Frustration symptoms and conditions

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.

I had the Mirena inserted last September. It was the most painful experience I have ever had! I bled for about 3 months straight, and have not bled at all since. For the first 6 months or so, my boyfriend experienced pain during sex. The wires were actually scraping him! I called the doctor and they said that the wires would soften with time - GEEZ! Since about January, I have been losing hair like crazy! I have to clean my brush every day and the bathroom floor is covered when I blow-dry my hair! I am also getting cystic acne, mostly on my chin. I have been severely depressed and angry all the time. I snap at everyone, and I don't know why. To add to the frustration, I am so bloated and I feel disgusting! As far as my sex drive, it has always been strong. However, half the time my body doesn't cooperate with proper lubrication. Anybody else have this problem? Let me know!

My 7 yr old daughter has been off of Singulair for 12 days now. The change in her personality is amazing. She experienced two nights of strange dreams and waking in the middle of the night. We put her back on Flovent once a day as a substitute. Her aggression and frustration went away within days. She is so happy and content with herself. I can see that she is no longer frustrated by emotions that she could not explain. She's silly, funny, happy. She no longer hates us, pulls her hair, or tries to slap herself because she's thinks she deserves it. She has been on the drug since she was 3-1/2. We were doing family therapy to try to help her. This is no longer needed. She's back to her old self. What a shame no one warned us of this potential side effect. I also wondered how I missed the news story since I just found this site in September 2008. The news story about Singulair came out in March - just around Spring Break. Since we were out of the country, I missed the news. Isn't that a convenient time of the year to break a story? I'm sure many other families missed the news.

I am replying to my first post here yesterday....So today I didn't give my 3 yr old son the singulair and do not plan on it ever again! I have to say though...I am very very concerned. I think tonight I truly saw one of the bad behavioral side effects :( He got upset over something so small. Said he didn't love any of us, he didn't want Chinese which is his favorite! He didn't want to do any of the things that we gave him options on that he normally would jump right up to do! This devastated me! I right away thought to myself is this going to get worse before it gets better? He is still complaining of back pain which I know that will take some time. He punched a little boy just before dinner in the neck. He walked out of the neighbors house to go home and usually I have to carry him out. This is seriously scaring me! I'm not sure what to do ? My fiance, his father, doesn't understand and started to yell at him for his behavior. (We don't get much time to talk and when I try to his dad just says he is ok but I know, deep down he isn't) I am the one with him everyday at home taking care of him. I am now being more patient with this behavior when normally I would lose patience and punish him with time outs. Do I continue to do time outs?
Why should I punish him when its not all him ? This is so unfair :( I mean, he is a boy and yes he acts like one. Doesn't share at times, hits sometimes, he is a or was a normal 3 year old boy. His dad will follow my footsteps on this as he see's how I handle things but I'm a little witty on how to handle it now. At this point I am babying my baby! I will tell him when things he does is not right but I'm at the point now that I don't want to send him to preschool! Do I inform the teachers? Can someone give me some words? Its just hard because he is my oldest and is only 3 so not only am I learning to deal with regular behaviors, I now have to understand how to cope and deal with this until its over. Thank you in advance very much for any help and advice!!!!

