Elbows symptoms and conditions

I was prescribed a 10-day regimen of 500 mg capsules, 3 times/day for a tooth infection. First dose at 9:00 pm last night (Friday). Woke up seven hours later with intense itching back of the neck and inner part of both elbows. No other symptoms. Spreading across shoulders and stomach. I'm taking generic antihistamine and applying calamine lotion. No really relieving the symptoms but I'm hoping they will subside my 9:00 am this morning. I'm glad I don't have to try to work in this condition. No plans to take a second dose.

I am a 52 year old female and my bad cholesterol is fine but my good cholesterol is low. I have been taking Lipitor now for a few years and have numb hands and feet to the elbows and knees. My feet are extremely sensitive, worse at night and now I'm getting sharp pains that feel like a bug just bit me. My tongue is also always numb and I do get migraines.I have insane stomach issues and food intolerance. I also take medication for high blood pressure, acid reflux, & thyroid. I have now been diagnosed with type 2 Diabetes but control that with diet so far. Until four years ago I had nothing wrong with me. I am slim and healthy. I had a lump in my thyroid which was removed and there was a trace of cancer. Then like dominos all the other conditions lined up. I have had MRIs and all the tests and doctors insist that I am not a severe enough diabetic to have neuropathy. I can hardly wear shoes now and it hurts when I wear runners while I walk and exercise. Does any of this sound familiar to anyone? I hate that my health has become so much a part of my daily life. Does anyone have neuropathy as a result of Lipitor and am I even taking the the right medication since I don't have high cholesterol?

THANK YOU SO MUCH FOR THIS SITE! I was beginning to feel that I was getting old too quick. I have been on Lisinopril for about a week and for the past two days I have had such severe muscle and joint pain that it even hurts to type this, it is in my hands, elbows, knees, and feet, and I look like a little old lady going to the store all hunched over and barely able to walk and I'm only 29!!! I don't care what my doctor says I'm quitting this medication today and going back on my old meds. Hopefully this excruciating pain will go away.

i started using nuvaring about two and a half years ago. i have always had a small problem with eczema (on the inside of my elbows only), though for the past two and a half years, it has consistently been flaring all over my body. it looks awful and has brought me to an emotional low that NOBODY should feel. i have spent thousands of dollars on medical visits (including a patch test - "inconclusive"), medicines (a variety of steriods, protopic, allegra), vitamins/teas/etc, and countless hours reading and online trying to figure out what could be causing this uncontrollable flaring. about two months ago, i decided to stop using the ring and see if it is the problem. so far, things have been clearly up, SLOWLY but there's some hope now. if anyone is experiencing these symptoms, i urge you to try and remove the ring, don't waste as much time as i did and have to recover from two + years worth of damage to your skin.

I have been on Yasmin for over 5 years, and just thought that I was a hypochondriac. After starting Yasmin I experienced severe nausea and unrelieved hunger pains. I saw a gastroenterologist who performed an EGD and Colonoscopy at the age of 20. It was normal and I was placed on Protonix to help with the GI issues. Also I have severe joint pains in my knees, hips, elbows and shoulders. I have been tested for everything from Lupus to Rheumatoid Arthritis, and it was all negative. I get headaches, have little sex drive if any, my skin is not clearer than usual and nor has it been since starting Yasmin. Thanks to all those people who have voiced their concerns and shared their stories, it makes us feel less crazy. I threw out all my birth control pills last night and I am going to try another form of contraceptive. I mean my headaches and chest pains have gotten so bad that they have forced me to go to the ER on several occasions. I DO NOT THINK THE BENEFITS OF YASMIN OUTWEIGH THE RISKS ASSOCIATED.

I am a 44 year old male, been on Lisinopril for almost 2 years. My insurance stopped paying for whatever I was on prior, and gave me this. I was told only side effect may be a dry cough. OK, never got the dry cough. Great I thought ! Last year, I developed a bilateral rash on both arms, and both sides of my waist. I dealt with it.. went away for a while, and now back with a vengeance... arms, elbows, buttocks, both sides, and chins... the scratching is unbearable.... Im guessing based on what Im reading on this site it could be the lisinopril ? Please comment back if you've had similar.....

