Clamps symptoms and conditions

I have PCOS, and was experiencing dysplasia of the endometrium. After some search, a doctor recommended the Mirena. This was November of 2008. The installation should have been a clue of things to come. I have never had children, and had a tipped uterus, and as a result they had to use the clamps that look like needle nose pliers to grab my cervix, and after 45 minutes of stuffing, got it in. It was excruciating. I was working out 6 days a week, 2 1/2 hours a day, and eating South Beach Phase 2- and had lost 80 lbs and had maintained for 1 year. I asked if it would in any way cause weight gain, and was told it would not. Within the first month my diet/exercise regimen failed, and despite working out 7 days a week and resuming Phase 1, I was gaining 10 lbs a month- which my Doctor would not discuss with me except to dismiss it. To make a long story short, after life threatening edema and bleeding 22 or 23 days straight and with my now discovered sensitivity to progesterone, I required a total abdominal hysterectomy to remove an enlarged, boggy, and fibroid riddled uterus. I am doing 200% better now, and I am sure there are some women the Mirena works well for, but I was not one of them, and I feel the Mirena actually endangered my life (that and the arrogant doctor who inserted it and told me to be patient. I had it in from 11/2005 to 7/2007- is that time enough?) Please, please,please. If something does not feel right, do not NO for an answer. I did not want children so I was okay with losing the ability to bear children, but having a TAH at 38 is a life change that most younger women would not want. Would I have had to have it anyway? Perhaps. But I could have been in a position to be navigator in my care rather than reactive as I was forced to be.

I got my mirena placed in April of 2007. The insertion is one of the worst pain you will ever feel in your life. Remember your contractions just before birth.....The pain is not to far from it. After going home the pain did not get any better. It was about to weeks before the pain was tollerable. It is an constant cramping sensation that you also feel in your legs. DONT do anything that involves you tightning your stomach muscles for about a month. I was a delivery driver and had to do heavy lifting. It was hell. I could not have sex for about a month.When I did try to have sex my husband was hitting the strings or the actual mirna not sure. When I went back for my month check up the doc cut the strings some more saying that might help. It did but when my husband goes in deep in certain positions he can still feel it. The up side to mirena is that you dont forget to take it. I have very light periods. There are some months i only bleed one day!!! Think long and hard before you choose to do this. They only thing that I am fearing now is when they remove it. I wonder what that will feel like. If everything goes well I will know in April of 2012. If anyone can tell me what thats like tell me please.

Had Mirena fitted 7th Feb 2008 and having it taken out on 12th June 2008. My stomach is huge despite eating sensibly and exercising. Also suffer from cramps on a daily basis, craved chocolate and have felt down in the dumps!! Can anyone tell me if having it taken out is as painful as insertion and will I bleed as much as when it was fitted. Am very nervous about the whole procedure.

Many thanks

Hi, I decided that I would write as this site has been really helpful to me. I too have had most of the side effects as a lot of you have listed. I had my mirena in for almost 3 years and I have experienced weight gain about 15 to 20 lbs, hair loss, definite lost of sex drive, bloated stomach (and I never had a stomach before), joint pains, very bad acne on face and back, constant bladder and yeast infections, I read where someone else had rough skin on feet and I also experienced that and never had it before, palpitations,chest pain, bad back pain, dizzy a lot, and tired a lot. Well I had mine removed 2 days ago and it hurt really bad. The doctor could not find the strings at first and had to probe around for a while and eventually used clamps to find it and pull it out and I was in severe pain but the doctor did find it and got it out.When I left the doctor, I was feeling pain down there but I could deal with it and started cramping right away in office. yesterday I was cramping bad in the morning and early afternoon and then it stopped. I also felt like I was about to get a migraine for the last 2 days. I have not had any bleeding yet and at first, like the day of removal I felt "funny" in my body but now I feel okay. I think if I would have left it in longer that I would have had to get an operation to get it out. The side effects just got worse and worse.Also I posted here a few months ago maybe around 6 months ago and at that time I was having a lot of these symptoms too but didn't think it could be the mirena but the bad acne and bloated stomach and weight gain =, I knew that was from the mirena. I too, like a lot of you have been to the doctor countess times for other problems just for them to say all tests are normal. I know that my problems came from the mirena, Well good luck everybody, I will post again later after its been out for a while for an update. God Bless

