Time in my life symptoms and conditions

Hi all, im so glad i found this site as many are too. Im 22 years old and was diagnosed with colitis at 14 and was put on 40 mg of prednisone to combat it. I can honestly say it generated the worst time in my life.. I went back to school and was overwhelmed with massive panic attacks feeling like my heart was gonna rip through my chest. Big moon face etc. I recently have had an attack and was put back on steroids its always my last last resort. I just feel very detached and anxious all the time constantly feel like im lost. I am now in the process of stopping them first day without 1 and I feel as explained. The worst thing is that no one seems to understand the effects, they cant understand why you'd rather be ill than go through with them. its not good for you on the whole. Good health is the unity and prosperity of all aspects; Body Mind Soul. Hope the best to all.

I am so glad I found this website.

After 2 years of being on Yasmin/Ocella, I have realized that my symptoms were entirely from this horrible drug.

Symptoms I experienced on Yasmin/Ocella:

-HEARTBURN! I had to have an endoscopy to determine the damage caused to my esophagus, and was on hard core antacid drugs for months.

-UTIs!! I suffered from a UTI pretty much every time my fiance and I had sex, and my Gyno referred me to a urologist. Mind, I had NEVER suffered from these frequently in any other time in my life.

-Strange heart beats - heart skipped a beat often.

-Anxiety, to the point of dysfunction.

-Back aches, kidney infections.

-Bladder infections.

-Depression - for instance, lying in bed for hours after my alarm went off, not wanting to get up.

-NO sex drive. NONE.

TAKE THIS DRUG OFF THE MARKET.

I have posted a couple of times previously about negative side effects, i.e. migraines, weight gain, acne, chin hair, eczema, lower back pain, no sex drive...and the list could go on. As a mature 36 year old woman I have educated myself over the past couple of years and can really only attribute all these issues to having the Mirena inserted 4 months after the birth of my daughter 3 years ago. Although at this time my doctors will not openly acknowledge these side effects, I am confident that one day they will. I encourage women to report adverse side effects to the FDA. It onlt takes a minute or two. Who knows, it may be the hormones or it may be the silicone plastic? It has to be something. It should also be acknowledged that some women, my very best friend for one, have had wonderful experiences with the Mirena. I really think it may just depend on the woman and her own body. I am having mine removed tomorrow after researching all of this for about 8 months. All I can say is, thank goodness. I am also scheduled for the Essure(permanent birth control). Food for thought for the older women in the group. Whatever each of you decide, realize you are not alone and you do not have to continue to feel the way you do if you believe that the Mirena could be making you feel so bad. Take care.

OH! I also had migraines for the first time in my life that started about 2 months ago! Nausea, lightheaded, and jittery too! Awful...just awful!

I am a 36 year old women that decided to start taking birth control for the 1st time in my life which was on aug. 1st. I decided this after having my last of 3 kids. my ob doctor prescribed me Yasmin, but I filled the ocella a generic of Yasmin. I was at first concerned a little bit about taking birth control due to my age. But my ob told me that if I smoked than there could be risks of the side effects of birth control. I do not smoke, drink, or eat badly.I used to drink coffee everyday, but stopped because of the b.c. effects. I am not overweight with no other health conditions, except now!!! I don't exercise much or sleep much because of taking care of the baby. I do stress and have anxiety at times. I have had a few mild heart palpitations in my lifetime that occurred at work.
I have never experienced so many and strong HEART PALPITATIONS until I was on the pill. I started experiencing them about 2 weeks after starting the pill they occurred about 3 to 6 times a day about 4 to 5 days in a row. I continued for another few days just to make sure, but still had HEART PALPS. I stopped taking the pill. on aug 17th. I was also more moody and felt like I had pressure in my head at times. I than got concerned and decided to take my blood pressure on aug 31st.which was at 133/88. I said to myself that i have elevated blood pressure that i never had before. I started to worry because i never had HIGH BLOOD PRESSURE. My BLOOD PRESSURE started to raise every day and reached 182/101. I was was so worried and stressed over this, because i know I did not have HIGH BLOOD PRESSURE before. I called my ob to find out my blood pressure before i started the pill and on july 27th it was 120/64 a great and healthy blood pressure. on Sept. 5th I went to urgent care they gave me a clonidine 0.1 to lower my bp when i reached 182/101. and did an ekg which was fine. my pulse if fine. They gave me lisinopril 10 mg to help if my blood pressure continued to be high. I did start it because if was like 172/96 which was close to this # everyday.It is helping a little. My pressure ranges from 128/80's to 156/90's. usually the 2nd #. It's rare that it hits lower. started meds on sept. 6th. I don't have any heart palps since about 3 days ago, which was 11th. but still have hbp. my primary dr does not think it could be my birth control, especially with being on for only 2 & 1/2 weeks. I'm pending blood tests right now. and my dr. thinks it could be my thyroid causing palps and hbp. my dr does not seem to think bc's can raise hbp. I read the package insert of bc's and read on internet it can. I felt completely healthy 1 month ago. and had excellent blood pressure.

