Doctor didn symptoms and conditions

Hello Everyone,

I've been doing some research on Mirena IUD side effects, and I'm so glad to come across these testimonials. I had Mirena placed in June of 2008, which hurt badly - something my doctor didn't tell me of until the procedure. Everything was fine most of 2008 but since January 2009 I have been extremely emotional and even was put on anti-anxiety/anti-depressant medication at one point. I have gained over 15 pounds in a year and can not get below a certain weight no matter how hard I try. My weight also fluctuates, which it never has before. I'm constantly gaining/losing 5-10 lbs, on a weekly basis. I have never weighed this much in my life, besides when I was pregnant, and it is really starting to bother me.

I've attributed most of my moods and "hormones" to being a single mom of two toddlers, financial stress, relationship stress with my ex and with my mother. I eat healthy and get exercise a few times a week. I'm definitely thinking removing the IUD would help my situation and make me feel like "me" again.

My question goes to the ladies that have had the Mirena IUD and have had it removed. Have you noticed a considerable difference, and if so, how long does it take for you to notice side effects starting to dissipate?

Thanks.

My allergies caused nearly constant painful sinus pressure, drippy nose (I should have bought stock in Kleenex to profit from my box-a-day use), asthma, getting gradually worse all the time--it was as though I'd had the flu for 10 years (I'm 54). I was taking Claritin in the morning and Zyrtec at night, which only toned down the most severe symptoms. I was on Prilosec as well, as one doctor though acid-reflux might exacerbate the asthma. My family and I are avid hikers, but I haven't been able to breathe well enough to join them for years, even with daily Ventolin and Flovent. I've only been taking Singulair for two weeks, but it has made all the difference. I feel "normal" instead of sick for the first time in a long time. So, for me, it does work. But my stomach's been killing me--like a bleeding ulcer (which I had 25 years ago). I'm hoping that will subside or going back on Prilosec (expensive!) will counteract it. I've also had the weirdest dreams--very vivid and disturbing. Because I did research online before taking Singulair (Doctor uttered not one syllable about side effects), I recognize the dreams are from the Singulair. Because I understand what is causing them, I can easily set them aside when I wake up. I think anyone who's had mental or emotion problems could be sent over the edge by the dreams unless they had a clear understanding and acceptance that the allergy drug caused them. I would be easy to think something was wrong with you to dream such bizarre, violent stuff. (I'd give examples, but I've truly trained myself to forget all about the dreams as soon as I wake us, so I don't remember the dream events now.) I'm quite concerned about children taking this drug. Maybe not everyone has this disturbing-dream side effect, but how could you explain them away to a four-year old? How would you even know if a younger child was having them? Even children old enough to comprehend shouldn't be subjected to horrific mental images, like the 16 year old above. A tip for people who Singulair helps, but they have the weird dreams--try Melatonin (over-the-counter supplement) at bedtime. I've used it to help me sleep in the past when life events kept my mind too active to sleep for several days at a time. Unlike sleeping pills, it doesn't make your tired the next day, you can wake up easily, and it's not habit-forming--it just lets you drift off on days you otherwise can't. Since I'm concerned about the long-term effects of anything taken frequently, I don't take Melatonin very often, but I did try it after the fourth day of Singulair dreams. I had no memory of weird dreams when I woke up, so it seemed to work, and I didn't remember dreaming the next night either. I only tried it that one day because, as I said, I've trained myself to not be bothered by the dreams.

