Proof symptoms and conditions

I am 45 and had the device inserted in June. Since then I have had an annoying constant red-brown discharge and my period three times. My menstrual cramps are definitely greatly lessened but what is freaking me out (apart from the discharge) is the anxiety I am experiencing for no reason. I am also feeling depressed. I am greatly concerned as being on the pill many years ago I had a mild stroke and my doctor assured me that the hormones ion the Mirena stay in the uterus. Why then the sudden anxiety attacks? I have always been a really laid-back person - I can only relate this sudden appearance of anxiety to the Mirena - it started about two weeks after I had it inserted.

I am now debating whether to ride it out - has anyone had the anxiety subside?

I'm loving it.

After trying every HRT and pill under the sun for surgical menopause, and I'm in my 30's, I'm glad I've finally found something that makes me feel better.

Trust me here. Everyone is different and it may take you a thousand different medications until you find the right one, especially with hormones, but when you find the one that works for you life as you know it changes for the better.

Don't listen to that bollocks about HRT or the Pill causing you breast cancer and death... not having HRT or the pill etc can cause you just as many difficulties. Some of you may get osteopenia, vaginal atrophy, and other things that are very private. Let's face it, death can come after you even if you're not on hormones, just look at a children's hospital if you want proof.

I wish all of you suffering from hormonal conditions a healthy long happy life. I know the journey there is hard, but never give up. Just try something else. Even giving hormone therapy a break for a few months and then trying a different drug or approach such as a smaller dose.

Perhaps it's not even your hormones causing the problem, perhaps you should seek a specialist physician, immunologist, endocrinologist or just find another doctor that understands what they are doing and actually helps you.

All of the above saved my life. All of it. Together. It is a long hard road ladies but it's your life.

Blessings to you all.

My husband has been on Simvastatin for a few years, six months ago his dose was increased to 40mg, since then he has become someone I don't recognize, we have been married over twenty years and he used to be a very placid and wonderful man. He is now both verbally and physically abusive, he threatens me with divorce on a regular basis. He lies about me to others telling them he does all the housework (never) there is never any food in the house ( Totally untrue) He disappears for hours on end, and sleeps much of the time. He can be quite plausible with other people but turns into a monster when he returns home. Doctor told me I don't think it can be the statin, don't believe everything you read on the internet! She said to be sure for him to come off it for a few weeks - he refused! His aggression is escalating and I now dread him coming home. he has odd moments of being nice but within hours he is back to being nasty. He had been impotent for 7 years but now during his "nice moments" becomes amorous! I am at my wits end, has anyone else experienced this!

I had mirena inserted in August of 2008, i bleed continuously for about two months after that my periods was really heavy. For me there was no hair loss, just stomach cramps and now i feeling like i'm pregnant, nausea also like morning sickness, but my thing is how can i be pregnant and this IUD is suppose to last for 5yrs. I'm seeing my doctor tomorrow and will post an update.

Like someone said maybe its time foe a lawsuit against mirena.

I have been on Singulair longer than I can recall... at least 10 years, maybe longer. My 7 year old son has been on it since he was probably 12 months old. Neither one of us have had any problem reported here. No depression, no sleeplessness (until I weaned him from naps, he slept up to 13 hours a day), no leg cramps, nothing. We are two of the happiest, most well adjusted people you could know. And, best of all, we haven't had any asthma attacks. Bottom line, different drugs react differently in different people. Don't let the post here stop you from trying a medication that for some could mean the difference between life and death depending on how asthmatic they are. As with any drug recommended by your doctor, try it. If you experience adverse reactions, stop it ASAP. It's that simple.

I took 400 mg of Topamax for about 5 months for migraines. It did help some when seroquel and verapimil were added to it at the end. I had a severe psychotic reaction and was diagnosed as bipolar. The dr wanted to put me on a high dose and let me spend the rest of my life twiddling my thumbs rather than admit Topamax was the cause. These psychotic event have been documented since the 90's.

It took me 3 years to regain my typing ability. I still scramble some words 4 years later. I proof read, but I may have missed some errors in this post. Thanks you Topamax!!

