Life style symptoms and conditions

I had mirena removed almost a week ago. One thing i wish i had been informed about before removal,is that your not supposed to have unprotected sex 7 days prior to it being removed. My DR told me to wait another 3 weeks, when I should be on my period, and have it removed, but because i have no transportation, I HAD to have it removed that day. I told the DR I would rather get pregnant than keep Mirena. I know everyone is different, and some are saying its not mirena, its our lifestyles, but I don't believe that. It amazes me how many women have complained about these symptoms, have tried to figure out where the depression, anxiety, acne, headaches and so on, are coming from...and how many found this website. How many women got their answers. Thats how it was for me. I had depression a few years back, I would say from my life style, but to look at my life now, I know how good I have it, and that this depression should not be a part of my life. I've made many sacrafices to be happy, and i have finally done it. I love my life. If mirena was the reason I was having all these symptoms, its gone now, and I can be me again! It really didn't hurt to have it removed, it was just crampy. I bled right away for 4 days. I had the worst depression in my life those 4 days. I couldn't smile, I didn't want to move, to go anywhere, see anyone. And I cried the whole time. yet, Sunday I woke up, and feel wonderful. I still feel foggy, and tired. But I feel one step closer to the person I was 2 years ago. Mirena didn't ruin my life, but i know that if I had kept it in any longer, it would have.

I have been on simvastatin for 2 yrs . The past six months have had foot pain my doctor described as neuroma.By the time I started physical therapy the pain was in my arch + tendons. I went to physical therapy for two months, the therapist became concerned when improvement peaked. Still have burning nerve pain. I think its time for natural supplements . I hear "red Rice Yeast" is effective.
S. M.

Can anyone tell me if you can just stop Lipitor cold turkey or do you have to stop it slowly? I have been taking Lipitor for 5 years now and I have been trying to find out what is causing my leg weakness. I mentioned it to my doctor who said it si just a fact of getting older. The problem is getting worse and I noticed it started about 3 months after taking the Lipitor and has steadily gotten worse. I am 49 years old a little over weight {which I am working on}. I also noticed my asthma which I haven't delt with since a small child has come back. This may or may not have to do with the Lipitor but the pain in my knees and legs I believe do. It really hurts in the joints of my legs and sometimes in my shoulder area.

I have a history of sinus infections. After two rounds of Augmentin did not clear up my latest one, my doctor finally gave me the steroid pack and Avelox. He had tried to avoid the steroids. I have had them so many times. I finished my steroids 5 days ago and my Avelox yesterday. I read the side effects and did as it suggested. Since it mentions low potassium would not be good I ate a banana every day and had some orange juice to keep my potassium levels up. The drug warms against taking any pain killers such as Aleve, Advil, etc. One earlier reviewer admitted taking Aleve and had a bad reaction... well.... bad move.... I have had no real side effects that I can say for sure are Avelox related. I did feel a little less focused at times, but was not obviously groggy or woosey. I did have a little abdominal discomfort that I usually do not have with drugs, but it was short-lived and only occurred 3 of the 10 days. Many people have bad effects because they do not follow the warnings against anti-acids, pain killers, low potassium, etc. Some people are more likely to react to any medicine, while others like me rarely have a side effect. My tendons did not hurt... nothing.... People who are out of shape, have a poor physical life style, etc. sometimes help contribute to the drugs reactions by being in basically poor physical health to begin with. America is one of the fattest, out of shape nations out there due to our abundance of everything. The majority of persons can take Avelox with no real issues. I will take it again. I truly feel concern for those who had problems, but sometimes we are partly guilty by how we don't take care of ourselves when we are well...... As with any drug, some persons will react no matter what... It's often just a matter of inherited genetics...... Be safe everyone, and take time to evaluate how you take care of your body and really decide to do better. For the record I am almost 58, 5-9 158 pounds and work out semi-regularly.... Take care of that temple God gave you. Its the only one we get on this Earth,,,,,,

Oh and by the way I have had the Gardasil shots and I have had NO side effects and I feel great!!! I think people are just looking for excuses to blame Gardasil!!

