First few years symptoms and conditions

I have had the worst year and a half of my life-it should have been the happiest! I was on Yasmin for about 7 years. This last year I had gotten engaged and was excited to marry the man of my dreams! The first few years on Yasmin everything was fine-I did not notice any changes. Over the last few I seemed to recognize some anxiety and started having panic attacks out of the blue. Well, in July 2008, I went to the Dr. and was misdiagnosed as having an ulcer-I really had mono and walking pneumonia?? I was having all kinds of anxiety and they could not figure out why I was sick. I went to all kinds of specialists-neurologists, cardiologists, gastroenterologists, etc. They said nothing was wrong. I received a call from a friend of mine who is a nurse. She knew of my symptoms that had compiled over the last year and asked if I was on Yasmin. She told me to stop the pill but I did not think that this was causing me all of these problems. I ended up having severe insomnia, massive anxiety and panic attacks, irritability, moodiness, muscle aches, night sweats, chest pains, racing heart, depression, the list goes on...I wanted to cancel my wedding! I thought that I was going insane! I ended up at a therapist looking for some help. She was able to help me get through my wedding (December 2008)-thank God!
One of my friends wanted to get off the pill to try and get pregnant and decided to do so after my wedding. After 3 months, she was able to stop her anxiety and depression medicine...correlation?? She was on Yaz!
I immediately stopped the pill (March 2009) -that was the icing on the cake! I have NOT had a period since March, I still have anxiety and am in fear every day that something is going to happen to me.I still have insomnia and feel scared that all of this is taking a huge toll on my body-especially my heart. I just want my hormones to go back to normal so that all of this will end!
Does anyone have a similar story? Any advice as to when I will get back to normal?
Please do not recommend Yasmin or Yaz to anyone ever! It has ruined my life in every aspect. It has affected my relationships, work, school, my well being.
I would love any feed back and/or comments-help!

I had Mirena now for almost 5 years and It has been absolutely WONDERFUL!
My monthly periods stopped after about 2 months, the only side effect I have is that I can tell a slight difference in my mood which my doctor said was common the closer I get to the end of the five years. I will have another inserted in October of this year.

Wow!!! I can't believe it! I just found this site. I've actually been on Advair 500/50 for years now, about 7 years at least. Just as a bit of a background, I'm 24 years old, used to be extremely active, played water polo, was on the swim team, and was just overall very active in high school. I've had severe chronic asthma since I was 8 years old, so in order to help me stabilize my asthma, my critical care pulmonologist put me on Advair. It was a "miracle drug"! However, while my asthma was under control, I was experiencing all these other symptoms that everyone else has been talking about.
Anyway, to make things worse, I just talked to my (new) doctor and she told me that the Advair makes it so that some organ (I'm sorry, I don't remember the name) actually stops producing prednisone (or the same stuff that your body naturally produces itself to keep your lungs working correctly) if on it for long enough. It makes sense because for the first few years it was prescribed to me, I really only filled the prescription as I was getting sick as a backup, but other then that I was generally under control. For the last I'd say about a year, I've been consistent and used it regularly as the doctor actually prescribed, every day, twice a day, whether I was sick or not. Now, I can't go even a week without it, otherwise I'm in the hospital.
During the last year or so that I've been consistent with taking the medication, I've had major depression, gained 45 lbs, fatigue, anxiety, dizziness, nausea, heart palpitations, heartburn, leg pains, sore throat, sinus infections (we just finally decided I was just allergic to our animals and I've been on decongestants for pretty much the whole year, doing sinus flushes, etc and I'm still all stuffy!), unexplained bruising, crazy mood swings, muscle pains, headaches, heartburn, etc. I thought I was just completely crazy, I kept believing it was all in my head!!!
I'm going to my doctor today and asking her to prescribe me something else. The funny thing was, I was just on my way to the hospital b/c my doctor's been treating me for the last 3 weeks for vertigo accompanied by the heart palpitations and the nausea, she finally is giving up and is sending me to the emergency room. I figured before I went that route, I'd look into it myself. Go figure!

It is so crazy that I found this site today, and super glad that I did....I should have went with my gut 3 months ago when I wanted to stop taking this pill...but now for sure I will!!
I originally started taking a Triphasil pill when I was 14..then it changed to Trivora, and I never had any problems with those pills....then when I moved to California when I was 19 I got greedy and wanted no periods (or short ones at least) so I tried Loestrin...which by the way made me bleed for 58 days straight...I thought I was going to die! So my doc prescribed me Femcon...and I said I'd try anything to get me to stop....It was fine the first few years but I was diagnosed with the first stages of Hypertension 2 years ago (age 24) and I blamed all of my bc symptoms on that! I thought, ugh I hate getting older cause now I have side effects like crazy...well I don't think its my blood pressure, and I wouldn't doubt that FEMCON has helped cause my high BP!!! Always tired, fatigue, WEIGHT gain like crazy, moody, ZILCH sex drive (poor bf), jawline acne (always was blessed with nice skin!), depression (poor bf again, we broke up constantly) and just recently nausea...no food can satiate me...I thought I was going crazy....Im getting off this crazy pill and hopefully I will get back to being normal...I'm 26...I'm not old!! This definitely is birth control cause I don't have sex, and I feel like a total fat @ss all the time!! It sucks!! I sure do feel like it and I'm stopping this pill today! I hope this site helped you as much as it did me!!