I was prescribed 750 mg Levaquin for 7 days for a bacterial skin infection that I got under my breasts from inverse psoriasis. I took one pill and it hit me like a ton of bricks. I was up all night long with feelings of dread and like I was on a bad acid trip. The next day, I was so exhausted, I could barely even lift my head off the pillow and literally slept all day. The day after that I was going through withdrawal-like symptoms and my husband finally took me to the ER. The nurse practitioner there told me she NEVER prescribes Levaquin because she sees so many patients coming into the ER who are experiencing horrible side effects. I quit taking it obviously but am still feeling shaky and weak. Also, today, both of my feet started feeling like they were asleep with the pins and needles feeling. Also, I have TMJ and my jaw is aching as well. All of this for a little skin infection that the doctor didn't even examine. He just got the results of the cultures back but didn't actually see the infection to determine if it actually needed something so strong. I am taking Keflex now which isn't near as bad and is helping just fine. The difference is the cost. I'm sure the doc got a huge kickback for prescribing the higher-cost Levaquin. I will not be seeing him again. All doctors are interested in is prescribing drugs. They don't ever try a natural means of healing which I do not understand. I am so frustrated...I hope this crap gets out of my system soon!!!

I too had bad rash experiences with Wellbutrin. I was on it maybe 3 weeks when all of a sudden, I started getting hives on my stomach and neck. Also my eyelids and lips blew up and i even went to the emergency room one day when the whole left side of my face felt swollen up like a balloon.
I was shocked when my doctor didn't think it was the Wellbutrin since that was the only thing that had changed recently.
Suffice to say, without her recommendation, I stopped taking Wellbutrin and have not had those symptoms again -- and it's a full year later!

I am 20 and I have been on Loestrin 24 Fe for almost 6 months now. Before that I was on Lybrel for almost a year. I started taking Lybrel because I had always had awful periods to the point where I would sometimes faint from the pain of the cramps and would pretty much couldn't function normally. Lybrel was fine for the first couple of months but I began to spot after 6 months and decided to try a different one. I was put on Loestrin and like other pills I have been on I had intense mood swings, felt more anxious, depressed, and had night sweats for the first 3 months. I had light periods, 2 or less days and then about 3 months ago, I stopped getting a period all together. I have had no spotting and recently I have started to have cramping around the time I should be getting my period, breast tenderness and bloating. These are all symptoms I have had on past BC too. I take my pill every day around the same time and have never missed a day. I like not getting my period but it does concern me a bit because my doctor didn't tell me that I would not get a period at all, he actually warned me that I probably have spotting for a while. Does anyone else not get their period on this pill?

I posted on June 08 ( 40 yr old moodyann)..... I got my the Mirena removed two days after I posted (june 10th) .... after reading all the stories here, I just wasn't willing to take a chance with all of the side effects..... I had it removed 1 week after it was inserted.... I don't know how much it cost initially or what bills I will get for the removal....

The day it was removed I felt fine... no symptoms or bleeding... in fact the doctor didn't warn me of anything to expect.... she simply said it was easier coming out than going in.....

two days after it was removed ( Friday June 12), I started bleeding heavy.... its a bright red color with a few small clots.... I get dizzy if I stand too quickly....

Does anyone know if this is normal or should I go back to the doctor?????

I was started on prednisone for Dressler's Syndrome.. a heart inflammation. I have been taking 20mg daily, now 10.. I am having severe muscles cramps and rippling in my legs.. achy all over ,sweating, peeing all the time.. I am miserable. Why do doctor's dole out this stuff with out a thought???

I've been on lipitor and other generic forms of it for the last 8 years since the age of 26. I started on 10mg then 20mg and later 40mg. About 4 years ago I started with severe stomach cramps. The pain is so bad that I have to go home in the middle of the day, I can't walk or sit straight the pain is that bad and NOTHING helps. On a scale of 1 to 10 I would probably put this at a 7 or 8. I would also be nauseous and be really tired. I have had countless opinions and tests done and doctors keep telling me it is an "enigma" and there's nothing wrong with me. We've treated it through coeliac diet, exercise, lots of water, but it never helped. About a week ago I stopped drinking my meds by pure chance. I have not had one incidence of stomach ache. My doctor tells me that it's not possible for the lipitor to be the cause. I am sure he's wrong. Has anyone had a similar experience?