Hi All, I am here for the first time in desperation trying to ascertain if my problems are Advair related. I have been on it for over 20 years (started as a study patient). I probably would be dead if it hadn't come along - seriously - and I had been on prednisone a lot. But, to add a voice to what others are saying, I can't sleep, and always wake with the most terrible headache, along with other general aches and fatigue. I was coping so so until I was rear-ended and developed some neck issues. Now I live with never ending headaches and fatigue and a tendency towards depression. Pain killers and sleeping pills get me through the winter months and then in the summer with lots of activity outside I rebound so that I can go through another yearly slide downward. What is really a killer is that I can't get going in the early mornings and have been hassled by my employer who has determined by a psychologist that I am a malingerer because there is little proof of physical illness! If I didn't have a history of having been, and still being, a very hardworking and persistent individual I would think I was going nuts (I'm 60). If anyone has a similar story, please comment further. Thanks

I read with interest several of the posts here. I have been on Lipitor for about 5 years. I have been experiencing leg pain, back pain, neck, and hand pain for likely 4 of the last 5 years. I have arthritis, I thought. Two weeks ago I ran out of Lipitor. I read several other forums where Vitamin C and Omega 3 were suggested as a possibles to replacing the Lipitor along with generous amounts of water. I said, What the hell, I will give that a try. Within days of stopping the Lipitor, most all the pain has subsided to the extent that I have not had to take any other Pain management medications at all. I was prescribed Perocet for the pain I have been experiencing. Two weeks ago, I had a tough time opening a bottle of soda, or even a relish or pickle jar. Today I can! Coincidence, I think not!!

I am so glad that I found this site and to see that there are other women out there who are having problems with the Mirena. I thought it was just all in my mind! I had the Mirena inserted in February 2008. Started having problems with high BP when pregnant with first baby and when I went back on pill after his birth BP wasn't doing any better. After having my second child, I contemplated about Mirena vs. having tubes tied. My OB said the Mirena was the perfect thing for me and was pretty much like tubal ligation, but without the surgery. I had no problems when Mirena was inserted..just bleeding (seemed like forever for me to stop bleeding) and the normal dizziness. For the first three months, I never knew when my period was going to be, but I just kept remembering what my OB said "your periods will be like nothing after the first three months." My periods did get a little better...however not the "light" or spotting periods. After the first three months, I started noticing that my hair was starting to fall out more but thought it was part of postpartum. I started feeling really tired, skin started to break out, felt depressed, my mind was racing, couldn't sleep, had problems remembering things (simple things), migraines got worse and more frequent than what they used to be before, moody, agitated, had chest pains, nausea in the morning (at one point I thought I was pregnant again!), stomach pains, diarrhea/constipation, kept having vaginal discharge (like when you are pregnant), came down with bacterial vaginosis, UTI's were somewhat common,no sexual desire and my BP was out of control. Seven months after having Mirena inserted, I started having sharp pains near right ovary. I had problems with cysts in right ovary before and had them removed so when the pains started, I had a hunch that most likely it was another cyst. My OB closed her practice so when I went to new OB for annual pap, I mentioned all the things I was experiencing including suspicion of cyst. I told her I had been experiencing all symtoms since Mirena was put in. She told me that she has never heard of the Mirena to cause symptoms like these. Told me that perhaps I was still having effects of postpartum and that my body was trying to get "back to normal" and get used to Mirena. Had all these blood test done and everything came back normal. I did have a cyst on right ovary and was told that it should go away within 2 months. Just had a follow-up ultrasound today (2 months later) and cyst is still there along with other cysts on right AND NOW left ovary. Most of the time, I am in a lot of pain especially on the right side. I was told to just take Motrin for the pain, but that nor heat packs work at all. I am really considering to have the Mirena taken out. I REALLY believe that the Mirena is the cause of my cysts. Is there anyone out there who have gotten cysts while with the Mirena? And has anyone experienced having no problems with cysts after the Mirena was taken out? Since finding out that I have multiple cysts on both sides and knowing that my doctor will probably tell me they will eventually go away on their own (first one is less than 2cm and others are smaller), I don't know if it is even worth keeping the Mirena in. I hate having all these symptoms...I just want to be "normal" again. BUT, IT IS VERY COMFORTING TO KNOW THAT THERE ARE OTHERS WHO ARE OR HAVE EXPERIENCED THE SAME. Now I can tell myself that it is not all in my mind and I am not going crazy!