Well, I am on my 2nd pack of this pill for the second time in my life. I started taking this pill about a year and a half ago and it was WONDERFUL. I was having the 2 days (sometimes less) periods which was great since my usual periods are about 14 days (yes you heard right) long and I have terrible cysts. I had mood swings and I was very lethargic and I had pregnancy type cravings for the first 2-3 months but after that, things were easy as pie :)
This 2nd time around I am not too pleased. While I am not having many really bad side effects (most of the same I had the first time)... I am having multiple periods! WHAT!!!! I am having at least 2 periods in a 30 day span. I didn't have this happen the first time around but it is getting a little ridiculous now. If the 14 day once a month periods weren't bad enough, I am now having 2 5-7 day periods which are more annoying than the long one-monther. Has anybody else had this problem? I liked the DRAW to this pill's claim to only have a 1-3 day period, but I am not having this luck this time around. HELP. Am I the only one??

I am so happy I found this site! I have only had the Mirena in for a little over a month but I have HATED this damn thing since the day I got it. For the first week I could feel the strings and they were so itchy! To the point where it was embarrassing to be in public because I would have to wiggle around a little bit to get comfortable again. I have bled non-stop for the month and a half I have had it and the cramps have been awful, despite my gyno telling me they would only be bad for the first day or two. I am exhausted all the time- I had more energy when my son was sleeping 4 hours a night- now he is sleeping 10 or 11 hours every night straight through and I am always so tired all day long. I am having panic attacks and I constantly feel like I want to pass out. The blurred vision and brain fog is terrible! I am literally scared to leave my house by myself with the baby because I am nervous that I will pass out when I am out alone with him. I have to do break up my grocery shopping into 3 small trips each week because if I am in the store too long I start to panic and get dizzy. Having the Mirena put in was the WORST decision I have ever made. This should be the happiest time in my life - I have a new baby, just graduated college, all in all life is pretty good right now. But instead I am MISERABLE! I have my annual exam in 2 weeks and I am having it taken out-if I can wait that long. I wish I had found this site before...I never would have gotten Mirena!

EFFFF Levoxyl!!! My life has been really, really difficult since being on this medication. Reading all of your posts truly makes me feel like I am not alone in my struggle, anger, and frustration! If we could only sit in a room and talk about this face to face, how much better we might all feel. I think there needs to be thyroid support groups. Does anyone know of any?

