Fertility symptoms and conditions

I've had most of the side effects mentioned in these posts. But the biggest problem I've had is the massive mood swings I've had. I'm talking really bad temper tantrums. Has anyone else had this? My oestrogen level is sitting under 130 which is way below the normal 750 - 1400 level. I am only 35, but in a psudo menopause state. I tell you what, if I cannot conceive once this thing is removed, I will sue the pants off them! How can no one tell me that I could LOSE my ability to conceive if I use this? I used to have normal levels and now I'm menopausal? At 35? Do me a freaking favor. Take this thing off the market. NOW.

ok, so I am 28yrs old just had my lap for endo on October 1 and my doctor has recommended lupron, and am going to be getting the med in a week to 2weeks,but after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do,and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? did any one have a baby after doing this. my bigs thing is being able to have a baby. Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

ok, so I am 28yrs old just had my lap for endo on October 1 and my doctor has recommended lupron, and am going to be getting the med in a week to 2weeks,but after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do,and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? did any one have a baby after doing this. my bigs thing is being able to have a baby. Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

Well, I am so glad I found this website. I am 39 yrs old and my husband is fixed....so I have no reason or desire to take any form of hormonal birth control. I never liked the idea of inserting a ring or taking hormones after the many female issues I have endure. I only agreed to this because I have painful ovarian cysts chronically, at least 6/year and 3 or 4/year that take me into my OB/GYN for a scan. I have previously had a tubal pregnancy (tube was saved because my OB/GYNs also specialize in fertility) and have had endometriosis. I have had 3 laperoscopic surgeries and 3 miscarriages. First for the tubal, second for follow-up endometriosis and third to remove a GOLF ball sized ovarian cyst to prevent ovarian torsion. Finally, I agreed for the 4th time to take birth control (previous attempts were thwarted by side affect from oral products. I used the nuvaring for 3 weeks and removed it today. Five days into the use I started cramping and bleeding AGAIN (10th day of my cycle). I have been bleeding, heavily for 11 days now, suffered dizziness intermittantly, have had a headache for the last 6 days and been more anxious, moody and tearful. I removed the ring today! I see my gyno on Tuesday. My cycle was predictable before, albeit painful and with ovarian cyst. Just want to say to all who took the time to share. Now I know it isn't in my head.

Thanks ya'll,
~ Texas Pharmacist

i also have been having pains in my back, i just cant wait for the day to end, some days i feel like i worked out all day. The things that i used to i don't do anymore like dancing,exercising and being more energetic. I haven't had trouble with the sex drive actually i want sex more and i don't have drywall either. I really have a sexual drive the week i take out the ring. this past two months have been the worst the for me, i taking to my doctor soon but every time i tell my doctor and i get checked for the problem the results are always the same that nothing is wrong. so what can i do

I just recently about 2 1/2 months ago switched from yaz to the nuvaring. Thank god. I have been struggling the last year with these symptoms: IBS, moodiness, anxiety attacks, palpitations, shortness of breath, headaches, SEVERE stomach cramps, and much much more. It started with taking a ride to the hospital because of what i think may have been an anxiety attack. but at that moment felt like a heart attack. I knew i was too young though. I have since been to my GYN doctor, he told me that it could not be the yaz. But i asked him to switch me anyway to anything else. i have been off for about 2 1/2 months and i feel much better. I don't have to not eat because i know my stomach will cramp. I couldn't even walk up the stairs at wet n wild to a ride because by the time i got to the top my heart would be pounding out of my chest, and everything would be blurry. ...just letting everyone know ...yaz is dangerous...and i do plan on getting a lawyer because yaz never said anything about these complications....

Ok, so I had this little "evil" thing put in May of 2007, at first it was fine and I hardly noticed it. Well, except for the not having a period, then having all the brown goopy stuff I suppose it was a period I guess. I went back and forth between nothing and episodes of this. I used to refer to my symptoms as having a "mock" period cause my body wanted to have one but I wasn't. I told my doctor I thought something was wrong at my annual in January of 2008 because I couldn't loose weight, I was tired, my migraines came back, my back hurt, my boobs hurt. She told me I needed to have my thyroid checked and ran all kinds of tests. I dismissed it all, but in the back of my mind I thought it was because of this little "evil" piece of plastic. I'm sorry but not having a period is NOT normal. I lived with the "side effects" and at my annual in February of 2009, I had gained more weight, even though I was taking fat burners, working out, and watching my eating habits. Then about 3 months ago, I started experiencing the worst pain possible. Always around the end of the month when I was having my "mock" period symptoms. It was so bad I could barely stand up. My mood swings were HORRIBLE, my husband and I fought a lot. It keep getting worse. After repeatedly telling him that I thought this was all due to this IUD, he dismissed it until this month, when I could barely stand up because of the pain. He finally said take it out. I am getting it taken out today at 10 am and I am counting the minutes. I thought I was crazy, and that this was all in my head. I finally told my husband that I am taking it out and our fertility is in Gods hands. I have an 18 year old daughter, and a 19 year old son. They are grown and gone, he has 2 children from a previous marriage that he never sees. I am 38 years old and have resolved myself to the fact that if I become pregnant it is Gods will for my life, but in the mean time I will be rid of this "evil" thing and all of the HORRIBLE side effects. To anyone reading this that is thinking of getting one, PLEASE don't, you will be sorry. I feel as though it was an ok option for me for about a year, not the 5 they say and it costs way to much money for only having a year. The side effects are horrible, you will experience them and you are NOT crazy.

