Docs symptoms and conditions

hello, i got the mirena in 2007 and after i got it put in a few months went by and everything was fine. then i started getting sick in the mornings and i thought great this birth control sucks i am pregnant again. but that wasn't the case because i took test and it said no and then the docs told me that nausea was a side effect so i figured i would just leave it at that. but it only got worse i started getting really bad headaches, pain in my stomache, sick all day long, and for some reason i couldn't eat more then once a day but i would gain weight i was depressed and i felt like a complete piece of crap. it also made me gain weight i am 22 yrs old and i have never weighed over 130lbs even when i was pregnant during the 2 yrs i had the mirena i gained 15lbs my expierence with the mirena was absolutely terrible if you ever got morning sickness that turned into all day sickness while you were pregnant this is exactly how the mirena made me feel bloated, painful and sick to my stomache i finally got the mirena removed because i just couldn't take it any more i have been off the mirena for 3 months now and i still can't eat much and it really bothers me i am hoping it gets better because i can't take much more of this. please let me know if anyone else expierienced this!

Folks, I was on this standard diuretic for about 6 years or so. For a very long time, I did not think it was causing any significant side effects (other than having to pee a lot). I was wrong. It gave me type II diabetes.

If you ask MOST doctors and nurses about this, they will deny it strenuously. As one very good PA told me, "diuretics are our first line of defense." An RN just two weeks ago thought I was crazy to blame my diabetes on it.

But it is not my imagination. The ALLHAT study -- which, if you cite, will cause most docs and nurses to shut up right fast -- is one of the most famous studies out there. It was huge, and its authors became strong proponents of diuretics. But the same study found that if you take HCTZ for five years, you have about a 12.6% chance of developing diabetes (versus perhaps a 1 to 2% chance otherwise). I am so angry about this because no one warned me. No one told me this, so I could never make an informed decision about taking this medication. Now I will be fighting diabetes for the rest of my life!

I haven't looked at the insert for HCTZ in a long time, so for all I know they're now finally listing blood sugar issues. But they said nothing when I started in 2002, and no one bothered monitoring by blood sugar either. Even when we finally noticed the glucose readings going up, no one said, "Oh, we should take you off that diuretic."

If you do some googling, you'll discover that there are a (minority) of doctors out there who are also very concerned about this. They argue a lot at forums for doctors. This business about diabetes IS a known side-effect. It's just, as I said, that too few doctors seem to be aware of it, or if they are, seem to feel the need to inform their patients before prescribing it.

Looking back at a post, it was 8 months ago when i first posted re long periods. and I'd had 3 two week ones then. So 11 months of bleeding...I've been to the docs, taken more hormones, different hormones, tried not having sex, tried having lots, but still bleeding and bleeding. Mirena used to be great. Have had it for over 3 years..... but it just stopped working. The acne has got worse.. the mood swings are worse, the dizzy spells before the "period" pain.....

I feel so guilty for recommending it to so many people as the answer... but it just isn't right for me anymore. Got an appointment to have it removed - scared of the removal pain and possible Crash... always struggled to keep hormones in check!

Thanks to all for their posts ... nice to know we are not alone. Would be nice to hear from anyone who has used Mirena to control Endometriosis.... or is thinking of it.... think it's pretty good... but hard to tell as it was inserted when I had my lapaoscapy and removed the adhesions. All Mirena side affects confused with endo.... but still think Mirena is the big cause.... enough is enough. Three years is a long time. (and a period constantly for nearly a year is insane!!) Good luck.....xx

Hello, my name is pam. About 6 weeks after my son was born I had made the choice to get the mirena iud. Well for 7mon after i got it I bleed. Also, new things started happening. I went to my doctor and discovered that I had an awful yeast infection due to the iud not being set right. He gave me one round of meds just for yeast infections. I went back for a check up and it hadn't cleared a bit. Got second round of med. Then about 2wks afterward I got a call from my doctor. He said that they found yeast infection, staff infection, and a strep infection that I am still having problems with after the level 4 anti-biotic that he gave me. I have headaches, body aches, no sex drive what so ever, mood swings that would send anyone away, and I am also on anti-depression meds ever since Ive had the iud.

I feel compelled to share my daughter's horrendous experience, which we (and some of our docs) believe was a reaction to Bactrim. Her chills, high, high fever, night sweats, itching and majorly swollen lymph nodes mimicked lymphoma. She had a biopsy of one of the swollen lymph nodes and it revealed Kikuchi' s Disease or Kikuchi-Fujimoto's Disease. Google it. Thankfully, it was benign and self-limited, but it made her very very sick and it was scary and most probably triggered by her allergic reaction to Bactrim - taken for acne. We will never take this drug again.

