Clue symptoms and conditions

Been on coumadin for a year, horrible medication. Have aches all over, legs, shoulders, back, always tired, want to be off this med. Was taking alternative meds previously...nattokinase, bilberry which are blood thinners but are also SAFE. Then I had no leg pain, no muscle pain. I now take vitamin e and fish oil with the coumadin, no interaction since I've been using them for a long time and are more beneficial than the coumadin as far as I'm concerned. What I need is a naturopathic doctor, but they are hard to find, regular mds have no clue about supplements..all they want to do is increase your prescriptions. Doctors try to scare people telling them they'll have a stroke without coumadin, but have no solution on how to prevent stroke, etc. without drugs.

I haven't gone through to read all of everyone elses side effects yet but is there anyone who is getting migraines because of this thing? i feel like my head is going to explode and the come so frequently i have never had this problem before getting the mirena i have no clue on whether or not this is what is causing them but i am hoping so, that way i can get it taken out! i go through spurts of depression too but im sure that it is because of the mirena but i will admit i do love the no periods and that it has done its job in preventing another unexpected pregnancy i just do not think i will make it through another headache!

Mirena inserted December 07, 6 mo. after my son was born. Was not even dressed after procedure when a severe wave of pain took over. Asked nurse, said "discomfort" was common. Thought to myself, I've had 2 kids, this isn't discomfort. She gave me a "super" Advil. No clue what it was, took it because I felt like passing out from the pain, Called husband on way back to work, in tears, thought I was going to vomit from pain. Got much worse, had to pull car over -- afraid I was going to black out. Mustered up strength, got to work. Took additional 3 hours for cramps to subside. Completely exhausted. Next night, out of nowhere, horrible, horrible pain -- never had ovary issues, but it was to one side, thought my ovary was exploding. Went to urgent care cetner -- didn't know what else to do. They took Xray (no ultrasound available), nothing out of the ordinary. Called dr. -- she was perplexed -- never heard of this before. Next 6 months a blur. Every single month, at completely random times, horrible pains would hit again - nothing I could do. So bad, thought I would wreck my car when driving, felt like throwing up from pain, had to lay completely still, take 4 ibuprofen and WAIT for it to go away--up to 3 hours each time. This left me exhausted and extremely scared for the next month. Waited the standard 3 months -- up to 6 months. Finally gave up, asked dr. to remove it. She did. Have not had a SINGLE episode like this again. IMy body doesn't react like this to new things, so I was shocked when my I didn't adjust. I have no other way to explain this, but I am interested why the side effects were so unheard of by my ob-gyn. She reported them to the FDA and pharm. manufacturer. WEIRD.

All i can say is WOW! i am so happy i found this website..
I too have suffered side effects and till this day am suffering from Levaquin.
In Feb of 08 i was diagnosed with Prostatitis and was given a 14 day dose of Levaquin. Hours after the first dose i started experiencing pain in my lower extremities,me thinking it was caused by the prostatitis i continued the doses.By the second dose i was in absolute pain in basically all my insides and started having this metal taste in my mouth.Not ever being allergic to any type of medicine i continued the doses only getting sicker and worse.By like the 6th pill i was having anxiety,insomnia,hallucinations,nightmares whenever i was able to close my eyes,partial psychosis,rashes on my face that would get bright red then go away and the skin would peel off.I would be so thirsty water couldn't quench it,suicidal thoughts.I developed a pain in my left calf and behind my left arm in the tricep that till this day bother me.Joint pain,ringing in my ears,excruciating headaches like someone was jabbing a knife in my head,lost 30lbs cause of the colitis it caused,neuropathy,and so much more,it was a total nightmare.
I went in for discomfort of my prostate and doctors couldn't understand why all the other symptoms only a week later,they were completely clueless and told me i was making this stuff up cause i was having an anxiety attack.. I was a perfectly healthy 33yr old before levaquin. The doctors sent me for test after test from HIV to LUPUS only to tell me its all in my head,that i was a healthy man to move on with my life.I would try to sleep and have all these terrible thoughts and would swear i slept for 3 hrs only to see that 20 minutes have gone by,i was gentle to the touch.My family had no clue,they thought i was going nuts.I was pretty bad for months after,the effects started going away little by little,i was back 50% to myself by like June of 08.Since,i still have the pain in my left calf from time to time,tremors,joint pain..I have since joined the gym and have been taking supplements that have helped a lot with my joint pains.
This stuff is poison and should be taken off the market..

