Stress symptoms and conditions

OMG... After reading everyone's stories... I know I am not alone. Mirena was placed on April 24th, 2008. IThe only reason I got Mirena is because I felt pressured into doing so. I have recently miscarried and was a little afraid to try and conceive again. I have two small kids already. I informed the doctor that I really may only need the birth control for a year or so and the doctor still insisted on this bull**** device. Insertion was horrible, they tell you to cough as if it will ease the pain. I have been having horrible pain that seems to be in my right ovary. The pain seems to be very sporatic and when it hits its just like a previous poster said ... LIGHTINING! I have large clots during and after my period. Not to mention when I am on my period I have the loudest odor ever. This is so not cool. I have an appointment to have it removed August 21st. I cannot wait any longer. As I am typing I am in so much pain. I have been under so much stress since I have had this thing put in. I am irritable, overly emotional, bitchy, and I have no sex drive. My husband is becoming extremely concerned at this point. Ladies... please beware. I really think I may have long term issues from this piece of crap. I will let you all know about the removal process.

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

Hi all, I have had the Mirena since May of 08. I had twins in Feb of this year and was given the little plastic ring for birth control. That gave me TERRIBLE migraines. i hardly ever even have headaches let alone migraines. It was impossible to take care of twin infants along w/migraine pain. I really shouldn't be on estrogen anyway because of a clotting problem in my family. So my doctor recommended the Mirena. I wanted it anyway because I can't remember to take pills now, (I'm a little busy.) Since I had it put in I have been losing my hair in unbelievable amounts which my doctor attributed to my just having twins. My depression and anxiety meds are NOT working anymore. My fourth and fifth toes on my right foot are completely numb and stiff, almost like I have arthritis or something. I have NO interest in having sex w/my husband. But after taking care of twins, who does?? Just kidding. I am not very happy with this IUD, but have decided the alternative (being pregnant) is not a better option at this time. So, for now I will continue to be a bitchy, balding, arthritic, celbate mother of two. Good luck to everyone else

I'm 21 yrs old and have been on Yasmin for about 3 years, I've loved it - well I thought I did. I have been with my boyfriend for 2 years now, and this past year has just been really hard. I'll love our relationship one day and the next not be able to stand it and I love him more than anything. Over the past year I've experienced extreme mood swings, anxiety, haven't been able to handle stress - I've been breaking out in rashes at least once a month and really think it's because of this pill. I've also lost a lot of weight in the past year, I've been getting headaches everyday some to the point that I have to go to sleep because I can't think it's soo bad, I've had no motivation to do anything I have always, up to this point, loved doing. I've tried many anti depressants and have been off of them for about 2 years now, and have been thinking of going back on them because of the thoughts and feelings I've been experiencing. I thought it was just me, maybe there was something wrong with me? I've been on this pill for so long, who would've thought that it's just now causing these symptoms?
Yesterday I layed out by the pool for about an hour and when I got inside I noticed all these bumps on my arms that itched really bad, but they also hurt, so this morning I googled "sun bumps" and found that it can be cause from birth control pills, so then I googled "side effects of Yasmin" and I found this site. I am absolutely amazed at how many other women are experiencing exactly what I've been going through! I cannot believe that doctors don't bother mentioning all of these side effects to you, I'm absolutely terrified to go off of them because of the weight gain and also the mood swings I will more than likely experience. I got on the pill so I would have a normal period and it's really helped in that aspect, the craping isn't as bad, but the mood swings have definitely gotten worse.
I have called and left a message with my doctor to speak with her about what I've been going through now that I have a pretty solid idea that it's being caused from this pill.

I was prescribed Levaquin in Feb./March for 30 days. I have had tremendous pain in my heels since then. I am walking slower as every joint and muscle in my body hurts. I can barely stoop down and it is getting worse. I can not sleep. I thought I was just going through some depression and stress until I started reading about it in the WSJ and now realize I fit many of the symptoms being discussed.
We all need to take some action as this is only going to get worse for everyone.
FDA?????????????????

When I started this pill, originally, when I was about 15, I bled for 5 days, and then after that I began to slowly develop a stomach ache. Further more, my appetite not only vanished, but when I did eat, I had constipation / the runs.