I really did think i was crazy. I found this website and started reading everyone's stories. well here is mine:
I got the Mirena September of 2008 right after my son was born. I have never been on birth control before.The docs really insisted i get the Mirena..so me thinking wow not having to take a pill everyday and 99.9% sure it works. Well stupid me i went for it. At first i liked it a lot didn't hurt when i got it, no bleeding it was great. Well now reading the side effects i am going crazy. I have these dizzy spells were i want to get sick, headache every single day, i got these rashes above my eyes and had no lcue what they were and now i wonder if its from the Mirena. Not wanting to have sex at all, i am always in a bad mood. Tired all the time, never want to go out, i wear t-shirts and short all the time, and last but not least I gain LOTS of weight like 25-30 pounds. i was smaller after having my son than i am now. I had to be on a waiting list to get the mirena so i guess i lost all the weight and didn't look bad at all now after getting it and can not loose this weight for anything. i am only 21 and i run everyday eat healthy bc my parents are health freaks lol. so on Thursday i am getting this thing outta me. I kinda want to schedule for and ultrasound to see if i have any cysits or anything bad bc its horrible.

I took levaquin (750) for a bronchial infection about 9 months ago. My doctor gave me individual samples with no info. on any side effects. Like most people, I trusted my doctor and took the pills without question. The aftermath has been a complete nightmare as I have suffered severe joint pain, depression and an atypical anxiety that at times that feels like a drug induced brain fog. I've seen numerous specialist searching for an underlying process causing the symptoms but nothing is ever found. Since the beginning I've contended that the Levaquin was at the root of my problem, but no doctor has ever given that thought any consideration. Prior to the Levaquin I was perfectly fine with no history of any joint pains or mood disorders. Does anyone have any ideas on how to reverse or heal the process?

I have an 8 yr old son that has allergies and asthma. The allergist recently prescribed Singulair which my son had taken when he was 5. We took him off of it back then due to anger outbursts. By the way, the Dr. said that was not a side effect, but nonetheless the issues subsided. When it was recently added back to his medication list, within 3 days he had anaphylactic type episodes 2 days in a row. The attack started with stomach pains, chest pains and then he couldn't breath AT ALL and turned blue! There was no time to call 911 so I gave him an Epi Pen. The attacks are still occurring yet milder and all his Dr.'s swear by Singulair and think I am crazy. I took him off Singulair immediately and we are still waiting for it to leave his system. I think that is why the recent episodes have been milder. He has been tested for all sorts of allergens which he did not come in to contact with prior to the anaphylactic events. We still have no answers and if I hear one more Dr. talk about how great Singulair is, I am going to freak out!! To heck with these drug companies and doctor's who get perks for prescribing medications without informing us of side effects.

Since on 0.175mcg of synthyroid after thyroidectomy and neck dissection two years ago, I have started to feel great fatigue? I can go to sleep at anytime during the afternoon. I also have a lethargy and malaise of the mind! If you mention this to the G.P., nurse or consultant you get vague looks!! Can anyone help?

I had my Mirena inserted in June 2009 and a few days ago and I started to feel numbness and tingling in my right arm,hand and fingers. Then it spread to my left arm, right side of my face and right leg and both feet. I called the OB/GYN to see if this was a side effect and they told me no. I am otherwise healthy and I even ended up going to the ER 2 days ago because the numbness was so bad. None of the docs said it was from the IUD. They ran all kinds of blood tests and an EKG which all came back normal. I went to the OB/GYN yesterday and had them remove the Mirena!! The OB/GYN thought I was nuts and said that my symptoms had NOTHING to do with the IUD...whatever!! I am so glad it's out and now I hope the numbness and tingling stops soon.

My husband stumbled across this website and first I would like to thank everyone who have posted their experiences on the NuvaRing. Because of you guys I now know I'm not losing my mind.

I started the NuvaRing March of 2008 and I started getting dizzy spells May 2009. I actually got my first dizzy spell when I was driving. Everything started to spin very fast!! My husband had to grab the wheel and tell me how to slow down and how fast to do it. That was the scariest thing ever!! My head felt a numbing sensation in my head. I had a pain above my left eye and it would shoot up my head and down my neck. The dizzy spells would come whenever, once every 8 days to twice in one day. I have had an MRI and an MRA done and nothing. The docs have had me on so many migraine meds to try to get a handle on this and nothing has helped. My longest migraine lasted for 14 days, that was in May. This month (July) I got a migraine on the 13th, took the ring out on the 21st, and had a dizzy spell this morning but this afternoon and especially this evening I feel amazing.