I'm only two pills into Biaxin for streptococcal pharyngitis (Allergic to Penicillin). Prescribed 2 pills a day for 10 days. It's 5 am and im really happy I found this site. Thank You all to start. After my 7 am and 7pm dose, I have already noticed insomnia and restlessness. Physically lethargic, but mentally energized. Like some others, I find I can't stay in one position in bed long before I have to move. One person noted sharp pains in legs and arms. I'm actually not looking forward to 9 more days of this. After only one dose, I experienced a sharp pain in my skin above my ankle. Felt a lot like a small hot ember was on my skin or a insect was stinging me. I have never felt something like this except for a time or two where I actually had an ember on me. I had no clue what it was and chalked it up to "getting older". I'll post again in a few days. Going to call my family Physician tomorrow since I was prescribed this in emerge away from home.

I am a single mother of 2 children, I wanted to quit smoking so my doctor said to try Bupropion ER150MG for a 1 week and 3days The first week it was 1 pill a day then 2pills from there on out. The affects hit me the second day it has helped with cutting down on smoking and it makes them taste very plain and nasty. I have these systems/side affects already>feel slow, dry mouth, horrible taste in mouth, food and sodas taste nasty food has nasty taste as well and headaches first week. Very emotional ever since I started taking 2pills, just a thought and I would tear up. Like today this morning I was emotional and around 1o'clock I was Bitchy and irritable. I feel drudged honestly. Totally not me I only get emotional when on my period and Bitchy hardly ever! Sleep well lets say I wake up a couple times every night since I have been on it period. I am a deep sleepier too. I have no clue on what to do if I should give it more time or tell the doctor I'm done? I just want to quit smoking with something thats not going to affect me like this. I have no anger problems or anything like that just smoking. I am actually under weight for my age I don't know if thats why it has affected me so quickly 5'5 and weight 107-109 26yrs old I have not been eating as much as I usually do and have a high metabolism and I seem that I have gained a pd or 2. Don't understand I just think it's mess me all up. I waited an hr or two later to take my next pill tonight and I felt so good like myself, I will also say it seems to leave my system within 9 to 10 hrs it suppose to stay in your system for 12hrs but not me. If anyone can help me on advice feel free to email me please ******Thanks Mel

Omg.... I've had the mirena for a few months now and have a lot of the same side effects as a lot of the other women that have posted. I had a bad rash on my face and I thought it was acne at first and I had no clue it was caused by the mirena at first until it got so bad I went to the dermatologist and he told me that is what is causing it and he said they have at least 1-3 girls coming into their office weekly with the same problem. Since then I have made my appointment with my OB/GYN to get it removed. It is just not worth it.

i was prescribed doxycycline for 7 days and it has really screwed my body up, i have experienced all the symptoms mentioned including a general strong feeling of unease and feeling like i have the flu as well as horrible reflux and stomach problems and its been 5 days since i stopped taking it and i am still experiencing these symptoms they seem to be just a little less severe. Can anyone give me any clue as to when i will recover from this or any steps i could take to help my body recover. thanks

Prescribed Bactrim for MRSA skin infection on my arm that I picked up at my local gym. Day 1 OK, Day 2 severe headache at the base of my skull. Day 3 continued headache, general nausea, gas. Day 4 I began to develop a low grade fever and dizziness. Almost passed out after walking just a half mile. Still a severe headache, weakness. Day 5 Headache, consistent fever of 103, chills and muscle aches, light hives visible, weakness, unable to sleep. Day 6 early am, couldn't sleep all night, went to the ER with the worst muscle aches and fever I have ever had. Hives now very clear and pronounced all over my torso. I was tested for the flu. Said it was not, but was a viral infection that was attacking my muscles. Muscle breakdown found in both blood and urine samples. ER physician changed medication to Clindamycin HCL. Told to stop Bactrim, but thought what I had was viral, not a reaction to the Bactrim. I continues to feel bad for a couple more days, but hives started to reduce, fever diminished and started to feel halfway human after being off Bactrim for a couple of days. Still not 100%. New med has it's issues too (have to take every 6 hours, can't lay down after taking it) and a nasty taste in mouth and stomach upset, loose stool. After 5 days of new med went back to my doctor. A secondary infection had set up in the Staph area. The fungal infection needed a different med. Now is 4 weeks later, after finishing all meds, still have an infection. Blood cultures taken to see if the infection is the staph or fungal. I have lost 8lb, have no taste buds, loose stool, severe stomach cramps/burning (now taking Activia to put back good bacteria in my stomach...no one told me to do this before!!). If Staph not gone, need IV antibiotic for a month. I am 50 year old female, but note I had taken this in my 30's without any problems. You can develop an allergic reaction to medicines previously OK for you. Beware of Bactrim. It kicked my behind!