I am totally blown away by what I've read here because I have one Avelox pill left and now I know the source of all these symptoms I'm having. I"ve got the blurred vision in my right eye; feel like my body's on fire episodes--esp hot hands and red palms; achey feeling in my joints; headache that comes and goes; neck pain; fatigue; disoriented fog feeling and decreased mental capabilities; anxiety attacks and depression; dry mouth and eyes (and I'm drinking lots of water); waking up sweating; ears ringing from time-to-time; pain in kidney area that comes and goes; and not wanting to eat. The fever in my hands thing is the worst. Never had anything like it. The anxiety side effect got me thinking that I was dying. After reading this, I'm glad I can pinpoint it to Avelox. I won't ever take this again and I'll tell others about my reaction so they can avoid this experience. I can only hope and pray that these symptoms are not long-lasting.

I'm really upset that my doctor didn't forewarn me about the potential side effects.

Hi everyone...I have had Mirena out for almost 2 weeks now and I am back to my normal self already!!! I haven't lost any weight yet but I know that will come off in time. I, too, am on YAZ and love it so far. I have my phone set to calendar so I remember to take the pill every day or else I will definitely forget.

The best part about being back to my normal self is that I am enjoying my children again. I don't treat them like slaves, yell/scream at them for no reason, or want to be away from them. There has been a remarkable difference in them as well. They are not so whiney and they have more fun with each other. A benefit to that is that my 6 year old who asked me a few months ago if there were any extra chores she could around the house is cuddling with me on a daily basis. She wouldn't do that at all before. She is doing better in school too. My 3 year old is listening better too. I love my girls!!!

So, I am more than happy that I got my Mirena out and equaly grateful that my doctor (who happens to be a man and a new doctor) didn't try to convince me to keep it in.

New life and new me, here I come.

This website is absolutely amazing to me...
I started the nuvaring in March of 2007, but got off of it after a few months because I had gained some weight. My doctor didn't think this was related (she is a wonderful doctor, and this form of birth control was also new to her), so in September of 2007, I got back on it. At this time, I had lost over 26 lbs in between the months I hadn't had it.

Since September of 2007, I have gained back 18 lbs, yet I go to the gym at MINIMUM 1.5 hours, 4 times a week, and that scale will not budge. I have done South Beach in the past with great success, but I could drink only water right now and not shed a lb.

Also, I've been in and out of the ob's office with Candida and itchy vagina in general for months. Now, reading these posts, it's all starting to make sense to me.

I was also diagnosed with hypothyroid. Which I'm starting to wonder if there is a connection.

My migraines were so bad last year, that I had to have Fiorocet prescribed to me to get rid of them.

And lastly, I feel much more tired than I have been in the last few years. I need my energy back!

Either way, I will be coming off the ring, again, this week, and my husband and I will be back to condoms. And I can't wait to see if I feel normal.

Been prescribed Flomax for urine spraying / retention problem. The doctor didn't think it was absolutely necessary, so asked me to take one pill every two days. Just took the 4th pills and had some bad side effects. Almost fainted twice. I have never fainted in my life and am physically fit, can run a half-marathon without any discomfort. Other side effects include dizziness and weakness, blurry vision, stuffy nose, etc. It doesn't seem to help on my spraying / retention symptoms either. On the days I don't take Flomax I feel perfectly fine. I will stop taking this medicine as the side effects are a lot worse than the symptom it's trying to cure.

