Severity symptoms and conditions

it's been about 2 months since my Mirena REMOVAL and I am just now starting to see a clearing up of my skin on my face and back. My skin was so bad. I had cystic acne on my back and arms and oily skin on my face and back. It's so nice to scratch my back without feeling thousands of bumps lining my neck and back.
*I feel better emotionally too. I am not getting irritated or angry as easily as i was when i had mirena in place.
*No more odor or discharge
*i'm still losing my hair but I think it's starting to slow down
*My knees don't hurt as bad as they used to.
In General I feel better and i'm getting better every week. I am sooo glad that i had it removed and that my life can continue now without such horrible side effects. It seems like it's taking a long time but that's ok as long as i'm making progress. I had it for 20 months so it will probably take a little longer to be cleaned out of my system .
Good Luck ladies.

I have had Mirena for 2yrs now and have been lucky enough to not have any side effects...at least I think. I am 23 and have never had a child and was suggested to use Mirena due to my horrible periods. I literally went to the ER a few times due to the severity of the pain. Now that I have it I do not have that sever pain anymore.

My question to you ladies is...Iv noticed, before but now more recently, that during intercourse if my partner goes too deep I get a sever pain. Also I will experience cramping the next day and begin to bleed. Almost as if the intercourse began a menstrual cycle. This happens even after I have a "regular" cycle. Has anyone else experienced this?

ok, so I am 28yrs old just had my lap for endo on October 1 and my doctor has recommended lupron, and am going to be getting the med in a week to 2weeks,but after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do,and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? did any one have a baby after doing this. my bigs thing is being able to have a baby. Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I am trying to find out if anyone has experienced 5 minute delayed reaction from Lamictal. My 18 year old son has been on Lamictal for over 3 years. He started out at 200 mg, had a breakthrough seizure after 1 1/2 years and is now on 600 mg. Since they increased him, he has episodes about every two weeks where he feels really dizzy and then forgets what just happened five minutes before. His short term memory is getting progressively worse. You wouldn't know anything is wrong if you were talking to him, but since he has had four grand mal seizures, he knows something is up. Any ideas would be greatly appreciated.

I stopped Yaz about a month ago after being on it for a year and a half and should have had my period a week ago. Freaking out, I took a pregnancy test but it came back negative and I couldn't think why I would be late.Even before I went on Yaz I always had very regular periods, always on time and always for the same length of time, Yaz did help with the severity of my periods and the length of them. My husband suggested that it may be something to do with me quitting Yaz...has anyone else who's quit taking it had these side effects??

I was prescribed Lisinopril last September due to hypertension level blood pressure that was at "emergent level" as determined in the ER. I had no other pre-heart attack symptoms other than headaches at night in sleep..

Prior to taking the RX I was doing 1 hr gym works outs 3-4 times per week, walk/jogging 3 times per wk 2-3 mi ea. NOW I'm lethargic and fighting to keep active. Joints are easily taxed and take several days to weeks to recover from what used to be routine.. Cough is dry and hits at night or day and leaves a general feeling of fatigue. Memory is impaired. Twitching muscles all over like little electrical impulses being shot off and extreme cramping of upper leg muscles when sitting down to stretch. Intermittent "heart flutters". Nothing I've every experienced before.

I'm heading in for followup now that I've read this forum. I had no idea of the severity of side effects. Here I thought I was being saved from eminent heart attack or stroke.

Raising two children and can afford to be lethargic or forgetful or worse.

Thank you all for your postings. You are indeed the life savers.

D.

I have been prescribed a 20 day course of flagyI. I was prescribed this med for a uterine staph infection caused by an iud...as you can imagine I was ready for any antibiotic that would bring relief. I tried a few antib's (Cipro, Macrobid, Doxycyline) before flagyl while the drs waited for the culture to return from the lab...flagyl brought immediate ( 24 hours) help with the staph but causes metal mouth, a woozy feeling and a strange aching in my feet. In my situation the side effects are worth it...Also the severity of the side effects have been temporary, as the bacteria die off the toxins they leave behind will leave your system and ease the side effects. It is important to replenish your natural bacteria while taking antib with probiotics in yogurt and supplements this helps me with the yeast problems also taking Caprylic Acid and coconut oil have kept yeast under control. Stopping your antib treatment before the course is through can cause a relapse in your symptoms worse than the original illness and can cause antib resistant bacteria...MRSA (bad stuff!!!) I hope this helps you.