I was on it for a year before stopping it for a few months, because I was becoming more moody than I normally am. For example, I would just start crying for no reason, or get very angry and hit people for no reason. Thought there's truly few good reasons to hit anyone.

I stopped the pills halfway through being 16. Stomach pain vanished, I began eating again, and having normal mood transitions.

When I started it up again, though, I bled for 18 days straight. Eighteen days of gushing blood all over the place. First 14 days was brown blood.

I stopped it after the 18th day, and got back onto it sometime in August. My everything seemed normal. Then the lack of appetite returned. And the stomach pain. The stomach pain actually got worse! I went to the doctor. Had to get a GI Series, drank a nasty barium solution, came up positive for... a stomach ulcer!

My doctor checked me for the virus, didn't have it. He chocked it up to Loestrin, though he said my stress probably made the ulcer worse. No less, he said it was all Loestrin's fault.

Recently, I stopped taking Loestrin 24 Fe again, with no intent of going back on it. And now, I have myself trouble breathing and some irregular heart beating, both which I plan to have checked out.

I do not plan to ever go back on Loestrin 24 Fe.

I did not enjoy explaining to people, at age 17, that the reason I couldn't eat spicy food or drink juice was because I didn't want to upset my ulcer, and needing to pop a Tums every two hours or so.

This is my story; if your stomach has been hurting, I hope you get checked for an ulcer.

I was given omnicef for a sinus infection, though I was told to take it twice a day , ive only been taking it once a day , due to an unnormal schedule... It has caused me to be so uncomfortable..I cant stand it. I have unbelievable abdominal pain, cramps ... but no diarrhea... Im constipated , one bowel movement a day ... and I also have the rust/ red stools. which is a listed side effect . Ironically, Before being diagnosed with all of this, I was in the doctors office a few weeks earlier complaining of stomach problems. . thinking I may have an ulcer, and my doctor told me It was only stress... yet he never tested me for an ulcer, no x-ray , nor an endoscopy. Now Im on some medicine that apparently may mess me up even more. WOW.

Zoloft. stress in colon sever, do not want to take any other drugs. will this subside with time? have only been on it 3 days, real tired today.

My Dad,a 78 year old highly functioning man, was admitted to the hospital last Wednesday evening, June 25, with a case of bacterial pneumonia. They gave him his first dose of Avelox, at 10:00PM. Twelve hours later, he was hallucinating, agitated, had an irregular racing heartbeat. He also had severe tremors, shaking. They gave him more medication for his heart and transferred him to the cardiac unit. They put him on a blood thinner, heart medication. Tested his heart and examined his brain. All tests came back negative. Thank God my father's heart is strong, or we probably would have lost him. 3 days later, I was on the internet researching Avelox, and noticed immediately that all of his problems were side effects of this drug. My family notified the doctor immediately and demanded that they switch my father's meds. The doctors did so reluctantly. They had never heard of these kind of side effects related to Avelox, even though it affects almost 3% of the population. My father had his last dose of Avelox on Sunday. Today, Tuesday, he is still having some "visions" and is confused. I don't know how long it is going to take for these side effects to disappear. The doctors are no help. This medication has caused my father and family severe stress, and prolonged his stay in the hospital. It has cost the insurance company extra money, since they had to do unnecessary testing on my father to try and determine the cause of his symptoms. He was also given additional meds that he never would have needed if they had just prescribed Zithromax from the beginning. AVOID AVELOX - IT COULD KILL YOU!

I had mine put in last August(07). Everything went fine and I have had no discomfort what so ever,Now I do have the small cramps letting me know when my period should start but its not a big deal. I got mine put in because of heavy periods. I have 3 kids and my tubes have been tied since 02. Periods are OBSOLETE and couldn't be happier,however,there is a small side effect I have had for about 6 months now. Very, Very low libido, I am talking once a month if my husband is lucky. I have been blaming it on stress of a 5 & 7 year old.The low libido isn't bothering me a bit but it is causing problems for my husband.Other than that,I think the Mirena is great!!

