Struggle symptoms and conditions

I've had the Mirena for 4 and a half years with no period. Reading here I realize a lot of my issues are related to the Mirena. Now ironically I am cramping, spotting/bleeding, and breaking out like never in my life. My stomach is always swollen and everything I eat creates pain. I do plan to have it removed ASAP but wondering if that will open the flood gates after so long without a period. I should mention I am in Menopause and some of my friends don't have a period anymore. Could I be that lucky!
It was a struggle to insert the Mirena and wondering if it generally isn't horrific to remove. I'm coming back as a Man!

i stopped taking bactrim yesterday, i couldn't stop spitting, my skin felt prickly, i woke up with swollen eyes and mouth, something i think im going crazy. Monday i couldn't sleep at all. I am so tired and its a struggle to keep my eyes open. Nightmares and paranoia keeps you awake. Chills and Hotflashing. Tingling in vagina. Today it feels like i cant get enough sleep. I have the worst taste in my mouth. I would not give this drug to my worst enemy. I don't know why they give it in the USA, if the side effects are this great

Ladies, I just want to thank you all for posting your experiences here. I was scheduled to get a Mirena but am canceling now. I haven't had a good feeling about it even though it was recommended highly by my doctor who I've come to trust. But in this case, after reading page after page of corroborating (and painful) stories, I am so relieved to know this is likely to make my life/health even more difficult than it already is. So I just wanted to say thank you ALL. And I'm SO sorry for each person's struggle and pain. :(

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

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

I started taking Levaquin for a sinus infection, a 10 day dose. I started noticing after a few days that I was irritable,depressed, aching and swelling from my wrist up to my elbow. After finishing my dose, the swelling went down. I am still having the pain. I have pain in my left shoulder, the cap of my shoulder. I have trouble sleeping because the pain gets extreme. I have pain in my right leg. The pain is on the back, the lower part--the achille tendon. I have trouble walking at times. The pain can be mild to severe at times. I even have the pain at night in bed. I didn't know what was wrong with me until a friend told me that these are some of the side effects of the medicine. If I had known, I would have never taken it. I feel like it is a struggle trying to get ready to go to work. I have yelled out loud at work because it would be so severe.

I have been taking Aviane for several months. My sex drive has diminished quite a bit and I am having trouble losing weight. In the past I've lost weight pretty easily by eating less and exercising, but since I've been taking the Aviane, it's been a struggle. I was on Yaz for awhile, but switched to Aviane because it's a $10 co-pay vs. $50, but I'm not sure it's worth it. Tomorrow I am going to call my doctor to see if I can switch back to the Yaz...

My name is Eric, I am 16 years old, I have been taking singulair for about 8 years I think, I was never one for having bad dreams, but that all changed. (right now) I searched on google "Singuliar bad medicine" and I found this forum. I am very happy to know that Singulair could be the reason why I frequently have dreams of myself being killed or people I am close to dying.

When I grew older, I realized that the dreams I had did not match up with any thoughts I had the previous days, this is when I began experimenting with Singulair. I would take it as prescribed, then not take it for X amount of days and would see what happened. After not taking it for 2 days in a row, I slept soundly through the nights and had no dreams at all.

I tell you this now, in hopes that it's not too late.. If you or someone you know takes Singulair, GET RID OF IT. The bad dreams I had were so terrible that often times I would lay in bed and not fall asleep for many hours because I was so petrified of what I might dream about. The dreams I had would seem never ending, and anyone who knows what I am talking about understands that having a long dream can be very painful (I have felt the greatest of physical pain, this mental agony is far beyond anything I could have ever imagined). These dreams still haunt me today and not only that, but they have changed me as a person. I would wake up sometimes from a spaz attack, (arm thrust, kicking motion, because the dreams were so real). If you think mentally you are able to handle this, then continue taking singulair it works miracles, but I promise you the pain will only get worse and worse, thank you for your time, and please talk to me if you have questions, I would love to help.