Ive broken out in a horrible rash with blisters and all-and all over my body with just extremely itchy red dots..i have no clue what its from..but im guessing nuvaring just started it 3 weeks ago.. My dermatologist has no idea whats breaking me out..i know now that it is nuvaring! Keep posting girls!

I have had problems with regulating my period since I was 15. When I was 17 I was on Depo (2 years) and it really screwed me up, I gained 40 lbs. and became lactose intolerant (don't ask me how that happened, i have no clue). I still have not been able to loose the weight. I then tried the OrthoEvra patch and I loved it. I went off bc because my insurance doesn't cover it anymore and i could no longer afford it. About a year and a half ago I was diagnosed with PCOS and my fiance and I decided that it didn't really matter if I was on bc, if I was able to get pregnant we would consider it a miracle. Over the last 6 months my mood swings and periods were so severe and painful that I have had to go to the ER 2x so we decided to try bc again, I was prescribed Femcon about a month ago. My first round of pills left me sick to my stomach every day and having migraines every couple of days. I started my second round yesterday and I have been so violently sick since swallowing the pill last night that I haven't slept and had to call out of work. I spent 6 hours in my bathroom last night and by the time i passed out I had thrown up blood twice. Ive never been this sick in my life and I'm waiting to hear back from my doctor to tell her I refuse to take this pill one more day.

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

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

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

I had the Mirena for 5yrs & had it replaced this past April. I had loved it (no menses) but little did I know of the adverse side effects that were plaguing me. I always had some depression, but wrote it off to cyclical hormones; cystic acne that seemed to be getting worse as the years went by; heart palpitations; NO libido; anxiousness. All this seemed to happen slowly over time for me. Once I had the new one inserted, I started noticing the part in my hair was becoming thinner, like balding; developed an eczema/rash on the back of my neck at the hairline; I felt like my hay fever was non-stop & got an ear infection/sinusitis for the first time ever; then the headaches which most recently turned into a migraine with visual changes coupled with insomnia. And I ached all over like I had the flu all the time. I had no clue that the Mirena could do this until I started researching & read the PHYSICIAN insert info! I discovered that out of 21 "adverse effects" I had at least 13 of them! I was mortified - being a Ob/Gyn RN, I felt I was really misled by the manufacturer & my doctors. I could not take the headaches & insomnia any longer. A week ago, desperate & could not wait until an appt., I went into the bathroom, pulled the strings myself & removed the sucker (being a RN, I have to tell you not to do that; I was willing to take the heat should something bad happen!). Over this last week, a HUGE difference for the better. NO headaches, insomnia, body aches, skin is clearing & my mood is getting better. I actually am feeling frisky for my hubby even (who by the way will be having a vasectomy in the next couple weeks & was fully supportive of me doing this). I am so disappointed as I LOVED the no period thing, but I am not willing to risk my well-being over that!

I am 18 years old. I started yaz three months ago. During my first month taking yaz, i had a really bad fever and started getting these electric shock sensations in my head. My heart was racing and I couldn't stop twitching. I was panicking and will skip the long er story but the doctor told me it was anxiety and an allergic reaction to my cough medicine and sent me home with vicodin and atavan. I got better and didn't have that sensation for the next week. However, I was growing increasingly anxious and panicky for no reason at all and would have long crying jags where I couldn't calm myself down. I am usually a very happy person, and I just feel so depressed. The shocks started coming again, along with the twitching and feelings of vertigo. I started thinking that maybe it could be the yaz causing it and went off it mid pack. I went to my doctor for the shocks and she had no clue. I had a mri of my brain and it came back normal. I have been off yaz for two weeks now, and have since seen a neurologist. She put me on an 80mg prednisone pack which she said would stop the shocks but only have me the worst migraine of my life and shaking so bad that I couldn't function or leave my bed for for four days. I went to a new neuro and am on an new migraine medication which seems to be working better as I am up and my headache is better. He seems to think the shocks are a result of yaz. Have any of you had this symptom, and the twitching? I feel like someone has turned an electricity switch in my body and I cant stop moving. I have no clue whats wrong with me and its really scary. The only way I can sleep at night is with ambien, and I cant stop twitching even during the day. If yaz can cause this why can they even sell this awful pill?