Hello, I have read over most of these side effects and i would have to agree and be afraid of most of it. See I was diagnosed with bronchitis/pneumonia, they prescribed me these pills along with steroids. I have not taken the steroids yet but I did take my first dose of levaquin about 12 hours ago around 8 pm. With my dinner and plenty of water and fluids. I went to bed late with my fiance but not cause of the medicine, we decided to stay up and watch movies. Although, it did help my coughing and breathing, I felt bloated or ballooned up all of a sudden and it was starting to hurt my stomach. I figured it was the food I ate and all the water I have been drinking. So, next I noticed some minor vaginal discharge of which looks like when I'm ovulation so I pasted that as that. Now I woke up at 5:30 in the morning when I went to bed at 2 am and I can't go back to sleep! I woke up from a nightmare to see things in the dark to scare the %$^* out of me. I had this really bad taste and dryness to my mouth I felt like it was suffocating me. I cant seem to think straight or type well (I had to go back and review what I wrote but I might not have gotten all my mistakes) I feel like I have ADD I keep forgetting how to spell simple words... I mean the list keeps going and going. I am writing now because I am currently on it. I will not be taking this medication anymore much less the steroids but if anyone reads this, I hope you read first then take.

I just read all of these posts and I have to tell you that I have been battling a so-called UTI for 3 weeks....I have been through two antibiotics, Cipro and Bactrum and I have had cultures come back negative...I have stomach pains in my upper abdomen so bad, nausea, loose stool. Dr's are still trying to figure out what the problems is; needless to say I am having this mirena removed on thursday and I have to tell you I CAN'T WAIT!!! This has totally controlled my life. I don't have any proof that this IUC is causing the problem but after reading all of this; word for word from other women, I'm sure it explains a lot. I wish I would have been warned of the UTI side effects long before I had it put in. I've had my Mirena for 2 1/2 years and I have been moody and no sex drive along with all of this and it makes me wonder...is this my problem. I'll let you know if I get better after Thursday.

I commenced Lipitor 14 years ago at age 47. At that time I was a regular tennis player, walker and generally fit for my age. No problem with Lipitor for the first couple of years until I began to experience hip and low back pain. My GP diagnosed arthritis. Gradually became worse and I started to gather injuries (over stretched ligament in right knee which refused to heal, plantar fasciitis twice) My back pain became far worse, I persevered with tennis believing that exercise would help. I began to "trip" on the carpet and going up stairs (foot drop). I was sent for a CT scan in 2002 which showed spondylolisthesis and root canal stenosisss. On advice from doctor I stopped tennis. Referred to a neurosurgeon who after several months carried out a laminectomy in July 03. Cleared to recommence exercise in December 03 which is when my nightmare commenced. I developed bursitis in one hip, stopped walking until it settled, then excruciating pain in feet, and then bursitis in the other hip and continuing foot pain. I developed rib/back pain, again diagnosed as arthritis even though I felt the pain was muscular. I had one session of aqua aerobics and woke the next morning with plantar fasciitis which continued for 3 months even with doctor, physio and acupuncture treatment. I was then referred to a Spots Medicine Dr who ordered bone scans/x-rays which revealed a stress fracture in my foot. In 2006 I began to notice that my right arm had a tense feeling all the time, I had a loss of dexterity in my right hand which assumed a claw like appearance and my normally neat handwriting became practically illegible. My physio recommended I see a Rheumatologist who said I had "no more arthritis than I would see in any 62 yo", he sent me to a Neurologist who after 5 mins diagnosed Parkinson's Disease. Within 7 weeks of commencing the PD medication I was experiencing Restless Leg Syndrome every night. The neurologist said that my condition had "progressed" and increased the medication - twice. I was then getting RLS DAY AND NIGHT and getting no relief OR SLEEP!!! Finally after 12 months misery my GP suggested that I try coming off Lipitor to see if that was causing my body pain. Within 6 days I felt better, my muscles became less stiff and relax. I went back to my Neurologist who refused to accept my claims, he insists I still have atypical PD (because I do not have tremors). I told him the cure is worse than the complaint and against his advice I weaned myself off PD medication and Lipitor. It was hard going but I NO LONGER SUFFER FROM RLS AND MY DEXTERITY IS SLOWLY IMPROVING. I still have dexterity problems with my right fingers but the tense feeling in my right arm has gone and my "claw" hand is starting to relax My muscles feel bruised all the time. I am still taking my blood pressure tablets and 150mg of Co-Q10 a day. I have been off Lipitor 9 months. It has been a painful journed for the last 8 years and a nightmare for 12 months. My GP has marked my records as "allergy to statins" but says she just doesn't know if I have Parkinson's. I know that I will never take this awful drug again. My cholesterol has skyrocketed but I will have to try and lower it naturally and take the risk. I constantly feel like I have worked too long and hard in the garden, all my muscles are so sore. I really need to know if this damage is permanent and if this drug has caused Parkinson's Disease itself or just PD like symptoms. I guess I will just have to wait and see. I don't think doctor's believe us when we say Lipitor is doing damage to thousands of people. They love it!! When we are aging we are not surprised to get diagnosed with arthritis and this is why we take this medication unwittingly for so long.