I had my Mirena placed almost exactly 3 years ago. For about the last year, I've had pelvic pain almost constantly. I've gone to my gyno and she's given me several ultrasounds. All show that I have multiple follicular cysts on both ovaries. I am starting to worry that I have endometriosis and my gyno won't give me a laproscopy to find out-you won't believe her reason. She says because I don't have a problem with fertility (I have 3 children), that she's pretty sure that isn't what's wrong with me. So, I was talking to a friend who has endometriosis and she gave me her gyno's name. I have an appointment on 18 August and the nurse told me to consider, in the time I'm waiting for my appointment, having my Mirena removed. I have battled depression for quite a while, I've never been able to lose my baby weight (my oldest turned 4 last month) and recently, my pelvic pain has become so bad that I have considered going to the ER a few times. Also, I have lots of cramping in my back. And something that I never considered being a symptom of the Mirena, I'm having a lot of trouble remembering things. If I'm trying to say something sometimes, I can "see" the word I want to say but I can't get the word out. But I've seen a lot of other posts here that describe the same thing. I was honestly afraid I had some horrible brain tumor. I have recently gotten divorced, so I don't need the BC anyway. I had another ultrasound last Thursday, with the same results, only this time, my gyno told me to go see a gastroenterologist (sic). Basically, I felt like she was saying "don't bother me anymore because I can't help you". She never, ever suggested removing the Mirena and stupid, gullible me never considered it because I trusted her that it's not the Mirena. However, now, reading these experiences that are so similar to mine (and my sister, who also has a Mirena and is having the exact same symptoms), I am going to call the gyno on Monday and tell her I want it removed at my appt next month. Thanks for sharing, ladies.

im currently on my fourth month of treatment with lupron and would like to know if anyone that had fertility problems was able to conceive after a course of lupron...? im 32 and have 2 beautiful children, but would like one more before i undergo a hysterectomy...i have been diagnosed with endometriosis, adenomyosis and severe pelvic adhesion's. i was in so much pain that it was ruining my life...the lupron has been pretty great this time around...six years ago i did it without any add-back therapy, but this time im taking progesterone along with it and the side affects have been minimal...still have mood swings and a decreased sex drive, but no hot flashes or night sweats. its definitely worth the pain relief...for me anyways.

I am in the middle of my second month after getting the first shot (for 1 month) and the second ( for 3 months). I have recurrent fibroids and ovarian cysts that caused a lot of pain and severe bleeding.
I was scared to try Lupron. I consulted with my uncle who is an OB/Gyn and he told me that the version they use now is very safe, with side effects like many other drugs...
My doctor gave me options for the treatment, but because I want to get pregnant again (already have a 2 1/2 yr. old boy), hysterectomy was out of the question. The doctor removed some of my fibroids laparoscopically before I got pregnant with my son, but since they "showed up" again, he recommended to treat them with Lupron instead of removing them trough surgery, because the surgery leaves scarring that can later interfere with fertility.
Anyway, YES I have experienced many side effects mentioned here: hot flashes, mood swings, a couple of headaches, and some "bloating". The worst side effect for me has been insomnia...but they really haven't been that terrible...you learn to deal with them. I am in no pain and didn't get my period this month.
I guess everybody is different and they experience everything in a unique way.
My suggestion is to try it if you really need it and weigh in the pros and cons objectively.
Good luck!

Wow, I'm a bit fr***ked out after reading all these posts. I must be one of the lucky ones, as well. I had my Mirena put on 1 year ago after my first child. It did not hurt and I have had very few of these complications listed. However, I have suspected that my weight gain and inability to lose was a side effect of Mirena. This is what brought me to this site. I've gain 15 pounds and no matter how much I exercise or stage myself...it stays! I also notice now that I read....that I have had a lot of hair loss. I now have a few questions:

I lost my milk supply after going on Mirena and my Dr. assured me this wasn't the cause. Anyone else experience this?