For reference, I am 23 years old. I got the Mirena IUD put in 1/30/08 and I got it taken out today. For the first several months i bled and cramped a lot. Once that passed, i was doing good and only spotted every once and a while. Well, for the last 3 months i got my period. It was heavy and I cramped a lot. During this time I also started feeling distant from my close friends and family. I felt a horribly weird sensation of a fluttering in my uterus, almost like when you are driving really fast and go over a hill, how your tummy gets that weird feeling. It felt much like that except it was in my uterus and it started happening all the time. I have also gained like 20 pounds. I haven't been able to sleep at night. I was having sharp pains in my ovary areas. I had it removed today after 15 minutes of my dr. stalling almost as if he absolutly did not want to remove it. I just kept repeating myself until he finally called in the nurse to observe. I am not good at paps or anything else that has to do with strangers invading my lady parts to begin with. So i was sorta freaking out in my own little world while he poked and prodded away. He was good about asking me if I was okay and if it hurt, but im not one to go and answer these types of questions when im in that much distress so it's okay if they talk but i don't like talking to them back. I'd rather they just get it done and over with. Well, I felt him tug and after a few good ones he got it out. That was a Horrible feeling! I almost cried! Then he just started talking to the nurse and since he is foreign i have no clue what he was saying to her, WITH the thingy still stuck in me!! I was so worried and this went on for about two minutes.. Then i asked if we were all done and once he took it out I noticed that the IUD was in a container but there was another small container with a bloody chunk in it!!! sorry if tmi...when i asked what it was he said that "a bit of tissue came out with the IUD and they were going to send it to the lab. I could tell he was trying to act like everything was fine but if everything was FINE...why would tissue come out too? I'm in a state of panic right now and don't know quite what to think at this point. I would NEVER suggest anyone getting Mirena. The bad side effects plus the removal are NOT worth it at all. This should be banned! If i would have known what i do now i would never have gotten it to begin with. I am now dreading the "crash" hopefully it isn't as bad to me as others. I am a single mother of a child with disabilities...if i get this "crash" thing, things are get difficult fast. Hopefully I start feeling normal again soon.

I went to the doctor one day they told me that nothing was wrong with me and that is was just in my head needless to say i had not urine for a day and my back was killing me so we i got home i went to the ER and they told me that i had a really bad kidney infection and bladder infection and a UTI ya it hurt like you no what. they gave me sulfamethoxazole to take for 14 days well in the first week i felt funny and i didn't seem like something was wrong with me So a week into the medicine i was a work and the inside of my mouth started peeling yes peeling like the top layer was coming off and i started feel really funny so i called the doctor and they said everything was ok that it was a normal reaction to the drug not being a nurse or doctor i believe them so in middle of the night my face was swollen i had a rash on my face and my chest. I immedity went to the doctor ( a different doctor of course) he looked at me and said what have you being taking i pulled out the medication out of my pocketbook and he look at me in shock and said i know you have not being taken this you you are highly allergic to the medication ya i said the same thing i had no clue but he gave me a shot of something and gave me prednisone i not feeling that will he said it would take a couple of days to kick in but hey i need something now!!!!

I sort of have a love/hate relationship w. this pill. I was on this pill after I had my 1st child. For those 18 mo. I felt great. I suffer from alopecia (female pattern hair loss) and this pill made my hair thicker and reduced the loss completely. I went off of it 3-4 mo. before easily conceiving my 2nd son. However, a month after I got off, I started to loose more hair than ever AND break out ridiculously for the first time ever in my life! The only reason I believe that everything turned around is because I got pg and we all know the good hair and skin that does for you. I am now done having kids and back on Yasmin because I was disparate to regrow my hair (which it helped again). It has been about 6 mo. and am starting to lose my hair again and have symptoms comparable to an ulcer. I'm just not sure anymore, but what i am sure of is doctors have no clue.

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

I had a mirena put in 5 years ago and had some weight gain and problems with ovarian cysts. My Dr. never told me the cysts might be related. They are extremely painful when they rupture - like having appendicitis. I had that one removed and then a new one put in three weeks ago. I have never been so sick in my life. I was unable to hold down food for 12 days and unable to get out of bed for 8. After that I started having severe ovarian cysts on both ovaries with one rupturing last Friday. I now have a metallic taste in my mouth that has basically destroyed my ability to eat. My breasts are very tender and I have had faintng spells. I am not sure if they changed the medication in the last 5 years but this is ridiculous. I think I am going to have this thing taken out at the 6 week check up. I am finished with kids and it is not worth it.

I have been on wellbutrin for four days. I can't think straight. My head feels like it is being compressed when I try to think. I can't remember most things. Someone asked me my mailing address and I had no clue. I've lived there for four years. I had to call someone and ask them my address. I couldn't focus. It was bad. By day three, I had started to get these itchy spots in weird places. Well, yesterday I quit taking it because I couldn't handle the weird feelings. Plus, it was making me suicidal. Today I wake up and my entire torso is broken out in a rash. I completely believe wellbutrin is to blame. If it wasn't the weekend, I would totally be calling my doctor. Guess I'll do that first thing tomorrow...