I got my Mirena IUD inserted at the end October 2008. I had a tubal ligation with the birth of my fourth child so my IUD was supposed to combat my battle with endometriosis. Needless to say, I am not pleased. After insertion I spotted for about a month. Finally that ended and I was blood free for about one month and as of January 1st, I am bleeding again. Happy New Year!!!! At first, I didn't know where to attribute my horrible depression, severe acne, and migraine headaches but now I have an idea since discovering this website. I am 31 and have NEVER suffered from acne not even during those adolescent years. The spotting is the worst. It is this horrible dark brown color with a horrific smell!!! I was starting to wonder whether or not it was actually blood. I contacted my doctor's office and was told that this was normal. I was given an antibiotic because they assumed the smell was from some type of infection. Well that didn't work. My doctor didn't want to remove it thinking that eventually my periods and bleeding will stop permanently. That day has not come yet, and I don't know how long I can endure. I really just want it out. I am tempted to contact my family practitioner and have him to remove it. I just know, I want it out!!!!!! I am just grateful for finding this site and finally realizing that it is not just me. I am looking into some herbal treatments to try to ease my discomforts with my endometriosis. I don't think I want to risk dealing with any more IUDs, birth control pills, or shots anymore. It just seems like to much to loose at this point.

I'm a 47 male and took Crestor for a year. I experienced muscle tremors, constant fatigue and muscle soreness. Not just a little sore but as if someone had hit me so hard as to leave a muscle bruise in both arms. One night my left arm and leg began to tremor and it was as if they were too heavy to move.

What I noticed was that all of my little aches and pains became severe aches.

I experienced blistering on my hands, a common side-effect of your liver rejecting the medication but my doctor didn't pickup on the symptom. Instead, he gave me a steroid-based topical cream that actually eliminated the blisters but they would return within weeks.

I experienced lapses in my memory and I started to forget words. I would forget the names of things and I found myself substituting the word 'thingy' when I could remember what something was called (like a phone).

I visited the hospital 4 times and my doctor countless time. Each time my doctor treated the current symptom and not the person as a whole.

It became too much to bare when I started having chest pains that felt like something was crushing my chest. At this point I started to do some research and found forums like this one.

During my time of the worse pain, I felt like I was actually dying. I started to get my effects in order and finalized my estate.

I stopped my Crestor about a year ago, after about 3-6 months my muscles began to feel better. After a year, I am finally starting to feel like my old self again (not that I was all that well before).

Statin affect people differently, but there is NO DOUBT that these drugs can have adverse effects on people. Listen to the commercial for Lipitor, "contact your doctor if you have muscle fatigue or weakness"......

I started Lupron in April of 2008. The year before this I worked HARD to lose 80 lbs. I finally got down to my goal weight because I was tld my endometriosis symptoms could be relieved if I wasn't overweight. I had a laparoscopy in March of 2008 confirming my diagnosis- Lupron was a last minute decision because of my age and status the doctor didn't want to do the hysterectomy right away. My endometriosis is spread throughout the body- including the lungs. While Lupron helped with the pain I was experiencing, it caused other pain. Pain that I can no longer even deal with. I became lethargic, depressed, and angry. My hair was falling out in large clumps. I didn't gain weight right away.. except a pound the first shot and three pounds hte second shot but I figured that was alright if it was only like 15 lbs total. I oculd deal with that. Here I am almost a year later. my last injection was in August. I gained a total of 47 pounds. I am a fat slob. I couldn't work out because my bones hurt so bad while taking the medication. No one around me knows what I went through physically. They al think that it was just some excuse to be a lazy fat cow but it truly HURT to move. Just simply walking from my bedroom door to my bed killed me. It hurt my ribs, my knees, my shins, my back. There were times when I couldn't even get out of my bed ebcause I just didn't have the energy. Then the depression started shortly after losing a large amount of hair. By now I am thinking about how ugly i've become on top of how fat I am. Nothing went right but my doctor pushed the shot. I figured hes the one with years of experience he couldn't possibly be this wrong. I trusted him. When I would go to him with complaints of my weight gain he would tell me to stop eating. The problem was... I wasn't eating. I was too sick to my stomach to bother. Then when I would get hungry i'd over eat. I bled a lot through the shots and I still had pain here and there but I was too afraid of what he'd put me on next if I complained. I started to forget simple things. My career was going down hill because they were sick of me not being 100% commited to my job any more. I cried all the time. I finally got sick of the weight gain while I was on my shots and I decided to work out regardless of how I felt and three times I passed out in the gym and was transported to the hospital where I had to listen to their advice on being overweight WHICH WASNT THE REASON I WAS PASSING OUT TO BEGIN WITH but no one wnats to hear what I have to say. Every one just assumed that I was this pig who never worked out in her life and over did it this time. What no one understood was that three months before the incident i was my average weight. I was tachycardic all the time- my normal resting heart rate while i was on my shots was 162. During a work out it would get up to 220!

