Perfect sense symptoms and conditions

Googled and found this site. Could not believe all that I read! I've been taking Lamictal for several years for Bi-Polar disorder. I also have GAD for which I control with another drug BUT...I guess it's been so long since I began taking Lamictal that I had forgotten, or did I ever even know, the side effects of it. First if all, the memory loss is incredible! Not being able to complete a sentence...never able to find a "word" that should be so simple to remember...going somewhere and within 2 seconds, forgetting what in the world I'm doing or where I'm going...happened today TWICE!
And to top it all off, my eyes are so bad...I didn't even attribute the L to this until I came to this site but it makes PERFECT sense! I feel such a sense of loss in my eyesight that it has begun to really scare me. I have not been to eye doc yet but plan too.
Also, someone mentioned in here that they feel the med just wears off before next dosage and that is exactly what I've been telling my doctor so at first, we just upped the dosage until I was on 450mg a day but even the, it still was not working. SO...now I'm decreasing and the doc added Depakote Er 250mg. But doc says I have to be almost completely off L to get fully on D. So...feel like crap a lot of the time!!
I'm like someone else on here who said, "just start fresh" and that is what I'd like to do but how do you go "cold turkey"? I know it isn't good! Even decreasing this L for the last several months has been hell!
I have been on a roller coaster of meds for 10 yrs. Have yet to find the "combo" that works! Sometimes I wonder if the diagnosis of BP was/is even correct.
Another person in here said he feels like he may have some side effects of OCD and I feel that way too. Nothing major but...enough for me to notice.
Damned either way, right?
One thing I DO KNOW is that I cannot take this eye problem anymore and now that I know my memory and all that other stuff has to do with L, I'm getting off it no matter what! I'm calling my doc tomorrow and we HAVE TO MAKE A PLAN!!!!!!!
I'm only 42 but my memory is that of an 80-yr old (except for my grandmother who died at 96 and could remember details of when she was 4 yrs old...lol) I guess it's good I can kinda laugh at all this but I DEF know it is not funny!!!
Anybody out there with insight to diff. meds...combo of meds?? I really am worn out!!
Right now, I am down to 375 mg of L and this has taken me several months now to decrease from 450mg...don't see the D working that well yet but it's only 250mg so...
I really am worn out!! My anxiety shoots through the roof bc of all of this! Esp. when I feel the L wearing off around 5p or so...
I'm game for any advice ( I did see where the one woman talked about changing the time you take this in the morning but that won't work for me)
Thanks!!

I have been on NuvaRing for about 3 years now and never really noticed any side effects. Normally, I have bad cramping and a heavy period, but NuvaRing relieved me of that. But for the past couple months, right before and during my period, I will get the most intense 3-4 day migraine/headaches. I have to constantly take Excedrin or something, the pain doesn't stop. So now that a couple months have gone by, I spoke with a girlfriend of mine she said that her old b/c used to give her headaches. I googled Nuvaring and headaches, and here I am at this site. I am so happy I found this site because I have had NO sex drive at all and I really thought there was something wrong with me. I am young, happy, in a beautiful relationship and my fiance thinks Im not attracted to him anymore. It makes perfect sense though, this has happened ever since the NuvaRing, i really just have no want or need to have sex at all-like its a task or something. Its horrible. And I saw several mention the discharge and the yeast infections and the UTI's. Wow. I have unlimited prescriptions that my gyn had to write me because I get UTIs. I keep asking my gyn what causes them and he tells me sex and not urinating after sex and blah, blah. I''ve heard every single reason and believe me, I avoid all of them and still get them. I am the most careful person ever because my UTIs are horrible. I wont have one, then BAM, it burns to urinate, i urinate blood, i go to the bathroom every 5 seconds, horrible cramps, paint in my back. Horrible.
Seriously though, I am in shock that it took so long for the headaches to start and for me to look into this medication more. I was 118 pounds when I started this pill (around 17 or 18 years old)...at 21 years old...I am 150 pounds. All of which, I definitely wouldn't blame on the ring, but never in my life have I gained so much weight for no reason. I was even working out at the gym and couldn't loose a pound. I feel like giving up, because by the time I get out of work all I want to do is sleep. I have zero energy, I am always tired and never want to do anything. And it seems like so many other people on this site have had these issues to. I hope my story helps someone else in their decision to stop NuvaRing. Thankfully, I just took out my last one on Sunday and didn't spend the $150 for a 3 ring refill. Crazy prices, especially when you pay good money for insurance.

I'm a new user of Wellbutrin. Unfortunately they've given me Budeprion (Teva) instead of the real thing.

I RARELY take medications, so when I do, I do A LOT of research to make sure it's worth it.

It's just not working at all. It's actually giving me severe mood swings. Enough that they are affecting my home life VERY negatively. Like.. I no longer have a home life. She's finally fed up.

Here is an article I've found about some pro research done.
******

It makes perfect sense, really.

I took one pill and ended up in ER with pain so bad through chest, back and stomach that I could not move. My liver levels were off the chart (10X higher than norm), causing my doc to call on Monday after she got the ER triage report. nobody believed it was the macrobid at the ER, and even my doc was skeptical until she looked at my blood test results from 2 mos prior and saw that indeed my liver levels are normally fine. Confirmed with a test that showed them coming back down over the course of a month. Then she found out that a side effect is hepatitis. gee makes perfect sense. why listen to me? Had I been physically able to finish course of treatment, my liver would have been destroyed.