I stopped taking singular, I never fall asleep in school anymore, my grades skyrocketed. I only have irritated eyes from not taking it, and sadly they hurt ALL THE TIME.

I'm 23 years old and had the Mirena put in 6 weeks after our first daughter was born. The first 2 weeks of having it were fine... other than a little struggle implanting it all was going well. Exactly at the 2 week mark I wound up in the ER with what I thought were a bladder infection, hemorrhoids, and swollen lymph nodes in my hip-flexors. Now none of this has been linked to the Mirena, so it could be a fluke, but none of the doctors could figure anything out! My urine sample was clean, my pap was normal, they couldn't find hemorrhoids, and it was a frustrating un-diagnosis. The doc sent me home with pain meds and a local numbing cream, but using the bathroom hurt so bad I had to bite down on a towel to pee! Taking a poop... HA... I've been putting it off for days because I feel like my rectum will tear open! Has anyone else had any of these things? Maybe I'm just ill with a strange disease, but this site has me curious if it isn't the Mirena!

I had my Mirena inserted 4yrs & 11mths ago. I believe this evil little device nearly cost me my life. A locum GP suggested it to me when I consulted her about tubal ligation. She said that as I was having heavy periods which made my varicose veins ache the Mirena may be a better option, so I went for it. It hurt having it inserted but the cramping after was a killer. My husband noticed a change in my mood within a week, at my six week check up he asked if it could be associated with the Mirena and was assured that it would be rare. The next six months I became more and more depressed to the point that I decided to commit suicide. Luckily my husband was one step ahead of me and I'm here to tell my story. Also have had migraines, weight gain, nausea, breast tenderness, but no period. I never associated any of these symptoms with Mirena (neither did my GP). As the five year life span was approaching I decided to go through the motions of having it replaced. Whilst looking on web for a local Gyno I started to read the horror stories. Today I had it removed, it was a little uncomfortable but I'm hoping it is going to make a difference to my long struggle to manage my depression.

I got Mirena 8 weeks after my daughter was born, March 3rd. The only thing that hurt about the insertion was when the doctor put the clamp on my cervix. Everything else I didn't feel a thing. I also took some Motrin before I went because I was super nervous. Afterward, I had cramps that felt like mild contractions. Nothing too bad. The only thing that bothers me about Mirena, is I've been spotting ever since I got it. It gets heavier when I work my abs. As far as losing weight or gaining it, I'm breastfeeding and it's always been a struggle with me to lose weight until I wean.

Since having the Mirena inserted 6 months ago, I have gained 30 lbs, my hands and feet swell terribly, I get headaches, suffer from insomnia, I have no sex drive, I cry all the time and other times I want to be as mean to someone as I can. I have developed heart palpitations and undergoing stress tests, ECG's, blood pressure monitoring. I have dry course skin and hair and developed acne and I either bleed or spot so have had to be monitored for low blood iron levels. I use to healthy and happy and feel like I spend all my time at appts or in hospitals. I have mentioned my beliefs concerning what the Mirena does and feel as though it reaches deaf ears. Today was a terrible struggle talking my ob/gyn into removing the Mirena. I will have to go for surgery to have it removed and have become very vocal about the Mirena overnight.

I had the MIRENA inserted in August 08. I have 2 kids (2.5 yrs and 1 yr) The 1st 3 months I spotted A LOT and now i get very irregular periods about every 3-5 weeks I'll bleed for about 3 days. I also have a constant yellowish discharge which I thought was thrush. But after being tested for that it has come back normal. I too have tonnes of hair loss and my hair just looks dull and lifeless. I did put on some weight at the start, but have since been on Weight watchers and I've lost 15 pounds, but it's been a struggle. I've had some mood swings and been very teary, but I just put that down to some recent family heart ache (my son was diagnosed with Autism in Dec) but I guess the Mirena could be adding to my stress levels and overall wellbeing. After reading all the other posts I have booked to get my Mirena taken about next Thursday. I'm not planning another pregnancy for a few years so I need to either get organized and take the pill or use condoms.... Oh the joys of being female!

