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Hi Joan:

I've had worse-than-average menstrual cramps and extremely heavy periods for as long as I can remember. I am anemic from it. I recently had a procedure to 'lighten my flow' and am waiting to see if it was successful. I was never diagnosed with endometriosis, but it has been suggested.

Tami (NJ)

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Hi Joan:

I've had worse-than-average menstrual cramps and extremely heavy periods for as long as I can remember. I am anemic from it. I recently had a procedure to 'lighten my flow' and am waiting to see if it was successful. I was never diagnosed with endometriosis, but it has been suggested.

Tami (NJ)

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Hi Joan. Well, as you probably know, I had endo. And I definitely feel there

is a connection to CU and endo AND to masto and endo. Too many women with

both conditions have had it. As for periods, mine were heavy, usually lasted

7 to 10 days, although did have them last a whole month a few times. Always

had severe cramps. I went on the pill when I was like 14 to try to regulate

my periods and alleviate the cramping, but it didn't help much and caused

migraines. Surprisingly, when I was d'x with the endometriosis, unlike the

norm of having heavy periods with it, mine had stopped completely.

Has anyone ever actually looked to see if you have endo? The only way, as

far as I know, is to actually go in and look, usually through a laparoscopy.

I have also read, now from several different places, that endo is believed

to autoimmune. Somehow I am not surprised...

Air hugs,

Jackie

Life is tough, but I'm tougher.

_________________________________________________________________

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Hi Joan. Well, as you probably know, I had endo. And I definitely feel there

is a connection to CU and endo AND to masto and endo. Too many women with

both conditions have had it. As for periods, mine were heavy, usually lasted

7 to 10 days, although did have them last a whole month a few times. Always

had severe cramps. I went on the pill when I was like 14 to try to regulate

my periods and alleviate the cramping, but it didn't help much and caused

migraines. Surprisingly, when I was d'x with the endometriosis, unlike the

norm of having heavy periods with it, mine had stopped completely.

Has anyone ever actually looked to see if you have endo? The only way, as

far as I know, is to actually go in and look, usually through a laparoscopy.

I have also read, now from several different places, that endo is believed

to autoimmune. Somehow I am not surprised...

Air hugs,

Jackie

Life is tough, but I'm tougher.

_________________________________________________________________

Join the world’s largest e-mail service with MSN Hotmail.

http://www.hotmail.com

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Hi Joan -

I do have horrible cramps for 2 days or so during my

period. I have been this way since I was 12 (I'm 38

now). I take one Advil every 5 hours during this time

and it helps about 80%. In total my period lasts

about 5 days and I don't think it's extraordinarily

heavy (how would you describe heavy?). What's worse

is the PMS I get starting 10 days before. I get

bloated, cranky, crampy, either go to the bathroom too

much or not enough, headaches, etc. This stuff seems

to have gotten worse as I get older. I don't think I

have endometriosis, nor does my doctor think anything

is wrong. She says if the pain is controlled by the 1

Advil, it is very unlikely that I have endo. Of

course I am not interested in going for a laparoscopy

to check it out. Being the health-phobic that I am, I

don't want to go for any unnecessary tests.

Am I the only one who can't wait for menopause to be

rid of all this nonsense?!

-Sheryl

--- Joan Passmore wrote:

> Ladies,

>

> I have a question. Do any of our female CU members

> suffer from worse-than average cramps or heavy

> menstral periods? This problem may be a totally

> unrelated to CU. I have never been diagnosed with

> endometriosis, but have had problems with heavy

> periods and cramps for many, many years. I have

> read

> that endometriosis is an auto-immue disorder and I

> was

> wondering is there was any connection to my problem.

>

> Thanks.

