Struggle symptoms and conditions

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?....

When I started taking it I suddenly started to fall asleep at odd times.Falling asleep in mid-sentence, when I would just sit down during the day, dizzy, disoriented. After I stopped, I quit doing that.

I've had Mirena for almost 2 years. I am bloated and fatigued. My joints hurt, especially my hips. I've gained 5 pounds and cannot lose it, even working out 7 days a week. I workout regularly but not with the stamina I used to have. I am 39 and in great shape. I can't make it through my classes the way I used. I struggle and it's very depressing. For the past few months my sex drive is zero. I am considering having it removed. Was it extremely painful?

I have only been taking Yasmin for a week. I am a healthy 35 year old woman and had not taken the pill in over 7 years. It is so OBVIOUS and striking that only after a week I feel terribly depressed and anxious. During the weekend, my heart was racing, I was crying and depressed for no reason. My "status" on facebook said "I feel lonely" until my friend asked me if I was taking any meds and all of a sudden everything was clear. It is so clear that the cause of this severe malaise is Yasmin. Yasmin caused me to be severely depressed and anxious in only a week of taking it. I will stop it immediately. I am also very upset at the nurse practitioner because I specifically requested she choose a pill that wouldn't cause depression! urg!!!

After being on Lipitor for over 5 years, I was told to stop cold turkey by my doctor after my routine blood test. Within 10 days I got blood clots and a pulmonary embolism. I had been on an aspirin a day for over 10 years, I drank cranberry juice often and always ate green leafy veggies. I never had any blood clots before coming off the Lipitor and I am convinced that it caused them. It has been a struggle with the pains in my legs ever since. Has anyone had the same or have heard of someone with the same side effect? ******

My 10 yr old is taking Concerta and it is the worst thing that i have every seen happen to a child. i am looking into ways to get him off the medication. it is horrible. he is fine during the day but in the evening he is a totally different person. Annoyed and irritated all the time, sad, angry, aggressive, mildly violent. he has melt downs every night and lately they have been lasting for 4 hours. no one is getting sleep and it is very stressful for the family. this drug should be banned....

I do not feel horrible but Im starting to experience a sort of constipation. I'll go a day and a half struggling to produce a bowel movement. Then finally I get a satisfying result. It's a struggle though. I push and push and push. I've been on 50 mgs for three months. I have to refill today. I will mention this to pharmacist. My appointment is not till the end of September.

My psychiatrist started me on Topamax 2 yrs ago for depression from being 75 lbs overweight. Started at 25 mg/day up to 50/day for 2 yrs. Lost 70 lbs and kept off with only minor side effects. Also took 150/day Wellbutrin during this time. (For being kind of a neat freak and washing my hands a lot.- didn't affect my social or work life much) Have slowly started gaining the weight back (+12 lbs). Seem to have built up an immune to the 50/day dosage over the 2 yrs. So he added 25 in the am in addition to the 50 I've been taking in the evening. (1 mo. ago) Having some strange reactions. My memory seems to be taking a real hit. I am a CPA (passed these exams 15 yrs ago) and now I'm studying for the Cert.'d Internal Auditor exams. I am having a great deal of trouble trying to memorize for these 12 hour long tests! I feel fatigued every day. My blurred vision (that requires reading glasses) has gone crazy. I can't read the song book at church at all. And I'm only 47!. I've had acne like bumps all around my nose and face. How could such a slight increase cause so much change? Also sometimes my heart feels like it is going to beat out of my chest. And I'm losing patience w/my 13 yr old son who's pushing my buttons to see how much he can get away with. He seems to sense that I'm not at my best. But if I go off this Topamax and gain back my 70 plds I know I will plunge into a DEEP depression. Has any one talked to their doctor about the possibility of these side effects going away after time? My tingling hands and feet did and my slight hair loss did. And my weight loss is trying to go away but I don't want that. I'm majorly concerned about the memory loss and blurred vision eventually going away. DALIAL

I am 30 years old and have never had any children. I had my Mirena inserted on on 7/18 (during my cycle). I know it has only been a week but I'm feeling a little concerned and confused.

While having it inserted I was SHOCKED by how painful it was. I, like many other stories I've read, felt like I was going to faint.

Sunday I woke up in at 5:30 a.m. in so much pain! It literally hurt so bad that it woke me up. The same thing happened Tuesday. Night time has been a struggle also. I resorted to taking Tylenol PM to knock myself out.

I asked my doctor to test me for all STD's to ensure that I would not have a PID, but I'm still apprehensive. I realize I need to give it time... but gosh it sucks being a girl! I'm glad I haven't had any emotional side effects and hope that I never do!