Since getting on the NuvaRing, like so many of you, my sex drive does not exist. It has caused so many fights between my husband and I. Its hard to tell him that he is still attractive but I can't explain why I'm not excited. So thank you for writing your experiences. He got to read that I'm not the only one and I wasn't making it up.

These last three months have been hell for my family and I. I have been like Dr. Jekyll and Mr. Hyde. So much tension has caused everyone to walk on pins and needles when they are around me.

So lets sum it up here, after being on the NuvaRing for 14 months I started getting dizzy spells, migraines, nausea, neck pain, twice I've puked because of the room spinning so damn fast, and very very VERY low sex drive.

I'M NOT CRAZY!!!! :)

I started taking Lisinopril two weeks ago for relief of high blood pressure. Male, 45, 260 lbs, family history of high blood pressure and stroke. After one week I began experiencing intermittent chest pain, tingling and numbness in my left hand, and sensations like shocks in my head.

I spent several sleepless nights feeling for chest pain, feeling my heart race, expecting my heart to explode and wondering if I should go to the ER.

I visited my doctor and expressed my concerns. She immediately performed an ECG and verified that my heart was functioning normally and that my blood pressure was down. She also indicated that it's not uncommon for vasoconstrictors like Lisinopril to allow stomach acids to rise in the esophagus. This can cause chest pain and affect nerves leading to the brain and to the arm. She prescribed Zantac 150 twice a day and asked me to call her at home 60 minutes after taking the first pill.

I filled the Zantac prescription (one of the $4 prescriptions you can now get most places) and took one immediately. Ten minutes the chest pain was gone. Twenty minutes later the shocks in my head were gone and my arm went from tingly and numb to just slightly achy. Thirty minutes later all of my symptoms were gone. After an hour I dutifully reported to my doc that she was a genius and on my Christmas gift list.

If you're taking Lisinopril and having chest pain obviously let your doctor know about it. Studies indicate that denial is a serious issue and a contributing cause in heart disease victims. Many of my symptoms were classic for unstable angina, which is scary. However, they are also common stomach acid symptoms for first-time users of a wide variety of high blood pressure medications. It's possible that a simple antacid could relieve your side-effects.

Now my goal is to lose 80 lbs so I can get off this medication completely. Working 90 hours a week (the highlights of which are travel, sitting at desks, and eating) isn't going to cut it any more.

Hi. I just had a laproscopy done 3 weeks ago for endometriosis. I am 26 yrs old and have been dealing with this pain for almost 2 yrs now and it is the worst pain in my entire life. My doctor is now suggesting Lupron because even after the laproscopy the endometriosis was level 4 and had bonded to my intestines and literally trapped my ovaries and uterus against the lining of my stomach. The pain was a 15 to say the least and the past 3 mos it had landed me in the E.R. Finally the docs figured it out. I started my period 2 weeks after the surgery and the pain was still pretty bad. An 8. Now I am seriously considering Lupron. My health is on the line and this pain is not right. At this point I am considering a hysterectomy if Lupron does not work. Any help suggestions please? Monday I follow up with the Dr.

I took wellbutrin for a year. At about month 6 of that year I noticed a spot in the center/ front of my head, (right before my hair line) thinning a little. Didn't think much of it; I had enough hair for three people, no joke. That is not the case today. I quit the wellbutrin and have been off it for a year and i wish i could write to tell everyone it grows back, but for the life of me I cannot seem to get it to stop falling. the top of my head is the worse but hair comes out on the sides as well. Ive tried everything from vitamins, holistic docs to just running everyday. Ive had thyroid tests, blood test... everything except hair loss drugs because I don't believe this is the case trust me. Even if it were it seems to ridiculous to treat the side effects of one drug with another that also has side effects.

i have had my mirena for about 1 1/2 months now, and so far i love it, i have had the spotting for the first month which doesn't bother me and now my period is on and i do have very bad diarrhea which im sure is associated with the period more than the mirena itself. haven't had any lack of sex drive in fact i 've wanted to have more sex, and i haven't' been irritable or anything else, so some of the side effects i believe everyone is having may be made up, think about it if you read over and over and over again how bad the mirena is your going to begin to feel that way i know if i tell myself that my arm hurts all day long then eventually it feels like it hurts..neways all im saying is relax stop reading these scary ass posts and do something to take your mind off of it, i know 3 other people who have the mirena that live down the road from me and NONE of them have had any of these problems...ladies i think you are just trying to find something to blame it on...

