Frustration symptoms and conditions

I stopped taking Aciphex and now try Zegerid because I was experiencing a lot of gas and pain in my stomach along with headaches, anxiety (shaking of the knee), depression, frustration, tight chest pain. The medicine seems to be quite strong.

Today is 10/28. I am Weezie1 and I posted on 10/26 about my severe drug reactions. They have gotten worse since I wrote my first post. The fever and chills are gone. But now I have been dealing with a rash/hives over all parts of my body. They are worse where close contact to sleeping clothing are - back, chest, neck. The one side of my face that I usually sleep on is purple every morning, along with that same side of my neck. I managed to get myself back to the doctor on 10/26 and am now on a 6 day dosage of steroids for the rash/hives. The steroids have stopped the hives from getting any worse. But it is taking awhile to go away. Any heat, anxiety, frustration brings them out again. I see I will be dealing with this for awhile. I go back to the doctor on 10/29 for a recheck. I lost 2 days from work because of this. My skin felt like it was on fire with hundreds of bee stings. Now I feel like I have a severe case of poison ivy. I have found some relief using Aveeno's oatmeal powder to do a bathtub soaking at night. Then I follow that with Aveeno's rich moisturizing lotion. The doctor may want me on steroids for longer than first prescribed.....not a med you want to be on for too long. All because of an UTI last week that could have been simply treated with a regular antibiotic if my doctor was not able to prescribe this sulfa drug to me on 10/19. Next time I will go with my initial gut feeling and refuse to take a medication when I see its extensive side effect list. I wish I had done so last week. I am suffering much more now than I was last week with my UTI. I filed an online complaint at the FDA's website. They mention it at their phone number that Weezie1 reported in my 10/26 posting here. I, unfortunately, expect to see additional patient complaints here every few days when I check back at this great medications site. And now I see that someone has internal bleeding. What next? A death? My blood pressure and heart rate were both increased for several days due to this drug. I could feel my heart pounding when I was sitting still and laying in bed. Thankfully, my BP is normally on the low side, but all the numbers went up by 10. We have to band together to get this crap off the market and out of the hands of doctors and unsuspecting innocent patients. Our voices will be heard if we speak in large numbers. Keep talking!Good luck to all.

I am so annoyed that this medication is still on the market.
What is it going to take for it to be banned??? It took me almost one year to get my life back together. The side effects from this medication are horrible. Only the people who have gone through them know how severe it is. I had anxiety, insomnia, chills, numbing in the hands and feet, palpitations, vomiting, tremors, twitching, vision problems and the list goes on. My body was out of control. My blood tests were even coming back with all sort of problems thyroid, high blood sugar etc. When retested a few months later, everything was normal.
It took me lots of hard work to get myself back to normal. Thanks to Chinese medicine/acupuncture I now have my life back.
Please don't take Avelox!!!!!

after 6 days of taking levaquin I developed severe shoulder and arm pain on both sides. Some days I can hardly use my arms. Lawyers don't want to take my case because I didn't suffer a rupture. What kind of crap is that? It's okay to have severe pain the rest of your life? My Dr. says it will go away. It's not. It's getting worse. Don't take this stuff unless you enjoy pain

I have no idea if this is the vitamins, but its the only variable thats changed in my life recently so I can't explain it otherwise, but I am extremely agitated in terms of frustration and anger. I could honestly rip something off the wall and smash it.

I, too, was told, only good things about mirena. I got it after the birth of my son, and had previously had a copper IUD, with it, I still gt my period, but no worse than before. Since getting the Mirena, I'd gained over 30 pounds (with no change in activity levels or diet), and have experienced frustration, depression, and am very self-conscious of this-from being asked if I was pregnant again, etc., as this make a very big difference on my 5'2 frame. I also never regained my libido. My gyn, Just told me last week that loss of libido can be a side-effect of mirena. My periods have been lighter, but still have the emotional side effect. I'm going to check with my ins to see if it will cover having it switched back to the copper one. I'd gladly take a period, than go on like this (as you can imagine how its affecting my marriage.)