I'm very curious to read all these side effects! I have some strange symptoms going on and it only occurred to me after weeks of them that they may be caused by the Mirena IUD. Apart from constant annoying spotting and a bit of a dull ache in the pelvis now and then, I thought I had no other symptoms but I can see that my fuzziness in the head, low grade anxiety and stress that I've been feeling lately may be related. I've also been ravenous and am putting on weight but can't seem to stop eating junk. My energy levels are low and I have body aches and fatigue and find it hard to work out. But has anyone had achy joints in the hands and feet? .....tight tendons in the ankles & archilles and sore bones in the feet.......a feeling like swelling/tightness in the joints in the hands? I thought I was getting arthritis but maybe it's related to the IUD. I'd appreciate any feedback. Thanks

I had started the nuvaring 4 years ago and had loved it! I had no side effects except tender, larger breasts. I am a natural 36 D so it is a pain for me to go up to a 36 DD. I stopped taking the nuvaring a year ago since I was not in a serious relationship anymore and I wanted to give my body a break from hormones. I just started nuvaring again almost 2 weeks ago. I find myself crying for no reason. I am moodier than I usually am. I find myself crying then laughing then being frustrated. I find myself not motivated to do anything but watch tv. As I do so, I find my thoughts wandering to pulling a trigger to my head. I have no stress or worries in my life, why would I feel this way? I just don't understand why nuvaring used to be the best birth control and now it is a nightmare.

I AM HORRIFIED AFTER READING ALL OF THESE! JUST TODAY SOMEONE TOLD ME THAT MY EXCESSIVE HAIR LOSS IS PROBABLY DUE TO THE IUD. I CAME HOME AND GOOGLED IT AND LANDED ON THIS SITE. I SERIOUSLY HAIR NOTICEABLE BALD SPOTS NOW. MY HAIR COMES OUT IN HAND FULLS ALL THE TIME ALL DAY. SHOWERS ARE A NIGHTMARE. THE SITE IN THE DRAIN IS NAUSEATING. WHEN I PULL MY HAIR BACK IT LOOKS LIKE I HAVE RECEDING HAIR LINE AND YOU CAN SEE MY SCALP THROUGH WHAT HAIR I HAVE LEFT. I HAD EXTREMELY THICK DULL HAIR BEFORE. I IGNORED THE OTHER SYMPTOMS AND FOCUSED ON THE HAIR LOSS THINKING IT WAS RELATED TO POST PARTUM AND STRESS.....LOOKS LIKE IT MAY BE THIS IUD THEY CALL MIRENA MAKING ME BALD. I AM CALLING MY OBGYN ON MONDAY.

I've been on in a little over one day. The 6 day treatment. 5mg pills-6 the first, 5 the second, and so on and so forth. I have been SO HOT! I didn't sleep for very long, and woke up a couple times in the middle of night burning up. For me, the mental side effects have been HORRIBLE. I'm a 20 yr old fairly healthy female. 5'3'' 110 lbs. I have had unbelievable depression.... really really irritable and angry. I've just felt like hitting someone 24/7. I don't want to talk to anyone, I just want to sleep, I can barely keep my eyes open. I don't know how I'm going to take 5 more days of this. I also experienced the extra sensitivity to heat that others described. I read online that photo therapy... or sun exposure will help speed up healing and can be used alongside prednisone. I just really want this all to be over with. I look like I have the plague, and I feel worse than I look on the outside. Every little stress or worry just makes me want to end it, though I know that that isn't the answer. I'm a Christian, and I'm just going to pray about it. God will take care of me. I'm BURNING UP AS WE SPEAK! I've also been extra thirsty and my skin feels so dry!

Wow, I am so shocked to read all your ladies' comments!

I just started using YASMIN about a week ago and suddenly I started feeling very anxious and depressed, at first I thought that it was because I recently moved to my current apartment and had a lot of stress.

Then the more I thought about it the more I realized that whatever was happening was not normal because that's now who I am. I felt it had something to do with the pill, but I didn't think the side effects could be so awful. I have breast tenderness right now.

I just went to my GYN today and let her know what was happening and all she said was that it was too early for me to be having those side effects and gave be a paper to go and get a blood pregnancy test done.

I am 27 yrs old and I had been off BC for a long time, but the pills I used years ago did not give me any of those side effects.