I have been taking 40mg Omeprazole (by APOTEX) for one week. At 3am Saturday 6/20/2009, I woke up with a severe itchy rash from head to foot. Over four hours, I took 125mg of Benadryl, but the rash got worse, At noon, I went to the Emergency Room at UPMC Shady side. They gave me intravenous steroids, but this had no immediate effect, After three more hours, they admitted me to the hospital. It wasn't until almost midnight before I began to have relief. I was discharged the next day. I have been instructed to never take Omeprazole again.

I have had the mirena for 2yrs. 1yr from the day my Mirena was inserted I was diagnosed with a UTI. Now 2yrs to date I have the same symptoms. I have had kids and did not have UTIs. My docs has taken cultures and they have come back negative. However, I know what I feel. I am really glad I found this site also. I'm really mad bc I have tired a few methods of birth control and they work well-the side effects always get the best of me after a year or two. Well thanks for the input and I am really thinking about taking this thing out.

i just had a baby 7 months ago and wanted to get the MIRENA b/c i never remember to take my pills....I got it inserted in Feb of this year.....i got it removed yesterday b/c of the same side effects that you all are having...when i was telling my doctor the reasons why i wanted it removed 1st she told me that it might be a problem b/c i hadn't had it in a full 6 months yet...then when i was telling her that i don't care about that i just wanted it out of me...she tried to tell me that it could be due to postpartum depression...i told her that i understand that but i wanted it out....she kinda offended me telling me that i might need to talk to someone...i know my body just like im sure you all know your body and i wasn't comfortable with it in...she did finally take it out and apologized if she upset me....i told her that it was cool i wasn't mad (cause that sucker was out!!!!)...these doctors and health care providers swear by this and like most of you have stated they don't think that one thing has to do with the other...ladies if your mind is telling you to take it out TAKE IT OUT!!!!!!!!!!!!!!!!!!!

I took yaz for maybe two weeks. after one week my breast blew up a cup size. they were so swollen! then i started noticing i was gaining weight but my diet hadn't changed. i started to swell all over within the next week. but what made me quit taking this pill was that i started getting these sharp intense pain in my upper abdominal region. it would come and gnaw at me for like 2-5 seconds then it would just go away. there was also like this temperature sensation anytime i would eat or drink anything. i've been off of it now for 5 days! i still have not got my period, my breast are still swollen, and my stomach pains are still there. i know im not pregnant, because i haven't had any sex! when is this going to get out of system or has it done something to me? i would imagine if you skip your period in one day and you can get pregnant in that one day... the pill should be out of your system! anyway- anyone else have this same situation?

Three and a half years ago i suffered a heart attack, i had three stents put in and was put on Aspirin 75mg, Cardicor, 1.25mg, Tritace 5mg and Lipitor 80mg. I was fairly fit at the time, didn't drink or smoke and ate properly.

But now i'm suffering, i've been to the hospital and my GP, but are told there is nothing wrong, my hear tis good. So why am i suffering with light headedness, pains through my body, back, neck, chest, stomach. So much so i thought i had gall stones or kidney stones. My right knee can't be touched, it is so sore. Chest heaviness, eyesight getting worse, slurred speech, depression i could go on.

I've said this to my doctor, he just brushes it off and says i'm on them for life, ....apparently standard treatment for anyone who's had a heart attack. I walk 5 miles a day, eat 5 or more fruit and veg, don't smoke or drink, do all what i'm meant to. My cholesterol is really low, but so is the HDL too. I was never recommended CoQ10 or a vitamin B complex.

It was my mother who told me to research the side effects of all the meds i'm on. I agree, we all want to live a long and healthy life, but at what cost. I am now of the opinion that doctor's are so use to thinking they are near god like, they have forgotten that we are individuals, that we know our own bodies. I'm sick of the fact that the large pharmaceutical companies send out there sales reps to doctor's surgeries and that is what is deciding what the patients end up taking and not the patient's problem.

DOCTOR'S WAKE UP TREAT THE CAUSE NOT THE SYMPTOMS!!!!!!!