Hi all,
I have spent the last 2 days on the Internet reading about Mirena; as a matter of fact, I had mine removed 2 days ago. For the last 10 months, my life has been horrible. I had the Mirena inserted in November of 2007, I was also coming out of a divorce, so I (and my doctor) was attributing my extreme depression, anxiety attacks to it. I started noticing that my hair was falling out and it just kept getting worse and worse. I went to see my doctor again and she said I had anemia (I was having very heavy periods and bleeding through my periods). Doctor said anemia causes hair loss. I went through different tests, saw a dermatologist, I always mentioned I had the Mirena, but no one seem to relate that to anything. I actually went on the Mirena site a couple of times, but the side effects listed there were very mild so I discarded the thought that the Mirena was causing my depression and my hair loss. There is no mention whatsoever about hair loss. Months went by, I kept seeing different doctors since my hair loss was getting worse and worse, my once beautiful, thick hair had become extremely thin, I have two holes on my scalp. I continued to bleed heavy and my ob/gyn said to give it some more time. My life was a complete mess, going to work was a struggle, dealing with my kids was a struggle, some days I would just lay in bed and cried for hours, I started to believe that my life had no purpose or reason. I was truly in agony, I am sure those of you who have gone through this know exactly what I mean. Anyway, I can't believe in all this months it never occurred to me to google mirena and hair loss....or mirena and suicidal thoughts, etc., etc. I thank you all for sharing your stories and I hope we can figure out a way to let all of those mirena users out there suffering that the answer to their agony is simply to have the Mirena removed. I look forward to my new life, new hair. It has been 2 days and I don't know if it is a state of mind, but I feel so much better already.
Thx
Jessica M.

These reviews are pretty scary to me ... I've been taking Yasmin for about 5 years. Late last year, I started getting what seemed like a full period (not just spotting) almost exactly two weeks into my pill pack. Then I'd get another full period when I got to the end of the pack, and I went ahead and took the sugar pills because I didn't want to mess around with my cycle (which I've done in the past, with negative results). My doc switched me to reclipsen for a month (which I've read bad things about too, but not as bad as Yasmin!). I've had NO sex drive for years now, which I've blamed on myself, but it's really affected my relationship w/ my fiance. It's hard because I just can't get excited. I loved Yasmin and recommended it to all my friends because it kept my water weight down. Last month when I went off of it, I gained about 8lb in just a few weeks. I attributed it to going on vacation and not exercising for a week (I normally eat very well and never miss a workout). But since then, the weight has stayed and is very slowly coming off. I'm a personal trainer and I never usually struggle like this. I've also been bloated and it seems like I have an excessive amount of abdominal bloating.
Anyway, after a month on reclipsen, I decided to switch back to Yasmin to see if the month on another drug "tricked" my cycle back into following Yasmin (wishful thinking!). Sure enough, got my period two weeks in. Also got lots of bloating, constipation (never normally a problem for me), and moodiness/ depression. I've had "stomach issues" for years, and I've even had a colonoscopy with no real diagnosis. My abdomen is always tender to the touch. I never would've thought Yasmin could be a cause, but now I really wonder. Also, in the last couple weeks that I took Yasmin again, I noticed days where it felt hard to breathe, and I just blamed myself and my weight, figuring it was the few extra things I ate that made me bloat. But now reading other experiences, I realize how unusual my recent experiences are for me. Now I'm not sure what to do -- I don't think reclipsen is a good answer. I want to go off pills completely for a while, but I'm really afraid of weight gain (Yasmin is addictive that way -- I love how it's kept my water weight down and I've been afraid to go off of it). Fortunately, I haven't had the blood clotting (to my knowledge) or acne. But I do have overuse injuries that never seem to heal -- now I wonder how much those relate to Yasmin. I won't be taking it anymore!

I am going to call my doctor tomorrow to schedule an appointment to get this removed. I got Mirena after the birth of my son in Nov 07. My period came on two weeks later and did not end until mid February. I called my doctor she assured me that this was normal to have "spotting" in the first six months. I went in for an appointment in January and she said that everything was fine. My cycle still continued for another three weeks. Not spotting but a full blown period. The benefits of this birth control made it worth trying to ride it out, so I did. Since then my waist has increased by 1 in, I have been depressed, it has been a struggle for me to loose weight. My sex life is almost non-existent. The reason I decided on this method of birth control is so we can continue with our normal sex-life without having to worry about an unexpected pregnancy. Now all every week or so I hear my husband ask how come I don't want him anymore. This drug is not worth the side effects. It has changed me into a different person and it is ruining my marriage. I was using seasonal before we decided to have a baby. I think I will be going back to that this week.
Don't worry, I've relocated since January and have gotten another GYN. I wish I would have found this site sooner. I see people writing about having a 14 and 18 day period. If I would have read this I would have requested that this be removed months ago. I went 78 days of bleeding.

