Heartbeat symptoms and conditions

Im so thankful i found this site, i was put on lisinopril about 2 months ago, i woke up one morning and felt dizzy took my bp and it was really high, i had never had problems before so i was surprised, went to the er where they check my blood and did an ekg, everything was fine, i have been so tired lately, my sex drive is completely gone, im having tingling in my hands every night, and my heartbeat is always elevated, my doctor is giving me an excuse of being over weight, well im only about 20-30 lbs over weight and never had this problem when i was 30 lbs heavier.. i have no energy to go to the gym, i was working out 3-5 times a week before, now i do good to get a full days work in, im always feeling shortness of breathe, im so sick of this, after reading this forum i have decided to stop taking it and hoping i get my energy back so i can get back to my life thanks to every one and their post.

When I had my last son, my obgyn did not inform me any negative side effects. I had previously used the copper T, and although I still got my period, mine aren't that bad, but still, my Ob-gyn assured my the progesterone in the Mirena would be limited to that area. Well 3 years later and I have had headaches, never got my libido back (which is hard on a marriage), and have gain about 30 pounds(with no change in diet or activity) from my 6 week post delivery check-up. I only have short spotting with Mirena, but would trade for a monthly period in a heartbeat if I could go back to my post pregnancy weight of 116 and get libido back. It was not until my check-up last week that I was informed it could affect libido. I'm 5'2", so 30+ pounds really shows, my mother and mother-in-law, both had made comments about "hoping I wasn't pregnant again. Its also caused a loss of self esteem and depression over all this. If my insurance will cover it I plan to go back to my old, 10-year copper IUD.