Wow, what an eye opening experience it is to read all these posts! I was just about at the end of my rope thinking something was horribly wrong with me. Now I firmly believe it's the Levoxyl that is wrong.

I went on thyroid meds about a year and half ago for just slightly under active thyroid. I was actually lulled into it because the Doctor assured me it was a completely safe medicine and taking it would help me lose weight. Always a welcome thing. So I started on 50 mcg. I noticed some degree of improvement. I was sleeping better and having more energy during the day. Next checkup, the levels are in the normal range but just barely. So he doubled the dose. Two weeks later I broke out in a horrible itchy rash. I actually thought about the meds but then I didn't change meds, I was just taking more. I called the doctor and he said, "No this medication won't do that." So I change detergent, soap, everything I could think of and nothing worked. Finally I said, enough and I skipped a dose. During the day the rash got a lot better. Next morning I took another one and within and hour I was itching like crazy again. I stopped taking them, waited a week and called the doctor again and told them. His reaction was "You have to take this." I said, No, I don't and I won't. He actually argued with me that the rash could not be caused by the meds. Now I realize at that point I should have called another doctor but he's in my town, convenient, yada, yada, yada. Anyway he called me in another med which he said was the same active ingredient but different brand. Enter Levoxyl. I've been on 100 mcg for 3 months during which time I have felt progressively worse. Most of these things I didn't attribute to Levoxyl until later. Initially I noticed I was having the hot/cold flash thing. I have no comfort zone. I'm either flushed and sweating or chilled so my nights are spent constantly either searching for cover or kicking it off. Next thing I noticed is that my breasts would swell. Naturally that was a concern but about the time I would decide I needed to see about it, they would be normal for a few days. Sleep? What's that? Tired all the time. Started having confusion and forgetfulness. I even told my co-worker I thought I was losing my edge. I was all of a sudden forgetting things I had done automatically for over 15 years. Then the really scary stuff started. I would wake up in the middle of the night with my heart racing and feeling like I was in a fight for my life. I was afraid to go back to sleep. Joint aches and pains across my upper back, my knee. Tingling in my feet. It just keep getting worse and worse. Still didn't think of Levoxyl. Then Monday of this week I didn't have a pill to take. I forgot to get it refilled. Monday at lunch I told my husband I felt better than I'd felt in months. Tuesday took the regular dose. By noon the mental fog was back, back was hurting and I just felt like crap. Tuesday night went to bed early because I was so tired. 11:40 woke up with the worse anxiety attack I've ever had. Heart was pounding and I was breathless. Wednesday morning I got up and the light came on. I did not take the pill. Entered Levoxyl in google and found this site. I am so angry at my doctor I can hardly stand it. I even went to the official Levoxyl website and all these side effects are listed except for the swelling breasts and confusion but I've noticed several posts here that list those. During those two days I didn't take the freakin' pill both problems improved greatly. This morning, I reluctantly took half a pill. I plan to to that every other day for a few days then skip two days, then three, until I'm off of it. I don't know at this point what I'll do about my thyroid but I won't take this stuff and I won't ignore feeling like crap again. This is crazy. Where is the FDA? Oh yeah, being entertained by the drug companies. What a shame.

Thanks to everyone who has taken the time to post here. It is a sad commentary when we can't rely on our doctors to take care of us but we sure can't. If he had just told me about the bone loss, I would never have started this drug in the first place. My Mother suffered with that and that is something I would not trade for a few lost pounds and a little more energy. No thanks.

Took Doxy for 2 years for Lyme and Babesia. Never had a problem with it. I stopped taking it for 8 months, then the Lyme disease symptoms returned. So I started back up on it. I noticed migrating pain in all of my joints...even every toe. I stopped taking it for a week and the joint pain pretty much resolved. I started it up again and sure enough, joint pain returned mainly in my knees and hands. Constant cracking of my thumbs, knees, toes,elbows. It also caused my tendons to become very tight and sore in my right hand. Making it hard to hold my dog's leash or open a door knob. Whether it was a bad herxheimer reaction or just my body deciding it was sick of this drug......I may never know.