I have had the Mirena for 3 or 4 years now. The first few years was great I didn't have any systems at all and i just loved it. Well over the past year I have had nothing but trouble I have gained over 30 lbs, I've became so depressed to the point I won't do anything get dressed, do my hair, leave my house, I break down and cry for no reason, I keep migraines, and I'm to the point I hate waking up. I've tried to talk to my Dr. about having it removed but they just make me feel as if all this is in my head so I keep it. They did tell me about another IUD called the Paragard which is what I want because it is non hormonal but they say they can't do it at their office and I can't find no one else to do it either. So I'm still stuck with the Mirena until I can get the Paragard. That's if I don't get fed up before than and take it out myself.

Nausea is the only side effect I have noticed after taking 300 mg of Wellbutrin for over three years now. The nausea is worst in the morning, after I take the pill. My stomach feels very acid, like I just drank a pot of coffee with no breakfast. It usually gets better if I eat something, although not always.
For the first few years, I also experienced decreased appetite - no complaints there! I lost weight, but this year I regained it. Not sure if the appetite suppression effect wore off, or if this year has just been really stressful for me.
I also found it impossible to smoke cigarettes - they tasted nasty. Another good side effect for me.
Overall, Wellbutrin has helped me with depression and social anxiety. Best of all, I have absolutely no sexual side effects, unlike with every other antidepressant I have tried.

I went from a rational non-emotional women to a crazy person!!! I feel awful. I would rather have pain than feel this way. I can't sleep though constantly fatigued. Achy body, headaches. Everything tastes like cardboard so I'm not eating well though I have gained a few pounds. I am severely emotional. I almost left my husband this weekend whom I adore, can't stop crying, very depressed and irritable. I want nothing more than to be alone and sleep, which no one can live that way. I am a mother of 3, a wife, and have a full time job. I can't function properly. I will never undergo hormone treatment after I get through this! I am currently on Lupron, just had laporoscopy 2 weeks ago for the 5th time all for endometriosis and I'm only 25. I started Premarin today to assist this anxiety and mood swings. Wish my family and I luck.

I have been on the Fentanyl Patch for about 5-7 years now, for a condition called Loin Pain Hematuria Syndrome. It's rare (but more people are showing up with it) that is not life threatening and has no cure, but consists of serious pain in groin (loin) area, side pain (near kidneys) and sometimes around to back. It also consists of mid to large amounts of blood in the urine, it's known have thin blood vessels in the kidneys that allow blood cells to enter urine, but no real known reason of its cause. I am still pain free (just have discomfort on the third day before I change to a new patch) but after the first few years have started to have a lot of side effects and withdrawal symptoms. I change my patch at night and on the first day (the next morning) I feel fine and have no issues except a little sleepy from the night before. On the second day I get very sleepy, anxious, somewhat agitated easily, and a little depressed. On the third day, when I have to change my patch that night, I am even more sleepy to the point where I can barely keep my eyes open and they are heavy, all through the day and evening, I too have some memory issues but are not as much as the other side effects, I get low grade fevers that I can feel change over different areas of my body, shallow breathing in which it feels like it is sometimes hard to catch my breath, urinating often with not a lot of urine coming out (on third day only), some body aches, worrisome, more depressed, and weakness. Then after I change my patch the third night and it absorbs, I am wide awake and can hardly sleep. I even wake up every few hours on the second night, but the night I changy my patch is the worst, so I am tired the next day which is the first day on a new patch and the three day cycle starts all over again. I like that I am pain free, but at what cost? I am going to talk to my doctor again and they cannot pinpoint the nerves or areas of pain so I cannot have a pain pump, and I changed to this because I was getting so much break through pain between any pill form of pain medications. I did not like having to take pills every 4-6 hours. Has anyone else had this on Fentanyl or had the condition I have?