EFFFF Levoxyl!!! My life has been really, really difficult since being on this medication. Reading all of your posts truly makes me feel like I am not alone in my struggle, anger, and frustration! If we could only sit in a room and talk about this face to face, how much better we might all feel. I think there needs to be thyroid support groups. Does anyone know of any?

I went back on Levoxyl about 2 months ago, because I was feeling tired again. I took myself off of it a year ago because I felt like I didn't need it anymore. I wasn't feeling great being on it and I had given myself a year on it already. Which by the way was a year from hell. I experienced depression for the first time in my life, gained about 20 lbs. from binge eating (never had an eating disorder or weight problem in my life), was fatigued constantly, then blamed myself for being so lazy all the time, lost friends because I canceled soooo much on hanging out, "I'm really sorry but I'm just not feeling good." Yeah that excuse gets really old to people with a normal functioning endocrine gland. Mind you I was diagnosed with this at 23. Sure I am mad that I have this problem, but when I am trying to get myself well and take the steps necessary per my doctor, it's really frustrating to just not feel like yourself. During the year off of it I took a natural thyroid support. Feeling fine, I slacked on taking the support thinking I had kick started my thyroid.
Two months of being back on it and I'm done! In a moment of emotional anger I threw my Levoxyl pills in the toilet. You know what they did...expanded to the size of a bazooka joe bubble gum piece. Uh that's big considering it's such a small pill.
I went to my doctor today because I've been experiencing bloating, pain and constipation for 3 weeks now. He told me to drink coffee and take benefiber, because perhaps I'm not getting enough ruffage in my diet. Just to see if I'm crazy about the expanding pill, I dropped an advil and tylenol in there. They simply fizzled down. I think these meds are making me bloated etc. and it's not worth it to me to feel this way. My body is telling me something is wrong and I need to listen!!
I eat right, take vitamins, drink PLENTY of water etc. and I still feel crummy.
I have been doing research online and have found a product called IODORAL. It is Iodine and Potassium Iodide. I have read many posts from people stating that this product has given them energy, helped with fatigue, their memory, overall well being. What was shocking for me learn is that Iodine helps fibristic breast tissue along with other parts of the body. Did you all know that 30 years ago breast cancer affected 1 in 20 women, and now it's 1 in 8 ???! Iodine used to be part of our diets. It has since been depleted from our soils and other foods. Bread used to be made with Iodine. Now Bromine is used in the baking process. Did you know that Bromine blocks the thyroid from producing necessary hormones for function. I bought myself some IODORAL and I'm going to see if it works. I am not a doctor but I am a person who is very in tune with their body. The bible says that there IS A CURE for everything on earth. I pray that all of you who have posted on here and are in discomfort do not give up your hope and find a different doctor or start doing your own research and be your own advocate for your health. There has to be something better out there! Something that isn't hurting our bodies! I am not giving up hope yet and neither should you!

My son was on singulair for most of his infancy (11 mos- 22 mos old) we took him off of it when I started staying home with him. He was in daycare and was having breathing issues. We would give him the singulair and Zyrtec every morning. He became a very despondent baby. He would spend the ENTIRE day in the rocking chair at the daycare. After months and months of the teachers telling me this we decided it was best I stay home with him. He came off of the singulair and things got so much better for a while, he began to interact with us and others, not fearful anymore, and slept through the night. However other things have grown to be worse, as he has been developing...every day he seems more difficult to deal with. Now, 5, he is angry, fits of tantrums and rage, can't cope with his emotions, he actually kicked me today during one of these fits. He has been peeing in his room when he is sent there because he has been punished for one of these outbursts. What are the long term after effects of Singlair? Has anyone had this experience? Could the singulair have been given to him too early and now caused some sort of permanent nero or psychiatric condition? PLEASE ADVISE!!!! This Mom is really frightened.