I quit Lipitor (40mg) five weeks ago. I believe I was on a trajectory to disabilty within a year.
The unbelievable left elbow pain has gone (maybe the cortisone worked!). My left knee feels "normal" again, not perfect but nearly like it used to be. Within a couple of days of quitting I had severe pain in my right thumb along the bone, then in the middle of my right hand, then between the first and second fingers in my right hand. I currently have minor pain in my right wrist (this is new) on the pinkie side and minor pain in my left shoulder where the arm joins (this has been intermittent for a couple of months). I am feeling much better - but would not be at all surprised if pain appears in another part of my body before this is all history! There is also plenty of joint clicking going on.
I believe I first reported pain to the assistant doctor to the heart surgeon two weeks after I had the stent put in and was put on Lipitor. I was also on various other medications. I had tingling on the ends of my fingers and toes at random - hard to describe but it was as if a fairly sharp object (like a ball point pen, say) was being pressed progressively harder from the end of the finger/toe and towards the rest of that finger/toe: and as the pressure increased it would suddenly become painful. It was not a tingling/numb sensation but more a tingling which increased sufficiently that it hurt.
I am only being so specific because when I described these "symptoms" the doctor shrugged. If anyone has had similar - and I have seen tingling mentioned here - please make contact with me as I do want to report my experience back into the medical community but find, an exact description difficult. Things never needed to have got so bad if this was the first warning.
I since asked my family doctor if my knee problem was Lipitor related and she thought not: I was referred to Physical Therapy. I also told the physical therapists (who thought my knee should recover much sooner, and were surprised that I had zero mobility pain) that I also had serious elbow pain.
The orthopedic surgeon I saw did not connect the elbow problem to Lipitor.
The heart surgeon (stent insert) could perhaps be the only person who I did not tell of the pains - I don't remember - but I may be so grateful to be alive - that he may be someone to whom I did not voice a complaint!
On the positive - five weeks later I am feeling significantly better.

Dear Silke,
That must have been very frightening for you! I do not know much about seizures. There appears to be many different kinds-- from "petit mal seizures" where the person 'tunes out in a daze' for a few minutes, to falling on the floor, to "grand mal" or "tonic clonic seizures" like I had where you fall unconscious, convulse, eyes roll into head, muscles contract, jaw clamps down on tongue. I was unsconscious for 15 minutes after the seizure and even after I reached the hospital I was groggy, confused, uncertain what was happening to me, etc. I didn't know who I was. In my confusion I assumed I was dying.
Yasmin is REALLY not worth all that! Silke is right-- there is no point 'adjusting' to this drug.

Good luck to every one of you! I'd get off of it while you have some semblance of health. If you later discover that your side effects were caused by something else you can always go back on it. I truly regret I ever tried it. The upside: just look how Yasmin is uniting the world in side-effects and ill health. :)

I started taking geodon a couple years ago when I had a "psychotic episode" so to speak. They diagnosed me with schizophrenia. They put me on geodon which did wonders for me and helped all my symptoms go away. I'm perfectly functioning and capable now. However, Geodon does have some side affects that I"m dealing with. It makes me tired all the time. I'm tired all day and can't sleep at night. It seems to be progressive as in the longer I'm on it the more I have to take. If I miss a pill I get very tense physcially like and my jaw clamps down. I also feel like I'm going crazy if I miss a pill. Thoughts start to race, however the natrue of the drug is that one pill missed shouldn't cause psychotic symptoms. I can't think as clearly because it makes it harder to think abstractly. I take it when I need the down feeling. Sometimes more then it's perscribed. I'm clearly addicted to it like somebody would be addicted beer or pot, perhaps psychological. I tried to switch to abilify and I couldn't function because of the hard with
drawl from geodon. Good luck at your venture with geodon