I began taking Wellbutrin 2 weeks ago and started on a 150mg dosage. I was on 150mg for one week. The second week, I went up to 300mg per the psychiatrist's instructions. I was feeling really angry some of the time and decided to stop the medication. Prior to the last 2 weeks I was taking 40mg of Paxil, which I stopped after the first week of being on Wellbutrin.
The anger was uncomfortable, I stopped taking the Wellbutrin and within 36-48 hours of being off this drug, my feet began to itch mildly at first. Within about 30 minutes of this "mild" itching, the sensations got worse. My feet felt like they were on fire. The only relief was putting them in hot water in the tub. I was screaming with frustration and pain. I attributed this to the cold turkey stopping of wellbutrin. But since I had been on it only 2 weeks, I didn't think anything would happen. Big mistake. After 2 hours of having feet in tub, on the phone with a 24-hour nurse advice line and pharmacist, I went ahead and took 300 mg. The itching stopped within 2 hours. This was a freaking nightmare ! So I am weaning myself off. The doctor who prescribed this, who I spoke with the following day, said...well..stop taking it. Doesn't make sense because when I stopped that's when the extreme itching happened. It's crazy. I'm weaning myself off and taking Benadryl. I also got some hydrocortisone cream. There are scabs on the top of my foot from scratching. No more. I've been on anti-depressants for over 10 years now and I want to stop ALL OF THEM. Within 2 weeks, I should be "clean". Just know that this itching...was so intense I was crying and screaming because there was no relief.

My wife is experiencing severe muscle pain in the back and rib area after taking this drug. Has anyone gotten better after they stopped taking the medication or is everyone still suffering?

Hi All - I have been off prednisone for one week and I am not doing as well as I thought I would be at this stage. My symptoms are not flaring, which is a very good thing but I am so tired and feeling very depressed and low energy. I thought I'd feel great once I was off the evil prednisone but so far I am feeling almost as bad as when I was on it. My moon face has not started to go away, which sucks, but I guess I have to be patient. I am so tired of this situation as it feels never ending. Part of the problem is I have continued to work throughout my ordeal, and it's been very hard at times to carry on like a normal person who is not sick. I have been sick since last November (with an autoimmune disorder) and I had really hoped by this time that I'd be on my way to being better :( Prednisone saved my life but the side effects are horrendous, as are the after affects of it. Good luck to all who are taking it. I share your pain and frustration.

I have now finished my fourth month on Loestrin 24Fe. Still no period. Prior to being on it, I was on Seasonale--now, sure it's great not getting your period for 3 months, but that is another side effect page! Since switching to LoE24, for the first 2 months I had CRAZY mood swings and 6 out of the 8 signs of peri-menopause (I'm only 37). I did find out that Seasonale has a higher dosage of hormones and LoE 24 has less.

When I first switched, I LOVED the Loestrin--it made me feel so much more alive and like me again from the Seasonale. After two weeks, I started the "yogurt-like" discharge that went on for two months--no, not a yeast infection or anything, just weird hormonal stuff according to my doctor. After the two months, the discharge and the major mood swings went away all of a sudden, I was just fine one day and those symptoms have gone. Still, no period...it's been four months and 6 pregnancy tests. Now, I'm still a little moody but I'm not sure if it is pill related or frustration at not knowing what is wrong.

A girlfriend of mine loved this pill, so I guess everyone is different.

Hi all! I am not sure this is a new side effect, but it certainly hasn't been the most pleasant one. I have had ZERO sex drive.

I had a baby in early Feb 08, had the Mirena inserted Apr 08. I thought my lack of interest was just being tired from dealing with the baby or frustration with learning how to be a mom and wife. Hubby and I had a little tiff over me not wanting to, again the other night, when it hit me. While plenty of the times I was tired or frustrated, more often than not, I truly just had NO interest. I would think, yeah, I could but I don't want to. This did not happen until after the mirena.

I was very active prior to pregnancy, during pregnancy and even after pregnancy (pre-Mirena). Heck, the baby wasn't even sleeping through the night then! He has for months and I still wanted nothing. I don't think I realized it was a possible side-effect. The pamphlets say - "this is not a complete list, please see your health professional"

As soon as I realized it, I called my OB to have it removed. They had a cancellation and I was able to get right in. After reading some of your posts, I am beginning to wonder if the fog I have been in can be attributed more to that as well. Time will tell.