Ive been off them since August and I haven't lost a single pound. I get up at 4am every day and work out. I park as far away as possible. I use the stairs instead of elevators. I eat healthy. I cut out extra sugars and stopped rewarding myself when I deserve it. I started these shots at 155lbs and today I am 215. Ive been on a strict monitored diet, diet pills and work out regimens and I am still 215. My knees kill me nad sound like velcro when I walk- ive even fallen a couple of times because they hurt that bad. My back still hurts and my neck still wont turn to the right completely because of a nerve that pinches or what have you in there that sends the sharp pain through my face when I move. I still have the depression but i think thats more because of my weight now than it is anything else.. and I finally ended up losing my job.

I recently saw my OB for a follow-up where he stuck me on yet another birth control. This one makes me vomit and gives me stomach cramps so Ive decided im done. I won't take another pill because its making me worse. Id rather have my uterus fall on the floor than pop another drug.

I have had THICK hair all my life. Was on WB XL (300mg) for 2 years went off because of memory loss. Was off for 6 months, felt good, but inevitably depression slowly crept back into my life. Went back on WB XL (150mg for a week, then 300mg). Been back on it for 2 1/2 months and just noticed 2 weeks ago that my hairline is thinning at the corners of my forehead. It's especially noticeable when wet or when the light shines down on my head. I can see my scalp. I have also noticed an increase in dandruff. Yikes! I am a hairdresser and it would be terrible for me to have bad hair while working with clients. Why didn't this hair loss happen when I first started taking WB XL 2 years ago? And why is it flarring up now? Is this a temporary side effect that will work itself out, or do I have to stop taking this drug? I'm glad that I am not the only one and that I am not crazy!

My brother passed away at 56 of a stroke. So after having my blood tests done, everything was high, cholesterol, CR Protein....doctor put me on 20mg of Lipitor....the very first day, I had severe muscle weakness in my upper thighs, back of my calves, pain in my knees, pain in my wrists, pain in my fingers. What a nightmare. I tried it for two more days, called the doctor told him, he said reduce the dose in half........not a chance, I told him I believe in quality of life, not quantity of life. I'd rather be dead, then live like that.......and yet the doctor didn't tell me to get off of Lipitor!!!

DO NOT TAKE THIS POISON!! I have spent the last 4 years dealing with
adverse side effects of this medication. I have central nervous system damage, digestive disorders, anxiety, panic attacks, dizziness, achiness-it feels like a really really bad flu. My dad who is a doctor didn't believe that Levaquin was the cause at first however he had a chemist look up the compound makeup and was told to never prescribe this or any other fluoroquinolone again (cipro, avelox, etc!) Side effects can last long after you finish this medication. Also animals can get this stuff so it can be in the meat you eat which will make you feel worse or it could kill your beloved pets. Do your research. Warn friends and family-even strangers. Make a mediwatch report. Helpful sites if you are dealing with poisoning.
There is also a yahoo group.