I am 26 years old with two kiddos.
It has been 4 weeks since the removal of my Mirena (it was in for a little over a year). So far, no more dizziness, nausea, joint pain, nor cramping. I made a list of all of my symptoms so that I can check them off when they disappear. Symptoms that I am still suffering from are: Eczema (fingers, arms, elbows, legs), tired, acne, cloudy thinking, moody, not much of a sex drive (but getting better), emotional, no patience, hard to focus, having and overwhelmed feeling...like I can't multi-task and handle lots of different things at once, just having no desire to clean up around the house...kind of and "I don't care" attitude. None of these symptoms were in my life prior to Mirena. I really hope these go away in the NEAR future!! I heard about the Mirena "crash", I don't think that I experienced that, just the same stuff with some symptoms vanishing. Best of luck to all and God Bless!

I just read about a side effect from another member
He talks of pain in his inner elbows. Oh my I have that too, and I thought
it was because I strained that muscle when doing work. But it was so long ago. I still have the pain and find it hard to pick up things. Now I read about someone taking the same medication as me and having the same symptoms. I actually only take a half of a pill a day, but now i will discontinue it until I see my doctor (also my sleep pattern has been affected)
I did not have this problem when I took Lipitor.
I am hoping I can go back to Lipitor but maybe I will increase my exercise and not eat anymore junk food and then not have to take any of this silly medication.

My symptoms are much like others described. I was prescribed Bactrim for a recurring UTI. I have never taken it before and have never been aware of any drug allergy. I took the Bactrim two times a day for five days. On the fifth day I began to develop a fever, with very cold chills, then very hot. The lymph nodes in my neck and the back of my head swelled up that evening and were painful when pressed. The next day I stayed home from work and my temp was up to 100.1. By evening that second day, I had developed rashes on my elbows and feet. They were itchy and raised. The next morning, which is today, the rash has spread to my shoulders, arms and thighs. It is not raised, but is a mass of small red dots. My face is also very red, and I think that my lips feel swollen. It has been good to read here that these are likely the result of the Bactrim. Much better info here than I got by calling the pharmacist! The only reason I looked in to it being a reaction is that my mother in law has had allergies to sulpha drugs, and has mentioned rashes. I agree that it is also interesting to here that it has happened to others either after the prescription had finished, or right around that 5 or 6 day mark.

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

Hi All,

I am so glad that I found this group of postings. For the past 5 days I have been experiencing muscle pain which began on the inside of my left knee day 1. On the second day I had significant pain in both calf muscles as if I had begun a new calf workout routine(I haven't) as well as pain in the large back muscle that runs down either side of the spine. Day 3 I noticed serious pain in my forearms and wrists. The forearm pain is causing hand cramping and my thumbs don't seem to function properly. I tried to sign a credit card receipt today and could barely grip the pen. I now have pain in my neck muscles as well.

I know I have taken Levaquin in the past 6 months, I am just not exactly sure when it was. I am definitely going to research that. I went to the Dr. yesterday to discuss my muscle pain. He took 2 viles of blood. He said he is going to check for Lyme's disease and other infection. I am hopeful it is not something serious. I must say thought, many of the posts above sound a lot like what I am experiencing. I am going to be beyond angry if I have a permanent condition from taking Levaquin. Some pain I believe I can deal with. It is the current poor function of my hands I am most concerned with.

I wish all of you the best in recovering. If my condition turns out to be something else I will repost.

My husband was given Levaquin and Prednisone in April for a bad chest infection. The last day of Levaquin, his knees began burning. He has been suffering with pain and cramps from his toes all the way up his legs. It has been in his fingers up through his elbows. He has shaking in his hands. He had an abnormal EMG. He has intermittent low grade fever. He started having trouble swallowing a couple of weeks ago. He now has to go to speech therapy because his tongue muscles aren't working correctly. He had none of this UNTIL he took this medication. The doctor now finally feels it is as a result of taking the Levaquin. The prescribing doctor had the nerve to lecture us about NOT stating he was allergic to the medication because he would be in the hospital with an infection otherwise. We are not returning to this doctor.