It took 3 years for me to be diagnosed with hypothyroidism and for a year I tried levethyroxine. This was a total waste of time. I was so exhausted the kids kept missing school, I kept walking into things, couldn't remember anything so I asked my doctor to let me try armour thyroid. This has apparently T4 T3 T2 and T1 and the T2 is the one that helps your metabolism (weight).
The change is nothing short of miraculous...I know it may not work for everyone but it is worth trying. I also had very extreme mood swings and the doctors were considering manic depression, but the latest thinking with that is to take your TSH levels higher before considering drugs such as lithium. I have just moved to Reading and my new doctor thought my T3 levels too high so reduced my armour dosage by half .....BIG mistake. Ended up in bed for days, couldn't remember which day it was, and the mood swings
!!!!!!! screaming, tearing my hair in frustration, punching my boyfriend. I staggered, literally, in tears back to the doctor who reinstated my original dosage of 2 grains one day 3 the next etc. For me my TSH has to be 0.1,
T4 around 14 and T3 around 8 to 9; basically on the high side but my blood pressure stays low as does my body temp and I feel alive again. It is worth trying different variations synthetic T4 AND T3, and don't rule out armour thyroid if nothing else is working after 6 months of use.

I have been on the Nuvaring for 7 weeks now and out of disgust and frustration I pulled it out. Will never take it again. I was supposed to have the Nuvaring in for 3 weeks then put another in for 3 weeks and then another 3 weeks after that THEN have my period. The dr. said you don't need your period soo often. Well I had my period every 19 days (instead of my 28 days) and the lasted 10 days!!! And very very very heavy with large clots. This ruined my vacation. I had to wear a pad and a tampon and change it every hour for 5 days. Horrible. Never again

MARCH 17TH MY MOTHER WAS A VERY HEALTHY ACTIVE FUN LOVING PERSON AS OF TODAY SHE IS TOTALLY CONFINED TO THE BED. SHE TOOK 4 PILLS OF LEVAQUIN FOR A MINOR CHEST COLD AND GOT A VERY BURNING RASH AND BLISTERS ON HER ARMS NECK AND CHEST AFTER THAT THE SORE THROAT AND EXTREME MUSCLE FATIGUE KICKED IN .HER DR. PUT HER OFF SHE WAS SMART ENOUGH TO QUIT TAKING THE DRUG ON HER OWN ON APRIL 8 SHE WAS HOSPITALIZED WITH THE ABOVE SYMPTOMS WHICH HAVE ULTIMATELY MADE HER UNABLE TO USE HER MUSCLE SHE CAN NOT SWALLOW HAD TO HAVE A PEG TUBE PUT IN SHE HAS NOW BEEN WEENED OFF OF THE 120 MG OF PREDNISONE SHE HAS BEEN ON AND NO END IN SIGHT ON RECOVERY. I HAVE NO MEANS TO TACKLE A DRUG COMPANY BUT I WILL TELL MY STORY AS OFTEN AND AS I CAN. 50 DAYS LATER WE ARE STILL TRYING TO GRASP ALL OF THIS

I've had my Mirena out for a week now and I'm very irritable and tired! I do feel relieved to have it out thought b/c all the bleeding, cramping, cysts and weight gain had been enough! I was wondering if anyone else has had the Mirena out and if you could email me and tell me what to expect for the next couple of weeks that would be great!! ******
Good luck to everyone!