I went back on Levoxyl about 2 months ago, because I was feeling tired again. I took myself off of it a year ago because I felt like I didn't need it anymore. I wasn't feeling great being on it and I had given myself a year on it already. Which by the way was a year from hell. I experienced depression for the first time in my life, gained about 20 lbs. from binge eating (never had an eating disorder or weight problem in my life), was fatigued constantly, then blamed myself for being so lazy all the time, lost friends because I canceled soooo much on hanging out, "I'm really sorry but I'm just not feeling good." Yeah that excuse gets really old to people with a normal functioning endocrine gland. Mind you I was diagnosed with this at 23. Sure I am mad that I have this problem, but when I am trying to get myself well and take the steps necessary per my doctor, it's really frustrating to just not feel like yourself. During the year off of it I took a natural thyroid support. Feeling fine, I slacked on taking the support thinking I had kick started my thyroid.
Two months of being back on it and I'm done! In a moment of emotional anger I threw my Levoxyl pills in the toilet. You know what they did...expanded to the size of a bazooka joe bubble gum piece. Uh that's big considering it's such a small pill.
I went to my doctor today because I've been experiencing bloating, pain and constipation for 3 weeks now. He told me to drink coffee and take benefiber, because perhaps I'm not getting enough ruffage in my diet. Just to see if I'm crazy about the expanding pill, I dropped an advil and tylenol in there. They simply fizzled down. I think these meds are making me bloated etc. and it's not worth it to me to feel this way. My body is telling me something is wrong and I need to listen!!
I eat right, take vitamins, drink PLENTY of water etc. and I still feel crummy.
I have been doing research online and have found a product called IODORAL. It is Iodine and Potassium Iodide. I have read many posts from people stating that this product has given them energy, helped with fatigue, their memory, overall well being. What was shocking for me learn is that Iodine helps fibristic breast tissue along with other parts of the body. Did you all know that 30 years ago breast cancer affected 1 in 20 women, and now it's 1 in 8 ???! Iodine used to be part of our diets. It has since been depleted from our soils and other foods. Bread used to be made with Iodine. Now Bromine is used in the baking process. Did you know that Bromine blocks the thyroid from producing necessary hormones for function. I bought myself some IODORAL and I'm going to see if it works. I am not a doctor but I am a person who is very in tune with their body. The bible says that there IS A CURE for everything on earth. I pray that all of you who have posted on here and are in discomfort do not give up your hope and find a different doctor or start doing your own research and be your own advocate for your health. There has to be something better out there! Something that isn't hurting our bodies! I am not giving up hope yet and neither should you!

I'm 47 yrs old now, & have been on Methadone since 92'. My journey with pain started at age 11 yrs, when i had a disease that totally screwed me up. From 11 yrs to 24 yrs, I was prescribed everything from Tyl #3 to Fentanyl patches. I don't know how many of you were around back then, but the 70's & 80's for pain patients wasn't easy. Lots of us put bullets into our brains because the Government made Doctors afraid to treat us "humanely" (so to speak). I was one of the lucky ones because I had outward physical signs of being in pain, so Doctors treated those outward pain symptoms. If i had not had those signs, I know I would wouldn't be here typing this now. I'm relaying this history, before my methadone side effects, because its important pain patients know something.

When I was 21 yrs old, got married & had a child. He didn't live very long, and it was at that point i started using my pills to stifle my feelings. At first I didn't realize what I was doing.. but.. it didn't take to long, and I realized it. Up to that point.. after losing both limbs, skin, and bone grafts, ulcer surgeries up the wazoo, fusions, countless medical procedures, hospitalizations, and operations.. to many to remember.. I had three surgeons, and a internist. All of them knew about one another, but it was up to me to keep each informed as to what they were prescribing.. and I didn't do it. Cut to the chase... About two years after my child dying, my internist retired, so I had to have my records transferred to another Doctor, at another Clinic. Everything with the Dr/ Patient relationship went well, up to about a month. One day.. Something in my head told me I should go to the clinic office, and read my records (i.e. Chart). So.. for the first time in my life, I listened to my head, and went into the clinic, told them what I wanted.. they directed me to medical records.. I told the lady there what I wanted.. she took me to a private room.. handed me a waiver to sign.. kind of stupid waiver, since I was reading my own file.. but.. none the less, signed it.. she handed me my three volume chart. It didn't take long for me to see why, and I'm sure most veteran pain patients will know why too. Right there in Bold Red on the very first piece of paper was "Drug Seeker! Abuses Opiates". Now.. I'm not saying I'm not deserving of that title, but what I am saying is.. "They don't let you know you've been labeled, they let everyone else know, but you." So.. If you are a pain patient.. read your chart once in a while, because once you get that title.. life gets much harder, & you have no idea how judgmental people (even Doctors) are. To most M.D.'s your too big of a liability, & a "criminal" Lastly.. be very careful with these medicines because, it's not that far of a jump from, you controlling them, to them controlling you." Once it happens, its not easy to turn it around again. From age 24 yrs to 27 yrs.. it was hell. I came close many times. Loaded my 30-06 three times, & My 45 twice that I remember. My wife came home early from work on that second time, and found one live round that had fallen on the floor, bent down to pick it up, then found the revolver under the couch.. took me to the hospital.. the E.R. doc admitted me for the pain, and actually treated it with Methadone. With the first dose, I noticed a relief, as I had never felt it before. Not all pain was gone, but after a could days of upping the dose.. it was. When my pain was controlled, it was time for discharge. The doctor that took over my care during admission sent me home with a week supply, & wanted to see me in a week. When I went to his clinic, he had read my previous doctors notes, & now wanted me to come off, & go back to something else. He told me, "that people like me, have to go to Methadone clinics to get methadone." I had been conservative with hiss discharge meds, so I left his office, went home, looked up the nearest methadone clinic, and stayed there for over 7 years (ME BEING STUPID AGAIN!). During those 7 years, I met 4 "pain patients" who were only guilty of being in pain, & having a doctor that didn't want to deal with them, so (like my doc) they mention the only real place, they can get it without bothering them (Methadone clinic). What I didn't realize until the day I walked out, and never went back (and never will), is that Methadone Patients are treated like criminals.. not patients.. AND by being a methadone criminal, you give your state permission to be part of your treatment (And believe me.. you may not see or hear from them,, but they know you by name). I found out after my pain doctor at the time got authorized to prescribe to me, supplemental Methadone at bedtime. After about a month, I get called into my councilors office, & she tells me "the State Methadone Authority says, I have to go back to Phase I because, apparently the pain doctor had been prescribing to other methadone patients without their permission, and that all of us patients had to go back to Phase I". There was no way I was going back to driving 90 miles a day 6 days a week, for something I had nothing to do with. I'm guessing the State was thinking I spread the news about my good fortune with this new pain doctor.. but everyone at the Clinic knew, I came there, sat & waited for my turn, & left. I might say Hi as i passed someone.. AND.. none of the 4 pain patients I mentioned above, were the patients being punished by the State.