>

> Joan

>

> __________________________________________________

>

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Hi Joan -

I do have horrible cramps for 2 days or so during my

period. I have been this way since I was 12 (I'm 38

now). I take one Advil every 5 hours during this time

and it helps about 80%. In total my period lasts

about 5 days and I don't think it's extraordinarily

heavy (how would you describe heavy?). What's worse

is the PMS I get starting 10 days before. I get

bloated, cranky, crampy, either go to the bathroom too

much or not enough, headaches, etc. This stuff seems

to have gotten worse as I get older. I don't think I

have endometriosis, nor does my doctor think anything

is wrong. She says if the pain is controlled by the 1

Advil, it is very unlikely that I have endo. Of

course I am not interested in going for a laparoscopy

to check it out. Being the health-phobic that I am, I

don't want to go for any unnecessary tests.

Am I the only one who can't wait for menopause to be

rid of all this nonsense?!

-Sheryl

--- Joan Passmore wrote:

> Ladies,

>

> I have a question. Do any of our female CU members

> suffer from worse-than average cramps or heavy

> menstral periods? This problem may be a totally

> unrelated to CU. I have never been diagnosed with

> endometriosis, but have had problems with heavy

> periods and cramps for many, many years. I have

> read

> that endometriosis is an auto-immue disorder and I

> was

> wondering is there was any connection to my problem.

>

> Thanks.

>

> Joan

>

> __________________________________________________

>

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So sorry to hear of your discomfort and I'm sure - some embarrassment Joan. Some causes of cramps can be Endometriosis, fibroid tumors, ovarian cysts, and other conditions.

My mother has always had extremely heavy flow and so did I until I had gallbladder surgery. Normally my periods even last 10 days to add to the misery. I was constantly having 'accidents' in public, etc.... It was horrible. Out of 4 girls in the family, not one of us gets cramps. Sorry, not rubbing it in but I do realize I am fortunate.

Anyhow..........After the surgery I now have a normal flowing, 5-6 day periods. I've never really known the reason for the immediate change other than docs telling me that it was possible trauma to my system. My system was in overdrive trying to respond to the gallbladder attacks.

Hopefully there is not anything going on with your body that you should need surgery. I know there are many here who have had endo. so I'm sure you will get many informative responses.

Until then, maybe try some Geritol or iron pills to lighten flow and heating pad, warm baths or Viburnum prunifolium (herbal remedy) for cramps. I doubt that Urticaria has any relation to your menstrual troubles although you just never know with this stuff. I have the 'Doctors Book of Home Remedies' around here somewhere. I'll try to locate it and let you know what it has for comfort suggestions. Sorry I wasn't much help to you this time. I felt the need to respond with something since I am familiar with your 'pain'.

I will pray for you to find a cause and/or solution to yet ANOTHER problem.

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Actually, I have less menstrual cramps than I did before the CU started.

Mine started after my first child was born and that was when my cramping

became almost nonexistent - 17 years ago.

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> Ladies,

>

> I have a question. Do any of our female CU members

> suffer from worse-than average cramps or heavy

> menstral periods? This problem may be a totally

> unrelated to CU. I have never been diagnosed with

> endometriosis, but have had problems with heavy

> periods and cramps for many, many years. I have read

> that endometriosis is an auto-immue disorder and I was

> wondering is there was any connection to my problem.

>

YES! Yes! I have had an ultrasound and a full check up..and no reason for

cramps that are so bad Im prescribed darvocet/ultram/ mega doses of

nsaids or motrin to manage. After quite a bit of time of dealing with

this.. I went on depo provera to stop my periods.. This is a good

thing..as I dont have pre time of the month break outs..and well birth

control is an ok thing too

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> Ladies,

>

> I have a question. Do any of our female CU members

> suffer from worse-than average cramps or heavy

> menstral periods? This problem may be a totally

> unrelated to CU. I have never been diagnosed with

> endometriosis, but have had problems with heavy

> periods and cramps for many, many years. I have read

> that endometriosis is an auto-immue disorder and I was

> wondering is there was any connection to my problem.