Wow. I have an appointment to go get my blood work done, because I couldn't for the life of me figure out why I feel the way I do. Until my friend asked me if it could be the Mirena... duh. I've had it now for almost a year. (It was put in after my second baby.) It hadn't even occurred to me before that it could be the culprit. I wake up every morning feeling like I just got hit by a bus. Anything but refreshed! I can be happy one second and then TICKED OFF the next. I never ever in my life would even THINK of swear words in my head. Now, it's a rare occasion when I DON'T freak out and kick walls and say every swear word I know. My vision is blurry. My neck is super stiff. My lower back always hurts. I get so depressed. People who know me are starting to notice that I'm not the same old me. My husband calls me crazy. My kids pray that mommy will stop being grumpy. I keep wondering why I hate my life, when everything is just what anyone would ever want. Hmmm.... something isn't right.

2 days ago I just happened to come across this website. I was in tears reading all of your stories. It sounded like it was me writing! You have given me the answer to all my misery over the past 3 years! My marriage nearly failed from all of this. I was married in July 2005, had a son in March 2006 and immediately had the Mirena IUD inserted. I thought it was the best thing on earth! No side effects... that I was aware of!! It all came on so gradually that I blamed my symptoms on post-partum hormones and a change in life-style. I remember I became a total bitch towards my husband very shortly after I got the Mirena. I gave up exercizing, ate like crazy (partially probably due to breastfeeding), and I had absolutely no sex drive, which was a 180 for me, because previously I wanted sex everyday! I blamed this on hormones too, or maybe my weight gain... just not feeling sexy anymore. When my son was 12 months old, I had the Mirena removed, only to try to get pregnant. We had a daughter in December of 2007, and I immediately had the Mirena re-inserted. As time went on, I was the bitch I was after my son was born.. again, I blamed it on my hormones. My back was killing me all of the time.. I blamed that on having to carry my daughter around. Then the insomnia hit me.. wow! I would lie awake in bed till 6:30 in the morning, and this was after my daughter finally started sleeping through the night. Maybe I had insomnia the months prior but never noticed because I was up all night long with my daughter anyways. I was miserable, depressed, moody, and incredibly mean towards my husband (thank God not towards my kids). He's a saint to still be here. Last summer I started getting pain in my joints. Some days I couldn't lift my kids because my wrist was so sore... or I was limping because of my hip or my knees. I was also incredibly depressed at this point. I was getting virtually no sleep, was pissed off at my husband all the time, and looking after 2 kids was draining me. My husband, being non-confrontational, was lying to me all the time try not to rock the boat. I found out he was lying to me, and I thought he was having an affair. I was crying all day everyday... finally after everyone told me I was depressed, my doctor put me on anti-depressants, and a bedtime pill called Elavil to help me sleep and to help with my joint pain. We went to marriage counselling (still are). After 2-3 sessions with an amazing counsellor, we realized I was not suffering from depression. Thank God, because the anti-depressants were making me even more miserable and I was binge eating like crazy! My husband and I, with the help on counselling, have since dealt with all of our problems. So why am I still so unhappy? Why is my join pain coming back? The Elavil is not working for my pain anymore. My body feels like I have the flu. Achy, but more intense and joint-specific. I have no energy or motivation to do daily tasks like laundry, clean the kitchen, or even take a shower and get dressed. When my kids wake from their nap, I feel like crying because I don't feel like a good mother is caring for them. 3 days ago I was with my husband and kids and had to leave because I began to cry. My husband came to ask me what was wrong, and I just said that I was in so much pain, I couldn't stand it. The truth, which I did not tell him was: I literally could not take another day like this. If I don't get better, I don't want to live anymore. I was not contemplating suicide, but I'll tell you this.. if I hadn't found this website when I did, who knows what I would have done!
Looks like I know how to make a long story even longer! LOL.
My husband and I went out for a romantic dinner on Friday to celebrate Valentines. I told him what I had discovered.. actually, I just handed him this website on my iPhone. AS he read your stories, we both were in tears! The last 3 years should've been the happiest of our lives, and we were robbed by this devil-IUD!!
Last night I couldn't take it anymore. I was crying and my husband said, "why don't you just go to a walk-in clinic and have it removed?" So I did! It was painless and I have no bleeding or cramping as of yet! I don't know if it's psychological, but I feel terrific today. My joints are achy still, but my mental state is on cloud nine! I have energy today and have been playing with my wonderful adorable kids all day. Let's hope it lasts. I will keep you all posted!
I hope my story helps someone as much as you have all helped me. You have saved my marriage, and probably my life. Thank you all!!