Just finished reading the posts and I feel like it was written about my 8 year old. I never connected the two issues of anxiety, frustration doing schoolwork, quick to tears and leg pains. I kept telling them they were growing pains. Last night he called me from his father's and said he has suicidal thoughts... not that he wanted to kill himself, just couldn't stop thinking about it... good lord. After months of dealing with him not wanting to go to bed and not feeling safe we have an answer. I told my ex husband to stop the medication today, I will post back after a few weeks to update the progress. I usually never post randomly on the internet, but this site might have just saved my son from emotional turmoil!

I had Mirena inserted about 3 months ago and have been consistently gaining weight since then. I initially wrote it off as anything else besides this drug because the pamphlet is very clear that weight gain is not a side effect and I talked to 2 gyns and they insisted the same thing. So I had my thyroid checked and started eating better and increased my exercising, I am a personal trainer so I already do these things pretty intensely, but I have stepped it up to slow the weight gain. I am up 8 pounds in three months which makes me crazy. Yet I am hesitant to get it out since it was so insanely expensive and not knowing for sure that it is the mirena. So any of you who have had it removed could you comment on if your excess weight that you did put on has come off or not. Besides this frustration, I have loved it, but it makes it difficult to build my business as a personal trainer if I am gaining weight.

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

I discovered my son's side effects from singulair a little over 2 years ago. He had used Singulair for approx 3 years. I did not recognize that he was suffering side effects until his ped increased his dosage to 5mg. At that point, it was loud and clear. I discontinued the Singulair in March 2007. The most significant improvements happen after approx 3 weeks. He was like a different child. Even after the 3 weeks, it seemed like he continued to improve a little every day.

I can tell you from our experience that my son suffered many, many side effects that i did not recognize. He had nightmares, anxiety, fear, frustration, leg pains, stomach pains, dark circles under his eyes, poor appetite, quick to tears and restlessness...just to name a few. On the higher dosage, he began to have a facial tic, dilated pupils and hallucinations.

I am thankful everyday for this website and some higher power that helped me realize what was going on and get him off Singulair. The first week off Singulair, he slept like an angel. No night terrors, no thrashing in his sleep. Week 2, he continued to improve in so many ways. It was nothing short of amazing. Week 3, he began to realize the changes in himself. Fears were a HUGE side effect for him. During week 3, the fears, ALL of them disappeared. He never spoke of them again. It was very strange and truly amazing.

I don't want to tell you to stop the use of Singulair. Only you know your child's health status. I will tell you that stopping Singulair changed our lives and saved my son. He suffered the assault of Singulair for 3 long years. Good luck to you all and your families. Feel free to email me if you have any questions.

This post is for the ladies who wonder will they feel better or notice any change after having the mirena removed. This is my own personal experience . I've had it out for about 2 weeks now after having it in for 3 1/2 years. I feel Great! I couldn't have a panic attack if I wanted to. I have had more energy, haven't had a headache. I have a returned sex drive. Sadly my hair is still very thin and patchy. The big kicker is I've lost 4 lbs as of today. My stomach now looks like I'm 3 months pregnant as opposed to 5 months. The big difference is noticed in my face and waistline. I don't feel so hungry all the time now and feel motivated to keep this going. I haven't had one heart palpitation since either. Yes I still yell sometimes, but not out of anger or rage. It's now to be heard over the yelling and screaming of my happy kids who used to cower because of my yelling that was so mean spirited and full of frustration from being so tired and feeling ill most all the time. I just worked last night 13 hrs got 5 hours of sleep today picked the kids up from school, played with them and cooked dinner to boot. I would have been in bed 2 weeks ago waiting for my husband to come home and rescue me. This has been my experience thus far and I keep posting to give those ladies hope that they can feel better once they get mirena removed. I hope others will have a positive experience with removal like I have had. Good Luck and Happy Recovery.