>

YES! Yes! I have had an ultrasound and a full check up..and no reason for

cramps that are so bad Im prescribed darvocet/ultram/ mega doses of

nsaids or motrin to manage. After quite a bit of time of dealing with

this.. I went on depo provera to stop my periods.. This is a good

thing..as I dont have pre time of the month break outs..and well birth

control is an ok thing too

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I started having heavy periods when I was 23. And then

around 2 years later cold urticaria started. Later it

was found that I had hypothyroidism. I am now on

levoxyl for almost 1 year. I saw improvement in both

my urticaria and periods while on the thyroid

medication. Now that I am pregnant, I have neither the

periods nor the urticaria. Don't know, what will

happen after the baby is born.

I sure think that menstrual problem have relation to

CU. However, both of these problems may be due to some

other underlying cause.

--- Joan Passmore wrote:

> Ladies,

>

> I have a question. Do any of our female CU members

> suffer from worse-than average cramps or heavy

> menstral periods? This problem may be a totally

> unrelated to CU. I have never been diagnosed with

> endometriosis, but have had problems with heavy

> periods and cramps for many, many years. I have

> read

> that endometriosis is an auto-immue disorder and I

> was

> wondering is there was any connection to my problem.

>

> Thanks.

>

> Joan

>

> __________________________________________________

>

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Hi Tami,

I am now convinced that there is an auto-immune

connection, we can't all be just a coincidence!!!!

I wonder if there is any " treatment " short of surgery.

Obviously the antihistamines are not helping with

this aspect of the problem. I have also had this issue

for most of my life, long before the CU reared its

ugly head.

Tami, I hope your procedure helped. Do you mind if I

ask what it was? Feel free to e-mail me directly at

joanie36109@... Thanks!!!

Joan

--- TamBar226@... wrote:

> Hi Joan:

>

> I've had worse-than-average menstrual cramps and

> extremely heavy periods for

> as long as I can remember. I am anemic from it. I

> recently had a procedure

> to 'lighten my flow' and am waiting to see if it was

> successful. I was never

> diagnosed with endometriosis, but it has been

> suggested.

>

> Tami (NJ)

>

__________________________________________________

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Jackie:

This is very interesting. How does one find out if they have endometriosis? Other than being opened up and having laporoscopy? They don't see anything on sonograms. I have pain with periods and was infertile after having one child. I've also had melanoma.

Tami (NJ)

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Jackie:

This is very interesting. How does one find out if they have endometriosis? Other than being opened up and having laporoscopy? They don't see anything on sonograms. I have pain with periods and was infertile after having one child. I've also had melanoma.

Tami (NJ)

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There IS a link between endometriosis and autoimmunity. In fact, studies

have shown that women with endo have a MUCH higher likelihood of developing

autoimmune disorders, as well as some forms of cancer. Interestingly, their

offspring have an EVEN HIGHER chance of developing these. From

http://www.endometriosis.org/html/press_release.html

ENDOMETRIOSIS FAMILY STUDY IDENTIFIES HIGH RISK OF CANCER AND AUTOIMMUNE

DISEASES

Press event, New York City, April 21st to release new data

New data from the world's largest research registry on endometriosis shows

that women with endometriosis and their families have a heightened risk of

breast cancer, melanoma, and ovarian cancer. There is also a greater risk

of non-Hodgkin's lymphoma in the families. These findings parallel other

work, including a study of 20,686 endometriosis cases in the Swedish cancer

registry which also found an increased risk of breast cancer, ovarian

cancer, and non-Hodgkin's lymphoma in women with endometriosis. Researchers

at Harvard Medical School have found an association between melanoma and

endometriosis.

In the new findings, the risk of the following cancers was greatest in the

families of women with endometriosis: 9.8% incidence of melanoma (compared

to 0.01% in the general population); 26.9% incidence of breast cancer (0.1%

in the general population); and 8.5% incidence of ovarian cancer (0.04% in

the general population). Because many of the women with endometriosis in

the study are young (teenagers, 20s and 30s), it is believed that over time

they may face the same risk seen in their families and in the Swedish

registry study, since most cancers are more prevalent in older age groups.