I plan on going back to the DR ASAP and let her know that I want a different BCP.

Wow, I can't believe how common my side effects are now that I've read these posts. Ironically, the drug "claims" to have very seldom side effects, but I feel like I've finally figured out what has been driving me crazy: Aciphex! I'm a 26 yr old female, teacher (medium stress, but now on summer vacation!), healthy - teach health and p.e., don't smoke, do drink and eat spicy foods occasionally. I'm not on any other meds.
I think I've been on aciphex for about 3-4 years now, and have taken it continuously. I was told to take it this way by my GI, even though I've read on the label recently that the med should improve your symptoms within two months. What are the long term effects I wonder? It's been around since the 70's, but that doesn't explain how it's affected me and others. Last night I took my first dose from a new refill around 5pm (usually take it in the am) and woke up with severe panic/anxiety around 12:30. I was thinking random thoughts that made me feel like I was gonna die! My heart rate increased, I felt itchy all over, my mouth was SUPER dry, and I had terrible insomnia (watched two movies, didn't sleep until 4 am). I also had a ringing in my ear/fuzzy sound like the drug was too strong. It was whack... This was the worst experience I've had from taking it and I KNOW it had to be the aciphex. The weird thing is, I've been taking it for all these years, but have only really suffered from anxiety about 5 times off hand (never pleasant). I used to think it was my birth control pill, but since I've been off it, I still experienced the anxiety/nervousness, so I'm attributing it to the aciphex.
I'm going to make changes to my diet and try acidopholus and other natural remedies to see how I feel. If I don't get these attacks anymore, I'll know why. I hope this is what it was so I know I'm not just losing it!! :) It's not worth my mental health, that's for sure.

HI I AM 37 YEARS OLD AND 1 WEEK AGO I WENT TO THE DR FOR HEADACHES EVERY DAY, AND MY DR TOLD ME IT HAD TO BE DUE TO STRESS, BECAUSE MY BLOOD TEST AND PAP SMERE CAME BACK NORMAL AND I WAS PERFECTLY HEALTHY. SHE PRESCRIBED CELEXA AND SAID THIS SHOULD HELP. ALL OF A SUDDEN I HAVE NO SEX DRIVE, HEADACHES, NAUSEA, DIZZY, LOSS OF APPETITE, SHORT OF BREATH, MOUTH IS DRY, VERY EMOTIONAL, MY WHOLE BODY ACHES. IM GOING TO THE DR. AND HAVING HER TAKE ME OFF I WOULD RATHER JUST HAVE THE HEADACHES. DOES ANY ONE ELS HAVE THESE SYMPTOMS?????

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?

female age 40 started zoloft 9mths ago ,after I found out my husband was having an affair for a year and he left me and our 3 kids for her and her 2 kids.I was so depressed and physically sick.I started at 50 mg and after 6 months the doc upped the dose to 100 mg.It does help me on the every day stress of going through a divorce and im not as depressed,but I find every thing is such a chore,my energy level is zapped and that some times can get me down.My favorite time of day is bed time ,because all I want to do is sleep!!!! I am wondering if I should ask my doc about switching to some thing else.

I actually LOVED the convenience of the NuvaRing. However, I felt that over time, my sex drive had deteriated, I was getting more moody and irritable, and tired all the time. After talking to my Dr., she suggested that I try a low dose pill for a while and see if that helps. Regardless to taking any form of birth control, she told me, the female body will still have hormone changes and other body changes that are not controlled by or a side affect of your form of BC. It could very well have been that my body was changing on it's own, and due to that, I needed a BC change as well. I see some of you blame the Ring for some symptoms that could just be natural to your own specific body type. Talk to your Dr. to see if a switch would be the right thing for you. There may be other factors like stress, depression, anxiety and anemia that make your symptoms worse, not your NuvaRing.