Wow, thank you all for your postings. I just wished I had found this before I had Mirena put in. I had it placed in Feb 2009, it's been exactly 5 months. I have been extremely tired and agitated. I didn't really associate this with the Mirena until reading the other posts. My hair comes out by the handful (with root attached), I never have solid stools, I have gained about 10 pounds even though I have been trying to lose weight through a diet and exercise program. All the weight is in my stomach and people keep asking me if I'm pregnant. I started to wonder if I could be seeing as I was crying all the time, extremely moody, and that I look at least 4 or 5 months pregnant. All pregnancy tests have come back negative. I got this put in the day before my fiance and I got engaged ( not knowing at the time) and last week we were about to call of the wedding because of my emotional state and constant conflicts. I have to wonder how much of this is caused by the Mirena. I have already made an appointment to talk to my doctor after reading what all these other women have been through. It's just so tough because with any type of birth control their are side effects so I don't want to make it out to be like this is the worst thing ever, it may be exactly what someone is looking for, but just be informed that there are some side effects because I like a lot of other women on this post was lead to believe that there were no side effects or very little side effects.

Well, my Fiancee (Sandra) started taking Topamax a few months ago. Her side effects have included: loss of energy, tiredness, tingling in the feet, nausea, chest pain, appetite lose, rapid weight loss, and a severe decrease in her sexual drive. The worst of the side effects is her sudden and unpredictable mood changes. She verbally assalts me and her children all the time. She is aggressive and picks fights over anything and everything. I love her with all my heart but I can not live like this. So bottom line, Topamax has gotten rid of her migraines and/or decreased their frequency and severity. And the cost of that benefit is the destruction of the relationships with the people that love her most.

ok, so I am 28yrs old just had my second lap for endo and my doctor has recommended lupron, after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do, my post-op surgery appt is this week, and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I was wondering.......it hurt like hell when it was inserted. For those of you that had it removed, "HOW BAD DOES THE REMOVAL HURT?" I am afraid to have it removed but know it is necessary.

I've called my doctor and am waiting on a reply from the nurse. I want my Mirena removed. I posted my symptoms on May 8th. I've had mine in for 4 1/2 months.

My symptoms are in order of severity:

*heavy bleeding 3 out of 4 weeks (pads or tampons with breakthrough bleeding and pantiliner 24/7)
*acne on my back, butt and jawline (going to Derm. and using ProActive)
*I've gained 15 lbs in the past 4 months and it won't come off
*headaches
*a sore spot in my spine (I was fearful I had cancer)
*facial hair
*bloating (I look 4 months pregnant 1/2 of the time)
*low libido
*irritable and moody more than usual
*sore breasts

Reading all this horrifies me since I have been on Remicade for almost 4 years for Crohn's and a still unidentified Inflammatory arthritis of some kind. I will pray for you all. But, on another note and by no means an attempt to diminish the severity of each account in this blog, I have had no such side effects and for the most part have had great success until recently. My Crohn's is and has been in complete remission since the beginning of the infusions. However, I have had increasing inflammatory issues in joints between infusions. I get 5 vials and they give me Solumedrol in the IV. I ended up in the ER last night because my joints were all frozen up and it was just unbearable. They gave me Solumedrol and Morphine, and I am 75% better today. The frequency and severity of the arthritis issues has gotten increasingly worse over the last 6-8 months. I get infusions every 8 weeks, and start to have severe joint pain after about 4 weeks. All that being said, it is appearing like Remicade is still working brilliantly for Crohn's but is having little to no effect on the inflammatory arthritis. The steroid they give during the infusion is what I think is doing the job for the joint pain since I was a 10 last night in the ER, and I am 3 this morning pain wise after getting the steroid. My case is unique and frustrating to the Rheumy b/c my sed rates and RA factures and C-Reactives are all relatively normal when I am in tremendous pain. So, they just ran alternate tests the other day to look into things like Myeloma and so on. I don't believe that Remicade has done any of this. I believe that Remicade's benefits for MOST people greatly outweigh the risks, especially when you are incapacitated with Crohn's etc. But in my case, it just does not seem to be working for my joint inflammation.

Thanks, everyone! My (brand new) doctor had convinced me that I was simply experiencing anxiety to explain my side effects. After being off Lamictal and all medications for several months, and then restarting on Lamictal only, I noticed all the following side effects, some of which I've had before, and some completely new. Also, the ones I'd had before came back at a level of severity which I had never experienced.