I'm a 35 yr old stay-at-home mom of two who was diagnosed with mixed connective tissue disorder over three yrs ago. But since I was 18, I've had scleroderma & rheumatoid arthritis when I was 23. I never took any drugs for either one up until May 2008. Although the worst things I've gone thru over the yrs were weight loss, stiffness and limited flexibility. The most dramatic change was my facial features. I've had old friends from high school ask me if I had plastic surgery! Other than that, I was able to get pregnant twice and have two beautiful boys. When my rheumatologist diagnosed me with MCTD in 2006, two yrs after my first child, it was very upsetting to know that lupus and sjogren's syndrome was added to the mix, literally. She wanted me to take prednisone and plaquenil. I said no way. I told her I wanted to try for another child and didn't want any drugs to ruin my chances. She assured me that I could take both even while I breastfeed! So I left and ended up with my second boy in 2007. But admittedly, both pregnancies took a toll on my body, the first one with MCTD and then the second one, I had gestional diabetes. A few months after birth, I felt the arthritic flares and the fatigue and sluggishness coming on strong. Without doing any research about either drug, I did consider taking it after I stopped nursing my second child and thought okay, two children are it for me and now it's time to take care of me. I was given prednisone at 5mg daily May 2008 for that entire month. I was very scared but I did it. I just didn't do it consistently. I would skip a day or two..or three...or four days at times before I would take it again. The rheumatologist didn't give me any warnings about side effects, skipping the dosage or tapering off. After I ran out, I decided I couldn't go back on anymore. It did ease the stiffness in my joints and gave me more energy but the mood swings, faster heartbeat and more than normal anxiety did not help. In the next two months, I experienced serious cases of heartburn and acid reflux and a series of episodes when I would gag on a bite of food and had to jump a few times to get it down. I felt a rush of such fear every time it happened that I knew it was the absolute worse feeling I ever experienced in my life. Then the worst happened last August when I fell asleep one one night after having a chocolate chip cookie. I woke up and couldn't swallow. I started drinking water but it was coming back up and out of my mouth. I panicked and screamed for my husband to do the Heimlich on me but it wasn't working. We called 911 and I started downing another glass of water. By the time they got there, I felt the cookie go down. It was something I never wanted to go through ever again. I saw a holistic chiropractor who specialized in kinesiology and other little rituals. He discovered a problem with my adrenal glands and digestive system. Soon after, I saw a gastroenterologist, had an endoscopy and Barium swallow and the diagnosis was esophagitis. It significanty showed how thin it was getting and why I had trouble swallowing. As of last November I was scheduled to have a three hour endoscopy to have a tube go down my esophagus to widen it enough to be able to swallow again. I was too scared and so it didn't happen to this day. You see I like to go the natural route but it is an expensive one at that. It really is my gut instinct that tells me that drugs like prednisone are killing more people than helping people live. But I look back to the fact that I still didn't know anything about it, not like I do now, thanks to the internet and websites like this. Then here's an absolute doozy for you! I was fine for a few months, up until a few months ago in February. My knees were in pain and stiff as a board, my arms were not happy as well. I couldn't take it anymore so I actually went back to my very first rheumatologist in March, who I saw when I was 25 yrs old. He did x-rays and then pushed for the prednisone. I broke down and decided to take it again. This time at 10mg a day. Now I know this is nothing and so was the 5mg from last yr but being only 102 lbs at the time, my body was telling me that it couldn't handle it anymore. I took it consistently this time and for almost two months. The last two weeks though I started to skip again. I also decided that the RA was too old school for me so I went to see yet another RA at the end of April, the one who diagnosed me w/MCTD three yrs ago. I figured the first one never changed so maybe she got better this time around. She took me by surprise when I told her I was taking pred and that she wants me to stop!! She specifically said, "it's an immunosuppressant, that wouldn't work for you."! What a joke!! So she just said to finish it off and start on plaquenil, another drug I dreaded to take. Again, no explanations about side effects or tapering off, I had like three pills left and just stopped. As for the plaq, talk about short-lived. I took maybe three or four and that was it too! I was angry by all the RAs and how they operate. Just take this and don't worry about nothing else. I'll see you in a few months. Then you go home and forget about it. It is highly unlikely with what came next for lil ol me. The first week of May, a pain started in my right ankle. It was more like an annoying sore pain so I tolerated it. By the end of May, I was hobbling on a cane and watched my foot go from normal every morning to an inverted position, w/ the sole facing my left foot. It was swollen, painful and I couldn't put any weight on it. After thinking I was going through an arthritic flare, I said to myself that this was no ordinary flare I've had in the past. I thought of prednisone and how it started after I stopped taking it. The plaq was not in the picture since it takes months for it to take effect. THAT'S WHEN I FINALLY SAT MY ASS DOWN AND STARTED SURFING. After a good three sleepless nights of reading pages and pages of info about withdrawal symptoms, tapering off and stories much like the ones I've read here, I flipped out and went on a mental rampage. I put two and two together about the link between my esophagus and stopping the pred last yr. I have no doubt that the pred f'd it up! Now after seeing one orthopedist (who didn't deal w/the foot/ankle but didn't know), having an MRI which showed torn tendons and ligaments and then being sent to a podiatrist surgeon (BIGGEST MISTAKE TURNED INTO A BLESSING), who decided to take the conservative approach by having my foot casted in a straight position. It was a procedure that I had to be knocked out for since I couldn't bear the pain of anyone moving my foot. That was June going into July. Removal day was the 23rd and lo and behold, hello inverted foot again. Not only did the cast feel loose but I felt my foot turning in it! The blessing was that I didn't have surgery and I didn't have it w/ this damn doctor! He then felt I needed to see a neurologist to rule out whether I may have lesions elsewhere in my body that could be the cause of my foot inversion. I said sure I will see one but I'm not coming back to you! I went to see the doctor I was supposed to see in the first place, an ortho surgeon who specializes in the foot & ankle. But boy he threw me for a loop! Not only did he roll his eyes at the idea that prednisone was involved in this injury, but that MRI don't tell the truth and so I don't have anything torn!! Based on my autoimmune history, he wants me to see a rheumatologist to rule out arthritis as the culprit. He also thinks seeing a neurologist will be a waste of time. He also mentioned the possibility having RSD/CRPS. Google it, it's not GOOD! I honestly hope that's not the case since I'm not in any pain other than the stiffness and non weight bearing pain I'm already used to. This ortho is supposed to be one of the best in the nation and I don't know if I can trust him either! All I know is the prednisone should be BANNED. BLACK BOX THIS BITCH!!! If I had the power and money to go after the makers of this drug, I would run them down for every dollar. I have my 22 month old who was just diagnosed w/PDD recently and I get angry w/the memory of that RA trying to get me to take the pred and plaq before I got pregnant again! My almost five yr old is wondering why I have to walk around in crutches every day and that I can't go outside to play with them anymore. It's been almost three months of this ordeal and it's starting to really depress me, my husband is trying his best to take care of me and the boys as well as my mother and mother-in-law. I have a great support system but I still long for leisurely walks by myself and taking the boys out on my own. I can only go outside in a wheelchair after my husband carries me down three flights of stairs in a no elevator apt. bldg. Life has changed drastically! I'm trying to stay sane everyday for my boys' sake and for my husband's. I do want to mention one last and most IMPORTANT THING. A website: ****** I started taking it two months ago and it has helped me tremendously so far, regardless of my situation. I developed an enlarged thyroid nodule back in February which needed a sono guided biopsy to see if it was cancerous and it turned out to be benign with normal thyroid function as of last month. As for my foot, I don't know what I may have if it's not arthritis related but I hope that LDN is working on it as of right now. For all autoimmune disorders and some cancers, anyone here should take a look at the website and read more about it. Thank you for letting me share my story :-).