Hello! My name is Lisa and I had a HORRIBLE experience with Yaz. I took Yaz for 2 months after 3 months of Seasonique. I had switched because Seasonique made me extremely moody (all of a sudden I hated everyone on the planet). My OB gave me a few months worth of Yaz. Within weeks I noticed a strong stomach pain. I contacted my OB and he thought I just had a stomach virus. This pain continued on for several more weeks. I called my OB again and he just said, "The pill doesn't do that." I got a second opinion from another OB and he also agreed.... "The pill doesn't do that." Then out of desperation I made an appt with my Fam doctor and he diagnosed me with Gastritis.... said that he thought my diet was the cause of my pain. Uh, let me mention this.... this stomach pain is so severe you literally CAN'T eat anything cause if you do, 5 mins later you will be in SEVERE pain. To get a better picture of this pain just think of glass shards piercing through your stomach walls (I thought just maybe I was getting an ulcer). My Fam doctor gave me a months worth of Aciphex (which never never never helped at all) and I also saw him twice more in that month (which was my 2nd month of Yaz). He got so frustrated with me... it was Gastritis and if I wanted it to go away I had to be willing to make changes in my diet (I still was not eating and was losing weight) and also be patient enough for the Aciphex to take effect. Finally, out of frustration I quit Yaz. Within weeks my stomach pain was completely gone.
Let me say this to all women reading this. I don't care what your OB says.
There is no need to tolerate any pain from a medication.... especially when there are other options out there. To have a doc tell you to "wait it out for a few months" is ridiculous. To not be able to eat for days or even weeks is dangerous to your health. I eventually googled Yaz + Side Effects and found that the severe stomach pain I was having was a possible side effect and it even instructs you to tell your physician if you experience such pain. Why is it I opted to tell not 1 but 3 docs this and no-one would listen??????? Personally I would like to see all 3 docs lose their jobs because they should have known this.
Ladies, tell anyone you know about this pill. Get the WORD out about this pill. I frequently go on Yahoo Answers and girls are always asking advice on birth control pills and I jump at every chance to spread the word. Let's get this pill OFF OF THE MARKET!!!!!!!!!!!!!!!!!!

I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

I just got a very condescending private message from a doctor on this site who said that while my articles from Europe are very helpful that I don't know what I am talking about and that I could mislead the public. Then I see how many parents and patients got a condescending attitude from their own doctors.

Well the public has been mislead but it is not my fault. I don't see any experts in this field stepping up to the plate to acknowledge that these side effects exist, have been reported by authorities in other countries, and that these experts are interested in learning why they are happening. This is an extremely widely prescribed medication that involves the lives of millions.

Merck's research director was quoted as saying that they know of no mechanisms by which these side effects could be related to psychiatric adverse drug reactions. That was a flat out LIE. So what if I quoted you a research article from China that was very complicated and yes, could possibly be misinterpreted by somebody? I just needed to give you an example. The only expert so far that had the guts to give you a truthful statement was Dr. J. Douglas Bremner. Thankfully, he corrected a misunderstanding about saying that it was "unclear."

I hope that we will all hang in there and something will be said by somebody, anybody on this site that will make the FDA listen and investigate Singulair (montelukast) all the way back to the very original studies done in test tubes not on people. And, then take a new look at it from the standpoint of what we now know about human genetics. I guess I will keep repeating myself about one size does not fit all.

I would also PRAY that all clinical studies on Singulair (montelukast) would be suspended until the FDA decides why these side effects occur. And that they would issue a statement to doctors to make conservative decisions regarding treatment with Singulair until the results of the investigation have been reported.

I hope that nobody thinks that I am trying to mislead anyone. The answers are either unknown or being hidden by Merck. How would I know the answers? I don't work for Merck. How many other people are out there trying to translate articles in foreign languages to see what's going on? American doctors are calling Merck and being assured that there is nothing to these claims.

I wonder how many experts there are that just don't want to be another Jeffrey Wigand or don't know what is wrong?

I know that I am ranting but somebody should do it.

My 6 year old son has been on Singulair for 2 years and I have noticed a big change in his behavior but it all started with leg cramps and falling down alot..I told my dr about what was going on but she told me that it was nothing to worry about that it is growing pains..Before he started the on the singulair he was always a happy go lucky kid never had problems with him back talking or ever really getting angry. Now that I read all these reports these are the problems I have with him now:
My child has never offered to hit, kick or slap me but in the past year he has gotten more aggressive not only toward me but others as well..
He is fearful of people now thinking that they are being mean to him or picking him out to pick on or make fun of.
He has problems of headaches on a regular basis but just thought it was due to his sinus infections...
I have also noticed that my child has started hurting himself like punching even slapping himself in the face when he gets really angery or fustrated about things..
Sometimes he has problems with nightmares but not that much..
He also has problems with stomach pain as well...
My concern is taking my son off Singulair with his asthma being under control right now and he just recently had sinus surgery but I think it will be the best thing for him just because I want my sweet child back not the aggressive and abusive child he is now.... That is why first thing in the morning he will be taking him to his dr to find another medication to put him on and take him off the Singulair....