One familiar side effect was hand tremors and general shakiness which sometimes also affected my speech. Even strangers would notice and ask me if I was ok. Luckily, this was during this past winter, so I would basically lie and just say I was cold and a bit shivery. Another familiar side effect that a lot of others are mentioning are cognitive issues and short term memory loss. Sometimes I felt like my tongue was lazy or I felt tongue-tied, and I couldn't get it to work right to say the words I was thinking. Sometimes, I just plain lost my train of thought or couldn't think of the words to express what I was thinking. I'd all my life been prone to mishaps of speech like occasional spoonerisms and such, but on Lamictal it was happening probably daily, and I'd even started stuttering. Teaching and explaining often difficult concepts and public speaking is part of my job, so this was causing me a lot of anxiety. I, too, completely blanked on spelling out words when friends and colleagues relied on my spelling abilities more than their computer's spellcheck. I also thought I was having sudden leaps in experiencing getting older (early 30's) because of my memory, I typically have an almost photographic memory and can picture where I saw my keys last or what have you, but all of the sudden I couldn't even piece the photo together anymore or it was foggy in my memory.

The newest side effect also experienced by others was clumsiness not only of my own body but of my surroundings. I suddenly noticed that I was doing things way more often like tripping, falling, stubbing a toe, nicking a finger, dropping things, etc. Where I was an excellent parallel parker before, I'd get out of my car and realize I'd parked 2 feet from the curb and crooked.

I decided to look up Lamictal's side effects after discussing this with my excellent talk therapist because I was extremely frustrated with my new doctor telling me I was just anxious and there was really nothing he could do for my (imagined) "side effects." And here everyone is experiencing the same thing. I don't think I should be made to feel like I don't know any better and that I should suffer the REAL side effects of this drug. I didn't study medicine, but I still have a degree in biology so I'm not so stupid that I'll believe anything any doctor tells me.

I think I would almost rather suffer a mild mood swing than suffer these side effects. I'm going to try to look for something else.

I LOVE LANTUS!!! I was diagnosed as Type 2 Diabetic in December 2008 when my blood sugar was 550 and I weighed 265 lbs. I am a 51 year old 6'tall woman. My physician prescribed 55units of Lantus am and again pm. My blood sugar now is between 80 and 110, and my weight is 180lbs. I take Lasix and Spironolactone for any swelling and have felt great ever since. I'm sure i'm very fortunate, but I must stress to be under the watchful eye of your Physician. Yes, there are other hormones that help with blood sugar levels, but please understand that it depends on the type and severity of you diabetes. I also can't understand anyone who has been told by two different physicians that she needs insulin but won't believe them. These physicians have nothing to gain financially from this. I just hope you have good insurance. If Lantus isn't right for you, fine, but PLEASE get professional guidence if you have Diabetes. The internet is NOT always the most informed source of information. A. in Austin

I share the scare - I developed a bacterial infection after surgery and had an allergic reaction to first two antibiotics so was given Avelox. About an hour after the 1st dose my eyes became bloodshot, my joints ached like I had the flu or severe arthritis and I started having jolts of pain in different places, legs, groin, neck. I became disoriented and developed tiny blisters on bottom of feet, behind knees, on neck they faded, and at base of my fingers. The second dose caused severe joint and neck pain, disoriented feeling and again blisters. My doctor had me break the pills in half to take twice a day with benadryl. I also took large dose of Ibuprofen an hour after taking Avelox. That helped lessen severity of side effects. Final straw was the fifth dose - took before sleeping, woke at 4am and could not move from neck pain. My husband pulled me up so I could use the bathroom with me crying from pain. Sitting on the commode, I threw up and started to pass out. I managed to get downstairs and take an 800 mg. Ibuprofen and passed out for about 30 seconds. We went to ER. The attending physician decided I was having a muscle spasm and dismissed my fear it was the drug. They gave me a muscle relaxer and sent me home. I slept like the dead. My doctor called me that afternoon and told me to stop the Avelox immediately. You can imagine after missing 5 weeks of work for surgery, then having to miss three days last week and who knows this week how bummed I am. I am 46, have a wonderful family (a husband and 4 kids), a job I love, and life is good. I hope my body can recover soon as I am not used to inactivity. I cannot seem to function normally anymore.

Started taking Topamax about a month ago for frequent migraines. I used to take Axert 2 to 4 times a week. If I did it at the beginning of a headache it worked very well, with little or no side affects- just got tired of having so many headaches. Started the Topamax and worked up to 100 mg per day (50 am 50 pm). Seems to control the headaches well, down to maybe one per week and I think less severity.

Side effects so far: 1. Perhaps some memory stuff as described by others (hard time spelling formerly familiar words etc... but doesn't seem real obvious to me (maybe to other!!!). 2. Diet Coke tastes terrible like everyone says!! This one hurts cause I love diet coke. The good news is that I don't notice the effect as much now a the first couple of weeks.
3. I have frequent (emphasis on frequent) diarrhea- like a couple times a day four to five days a week. This one doesn't seem much better. Now there has been some associated weight loss as reported but Im not sure that is due to reduced appetite or daily diarrhea or both. Either way I was glad to loose the ten pounds I needed to loose anyway, just wish I could do it without spending so much time in the bathroom.
Have not had any of the tingling in the hands or fingers that others have reported.