I got mirena almost two years ago and my periods defiantly got lighter. They only last like 3 or 4 days, but after finding this site i know now that all the other stuff is caused by my magic birth control. I started to get pimples all over my face and i never had acne even as a teenager. I have sore breasts and they feel like they double in size for about a week and a half every month. I have mood swings so bad that my fiance thinks im crazy and need to see a doctor. I have noticed that i loose about two handfuls of hair a day in the shower, i have gained probably 40lbs and my life style is no different now then before i go mirena. My back hurts all the time, i noticed that i have facial hair that i never had before, and i feel depressed a lot of the time. I am glad i found this cite because now i know it is the mirena and im not just crazy.

I have been on Yasmin for 2yrs. now. I went to my doctor recently to check my thyroid out because I've been experiencing hair lose.My thyroid is normal and now I'm thinking about getting off the pill. I'm only 24yrs.old I work out regularly and eat healthy so I know it has nothing to do with my life style.It also seems like my sex drive is not where it should be.

I have been taking Simvastatin for 2 mos & I have been experiencing horrible insomnia,fatigue, and frequent nocturia with urgency. I would particularly like to know if any one else has experience the urinary urgency?

Ladies! I think it is wonderful that we are sharing our experiences here and helping one another. I felt it is necessary I share my experience as well. Thank You to all you ladies who have posted. You have helped me.

Got Aviene from my pharmacist saying 'it's same as Alesse, it's cheaper and the drug company covers this versus Alesse.' How dumb of me not to research this despite the fact this came without a box and instructions.Where is this made? Read up on it etc... things one would do BEFORE trying something. I did not do this and this has cost me.

I noticed changes as you all say you did as well. I have been taking the pill for 3 months. I work out as much as I can so about at least 3 times a week, I had a energy loss, I felt in an unexplainable way, just tired and irritated by the day. No, this is not normal for me. I got a great deal on a scale and stood on it and couldn't believe a 20 pound weight gain. This was not exactly a surprise since my clothes don't fit well and I am very uncomfortable. However, this still didn't make sense b/c I have breakfast and it's not junk, toast coffee or eggs with it or serial. For the last 3 months I made healthy lunches, I cooked ahead so took fish, chicken, rice, whole wheat sandwiches, orange juice, water, milk to work. No junk, no pop, no over eating. Had fruits and veggies. I was glad I was keeping up with this but to gain weight from it? I have a full time and a part time job keeping me busy and this life style, what I did for the last 3 months always included weight LOSS not GAIN. I am pretty pissed about this. (Of course, I am on Aviane, we are all pissed off, haha but not really haha right?) I have major issues with my face, considering I am using the same wash... no change...Anyway.. you're all seeing something doesn't' make sense. I have actually had bloating. Major bloating. 3 weeks. Never had this before. I took over the counter aid, that did help. I am 30 I never took over the counter aid.. let's not mention what I took but it helped.

Listen everyone, get off this pill. I will never take this pill again. I have 4 left this month and forget it I'd rather get my period tonight and anticipate change to occur.

On my way home, as usual of late, I tried to figure out WHAT is wrong with me. In conversation with a cooworker I mentioned the 20 pound weight gain and all and she said 'so much in such little time?' I was thinking about it on my drive home... I am at 2 new jobs and have stress but... to gain this much... and it dawned on me. I CHANGED MY B.C. It HAS TO HAVE something to do with it. I came home and goodled. You can't find anything on Aviane but negative comments. You go on Alesse... oh! a company website at least shows up.

Thank you Ladies... I believe I am having the same reaction as all of you did and I do sincerely Thank everyone for taking time out to post. You have helped me and I do think this B.C. is the reason for my current state.

I'll post in a week or two and then after a month to provide an update.

Take care Ladies!