I am a 32yo male and a Paramedic and it has been a living hell for the last two years. Here are my side effects and then my story. Anxiety, anxious, Irritable, high heart rate, leg calf pain, horrible sleep, bad nightmares, depression, suicidal thoughts, thoughts of hurting people, hate being around people, fear of heights (I used to rock climb daily), dizzy- if I move my head too fast or spin around with my son, weight gain(could be unrelated) arm cramping, frequent urination, and mood swings from crying to anger in just a few minutes. Not like me at all! First few years looking back, I was just became irritable and short with people. The last year has been horrible depression and anxiety along with the other side effects. I like many of you who have written here have had many of the exact same side effects. I had a stressful job at times and worked 24 hour shifts. I have always loved people, and enjoyed meeting new people. Not any more!! Two years ago my mother who lives 3.5 hours away asked me why I was in such so anxious all the time. She said, you are not the laid back and carefree man I know. I thought it was just due to some stress about being recently married or the job. The changes took time and I did not realize them or see them. Looking back, others knew something had changed.
Knowing about medications for my job and how to research them, I looked into every possible side effect and how Singulair worked before I started taking it. Looked good in 2004 with no major side effects. A little over a year ago my father became sick. He was going to battle cancer, but before he could, he would find out he needed a heart valve replaced. He got the surgery, went into cardiac arrest at home a week later, and was given CPR by my mother. A local police officer shocked him and got the heart out of V-fib. I slept with him in the ICU almost every night. He died a week after that and my wife was 7 months pregnant. Talk about stress. The baby came and I stopped working to raise our new little boy. I became short with my wife and started to pull away from being around people. I started to have bad dreams with twisted and morbid outcomes. I had suicidal thoughts out of nowhere and would wonder, where did that come from. Just as soon as they would come, they would be gone or I would think about something else. I got dizzy all the time and started to get carsick if I wasn't driving. I used to be able to read while riding backwards or sideways in the ambulance without a problem of feeling sick. That was not like me at all. I would snap at anything and became almost OC about everything. Thinking all this time the last year that I was just depressed about loosing my father whom I was very close too. Our little boy ended up having some medical problems and the insurance company would not pay the bills. More stress! My wife an EMT-Intermediate blew out 2 disks in her back on an ambulance run, more stress again. More insurance problems. I became a basket case! More anxiety, more depression, never got a full night sleep, mind racing, calf pain soo bad I would ask my wife to rub them, arm pains and finger joint pains at night. I also had a high heart rate of 100 almost all the time. Heart palpitations and a few times it felt like my heart was empty off all the blood and would beat very hard in the middle of the night lasting only a few seconds to a minute. Weight gain, moody all the time. I thought just due to all the normal stress in life.
Two days ago I went for a hard hike and came back with a pounding headache. Excedrin always does the trick for me. Not this time! I had seen a second of a news where the anchorman was talking about Singulair. Googled "Singulair problem" and found this site. I freaked out!! Almost all of you are talking about all the problems I have had as well!! This medication is making us go completely mad!! Tried to go to bed two nights ago and my mind was just racing. It has been Singulair the whole time. The only medication I take. It has made me nuts. My head was pounding the worst I have ever felt and my heart was coming out of my chest. I was awake since 3:30am and read the story of Cody Miller. This poor boy had no chance with this drug. He brain was not fully developed like an adult at just 15 years old. He wouldn't be able to fight the suicidal thoughts like I can. I have been to a lot of hangings, suicide shootings, and drug overdoses. I have seen plenty of death.
I called his mother a few hours later and explained to her that by them going to the media and getting the story out, prompted me to look into Singulair side effects. And that they just saved my marriage and my life. I explained to her that she did nothing wrong by giving Cody the medication for his allergies. It works great for the asthma and allergy symptoms for me. But, it ruined the last year of my life! I felt like I was going to have a stroke shortly after talking to her. I had my wife check my blood pressure and it was 154/100 (normally 120/82). Got grandpa to watch the boy and went to the ER. After my lab results came back and talking with the doctor, we decided it was a panic attack and who knows what the side effects of coming off this drug will be? I had stopped taking it the night before. Thanks to all of you who posted here and thanks to Kate and David Miller for speaking up. You saved my life. This medication got worse over time for me. It got worse as the stress level went up. I have been off it for two nights and already feel much more calm and was sleeping fine, until the little boy woke up and wanted a hug, or bottle. I hated almost everyone, I was short tempered, anxious, OC, and wanted to hurt people for no reason. I want my life back. I want the old me, the care free happy go lucky guy! I already feel better and will write hear as the days and weeks go by. I will never take Singulair ever again!! Not one stupid pill!! Look to those close to you and see if they notice changes. Even those of you who have been on it for three years like me. The drug company knew what was up the whole time. Bad men and women who want money over telling the truth. Maybe not everyone taking Singulair will ever have the side effects soo many of use have been living with, but to those of you that notice changes! Throw this medication away now and never touch it again. Get your life back!!! Be the old you again. I will go back to Albuterol (the only medication I used to take). Read the stories about the two year olds and the five year olds that cry all the time and are angry all the time. Little kids tell it like it is. It's not until they get to work for large drug companies as adults due they lie about side effects and wait years to publish paperwork saying that post marketing research shows all these negative side effects. They knew all along.

I have been reading all the entries for this website and thought I would pass along some useful information. I have been on Levoxyl for 8 years now and have had lots of the symptoms that all these people have had. I then had an appointment with a great Endo doctor at the *** and discovered some interesting things. There is a number "range" they put all people into when checking your TSH levels, only problem is each person is different and even though the doctor may say your in the range, it may not by the right dosage for you. Unfortunately the only way to determine the correct range for you is to experiment with the dosages and it takes 3 months or more for your body to adjust. Also, thyroid hormones are accumulated in the body and depending how active you are is how you may feel. The hormone pill you take today will not be used by your body for up to 10 days, so if you feel good for a few days at rest, then exercise the next day you may feel drained. It will take a few days for your body to replenish the stockpile of hormones to feel "normal" again. A working thyroid makes hormones as needed, yours now does not so this is why so many people feel fatigued, or racing heart beat if they don't get enough exercise. I also had leg and muscle pain. The medication depletes your body of Calcium and B complex especially B12. My leg and muscle pain have disappeared. I still get headaches, but much less with the B12, and some days I still feel tired but I say again, your body cant regulate its needed thyroid hormone and a synthetic pill is only a substitute.. You will always have some side effects. Hope these tips help someone.

I had my Mirena inserted on Dec 5th at which point I was 6 wks postpartum. The insertion wasn't that bad. I expected it to be a lot worse as my Dr. told me it would be. I had slight cramping a few days later. I spotted for 15 days with mild cramps that are still ongoing. They last about 2 minutes or so. I have noticed that I feel much more "spacey." I will give it time to adjust before I make another rash decision to have it removed. I have read all the problems posted on here and it does scare me. I have not noticed any signs of depression, nausea, or headache. I am experiencing insomnia, but I have a new born. I listen for him while sleeping and have not gotten back to a normal sleep routine. I apologize for all of you who have had such a terrible time with this form of birth control. I thought I had done my research and now find that there is so many more negatives. I am willing to make a few sacrifices for a worry free sex life. I don't feel that the Mirena has altered my sex drive or my sex life; my kids on the other hand have and do. For those of you who are wondering whether it's right for you, you have to decide for yourself. Is it worth it? I think it is. I may not feel that way three years from now, but seriously I don't plan to keep it in that long anyway. I will probably be planning child # 3. I have noticed that it seems to be great for most women for the first few years and worsens over time. So maybe my method to this Mirena madness may prove to be fruitful.

Hi all. I was diagnosed 3 or 4 years ago with epilepsy. So far, I have on about 5 different epilepsy meds. I can't recall the first 3 but had to get off them because of physical side-effects. My last one was Dilatin which worked pretty well for a year. I slept great - 8 hours on the dot. Then, I started to have short seizures that began to successively lengthen. So, I was switched to Keppra.

I started at 250mg/2xday on Keppra and now am up to 1000mg/2xday. I also started taking B6 100mg/day. A couple of days after starting Keppra, I started to get slight headaches. These went away after about 2 weeks. I also got a numb patch on the same place on the bottom of each foot. When I went up to 500mg/2xday, the numb patch spread, I started to feel off-balance, and I started to get the "rage" symptoms. I went up to 1000mg/2xday and most of the bottom of my two feet went numb and cold, I began to get slight tingling in my fingers and a mild case of tightness in my chest. I still felt off-balance and the rage symptoms were there. It began to get hard to get to sleep and I would get up unnecessarily early and not be able to fall back asleep. I want off this med. Maybe it works great for other people but for me it I take it at the levels I need to, I won't be able to work or do much of anything.

I live in the UK and receive an annual kennalog injection for hayfever.

Described as using a giant hammer to crack a nut! my first injection was about 10 years ago and the effect was absolutely amazing, my hayfever cleared up instantly.

During the first few years the only side effects i noticed were increased agression ( i am normally calm !! ), really bad headaches and the increased number of bugs/colds due to my immunity system being broken down. What i did notice is after a few years the injection has a lesser effect, it still works wonders but not as good as the first few times.

Last year i had a massive bust up with my doc as he refused to give it to me. I cannot do my job with hayfever so eventually he gave it to me on the condition i signed a disclaimer as it is no longer recommended for hayfever.

I usually dismiss all normal hayfever tablets but this year I have decided take docs advice and am using tablets first before i go back begging for my injection.

The tablets i am using are called Neoclarityn and are only available over the counter.

Into June and all is ok so far apart from a bit of asthma.

Anyone else using anything else other than kenalog for hayfever??

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