Hi everyone, I’m 24 years old and had healthy periods prior to starting Loestrin 24. I just stopped taking the pill yesterday after 2.5 packs. Although it’s recommended to stick with any pill for three months before making a decision, it’s just not worth it to me. Here are my observations. The first month on the pill I was extremely moody and scarily depressed. Although I can get frustrated easily, normally I would keep that frustration to myself and get over it. After about two weeks on the pill I was overreacting to nearly everything, I cried all too easily, and unfortunately I lashed out at those close to me when something wasn’t to my liking. All of which I thought was totally rational at the time, and only later did I regretfully play back certain incidents in my head and wonder why I had been so upset. I have a fairly demanding job with long hours and stress both at work and at home with my roommate. The best way I’ve found to cope with that stress and to keep my sanity is through regular exercise. Again, within the first month of being on the pill my energy dropped drastically, and I felt lethargic nearly all the time. Even getting up from my chair and going to the bathroom while at work seemed like too much effort (and I used to relish going to the bathroom just for a break from my desk). That said, I forced (and I mean forced!) myself to continue my regular exercise routine, because my sanity was already waning. In fact I found this forum in that first month because I was trying to figure out why I was so lethargic, and wanted to know if that was a common side effect of this pill. What else? I developed a ravenous hunger. I constantly thought about food (especially sweets). I already have an unhealthy sweet tooth, but prior to the pill I had some semblance of self control, but I lost that while on this pill. My breasts got bigger (which is nice although they’re sore all the time), but luckily I wouldn’t say I’ve gained too much weight. My lower abdomen, however, started looking bloated and distended. What I found really bothersome was that I never felt satiated. I would eat and eat and eat, and when I should have been full, I’d already be thinking about other things to shovel in my mouth. It was hard to think about all the food I had eaten through the course of a day, and yet not ever feel satisfied. And here is my biggest complaint: during the first month on the pill I spotted on and off, but I had read that that was normal and as promised, I had a very short period. That was nice. After the second week of my second pack of the pill I was bike riding with a friend and felt distinctive period cramping. I dismissed the sensation since I was mid-pack. When I got home and went to the bathroom there was a glob of fresh blood in my underwear. I then continued to bleed (not heavily) for about two weeks until I hit the placebo pills and had my period. That really really pissed me off, especially because I had planned a camping trip with my boyfriend during a time that I shouldn’t have been bleeding. Anyway, I was almost ready to go off the pill, but decided to give it one more month. I started my third pack and everything was basically hunky dory (despite the ever present hunger, sore breasts…etc.), and then one morning I went to the bathroom and found that I had started spotting again…less than two weeks into the pack. I said f*&# it. I’ve never liked the idea of introducing hormones into my body, and I really don’t like not ovulating. I went on the pill because I wasn’t ready for an IUD. Now I am. I had come to accept a lot of side effects on this pill, but bleeding for two weeks straight is not OK. I bet my body would have eventually caught on to the routine, but I’d rather try a different method, and I’d rather get back to ovulating normally.

severe short term memory loss, notable irritability and aggression. I've been on 1-2mg a day for a year now and prior to that I was on .5mg a day with memory loss issues even then. If anything, I'd say the higher the dose, the higher the aggression, lethargy, confusion, and irritability are. Also I have blurred vision but since I am on adderall, that tends to go away shortly after I take it. For me the side affects outweigh the risks...Klonopin slows my racing thoughts and practically erases my overwhelming social anxiety and panic. I also have very, very few intense panic attacks anymore, maybe twice a year? This sure beats twice a day...With school it is hard, I am a senior in college and the memory thing is quite the frustration. But, like I said before, it outweighs the risks to take this drug. I also used to be a drug addicts and have had no issue with abusing this drug. I respect its limitations for it resects me by helping me, literally. Hope this helps.- H. in South Florida.