I had Mirena inserted after the birth of my 2nd daughter - November 07. Things were going ok (at least that was what I thought) until about two months ago. I really did not think about the Mirena much. Maybe that was because my sex drive has been soooo gone that I have only used the benefit of the Mirena about 3 times. The problems I guess really started when my period disappeared. That happened 3 months after I got in inserted. I thought that was going to be great because my periods usually last 7 days from start to fully finished. But with this thing, I did not bleed but I definitely was still having a period. Bach aches, mood swings, headaches, bloating, etc. I started to think something was really wrong when I got a headache that lasted about a week, and I don't normally get headaches that last longer than a few hours. I could not figure out what was wrong with me. I even went to the emergency room to have them tell me that there was nothing wrong and it was probably just stress. I started to think that maybe it is the Mirena. I started doing searches on the adverse side effects of the Mirena and thank God I found you guys. I have most of the symptoms described here and other Mirena side effect pages. I will be having this awful thing removed in about two weeks. I don't know what my husband and I are going to do about birth control. We both do not want anymore kids but I am only 28 and do not want to have my tubes tied.
Headaches
Joint Pains
Low Back Pain
Mood Swings
No Sex Drive
Massive weight Gain (I have not lost any of my baby weight plus i put on a few more pounds)
Breasts Double in Size
Fatigue
Dizziness
Depression (low self-esteem)
My feet have even grown (probably because of the weight gain)

Hi all, I was amazed to find this site. I too have had a rough life for the past eight years! I am going to be 39 in a few days but this story starts back in August 21, 2000. The day that put me in HELL for the next eight years and still going through it. Prior to this day, I had a lot of UTI's and Pneumonia and several times prescribed both Levaquin and Cipro. I did develop Achillies tendinitis but I thought this was due to my active life style, see I was an LPN and a firefighter. So I went for treatment to fix the Achillies tendinitis. This was a foot Dr that of course gave me a cortizone shot in it. I cant remember how much earlier this was that this took place and I am still not sure if this is what did it but as I am thinking back these are the things that come to mind. On August 21, 2000 I was on a fire call and my right Achillies tendon popped off the bone! They took me away by ambulance. The Dr in the ER said to go home with an air cast on, eat or drink nothing and come back in at 10:00am and they would possibly do surgery. Well, I did just that. The orthopedic Doc said oh yeah it is achillies rupture will have to go in and tie back all the little fibers. So away to the operating room I went. They gave me a spinal and just knocked me out. I was awakened suddenly by my Dr. voice loudly saying " Holy shit it peeled off the bone!" And another nurse saying let me see! I came up on my hands and they grabbed me put me back down and knocked me back out! (I still have night mares over that!) Anyway, I spent the next 3 months in a cast. During this time, I was told from over usuage of my left foot, I now was developing tendinitis in my achillies tendon in the left foot! Which this sent me to a wheel chair. They took the cast off in 3 months then I was still no weight bearing for another month. Then i had physical therapy for about 6-8 months with little improvement. I complained to the Dr about the left achillies tendon and he said he would not do anything about it unless it too popped! So now many Dr later, and many many medications tried and many surgeries later, and now diagnosed with Lupus, Sjogrens, and Fibromyalgia, the most my rheumatoligist says is I have a connective tissue disorder, and taking cancer medication (Methotrexate) I am now disabled at 39! My life taken from me. I have situational depression, panic attacks, sleep trouble, Suffer from post traumatic stress, nightmares, basically my life is a mess and it is over. On July 1, 2008 I had to go to the ER cause I was sick. I had been run down and feeling bad and sleeping a lot, disoriented, couldn't stay awake. They found I had another UTI and a sinus infection. The Dr Says we will put you on Levaquin and that should take care of both problems. So he left, it took me a while for it to sink in that I should stay away from that drug, so I caught him and told him, he said to me that this was only found to be in kids while they are young and developing that it causes tendon rupture, and besides he said, one dose will not hurt you. I took 5 pills, one a day. Since then I have been in so much pain all over my body it is unreal! It still took me days to figure out that it was the Levaquin doing this to me! I feel like at random someone is sticking a knife in different muscles in my body! I felt like I had done Tie bo for 24 hours straight! Even my butt muscles hurt so bad to sit here and write this email! I have days when I cant even use my hands! Write my name with a pen. I am not sure if this is all due to these drugs, but I am most miserable and not a bit better. I may have just made it worse by taking this last round of them. Has anyone else had this kinf of symptoms?