My neurologist put me on Prednisone for cluster migraines. I started with 80 mg for 2 days, 60 mg/2, 40mg/2,20mg/2. It was so effective at keeping the cluster attacks from coming. I was so thankful to finally have something to stop the attacks. I have suffered with CH for 20 years and other than pain medication to abort an attack I never had anything that worked as a preventative. After taking the prescribed dosage I stopped taking the Prednisone. My neurologist warned me that this drug can be very effective short term but I would not want to have prolonged use because of the side effects. Unfortunately, when I stopped taking it my cluster migraines came back full force. So I went back on taking 20 mg daily. That was a BIG mistake. At first I was euphoric, on a constant high. I had so much energy even though I would only get about 4 hours sleep because my mind was racing from 2:00 am into the early morning hours. I would wake up with night sweats and needing to urinate 3 times per night. My face got puffy, I had terrible heartburn, increased thirst and a decreased appetite. My family was watching me wizz around like the Tazmanian Devil wondering why I was acting so bizarre. I thought I was seeing things so amazingly clear! The worse part of all is the itchy, red rash that started on my elbows, then knee caps. It has now spread up and down both arms and legs. I went to see my GP and I told him that I have never had any skin rash like this before. Could it be the Prednisone causing it? He of course said it was unlikely because Prednisone is used to clear up skin problems. Now having stumbled on to this site I realize that it must be the Prednisone doing this to me. I am unfortunately going to have to suck up the pain of the migraines and let them run their course until they leave me for a few years. I'm so disappointed that Prednisone isn't going to be the cure after all.

I had my Mirena put in 10/08 at the end of my period, after having my youngest in September 2008. I had bleeding for about 6 months daily, heavy at first and then just enough to be annoying. I had some random nausea during the bleeding period. Since the bleeding stopped in May 2009 all the wonderful symptoms started. I suffered from nausea and bloating every day, all day until just last week. Then last week the nausea went away (mostly) and the constipation started. What a nice trade off. We were in Wisconsin Dells the past few days and I started experiencing pain/numbness in my hands that went to my elbows and at times to my shoulders. I don't know if this is related to the Mirena or pushing a heavy double stroller all over and up big hills. I have had pain/aches under my armpits right next to my breasts for a month now too, along with shoulder and collar bone pain. There is occasionally pain in my breasts similar to the letdown pain I experienced while nursing ( stopped month ago.) I had an ultrasound last Tuesday and the Mirena in in the right place and I am definitely not pregnant. My ob/gyn told me to follow up with my PCP as none of these were Mirena symptoms including the nausea. My PCP gave me a stool softener and did a chest xray which was normal. I was beginning to think I was dying or had some deadly disease until I found this website. Oh yeah I forgot to mention the awful headaches I've been getting on and off, I think looking back mostly at the beginning/ middle of my cycle. I still have spotting on and off and get a really light period every 21- 26 days. The minor things I have noticed are oily hair, light acne and irritability. I have an appointment to have the Mirena taken out next Monday. Has anyone else experienced these symptoms together? Also could somebody please tell me more about the Mirena Crash? My ob/gyn just said to expect a long heavy period. I want to know how long it will take to feel normal if these issues are Mirena related. I would love to get some opinions from other Mirena users. My email address is ****** Thanks!

Wow, I'm so glad I found this site!
I was diagnosed with pleurisy 2 and a half weeks ago following a virus, a few weeks before, so naturally, as my asthma nurse has always told me, I've doubled up my Advair (or Seretide as it's called here in the UK!) for that entire time.
Previously I was taking one puff once a day in an evening which I never had any problems or side effects with, it just controlled my asthma really well. Now I'm taking 2 puffs twice a day (morning and night) and for a few days now I've been having terrible joint pains in my hands, feet, elbows and knees. Have been searching the internet for what it could be and think I might have found the answer! Hopefully if I decrease my meds back down the pain will improve!
Like a lot of people on here, though, I was NEVER told about any potential side effects to Seretide, just that it was a wonder drug.