--By meeshes617

Just reporting back with some information.
I've been off of Yasmin for over a month now. Overall I've been better but there have been a few "relapses" where I've become so dizzy/lightheaded that I hard-core started to panic. Those days can be disheartening.
I've read some previous posts from an RN who said that Yasmin in particular, suppresses your androgens (testosterone) which causes many of these symptoms. This also explains why sometimes it takes a while for these symptoms to "catch up" I know I was feeling great when I first started.
I'm a lot better now that I stopped Yasmin, but I know it's going to take up to six months to get back to normal. Have your doctor check your hormone level. Even if it's " low normal" that isn't healthy for say, a 20, or 30 year old.
For herbal supplements I would suggest Ashwagandha. It's supposed to help production of your androgens. Also keep hydrated and have plenty of Omega-3 fatty acids.
What I also encourage is to talk about your situation. Once you open up, you'll never know who you'll find that had the same issue. We women can be a very helpful resource for one another.
I'll keep you posted on the progress and I hope the best for all of you.

I was on Orthocept pills for 10 years with no problems. Short, light periods, no PMS. I can have a temper, but it was when I was younger and in the middle of a fight. That being said...I gave birth to twin daughters in November 2005. 9 months later, I stopped breastfeeding and had to go back on birth control. My old pill didn't work and neither did 3 others (included Yaz). I bled almost the entire month. I was crabby and irritable, but mostly frustrated. It was a horrible 1 1/2 years. 6 months ago I was put on Nuvaring because it should produce no side effects for the most part. Besides heavy discharge (which I could live with if I wasn't bleeding all month), I had heavier periods. I also noticed I was starting to get some nasty PMS, which I've NEVER had in my entire life. I was moody and irritable and cried even more easily than normal. Lately, I've been lashing out at my sweet girls and yelling at them. At first I thought it was because they are going through the difficult "2's" and mealtime is a struggle. I thought, they are more challenging so my patience is worn a little thinner. My husband has a different story. We've both noticed nasty mood swings and it's gotten to the point in the past month that I feel bi-polar. I really feel out of control. My doc said to go off it for a few months to see how I am. This is my "period" week and all of a sudden I've had a little period. I haven't been able to get my hormones under control since giving birth and it's frustrating. My husband wants his wife back and I don't want my girls to remember me yelling and crying for no reason. THAT'S enough to make anyone depressed on their own. I'm not sure what we are going to do for birth control at this point (condoms I guess...which is no fun when you are used to not using them). I will see what happens. I hope it's not the Nuvaring, but after seeing these posts, I feel a little better knowing I may be able to get rid of some of my craziness over the next few months as my body goes back to "normal". Good luck to the rest of you as well. I love being a woman, but boy, we get the short end of the stick sometimes!

I was Dx with Asthma in 98 after having bronchitis for the first time. I am not a smoker but Asthma does run in my family. I have been taking Advair 500/50 for 3 years and as far as controlling my Asthma I am so HAPPY to be on it!(I am 40 years old). In the begining I did struggle with side effects of heart burn,& tooth pain but that has subsided. The only side affect that has really affected my life is the loss of cartledge in both of my knee's. Granted I had a history of Femoral Patella Syndrome prior to taking ADvair, it just seems like the medicine has sped up the deteration. But Honestly. It has worked so well to control my Asthma, and nothin else seems to be stronger. I will have to choose breathing over my knee's.

After reading this website and struggling with some pretty severe side effects with our son over the last 5 years, we decided to replace Singulair with a different asthma med. Guess what? After 2 weeks, we saw a TOTAL turnaround with our son! It was like night and day. I can't believe we let our son struggle with this side effect for 5 years. Singulair DID work great for our boy, but it just isn't worth the side effect that he had.

I would like to share this information with everyone. First, I would like to caution all that it does not prove anything regarding the negative side effect of Singulair but it does suggest that there might (only might) be a physiological cause for any side effect that could be attributed to brain function.

A Chinese team has been studying the receptor (Cysteinyl leukotrienes receptor 1) that is targeted by Singulair and is responsible for the method of action that makes Singulair successful. Here is one of their studies.

