely recovered.
©Abbot Laboratories, Limited LUG/4A01 – April 1998
Information About Lupron
This article contains information on Lupron that I have gotten from the Inserts that came with my first Lupron shot.
From the Patient Information Insert that came with my Lupron shot:
-it is for intramuscular use only
-it comes in 3.75mg (1-Month slow release) and 11.25mg (3-Month slow release)
-it’s limited to women 18 years of age and over
-the proper use of Lupron Depot:
-very important your physician checks your progress at regular check-ups
-you might get a local skin reaction: itching, redness, burning and/or swelling at the injection site; the reactions are usually mild and disappear within a few days; if they persist or worsen, tell your physician
-you might get hot flashes; if they continue and make you feel uncomfortable, tell your physician
-if you develop: severe bone pain, severe hot flashes, heavy sweating, severe pain in the chest or abdomen, abnormal swelling or numbness of limbs, persistent nausea or vomiting, rapid heart beat or nervousness, contact your physician immediately
–if you think you might be pregnant, contact your physician immediately
-always remember to:
-check with your physician or pharmacist before taking any other medications, including non-prescription (for colds, nausea)
The above information was from the Patient Information insert distributed by ABBOT LABORATORIES, LIMITED October 1999
From another Information Insert that came with my Lupron shot:
Lupron Depot is also known as leuprolide acetate for depot suspension; this is a synthetic, nonapeptide analog of naturally occurring gonadotropin-releasing hormone (GnRH or LHRH)
-it acts as a potent inhibitor of gonadotropin production when administered properly
-it exerts specific action on the pituitary gonadotrophs and the human reproductive tract
General Warnings from the Insert:
-isolated cases of short-term worsening of signs and symptoms have been reported during initiation of Lupron therapy
General Precautions from the Insert:
-those on Lupron therapy should be assessed on a regular basis by their attending physician
- Changes in Bone Density
- Changes in Laboratory Values during treatment: Plasma Enzymes, Haematology, Lipids,
- The safety of re-treatment as well as treatment beyond 6 months with Lupron has not been established.
Adverse Reactions:
-body odour, flu symptoms, injection site reactions, palpitations, syncope, tachycardia, dry mouth, thirst, appetite changes, anxiety, personality disorder, memory disorder, delusions, insomnia/sleep disorders, androgen-like effects, alopecia, hair disorder, nail disorder, ecchymosis, lymphadenopathy, rhinitis, ophthalmologic disorders, conjunctivitis, taste perversion, dysuria, lactation, menstrual disorders
-mood swings, including depression, have been reported as physiological effect of decreased sex steroids
-the following symptoms have been reported by patients while using this medication, but the relationship of the symptoms to Lupron hasn’t been established
-symptoms consistent with fibromyalgia (joint and muscle pain, headaches, sleep disorders, gastrointestinal distress, and shortness of breath)
The above information was from an insert that was distributed by ABBOT LABORATORIES, LIMITED July 1999