Passion symptoms and conditions

Hey, am I glad I ran across this. I too had BAD experience with Lamictal; anything over 75mg gave me depressive / fatalistic dreams if I took it at night. Doctor suggested taking it in the morning, that helped, eventually up to 150mg. All this for *suspected* bipolar II. All that really happened is that the med flattened me out too much- I didn't care much about anything, no passion or motivation. Optimism? What's that? Then the OTHER fun part - coming OFF the drug. Whoooo boy. Wasn't so bad coming down from 150mg to about 75mg. THEN I got hit with a LOT of anger, anxiety, insomnia, tremors.... I wound up going into a Partial Hospitalization Program for 5 weeks. I am now 100% OFF Lamictal. Thank God.

I always had irregular periods, maybe 2 a year. And my periods didn't affect me at all when I did have them, it was just another day. I was very normal.

Started taking Sprintec 2 years ago. Gained 5 lbs, (no biggy), and very gradually starting getting depressed and dry down south. Periods gradually got more uncomfortable too. Now when I'm wet all I gotta do is touch myself and I go dry. Now I'm a psycho who wants to kill myself and I hate sex with a passion. I hate being a woman my periods are SSSOOOO unbearably uncomfortable with the bloating and the murderous cramps.

Thanks Sprintec.

I took Yaz for a couple months and was fine during that; however, about a month ago my doctor switched me to Yasmin(I have been on BC for years however, the ortho brand). I've been in the most pain in the past month than I ever have and I'm usually pretty good with pain and just try to take advil or something... but the symptoms have only gotten worse. I finally decided to google my symptoms and I found a lot of people on Yasmin had very similar symptoms. I have the worst anxiety like there's a lump in my throat and sometimes I'm literally grasping for air and I always try to drink a lot of water or cough or eat or burp to make it go away but it doesn't until I wake up the next day (sometimes). Also, I have never ever experience migraines in my life, but the past month I have the worst headaches imaginable. It happens at least 4 times a week; at first I thought they were caffeine headaches because it would sometimes help, but the past 3 days my headache has pretty much been constant (usually located near my temples/eyes). I take probably 8 Ibuprofin a day and drink an excessive amount of caffeine hoping it will make it go away, but it doesn't. Along with these problems I've been feeling lightheaded more often and usually have to sit down immediately or else I feel like I'm going to faint. The biggest/scariest symptom is my heartbeat and chest pain. Heart disease is extremely dominant on my moms side and almost all of her siblings have already had at least one heart attack. Lately my chest will hurt extremely bad, then I feel like my heart rate is just freaking out; I can feel my heartbeat from anywhere on my body and it's very intense. And then because of all of this going on, I always start to freak out and realize i'm getting extremely anxious so I try to make myself take deep breaths but nothings works. The past 4 nights I've been up til like 4 a.m. because my heart rate is so high and my chest hurts so bad in every position I try to lay in that I'm constantly moving. I never thought about going to the doctor because I thought it would get better but now I'm starting to think I should... I'm just wondering if anyone else has/had any of these problems from this medicine and if you've done anything to get rid of them.

(a couple other minor symptoms I've noticed recently are: joint pain and rapid memory loss (I'll be in the middle of a sentence and completely forget what I was talking about and blank out))

This drug works great for like one year. Then, it wears off and you feel on auto-pilot. I was on this for 3 years and at the end it does not work, you just function with no passion at all, always tired no matter how much sleep. With a physician's help, you can taper it down safely and get off of it. I felt so alive and awake once I got off. bottom line, if you need it short term for something like post partum depression, it is good to fight off anxiety, but long term, you are not enjoying life to its fullest....it is a drugged life experience.

I have been taking Nasacort for only a week. I developed a rash on my forearm 2 night ago and decided to stop taking the Nasacort and Amoxicillin. I noticed last night that I couldn't taste my food. I could only sense the saltiness. PLEASE LET ME KNOW IF ANYONE HAS REGAINED THEIR SENSE OF SMELL/TASTE. I'm in the restaurant business. My sense of smell and taste is my livelihood.

I am a 65 year old female taking 20mlg of lipitor for almost 10 years. All of a sudden I started having severe pain, shaking and weakness in the calf muscle. The pain is unbearable. Doctors after doctors including a cardiologist, rhoumatologist and internist don't know the reason. I have stopped lipitor for 3 days. I cry and pray to god to help me everyday. I cannot exercise which is my passion for many years. I am hoping the lipitor is the reason and not something else. I have to wait and see. But I suspect it is.
SR
I do have nausea, depression and low back pain and arthritis and frequent headaches.

I have been on prednisone for 5 1/2 months now, I was hospitalized starting in February until like the 25th of March for a bad exacerbation(sp) of my ulcerative colitis. I have taken prednisone for 9 1/2 months out of the last 17 months. I have experienced everything from growing facial hair I don't want to loosing what hair I do in a short period of time. Most of my hair loss started after I weaned off the prednisone about one week ago, or lets say it got much worse. I also while on prednisone got have got to experience the lovely side effect of pysicosis(sp) and am on meds to couter react what it has did to me. This is a evil and horrible drug, I hate it with a passion for all the harm it has did to me. I now have joint pain, restless sleepless nights, night sweats, tremors, not to mention the rapid weight gain. And to top all this off I am still not in remission, so this drug was used all in vain. Please be careful using this awful drug and if you have to use it, only use it for a few weeks at the time and not long term...the side effects can be horrendous and sometimes like in my case permanent to some extent. I do wonder about the hair loss, it has been worse this time than ever...I hope it stops soon.