1: Neurosci Lett. 2004 Jun 17;363(3):247-51. Links
Expression of cysteinyl leukotriene receptor 1 in human traumatic brain injury and brain tumors.Zhang WP, Hu H, Zhang L, Ding W, Yao HT, Chen KD, Sheng WW, Chen Z, Wei EQ.
Department of Pharmacology, School of Medicine, Zhejiang University, 353, Yan An Road, Hangzhou 310031, PR China.

Cysteinyl leukotrienes (CysLTs) are potent proinflammatory mediators. CysLT receptor 1 (CysLT(1)) is one of the two CysLT receptors that has been cloned. Although the expression of CysLT(1) in the brain has been demonstrated by Northern blot and RT-PCR analyses, the location of CysLT(1) in the brain remains unknown. The objective of this study was to examine the distribution of CysLT(1) by immunohistochemical analysis in human brains with traumatic injury or tumors. CysLT(1) was expressed intensely in the microvascular endothelial cells in both normal and abnormal conditions. At 8 days after traumatic injury, microvascular regeneration was found and all of the endothelial cells highly expressed CysLT(1). In gray and white matters of the normal regions of the brain, CysLT(1) was expressed weekly or not at all. However, the CysLT(1) expression increased in the neuron- and glial-appearing cells in gray and white matters after traumatic brain injury. CysLT(1) was also detected in astrocytoma, ganglioglioma and metastatic adenocarcinoma, and the expression in the neuron- and glial-appearing cells around brain tumors increased robustly.

PMID: 15182953

Here is the relevant part of the study.

"Although the expression of CysLT(1) in the brain has been demonstrated by Northern blot and RT-PCR analyses, the location of CysLT(1) in the brain remains unknown."

That sentence says that these scientists believe that CysLT1 exists in the brain but they don't know what the location in the brain is.

It is logical to assume that if a receptor exists in any part of the body that it has a function in other words it does something or tells some other part of the body to do something. So we don't know what part of the brain or what the receptor does in the brain or what the effect on the body is if the receptor does not do it's job.

We do know that Singular (montelukast, Cysteinyl leukotriene receptor 1 antagonist) blocks this particular receptor so if the receptor exists in the brain that it COULD BE POSSIBLE that Singular prevents this receptor in the brain from doing it's job whatever that is.

I know that it is difficult to argue with doctors. This drug has been around a long time. It would be difficult to understand why we are just learning about problems after so long a period of time. I can see from all of these responses that these problems are very real. Of course, we have no idea if Singulair is related or not. But if you need something supportive to show that it is not impossible for them to be related even though there is no proof that they are related, you could print this out and discuss it with your doctor.

This isn't proof of anything but at least it might be a clue.

Hi
I posted my story with my son on March 29th approx. at 11 something. My story is talking about my 15yr old son and his struggle with his emotions and drugs. Is there someone out there that may be going through the same thing? I am desperately struggling with this. I need to know if there is someone else that is going through this. If so, PLEASE email or reply to my story.
Thank you

I have an 8 year daughter who has been on singular since the age of 4. I began to notice behavior changes, but contributed it to me being a single mom, and her aneixty about school. She became very germ a phobic and these behaviors became worse when she began displaying aggression towards me and her grandmother, not wanting to go to school, inability to focus and very "worried" about getting sick and dying. She is now in the 3rd grade and was diagnosed w/ aneixty disorder and ADHD and is taking two different meds for this. It does take much to get her upset and she often describes herself as a horrible person, and she "hates" her life. This was a very happy infant, and easy going child. Now it is a struggle everyday to keep everything "under control" and her stable. I wonder. Many of the stories that i have just read are so similar to mind and I know how difficult it is. I did not give my daughter her singular as she has mild allergy induced asthma and I will be consulting my Pediatrician ASAP, to find other options.

I have been on Warfarin since the end of Aug. 2007 when I had my mitral valve replaced with a mechanical valve. I will be on it for the rest of my life. My doctor.'s all assured me there were no side effects other than the bleeding risks. I now know this is not true. The side effects I am dealing with make me sometimes wish I had chosen a tissue (pig) valve, even though I would be guaranteed another heart surgery within ten years. I am 39 years old and a mother of two young kids. Since being on Warfarin I have experienced various body aches that come on suddenly but don't stay long; extreme hot and cold; itchy hands and feet; dry hair and hair loss; seeing "spots" usually followed by a headache; very thirsty; ongoing bowel troubles, possibly developed colitis; but the worst side effect for me is the fatigue and depression. I feel like I traded in my old self for my mechanical valve. Like I said, I'd have to have a tissue valve replaced eventually, and as bad as heart surgery is, I'd rather have 10 happy years w/out Warfarin than this struggle I deal with almost everyday. My brother is a surgeon and even he buys into the "no side effects" b.s. I work out as much as I can, which used to make me feel great, now I feel like it helps me get by but not the positive effect it used to have on me mentally.

Folks, I have put several posts and replies on here. I am trying to be advocate as much as I can. My family went through hell with this drug and my 4 year old. He has been off it since October of 07 and I can report that he is about 90% recovered. I finally have my son back!! I am a paramedic and have seen these effects on other children first hand! Aspartame is in almost everything. Sure some kids may be having a reaction to that. Most likely not. It may be the inert ingredients. Most allergists do not test for that. However I would be willing to put money where my mouth is and say that neither one of these scenarios is the case. Merck knows what is going on and has failed to do anything. WHY you ask because Singulair is their number one money maker!!!!!!! Please read my other posts. Yes I am very passionate about this. My innocent 4 year old had his world stripped from him. He could not understand the thoughts or pains he was going through. It was overwhelming. No child should have to go through that at any age. Just ask the mother on this board who lost her son from this drug. Trust me folks it can happen to you!! No parent wants to ever face that. It is unbearable. I have seen it first hand, more than I would ever like to. The only thing that we can do as parents is protect our children. Be an advocate. Contact your Attorney General, The FDA. Heck I even wrote Bill O Reily. Maybe if enough of us do that, things will change. My hope is that other parents as ourselves have done stumble upon this website and realize the problem at hand!! Best of luck to you all. My heart is with you as I know this can be a very challenging struggle.

My son was diagnosed w/ ADD/ADHD when he was 7. My husband and I were not advocates of giving drugs to a child and avoided it for some time. But as I watched him struggle and become depressed because he couldn't focus, etc .etc, I remembered what it was like when I was his age. (I am also ADD). You can say what you want about drugs but when my little boy was looking up at me crying and pleading for help "please help me, please...please come to school with me and tell me what to do, remind me because I forget what the teacher says right after she says it".... To see him struggle like that at such a young age we had to do something. He was a very confident and happy kid prior to starting school and after being in school for a few years being the kid that was always getting corrected by the teacher or being called out more than others for not paying attention was taking it's toll on his personality.
He did not start out on Adderall, but another Ritalin type drug. But it made a drastic change in his life - he was happier, able to focus and his self esteem came back. Later he was changed over to Adderall. He said it didn't make him feel nervous like the Ritalin type drugs. I am also on Adderall and it has made such a positive difference in my life as well. I didn't realize how much I had to struggle to stay focused, how much I procrastinated and how overwhelmed I used to feel on a regular basis until I stopped having those issues...what a relief!!! I don't have the stress eating issue anymore because I don't feel as stressed. The only side effect I noticed was my eyes getting red and a some dry mouth.
Adderall has a calming effect on me, I don't feel nervous, I don't feel detached, or any of that stuff several other folks wrote about. My son doesn't either, he is calm and happy and is doing great in school. Neither of us have any issues when we don't take the medication - as far as craving it, etc. In fact, from the initial research I've done and my own personal experience,many who are truly ADD and not misdiagnosed are less apt to become addicted than those who are not truly ADD. When we don't take it we might be a little less apt to remember that important thing we were supposed to do because we got distracted! But we don't seem to have any other withdrawal symptoms or tiredness, etc. So far it has been positive choice.

So for all you people having social issues, hearing voices, having chest pains, feeling strong urges to take the medicine even when you don't want to - YOU PROBABLY SHOULD NOT TAKE IT! All medications effect everyone differently and not all people can take or tolerate the same medicine. And for all you folks that are able to spend 10mins w/ your kids and get good results...well good for you, but DON'T JUDGE those of us for which that technique didn't work. During the summers we usually don't make him take any medication and we spend a lot of time talking through the issues that arise, practicing focus without medication, etc. We spend a lot of time reassuring him that it's OK to make mistakes when you're trying to change your behavior and that we love him just like he is. We hope that eventually as he matures that he will find it easier to do this on his own with out medication to help. However, if he doesn't, then I would rather see him be happy on medication than to struggle and be depressed without it.

Peace.

WOW! I am so glad that I found this web site. I have had the Mirena in for almost 3 yrs. I thought I was crazy with the side effects. In the beginning I just kept telling myself to give it time. Well, again three years later I finally have come to terms with the fact the Mirena is just not for me. I did not notice a weight struggle. Depression seems to get worst. Mood signs are unbearable for myself let alone for my kids and hubby. When I told my doc he suggested depression meds! No thanks. Looking forward to removing the Mirena in February.