In the Swedish cancer registry study, the average age of cancer diagnosis

was 52. Unfortunately, the mean age of cancer diagnosis in women with

endometriosis who had already been diagnosed with cancer was substantially

earlier than in the general population. For instance, the average age of

ovarian cancer diagnosis is 52; in this population of 4,000 North American

women with endometriosis the mean age was 34. Breast cancer in the general

population is most often diagnosed in middle aged and older women. In women

with endometriosis, the mean age of diagnosis was only 39. Another

startling finding was a 42.2% incidence of diabetes in the families of women

with endometriosis. The general incidence of diabetes is 5.9%. Other

significant findings in the study include a high rate of thyroid disorders

in women with endometriosis as well as in their families:

Women with Endo

Their Families

General Population

Hypothyroidism

6.8%

15.1%

1.9%

Hyperthyroidism

1.5%

6.3%

1.1%

Hashimoto's Thyroiditis

1.8%

1.9%

0.01%

Other autoimmune diseases with significant incidence in the study included:

Women with Endo

Their Families

General Population

Rheumatoid arthritis

2.0%

17.3%

0.8%

Lupus

0.8%

5.8%

0.05%

Multiple Sclerosis

0.6%

4.8%

0.1%

Meniere's disease

0.9%

2.8%

0.2%

Only physician-diagnosed cases of cancers, autoimmune and other diseases

were included in the data.

" Unfortunately, these findings underscore all too well what women with

endometriosis have been saying since the beginning of the Endometriosis

Association in 1980 endometriosis is a much more serious disease in many

women and families than has been thought in the past. We all need to be

more vigilant for our girls as they enter adulthood and for our families.

Obviously, this study calls for additional research, " said Lou Ballweg,

President of the Endometriosis Association.

A number of the cancers and autoimmune problems seen in women with

endometriosis and their families have been linked to environmental toxins.

Research conducted by the Association beginning in 1992 and the National

Institute of Environmental Health Sciences, the Environmental Protection

Agency, and others since then has pointed to dioxins as a possible trigger.

Dioxins (including dioxins, PCBs, and furans) are organochlorine chemicals

which have been produced and widely disseminated in the environment

primarily since World War II, although PCBs were first produced in 1929.

[PCBs were banned in the U.S. in 1979 and in Canada in 1980, but still

persist in the environment. Organo-chlorines accumulate and remain in fat

tissue in animals and humans for long periods of time. These chemicals have

been found to cause cancer in prior studies, including Vietnam war veterans

exposed to dioxins via the herbicide Agent Orange. These veterans were also

found to have a 50% greater risk of diabetes.] As the authors of the study

utilizing the Swedish cancer registry wrote, " Recent observations that

dioxin, a well-recognized immunosuppressive agent, is associated with both

non-Hodgkin's lymphoma and endometriosis may indicate that shared

environmental factors may be responsible for our observation, an issue that

deserves investigation in future studies. "

To further research on endometriosis and related health problems, the

Endometriosis Association, in partnership with Vanderbilt University School

of Medicine, is launching a major new research initiative. Vanderbilt and

the Association will build a multidisciplinary team to examine endometriosis

from all angles, including the immune aspects which seem most promising for

understanding the cause and cure for the disease. Vanderbilt has committed

$2 million in funding, extensive institutional support, and state-of-the-art

laboratory facilities. In addition, Vanderbilt brings to the research

effort a coveted NIH grant to build a women's reproductive research center,

providing an additional $3.75 million over 5 years for Vanderbilt's efforts.