Im a Spanish 22 year old girl who just had my first dose today. I had side effects such as dizziness, nausea, vomiting and sweating.

Can I still take the second dose??Will I have side effects again?Will they be worse?

I had Mirena put in five days ago. I have had cramping off and on. I finally did a complete workout on my pilates reformer and did just fine. I have yet to see what having sex with my husband is like with this thing in me. I am a little scared about pain. I do feel bloated. I will keep everyone up to date on how I am doing. I sure wish I had come across this website before I decided to put this in.

I was given a 10 day dose of LEVAQUIN for a mild bronchitis/respiratory ailment on Jan. 29, 2008. I took 1 500mg pill for the full ten days. Three days after I stopped taking this medication, I experienced incredibly painful swelling in both knees. I could barely walk, and couldn't bend my knees. I was scared, upset, and in absolute misery. I spent a week literally throwing myself backwards onto chairs. It was unbelievable. When I could finally get to my normal health care provider 5 days later, she immediately identified the culprit as the Levaquin I had taken. She said she knew it to cause people's tendons to burst. It was obvious since it was both knees that it was not an injury and I never had any other problem with my legs. I am, or shall I say I was an avid walker. I was told to see an orthopedic doctor if I had not improved in one week. I had not improved in a week. The orthopedic doctor sent me for an MRI which showed irreversible, permanent cartilage damage in my left knee. The right knee he didn't MRI at the time, saying he could determine what he needed to know from the one knee and would only be able to do corrective surgery on my knees in 6 week intervals. This horrible drug has permanently altered my way of life. I was a 53 year old active, ambulatory adult who would walk miles a day. Two months later, I still have constant knee pain, cannot stand for long periods of time without leaning on something and can no longer kneel, etc. I can only walk around a bit and if I'm on my feet for long periods of time I experience knee, ankle pain and swelling. I sent a report to the FDA who obviously cares nothing about this situation, since I'm not the only unsuspecting person to have this happen. I've been studying this drug now and there was evidence in animal clinical trials of joint and tendon damage, To me it would have been no different an experience if someone had come up and hit me with a baseball bat across both knees. I am permanently damaged from Levaquin. I think it's criminal this drug is given to younger ambulatory adults at all.

Hi I have severe lower-back cramps and ache going all he way up to my shoulder blades.
I guess its from the Euthyrox 25micro grams(Livothyroxine sodium) which I am taking now for over a week.
I was diagnosed for hypothyroidism and my T3, T4 levels were marginally high so my practitioner started me on the lowest dose.

But this side effect is quite disturbing and need to get rid of this to handle the work pressure in the office.

thanks
Abhishek

We lost our home to a house fire this past August so when my 8 year old daughter experienced severe depression, night terrors, and was constantly acting out we naturally blamed it on the house fire. The odd thing was that she had the "normal" depression immediately after the fire and started to become herself again. Several months past when she started this severe depression and horrible behavior. We brought her to a psychiatrist because this was just not the depression she was experiencing after the fire.The psychiatrist diagnosed her with post traumatic stress disorder and explained that with children it can take months for this to "come out". Well, with allergy season on us in the South, my daughter started her Singulair treatment the exact time of this recent behavior. Needless to say, we are taking her off the Singulair, I will post again to let you know if she makes a turnaround.
---by rlhulsen

Our daughter has been on Singulair for four years that we can recall and are in the process of obtaining medical records to find out for sure.

She was diagnosed with A.D.H.D. when she was first starting school and allergies in the first grade. She was on liquid Claritan-D up until she started Singulair (4 or 5 Yrs ago).

Since she began taking the Singulair along with her A.D.H.D. meds. she has become very depressed, anxious, and sometimes extremely angry for no apparent reason.

Her elementary school career thus far has pretty much been a total waste because she does not pay attention or is outright defiant. And She has started stealing from other students.