Soon after receiving the first of three Gardasil vaccinations, my daughter started experiencing daily headaches which progressively worsened. Her doctor said that it wasn't likely to be a side effect of Gardasil. Over the next year, she was referred for vision testing and had a CT Scan and MRI to try to diagnose the chronic headaches which had become quite severe and often debilitating. No cause was found. She was given prescription after prescription which didn't help- and often generated additional side effects that made her feel worse. A year later she still has undiagnosed headaches and takes a prescription medication twice per day to lessen the severity of the headaches. Only recently did we find an article relaying the same story- linking the headaches to Gardasil vaccinations. With no health issues prior to the vaccinations, no underlying cause found following many tests, doctor referrals and medications, and the fact that this all started immediately following her first dose of Gardasil, we suspect this is what instigated the headaches.

so, I was prescribed Avelox a week ago to clear up an infection caused by a ruptured ovarian cyst. I went on-line tonight because each night since I've started the medicine, I sleep less. I have turned into a total insomniac. I remembered the name AVELOX when my doctor prescribed it but I couldn't remember if I had any issues with it when I took it last, or when I even took it last. After reading your posts...it came back to me. About a year and half ago, I was prescribed Avelox for a kidney infection. Within a couple of days after taking the medicine, my right arm became completely inmobile and it was painful to even try to move it. I also had terrible abdominal pain. I went to the ER, only to have them ask me if my "home life was OK" or was I "depressed". They checked for the kidney infection but found no trace of one. I left the ER with no diagnosis...except they thought I was crazy. Gradually, after a week on Avelox, my arm pain went away but the abdominal and lower back pain became so bad that my doctor admitted me into the hospital. He feared the kidney infection (which the ER couldn't find) had gotten very bad. I was there for 3 days and they couldn't find anything wrong with me.They again couldn't even find any trace of a kidney infection. I was not eating, not sleeping, feeling constantly sick to my stomach and dizzy...and the abdominal and lower back pain was incredible. The doctors again were talking to me like I was a crazy person. They couldn't find one thing wrong besides a little dehydration.
I stopped the Avelox while in the hospital after no kidney infection was found. After a few days off the medicine I gradually felt better. Two days after leaving the hospital my doctor called and said that one of the tests they did said I could have possibly been exposed to Mono, so they chalked the who experience to being a possible case of Mono. That never made sense to me...but after reading your experiences, I'm sure it was the medicine. Now after remembering that I had taken this medicine before, I also remember sitting in the hospital drinking coffee! The prescription on the bottle I got last week reads "avoid caffeine". I know I drank coffee when I was on it before and I don't recall any warning about caffeine with Avelox last time. That said, I tried drinking a little coffee the 2nd day I was on it this time (I need my coffee, even though it said no caffeine). I was sooo jumpy, hands shaking, heart racing and lightheaded - like you feel if you drink many cups of coffee with no food - but I had only had a couple of sips. I haven't had any coffee for the rest of the days I had been on the medicine and I haven't felt that way again. I have also been drinking tons of water because the Avelox is making me so damn thirsty. My hands, lips and even my eyes are dry. The issue I am having with Avelox this round is flushes. One minute I'm fine, the next I'm flushed and my face is hot like I was running a marathon, but I was sitting still. Maybe with no caffeine and tons of water, you might feel better while you are waiting for this Avelox poison to get out of your system. Hope that helps. I'm going back to not sleeping...(It's 1:30 am ~aaarrrggghhh)

I'm 43. Started taking Singular about 10 years ago. I think that's when it came out. Over time, I've developed panic attacks, mild depression, mood swings, panic disorder, muscle twitches and cramps, and agoraphobia. I finally slowly took myself off of all medications after doing The Allergy and Asthma Cure - a great book and it helps tremendously!

After being off of the Singular, my symptoms listed started going away. i stay have agoraphobia because that's a learned issue from fear of having a panic attack. All doctors and pharmacists say there's no link. I know lots of adults who have gone through this only to get put on Xanax and antidepressants. Try to go as natural as you can. All of these meds have fried my body. Diet is huge to! I've substituted goat's milk for cow, Try it!