WOW!!!! I wish I found this website months ago!!! I started taking Yaz 8 months ago. I consider myself a very healthy person, I workout intensively 5 times a week, eat right and have a healthy lifestyle and wonderful people in my life but around 8 months ago I started getting sick all the time, feeling depressed and in a fog, not wanting to get out of bed,getting bad headaches all the time, increasingly anxious and stressed and gaining weight and not being able to lose it. I have a very comfortable and happy life and have nothing to be depressed about so I couldn't figure out why this was happening. I've gone to the doctor many times and had every blood test known to man done and still no answers, I even started going to a therapist. I couldn't figure out why I had lost interest in life and every day had become a struggle. No one ever considered it could all be related to a drug side effect. I called my doctor and I'm going to stop taking Yaz and hopefully this is the answer to what is going on with my body. I will keep you posted!

I've been on Femcon for about a month now, and so far so good. I started out on OrthoTriCyclen which made me vomit several times a week, so, strike one. Then went to Yasmin, which was okay, but decided to switch to Seasonique (sp?) for the convenience of a few periods a year, but it made the skin peel off my face at an alarming rate. I was then switched to Yaz, that was great except for one thing: It stole away any sex drive I may have had--no good. Because of this, my doctor switched me to Errin-a progesterone based mini pill-which did give me back my sex drive, but also made my acne horrific, the skin on my scalp peel off, and my breasts painful. Needless to say, it has been a long and difficult struggle with the world of oral contraceptives, so here's hoping that Femcon works out for me!

Someone PLEASE help or offer assistance! I have been on 50mcg Synthroid for about 1.5 yrs now and have gained about 25 pounds!! I am a very, very active triathlete, not just your 30 mins on the treadmill kind of girl. How about running 5-6 miles, riding my bike 40-50 miles, and swimming all about 3 times per week!! How can a human being continue to gain weight at this activity level? I am considering just stop taking it, cold turkey. Has anyone tried any of the supplements for thyroid support, or natural meds? If you've got any suggestions, I am open to just about anything at this point!!

I started taking Zoloft in Aug 2007 because I could not get sleep at night...tossing and turning - thinking about all the stuff I had to do the next day. Within a few weeks - that was so much better - my moods were better - and my performance at my profession was better because I could actually relax at night. I had lost all the anxiety that I have had all my life - and couldn't believe that there was something out there that could help me so much. I, at the time, would never in a million years think about stopping this medication. HOWEVER, fast forward to Nov 2008 - the zoloft is still working great - but my sex life with my husband is so bad that it is more like work for both of us...and reaching orgasm was almost nearly impossible. I just didn't desire sex...which is highly unusual for me. These affects of the med increased over time - and I was willing to deal with them - but the thing that changed my mind about it all was my weight gain. I chose to take Zoloft because it had the least chance of weight gain...or so I thought. I had gained 30 pounds since I started taking it. I wasn't working out as much - and so I thought that was it...but when the scale hit 200 - and then 210...on a frame that should be no more than 140 (I was a bit overweight when I started it) I freaked out. I had been working out and eating really well for three months, no alcohol - no extra hidden calories - to the 210 mark - and I had gained weight during that time. I was talking to my doctor one day and out of the blue complained that I had gained so much weight and it was really starting to bother me. He said, "oh yeah, that can happen on ssri's - in some people they can pretty much almost shut down your metabolism". I was in shock...he knew my struggle with weight to begin with - and here - now a year and some later told me this. Needless to say - I felt betrayed, but was then determined to get off zoloft. And so I have been with his help..and it has been one of the hardest things I have ever done...and I am still working on it. It has been two months and I am slowly weening off. I was on 100mg per day - and dropped to 50mg, and now I am taking 25...I get dizzy, the mood swings are awful...AWFUL - but I am doing it...and I will not ever take zoloft again. I never realized how addictive this med was - and just how much it affected me until getting off of it. However, the one thing that I have found to help with the withdrawal symptoms - even the dizziness is working out. It has been my saviour.
Just thought I would pass this along. The honeymoon period is great with Zoloft - it is when you see your body out of control that puts it all into perspective. Every person's body is different, but if you notice that you are gaining weight for no reason - and can't seem to lose it - tell your doctor. There are other drugs out there to help with symptoms that zoloft relieves that do not cause all these side effects...the ssri's just tend to work more efficiently. For all those with decreased sex drive - wellbutrin does not affect this or weight...but isn't as good about sleep.