I have been on Topamax for 2 1/2 months. My dosages have been varied due to side effects that scared the daylights out of me. Never more than 100 mg a day, at which point I was a vegetable. After such terrible side effects - pressure in the eye, blurriness, loss of speech, coordination, complete exhaustion, inability to work, stopping mid sentence with inability to complete sentence - I finally had it. I talked to the doctors all along that I was terrified what was happening to my mind and body but they just said it was too soon to tell if the meds were working or not.
Out of pure frustration and concern for my own well being, I decided to try to taper off Topamax and then stop completely. I lost feeling in feet and hands, pins and needles, weakness in feet and hands as well as spasms- lovely. Frightened me so much I wound up in emergency thinking something else must really be wrong with me. MRI said all was fine as regards to MS or stroke, etc. Whew!
Continuing to withdrawal and mad as @#*! that the Dr.s don't know what they are prescribing to poor patients, Topamax is a dangerous crap shoot. Funny to me how something as horrible as this drug can be prescribed in our government, yet medical cannabis prescribed properly with little to no side effects is a crime in most states.
What have I learned from this experience?...be your own advocate. Don't let anyone ever push you into saying something is black when you clearly see it is white. Get angry, state your feelings if you feel you are being harmed and brushed off and not helped. You still have the brain cells in you to make good decisions though Topamax and pressure from others about "not taking your meds" may knock you confidence for a loop.
I'm thankful I live in CA where I can make legal choices that are not available to others in the USA. Shame on the drug companies, shame on the Dr.s that need to do their homework, shame on our FDA for letting this horrible drug on the market whilst holding back natural herbal relief that grows right out of the ground for all to use legally. Shame on me for not doing my homework earlier and doubting myself and letting other decide for me for so long now.
Good luck, hope you all find some comfort and fire in this message. We are our own best advocates. No one knows us better than ourselves. Freedom of choice is a wonderful thing - so thank you makers of Topamax, for helping me to find the strength inside to tell you....JUST SAY NO! to drugs - your drug in particular. May you be recalled and not harm any others, and may your profits plummet as you have make you $ on the suffering of so many others.

I had my Mirena inserted in January, 2 months later i stopped bleeding, i have spent several days waking up with the same type of nausea i had when i was Pregnanat. 10 days later i experienced excruciating pain in my left side of my abdoment that is so intense it makes me double up, it feels as if something goes pop before the pain relapses this happens every 3 weeks, i have a dark discharge every 3 weeks that lasts for 8-10 days, i have lost my sex drive altogether, my tollerance level is less and frustration comes easy. Over the last week i have experienced contraction like pains that last about 20 minutes. I went to my local gp's to get it checked 8 weeks after insertion, i was told my Gp isn't qualified to do this i would need to go to the sexual health clinic and see the nurse there....

This is my third post: I just returned from the OB office after having the Mirena IUD removed and would you believe it took 2 doctors, 2 nurses and an ultrasound tech 4 hours to get this damn thing out! I'm not kidding, it was like a fishing expedition in my vajeje...ridiculous! Apparently, the string was very short, thus the little culprit migrated far into my nether regions where, much to the frustration of the OB staff, it avoided capture for many hours. They finally numbed my cervix, used frighteningly large salad tong-like forceps, all while watching the ultrasound to try and snag it....this was NOT at all how I wanted to spend my day! I can safely say after this experience, I will never have another IUD of any kind shoved up in there! I can't tell you how relieved I am to have it out...maybe now I'll get back to normal...here's hoping! May all your Mirena removals be uneventful!

I am a 25 year old with Factor V Leiden and was told by doctors that the Mirena would be the best birth control for me since I can't take BC pills anymore. I had the Mirena inserted Nov. 2008 and am having it removed next week. I have had a horrible experience with it. My obgyn told me that the chance of experiencing any side effects was rare since the hormone stays in your uterus. The insertion was extremely painful which I expected since I have never had a child. In the past 4 months I have gained 15 pounds despite regular exercising and eating a low calorie diet, I have a constant stinky discharge, acne across my chin and sides of my face, my hair is falling out, I have no energy and am incredibly tired all the time, have been experiencing nightmares, and have sharp cramps that make me double over in pain. I am a newlywed and have never had any psychological issues. Now I am in therapy for anxiety and depression and after reading all the posts, I now am convinced that this is also a side effect of the mirena. I used to have a healthy sex life and now I have no desire to have sex or be touched by my husband with is causing tension in our new marriage. I was trying to stick out the side effects to see if they would go away since I paid so much money ($600) for the mirena. When I spoke with my obgyn about my side effects she said they were not caused by the mirena because the hormone is directly in your uterus. I am so frustrated! I feel like I have been lied to by my doctor. I am hoping that after removal of the mirena I will feel like my old self again!