Thank God for the internet. Seriously.
I am really trying to give Mirena a fair trial, however, some of the side effects are worrying me.
I have been having hot flashes (I just turned 40), my mood swings are disturbing, and my breakthrough bleeding happens often without warning. I also have the weight gain. However, to be fair, I don't know that I can really attribute my weight gain to Mirena. This is pretty important; has anyone else out there experienced addiction feelings? To cigarettes? Alcohol? I have never had strong urges for drugs and alcohol, however, I have lately... Again, can you really say that Mirena is to blame?
The upside is that my periods are, blessedly, light. This is a definite upside for someone who had heavy periods. I also don't feel the strings, nor does my husband. After reading some of the postings on this site, that concerns me.
Thank you.
MaryKay

It all finally makes sense!!! I'm 26 yrs old, have been on 3 bc's in my life for Polycystic Ovarian Syndrome and this past bc was Yasmin. Weird things have been happening and I never thought to link them with the bc but after reading all of these stories it makes perfect sense. Here I'm thinking that I have severe IBS and zero sex drive b/c I'm just a medical disaster but these other woman have opened my eyes. The worst side effect of all is the story that I am about to tell you and I hope that nobody else has this problem. My gyno put me on Yasmin the 8th of Aug. ('07) and at the end of Aug. beginning of Sept. I noticed a big sore knot on the back of my ankle. I thought nothing of it until another one appeared under the skin of my other ankle. I went to my doctor (who is my regular and gyno) and she told me that she didn't know what these lumps were but were NOT caused by my bc. She gave me antibiotics and sent me on my way...one knot went away and another larger one appeared. I went back to her and she gave me a 2nd dose of antibiotics, one goes away and 2 more appear. So this time she sends me to an Orthopedic Specialist who takes x-rays and has no idea what is wrong. He tells me to go see a dermatologist. I went to a dermatologist 2 weeks ago who tells me that I have a blood flow problem. My blood is thick (never had this problem in my life) and has problems flowing back up from my feet in my veins. He diagnosis me with Lipodermasclerosis...ok, so I ask him if this could be caused by my taking Yasmin...YEP! So, I stopped my bc that night. Now I am going to wait the three months for the Yasmin to completely leave my system before I know for sure that this was the cause of the knots on my ankles. Please let me know your thoughts and if anyone has had this same issue. Thank you!

I'm so happy I found this site. I've been thinking I'm crazy or just getting old for the last 3 years while on Yasmin. I started taking it at age 29 and almost immediately after started having mood swings, extreme irritability and depression. I had previously been on Ortho Tri Cyclen and the Ortho Cyclen before Yasmin and was on them for MANY years and never had one side effect. I only switched in the first place because I like to have very very few periods and I run all my active pills together to forgo periods very often and I was having breakthrough on the Cyclen. Hence, the Yasmin trial.

I'm actually a doctor (which is why I CANNOT have frequent periods with all the accompanying issues), but I didn't even realize the possible connection between IBS and Yasmin. This needs to be studied and taken seriously. I never once had IBS symptoms until a few months after starting Yasmin. Now, 3 years later I have almost constatnt trouble, to the point everytime I eat I run for the bathroom, yet my weight has never been higher. I asked a GYN friend at work if they could be related and she said definitely no, but reading all of these "real life" examples, coupled with my own experience has made me think otherwise. Often, the symptoms will occur shortly after taking the pill, even when I haven't yet eaten breakfast. It's crazy!!

I'm going to switch either back to Ortho Cyclen or to something new ASAP and will report back. I'm both excited at the thought that my "IBS" might really be Yasmin related but also scared that it might not go away and therefore might really be IBS. I'll report back... It honestly never entered my mind that all of it could be the Yasmin. I had just moved, started a new job in a town I hate and I thought it was all stress related.

I've also had an interesting side effect no one has mentioned yet- my hair texture has dramatically changed. It isn't falling out, but has gone from VERY curly with a nice soft spiral curl pattern to very dry, straight and hard to manage. Nothing else has changed and now I'm wondering if it's not the DRSP. If pergnant women can have hair changes, why not women on the pill?? It's all hormones.

As always with a drug, there are always possible side effects. No one drug is perfect, and humans are so complex in their make up and they way they process drugs. Therefore, please don't judge your family docs or GYNs too harshly as not even the best doctor in the world can predict every side effect.

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.

I am soooo happy I found this site. I marked it on my Favorites. I am an active 57 year old woman and have been on singulair since 11/2002. I have also gained over 20 pounds. I can't fit into any clothes and I just can't seem to get the weight off no matter what I do. I would stop taking singulair for several days and noticed I could shed a few pounds. Then I would go back on it because I thought I would have trouble breathing. I only have a mild case of asthma. I did a Find on the word "weight" on this site and I was absolutely amazed at how many hits I got. Singulair is the culprit. Most of my weight gain is in my middle area. My dr. now says I am pre-diabetic and put me on another medication to help lose the weight...NOT working though. I am stopping this medication as of tonight 2/22/2005. What triggered me looking online was the montelukast "sodium" Sodium (salt) is a water retainer...makes perfect sense.