I've had my mirena in for 4 years now..and can relate to some of the symptoms mentioned. It never occurred to me before that mirena may be the cause. I'm extremely exhausted all the time. I'm a mother of 3 and I maintain a very healthy lifestyle. I go to the gym at least 4 times a week and eat all the right foods. Instead of my workout leaving me refreshed(as should) it nearly takes everything out of me. The rest of the day is a total struggle. Its like ive used up all the energy available to me. I turned 33 less than 2 months ago. I taught of aerobics prior to the birth of my 4 year old son. I had my mirena inserted at my 6 wk checkup. I lost my motivation to continue my workout habits..yet still maintained an active lifestyle without the intensity until 6 months ago. I was 112 lbs @ 5'1 when I got pregnant with my son. I was 144lbs when I delivered. I was down to 120 at my 6 week checkup...and still haven't budge from there! (after the mirena). I'm bloated all the time. As others have said...looking like they're 3 months pregnant...thats me! I've also have swelling in my hands and feet randomly. (mostly my hands) My periods are light..spotting mostly and come approx every 3 weeks. My breast become extremely tender a week prior to. Sleeping is not a problem here...I'm practically out before my head hits the pillow. I often have trouble focusing and feel lightheaded. I also hope to have another child next year some time being that I am remarried and my husband doesn't have any children of his own. After reading some of these stories I'm wondering if that will be possible. In the past...my husband had often complained of feeling scaping during intercourse...yet hasn't felt it in quite some time. I wonder if that's good or bad? I hope I don't have to get mine surgically removed! I'm scared now! If anyone can relate to me...please comment.

I have always had and currently have the side of effect of extreme fatigue associated with the use of synthroid and now Armour thyroid replacement as well.
Whenever my tsh reaches normal levels I become increasingly fatigued. Now I an hardly stay out of the bed and yet my levels are normal.
I have Hashimoto's Disease and am menopausal with severe insomnia to cloud the issue. But the fatigue associated with thyroid replacement is longstanding and has occurred for about 15 yrs. For many years, I would stop taking the medication because of it. My doctors do not believe that the fatigue is related to Synthroid which I find utterly frustrating. Will be looking for another endocrinologist soon. Has anyone out there experienced this side effect of extreme fatigue?
Any input would be greatly appreciated.

I had muscle aces and pains most of that time but near the end of the 3 weeks I would loose the use of my left arm for periods. I would feel faint and very weak. I have had restless leg since I was a child but my legs got much worse during the 3 weeks. Finally I remembered that if you had muscle weakness you were to stop Zocor so I did. The daily muscle weakness gradually went away but I developed severe restless leg and had to go on Requip. I also started having face spasms and “turrett” type spasms in my legs that would travel up into my arms and hands. My hands would clench and I couldn't talk plain. My head would jerk and my body would shake inwardly as if I were freezing. These symptoms were worse when I was stressed or got too hot. Eventually I had to quit my job, it was very high stress. Five years have past. I now stay home and garden and paint. I very seldom leave my home and my stress level is low but when I do get into a stressful situation I still have to deal with the “loss of control” over my body. My sleep is a nightmare every night. My restless leg syndrome is getting worse and I've had to increase my Requip and will probably have to do so again soon.

My cholesterol is very high and my doctor keeps trying to get me to go on some meds for that but I would rather die than add to the painful, exhausting struggle I go through now because of what Zocor did to me.