Also, I'm concerned about the effect this will have on my next pregnancy. What has been your experiences once you've started trying again? I was told I would have no problems and should go off 1 month before TTC, but now I'm pretty worried!!

ok, so I am 28yrs old just had my second lap for endo and my doctor has recommended lupron, after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do, my post-op surgery appt is this week, and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I just went in for my second shot of Lupron (out of a series of 6) for treatment of stage IV endometriosis. The most noticeable side effect I experienced was during my first menstrual cycle after my first dose of Lupron. I had never experienced menstrual pain or cramping (even though I had advanced endometriosis) until after Lupron. I have a fairly high pain tolerance and yet the cramping for the first 2 days of my period were almost debilitating. I had extremely heavy bleeding and have had spotting daily ever since (app.18 days). I have gained about 3 pounds because I have no energy at all. I'm usually active and work out 4-5 times a week but by the time I get off work, I'm too fatigued to do so (hence the weight gain I guess). I have hot flashes and night sweats all the time. The most recent side effect is high blood pressure. I have never had high blood pressure in my life (I'm a healthy 25-year-old woman) and when I went in for my 2nd Lupron shot today, they told me I all of a sudden do. I don't seem to have mood swings but do feel depressed and sometimes more anxious than normal. I have experienced a decreased interest in sex as well.

I've been searching for answers on LONG TERM side effects of Lupron hoping that it could give me answers as to what's going on in my body now!
23 yrs ago my fertility dr. gave me Lupron to inject MYSELF EVERY DAY (experimental back then). I had SEVERE endo since the age of 16 and was fighting that as well as trying to get pregnant thru invetro. I was 26. At 29 I had an emergency hysto. Now at 48plus I have chronic tendonitis where the tendons will shred off of the joints. I have been diagnosed with C spine and T spine disease, osteoarthritis and a mystery that I'm going to have to go to the Mayo to figure out (hopefully). I have tumors that are growing in my lower back...growing around nerves, tendons and bone, They aren't sure why they are there, why they are growing, or even what they are. Surgery removed 2 of them...but pathology shows foreign matter other than tissue/bone. All they DO know is that it is not cancer. One year ago I started losing weight (25 pds) for no reason. I'm now holding my own at 112 and hoping to figure all of this out. I can't help but wonder if Lupron or any other experimental drugs I was on has something to do with this. Is there anyone out there that used this drug so long ago??

I want to share information with everyone regarding the filing of Vaccine Injury Compensation (VIC) claims. I realize that many of you have probably already initiated action, but, if not, you may want to consider doing so.
I have posted a couple of times before regarding my daughter's reaction to Gardasil. Here's a brief summary: At age 19, she had 2 shots (Sep & Oct 2007). For 9 weeks in late 2007, she suffered severe GI problems, along with many other incapacitating symptoms, but no seizures. She recovered from the constant GI problems but has continued to experience occasional flare-ups. (Prior to the shots, she had NO history of such problems.) She also began to experience debilitating problems during menstruation, and in Oct 2008 her annual pap test showed precancerous cells, as did a follow-up pap test in Feb 2009. (In Sep 2007, she had a normal pap test.) Her next GYN appt is in May.
In light of her continuing problems and the alarming information in the Jun 2008 Judicial Watch Report regarding (1) the 44.6% increased chance of developing precancerous lesions if certain (undetectable) conditions existed prior to vaccination; (2) the fact that Merck does not know if the Gardasil vaccines are carcinogenic; (3) the fact that it is unknown if Gardasil will have long-term effects on fertility; (4) the fact that the final report on Gardasil's safety is not due until late 2009; and (5) etc., etc., etc., we have decided to file a VIC claim. She is still on our insurance bc she is 20 and a full-time college student, however, her future insurability once she becomes independent is a concern.
Information on filing claims is at www.hrsa.gov/vaccinecompensation. I called the Clerk of US Court of Federal Claims at 202-357-6400 and within minutes he e-mailed me a list of attorneys who specialize in VIC claims. I called a nearby attorney, and he returned my call in less than a day and provided very helpful information. Generally speaking, claims must be filed within 3 years after the first symptom of vaccine injury and injury must last more than 6 months, or claims must be filed within 2 years of vaccine-related deaths. (This is not intended to serve as governing guideline; please refer to the website for complete information.) So, in my daughter's case, the 3 years will be up in Oct 2010. The attorney advised that we need to get started now to collect all the medical records and allow at least 6-8 months for review and processing (after medical records are obtained). The up-front cost is minimal ($250 to file, but assistance is available in cases of financial hardship, some doctors/hospitals may charge for records reproduction, but that's about it, as it was explained to me.)
I know that many of you are still trying to get your daughters through their Gardasil ordeals and may not have a lot of time to devote to this, but I wanted to alert you to the time limitations. Unfortunately, none of us know what complications our daughters will experience in the future from Gardasil, so it's something we should all consider.
Good luck to everyone. I pray daily for the thousands of girls who have been injured by Gardasil.

I have had the Mirena since October, 07, right after my daughter was born. Very easy insertion. I have had the usual problems with weight gain, acne, moodiness. I went to get my IUD out on Monday, 3/23. My doctor couldn't find it and I was in agony as he tried to "tease" the string back down out of my uterus. I had always heard the removal was the easy part. I went back today after doping up for the pain, and after thirty minutes, my doc still couldn't find it. Now I have to have an x-ray and surgery done to remove the stupid thing, which has either imbedded in my uterus or perforated into my stomach cavity. It is supposed to be very rare, but it has happened to me, and I just want the thing out of me. I want to get pregnant later this year, and am fearful for my fertility. Think about that very carefully, anyone contemplating it. I had no idea that could happen or I would have NEVER gotten it to begin with.

Before I had my son I had been on Orth-TriCyclen off and on for about 4 years. My periods were always normal and when I went off the Pill it was so easy to become pregnant. After my son was born in Dec. 2007, my doctor recommended Yaz. I've had all the symptoms everybody here has talked about: anxiety, depression, weight gain, very high blood pressure, no sex drive, and just overall not feeling like myself. I just attributed it to post-partum and my body trying to readjust to not being pregnant. But the biggest fear, but secret relief, was the fact that I NEVER HAD A PERIOD!!! not once!!! I think I spotted twice in the course of a year. I would like to get pregnant again in June so I went off Yaz in January. It is March and still don't have a period - don't get me wrong it is kind of nice, but I am also very worried. My doc says its normal, and to just give it time, but I still feel worried that Yaz may have messed up my fertility and I may have a hard time getting pregnant again if I don't get my period back. I haven't received any good info about this - maybe someone else is in this situation -

Hi
I did find that life with the MIRENA coil got better as time went on... I had mine from about 4 years ago and had it took out jan 15th 09. A few problems at first, agony putting it in, unable to drive home, my partner had to come and get me. Thats the main reason I didn't get it taken out because it was agony for days! Then I had the terrible acne and weight gain, periods stopped, and no sex drive. But these did go away and it was fine after about 6 months.
I was told that fertility returns to normal right away... but that doesn't seem to be true, I have not had a period yet so was a bit worried, looking at this site and others, it seems periods can be slow to restart and irregular after that. Has anyone else experienced delay in periods starting again after the Mirena was took out? Would be good to hear about this so I don't keep worrying about this.

I had my mirena inserted about 13 months ago before Christmas after the birth of my 2nd child , I was naturally shedding the baby weight until Mirena came into my life and then I gained 10lbs effortlessly within 2 months! even though my diet is always the same (I am coeliac). I had to start working out running 4 times a week and gradually have lost 8lbs but its been a huge battle.
Last May I woke up one morning bright red covered in a sunburn type rash all over my body it was scary, my joints ached so bad and my hands and feet were really swollen as if my body was reacting to something.. my gp did some blood tests and nothing it kept happening for 2 weeks and then the rash went,..I put it down to a virus at the time but felt as weak as a kitten and suffered night sweats, anxiety and flu like symptoms for months.

Ive had to really fight to keep up my running because most of the time I feel tired and depressed and run down and I have awful PMT the past few months have been dreadful I feel rubbish most of the time..everyone is getting on my nerves, I have little sex drive too and I am sure its down to the Mirena..its side affects remind me of the mini-pill which I took once for a few months it sent me so extremely loopy (paranoid and anxious) that my husband flushed them down the toilet!! well I think its the same/similar type of synthetic hormone that my body DOES NOT agree with.

I saw my Gp the other day and asked her about the side affects and she still said that I shouldn't have any after a year and it was very rare but after reading about it on here I cant believe it... its obvious and Im getting it removed. Ive had over a year of feeling terrible and various ailments so much so that I think my immune system (which is already sensitive) has suffered.