I was on prednisone while getting over pneumonia to help with my breathing. I was only on it for 7 days and the doctor didn't have me go off of it gradually. I missed the last dose on the 7th day and by bedtime, my muscles were sore enough it almost hurt to lay down. I took the last pill that night before I went to bed and had no muscle soreness in the morning. After that, the muscle soreness came back, along with dizziness. My pulse was also higher than normal. Two days later at night, I was still having muscle soreness and dizziness, although not nearly as but, but I was having a lot of trouble breathing and my pulse would refuse to go below 100 no matter what I did and the problems continued thought the night. The next morning I went to the clinic that prescribed me the predisone because the information they gave me said to see a doctor if these problems persisted. I told them I thought I might be having a predisone withdrawal because my mother, a nurse, said it was the most likely problem from experience. They completely ignored that saying it had been several days since I've stopped the steroid and kept asking me about my asthma (inhalers weren't working and it was definitely not an asthma attack -- I've had plenty of those, to all different degrees) and ended up giving me medicine for anxiety, which helped the closing of my throat, but none of my other symptoms. Three days later, my resting pulse is down to 80, but my breathing is so much worse than it would be with just my normal asthma and taking my inhalers as much as is allowed. I had no noticeable symptoms when I was on the prednisone except being less able to sleep. If it keeps up, I intend to go to a different doctor to see what is really happening, but I don't think it's 'normal' to have the withdrawal symptoms for this long after only having it for 7 days. I know I took it when I was younger (I'm 22), but I don't remember ever having issues going off of it before.

Hi, Ive had the Mirena for 2 weeks now and it has been TERRIBLE, I have had terrible sharp pains off and on... I have never had kids but is a contraction like the pain that I am feeling? My doctor suggested that I have it put it since I felt sick with the pill and specially if I am not ready to have a baby yet. I've been married six months now.... I don't know if this will go away and I don't know what to do, the only thing good about this is that my sex drive is much better, lol... but this is terrible what should I do? Should I have it taken out and will it hurt?

TOOK IF FOR 10 DAYS...ON DAY 7, NOTICED MY RIGHT NECK WAS PUFFY AND SORE (ONE OF THE SIDE EFFECTS) AND ON DAY TEN, I HAD RED SPOTS ALL OVER MY BODY, FACE WAS FLUSHED...HOWEVER, WAS NOT ITCHY. DOCTOR DIDN'T BELIEVE IT WAS AN ALLERGIC RXN BECAUSE IT DID NOT ITCH. THE PHARMACISTS I WENT TO SAID THEY SEE IT ALL THE TIME AND IT DOES NOT NEED TO ITCH TO BE CONSIDERED AN ALLERGIC RXN. THE DR PRESCRIBED CLARINEX FOR THE SPOTS.

I just spent $40 on a 10 day supply of Levaquin (750 mg). I am so upset - for one I am out $40, and now I don't want to take it. Of course the pharmacist will not take it back. I am a 30 year old female, (weigh 105 lbs) and have had serious reactions to medication before. To top it off I have fluid in both ears, which is why I got this medicine in the first place. I am assuming that most of you would tell me to stay away from it. I feel like I should try it since I spent all that money on it, but I am afraid to now. Any thoughts from anyone. I can't believe my doctor didn't say anything about the possible side effects.

I took the generic for Norvasc (amlodipine)for 2 months and all I have
to say is the stuff is pure junk.
I felt absolutely AWFUL.
I felt like I had been poisoned.
My lips and tongue swelled,canker sores on my tongue
and I became horribly depressed.
What a bunch of BS!!!
I'm not taking anymore of these poisonous substances!

I had Mirena put in 6 weeks post pardom with my third child with a c-section. The insertion was the worst thing ever!! And my Doctor didn't warn and I almost pasted out. I have no sex drive, painful intercourse, vaginal dryness, burning during urination, massive head aches, blurry vision, mood swings, emotional distress and serious weight gain problems. I too was coxed into this option by my doctor and he said it was so easy and had almost no side effects. I guess this is what I get for taking a mans word!!! I do however have little to no period, but now I am wondering if that is the problem. I mean our bodies our supposed to go through cycles....maybe this thing really screwed something up. I am calling my doctor tomorrow to schedule having it removed. I am hoping I can get my hands on a valium first though....it hurt like Hell last time. I guess I should have looked up some of this stuff in the first place...with what I see here, I would have never had this thing put in.