Thank God for each and every one of you'll who posted!! I am a 31 year old female who has consumed this poison since March 08. My PCP had started me on the Lisinopril 40mg and eventually increased it to 80mg per day.
OCTOBER 2008-
I begin having "flu like" symptoms which I started taking over the counter medicine for.

NOVEMBER 2008-
I was becoming worst so I went to my doctor (the one who prescribed this mess) and was told it sounds like bronchitis so she prescribed a "z-pack" (which is a 5 day course), "cough syrup", and stated to "quit smoking".

FIVE DAYS LATER-
I went back to my doctor with the same complaint chronic cough and now shortness of breath. I was told that since the "z-pac" didn't work it may be "asthma"!! SO of course I was prescribed more drugs one being one called "Augmentin" (which is a 10 day course), and an inhaler now for asthma!! I was ordered to have a "chest x-ray", and another script for more cough syrup with codeine!!!!

SEVEN DAYS LATER I WAS IN THE ER-
I felt as if I was dying! I was so scared and did not know what to do. I couldn't even go to work all I could do was cough, gag (sometimes vomit), and gasp for air!! I knew something was terribly wrong. The chest x-ray was clear other then a small amount of inflammation. I was prescribed yet more pills this time a 5 day course of "steroids" for the inflammation, more cough syrup, and was told I didn't need the inhaler!!!

1 WEEK LATER IM STILL COUGHING-
I was beginning to think that this condition was smoke related and begin to feel depressed as if my life was over. I decided to quit smoking as of 12/19/08, however the gagging cough and shortness of breath is still present.

I GOT A 3RD OPINION
I went to an internal medicine doctor (just 6 days ago) who stated that it appeared to be the Lisinopril the whole time and to stop taking it immediately. I was prescribed a medication called "Diltiazem" generic for " Tiazac" but the insert mentions cough as a possible side effect for this medicine as well. I am to weak, broke, and cautious to take another one so quickly. I'm still coughing as I type this!! I think I will just stick to my fluid pill and a better way of living before I continue to put this stuff in my body. To sum up this whole coughy blog, please, please think twice before taking this or any other medicine, trust me it will save you a lot of health problems and medical bills. And finally if your doctor wont listen, don't hesitate to get a 2ND OR EVEN 3RD OPINION IF NEEDED!!!!!

Hello Everyone,

Reading your stories has brought tears to my eyes. I have received my first shot two months ago, on October 20th. Since October 24, I have had nothing but struggle. I am 25 years old and have been in good health my entire life. The only thing I have ever had a struggle with was UTIs, approximately 2 times a year. However, they were gone with the first dose of antibiotics, within 24 hours. Couple of years ago, my gynecologist had completely cured me from that annoying disease through a course of medication that I took for two months. That was not a very easy process but I was free at last. I did not have a care in the world. However, my nightmare came back after the first Gardasil shoot. Exactly three days later, I woke up with severe pains in my lower abdomen, as well as all the other common symptoms of a UTI. Honestly, being as careful as I always have been with UTIs, I did not put Gardasil and this infection together. I went to my doctor. She tested me for a UTI, said I had a small presence of bacteria in my urine, and released me with a prescription for Macrobid. After a week of taking the meds, things were not looking up. It has been two months, and things have not gotten better. About two weeks ago I started searching for other causes of this pain that is resisting going away. I have been on three courses of antibiotics and going back to my doc tomorrow, after coming across this discussion. I have never experienced pain like this before, having considered myself a veteran of UTIs. I thank you for sharing your stories and advise everyone to think twice about having these shots or taking your children. I am not going back for another dose of this nightmare! I don't even know when I will feel normal again. Everyday starts with a thought: "Will I feel pain when I go to the bathroom today?" I am now completely sure that Gardasil had everything to do with my recent condition.

