Dealing with depression symptoms and conditions

I have been on the nuvaring for a little over 3 years now and have never thought to search for possible side effects until now.
I am constantly tired, I never want to do anything, My body aches. I have NO sex drive. I'm always dealing with depression. I randomly cry for no reason. I've ruptured a cyst on my ovaries which landed me in the ER...
Finding this site is making me really rethink my bc choice. I love the convenience of the Nuvaring, but I miss having energy :(
Any suggestions on what i should switch to?

I don't know what is wrong with you people but its like you can't handle anything. I had the mirena put in November last year and yeah ok i had cramping for the first month or so and yeah i had spotting. But unlike some of you fools i knew what the side effects were i read what came in the package which means i knew what to expect before i got it put in. And yeah there are loads of possible side effects but if you read everything and know what could happen you shouldn't complain if something does happen. Not everyone who has the mirena has these things and for people who are considering it i would recommend trying it and after 3 months if it doesn't feel good then get it removed. That especially goes to people that have just had a baby... i mean really in the first 3 months after having a baby who is really seriously interested in sex right away. The reason i am here was to see if there was more information about them now because UNFORTUNATELY i had to have mine removed for an operation. I had a cyst on my fallopian tube which was not mirena related. In fact almost all women get them when they are menstruating but they go away. Unfortunately with me they don't go away and this is the 2nd cyst to be removed in 3 years. I am planning on getting a second mirena inserted next week. Because frankly i find it ideal. And yeah i may have had mood swings on occasion while i had it but come on think about it what woman doesn't have mood swings. So sure you can blame everything on the Mirena but for the most part besides then for the people where the mirena got stuck or moved during the time you had it... its all in your head. And like i said before i would recommend the mirena and if after 3 or 4 months it doesn't suit you then go for something else... but don't dismiss it because some people have too much time on their hands and like to spend it whining over everything on the net. Remember with the Mirena you have a 50/50 chance of having symptoms or not. Take that risk before taking the risk of going on the pill and forgetting to take it or going on depo provera and putting on 20 pounds.

Some of these stories read like a diary of our life.our son went from a reasonably confident, happy, somewhat easy going 10/11 year old to a now 16 year old with no confidence, somewhat paranoid, dealing with depression and tremors so bad that he could not hold his pencil to draw a straight line in drafting. He often says he hates his life, can't see any hope for the future and feels he is a failure- he is an honors student with a nearly perfect 4.0 average, yet he is never sure it is enough.

some of it we put down to being a teenager, who had inherited hubby's fathers shaky hands. some we figured came from my dad and his troubles with ocd and depression. i have worried, cried, prayed, ranted and begged for things to be different for him.

what changed at 10/11 years of age? he started taking Singulair. at first a low dose but about 3 years ago the doctor uped the dose to full strength, the symptoms also escalated - however he had entered the teenage years and changes they go through.

the allergist last year,put him on Pulmicort and at that point did not need the Singulair but through a misunderstanding we kept giving it to him. hubby is a pharmacist and questioned it, he has never been wild about Singulair because he says it opens you up to infections.

which may answer a secondary question of why he has had more cases of bronchitis and has had 3 bouts with pneumonia, more since the dosage was raised.

i have to wonder if the history of depression in our family made our son more open to the symptoms and side effects of the Singulair. the suicide part of it really scares me as my uncle and aunt both committed suicide, we didn't need any push in that direction. we have talked extensively about it and he assures me he does not consider it an option.

i know some kids take it no problem, but this recent set of reports, and the fact that the FDA has changed the warning labels 4 times in a year, causes me to take notice for him

please pray that we can see some improvement as he is now off of the Singulair. I stopped mine last year due to recurring ear infections. now i am especially glad i did. i have felt very hopeful today that this may be an answer to prayer. two days off and he had a good day today.

I'm a 35 yr male and have been dealing with depression/anxiety for years due to current & past issues in my life. This post IS dealing with singulair side effects but want to give some history as to why I think it's singular and not something else. For the past 2 or so years I've been using xanax which has worked fairly well in controlling my anxiety, but my doctor preferred I stop taking it because of it's potential for abuse. I've been on SSRI's before and I hated them, so I did some research and decided to try wellbutrin which works differently from the SSRI's. I was still using xanax while ramping up on wellbutrin the end of February. To my relief, the wellbutrin started working wonderfully - felt like I could cope with life, increased energy, better mood, with no negative side effects (actually some positive ones) - the only problem I was having is I traveled during this time frame and developed a bad case of sinus rhinitis due to the climate changes. I've had chronic sinus problems my whole life so it's no surprise. I tried most otc meds and nothing was helping. In the meantime I was feeling so much better (other than the rhinitis) that I decided to start tapering myself off the xanax. When I got to the point where I'd stop taking the minimal dosage I would start getting physical withdrawal symptoms (headaches, dizziness, etc) which is fairly common after taking for a prolonged period of time. The side effects were strictly physical - no excessive anxiety or psychological craving My sinuses were still really bothering me so I had two reasons to visit the doctor - try to get something to relieve my sinuses and to get a short supply of a benzo with a longer half-life to ease the withdrawal from xanax. The doctor gave me a prescription for a month of diazepam and 9 weeks of singulair samples. That was 3 weeks ago. I immediately begin using the singulair, but still had some xanax left so I decided to continue on a minimal dosage and use it up before I went to fill my rx, which I just started several days ago. Coinciding with when I started taking the singulair, all the positive benefits I was feeling from the wellbutrin just suddenly stopped. My depression and anxiety came back worse than they were before - another persons post describes the change in me: feel very anxious, fearful, reclusive, depressed, that everything is going to go wrong, or is always wrong. I'll have extreme anxiety about small everyday things. I’m unable to concentrate. I've also become more irritable, argumentative, and aggressive. I have difficulty falling and staying asleep. I also experienced a very noticeable decrease in sexual energy after a very noticeable increase which is a side effect of wellbutrin. I can even understand the rationale for suicide just to be free of this emotional nightmare - not that I would do it - but can understand it. I couldn't figure out why I went from finally feeling good about life to suddenly feeling worse than ever before. I guess I didn't realize it right away because my sinuses were much better, but I know these symptoms began occurring very shortly after I started to take the singulair. I was trying to figure out what was going wrong with me and yesterday I did a web search on 'singulair side effects' (since it’s the only variable I could think of that changed within that time period) and came across this site and several similar ones. It blew my mind how many people were talking about the exact things I was feeling. Yesterday was my last dose. Does anybody know how long it takes for this crap to work its way out of your system after 3 weeks of use???

I have been taking Effexor for around 2 to 3 years for depression. I am currenty taking two 150 mg at night, though I was told to take one in the morning and one at night... I found it easier to take them both at night. The only side effect I am sure comes from the Effexor is the reduction in my libido (and I am female). Effexor is the only anti-depressant I have been on, and I think I got extremely lucky in that I found the one that works for me on the first try. I also see a psycho-therapist, and between the two, I feel I have managed to get a better hold on my life. I am a thirty-five year old mom (married, and with a seven-year-old daughter) and I have "almost" nothing but praise for Effexor.

HOWEVER, I do know that the withdrawal side effects are terrible... I have missed it for up to three days when I went out of town and forgot my medication. I can usually miss one day and the side effects will most likely just be a bad headache, and maybe a little nautious. But when I missed three doses:

Missing one dose at night: I had a headache the following day.
After missing two doses: The headache became worse, I would occasionally get dizzy spellls, and I started getting very emotional - swaying between sad and cranky.
After missing third dose: The headache became worse still, and was aggravated by light - I wanted to just keep my eyes closed. I felt dizzy and nautious - nautious to the point I couldn't tell if I was going to throw-up (never did).
Oh... and I should add that the dreams while I was off the medication were incredible... like watching movies... so detailed and complex. I usually don't remember my dreams... but these I could recall... not in perfect detail... but they were amazing.

After I got back home and took my dose that night: I missed three days of work while being back on the medication. I was nautious, had a terrible headache, wanted to just stay in bed, I was no longer ultra sensitive emotional-wise - but I was ultra-pissed-off. I became very angry that I was on a medication that was addictive after having been told it was "not addictive". I was angry that I have never had an addiction before, but now suddenly I was addicted to a prescribed drug. I don't smoke, I only drink a couple of alcholic drinks in a month (socially), no canabis (pot... is that an out-dated term? ... everyone here says canabis), or any other illegal or legal addictive drugs... the only other drugs I take are allergy (Clarinex) and birth control (Nuva Ring), neither of which are addictive.

That whole experience was months ago, and now that I have had time to calm down and get a clear perspective on the situation... I wouldn't stop taking Effexor for just being addictive... and YES... it is addictive... I don't give a rat's ass what any "expert" says about it. If you can't stop taking something without your body freaking out... then IT IS ADDICTIVE.

I don't know that I will ever be able to stop the medication. I go back and forth as to how I feel about this. At times it bothers me being so dependant on a medication... but on the other-hand, I'm dependant on the allergy medication, and that doesn't bother me, so why should I let being dependant on an anti-depressant bother me? Who cares what everybody else thinks, right? - - Boy, that's loaded...

Effexor has helped me tremendously. My thoughts about death are very infrequent. I don't feel like crawling into a hole and disappearing all the time. I have found "my voice" with the help of this drug and my therapist to voice my opinions more often to help me from not feeling so trapped and helpless in situations. It does cut down on emotional sensations... I don't feel overwhelming sad at all the terrible things I hear on the news. And I don't cry at sappy commercials and movies any more (Thank you!). For the first time, I feel much more in control of my feelings and my life.

So, I can understand the anger in a lot of these postings, but I would like to add, that I don't think the people who have benefited from Effexor are posting here. They have no reason to be looking for this site. I found this site when I had been angry over finding out it was habit-forming. I believe Effexor has probably helped a lot of people - and it isn't an "evil" drug... it's just a drug. For some, it just isn't the right drug.

I should add, that I'm on here today because I've recently started experiencing night sweats, but I wasn't sure if it was a side effect of Effexor or not. I hope that it is a side effect of Effexor and not a symptom of menopause... cripes... I'm only 35! The first site that popped up after searching under "Nightsweats" was about nightweats being a symptom of perimenopause or menopause... ugh!

But if I have to weigh the benefits I have experienced using Effexor, with the downfalls: addictive, sexual side-effects, and maybe night sweats... I still am of the mind that it is a good drug for me.

I wish all of you luck in finding what helps you most to be happy with your life.