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

hello i am a 28 year old mother of three i am going to school to become a nursing assistant just started my clinical.i have not been feeling good for the past 4 weeks went to my doc and asked for them to test my urin they took it and only did the dip stick instead of sending it to the lab the doc called me about a week later and told me everything looked good i said to him are you sure i feel like i have a uti so he told me if i am still not feeling well come back in in about a week so a week passes and now i am having pains in my back and trouble going to the bathroom so he does a (ua) i go to the lab to give urine and he put stat so the women said it should be back by tomorrow i called my doc the next day the receptionist says yes your results are in so i told her i am coming down cause she couldn't give me the results over the phone so i get ther and she tells me well it came back abnormal which i knew didn't have to pay $80.00 to tell me that i was the one telling the doctor that so anyway she tells me the doctor is in with another patient that i will have to wait i said oh no i feel like i am dying i am having so much pains in my kidneys so she said ok 1 min she got the doctor he called me down to his office and said well it looks like you had a uti and now it seems a little worse than that it might have traveled into your kidneys so i said i told you a few weeks ago when you said my urine came back fine i was in a lot of pain so now what he told me he was going to put me on levaquin 500 mg for 5 days and lets see how that works and to come back in in 2 weeks to take a repeat ua so i said ok got the prescription filled $50.00 later went home and read all the side effects and was so scared to take it but i was in so much pain and hearing about the actress who died of a ut i was so scared but i took it even know in my heart i knew it was not going to respond to me ok well let me tell you i almost had to quiet school i can hardly take care of my children just to walk up the stairs to go to the bathroom feels like i have been running a marathon for 10 miles we are a young couple and parents of 3 and i am a homemaker till i finish school so we live on my husbands pay check which really is living week by week nothing in saving cause we need every penny for bills and food but now i have been in so much pain not sleeping a wink cause i am so afraid of the nightmares that he has been home and not working which means no money is coming in at all i mean how do you tell your children well sorry i have nothing here and no money to buy you juice boxes for school i just really wanna give up i feel like i became a failure to my husband and children if i wasn't so sick he could be working and at least we can have the basics how do i tell them that we are almost out of oil and might not be able to have hot water i mean my life seems ruined all because of this drug i can not believe it i wish every day if i do fall asleep mybe it would be in my childrens best if i do not wake up but then feel like how can i even think that they love me no matter what i don't know i just can not even believe that my life turned around like this in the matter of a week how can this happen i really need help if anyone is out there please help i just wanna end it but i know deep in my heart my kids need me what to do

I started the Yaz . First BC ever for me , Im 38. I did try the Nuva Ring once but stopped after 2 weeks because of a burning sensation down there. So, not ever searching symptoms, side effects on line ever for any BC I decided to take this Yaz , recommended by my doctor explaining if I had PMS , Yaz may ease that as well. Ok, sounds great. Also I was told Yaz had a diuretic in it too , which was a plus to me because I tend to hold water , bloat a lot during the month. So, Im happy go lucky thinking wow, this is great. My face cleared up , I felt the bloat going away, Boy was I in for a surprise !
The second month of a pack is when I went down hill and fast ! Depression hit me so fast out of no where...I never had a clue a BC could do this ! I started having bad dreams every night. Bad headaches. Like the kind where I was holding my hand to my head constantly. Emotional. Snappy , grouchy. Irritated , impatient with my boys. I felt like ripping my hair out. Weird I was.....then is when I stared doing research online.
This is so sad to me , now I think of all the sweet young girls getting on these and feeling these side effects and not even knowing it is the BC. I have boys but I would be devastated if I had a daughter and had to worry about preventing pregnancy. I stopped taking them and had the Essure done to avoid ever ever having hormones in me again. I am so so sorry for the millions of women who have been on BC and had to suffer from this. It is not you , you cant help be witchy....it is the BIRTH Control !!

I was on ortho tri-cyclen lo from the time i was 16 til i turned 21... i liked it.. my sex drive was awesome, but it did make me horrifically moody during my period. I have currently been on the nuvaring for 2 months, which has it's perks (you don't have to remember to take it, i have no cramps or moodiness) but my breasts throb 24/7, im hungry ALL the time (like starving), i'm bloated, get gas about every day after i eat dinner, i've gained a few pounds, i wake up 3 times in the middle of the night, and i have next to no sex drive.. and when i do, sex is dry and it burns! So i'm going back to ortho... i will for sure trade weight gain and dry painful sex for moodiness on my period! I really don't think there is a bc without side effects, you just have to try a few and see which one you hate and which one you can live with. All in all... ortho tri-cyclen lol has been the best one!