I took Levaquin 750 for 10 days for a sinus infection. I took first 5 doses, went to see my doctor again 6 days later because I was still sick. She prescribed again 5 does of Levanquin 750. I am still coughing and I feel very tired. It did not help at all. I am still sick and I have muscle pains in my two calves and stress Achille tendon. I am a runner and I have sometimes problems with my calf: I have been not running too much recently and I was wondering how come suddenly I had those muscle pains in both my calves. I am not sure if it is related to Levaquin, but when I read all those comments, I am worried. Why I have been prescribed this antibiotics if it is obviously dangerous?

i'm so glad i found this site. i've been using the nuvaring for around five years. i can't remember exactly. i thought it was great at first. i get really sick on other bc. but i started getting leg cramps recently and i also had a gallbladder attack and they found three small gallstones. i'm a very healthy person so i was concerned but i didn't relate these things to nuvaring. my boyfriend moved out of my apt. we had been together for 7 years and living together for almost 3. i'm starting to go back and realize the depressed feeling i've had for years now. i didn't realize it could be NR. i lost my motivation, i was performing terribly at my new job that i started 3 years ago (couldn't focus the way i should and i always do well at work) luckily, i still have my job but it's been a struggle emotionally. i wasn't' really interested in anything and couldn't get back into my own personal artwork. i thought i was depressed in my relationship and work but now i'm thinking again this might be the nuvaring. could all of the 'bad luck' i've had in these last couple of years be that? it's hard to blame it on that but reading everyone else's reviews is starting to really scare me. i knew something felt off but i didn't know what it was. as the years have gone on i have lost my excitement for things. arghhhhh! this is so frustrating. i only started looking up nuvaring side effects because i heard something about blood clots and i started getting bad leg cramps. i played competitive tennis when i was young through college and other players would get leg cramps but i never did. now i'm getting them and i work out a lot.

To the best of my knowledge I never had any of the 'immediate' symptoms.
My problems are probably due to the fact that I was prescribed Cipro 3 possibly 4 times from Aug 06 - Dec 07 and then finished up Dec 07 with a round of Levaquin. My father is over 60 and was recently given Levaquin and had immediate and serious problems. He is seeing a doctor recommended by the CDC today. Yes, he is even working with the CDC on
this one. Due to all he is being told he is convinced that the medication is behind my medical decline as well. Since taking these medications (symptoms started slowly in 07), but after taking the Levaquin at Christmas time I never got up from the couch. My thyroid gland has quit working, my adrenals are shot, I have been diagnosed with fibromyalgia, chronic fatigue, blew out 3 disks in my back, vision is deteriorating rapidly, and really so many things I can't list them all. I had a complete physical
in Oct 05 and was given a perfect bill of health. Through Aug 06 I was riding my bicycle 33 miles per week. I'm still trying to figure out what hit me??
What my father has been told is that in some individuals Levaquin will attack the glands (like the thyroid) and will compromise the immune system. This damage appears to be permanent. All I know is that I went from being extremely healthy to terribly sick. If in a day's time I have enough energy to load and unload the dishwasher it is a banner day. I can
not work and seem to get worse instead of better as each day passes.

My husband also had pneumonia at Christmas and took Levaquin but does not seem to have had an problems. I suspect it was possibly the cumulative effect of having basically 4-5 rounds of the antibiotic in a years time. According to the people at the CDC that have spoken to my father the symptoms that I have can all be traced back to the medication. One never knows what effect a medication will have. Just please be careful when taking this medication, and limit how many times you take it.

WENDY.... IN UR POST ABOUT THE BLOOD CLOTS IN THE LUNGS.. WHAT WERE YOU FEELING THAT MADE YOU HAVE TO GO TO THE HOSPITAL? THIS PILL IS A LIFE RUNNER....I FEEL FOR EACH AND EVERYONE OF YOU... ANYONE THAT EXPERIENCED THE ANXIETY/PANIC ATTACKS ON THE PILL... AFTER STOPPING YASMIN DID THEY GO AWAY?....