I have been in a serious relationship for 5 years I was on the pill for at 7 years when we got married in June we decided it was time for me to stop taking the pill.. I had my first Gardasil shot and everything was fine just really sore injection site and sore arm. When i went to get my 2nd shot they made me sign all the paper work again to get the shot.. I asked it it was standard procedure to resign these papers and she said no why.. I said because i have done this once and this is my 2nd shot.. She insisted that it was my first. When i got done i asked the lady at the desk and she said she had no record of it and i was like well something is wrong here you may have no proof but i know because remember my arm hurting.. She finally had to call my ins co. to see if they billed me once before.. Lo and behold i was right! I just go t my 3rd shot right about the time my period was going to be here and it has been 2 weeks and I still haven't gotten my period which is really unusual because I am always on time.. I have taken 3 pregnancy all which are negative. However last month my husband and I were really active during that "Window" to get pregnant. I was talking with my mother about it and she said that she had to get a blood test to show that she was pregnant with me.. So i don't know if i need to get blood taken or just think my missing period is because of this damn drug.

4 months ago started on preastatin 20mg increased within 1 month to 40mg; could not stand up without help; stopped statins at that time. CPK done 157, this was done to show me I wasn't in danger of rhabdomylysis, I continue to suffer with swelling R leg and severe pain. Leg is still swollen 4 months later.....I am professional RN in ICU ,,can't really do my job as necessary...Should I file for disability; or does someone have an answer to provide relief for this malady???

I have adult onset asthma that has gotten progressively worse since I moved from a small Midwestern town to a larger city in the Sonoran desert. On account of this progression in asthmatic symptoms and flair-ups, I switched from Flovent 220mcg to Advair 500/50 about a year ago. For a long time, Advair really seemed to be helping my asthma. Outside of gaining 10-15 pounds in this year (which I asked my pulmonologist about and was assured that inhaled steroids cannot be responsible for), I have fortunately not had many of the aforementioned side effects. However, in the past month after experiencing a bad flair up while studying abroad, I have developed severe heartburn, nausea, acid reflux, a sore throat, and mouth sores. I take the medicine as prescribed and am always sure to properly rinse out my mouth, having been warned about this. After reading everyone else's entries on this site, I am now curious if Advair is doing more harm that good.

I've been on Levaquin for only 2 days, combined with Prednisone... Taking them due to a nasty sinus infection. One of these two meds is making every joint in my body hurts, as well as me having lost almost every bit of my sense of taste. I ate general tso's chicken today for lunch and could not taste anything, so as an experiment I ate one of those little red Chinese peppers that I normally throw out because they are WAY too hot - I couldn't taste a thing. Last night I had to drop the air condition down to 68 degrees as one of these two meds made me sweat very heavily and uncomfortably hot.

I have only been taking singulair for about a month. I have noticed that I have become more irritable, grouchy, hateful and just numb, not really wanting to be around anyone, not caring about anyone else's feelings much. I also noticed I have become extremely lethargic, to the point of falling asleep at work as well as heart palpitations and stomach pains. I just started new birth control pills so at first assumed they were causing these side effects, that is until I looked up the side effects of this drug! I have over half of the side effects so I stopped it immediately and can already tell a difference in my mood. I have to sons age 11 and 14, both who have asthma and allergies. The took this medication for a few years with no side effects but have not taken it for about a year now. My youngest son however, has been diagnosed with ADHA and ODD and possibly BiPolar disorder. As I read the other posts, I realize the description of how their children act while on this drug is exactly how my son acts. I wonder if there can be irreversible permanent damage from taking this medicine? He has been on a number of ADHD drugs, none have helped except to make him stop eating and lose weight and he is small for his age, so I have taken him off everything. Has anyone else out there experienced what could be permanent damage from this drug in their children? Even after being off the drug for a year or so? If it could make me miserable within a month, what can it do when one takes it for years? Its sometimes hard to tell the effects of medicine on small children. My son prob starting taking it around 4 yrs old and took it til he was about 8 or 9. Just wondering if anyone else out there has had this happen to them or their children.