I can hardly believe what I have read on this board. It is my son's story repeated over and over again and the sad fact is that I never put 2 and 2 together until I saw the news stories last week. My son has been on Singulair for years (he is now 7 years old) along with other drugs for asthma. We recently started taking him to a therapist because of his extreme unhappiness, violent temper tantrums, bad nightmares, many tics, and overall negative attitude. I took him off the singulair 5 days ago and cannot believe the results so far. My son is not affectionate in any way, does not even like a simple pat on the back, no hugs or kisses for sure. Two days ago he came over and gave me a kiss and a hug out of the clear blue. I cannot express enough what this meant to me. I have 3 other children that can't get enough of hugs and kisses, but coming from my 7 year old it just brought me to tears. The hugs have continued and he even told me that he loved me. The therapist had me convinced that he had a sensory deprivation disorder... until now. I cannot believe that until now I have not heard anything metioned in the news and that the medical professionals are so quick to dismiss claims against Singulair.
I am so thankful that I have found this website and for all of the people that have taken the time to include their experiences as it is evidence that there are serious problems when it comes to prescribing Singulair to children. I cannot help but to be saddened when I think of all the years I have lost to this with my son. All the time spent in frustration and tears over what I thought were serious behavior issues on his part. Not to say that I never expect any negative behavior out of a child, but certainly not like I have had to endure in the last years. The last few days have been amazing...I pray it continues. Shame on Merck for not being forthcoming and only keeping their bottom line in mind.

My daughter who is ten has been taking singular for two years. My uncle and my mom had both told me about the recent report. I was outraged. Since I didn't see it myself, I got online to check it out. I am so pissed off. My daughter has at times seemed to be depressed, my husband and I just thought it was a phase. She was never consistently depressed, more of an up and down thing. And she was fatigued from time to time. I never made the connection to Singular. I mean seriously it's an allergy medicine. And I always read the label. Never once have I ever seen a label say " may cause depression, or suicidal thoughts." I immediately took her off of it. Her last dose was 3/27/08. I noticed a difference almost right away. With in a day or so she seemed to be happier. I am so pissed off at myself and the doctors. of course I would have no way of knowing singular could cause this. I guess as a mom I feel like I should have know. I feel horrible!! Never once have they ever said anything of these reports. The FDA will be hearing from me. They hand out the medications like candy and have no idea what it really does to people. I just PRAY that my daughter, my nephew ( who was also on it for quite some time) and all these other kids out there have no lasting side effects from this medication. God Bless you all I will be praying!

