Hospital emergency symptoms and conditions

MY STORY

My Mirena was removed on 29th May 2008.

I had the Mirena put in four years ago,I had terrible pain the day after, it was that bad I was going to go to the hospital Emergency to get the thing out but I put up(the worst thing I done in my life, Im paying for it now) with it and it and the pain got a bit better,had a lot of bleeding (spotting) for the first six months and then it finally went away. For the first year I thought Mirena was Great but then the problems started.I started to gain a lot of weight,facial hair,Very sore breasts, I also had a lump removed from my left breast a couple of years ago, but I didn't know until recently that it was most likely caused by Mirena. Some of the other problems I had, My stomach bloated, I look like I'm six months pregnant ,I have a cyst on my left ovary,dry skin,acne,strange depression,headaches,and the Worst of all I had to have my Thyroids REMOVED on 1st Nov 2006 and I'm pretty sure that was caused by Mirena as well, so now I have to take thyroid Medication for the rest of my life,I had the Mirena removed as soon as I done some searching on the internet for my unexplained medical problems, mainly my weight as I had weighed about the same my whole adult life and now I had put on a few stone and now I have to try and lose it,as for my thyroid I have trouble getting the Meds right its a real pain,blood tests all the time.I just don't feel I have much left in my life,depressed,sick all the time. I eat well as I have high cholesterol so its not that I over ate,I noticed you do feel a lot more like eating sweet things. I found a site called ****** and found out there are thousands of woman,girls with the same problems as myself and that there is a class action law suit going on to Sue. Its worth having a look at this site it helped me a lot.I feel so bad I don't go out anymore I don't see friends or family I'm to depressed about my weight now. I am in the process of trying to find out if there is a Class Action Law Suit in Australia.If anyone knows of a Class Action in Australia could they Please let me know. After having the Mirena removed about 6 weeks ago I thought I was doing ok only a bit of spotting,but about 3 weeks after having it removed I got my period and the pain was unbearable,I was in agony stomach cramps and I bleed so much I thought I was going to die from blood loss,also the scariest was the huge blood clots,very scary,must of been four years of period in 1 week I couldn't believe how bad it was, I felt really sick and weak,but thank goodness its eased off now after a week. I just hope now I might slowly start and feel like my old self. Im also on medication for heart palpitations,I get Heart palpitations (SVT) a few times a week,I had my heart palpitations just after my thyroid removal op and was put on ecg and my heart rate was 176 Beats per Minute I was rushed to Intensive Care and I had to have an injection called Impending Doom (It makes you feel you are going to die) to slow my heart rate,it worked and I was kept in intensive car for 3 days,very scary thing to go through I hope I never have to go through that again,my heart palpitations got worse while I was on Mirena and now I also take Magnesium to help control them as well as Metoprolol which I have been on for some years and I recently read that if you are on Mirena it increases the side effects of Metoprolol.

So if you have had any bad experiences with Mirena please let us know,it will help others with their problems, hopefully. I just wish I never got Mirena and my advice is DON'T its not Worth the risk,if the Doctors had of told me about the BAD side effects I would NEVER of had it put in. Sorry about going on so long, Good Luck to you all,

Thanks Net.

google mirena-side-effects.****** (a mirena help,info site)

UPDATE

I have had it out nearly 3 months now my painful breasts feel normal again,I haven't lost any weight yet, but will soon hopefully,I do feel a lot better but still get some of the symptoms back just before my period.

I get sooo mad when i think of what Mirena done to me and all the other women and how bad some of their side effects have been. I get mad when i read some of the other ladies stories and the terrible things they have gone through ,

Perforations,Miscarriages,IUD's lost in their body,

Hystorectomy,and the rest. I want to wish them all the best, and we WILL get Better and Bayer ,Mirena will PAY some day for what they have done to US..

My GP put me on Advair in the summer of 2006 because I was having trouble with so much phlegm in my throat and losing my voice by using Combivent. I also have a weakened voice as a result of asthma medication. For the first three weeks the Advair was great. Then one weekend at our cabin, I had a severe asthma attack -- to the point that my husband wanted to pack up and drive an hour to an hospital emergency ward. I thought it was from something in the cabin or in the air. As a result of some research on Advair, I truly believe that it was from taking this medication. Not realizing this, I have continued to take Advair at the advice of my GP. I then noticed that my skin was very itchy, mostly on my legs at that time. My GP said it was excema. It started spreading to my hands, wrists, elbows. I started reading about the side effects of Advair -- from the insert that comes with the discus -- itchy skin is one of the side effects listed. In December 2006, I went to the lung specialist that has been treating me for asthma for several years. I asked him about the itching and mess on my wrists, etc. He indicated that it was excema and not a reaction to the Advair -- and proceeded to write me a presription for more Advair. In January 2007, I went back to my GP because I couldn't stand the itching and red blotches anymore. She wouldn't give me anything to relieve it, but sent me to an allergist. I asked him about the mess my skin was in and he told me that it was very rare that someone would react to Advair in this manner and he didn't think that was the cause. He decided that I was allergic to dog and cat dander. Just the other day I was finally sent to a dermatologist. She was appalled at the condition of my skin, as the ithing and redness had now started to spread to my upper arms, under arms, breasts and stomach area. I took some research about Advair with me to this appointment. She has now taken me off the Advair for a two week trial and given me an ointment help with the healing. Finally, a specialist that really might think the Advair is the cause of this itching all over my body. I sure hope that these doctors will realize that I really have an adverse reaction to Advair and will find another medicaiton that will be suitable, but not cause the problems I am having now. my voice is still strained, but I am sure as the Advair leaves my system, this will improve too.

severe chest pain, cold sweat, nausea, vomiting, going on for hours! Went to hospital emergency twice before I realized I was reacting to the doxy (for Lyme). Never really got rid of the Lyme but with the doxy I literally thought I was dying - and I am not a pain-freak. Have a pretty high threshhold but was unable to walk or use the phone to call 911 when I was alone with the attacks. (Yes, it took me a couple of times to realize I was having a reaction, not a heart attack).

BTW, I have looked doxy up online as an antibiotic and these kinds of side effects are typically not even alluded to much less discussed. Shameful!