My 10 year old son has taken Singulair on and off since he was 5 years old and has been on it for the past 3.5 years. My son at an early age was affected by a bad marriage and then the divorce when he was 5 yrs old. So we always suspected that his behavior issues were caused by this and I had done everything I possibly could to give them the help he needed to get over and through his issues. He was held back his first year of Kindergarden and during his second year midstream he was placed in a special class for behavioral problem children. Nothing ever seemed to help him, everytime we would see some progress and encouragement we were always blind sighted by a behavior that was always worse. Two steps forward and them 5 steps backwards. I always knew that his problems would never get better overnight so I just kept on going. He was diagnosed with ADHD but because he has some ticking issues I had to put him on Strattera which was did not do a thing for him. I always described him as my Dr. Jeckyll/ Mr. Hyde child. He could be really good and sit still and behave but I think he had to try really hard to do so. He eventually was always overpower by the impulse to show negative behaviors. Defiant, extremely impulsive, always negative and completely miserable all the time. He also went through phases of compulsions. There was always a compulsion of the month- germs, bathroom habits, noises, repetitive words. He hated school and always complained of a stomach ache which i thought he was always faking to get out of school. He had confrontations in school everyday for most of the day. I often thought some of this was because of being tired all the time. We had battled over bedtime every single night. He was terrified to go to bed alone, I tried everything to get him to sleep alone. I wore myself out falling asleep next to him, I would then go to my own bed only to be up with him half the night going back and forth. I gave in many a night and slept with him just so we could get a good nights sleep. At age 8.5 I finally got him to go to sleep alone but the lights haf to be on and he has to know that I am still awake before he will fall asleep. He would always say he didn't want to go to sleep because when he does he has bad thoughts about me and people that he loves. He always had an extremely hard time excepting the word "no"- he would flip out and hit his head with whatever was handy, throw things, break things, scream holler etc. It would take hours to get over it. When he did he would be very remorseful and lovable. He was always in turmoil. Finally in February of this year, this graduated to a new level where he would want to just kill himself and would actually go and pull a knife out of the drawer and just shake with anger as he held the knife to his throat. I was terrified although i really didn't think he was going to harm himself he just wanted to scare me. Then at the end of March when i first heard the news about the possible side effects of Singulair, I had only heard about the suicide effect. Oh great just what I needed was this medicine causing him to do that. The doctor was thinking about taking him off if this summer because he wanted to see if he out grew his seasonal allergies so I took him off immediately. Well I had no idea about the other side effects until my son turned into a completely different kid. School noticed a huge difference in him! His grades went up, his is able to control his behavior, he is happy he is NORMAL. I never suspected this drug as the culprit due to the timing of taking it. Our lives have changed completely. When i first found this site, it seemed as though some of the parents were writing about my child. It is amazing. My son still has some old habits to break but overall he is a wonderful and normal 10 year old boy. He did not outgrow his seasonal allergies but Allegra seems to help in through it. I get so angry- his whole early childhood was ruined by this medicine. He is a labled kid in our school system. This whole experience has opened up my eyes. Thank you for letting me share my story.

Hi everyone
My little boy who is nearly two was put on Singulair as a preventative.
I did check on forums when we started using Singulair and I was concerned that there has been descriptions of negative affects. Always trying to be objective I rationalised that the people in this forum are a small part of the greater Singulair population and as a result there was a low risk of negative affects on my little boy.
I have to say I think I was wrong. As soon as he was using Singulair, he had restless nights of sleep. Every night he would cry off and on until 2am and I guess he was so tired he slept. During the day he was very short tempered and became upset very easily. We put this down to tiredness. After 10 days of the lack of sleep for parents and little one, we told our doctor.
He advised to take him off Singulair for 5 days and make observations and then put him back on. Last night, his first night off Singulair was bliss. Not a sound. He had a great sleep. As I type he is now having another great sleep.
Let us see what happens after 3 more days and after putting him back on Singulair.
It would seem that if we are correct and that Singulair is a cause of an issue for my child, am I a quasi beta testing laboratory for a drug?
We are from Australia.
Thank you for reading.

When i was 13 i was put on paxil for major depression. I stayed on it till i was about 17 after a downward spiral of depression that lead to a suicide attempt. After that the doctors decided that Paxil wasn't benefiting me anymore and decided to take me off of it, cold turkey. At that time i was on 40mg.
I started getting zapping headaches, muscle spasms, i was sensitive to light, my body ached, i had hot flashes, pretty much anything over stimulated me... i was irritated with just hearing anyone talk, i was completely out of touch with anything around me and i didn't feel like i was real.. I basically shut myself in my room for over a month getting over paxil. My family was afraid i was planning suicide.
After that, it's made me afraid to take any of my prescribed antidepressants, but i just cannot go through that again. At the time they put me on it, there was nothing that said that it was addictive, i was even told that there was no proof that it was addictive.
Also, I still experience the headache zaps to this day, and im 22 now, and i never had those type of headaches before paxil. I really think my mental illness is a lot worse from paxil. I have depersonalization disorder now, my short-term memory's crap, im more uncoordinated, im a lot more depressed and social phobic.. i know part of it could be from not taking any meds at all.. but i know that paxils really screwed me up, and i would have been a lot better not taking it at all. I just wish they would have warned me before putting me on it, or warning me before taking me off.