48 year old male - Hello all, I started with 10mg zocor (Simvastatin) off and on for about 2 months. No real symptoms other than it made me very nauseous. My cholesterol sky rocked and my doctor informed me that I needed to take it regularly and also increased my dosage to 40mg. I have been taking it religiously for about 3-4 months now and my cholesterol has improved very much, but about 2 weeks ago I started feeling pain in both my inner elbows, at the joints and along the sides. Its hard for me to lift things at times. Sometimes it’s a burning sensation and sometimes its sharp pain. My Doctor informed that it was the simvastacin and now wants me to change my meds to Lovaza (900mg omega-3 ethyl esters). I am going to stop using the zocor, but what do you guys think? Is there something better for me too use?

I took 500 mg of Levaquin more than two years ago and am still have severe tendon problems. I was a runner and triathlete. Now my hips and elbows ache so bad that just daily routines are difficult. I have heard that Levaquin has a dispropriate effect on athletes. So if you are a runner or triathlete do not take this drug. YOU WILL NEVER BE THE SAME. The information provided by the manufacturers regarding the side effects is false. The incident of injury for certain groups is much much higher than they report.

I am 26 years old, 5’6” and weigh 112 lbs. I have had the Mirena in since June 2008. Where do I start? This IUD was suggested to be by my OBGYN after the birth of my second baby. I really trust my OB so I agreed to have it inserted. I made a quick decision with LOTS of emotions behind it (I got pregnant with my second baby when my first was only 5 months old…so I was a little freaked out by the thought of getting pregnant for the third time in the near future). I can only take one other hormone-based form of birth control (the pill with NO estrogen), so this seemed like the answer to me. I was given a Mirena pamphlet from my OB, and it did NOT list several of the side effects that I have experienced over the last year. The insertion was indeed pretty painful. To me, it felt like I was having pretty strong contractions. It took about 20 minutes from start to finish. I had cramping and steady bleeding for the first 3 months. I then had no period for about 6 months, which was nice. I did, however, completely lose my sex drive. I am always tired, moody, irritable, and emotional (all of which are not common for me to experience on a regular basis). I have trouble focusing and thinking of the right word I want say. I have mild but annoying acne on my face and neck, eczema on my hands, elbows and a few spots on my legs. I have knee pain when I run/jog, and I just don’t feel like myself. I am in perfect health otherwise, and no history of the above symptoms that I listed. Currently, I have a normal period every month that lasts a week (before they only lasted about 4 days), then a week after it stops, it starts up again. I called my doctor and they say that’s normal. After intercourse, I have cramping and bleeding (that’s a fairly new symptom). So imagine having sex when you don’t feel like it whatsoever and then knowing that you will have cramping and bleeding afterwards…sign me up!! My husband has been so patient with me, but has finally had it. He wanted me to look into it and make an appointment. I am so thankful that I found this site. I was so worried when I didn’t have a sex drive and I felt myself blaming my husband for things that I assumed he was thinking. I have been praying about it and know that God led me to this site to see what other women are suffering from and going through with this IUD. Aside from all of its nasty side effects, I wanted to let all of you know what I have discovered could happen to an unborn baby if the mother has an IUD. First of all, if you become pregnant, you need to get down to your doctor right away and have it removed. However, there are no guarantees that during the process of the removal, they won’t bump the baby causing either a miscarriage or birth defects. That just breaks my heart. To me, it’s not worth it. The other thing that worries me is that, after getting it removed, are my chances of having a perfectly healthy baby in the future lessened because I had a foreign object inserted into my body? No one can say for sure. It’s just something that time can only tell. I really would discourage with all of my heart, NOT TO GET THE MIRENA or any form of IUD.
Anyway, I have an appointment scheduled on August 18 (wish it was sooner). My insurance doesn’t see this as an emergency or life-threatening, so I have to pay my full detectable of $200 to have it removed. That kept me from doing it a few weeks ago. I now know that you can’t put a price on the happiness of your marriage, your health, and the health of the baby that you could very well become pregnant with. I wish you all the best and will definitely update you on the removal and how I feel. God Bless. SAO