The Country says, "its doing better when it comes to treating chronic pain patients." and to a point, I'd say its better.. but there are still miles to go.

METHADONE SIDE EFFECTS:

Someone here mentioned that by taking methadone, he doesn't feel the need for any other opiate. Thats very true. I felt it, & its why they use it for heroin addics. THe first month, I felt really sedated after about 20 minutes of taking it.. But that went away, & now all i get is pain relief.

Constipation-

When I have a operation, I stop taking them about two days before. Three if its possible, because its also true.. after the operation the pain increases, but you get little pain relief from anything.

I can't think of anything else.. except.. soon my only doctor since being on methadone is leaving to another State 3000 miles away, so soon, I'll be back to unthinkable thinking again, I'm sure. Who's going to take a past "drug Seeker-Methadone clinic patient? No Body that doesn't know me.. thats for sure.

I'm sorry this is so long. Good-Luck All

I am a 24 yr old mother of two, and my family is incredibly fertile, so I hav to be on BC. I had mirena put in last Friday at my six week postpartum appt. It was highly uncomfortable going in ( I am very sensitive though), and when I sat up I immediately asked the Doc if I was supposed to feel it in there. He said there was no way, and that should go away. I started spotting and continued to do so for two days, until I started bleeding HEAVY on the third day. My lower stomach and back have been killing me ever since. I have even resorted to taking my leftover pain pills from delivery! My sex drive dropped off immediately (very unlike me) and for the first time in my life I was really having "depression" symptoms. I am normally such a happy person. Needless to say I had it removed a week later (yesterday) and my libido returned that day, and I am my happy self again. I am still bleeding very heavy however, my uterus and back still ache and last night the pain was shooting all the way down my legs, so bad I couldn't sleep. I have some kind of nerve sensitivity disorder ( I feel things other people never feel). So I should have known better than to have some foreign object shoved inside my uterus. I couldn't be happier that it is out, and I cannot wait be back to "normal" again. I am happy for all the women it works for, but it sure seems like this is a big pain for a lot of women. I wish I had done my research first! BC pills it is for me!

I'm 27 years old and have been married for 2 years. In May I decided to get on female birth control for the first time in my life to regulate my 7 day period. The first month I felt like a mental patient, lol. I'm already an emotional person so when I started the pill I swore I would stop it. My nipples looked deformed because they were so swollen, I was depressed and nausea. I decided to stick it out because I wasn't taking it at the same time everyday. So I regulated myself with an alarm clock and the next month everything was wonderful. My period only last 4 days, and all of my symptoms were GONE!!! I'm now at the end of my fourth month and my period has come early which is freaking me out because I have never had an early period in my life. I've read about spotting on this product, but I haven't spotted EVER not even in the four months that I've been taking the pill. Other than my first month of horror and my recent early period everything else on loestrin has been wonderful.