My daughter had her gardasil injections in 2007 at age 16. Until then she'd had 3 years of normal regular periods. Since then her period has all but stopped, just appearing every 4 or 5 months for a day. We are now worried if this will effect her fertility.
Since the injection she has also developed vairly severe acne.
She has also had 2 episodes of passing out and seeming to have a seizure after just 2 alcoholic drinks. The doctor says none of this has anything to do with the vaccine, however I am sure that the sudden change in her periods came directly after her first shot. Qld. Australia

I started taking Yaz about a year ago. I started taking it around the time my brother died in a car accident. I thought that my loss of libido, tiredness, lack of interest in everything, emotional outbursts, arguing with my husband for any reason, crying over nothing, unable to concentrate while studying and unable to remember a thing were all because of my brothers death. I am now thinking that this may be due to Yaz. Does this sound like Yaz side effects? or am I suffering from depression because of my brothers death. I just haven't felt right lately and I cant figure it out.

i was on Yasmin for 3 years - thankfully the worst side effects i had were low sex drive and dryness. i did have a couple scares where i thought i had a clot, but i got it checked out an it was nothing. i got off the pill a month ago. i feel fine. i've been a bit moody and i cry a lot over nothing, but i attribute that to my body readjusting. i haven't had a period yet. i'm a bit nervous about that. i do feel i've gained a small bit of weight.

for all of you who are reading this - there ARE alternatives that are safe and easy. i just bought a fertility computer called LadyComp. it's expensive, but when you think about the side effects it is saving as well as the monthly expenses for the pill, it will eventually save you a lot of money as well as your health. it's not sold in the states (cuz pharmeceuticals rule the country and won't allow something like this) but you can buy online from England or Canada. it's just as effective as the pill and SO much safer for you!!!!

The gynecologist examined me and refused to insert a copper IUD because he said my uterus was too small. After I got dressed, he handed me a FREE SAMPLE of NuvaRing. I said : "But I don't want to use hormonal bc." He said : "This has less hormones and doesn't go through the liver." Well I guessed that was a GOOD thing, which he wanted me to believe of course. The mood swings, serious anxiety, irritability (I would go as far as to say, anger and impulse control problems) and burning vaginal pain during sex seriously affected my relationship with my boyfriend. We may even be broken up now and I blame it partly on NuvaRing and other hormonal bc I took after my 2 months on NuvaRing. I am so sad that I had to go through all that! I wonder how many gifts the doctors get for giving us the prescriptions of bc. Anyone interested in non hormonal bc? There is the cervical cap in many varieties and sizes. It doesn't affect sexual spontaneity because you can insert it several hours before sex and you can have intercourse several times with it on. You can even keep it in for up to 3 days.

I used nuvaring for 7 months straight and never had any problems. My period always came exactly the same day every time and I loved that since without it im pretty irregular meaning I could get my period between usually 3-5 days after I was supposed to. Last month I decided to stop Nuvaring and had my period exactly when I was supposed to have it (September 8). It is now October 10 and I still haven't had my period. I just had sex twice a week ago and with a condom. I'm also feeling some cramping like when I usually get my period only that when i usually feel that, my period comes within minutes but I've been having this cramping the whole day. i also have been peeing very often today. Yesterday (Oct 9) I took a pregnancy test and was negative. Why am I having cramping? Why is my period already 5 days late? Why do i have to pee so often? Is this because I stopped using nuvaring a month ago?

I had Implanon inserted in June 2008, I just had it removed Sept 17 2008. The first side effect was that I gained weight. My appetite increased and I felt like I was constantly hungry. Within the first month I got an Urinary Tract Infection, the infection was so bad that it transferred to my boyfriend through sex.. After a month I started bleeding and it lasted 4 weeks, not spotting just bleeding. I lost my drive for sex, I felt bloated and was too tired ALL THE TIME!!! I was crying over everything, I felt depressed and stressed about everything, my head hurt all the time. My whole body just felt off. I wasn't myself at all. One morning I woke up with a horrible sore throat. I went in for strep test and tested negative. They said it was just a viral infection. A few days after that my muscles started to hurt. My left knee and hip joint began hurting so bad that it was hard to walk and get up out of bed in the morning.(The Implanon was inserted in my LEFT arm). Occasionally I felt tingling in my left arm and fingers. I then notice my left ankle was getting swollen and at that point my whole body felt like it was shutting down.I started to run fevers and thats when I looked up the "possible side effects of Implanon" online. As I read I realized that I had every single side effect even the uncommon more severe ones, but it seemed like my symptoms were multiplied by 100. I called my doctor and she immediately had me come in to have the implanon removed. Today is Sept 22. I have been on bed rest since the implanon was removed. It turns out that my body had rejected the Implanon, treated it like was a foreign object.