My son is 10 years old and has severe allergies and asthma. He was hospitalized when he was 5 for asthma and at that time put on Flovent 110 mg twice in the morning and twice at night for awhile this seemed to work around the age of 7 he was put on Singular 5 mg to help with asthma and also his allergies. After a short period of time he began to complain of stomach pain he would get nauseated and sick with a 10 minute car ride, we took him in to the pediatrician and was told that there was no obvious cause and to basically deal with it. Around this same time he also began to have trouble in school he was not able to pay attention and was falling far behind we tried tutoring, extended day classes anything to keep him up with his other classmates. Needless to say all our efforts did not work and he got worse he was now moody and withdrawn. We thought it was his frustration with school that made him short tempered and emotional. At every parent-teacher conference it was the same report; being told how bright our child could be but his lack of focus and emotional state prevented this. My husband and I decided that we needed to be proactive and made an appointment with the pediatrician again we discussed all the issues and told the pediatrician that his mood has changed and he could not focus that homework was a battle each night usually resulting in a major meltdown. The pediatrician diagnosed my son with ADHD with ODD. Never would I have thought that my child with have behavioral or anger problems and I had a hard time coping with the idea at first but tried to make it okay for my son I did not want to make him feel like he did something wrong or that he was broken. The pediatrician prescribed Adderrall 5 mg at first and after three months we revisited and the dose was adjusted to 10 mg. School made a dramatic turn around and we were hopeful, however his mood was still all over the place he would get angry over small things, have a meltdown, and at some points would just wake up in a fowl mood and when asked what was wrong he could not explain it he just was not happy with anything. In the background of all of this was his asthma he was hospitalized again in when he was 8 after being discharged he was put on Zyrtec as well. So now his meds were Flovent 110 mg, Singular 5 mg, and now Zyrtec 10 mg. It was all overwhelming for all of us but we were trying to make it okay for him. He began to complain of restless nights, headaches and would get dizzy for no reason. Here we go again back to the doctor they attributed everything to the Adderrall. He passed out one day at daycare and we rushed him to the ER they did an EKG and found nothing and told us he was probably dehydrated. He constantly had a fowl smell coming from his mouth we asked his dentist they found nothing no cavities we asked the pediatrician no reason; no matter what we tried we could not get ride of it and he brushed, flossed and rinsed with mouthwash everyday three times a day. I was not making any connection on the side effects I guess you could say the left hand was not talking to the right. After we had wildfires that burned almost the entire city he had another asthma attack that lead us to the ER again after being treated we were assigned to a pediatric pulmonologist that added Nasonex to the regiment. Then in January we had him tested to learn what exactly his allergies were and was advised they wanted him to come in for allergy shots one in each arm once a week. In March 2008 we went in for his first set of allergy shots and right after had an appointment with his pulmonaligist he had a bad reaction to the shots and they changed his meds again. Now he is on Advair 250/50, Singular 5 mg, Zyrtec 10 mg, Nasonex, and Adderrall 10 mg. We decided to hold off on the allergy shots until he can better tolerate it. This entire time there has been little improvement on his attitude and he is withdrawn and seems disconnected now. When we try to talk to him he simply says he doesn't know what is wrong. It is all a roller coaster ride. Then on March 26, 2008 it all changed for me, I had put the kids in bed as normal and about an hours later heard someone up and in the bathroom I went to go check to make sure no one was sick and found my son in the bathroom and it appeared he was washing his hands and I asked if he was okay. He told me he was washing a cut, I looked at it and asked what happened he was hesitant and then pointed to his arms; he had bitten up and down both arms and on his hands to the point of bleeding I was shocked and did not really know what to say. We talked about it and he told me he could not control himself and even when he wanted to stop biting himself because it hurt could not resist the urge to to it over and over again. We talked calmly and after a long conversation he told me he needed to talk to someone about his problems. The next morning I called the pediatrician he said he could see him on March 30, 2008. On March 29th I heard about the side effects of Singular and was so shocked and angry how come no one told me what this could do to my baby; I wondered if he had never started this stupid drug if he would have been put on Adderrall. I would not let him take Singular that night or any night after. I will never let my son take this drug ever again. The following day I took him in for his appointment and after discussing everything the pediatrician agreed that it is best to leave him off Singular. I am taking my son to see a child physiologist as well. I am so upset that I did not make the connection myself.

We all experience similar problems. I think most of it is from frustration and is affecting us all mentally. You go to the doctor pay your co pays,blood work,and your prescriptions. Then patiently wait for change for the better. Go back and do it all over again every few months. You pay all this money and you still feel miserable.I feel like a lab rat sometimes.My muscles hurt,feel tired,can't lose weight.Don't feel like doing somethings I use to enjoy. I been on this stuff 3 yrs and my doc has me taking 300 mcg now.Wish I have some answers!