Wow, wish I had read this a long time ago. I have been on Vytorin 10/10 for 2+ years. Have many of the same complications as posted by others. Numbness in the hands and arms and severe joint pain in my elbows(I am not a tennis player, or anything remotely close to that) has just started to increase over the last month. Never made the connection until now. And the sleepiness!...I just feel like I could sleep all day everyday!...Now, this is one that I haven't seen in other posts, and am curious if anyone else has noticed capsule shaped things in your stool? They are almost a yellowish color and I would say about the size of a ring finger tip from the top joint to the tip of your finger? Part of me just assumed it was the Vytorin taking the cholesterol out of my system, but now I am worrying it could be something more. Any replies are appreciated, and last night, I took my last dose of Vytorin!

I was on levaquin august 2008 for a sinus infection. After about day 5 is was in pain. My joints ached terribly. My knees, my hips, my wrists, elbows and fingers. I have undifferentiated connective tissue disease with lupus like symptoms. I thought that maybe the levaquin made me flare. I stopped taking it on day 5 and after a week felt somewhat better. I am on meds for joint pain for my autoimmune condition but still had the joint pain with the levaquin. The physicians assistant that I saw said joint pain wasn't common. From what I'm reading here it's very common.

I was prescribed Simva 30mg to replace Lipex which is no longer government funded 6 weeks ago. Since taking this medication I am waking up with tingling in my elbows and fingers blurry eyesight and what really worries me and no one seems to have mentioned is low body temp 34.2 and then a reading of 34.8 now averaging around 35.2

Please is anyone out there suffering from low body temp

I started feeling much better very quickly after being off Lipitor now 7 months. However, the symptoms I had using the RX has cause significant problems. I fell so many times with my weak joints and muscles, that I had severe problems. I now need to have knee replacement surgery after falling so many times injuring my knees and weakened muscles to support myself. I am getting cortisone shots in that knee, as well as physical therapy. My MRI shows a torn meniscus, stretch PCL very thin, cartlidge loss and debris, still swollen with csyt after all these months. With no meds, and lack of being able to exercise, I now have hig-chol back. On and on it goes.... a real catch 22. Take care of yourself, watch out for symptoms. I ignored sx's thinking it was stress but after reading adverse reactions, it fit me to the T.
My original posting re: Lipitor is Forestseaski on Jan. 2, 2009

C.

This is the second time i'm writing on here. I posted my Mirena side effects a few months ago and thought i'd update my side effects....

before i had the mirena put in i was doing GREAT losing weight right after my 4th baby. i actually lost 15 lbs and weighed less then when i got preggo. within a 3 week period of getting the Mirena put in, i gained 11 lbs! and my dieting and exercise wasn't doing much good. my doc recommended that i watch was a eat a little more carefully and exercise MORE.... how much more do i have to watch was i eat and exercise?? anyhow, its been almost 6 1/2 months since i had it up it and im just experiencing more and more side effects. now i had what looks like a really bad case of eczema all over my body. especially on my knees, elbows and my knuckles. my scalp is really itchy, i've GAINED 30 lbs, my hair is falling out like crazy, by bones are killing me especially my lower back, ankles and shins, my mood swings are horrible i feel like im PMSing all the time and when i get my period which is still messed up and lasts for 2 weeks i get even moodier! i am always really tired, i feel like my chest is about to explode, whenever i eat i get really nauseous, i feel depressed all the time and have bouts of crying spells.... i've always had migraines but the mirena seemed to make them EVEN WORSE now. IDK, i've just about had it with the IUD. the only good thing about it is...im not pregnant!! and i don't understand why doctors keep brushing all these symptoms off as if we are all crazy when we say we are experiencing something that we know wasn't there before the IUD...