I was prescribed lipitor, took ONE pill before I went to bed and woke up in the morning with severe pain in my right shoulder. I searched for lipitor and found so many side effects I have not taken another lipitor and will not. The pain moved to my left shoulder quite soon. Now it doesn't really hurt but there is a lump above my left shoulder blade, I was pushing on it and lifting my arm up and down hoping it might losen it up but the lump grew bigger. I quite often feel numb and week on my left side, kinda scary like I'm having a stroke. This has been going on for awhile so I don't think I'm stroking out or I would be gone by now. I do have high blood pressure, I think this ONE little lipitor pill made it worse as it's higher than it used to be. Maybe from stress as this shoulder problem and numbness upsets me from time to time. I also developed arthritis in two of my fingers, I have been taking FLAMMAGEN 1500 from the health food store and it has helped my fingers considerably, thank goodness. I'm not mentioning it to my M.D. as he was so excited about putting me on this stuff, poor guy is brainwashed. It really is a sin that our M.D.s are used in this way by big money pharmaceutical companies.

Hello,
Just thought I would add some pro nuvaring commentary to the chorus of horror stories here. I've been on the nuvaring for about two years now and so far I have no babies (yay!) and no side effects I could confidently link to the ring. Like most women I get headaches (about once a week or so), experience pms, and my sex drive is not what it was in the first few weeks of my relationship but I'm unwilling to ascribe any of these 'side effects' soley to the ring. In particular I find it difficult to believe as some of your postings indicate that the side effects of the ring seem to be worse than the pill- depression, weight gain (in one post 40-50 lbs!), headaches, etc. when the dosage or hormones is lower. So I guess simply put, I am satisfied with the ring and although it's not my place to criticize another woman's choice of birth control, I wouldn't let these posts scare you away from what is, in my experience, the best form of hormonal birth control based on its user-friendliness and lower dosage of hormones.

I was given a free sample of Topamax to help with neuropathy, but while I still feel the neuropathy pain, I have so many side effects. It's been several weeks, and family members are concerned with the changes in my behavior and ability to function. My wife is afraid to let me drive, and worries about my performance at work - the stress is hard on me.

I've had severe moments of panic, agitation, rage and thoughts of suicide.

Since I can't tell that it's really treating the pain, I want off of this medication.

This website has been a blessing for me - a person who seemed to feel crazy for all the symptoms I was having. I had mirena put in place in March 2008 after the birth of my second child in December. I was so excited that I didn't have to worry about birth control - I could focus on taking care of my family and work, etc. I couldn't have been more wrong about it. All was fine at first until April of 08 (two months later). I started to notice a red, bumpy rash on the trunk of my body. It progressively got worse with each passing day. It began to look like hives on my legs (behind my knees) and then on the inside of my arms. It has gone all over my back and finally to my face last night. I looked at the mirena website and it said to call your doctor if you had a rash with hives. So I did and they assured me that mirena WAS NOT systemic and couldn't be the problem. They maintained that it was probably an outside source. Instead they offered an anti-depressant. I needed something to help with what I was going through, so I started on Lexapro. That has been the only positive thing that has kept me from falling apart. What's the use in calling them if they don't listen to you? I have finally decided to have the mirena taken out in two days. I am so ready to get back to feeling normal. I was wondering if there was anyone else out there with similar side effects with the rash. If someone would have told me that this was a possibility, I would never have signed up for this!!!!!!
I will post again once I have it out and give an update!!

Reading these postings have brought me some comfort. At least I know it is not all in my head and that Mothers Intuition is still a strong powerful gift! My 4 and 6 year old were given Singulair. My 4 year old daughter came down with her first ever case of swollen glands. She could not eat any food and spent the next 2 months drinking from a straw. All tests came back negative, antibiotics didn't work, steriods didn't work and the ENT said I should remove her tonsils. After 2 months of being on all kinds of meds and her steriod treatment was done I decided to take her off Singulair. I just thought her body should be drug free for awhile! Within 2 days she was completely "healed". I will never give her Singulair again.

My son is 7 and I have just decided to stop his treatment of Singulair also. He has constant complaints of belly aches, grey stool, trouble sleeping and sudden tears. I just thought it was stress with school work, peers, etc. but I don't think so anymore. We seem to try to "understand" why our kids are having certain stress like symptoms but I think we need to look at our medicine cabinets first. They are small people on strong meds and I just don't think their systems can handle it. I think I am going to visit a nutritionist not pediatrician the next time I need help!