Hello Ladies, I am also a victim to Mirena. I am a married 30-year old women with three children and have been with my husband for 15 years. I have never felt the way that I feel today with the Mirena. Like most of you I didn't want to tie my tubes, but is very sure that I do not want anymore children. I figured I would try the Mirena for five years and then see what I want to do at that point in time. My list of symptoms are headaches, severe fatigue, bloating, cravings, acne, mood swings, dizziness, memory loss, painful intercourse, depression, nausea, vomiting, weight gain or loss (weird), thinning hair, severe backaches and cramping, pregnancy symptoms like not being able to brush my teeth without gagging and the feeling of a baby kicking inside my belly, lack of sex drive and last very little appetite for food. I thought I was going insane until I found this website. Thank you all for posting your symptoms you may have saved my marriage and my children from hating me. My mood swings are ridiculous, I mean down right MEAN for no reason. My husband and I have decided to have the Mirena removed and he will get a vasectomy. He said I have been through enough and God knows I didn't want to try anything else. So thank you all. Also for the young lady who works in the health field and has only had the Mirena for "I'm 21, relatively healthy, and never had children. I work in healthcare and see people react like this all the time-no tolerance to pain, and just wanting an excuse as to where some of their "pains" come from" discuss your issues if any after a couple of months. I hope you don't have any problems. But I know for a fact that before the Mirena I too was a healthy women who had never taken medication not even to have my three children. So I think I can handle pain very well. These symptoms are real at least for me. But good luck with you. To all the other ladies, follow your gut instinct. You are the only one who knows what your body is going through and can correct it. I will follow up once I have had the Mirena removed. Thank you all.

My son is 8 y/o (almost 9). We love Singulair, he has been on it for years (at least 3 years). He can go about 4 days off of it and then his asthma flairs up again and we are up at night coughing. However after reading some of the posts I figure that I would throw in my two cents because some of these posts have been eye opening. We just recently went to an allergist and he was diagnoised with more severe ashtma then we expected so he was put on Allegra and Advair to go along with his Singulair and Albuterol (we dropped Claritan for the Allergra). In the last year my son has been experiancing horrible moods to the point that at 8 y/o I wonder if he knows what suicide is because the moods have brought him to a level that makes me very scared for him. We have recently decided to bring him to a therapist to talk about the moods and the behaviors he is experiancing at school and home. The negative attitude, the anger and frustration, the short temper, the night terrors, and night walking. He has also had over the last 6 months that 'stitch' in the side that another person was talking about. We took him to the ER once for it because we thought he was having an appendicitis attack. However he was not and we have had recent attacks like that. Like I said, I love Singulair, it was and sort of still is our dream drug however after reading this I wonder if it is not. My heart is crushed that a drug I thought was great for my son maybe the one thing that is hurting him. I am going to talk to his allergist about it and will try to take him off of it to see if it makes a improvement. Thank you so much for opening my eyes and maybe finding me a solution to it all.

Severe Depression: Our 18 year old daughter started taking Levaquin as prescribed to treat her pneumonia (brought on by Influenza-A and accelerated by her asthma). Within four -five hours of taking the first dose, a sense of panic and frustration hit. Thinking she was stressed as one normally might be over missing college classes and the thought of what she had to do to catch up on her work, we continued with her second dose. Within two hours of that second dose, she was unable to stop crying, unable to sleep without nightmares and truly unable to cope with the situation. After a call to the pharmacist and then to our doctor, her medication was immediately changed. Within 12 hours after taking that last dose of Levaquin, she returned to her normal personality and has since continued to recover from her pneumonia, has returned to college, and resumed her life. I have never seen anything so frightening as the side effects of this medication on our daughter. Neither she, nor anyone else in our family, will take Levaquin in the future... or any other drug in that family of medicines. Be cautious if prescribed, avoid if possible.