I have had a total of 5 kenalog injections in my back for no disk left between two vertebrae, doc says fused naturally and no movement. I still have pain. I am scheduled to have yet another shot in the neck area, 5 bulging disks causing pain around the shoulder blade. I have less sciatic pain, but I have HEADACHES for the 3 months since the first shot, they don't go away. No OTC pain relief works for these headaches. The doc says the kenalog does NOT cause headaches, I know these guys lie or don't care about the FDA list of side effects. I am hesitant about getting another shot. He wanted me to have this one done under sedation, I declined, since I had the others without. He said more sensitive area and don't want you to flinch. I also get, I assume kenalog injections in both feet for morton's neuroma. Left foot shot worked. Right foot 3 shots and still hurts and numb, they can't seem to get it right. I am tired of getting the shots, and today I went to that pain management doctor and forgot to ask him how long can I expect the shots to help the pain, years? months? or weeks. I barely do anything anymore, afraid to bend, or even move. I had to go to ER first time for my back on 2/14/09 and sent to different docs and finally pain management. For those of you whose docs don't order an MRI for you, I wouldn't have the shot. I had and MRI of the back and neck and this doctor gives the shots while I lay on a fluoroscope table, I can see on the screen in front of me where the doctor is injecting. Hit and miss without an MRI is just not medically correct. Good luck to all and gonna think about whether to get another shot next Thurs.

I made an appointment today to see whats going on.I have been on yaz for about 3 weeks..yes i too have all the same symptoms however i also have a horrible pain right in between my breast..it feels like someone is standing on me.i wake in the night in tears cause i cant roll over i cant pick my 3 kids up cause the pain is always there.... maybe its something else but at the same time im thinking it might be this pill.. as of today im off it.. and when i find out what my doctor says i will let everyone know.. i personally think out of the blue im seeing all these commercials on this pill and doctors are pushing it like crazy so im feeling a little like a ginny puig and no one will tell us this pill is causing all this crap in our lives! so im off to
the docs to see whats hes going to say not too hopeful...

Was prescribed Sulfameth/Trimethoprim for acne when erythromycin and doxycycline were not enough. Dermatologist simply asked "Is there anything that are you allergic to?" I said, "Not that I know of." Took it well for first six days. Looking back, I felt probably the most lethargic during this time, at a job that I loved the most. On the 7th day, after having a great time with the new love in my life, I noticed a heaviness, tingling, and warmness affecting my legs. Went into work feeling too warm. Left about 20 mins in. Had incredibly bad fever this night. Went home, took another Sulfa/Trimeth pill (hadn't linked the problem). Woke up about two hours later, worse than ever. Flu like symptoms, blurred vision, couldn't sleep, and red rash developing over body. Took next night off of work. Went into emergency room with a panic attack and left side of body numb. Docs didn't know what it was. Blood pressure: 159/100 Temperature: 104 F Rapid heart beat. Completely dehydrated. Fever continued ... released same day and told to take Tylenol for fever. Stayed off sulfa/trimeth for two days. Got much better. Just took it tonight (foolishly) then found this page. Now realized that my body has been rejecting this drug. Currently itchy and cannot sleep. Took vicodin and ibuprofen - no effect to counter this drug. Must wait for it to leave the system. Will contact dermatologist in the morning about my allergic reaction to sulfa. Also experienced severe depression on this medication.

hip bursitis- getting shots every 6 weeks for over a year. Shots are extremely painful.I actually cry while getting it. It hurts that badly. Day of shot-throbbing pain in hip, radiates down leg, fatigue headache.
2nd day- facial flushing,headache,fatigue,slightly lessened pain, knees now swollen
3rd - all symptoms slowly start to subside
My last shot was the worst. Left the Docs and felt soo tired, in pain and upset from how badly it hurt. Drove right up a curb.(im ok) Couldn't wait to get home to sleep. I was worthless to 3 kids until next day, weird, its the first time thats happened.

have been taking 20mg for about two weeks. a couple days after i started taking the stuff i started experiencing chest pains at night that would wake me up, coupled with leg pain. it's getting worse; now, after two weeks i am having severe lower back pain that radiates down both legs, similar to sciatica, happens at night but continues throughout the day. also leg spasms at night. i am stopping zocor today. can't face this pain anymore. i have bad knees, and recently had to have a cortisone injection, but this new pain is worse than the knees. owing to the chest pains, i had a stress test today at the heart group, and had such difficulty walking that i could barely make it down the hall with my cane. three of the nurses there said they hear this all the time about the statins, and that the doctors don't want to listen to the complaints but the nurses all agreed that the statins are the culprits. results on stress test were fine.