I was diagnosed with 'a "spot" on my chest upper left, after doing an x-ray.I had 100.4 fever really bad chills and sweats, terrible loss of appetite. I am 41 years old. No diagnosis given at initial visit. After 5 days of Levaquin 500, I felt that the dose was too low as I was not improving. When I called my doctor he said, we usually given 750 mil. I thought, well why didn't you do that in the first place? I would be over this thing by then! I was hacking and plenty of phlegm greenish yellow was coming up. He said to use Mucinex DM and Ambien to sleep. Ambien didn't work so I discontinued it. Don't recommend Mucinex at night it keeps you awake, daytime fine. I felt depressed, super fatigue and very anxious, with difficulty sleeping, but thought that is the way everyone feels when sick. I had trouble having my twins jump on the bed to see me, do to the aches, again I thought that is from the illness, now I wonder if these symptoms were exacerbated by the Levaquin . I had the original script that Dr. told me to refill, it was for 500 mil, so he said do another course of that for another 5 days, 1 per day. I did, at that point 10 days total. Still wheezing, I called and said I was still not any better after 10 days of Levaquin 500 and in bed all of the time. Finally I asked him what was wrong, 'bronchitis' he said. I never had it before but I started looking it up before he told me as it had to be that! He said do another 5 days of Levaquin 750. Very hard to get rid of cough still there, however weird wheezing slowly getting better. It is weird though, I have incredible pain on my lower right ribcage from my back radiating to the front. I think it is from being in bed so long, but hope it is not from the tendon issues people are talking about on this forum. My friends who had same symptoms one week before me, (her family and I got bacterial bronchitis from her 4-1/2 son on a play date we had the week before Thanksgiving) was prescribed Amoxicillin 250 per day and was over it in 1 week! My doctor said he didn't like the way Amoxicillin worked over the gastro track. My opinion, stick with the tried and true meds. unless we all become immune to everything, Amoxicillin worked for me with other illnesses in the past and that is what I will be requesting next time! Hopefully there wont be a next time! Good luck everyone. I hope and pray we have not suffered permanent damage from Levaquin!

I am not currently using nuvaring anymore because of a side effect I haven't really found anyone else experiencing. I would like to share my story and if anyone has had the same or similar symptoms please let me know because I am totally bewildered about it. I started using nuvaring after the birth of my daughter in December. I was on the ring for about one to two weeks. At first everything was fine but I started to experience very unique chest pains. The best way I can describe them is they felt like they were in the tissue and flesh in between my skin and my rib cage, and it felt like the area was being squished in a vice, and then my back would start to hurt alot. They first started about once every other day, but then got more frequent to the point when I stopped they were constant. I could not sleep because the only comfortable position was to sit down hunched over with a pillow on my stomach, with my back up against my headboard. My husband brought up the point that it could be the ring, and at that point I was willing to consider anything. I quit using the ring, and the pain stopped, for a little while. But it is still ongoing to this day. Although it only happens about once or twice a month, the pain is no less severe. I am sure it was the nuvaring or the ingredients in it that has triggered this because I have never had this problem before using it. Please if anyone has any advice or ideas, your help would be very much appreciated.

Monthly wicked migraines, right before period starts. Sometimes lasting on and off for 2 1/2 days. I had one so bad I had to go to the ER. I've never had problems with migraines before in my whole life. A few were very bad and makes me not want to do anything all day. I went to the neurologist just to get a pain medication for this.

Also was diagnosed with allergies last summer because I had 2 bad sinus infections.

Recently I have started to have acid reflux every night and now sometimes in the mornings. This sucks!! I am getting this removed.

I did several internet searches over the past several months and all these symptoms are caused by progestin (levonogestrol). This is not worth it.

I've had this thing in for over a year now, but all these symptoms appeared after getting this thing in.

Ive also been very moody around the time of the month, super irritable and bitchy.

My gyne suggested to take another drug to counteract, (basically prozac with another name) but that's like taking speed to counteract a downer. No thanks!!!!!!!!!!

I got this thing put in because of heavy periods, but it is totally NOT WORTH IT!! My health has suffered because of this.

I suffered with pre-menopausal symptoms for 2 years before having the Mirena inserted in May 2007. My symptoms included bad menstrual cramping, heaving bleeding, hot flashes, night sweats, moodiness and lack of libido. But since having the Mirena all those symptoms have gone away. My OBGYN is using it for Hormone Replacement because I am too young (34 yrs old) to have menopause. I felt a lot better after about 3 months, I still have some side effects like hand numbness (mostly when I wake up in the morning or at night). Every couple of months I have some mild break through bleeding and I have PMS symptoms before it happens. I would have gone crazy without Mirena. I do have 1 symptom that I haven't heard anyone mention. Increased bladder infections, I don't know if this is caused by the Mirena or maybe its something else. If anyone has had this symptom can you post it?

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona