Mean time symptoms and conditions

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

I have had my Mirena for 3 yrs. (Oct 2006) For a long time my doctor, nurse and I joked about how I was the poster girl for this product. I didn't have much cramping with insertion, had one slight period a month later, and have been period free since December '06.

A few months later I broke out with the cystic acne and they put me on Yaz. It seemed to help for about 6mths. I then went off the Yaz and was fine for a few months, until I broke out again. This time Yaz didn't work. I've delt with them ever since. In the mean time I started having troubles falling to sleep. It was very sporadic at first until this past Jan. (09) My doctor put me on 10mg of generic Ambien. In July she cut me off. I had a full blown panic attack! The next day I contacted another dr who doesn't have a problem with me being on them. She put me on several anti-depressants until we found one that seems to be helping.

I have always been a people person, full of life and love for everyone! Now, I dread going to the store, or taking my boys (11,9 & 4) to soccer practice/games!

My husband has mentioned from time to time that I complain of a lot of headaches. Come to think of it now, they happen nearly every day to one extent or another!

I've been researching the Mirena the last couple of days because of the acne and sleeplessness. MOST posts talk about the symptoms beginning right away, making me think I was crazy and just looking for a reason to feel this way!

My husband has been my rock and is very supportive of me. He has no problems with me taking it out, but will NOT get the sweet lil V done! ugh If I can get this out and have the acne clear up. I'd be HAPPY!

First symptoms: Acne
Then: Sleeplessness, Headaches, back pain especially lower, mood swings, anxiety/depression, oily hair, uncontrollable crying... I'm sure I could go on. The symptoms don't have to be instant. In my case they came slowly...

GOD BLESS!

I recently back in April of this year received Cyberknife radiation for Adenocarcinoma with metastasis to my brain. After surgery to remove my brain tumor in March of 2009. I went though whole brain radiation and the Cyberknife to my lung. The doctor was very adamant that as the lung heals from radiation you will develop what they call wet lung or neumonesis sp? This will have to be treated separately, or severe coughing would continue. My primary care doctor in the mean time put me on Lisinopril 20 mg for hypertension. I have not gotten a good nights sleep in 2.5 months since, then came the pneumonosis. This cough persist to this day waking me from what little sleep I do get, and amazingly am now suffering from joint pain especial in my hips. It's to the point I can't even cross my legs anymore it hurts. When discussing this with my primary she says its in my head as of today and reading this site and side effects I am taking myself off of Lisinopril and will seek a second opinion, even a third if need be thank you all so much for posting your side effects from this drug.

I too have been experiencing the same side effects listed by most of you. I have also been seeing a gastroenterologist for about 9 months now because of stomach issues. All symptoms point to gallbladder disease but the tests come back normal. I called my gyne today and they seem unconcerned with what I have told them and advised me to continue to take my pills until my annual visit in October. I'm done with this pack on Saturday and am thinking of going sans pills for the next month until my appt. Any advice on what pill I should switch to when I do see my dr.?

I have had the Mirena for about 3 years now, I first started having noticeable symptoms about 6 months ago. I started having panic attacks out of left field. I am a very happy person, with a good life so I could not understand what was going on with me. I thought I was going crazy. My daughter had to go with my mother for about 2 weeks as I didn't want her to see me the way I was: having panic attacks, paranoia, depression, crying fits. I was put on celexa to help these problems. It worked for the panic attacks, but I'm still moody and can only sleep if I take a 2.0mg of klonopin. I have never had these problems before. I cannot say it was the mirena, but I doubt I have any other reason for it. I recently started getting really bad cystic acne on my face, chest, back, and even on my scalp. I have gained about 25 pounds and cannot get it off for the world. I only have one daughter and a lot of help from my husband and my mother, so I can't understand the feelings of fatigue that plague me. I have a horrible year. Just the anxiety and panic attacks alone have changed me completely. I thought I was abnormal and sometimes just wanted to die. I do feel better, but as I read, I wonder if taking it out will help with the weight, acne and fatigue as my other problems seem to have just vanished after only 2 weeks on celxa, which I thought strange but was thankful nonetheless. I spoke with my doctor today about removal and she gave me a rx for the acne and said we should think about it.... I think I'm all thought out.....

Ok, so I had this little "evil" thing put in May of 2007, at first it was fine and I hardly noticed it. Well, except for the not having a period, then having all the brown goopy stuff I suppose it was a period I guess. I went back and forth between nothing and episodes of this. I used to refer to my symptoms as having a "mock" period cause my body wanted to have one but I wasn't. I told my doctor I thought something was wrong at my annual in January of 2008 because I couldn't loose weight, I was tired, my migraines came back, my back hurt, my boobs hurt. She told me I needed to have my thyroid checked and ran all kinds of tests. I dismissed it all, but in the back of my mind I thought it was because of this little "evil" piece of plastic. I'm sorry but not having a period is NOT normal. I lived with the "side effects" and at my annual in February of 2009, I had gained more weight, even though I was taking fat burners, working out, and watching my eating habits. Then about 3 months ago, I started experiencing the worst pain possible. Always around the end of the month when I was having my "mock" period symptoms. It was so bad I could barely stand up. My mood swings were HORRIBLE, my husband and I fought a lot. It keep getting worse. After repeatedly telling him that I thought this was all due to this IUD, he dismissed it until this month, when I could barely stand up because of the pain. He finally said take it out. I am getting it taken out today at 10 am and I am counting the minutes. I thought I was crazy, and that this was all in my head. I finally told my husband that I am taking it out and our fertility is in Gods hands. I have an 18 year old daughter, and a 19 year old son. They are grown and gone, he has 2 children from a previous marriage that he never sees. I am 38 years old and have resolved myself to the fact that if I become pregnant it is Gods will for my life, but in the mean time I will be rid of this "evil" thing and all of the HORRIBLE side effects. To anyone reading this that is thinking of getting one, PLEASE don't, you will be sorry. I feel as though it was an ok option for me for about a year, not the 5 they say and it costs way to much money for only having a year. The side effects are horrible, you will experience them and you are NOT crazy.

Okay, I'm 17 and have been taking Loestrin 24 Fe since early February.. This is my first birth control, so I wasn't quite sure what to expect.. but so far I can't recall any serious mood swings or crazy depression.. however, I am on my 4th pack or so and for the first time, I have yet to get my period and I am on the 3rd day of my 'reminder' pill.. My boyfriend and I use protection and I have heard that this missed period is a common side effect, but in the mean-time, I'm still going nuts! I'm just a nervous wreck and don't know if I should be.. Is it normal to miss my period this early since I've only been using Loestrin for 4 months??

Hi, I have had my iud since 2-14-2007. Just last year all my side effects that everyone has had have stopped-just plus size, alot of belly fat. Seems like I am having another baby ,looks like it anyway. No periods every now and again spotting, mild cramping. If you have a choice and you can use something else that you know worked well for some one else- use it. If you can take the weight gain, bloating, cramping, mood swings ,etc for how ever long than do it and find natural supplements that might help your symptoms . Just because you know it is closer to permanent, you have talked to your doctor everything looks fine ,blood work normal-give it time if your comfortable. I hated what I went through. I made it through it without having anymore kids right now. So in the mean time we just need to decide - If we want more kids -have two. I was yelling at my kids and in pain and just knew I couldn't afford to have anymore so it is worth something to me. I just managed with herbs and vitamins and a good support system. Now that it has worked and the side effects are over I would remove it for the weight gain issue. Thankfully my husband is supportive. Thankful to that I am still mother of only two. Wish you all the best.

Unfortunately I've had to stop the Lupron injections. I lost my job and with that my health insurance. I am wondering can anyone tell me when I can expect my period to start again?

November 6, 2008 was my last injection and it was a 3 month dose. It is May 2009, I am 39 years old and I have not yet had a period. My fibroids ae back to their large abdomen filling size so I am very worried.

Not having insurance or adequate funds has reduced me to the internet for research first before venturing out to a doctor as a "self-pay" patient.

I have had pain in my knees and legs after taking levaquin for pneumonia for 10 days. I am weak. It is hard to get up and down and very painful with steps of any kind. I am very depressed from the pain and inability to find anything that will help. I have been to an orthopedic doctor and had X-RAYS. Just given anti-inflammatory. No tendon or obvious reasons for pain. What do you do now? Who do you go to for help? In
the mean time, my breathing at night has gotten worse again.

I have been using the NuvaRing for about 6 months now. I thought it would be a blessing because I would not have to take a pill everyday. I am 23 years old. Have a fantastic serious boyfriend. and NO sex drive. I have always been a happy person, so this behavior has been obvious to not only me, but others. I have been considering going to see a therapist because i just can't seem to get out of this "funk". And thanks to all of the posts, I now think I have a legit answer to my behavior. Besides having little, to no, sex drive.. I have been having waves of depression, headaches, moodiness, feeling anxious, fatigue, weight gain, (looks like someone put an air pump in my face, ugh.) and plain weird thoughts. I really just feel out of my body, just not with it at all. I have tried diet changes, regular exercise, etc. Basically, trying to fix my depressed feelings/anxiety without having to see a doctor or get on another medication. Does anyone know how long it takes to get the NR out of your system. Just ready to get back to normal!!!

My story started about a year and a half ago. I got my first kenalog injection for ORAL LICHEN PLANUS and was told that it was safe enough to give to his own wife and kids and he convinced to take it. But little did i know that it was going to leave this huge dent in the top part of my right arm. The doctor said it would fill in but would take awhile. So in 4 months i went back for my second injection because it seemed to help my mouth but then strange things started to happen. I take blood pressure meds and have for 14 years and never had any problems until that second shot and my BP started to go up and down and i mean very low and very high. I went to my family doctor and he wanted to try other meds and i said no so he sent me to heart doctor and that was a waste of time and money. I just waited it out and in the mean time i stared to to drop a lot of weight and couldn't figure it out. Now it was time for third shot and by this time my weight started at 145lbs. is now 119lbs. The doctor said my problems are not from the shot. So my health started going down hill and my bp is now very high all the time and still losing weight. Guess what its time for fourth shot and i now weigh 109lbs. and i told myself no more shots because in the end every shot i took started to not help my mouth anymore. Well its been 5 months since my last shot and my bp is normal now and my weight is at 115lbs. I still have the dent in my arm. This is a very dangerous drug and i advise no one to try it. Someone needs to take it off the market. And before i forget- what it has did to me is i have very bad bone and joint aches but i hope in time it leaves and blurring vision and headaches everyday. I just want it out of my system.

This is amazing to me to hear all of these side effects from the yaz. I have been experiences all of them but really didn't make the connection. I have been experiencing knee joint pain since I have been on these pills but really didn't make the connection. I only started researching this since I received an email from someone about yaz and the warnings about it. This message went into my spam out of the blue, and I opened it to read it. That was about a month or so ago, and I am scheduled to see my doctor in a month or so and I don't want to abruptly discontinue without having a plan. I am 46 years old and was an anemic due to heavy periods, so this was the solution to get my blood count up to what it should be. This was a real issue because I had to have emergency surgery but had to have 2 units of blood before the surgery. So after that, it was suggested that I take bc to control my periods. I really didn't want to do this but I had to for the mean time and I have been on them for about 8 months. My blood count is back to normal now but I have to figure out what else I am going to do because I cannot continue on these pills now that I see what it is doing. I will be going into menopause soon also, but that's probably not until 5 more years and I am not going to take these all that time. I have some decisions to make.

I started taking Yaz about a year ago. I started taking it around the time my brother died in a car accident. I thought that my loss of libido, tiredness, lack of interest in everything, emotional outbursts, arguing with my husband for any reason, crying over nothing, unable to concentrate while studying and unable to remember a thing were all because of my brothers death. I am now thinking that this may be due to Yaz. Does this sound like Yaz side effects? or am I suffering from depression because of my brothers death. I just haven't felt right lately and I cant figure it out.

I have contacted an attorney in Delaware who is willing to pursue a possible class action suit. I explained my side effects from this drug and told him of the countless others that are suffering as well. He said if I was willing to do the "legwork" and gather up names of others who would like to join this suit, perhaps we could get a class action started. If anyone is interested please reply by contacting me at ***** Please be sure to type "Kenalog" as the subject and include your name, email address, and a description of your experience with Kenalog. I will than gather your responses and forward them to the attorney. He will than contact you individually, so please include a contact number. This will take some time. So please be patient, as you know these cases take time. I have spent 15 months trying to get some kind of help from various doctors, to no avail. Someone needs to step up and take responsibility.
Hope to hear from many of you. Thank You

I was put on Yasmin not for birth control but for the beginning of fertility treatments. I was on Yasmin only 1 months. After about 2 days I started getting symptoms. I called the Pharmacist and my fertility doctor and they both told me the pill wasn't the culprit. But after the 20th day I just couldn't take it anymore I went off of it. After starting Yasmin I had TERRIBLE Panic attacks, Anxiety ( still have to this day two months later), Heart Palpitations, leg cramps, boobs hurt, breathing trouble ( still to this day), HORRIBLE thoughts, adrenaline rushes all hours of the day, tingling in my hands and feet, my mind feels fuzzy, no appetite, no sex drive, depression, crying fits for hours, I felt like i was going insane.... You name it I had it. I stopped the pill two months ago and I still have the horrible anxiety/attacks, feel like i cant breath properly, OCD about my breathing.

I went to the hospital and got checked for blood clots in my lungs, legs, Asthma test, EKG, blood tested, was put on heart monitor all came back normal. I have started seeing a therapist, on depression meds and none of it is working. I feel like this pill has ruined my life and i wasn't even trying to stop life i was trying to help create it.

Here i am two months after stopping the pill and yes some of the stuff has went away but i still suffer with Anxiety from the time i wake up in the morning till the time I go to bed at night. And sometimes I wake up in the middle of the night with anxiety. My head is getting a little clearer and I am not as depressed as before. But I am just praying that this anxiety goes away. I have NEVER been a person who can't handle stress or gets anxiety/panic attacks and since it started it hasn't stopped. I am so very weak, muscles ache so much which i think is from the anxiety attacks and the muscles tightening.

So if you have this... you are not alone! I am suffering with it everyday. It is so debilitating I cant do much. Has anyone else had this months after stopping Yasmin?

I am replying to my first post here yesterday....So today I didn't give my 3 yr old son the singulair and do not plan on it ever again! I have to say though...I am very very concerned. I think tonight I truly saw one of the bad behavioral side effects :( He got upset over something so small. Said he didn't love any of us, he didn't want Chinese which is his favorite! He didn't want to do any of the things that we gave him options on that he normally would jump right up to do! This devastated me! I right away thought to myself is this going to get worse before it gets better? He is still complaining of back pain which I know that will take some time. He punched a little boy just before dinner in the neck. He walked out of the neighbors house to go home and usually I have to carry him out. This is seriously scaring me! I'm not sure what to do ? My fiance, his father, doesn't understand and started to yell at him for his behavior. (We don't get much time to talk and when I try to his dad just says he is ok but I know, deep down he isn't) I am the one with him everyday at home taking care of him. I am now being more patient with this behavior when normally I would lose patience and punish him with time outs. Do I continue to do time outs?
Why should I punish him when its not all him ? This is so unfair :( I mean, he is a boy and yes he acts like one. Doesn't share at times, hits sometimes, he is a or was a normal 3 year old boy. His dad will follow my footsteps on this as he see's how I handle things but I'm a little witty on how to handle it now. At this point I am babying my baby! I will tell him when things he does is not right but I'm at the point now that I don't want to send him to preschool! Do I inform the teachers? Can someone give me some words? Its just hard because he is my oldest and is only 3 so not only am I learning to deal with regular behaviors, I now have to understand how to cope and deal with this until its over. Thank you in advance very much for any help and advice!!!!

I was put on synthroid a year ago, due to a tsh level of 87. I pretty much felt better right away after taking it. First I took 50mcg and then it was upped to 100mcg. Everything went well until I had my latest tsh test. The level was going up again (tsh 5.4) so the doctor decided to put me on 125mcg. After about a week I began feeling like crap. Slugglishness, tiredness, muscle pain, joint pain, and it became progressively worse. I have an appointment coming up thank god. In the mean time I read 3 books on thyroid and it was mentioned that most people don't benefit from just taking T4 (ie. synthroid), despite the fact that the pharmac. and some docs say that body breaks t4 down into t3.
Some people's body cannot successfully break it down enough, some are cellular resistant to thyroid hormones, and those people absolutely need t3 in order to not develop Hypometablolism. The cell need the T3 to function. But unfortunately one can be hypo and still have good TSH levels, because this particular test only tests if there is enough T4 in the body.
Unfortunately, it's so hard to explain that to mainstream doctors.
One doctor I read about said it right: Don't just treat the test results but also the bodily symptoms, for everybody is different anyways. Just like our finger prints are unique, so is our hormonal metabolism.
I'm going to try to talk to my doc about this, but if he doesn't listen I will look for another doc until I found one that will. Good luck to all in this hormone jungle.

I took it for one month only. In the first week I was extremely fatigued but ignored it. Then I got stiffness in my fingers. I started getting cramps in my feet and legs. I stopped the medication after exactly one month. It has been one month since I stooped taking it. But my symptoms have not gone away. My arms and legs are still stiff. I develop severe pain in my left arms. There is a terrible tingling sensation in my body when I sleep. I am going to see a neurologist next week. I hope there is no permanent nerve damage. I have started taking Lyrica 50 mg in the mean time to get rid of this tingling sensation.

I got Mirena put in on July 5, 07...never had a child but Dr. said since I was 36 and not planning on having children, Mirena was a good alternative to the pill which I had been on since I was 19. On the pill I had very light 2-3 day periods and with diet and exercise, could lose weight. Now, almost a year on Mirena...the only good think that has gone away from when I was on the pill is the migrane headaches that I was starting to get on a monthly basis...but, in their place...I have gained weight, tired, have acne, cramps erratically throughout month, never know when my period will show up...some months it does not, some months it lasts 4 days (like last month), and I always feel bloated - esp. in the abdomen. I've even wondered on occasion...am I pregnant?? why do I feel so bloated?? One other weird thing, since I started running this year, I get this weird sensation that I have to go empty my bladder...this also occurs while doing intense stomach crunches...but it is not incontenance..nope never have bladder problems...it is just this funky feeling - sometimes almost a burning feeling around my uterous. Have not seen anyone post this - but it did not happen before Mirena when I ran or did sit ups...now it does - doubt this is coincidence.

Some of these symptoms truely could just be simply the result of ovulating again - that is what my Dr. told me...that on the pill I never released an egg...so now my body was getting used to ovulating again. Well...if that is the case, I just can not stand it anymore...I get it removed June 26th - next week so hopefully I'll be able to post back that these symptoms are gone or have removed. Going to go on the pill again...which has its own side effects...but I sure did not have as many when I was on it. Husband has offered to go under the knife to take care of him...but I'll see how the pill does again. Hoping to reclaim my life and actually lose weight as I've been dieting and exercising while on Mirena to no avail!

Does anybody have anything GOOD to report about Mirena?

I got my mirena a week ago today. I'm not sure if i'm just being a Hypochondriac - or if I just have a lot going on in my life, but I feel that fog that other women are describing, and I swear I feel like i've gained 5 lbs in a week because i'm so bloated. ?? I scheduled a follow-up for exactly 2 weeks to discuss symptoms with my Dr. I'm scared now! I wish I read these reviews before I got the mirena!!

I spent the weekend reading about the development of Singulair. The early studies recognized that the first phase of the acute asthma response bronco-constriction was probably not caused by leukotrienes. They identified histamines and prostaglandins as the probable sources. I don't think that changed because the Singulair literature states that it should not be considered as a treatment for that. Leukotrienes were a source of inflammation caused by eosinophils and mast cells present in greater numbers (than normal) in airway tissue. So, it was beneficial to find a way to decrease that.

The cysLT1 receptor was identified as source of the signals that tell the cells to produce leukotriene. The receptor, a gene, consist of 337 (they think) amino acids. They modified a compound that would bind to that receptor thus blocking the cells ability to produce leukotrienes. This compound is very specific. It was formulated to bind to the "model" receptor. This compound will not even bind to cysLT receptor sub-types. (That is the good thing.) There is an enormous amount of research that discusses the genetic variability of the chemical reactions that occur in the leukotriene (calling it this for simplicity) pathway. We are also seeing that a number of researchers would like to use gene profiles to predict whether patients will respond favorably to different asthma/allergy drugs. ALL PATIENTS HAVE A RIGHT TO KNOW IF IT IS INHERENT THAT SOME PEOPLE WILL NOT RESPOND TO SINGULAIR OR RESPOND ADVERSELY.

There are many studies from the 1998 era that conclude that montelukast is not effective for everyone. Those researchers stated that it can be predicted that those people who are going to respond favorably will do that within the first 14 days or so. That conclusion would be consistent with a genetic component for efficacy and safety of Singulair. Those doctors concluded that those who did not respond within that time frame should not take Singulair for fear of harming them. That makes good sense.

The Italian researchers wanted to know if there was more going on than blocking leukotrienes in the action of montelukast. They set up a "test tube" study regarding montelukast, the cysLT1 receptor, and some t-cells that they selected. Why? Researchers always have something on their minds. They observed the death of these particular t-cells.

Montelukast is a quinoline. We basically know of quinilines and quinolones as compounds that were invented as broad spectrum antibiotics. They work because they interference with bacterial DNA so they cannot replicate themselves. Montelukast is a quinoline modified to bind with the cysLT1 receptor (a gene) and prevent that gene from activating. That's consistent with what a quinoline/quinolone does.

So what does montelukast do in blood plasma if it does not bind to the receptor because of genetic mis-match? (If montelukast does bind, then a chemical reaction has occurred and the liver will break down the by-products. Montelukast metabolized in 10-12 hours.) What happens if it doesn't bind? How long before it breaks down? Does it produce toxic by-products?

I want to know what happens to lymphocytes such as t-cells just because montelukast is a quinoline. Maybe nothing but what's up with the Italians researchers? I want to know if montelukast has the capability to interfere with lymphocytes who can clone themselves. That could be a good thing under circumstances when these lymphocytes are causing inflammation. But it could be a bad thing in the case of normal individuals with no problems.

I want to know if the bad side effects are due to the fact that the body has to break down and metabolize a quinoline that did not bind to the receptor for which it was created. The side effects of Singulair are strangely similar to what is observed in the quinolones such as levaquin. I have not as yet been able to compare montelukast as a quinoline to levaquin as a quinolone. I am hoping to find something on these categories. There may be no reason to worry that they cause similar damage. But frankly, I think that there is. There is some terrible chit happening to some people. The scariest is the neurological damage.

All of these questions would be in the everybody pharma knows to ask category. I don't know where the answers are. I haven't found them as of yet. Maybe there are no answers. We have to remember that Singulair and Vioxx were released in the same year. They have continued to be drugs under the current executive management of Merck. If the Vioxx marketing promoters had their ghost writers, why not the Singulair marketing promoters. The genetic component appears to be widely accepted but we haven't heard one thing about even that.

I think that it is sad that maybe the marketing of Singulair as one stop shopping for asthma/allergies may have destroyed the original concept. I really think from reading the original work that they knew that they couldn't engineer a drug for one size fits all. Everybody gets harmed when information is withheld.

Shame on the allergist who yelled at the mother who wanted to discuss issues. Does he know exactly who is allergic to Singulair and who isn't? Get him a dunce hat. Just because Singulair is marketed for allergies does not mean that you cannot be allergic to it. See the power of Madison Avenue? The ad agencies focus group these drugs to death. The ad agencies cleverly craft the product information. A good piece of legislation would be to prohibit consumer drugs ads.

i am on my second pack of Yasmin. In the beginning,i got really sick to my stomach, probably because my body was getting used to the pill. As soon as i began the week of sugar pills, i had terrible headaches on one side of my head. the headaches lasted about a week, and by the end of it, i was ready to lose my mind. now, today,i woke up and began feeling very dizzy and numb all over my body.after a few minutes my vision was fading until it got to the point where all i could see was outlines of things. Everything looked like a picture with really high contrast.i looked at my mom and her face was bright white with black detailing. it was really weird. i also noticed a sort of white glow all over everything. i was so terrified. i am not the type of person who ever faints or anything, so this was really odd. it went away after about 5 minutes, but it was so scary that it felt like an hour had passed. I'm not 100% sure if this is caused by Yasmin, but i haven't done anything different that would make this happen to me. i am going to the doctors, but in the mean time, i'm going to stop taking the pill. please let me know if anyone else has had an experience like this

I am a 34 yr old mom of 2 and have had my Mirena for 4 and 1/2 years. I actaully have been having a great experience, but again, have the same weight gain issues with almost no loss, no matter what. MY BIG QUESTION: has anyone else experienced mysterious vaginal discharge and symptoms? Starting about a year ago, I began having mystery discharge and have been to 7 different doctors who have tested for everything under the sun, and FOUND NOTHING. they can see it, keep giving me yeast treatments. etc, but in 2 or 3 months, it is right back. There is a pungent fish odor, especially after sex with my hubby, which Dr's have been saying is normal... MAYBE NORMAL FOR THEM, not me!! I actually thought it was due to a lack of hormones now that my IUD is ending is life.. However, I did have a couple of crazy panic attacks, which I have never had, the dryness for sex and friction is intense, and my hair has been thinning, which I thought was just me... Can anyone let me know if you've had the vaginal symptoms... I know no one wants to talk about it, but I have to ask!!

I have a 15 yr old son, that has been on Singulair for 4 years. He used to complain to me about not being able to sleep through the night, he couldn't concentrate at school. He was an honor roll student. Then he became short tempered. He also isolated himself, and no motivation. He would not want to do anything. He was depressed. Does not want to shower or anything. He has absolutely no self worth. He would talk about having these problems and I would just say to him that maybe it was just the changes going on. New school, changes to his body, it's just those times where changes and expectations are harder. Some handle it better than others. Than everything just continued to go down hill. My son is very intelligent, so when mom did not listen, he decided to self medicate. Went online to try find out what was going on. Tried to find what would help him. He learned quite alot about pharmacology(spelling???) at any rate he then started experimenting with other drugs. Prescriptions drugs. He just wanted desperately to be happy. I found out about this. He was getting into trouble at school, grades fell. So we then sought counceling and then a psychiatrist. They put him on all kinds of meds. Prozac, Ridilin anti pshychotic drugs. You name it my son has probably done it. Now my son is an addict. I now hear all these things about Singulair don't know what to think.??????? I have had him a drug treatment program of which he was kicked out for overdosing. Then, the hospital of which just put him on more drugs. I don't know what to do. He has asthma, when he does not take his Singulair the asthma really kicks in. I know this we are going to look for something else to treat his asthma. I need input. My thoughts are simple. I believe that it is possible that the problems my have started with Singulair but then my son took a step further. I think to try to survive. But in the mean time he is now an addict and I'm scared of whatever permanent damage that may have occured over the years. Are there any other parents out there, that think their teenager might be going through the same problems? If so PLEASE reply to this message.