I am sure that all kinds of people told Kate Miller that Concernedcitizen was a cuckoo or a Merck competitor. I haven't been employed by a pharma company in many years. Everybody ever employed by a pharma company higher than a certain level (practically the mailroom) knows this stuff and what to look for.

I think that I am about ready to say my opinion on how montelukast works and why these problems develop. It will just be my opinion. I need to try to find actual proof but I may forego that and just say it soon.

Hello All,

Regarding the first post I wrote, immediately below this one: I meant to say that I noticed the depression and anxiety increasing when I INCREASED the JANUVIA dosage from 1/2 a tab twice a day to 1 tab twice a day. I had thought that the SINGULAIR was the only reason for the depression and anxiety increasing/resuming but instead it went something like this: I began JANUVIA then started the SINGULAIR; perhaps the JANUVIA woud not have started the increased symptoms/side-effects until at the higher dose which I now take OR until COMBINED with the SINGULAIR. In either event, I now have see these symptoms of depression and anxiety returning and increasing, significantly, and have thereby stopped the JANUVIA until at least one week has transpired; whereupon I will begin it for a few days and note all side-effects and symptoms to present to my physician as proof of a pattern from the ingestion of JANUVIA.

Again, thank you for reading this and may you all have much better health and wonderful, health-conscious lives!

After only ONE tablet my husband took for his bronchitis he got SO dizzy, disoriented, nauseated, he threw up several times, couldn't walk or talk- this is freaking poison, that's right! Looks like somebody is using people as guinea pigs for their experiments. Does anyone know how to file a lawsuit against the stupid doctor, who prescribed Levaquin to my husband & what proof do we need?

concerned citizen,i enjoy reading your posts and research you have been so helpful,but i do have to say,i do expect the doctors that write prescriptions to do their homework and research on these drugs,i do feel that they should be extremely knowledgeable about what they are giving our children,that is why i pay them the big bucks.I told them of my concerns and they poo pooed me,when as it turns out now i was quite possibly right,i will asked them to do another blood test now he is not on meds,and if as i suspect it has gone down i will loudly shout i told you so and demand answers from them.I so often questioned the meds and was always made to feel dumb,Ignorance is not a defense and someone was very ignorant

I had my Mirena IUD removed on Monday, May 5, 2008. I had it inserted on November 10, 2005. I was having major side effects from the birth control, and every doc I went to said that there is no way that Mirena would cause the side effects I was having because the "progesterone amounts are too low to cause these side effects". I have had the following side effects:
WEIGHT GAIN
JOINT PAIN
LUMPS IN BREASTS
BREAST TENDERNESS
HUNGER (as if i were pregnant)
DEPRESSION
LOSS OF SEX DRIVE
HAIR LOSS
SWOLLEN ABDOMEN (BLOATED?)
HEADACHES
GROUCHY/ON EDGE
ACNE
CYST (had a couple weeks ago... i was on vacation in Vegas and had a cyst burst.. never had these issues... this was the last straw)
STABBING PAINS IN ABDOMEN AND IN AREA OF OVARIES
PMS SYMPTOMS EVERY OTHER WEEK FOR TWO YEARS
BREAST GROWTH D TO DD
VAGINAL BLEEDING AFTER INTERCOURSE
FATIGUE
TENDERNESS OF ABDOMEN
BACK PAIN
HIP PAIN

As of today, Friday, May 9, 2008 (4 days after Mirena has been removed) I have lost 9 pounds. I am sure this is probably water weight? I am feeling a little better every day. The night I got home from having it removed, I had major mood swings... would be happy one minute and crying my eyes out the next!!! I would not recommend this IUD to ANYONE.. not even on my worst enemy (if I had one). This needs to be taken off the market. It is not safe! I have spent thousands of dollars on ultrasounds on my breasts (thinking i could have cancer because the lumps i had in my breast) and on other doctors bills to figure out what was wrong with me.. only to find out that "Mirena is not the cause"!!!!