I was given this shot by an idiot of a Dr who told me that it was "for inflammation". He never told me it was a steroid and even though I asked repeatedly about side effects, I was brushed off with "if you don't have a reaction within 15 minutes, I would not have any". I wish I had trusted my gut instinct and never let him do it. I have only been on it a week so it hasn't dented YET, but I have mood swings, irritability, insomnia, jitteriness, dry mouth, racing heartbeat, and though I am eating only 1200 calories a day, I am already gaining weight. Does anybody know if there is a way to get this out of your system faster? I had a hysterectomy so I do not have the bleeding issues.

I am so relieved to hear that so many people have experienced significant WEIGHT GAIN while on this drug. I weighed 150 pounds when I got pregnant and was 183 when I gave birth. I got all the way down to 152, when I became depressed and suffered from severe anxiety. I have gotten as high as 210 lbs, and my life has been miserable because of my attempts to lose weight and NOTHING WORKS! I can do an hour of spin class (supposed to burn 500-700 cals), lift weights, eat perfectly for weeks and step on the scale and lose NOTHING! I even hired a personal trainer and I think she thinks I am lying because she sees how hard I work out, and nothing changes. This is so depressing, I am embarrassed to go in public or even look in the mirror. I have decided to wean off although I have been taking this med for 10 years. It did help the depression, but now I am so depressed from this weight it is not worth it. Thank goodness I found this thread, because maybe I am not crazy!!!! Is there any chance I will ever lose the weight, or is my metabolism ruined for life?

I just wanted to post my experience/perspective. I am 30, never had children...

For the most part I love my mirena and would get it again in a heartbeat. Negatives: I have had it for over 2.5 years (I had to get it reinserted after the first month because it had started to expel, but the removal was pain-free and the reinsertion was less painful than the initial insertion). My period does generally last 8-9 days (compared to 3-4 before); BUT, I love that I only have to wear a pad or pantyliner because my flow is so light. My cramps are not necessarily worse, but different--I swear I feel myself ovulating!

Positives/Neutral: I have actually lost weight since getting my mirena (about 30 pounds), but this is because I joined weight watchers not because mirena helped me lose weight :) I have always shed a bunch of hair and haven't noticed a difference. My sex drive has been low lately, but I think it's because my significant other gets home from work after I'm asleep so my motivation for sex succumbs to being tired. My period is so light that I only have to wear a pad (first time since 6th grade!). I've always had some acne since I was about 11 and have noticed no changes. My significant other can't feel the strings because they are way up by my cervix (I have to struggle to feel them to check that it is still in place). I love not having to remember a pill--I am very forgetful and busy!

It's nice to know that I'm not alone..

I got Mirena in November 08, and since then I've developed a plethora of unpleasant side-effects. Initially, I couldn't put them all together. As I'd had a fainting spell and some restless legs a few months prior to getting Mirena, I've been concerned that all of my symptoms were stemming from a nutritional deficiency like folate or b12 anemia. Nothing seemed to quite fit exactly right though, and I take vitamins regularly, so I was perplexed until last night. After googling "tingly feet" and "heartbeat" I stumbled onto one of these forums.

I have felt like a crazy person all of this year, and I am now quite certain that it's from Mirena. Feeling foolish that I didn't see this sooner.. but I guess I we perceive what we want to, and I was happy to have easy birth control.

I've NEVER had heart palpitations, this kind of foggy-headedness, anxiety like this, unexplainable nausea, tingling in my feet, or depression before. My dizziness and fatigue alone had me fearing for my health, and my extreme mood swings had me fearing for my life.

I'm getting this removed as soon as possible.
Clearly I could've done my pre-Mirena research better, but the pamphlet and pep-talk I was given did not mention everything that I've been going through. I'm a little pissed, to be honest.. but mainly relieved.

I think I'm going back to the Nuvaring.. I'd rather bleed than be a dysfunctional, ill, zombie-person.

Holy crap! Thank you all for helping me to justify my pending MIRENA removal on Wednesday, June 17th. I thought I was pregnant again - but I wasn't. Instead, via ultrasound, they found a large cyst on my ovary - the kind that's an UNDEVELOPED FETUS - it can have hair, fingernails, teeth and sweat glands - but never had a heartbeat! I have to live with this til it goes away or they decide to remove it... It's really sad for me to think about a little one that tried to make it but didn't...

After insertion when my son was 8 weeks old (he's now 20 months old-I've had this for a year and a half), headaches, incredible fatigue, weight gain - never lost the baby weight and gained more, low back pain-constant dull achiness, high blood pressure-mine's always been very low, incredible moodiness (I threw a carseat at my guy), huge depression swings-got a new anti-depressant, anxiety attacks, horrid cramping... The only good thing was no periods.

We decided to have them take the Mirena out so I can be "me" again. We decided that having what could have been a baby sticking around inside of me was unacceptable. I just hope I can be fertile again as I'm already 40 and we might want another.
Thanks again for helping me confirm that it's not all in my head!!!

Less than 2 months after taking Lipitor I have been experiencing intense weakness of the legs, especially the hip area. A normally avid walker, last week really woke me up when I was unable to walk over 40 feet without having to stop from sheer leg exhaustion. I'd have to actually lean on my partner until I could manage to shuffle again- a shuffling gait is what I had to resort to just to make it back to the car.
This is bullshit because even though I've had some angina symptoms, right up until I went to the hospital I was able to hike; was still relatively strong.
So today I have spent hours researching side effects and have seen on this site alone many mentions of intense leg weakness and pain with Lipitor.
This, along with simultaneously educating myself on the truth about high cholesterol has convinced me to gradually cease taking this medication.

Instead I will replace with sufficient quantities of VitC, buckwheat combined with gingko, and of course I can never stop with the garlic because it is delicious.

The purpose of prednisone for sinus sufferers is to open up the sinuses. Now, I have found that 40-50mg a day is usually QUITE sufficient to do that. (For me – everybody is different) And, as I get better, I taper off each day to 30mg, then 20 as needed. What doctors forget is that people react very differently to medications. Why take more when all it does is make the side effects worse? The doctor doesn't know how you feel, YOU know how you feel. Don't blindly take this dangerous medication, LISTEN to your body.

If you have taken 40 mg, your sinuses are completely open, and your heart is starting to race, do NOT take any more that day! Or, at the very least, wait till it stops and then take 10 mg or even 5 to see how you do. I advise never taking all your prednisone in one dose - try to space them out over the day so you can see how you react. Never take any later than dinner so you can give the side effects time to wind down if you experience them.

In summary: I have found that taking unneeded prednisone after you have achieved the needed relief will not do much good, if any. However, the lack of sleep will be very detrimental.

One final tip: I have found that after I start to get better, 20mg prednisone taken with a couple Sudafed is about as affective as 40mg prednisone. However, be VERY careful combining medications if you get fast heartbeat! Two examples are cough medicines and (especially) Sudafed! I advise trying a half dose of Sudafed (1 pill or half a 12hr pill - 12hr pills are great for nighttime) first if you are on prednisone. You can always take more, but you can't un-take a pill.

Disclaimer: I've taken prednisone many times, but I'm not a doctor, yada yada...

Other than weight gain, mood swings and heart palpitations, my most disturbing side effect has been a pulse/heartbeat at the back of my head. Has anyone else experienced this?

Wow, I can't believe the bad experiences everyone has had. I guess I was one of the lucky ones because my experience was WONDERFUL! I had it inserted about 2 months after baby #2. I lost all 60lbs I gained during pg PLUS and additional 10. I have to admit the insertion was awful but the almost non-existent periods for 5 years were wonderful. If my insurance hadn't changed, I'd have another one in a heartbeat. I don't want to be on the pill because I just had an allergic reaction and my husband is resistant to get his end taken care of. So, we're still looking.............

OMG...Seriously...People do NOT know of this site and are just beginning to put together all of these life altering side effects and look for answers. Again I am open to and have tried all sorts of new and innovative medications because I truly believe in the science.

My Daughter just turned 17. I have been a single Mom her entire life as her father is deceased. I have done it all carrying 3 or 4 jobs to pay for college tuition and the costs of raising a child. Carried a 4.0gpa for 4.5 years while raising a highly spirited red head single handedly in a college town where I knew no one. She is an amazing high honor student who is community and civic minded and is truly the most responsible person I have ever met.

I now work from home for the first time with a home daycare. I have little one's leaking or spewing on me daily just to be able to still enjoy the things my daughter now deems *gay* or ...*totally gay*.

For the first time in my life I have found a great man and truly in love but have ZERO desire to start over...this is perfect...I get to play with kids all day and send them home at night. all the fun and i get to sleep in and not worry about rising college tuition costs.

I'm 37 and about to have my life to myself for the first time...in...well...MY LIFE. My daughter will not be lingering she has plans and goals and is headed off to start her life soon after graduation next year and I have an account I have been stashing away since she was little for someday for...ME.

I would absolutely in a heartbeat rather deal with an unplanned/unexpected pregnancy than spend one more second of my life with that device inside my body.

My fever finally broke today...thought it was that *flu* i'd had back in February.

Listen to your body and do not let any Doctor try to make you continue to take a medication you don't want to take. I went through this way back when the Norplant made me gain 75lbs and bleed for 2 years while i fought with my insurance company because I had signed a contract stating I did not want children within the 5 year period for them to pay to have it put in. It requires COURT ORDERS to force you to take medication against your wishes.

when I came to this site I was still believing it was something else or I just needed to give it *more time* to adjust or whatever. No. just as some people tolerate medications and others have allergies. I believe my body was *allergic* to this device and was REPEATEDLY openly telling me to have it removed. I was lucky my *family practitioner* was booked solid the morning I finally did the math and *freaked out*. I got a doctor who turned my 15 min check into almost 2 hours of *what should we do * and *these are your options* she handed me to oxycodone and left me for 5 minutes to *prepare* for the removal, has had enough experience in last 6 months she said to know I needed some time to prepare myself for if nothing else the pain. let alone...omg...what might come next...after removal. she also told me she would only give it two *tugs* as I hyperventilated and if it didn't release she would reschedule and SEDATE me.

I'm venting and i'm sorry. It's the first time my brain has been clear enough to think since Dec 4th of 2008. I thank goodness I found this site and took some time to think about all of this and have it out first chance I got.I fear the long term effects and i'm certain my easy removal was due to it's short time and my body's good sense to try to get it OUT. I thankfully had no infections and again, removal is so NOT the *Want to kick your Doctor in the face* ordeal the insertion is.

I can't wait to see the responses from those who are nieve enough to believe that everything works the same for everyone, and I hope they hold on to my email address to keep me updated in a year or so when they too are finding themselves at a complete *loss* for their sudden lack of desire to live...or daydreaming of maiming those they once cherished.

sorry for the rambling...gotta love hormones !

I think Yasmin is great. I understand, though, that not everyone is going to react the same way to a certain birth control pill. I have been on some that have made me pretty close to impossible to live with. I do, however, have a problem reading about all these so-called side effects of Yasmin that can be attributed to something else.

For one, Caffeine. Birth control slows the metabolism of caffeine in our bodies, making that one cup have a much stronger effect on our bodies. If you drink caffeine daily, look at the symptoms of too much caffeine, as that usually amount before Yasmin can now be an overdose for your body.

Symptoms of too much caffeine:
-Jitteriness
-Difficulty sleeping
-Headaches
-Anxiety
-Flushed face
-Nausea
-Accelerated heartbeat
-Increase Blood Pressure
Etc. (look up in google more if you want)

So if you experience any of those symptoms on Yasmin and drink caffeine of some kind, try cutting back first. It might not be the Yasmin. Any birth control will increase the effects of caffeine on your body. (Some possibly more than others)

Secondly, look at how much water you are drinking. Yasmin has a diuretic in it, causing our bodies to lose more water. Are you drinking enough to replenish what is lost?
Symptoms of dehydration include:
-dry mouth
-the eyes stop making tears
-sweating may stop
-muscle cramps
-nausea and vomiting
-lightheadedness (especially when standing).
-The body tries to maintain cardiac output (the amount of blood that is pumped by the heart to the body); and if the amount of fluid in the intravascular space is decreased, the body has to increase the heart rate, which causes blood vessels to constrict to maintain blood pressure.

Seriously, if you are thirsty, don't reach for the soda. Grab some water. It might be what you need.

So, again, I know, not every birth control will work the same for everyone, but at least look at what you are doing first to see if it's you or the birth control causing the problems. Don't blame Yasmin for giving you anxiety when it could easily just be the amount of coffee that you drink.

If you've cut back on caffeine (for more than one day now) and been drinking more water and you still have problems, switch, by all means. But make sure it's not something else first before blaming the birth control.

I took it for 3 days with extreme nausea, some heart racing, palpitations, headache, restless leg and insomnia. Then 4th day, I was afraid I needed to go to the ER - extreme heart racing, palpitations, numbness in left arm, tingling in hands and feet and feeling like I was about to faint. I waited it out for an hour and a half and is slowed down. But now after about 18 hours, my fingers are still tingly and feeling heartbeat in my neck.

My dermatologist prescribed it for an infection after a derma-filler injection. The side effects were not discussed. My ENT agreed that the med was best for my infection but did not seem concerned over the initial symptoms.

I have a heart murmur and cannot take anything containing pseudoephrine - this med acts like a mega dose of it!

I took Yaz for a couple months and was fine during that; however, about a month ago my doctor switched me to Yasmin(I have been on BC for years however, the ortho brand). I've been in the most pain in the past month than I ever have and I'm usually pretty good with pain and just try to take advil or something... but the symptoms have only gotten worse. I finally decided to google my symptoms and I found a lot of people on Yasmin had very similar symptoms. I have the worst anxiety like there's a lump in my throat and sometimes I'm literally grasping for air and I always try to drink a lot of water or cough or eat or burp to make it go away but it doesn't until I wake up the next day (sometimes). Also, I have never ever experience migraines in my life, but the past month I have the worst headaches imaginable. It happens at least 4 times a week; at first I thought they were caffeine headaches because it would sometimes help, but the past 3 days my headache has pretty much been constant (usually located near my temples/eyes). I take probably 8 Ibuprofin a day and drink an excessive amount of caffeine hoping it will make it go away, but it doesn't. Along with these problems I've been feeling lightheaded more often and usually have to sit down immediately or else I feel like I'm going to faint. The biggest/scariest symptom is my heartbeat and chest pain. Heart disease is extremely dominant on my moms side and almost all of her siblings have already had at least one heart attack. Lately my chest will hurt extremely bad, then I feel like my heart rate is just freaking out; I can feel my heartbeat from anywhere on my body and it's very intense. And then because of all of this going on, I always start to freak out and realize i'm getting extremely anxious so I try to make myself take deep breaths but nothings works. The past 4 nights I've been up til like 4 a.m. because my heart rate is so high and my chest hurts so bad in every position I try to lay in that I'm constantly moving. I never thought about going to the doctor because I thought it would get better but now I'm starting to think I should... I'm just wondering if anyone else has/had any of these problems from this medicine and if you've done anything to get rid of them.

(a couple other minor symptoms I've noticed recently are: joint pain and rapid memory loss (I'll be in the middle of a sentence and completely forget what I was talking about and blank out))

Hi Ladies,
I have also been having some problems with my Mirena. I had it implanted in November 2008. Since then I have had severe cramping, with pain that goes down my right leg. I can cramp at any time during the month, not just during the period. I feel like I am really tired,weak, and fatigued sometimes too. I have ringing in my ears that sounds like a heartbeat.

But to me, the worst thing that has happened so far is having longer periods. Sure enough, the period is light enough for me to wear a pantiliner the whole time, but they tend to last forever. The first period lasted for over a month. The second one for almost a month, and now this third one has been going for over a week now. I had the Mirena implanted so that I could have a more free sex-life with my husband, but being on my period all the time definitely defeats the purpose. My doctor said," Oh well it says it in the pamphlet: where it says may cause spotting or bleeding in between periods." I told her, yeah but you didn't tell me a period for a whole month straight. She said that there are some women that this same thing has happened to, and even a woman that had a 3 month long period.

Sometimes, I feel like my doctor tricked me into this and didn't really tell me all the risks and things that could happen to my body. And she definitely didn't tell me it would be as painful as it was when I had it put in.

I am still debating about having it removed because I like not having to take pills everyday. (That's how I got in trouble the first time.) But it is definitely very irritating to my body.

For those of you who say that your husband can feel the Mirena, you can have your doctor to shorten the strings. That is what my doctor did for me, and I never had any complaints.

I was recently diagnosed with ulcerative colitis and was hospitalized in March 2008 for pancreatitis - a reaction I had to Asacol. A week later I was discharged then went back to the hospital a day later for a severe flare-up. There, they started me on antibiotics and prednisone through an IV. When I left the hospital I started taking 40mg. The initial side affects were severe sweaty palms, racing heartbeat and dizziness. Within 2 weeks I started experiencing insomnia, acne, hair loss, extreme mood swings, depression, anxiety, and was OCD on top of the sweating to where the skin on my palms was starting to peel. It suddenly got out of control fast. I became suicidal - nearly attempted suicide twice. I was paranoid, had severe lack of concentration to the point that I felt cognitively delayed, couldn't do anything on my own, lacked emotion, and felt that I WAS crazy. Luckily my family was very supportive. During the second suicidal attempt they begged me to stay at a psychiatric hospital. I did and was there for about three days. A week later I was finally completely tapered off prednisone. Within 2 weeks I was completely normal and back to myself. My three months of hell was finally over. I tell myself I will never take prednisone ever again but the truth is it might be the only thing down the line that can save my life. I hate this drug and I don't recommend anyone take it unless it's the last option you have.

My 13yr old niece has always been a healthy, active and straight A student. Then on 11/5/08 during a routine physical, she received her 1st dose of Gardasil. On 11/28/08 she started to complain that she felt weak and had a headache. Since it was 2 days after Thanksgiving we thought that she was tired from all the holiday activities. On 11/29/08 she had a headache and stayed in bed all day. She got up that afternoon & had 2 seizures. She was rushed to the ER.
As of today, March 8, 2009 she is still in the hospital in Intensive Care Unit. She has been in critical condition since. Within 2 days after her seizure, she lost the ability to eat,speak,walk and communicate in anyway. She is completely unresponsive. She is on the ventilator, she is basically in a coma. We do know she has an viral infection with a shadow on the left side of her brain. All of the testing that has been done all show negative for any illness or diseases.
We are still unsure if she will come out of this. This has been completely devastating to our family.
We have no answers from doctors. Even though we know in our hearts that this was a side effects from Gardasil. I don't know if they will ever fully admit it.
We are left to watch and wait. That is what the doctors tell us daily..

I also was prescribed Levaquin for a sinus infection. I have a PAINFUL tingling sensation in my hands, feet and legs, as well as a rapid (POUND OUT OF YOUR chest) heartbeat. When will it go away? The doc said as soon as it was out of my system, the symptoms would stop. How long will that be?

I never ever read side effects listings, and I didn't when I took this medication, either. One hour after I took this medication, I felt hot and became very irritable, then my face turned bright red, and my blood pressure went so high I could feel every heartbeat, and heard ringing in my ears. I had complete brain fog, and barely remember the evening. I became angry and snapped at everyone. I was jittery and anxious and barely able to sleep. Two days later, I am still feeling some of the jittery, foggy feelings.

I have read soo many negative responses in regard to this medication you would think these people are all in the medical profession and could diagnose their symptoms as being avelox triggered.For a few of these people that could be true but unlikely.People have this tendency to read about side affects and believe they are having them.For a minority of people thats true,thats why they are called side effects.I have been taking this drug for 4 days now and I am feeling great!!! I started out with body aches,fever,severe sore throat and sinuses that would not stop.By day 3 only minor sore throat remains.

I am so relieved to have found this web site! I had my Mirena IUD placed in early October 2008. It hurt a bit when they put it in like birthing cramps. I had some cramping for about a week but it was tolerable. I had spotting for about 3 1/2 months. I had one period about a month after placement which I experienced the worse cramps than ever before. Since then no periods and no cramps. Every now and then I will get some spotting, but no big deal. I have noticed an increase in acne but it's livable. I have had headaches of which I never got before. I haven't slept soundly for the past 10 years after my husband died because I know I am the only one here to protect my children should anything happen during the night. So I wake at every sound and make sure all is ok then go back to sleep. It's been different since the Mirena IUD. It's gotten much worse. It takes me a LONG time to get to sleep and when I do, my night is filled with intense, long-lived, vivid nightmares! (up to 4 a night) After which it again takes me a while to get back to sleep. What I am incredibly concerned about, though, is the emotional side effects that I have experienced! I have slowly become a basket-case. I have at different times experienced the following side-effects : anxiety, minor paranoia, racing heartbeat, MOOD SWINGS! unexplained crying episodes, foggy thinking, and panicky feelings. They don't all come at once and when one would occur, I dismissed it as weird or due to stress or whatever. I am not sure how long I have been experiencing them because it happened so slowly. It sort of all snuck up on me. However, in the last week or two, they have really made an impact! Two weeks ago, I remember telling a friend at work that something was wrong with me. She said "Oh you are probably just stressed or something. Don't worry about it." I said "No! I really think something is really wrong with me." I was scared to push it because, I don't know, I didn't want to sound like a freak. Then came this last Friday. At work, on my lunch hour, I just sat and cried for no good reason! Friday night it was unbearable. I HAVE NO REAON TO BE DEPRESSED! Saturday really scared me! I felt like I couldn't live this life! I was a mess!!! Thank God for my friend whom I called out of sheer desperation and who talked me through it! I had previously wondered about the effects of the Merina IUD but Saturday evening I immediately began to do the research (in between my crying fits that I had no control over). I found a little bit of info but just basic stuff like it can cause "depression and other mood changes." I knew something was terribly wrong with me and I needed to find more detailed info! (I am normally a fun, happy, in-control, go get 'em kind of person. I have to be. My husband died 10 years ago and I have had to raise my three children completely alone. A person has to have it "all together" to accomplish what I have accomplished! Let there be no question about that.) Now it's Sunday and I woke up this morning no better off. The crying fits have been even more often and all day long! My children have been scared for me because they know this is NOT my normal behavior! I just told them I would be ok. They have hung in there with me all day! I knew I had to just roll with it until I could get to my doctor tomorrow because there is no controlling them. I finally came upon this website this morning! OH! THANK YOU ALL SO MUCH FOR SHARING YOUR STORIES! I thought I was going crazy! I will be on my doctor's door step first thing in the morning to have this beastly contraption removed! They WILL fit me in their schedule because I WILL NOT leave their office with this IUD in my body! Sadly...Valentine's Day is around the corner so too bad for me and my boyfriend! I can't handle another week with this...so I have to do what I have to do! I understand that some women have good stories to tell about their Mirena IUDs but they seem to be few! If a woman was contemplating it and asked my opinion, it would be this.."Do what you think is best, but weigh the consequences first! I personally regret having it! It's been hell!" All I hope now is that it doesn't take much longer to get back to normal after the IUD is removed because I can't live like this! I hope I have helped another woman like me in writing this.

I have had 3 injections of Lupron. The first one I felt no side effects, the second came with miserable hot flashes, and with the third my life changed dramatically. Along with the hot flashes, were insomnia, extreme anxiety attacks and a racing heartbeat. I will not take this drug again. It has been over a month since the last injection and symptoms have not gone away. I was prescribed xanax for the anxiety and ambien for the insomnia. They help, but after 3 weeks I am still miserable. Does anyone know when this stuff gets out of your system?

I took my first 500mg Niaspan ER at about 1130 after eating an apple. At 0115 I woke up and my body from head to toe was on fire internally. I got up out of bed went to the bathroom looked in the mirror. It looked like I had a bad sunburn from head to toe plus my face,arms, hands upper torso were swollen. I do not recall any increase in my heartbeat. I went to the ER and by the the time the doctor came around I was some better. I did experience severe itching and cold chills for a while. I did not know about the aspirin for help. Am awaiting further directions from my cardiologist. I have never experienced anything like this before.