Never before has a major medical institution made such a bold commitment to

solving the medical and scientific mysteries of endometriosis. " This

represents a new concept in endometriosis research, indeed, for research

generally, " said Osteen, Ph.D., Director of the Women's Reproductive

Health Research Center, Vanderbilt. " Academic research centers are

constrained by the lack of traditional funding sources for a core group of

interdisciplinary scientists focused on a single disease entity such as

endometriosis. The pathophysiology* of endometriosis suggests that

endocrine*, immune and environmental elements can each contribute to the

disease process. We will be able to support the work of a consortium of

world-class researchers with backgrounds in these diverse disciplines.

Working in concert, these scientists will be dedicated to developing

research-driven therapeutic strategies for the successful treatment of

endometriosis. "

Lead gifts for the Association's $2.6 million campaign, called the

Millennium Campaign for the Cure, have already been received. A gift of $1

million is being given by Harry and Betty Quadracci and their family. Harry

Quadracci is President and founder of Quad/Graphics, a four-color printing

operation employing 12,000 worldwide. and Betty Quadracci will

chair the Endometriosis Association Millennium Campaign for the Cure.

Quadracci works as a Corporate Sales Executive for Quad/Graphics

in the New York City sales office. Betty Quadracci is President and

Publisher of Milwaukee Magazine, and President of Quad/Creative, a graphic

design studio. Says Quadracci: " As a woman who has endometriosis

and has had to deal with its consequences, I realize I'm lucky. I have the

financial resources and family support to help me physically and

psychologically. Unfortunately, there are many women who have cases ten

times worse than I do and don't have this kind of cushion. So, it's become

very important to me to get involved in this campaign. I know what it feels

like to have this disease and I know how important it is to find a cure. "

Ballweg praised the Quadraccis, whose gift is the largest private donation

for research on *pathophysiology: Derangement or alteration of function

seen in disease *endocrine: hormonal endometriosis ever. " This generous

gift by Harry and Betty Quadracci and their children represents so much hope

to families affected by endometriosis everywhere. Their leadership will

inspire others to give and to become more aware of this often neglected and

overlooked disease. "

Another major donor to the campaign is H. Dickinson, New Jersey. Ms.

Dickinson, a member of the Association's board, also funded the H.

Dickinson Research Chair of the Endometriosis Association at Dartmouth

Medical School, where the Association has funded research since 1994.

Additional significant donors include Searle Pharmaceuticals, contributing

$150,000. Searle makes a drug, Synarel, used in treating endometriosis.

" With two exceptional organizations Vanderbilt University School of Medicine

and the Endometriosis Association dedicated to a common goal eradicating

endometriosis there is now hope for the millions of women, girls, and

families worldwide who suffer from this debilitating disease as well as the

frightening specter of cancers, autoimmune diseases, and other health

problems, " said Ballweg. Contact headquarters for further information,

including cancer, autoimmune, and data charts.

NOTES FOR MEDIA:

The Endometriosis Association was the first organization in the world

created for those with endometriosis. As a non-profit, self-help

organization of women with endometriosis, doctors, researchers, and others

interested in the disease, it is a recognized authority in its field.

Founded in Milwaukee, Wisconsin in 1980 by Lou Ballweg and Carolyn

, it is now a worldwide, independent organization with some 300 groups

worldwide.

The Association has created the world's most comprehensive data registries

on and about women with endometriosis. The data registry tracking cancers

and other diseases was created at the request of the organizers for the VI

World Congress on Endometriosis with funding from Zeneca Pharmaceuticals,

which makes Zoladex, a drug used in treatment of the disease. Data on

symptoms, delays in diagnosis of endometriosis, and attitudes toward

endometriosis was presented at the VI World Congress on Endometriosis. In

addition to a wide range of literature, videotapes and audiotapes, the

Association has also published two books: Overcoming Endometriosis and The

Endometriosis Sourcebook.

Endometriosis is a hormonal and immunological disease in which tissue

similar to the lining of the uterus is also found in the abdomen, on the

ovaries and abdominal lining, bowel and bladder, resulting in internal

bleeding, formation of scar tissue, inflammation and other medical problems.