My suggestion to women who are on their first pack is try to tough it out, you will feel horrible the first month but just apologize to whomever feels your rath and remember your body needs some time to adjust. I'm a victim of horrible menstruation, and so is my mom. Since I was 9 years old I used to get 14 days of cramps and 7 days of bleeding. I would pass out all the time on my period and my husband and family was very upset since he or others would find me blacked out at home, work, the salon, at the zoo, in the shower, and once my neighbor found me. Loestrin has DEFINITELY changed my life for the better, so stick out that first month ladies its worth it. I hope my experience helps other women who are scared and feel like the symptoms won't end.=)

I have been reading all of your Simvastatin experiences with high interest and would like to share my adventures with all of you as well. My story began seven years ago when I was relatively healthy and enjoying life. My doctor prescribed Lipitor for my elevated cholesterol and two months later I found myself in the emergency room after having a severe bout with vertigo for the first time in my life. I have since spent the last seven years fighting this debilitating illness which continues to haunt me after having seen every top neurologist in my area and having taken every neurological test available. It would be as difficult to convince me that I was not somehow "poisoned" by Lipitor as it was for me to convince my doctor.

I was eventually prescribed Simvastatin 40MG and seemed to stabilize for a few years even though my dizziness problems persisted. Suddenly I began experiencing bouts of upset stomach and severe lower abdominal pain. I allowed my doctor to order basically every nasty test known to man in an effort to discover the cause of this new problem, but all have come up negative so far. Eventually I began to experience total exhaustion in the middle of my work day, not to mention the back, neck, and muscle pain that has been described so vividly in this forum. Basically, I have become a 53 year old man who feels much older, has absolutely no energy, and rarely has a day when I can honestly say I feel alive and well.

I am not a doctor and I can't honestly prove that Simvastatin is the cause of all of my problems. However, I do have common sense and after reading all of your thoughtful comments on the subject I would be foolish to at least not suspect that the drug may possibly be making me less healthy and not more healthy. Thank you all for opening my mind to this possibility and I certainly plan on discussing this with my doctor very soon, who may no longer by my doctor should he continue to insist that I take this nasty drug.

This is my less than 24 hour update from yesterday since I had my Mirena removed. I had my yearly appt. yesterday and explained to my dr. all the problems I've been having over the last year. I thought he would try to talk me out of having it removed but he was very sympathetic and removed it without question. So, I'm definitely relieved about having it out. I'm sure it will be a while before I will be able to notice any changes that I can directly relate to the Mirena coming out. But, I can tell you that my husband and I can already tell the difference during intercourse without the Mirena. It is so much more comfortable so, we are very excited about that! I requested Yaz for birth control since I've been on it before and never had these emotional issues while on it. He also gave me a brochure and DVD on the Essure which is the in-office permanent sterilization procedure. So, I'll be doing research on that to see if that will be a good thing for me to do.
Another thing, too, during my gyno exam, he found a lump in my left breast. I have never had any problems and definitely no history of any kind of cysts. I'm not blaming the Mirena but all of this is just way too coincidental. Now at 35, I'll be having a mammogram and ultrasound to determine what this lump is. I'm just praying hard that it won't be anything and definitely trying to stay positive. I'm just very relieved to have the Mirena out and I will stay posted as to any additional changes in the future.

I've been on the NuvaRing for 2 years now. I think it reacts differently to everyone. It has made my life much better. My periods are shorter, lighter and less painful. I used to get sore muscles and sore breasts a few days before I started now I have none of that. I'm not moody and for the first time in my life I don't have to spend the first day of my period in bed. My body adjusted to it quickly and I didn't have any spotting. I still have my sex drive and there is no pain during sex. I have a lot of stomach problems (bad gallbladder) and if I were on an oral contraceptive I would likely be pregnant because my body wouldn't absorb the pill properly. This has been a lifesaver for me.