the pediatrician prescribed singular for my dd when she was 12yrs old for her asthma. she described it as being safe. that same year dd started having problems in school and seemed depressed. I talked to the doctor about it thinking maybe it had something to do with her adhd medication. the doctor thought maybe it was just normal teen behavior and dd trying to adjust. eventually we took dd to a therapist and things seemed to get a little better. then dd started complaining about stomach pains, she talked about strange dreams at night and would wake up in the middle of the night. Then the tantrums started, wild out of control tantrums. she would scream, throw things, destroy things, she talked about wanting to die, how she hated her life. again I went back to the doctor her adhd medication was adjusted and I also got her back into therapy. therapy was helpful but we continued to deal with the wild tantrums. we kept trying to seek help and answers but to no avail. we were beginning to think dd was suffering from a mental illness. the doctor told us to keep an eye on it and the next step would be maybe putting her on more medication. In the meantime dd became anxious, she had an anxiety attack at school, she would get in arguments with her friends and become very irrational, she continued to be angry at home, she destroyed things in her room and punched a hole in the wall. When I would look in her eye she had the look of a wild animal. my doctor began to think it was merely teen rebellion and we needed to get tougher with her. Never did it ever cross my mind that it could be something with singular till I heard about the study on the news then it all clicked. before singular my dd was an above average student who was liked by teachers and students alike. teachers talked about how well behaved she was and she was a leader. she was very active in various activities at school. Now she has become nervous and suffers from anxiety attacks, she has out of control tantrums and anger. her friends frequently avoid her or her calls because she has become so moody and angry. she frequently complains that her stomach hurts and feels like she's going to be sick. she screams and talks about wanting to die and that we don't love her. till today I had considered this drug to be safe and very useful in controlling her asthma but after doing more research i'm beginning to wonder if it's worth the risk.

I had the Mirena inserted six months ago. Since then I have noticed a huge change in myself. I am very moody and irritated all the time. I feel depressed most days and want to lie around all day. I have no motivation or real care for the important things (ie, laundry, dishes, housework). I feel like I'm on really bad hormonal rampage 24/7. I wake every morning with a headache. I have no interest in sex. I don't feel turned on and could care less if I ever got it. I have not experienced any weight gain, thank goodness. I am easily overwhelmed by the tiniest things. I have three children and it's all I can do to tolerate them each day, which is so unlike me. I do not have ringing in my ears, but I am very sensitive to loud noises and get easily aggravated by toys that make noise and loud laughter. (Not good for a stay at home Mom) I have thoughts of throwing and breaking stuff due to my frustration and I have no idea what I'm really frustrated at. I am definitely a different person since the Mirena was put in. Also, I have been having really bad pain in my wrists. They almost feel sprained. I am having it removed ASAP. I miss the old me. It's been so long, I've forgotten how to be happy and have a wonderful sex life with my husband and have fun with my children. I will be having a tubal. Bad periods, to me, is way better than a chemical imbalance due to hormones. The headaches alone are enough to make me go insane. I have done lots of reading on Wild Yam. For all you ladies that have bad periods and are using the Mirena to fix it... look into Wild Yam. It's suppose to lighten the flow and symptoms of a period and boost your natural sex drive. Most importantly it's NOT a drug.
Good Luck to you all!

yes, I two have had the back pain screaming at my kids no sex drive also, the acne wow big red pimples with scaring never before have i had this in my life i had the mirena for 2yrs i have no insurance so i pulled it out myself but have a lot of bleeding at times with clots i am scared out of my mind but i have no money to go to a gyn so, can someone help what should i do i was gonna wait a week or so, to see if bleeding stops if not don't know what i should do i have had it out for 4dys and I feel great I swear I can feel the difference so, much more relaxed and not screaming.. I wish i would of never received this IUD it's been a long 2yr nightmare!!