Typical symptoms of endometriosis include chronic pain (particularly

pelvic pain), period pain, pain with sex, infertility, painful bowel

movements with the period, painful urination or other urinary problems with

the period, chronic fatigue, chemical sensitivities and/or allergies and

other allergic diseases, and sometimes, other diseases as noted earlier.

Endometriosis is usually treated but not cured with pain-killing drugs,

surgery, and expensive, powerful hormonal drugs. Most women and girls with

the disease undergo multiple treatments and must cope with the effects of

the disease for many years. An estimated 5 1/2 million women and girls in

North America have endometriosis.

REFERENCES:

Brinton, L.A. et al. (1996). " Cancer risk after a hospital discharge

diagnosis of endometriosis. " American Journal of Obstetrics and Gynecology,

Vol. 176, No. 3, pp. 572-579.

Cummings, A.M. et al. (1996). " Promotion of Endometriosis by

2,3,7,8-Tetrachlorodibenzo-p-dioxin in Rats and Mice: Time--Dose Dependence

and Species Comparison. " Toxicology and Applied Pharmacology, Vol. 138, pp.

131-139.

Henriksen, L. et al. (1997). " Serum Dioxin and Diabetes mellitus in

veterans of Operation Ranch Hand. " Epidemiology, Vol. 8, No. 3 pp. 252-258.

Hornstein, M.D. et al. (1997). " Association between endometriosis,

dysplastic nevi and history of melanoma in women of reproductive age. "

Human Reproduction, Vol. 12, pp.143-145.

Osteen, K.G. et al. (1996). " Dioxin (TCDD) can block the protective effect

of progesterone in nude mouse model of experimental endometriosis. "

Presented at the American Society for Reproductive Medicine Annual Meeting.

Rier, S.E. et al. (1993). " Endometriosis in Rhesus Monkeys (Macaca Mulatta)

Following Chronic Exposure to 2,3,7,8,-Tetrachlorodibenzo-p-dioxin. "

Fundamental and Applied Toxicology, Vol. 21, pp. 433-441.

Rier, S.E. et al. (1995). " Immunoresponsiveness in Endometriosis:

Implications of Estrogenic Toxicants. " Environmental Health Perspectives,

103 (Suppl 7), pp. 151-156.

GLOSSARY:

Autoimmune disease: A condition in which immune cells mistakenly see the

body's own tissues or cells as foreign and attack them, resulting in

inflammation and autoimmune diseases such as rheumatoid arthritis and lupus.

Hashimoto's thyroiditis: An autoimmune thyroid disorder characterized by

production of antibodies against the thyroid.

Hyperthyroidism (or overactive thyroid): A condition in which the thyroid

gland produces too much of the thyroid hormone.

Hypothyroid (or underactive thyroid): A condition in which the thyroid gland

produces too little of the thyroid hormone.

Lupus: An inflammatory disease, generally occurring in young women, that

causes deterioration of the connective tissues and may attack soft internal

organs as well as bones and muscle. Symptoms vary widely but may include

fever, rash, abdominal pains, weakness, fatigue, and pain in joints and

muscles.

Meniere's Disease: A sometimes disabling disorder of the ear, causing

hearing loss, dizziness, and ringing in the ear (tinnitus).

Multiple sclerosis: A chronic, often disabling disease attacking the

nervous system. Symptoms include: numbness of limbs, slurred speech, muscle

weakness, unusual fatigue, etc.

Non-Hodgkin's Lymphoma: Cancer affecting the lymph tissue; mainly found in

patients over 50 who are immunosuppressed.

Rheumatoid arthritis: A chronic disease characterized by inflammation,

stiffness and often, deformity of joints.

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Thanks a lot for all the good wishes. I'll keep

you all posted. I have derived a lot of strength and

support from this group in fighting with my urticaria.

These days I am hive free. But I have read many times

here and elsewhere that hives will come back as soon

as the baby is out. I am just keeping my fingers

crossed.

Once again, thank you all.