I have had asthma since i was 10. I am 44 years old now. I have never in my life been on prednisone this long (since Feb 2009). It is now July 11,2009. I was admitted to the hospital for IV steriods (prednisone) because for the first time in my life the general 10 course with the pills wasn't working. so there i was on 165mg of pred every 6hrs. After eight days in the hospital i was released and was to take 40mg for five days and decrease by 5mg until done. I didn't do to well and had severe exhaustion where i couldn't even walk 2 steps the next day. so I went to my pulmonary dr. who said he noticed a severe anxiety side affect in me from the drug and said i needed to get off it as soon as possible, he had me drop my dose every day by 5mg. TO FAST! I had breathing problems again, started over going slower, got down to 10mg and had to jump to 40mg again! side effects for me are severe anxiety (which i have to take ativan for) and especially massive painful foot cramps. My hands will cramp to while trying to write, but the foot cramps and the feeling of being wired are the worst. I am still trying to wean off....sometimes i wonder if i will ever finally be off this stuff. I just want to cry sometimes. It feels like being pregnant and going thru post partum at the same time

I had the Mirena inserted back in March (2009) and I had some problems the first 3 weeks of having it in, but everything seems fine now. My periods are regular, not heavy, they don't last a full week anymore, I got off the iron pills I had to take prior to the Mirena because I was bleeding bad, had softball sized clots, it was just awful. Now everything is so much better. Only thing I have is headaches during my periods when before it was severe cramping. I don't mind the headaches so much, one Tylenol and I'm good in 30 minutes. Every woman's body is different, some have bad effects from Mirena, others don't. And believe me, I had a bad time in my life with my body, and since I got used to the Mirena, everything changed for the better. I'm glad I got it.

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

IT'S OUT!!!!!!!!!!! What a mess I went through. For those who missed my prior posts, I got my Mirena in June 2008 after I got married. Even though I'm 29, I'm a medical student and not ready for a baby.. Within weeks I had oily skin, oily hair, hair loss, sore breasts, and no sex drive at all. But I never had a single period after the second month, so I was happy!

By August or September I was gaining a lot of weight (20lbs) and started feeling "brain fog" and fatigue. By December and January I was seeing neurologists for SEVERE migraines and dizziness. In April I developed symptoms like MS such as tingling/numbness in my head, face, and one foot... profound fatigue, and incapacitating dizziness.I've had every test done from thyroid workups to MRIs/MRAs and nerve conduction studies. I was on 3 different migraine prescriptions and was even getting nerve blocks in my neck for them.

In May I became withdrawn, irritable, depressed, and had anxiety attacks. I'm not ever a moody person, and never had PMS. But here I am, crying for no reason, yelling at my husband, snapping at my mother, and SO FREAKING EXHAUSTED that going to work is impossible, driving the car seems dangerous (severe brain fog.... like I'm drugged), and even just doing the dishes or feeding the pets takes all my effort (with tears) to complete. I don't feel like myself at all.

I found this website and thought perhaps all these symptoms were from the Mirena. So I found a new OBGYN who was awesome and said he'd take it out. I went to have it removed but the first a$$hole who put it in for me cut the strings too short so they could not be grabbed. The new doc tried to reach them but couldn't. I ended up having to have THE MOST PAINFUL PROCEDURE OF MY LIFE.... I had to take cervical dilation pills and then get a hysteroscopy which is where they shove a camera into your uterus to look around and find the little sucker. The cramps were unbelievable.... 10 times worse that getting it placed. (Mind you I've never had children so it was really bad). After he found the strings, he grabbed them and pulled. I thought I was going to die.... my poor cervix had a scope in it, an instrument holding it still, a dilator in place, a speculum in the hole, and then an instrument went in along side the scope and pulled the little bugger out. AHHHHHHHHHHHHHHHHHHH! I was in a hot sweat worse than menopause I bet!

So here I am, home, bleeding, only minor cramps. But now I wonder... how long will it be until the depression and brain fog go away? I want to be myself again. I want to be happy. I want to laugh instead of cry. I WANT TO HAVE ENERGY. My greatest fear is that I went through all the pain of putting it in, taking it out, and the cost, and the depression, fatigue, and brain fog won't go away, meaning it wasn't the Mirena to begin with. (If that was the case, I could have dealt with the weight gain, oily hair, and migraines as long as I had the nerve blocks). But I find it hard to believe that the Mirena is not the cause since so many of you women say the same thing. BUT.............. most of you had the Mirena placed after having a baby, so it's possible it was PPD?

THIS IS MY QUESTION TO ALL OF YOU OUT THERE.... did any of you WHO HAVE NEVER HAD CHILDREN have these things after getting the Mirena? Also, isn't it weird that the severe fatigue, depression, and really bad brain fog started after 9-10 months of having it and not sooner? I was on OCPs before the Mirena and did fine.... but this time I am so depressed and irritable, dizzy, and FREAKING TIRED TIRED TIRED.