GOOD NEWS THE FDA HAS GIVEN BAYER A WARNING BECAUST THIER ADVERISING WAS NOT SAFE FOR THE PUBLIC.
You can find the exact wording at fda.gov under "drugs" than under "consmer" {info or something},
once you're there search Yaz. Anyways I plan on contacting all the lawyers that I did a few months
ago to let them know bayer was warned that their advertising didn't warn women well enough of the
potential dangers. I believe Yaz should be off the market or at bare minimum have MUCH MUCH better
warnings. I am apparently not the only feeling this frustration so I think we should all contact
the same lawyers and anyone who wants a list from me please e-mail me and if the lawyers hear from
all of us and know about the warning the least that would happen is they would be prepared when
more problems were addressed by the FDA and I think we all know what the best out come would be.
IF YOU WANT YAZ OFF THE MARKET PLEASE CONTACT THE FDA, FDC, AND BAYER { EVEN THOUGH YOU'LL FIND
BAYER DOESN'T HAVE ANY INFO FOR YOU}. Let me know if you want the lawyer the list. Thanks to
everyone who has already contacted the FDA {who knew it would really work}.

i had the mirena for 9 months and that enough i had cramps, dizzy, headaches, nausea, backaches and worst depression. i fought w/ my husband everyday, i hated life to the fullest, i was very sad and i would cry for no reason. i knew something was wrong and i realize it was mirena. i had it taken out today, i plan to patch things with my husband if its not to late. hope this helps anyone that plans to use mirena, DON'T USE IT, IT WILL RUIN UR LIFE.

I have had my Mirena for 23 months - placed 6 weeks postpartum. Like most, I too experienced the usual breakthrough and almost consistent bleeding/spotting for the first 6 months with cramping, headaches, and weight gain. What I have also experienced is an overwhelming sense of exhaustion that has not improved but gradually worsened.

Around 4 months PP I realized that something was off in my body. I did not have any energy, didn’t feel like myself, super emotional and no matter what I would try I could not gain motivation to accomplish the task of maintaining my house. I was struggling with a feeling of fogginess and cloudy thinking. I've experienced hair loss, increase in breakouts, dry and splotching skin.

During the first year I would have 1-2 good days in a week where I felt energized and I would be fooled into thinking that I was on my way back to the old me. I could accomplish things, rationalize clearly and deal with life. The rest of the week though would slowly slip back into a drained, over emotional foggy state. At 15 months into having my IUD in place, my days of productivity were dwindling further and further apart.

I have been blessed to have a husband that truly loves me. However, even still he has had a hard time comprehending what I have been dealing with and it has taken a toll on us. He will often say you are just not a happy person no matter what. I know that I am not unhappy with my life in general, my husband or kid and yet he is right. This thing robs you of your happiness and sense of self.

For the past 2 years I have said over and over again that I know something is wrong. I simply don’t feel right. I have been very aware of the changes within myself. I have struggled to be an active parent to my child and I have struggled with the most basic tasks. Things that use to take me 1-2 hours could stretch into days now. I was once this extremely productive individual that now barely is able to get the simplest of things done. I literally put all my effort into trying to accomplish things yet it barely makes a dent.

Until I started doing some reading, and I have found there thousands of women going through the same stuff I am, I really felt like I was going crazy. These symptoms are so subtle and similar that they most often get passed off as PPD, or dealing with the pains of motherhood and stress of life. Up until 2 weeks ago I couldn’t even verbalize the fact that no matter how much I slept, took vitamins, or exercised that I still felt tired all the time and was experiencing an inability to be productive.