Nilima

--- Ersan and Ilgar wrote:

> YIPPEEEEEEEEEE Congrats on the baby on the way. You

> know Nilima we will all

> want PICTURES!!!! My Olivia was a May 25th baby. I

> am sending big wishes

> for a pleasant hive free pregnancy and a healthy

> baby. Much Love,

> ~Alena's Mom

> Re: question for females

>

>

> > I started having heavy periods when I was 23. And

> then

> > around 2 years later cold urticaria started. Later

> it

> > was found that I had hypothyroidism. I am now on

> > levoxyl for almost 1 year. I saw improvement in

> both

> > my urticaria and periods while on the thyroid

> > medication. Now that I am pregnant, I have neither

> the

> > periods nor the urticaria. Don't know, what will

> > happen after the baby is born.

> >

> > I sure think that menstrual problem have relation

> to

> > CU. However, both of these problems may be due to

> some

> > other underlying cause.

> >

> > --- Joan Passmore wrote:

> > > Ladies,

> > >

> > > I have a question. Do any of our female CU

> members

> > > suffer from worse-than average cramps or heavy

> > > menstral periods? This problem may be a totally

> > > unrelated to CU. I have never been diagnosed

> with

> > > endometriosis, but have had problems with heavy

> > > periods and cramps for many, many years. I have

> > > read

> > > that endometriosis is an auto-immue disorder and

> I

> > > was

> > > wondering is there was any connection to my

> problem.

> > >

> > > Thanks.

> > >

> > > Joan

> > >

> > >

> __________________________________________________

> > >

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Thanks a lot for all the good wishes. I'll keep

you all posted. I have derived a lot of strength and

support from this group in fighting with my urticaria.

These days I am hive free. But I have read many times

here and elsewhere that hives will come back as soon

as the baby is out. I am just keeping my fingers

crossed.

Once again, thank you all.

Nilima

--- Ersan and Ilgar wrote:

> YIPPEEEEEEEEEE Congrats on the baby on the way. You

> know Nilima we will all

> want PICTURES!!!! My Olivia was a May 25th baby. I

> am sending big wishes

> for a pleasant hive free pregnancy and a healthy

> baby. Much Love,

> ~Alena's Mom

> Re: question for females

>

>

> > I started having heavy periods when I was 23. And

> then

> > around 2 years later cold urticaria started. Later

> it

> > was found that I had hypothyroidism. I am now on

> > levoxyl for almost 1 year. I saw improvement in

> both

> > my urticaria and periods while on the thyroid

> > medication. Now that I am pregnant, I have neither

> the

> > periods nor the urticaria. Don't know, what will

> > happen after the baby is born.

> >

> > I sure think that menstrual problem have relation

> to

> > CU. However, both of these problems may be due to

> some

> > other underlying cause.

> >

> > --- Joan Passmore wrote:

> > > Ladies,

> > >

> > > I have a question. Do any of our female CU

> members

> > > suffer from worse-than average cramps or heavy

> > > menstral periods? This problem may be a totally

> > > unrelated to CU. I have never been diagnosed

> with

> > > endometriosis, but have had problems with heavy

> > > periods and cramps for many, many years. I have

> > > read

> > > that endometriosis is an auto-immue disorder and

> I

> > > was

> > > wondering is there was any connection to my

> problem.

> > >

> > > Thanks.

> > >

> > > Joan

> > >

> > >

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Um, as far as I know, the only way to make a positive diagnosis is through

actually going in and looking...

Air hugs,

Jackie

----Original Message Follows----

From: TamBar226@...

Reply-To: urticaria

To: urticaria

Subject: Re: question for females

Date: Thu, 3 Jan 2002 18:07:37 EST

Jackie:

This is very interesting. How does one find out if they have endometriosis?

Other than being opened up and having laporoscopy? They don't see anything

on sonograms. I have pain with periods and was infertile after having one

child. I've also had melanoma.

Tami (NJ)

Life is tough, but I'm tougher.

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