We elected to try natural treatment for the A.D.H.D. with limited success and now we know why! The Singulair is counteracting the treatment! I would bet my last dollar that she will improve without the continued use of Singulair!

Before she started taking the Singulair she was always an outgoing kid that loved life unconditionally and now she is always down in the dumps and struggles through the school day and it is putting pressure on us as parents because the school gives her detention for not completing work or acting out in class etc.

She frequently complains of tummy aches and headaches or joint pain.

I feel really horrified as a parent because I argued with her just this morning and made her take the Singulair before school!

Even if taking her off this med. changes her future it won't erase the memories of her childhood school years that should have been some of the happiest times in her life and are now just painful ones she will try to forget!

We all need to find other parents in our own towns and get together a group and contact a lawyers office and file class action suits against the monsters who created this mess!

I have been on Lisinopril since the first of November. I had a dry cough at first but nothing really bad. After about three weeks I got a fever and sick for about a day and 1/2. The fever went away but I had shoulder and back pain (between my shoulder blades) The doctor listened to my lungs and told me I had pleurisy!!!! Treated me with antibiotics - got a little better. The soreness still there in my lungs up into my neck - some chest pain. Went to the ER - took chest x-rays.. found everything normal. Still coughing - congested all the time - I am 41 years old and I WAS on 5mg of this drug 1time a day. Not a lot at all but the ER doctor took me off the drug. He said after about three days the drug should be out of my system and then I can evaluate whether it was the lisinopril causing my lung problems. Also I have noticed that I have been having anxiety and worrying about things to excess lately, which is not like me. The anxiety started about a month after starting the drug. Maybe it is from the physical problems that I have been having. I was very healthy before all of this - I am very active and a non-smoker. Since these things starting happening I feel like I have aged 10 years!!! I also have some troubling getting air sometimes - like I feel as if I have to take a deep breath. Anyway - this is the only drug I am on so it only makes sense that it is causing all of this. The first night I stopped taking it I had terrible dreams - anyone else had this after stopping the drug?

I was prescribed to take 30mg/day (Prednisone) to try to reduce the inflammation brought upon by Ulcerative Colitis. I have taken Prednisone before....up to 60mg/day, when I was first diagnosed with UC. I don't really remember all of the side effects I experienced, but I do remember my calves and feet swelling, a bit a of moon face and very little weight gain due to the UC. Does anyone have any suggestions to how/and when I should take the daily dose of Prednisone (early morning, with food...what kind of food)? Also, I would love to hear from anyone with Ulcerative Colitis and how they are coping with the disease. From their diet when in remission to during a flare-up! Thanks...

I was on a Beta Blocker and was having side effects that were effecting my sex drive. My blood pressure has been going done. I have also lost 30 pounds and am doing some what regular exerise. Since my BP was getting better readings my doctor switched me to Lisinopril 10 mg. I have not had any bad side effects on this. Maybe I am lucky and only need the 10 mg and that dose doesn't produce some of the side effects I have read on here. Don't assume you will have the same effects as someone else. You don't know what other drugs they are taking or what their life style is. Do monitor your BP, weight, sleep, and any side effects you feel and discuss these with your doctor.

I have been on lisinopril 20mg for a couple years. Took a more expensive med for 8 years prior to lisinopril. The dry cough has been my most persistent side effect. It's worst in the mornings. The last couple months I have experienced a very unpleasant taste in my mouth. Hard to describe, kind of bitter or acidic. Not all foods are the same, coke & pepsi are the worst. Sometimes the tase is present in my mouth even if I'm not eating at all. I don't know if this is related to lisinopril. It's the only med I take, except for vitamins. Has anyone experienced this?

I have gained nearly 40lbs in almost 2 years since I got my Mirena. Nothing about my life style has changed. I have tried everything to lose the weight and can't drop a pound. I never know when i will get a period and never know for how long. I am extremely depressed and need some advice. My gyno says that there is no way my weight gain is from the mirena and all my blood work has been normal. HELP!

I have been experiencing severe hair loss and thought it was the Fosamax, so stopped that drug, but the hair loss is continuing. I have found only one article relating Singular to hair loss.