:( How long until I feel better if it was the Mirena?

Today is a new beginning for me after finding this site about the harmful side effects of Lisinopril and all this time I thought I was going crazy. I was put on this drug in 2006 for elevated B/P of 130/90. I had just recently completed 20 years in the Marine Corps and was in the process of starting a new career so of course I was going through a very stressful time in my life which may have been the cause of the recent spike in b/p. I went to see the doc for a checkup and she put me on 10 mg of lisinopril. I first noticed the dizziness soon after taking this drug. I was working out with some Sailors since I got a job working for the Navy and we had a bet on who would finish first in a three mile run. I thought this would be easy for me since I used to run everyday as a Marine with run times of under six minutes a mile but this time it was different. I was the first one to the half way point but then my body began to shut down to the point I could barely run. Everyone passed me by and when I crossed the finish line I had to sit down cause I thought I was going to pass. Let me remind you that this was only a three mile run, I was used to running thirty to forty miles a week. It is 2009 now and I very rarely workout due to the pain I experience afterwards. I have the constant feeling of gagging and I thought it was allergies but I refused to start medication for that. I remember the times that I used to stand up at work and shake my arms out because of the numbness in my arms and hands. I always have the funny feeling with the left side of my chest not sure if my heart is just going to give out on me. My wife always notices how I'm always massaging my chest muscle. I tell her it must be arthritis to quell her suspicious. I too had to remove my wedding ring due to the smelliness in my hands something I never had to do even while serving my country overseas. Thank you all for your posts, you have turned the light on for me to all the aliments I have been feeling these past few years. I have been off lisinopril for three weeks now and I am already feeling like my life is coming back. Hopefully, I'll be able to run that marathon that I always dreamed about. Again, Thank you all!

I was on Yasmin and then YAZ for about 5 years and started when I was 19, and am now 24.

ON YAZ: I got a lot of urinary tract infections, had mood swings, depression, snappiness, and anxiety. I also felt swelling and occasional bruising in my legs ( started when I was 23). I stayed really thin and never felt bloated (5''7 120). I also never got pimples.

OFF YAZ: I have actually gained a few pounds and I KNOW its from going off the YAZ because it happened almost instantly. (5"7 126) YAZ does have a diuretic in it, so it really does help with the water retention. I feel bloated for the first time in my life. I broke out a little bit on my face and back. However, my mood swings have gone away, and my depression and anxiety have been almost non-existent. I am so much happier! I no longer feel swelling and bruising in my legs. My Urinary tract infections are gone as well.

Overall, I am a little bit chubbier, and have a few more pimples. But- I am happier, less irritable, anxiety free, and generally have a better, healthier outlook on life. The swelling in my legs and UTIs have also disappeared.

Any suggestions on a new BC?

im a twenty four year old student on paxil since i was fourteen.
coming off this medication is nearly impossible, i have tried at least ten times. The reason i have decided to come off it for good is because of memory loss. I can spend up to one hundred hours studying for a test and still only get about seventy percent.
Another reason i have decided to come off paxil is tooth decay. I now have a cavity in every single tooth and have lost three teeth due to paxil.
A common side effect of paxil is dry mouth. With out salivia in your mouth, it becomes difficult for your mouth to wash away bacteria, leaving you with tooth decay.
Im coming off slow, cutting up pieces of paxil to take each night, about two milligrams less per night. Ive been all the way up to sixty milligrams and im now down to twenty and hopefully will be free and clear within a few months. This is not a medication you can come off by cold turkey. you must cut it down very slowly

I had the Mirena IUD inserted on April 1st 2009 for treament of endometriosis, nearly a month and a half ago, and I am absolutely miserable. I thought I was completely losing my mind, only to find out from finding this site and others that I am not alone. The worst of my side effects are the EXTREME anxiety and now depression. I have had a history of both from time to time in my life but nothing like what I have experienced since the Mirena. Also, my hair is falling out like crazy, my face is breaking out everywhere (never before), and worst of all I've gained 7 lbs since I got this thing put in. I felt ravenously hungry almost immediately, I never craved sugar and food like this in my entire life, not even when I was pregnant. I too was fooled by my OB in that I would experience little to no side effects as I cannot take BC due to the effect of hormones. She said that the Mirena is a localized synthetic hormone within the Uterus and would not at all enter my blood stream. ARE YOU KIDDING ME! I'm a basket case, my 3 yr old told me that she misses her mommy, that I sleep too much. That is what finally brought me to researching my symptoms and the Mirena it was the only thing new that could be related and so it was. To summarize my side effects in order from worse to much worse: weight gain, hair loss, cramping, bleeding constantly, libido decrease, extreme tiredness, severe mood swings, depression, blurred vision, sever migraines (no previous history) and the very worst of all the ANXIETY. I'm generally a very happy positive person and lately I can't even stand myself. I often times ask myself when will I ever feel normal again. My OB refused to take this thing out after I went in for an office visit a week and a half after insertion. She said let's not "throw the baby out with the bath water" and give it till 3 months before we can say for sure that I'm experiencing this from the Mirena. Whatever, it's been 6 weeks and getting worse. Finally today I took some blood tests to prove that I'm not diabetic, that I don't have a thyroid problem and that my CBC is fine. Then finally she will consider removing it, well newsflash lady, I'm going to demand it be removed immediately. If not, I'll take it out myself.

I took Loestrin 24 for 5 months before I saw any side effects. I’ve always been a cheerful, healthy person. I’m healthy. I run track for my college. Everything was going great until for some reason I just didn’t want to see anyone anymore. I was constantly tired and lazy. My sexual drive became zero and I would fight with my boyfriend for no apparent reason. It was terrifying. Almost two weeks ago, I had a panic attack for the first time in my life. I thought I was having a heart attack. My left arm, chest, and back hurt. I couldn’t sleep. I had heartburn. So, I decided to go home and talk to my parents who comforted me. They also saw a change in my personality. My mother and I wouldn’t argue anymore. She would just say something and I would cry. I was depressed and kept on having anxiety attacks. At first I thought it was from caffeine but when the symptoms still persisted, I looked toward the birth control. I completely stopped it last Wednesday. Now, everyday is an improvement. I am much happier than I was. I felt a difference around 2 days after stopping the pill. Never take this pill. It’s terrible and no one should feel the way I have in these past two weeks.

I'm just in shock.
I can't believe that this sort of thing can go on.
My experience is all over this page. And the seven after it.

I graduated high school with a 99 GPA and was at the top of my class.
I was accepted to medical school along with my admission to college.
I started Yasmin at the same time.

All of a sudden I was getting classic migraines multiple times every month.
Soon, Yasmin became Yaz. Okay, fair enough, nurse says to switch, I'll switch. Yaz is said to be safer.

Time goes by... I'm irritable, I've lost my sex drive, I'm dragging myself out of bed in the morning if I get to classes at all, but I miss lots of them.
My GPA falls from a 4.0 to a 3.6.

I had to come home last semester because of how sick I was. Nurse says that the doctor wants me off Yaz because of the risk of classic migraines.

Liver enzymes were screwed up - fatty liver at 20?? - and cholesterol is backwards. My heart races a lot, too.
My anxiety is out of control and I'm depressed for the first time in my life.

I've been off Yaz since November of 2008 and still haven't had a period.
Additionally, I still haven't MET my gynecologist, despite asking repeatedly if I can see her.

Now she's ruled out PCOS and all other causes and wants me to "jump start" my period with more synthetic hormones.
This feels so wrong.

I have IBS, nausea, back pain, and abdomen pain. This is all just too much. I'm disillusioned with the medical field now and am having a hard time accepting that I wanted to put myself in a position in which I'd have to either perpetuate the problem or fight it. It doesn't make sense.

There needs to be a lawsuit, and now.

April I started Singulair last Thursday night and felt tired and depressed
29th on Friday but thought it was something going on in my life. On
2009 Saturday, I had severe, throbbing headaches all day but took the
Singulair for the third night. Sunday, I again had throbbing head- aches so looked up this web site and thought, "Aha!" I stopped
the medicine but had dull headaches on Monday and felt tired. On
Tuesday, I woke up and had trouble breathing. I went to the doctor
who ended up putting me on a nebulizer, giving me a shot of
steroids and prescribing an inhaler that I'm to use 3 times a day as
needed until the Singular is out of my system. I was only put on
the Singular in the first place because my doctor thought my
hoarseness might be from an allergy. What a nightmare!
I also suffered from apprehensiveness, and also
sleeplessness, and a fever. Never again!