I had severe stomach pains for 2 weeks when I switched to ER. However, I was able to regain control of the epilepsy when the depakote stopped working so well after 15 years.???
I have gained 80 pounds on depakote and ER over the past 20 years but I cannot fairly blame the drug for that. I have also had bouts with depression-like symptoms (never sought help) but again, who is to say that can be blamed on the drug? While I have lost hair, I still have more than many 40-year old men.
When first going on Depakote 20 years ago I slept for days it seemed. I have never felt as though I had the same energy level as before starting the medication but it has been so long and I am so thankful that I can lead a normal life without seizures by using the med.

Where do I begin?

I can’t tell you all how appreciative I am to find this site! I have been on the NuvaRing for nearly three years and was ignorant enough to never attribute my increasing problems to this terrible medication. In all fairness, I must admit that the initial reason I decided to use the ring was because I had even worse results with three different types of pills. My doctor then prescribed the ring, telling me that it would have the very least amount of hormones of any birth control. What she didn’t tell me and may not even know is that some women can not physically handle any type of added hormones at all in their body and must use a non-hormonal method. Why don’t they warn us of this?!

I come from a generally nervous and careful family. You could say they take life very seriously and perhaps too much at times. However, I myself have always been very social, productive, and had a passion for life. I used to love to write. I was good at it. When I started taking birth control, I was busy planning my wedding and so I just figured all the stress and business of life was taking all the fun out of everything. When I did get married, my sex drive tapered drastically (with the exception of my “free week” when it’s at its highest all month long, but still not what it used to be). I stated suffering from severe abdominal pain at certain yet random times of the month. One month, it got bad and was associated with a mild fever. The doctors did an emergency appendectomy on me just as a precaution. It turned out my appendix was fine and never needed to be pulled! Since the beginning, I’ve suffered the same pain almost every month. Not a month goes by that I don’t have weird things happening to me physically. About a year ago, I started suffering terrible panic attacks! I get extremely dizzy in stores, in traffic, while eating, lying in bed and it happens completely randomly. I suffer terrible leg cramps at night during the week of my period. They’ve gotten so bad that I wake up crying sometimes. I never used to grind my teeth and now I have TMJ! I’ve become overly paranoid and find that at certain times of the month I have more courage to do things I know I shouldn’t ( I have crazy thoughts), while at other times, usually right before my period, I’m afraid to do anything at all. I become obsessed with the thought that I’m dying and I suffer from extreme panic attacks for no good reason at random moments. Rarely, but on occasion, I feel completely normal and just wish I could stay in those moments for good. I suffer from: night sweats, bouts of intense emotion and sadness at the start of my free week, nausea upon insertion of the ring, lethargy and the feeling that my body is held down by weights. My appetite fluctuates greatly from day to day. One day, I’ll eat very little, and the next I’ll want to eat everything. Also since I’ve been on birth control, I’ve developed what you could call an eating disorder. I argue that I don’t have an eating disorder simply because I know that I am not myself on birth control. I haven’t always been this way, and I look forward to the day when I’ll be back to normal. I’ve grown so neurotic that everything in my life is just one big disorder! Doctors can only seem to diagnose what they can see, and so naturally they label me anorexic at 5’7 and around 90llbs. Two and a half years ago, I was a thin, normal girl at 105lbs. The pill made me gain about ten pounds, and since I’ve been on the ring, I’ve lost more and more weight as I’ve grown weird about everything in my life including food. I don’t use laxatives or throw up my food; I’m just a strict eater, disciplined to a fault and with more self control than one should be allowed to posses. I hate my life now. I’m terrified of having an attack in front of people and my daily life has become unpredictable and daunting. I want to be normal. I don’t want to have another dizzy spell ever. I hate it! I feel for women everywhere who are put on such drugs. I did decide to contact NuvaRing first, even before I found this site. I figured they could provide the best answers. Since it’s the only form of medication I take continually, (I’ve decided NOT to follow doctors orders to take the three different anti-depressant meds they’ve prescribed to me in the past two and a half years) I started to wonder if this was the cause of my problems. A representative of the drug told me that there have been no known reports of dizziness, my main complaint. This made me feel alone in my frustration. Now, either she was out right lying to me or the company hasn’t been notified by patients like us who suffer everyday from the adverse reactions to the hormones unnatural to our varying bodies. Regardless, this will be my last month on the ring. I’m pray that I can go back to life as I knew it. I don’t know if that’s even possible. Right now, that just seems like a dream.

Im from Cork,Ireland.I was put on Seroquel to treat my Body Dismorphic Disorder.I have really disliked the way i look for years.Hated the way i look in fact.I was very badly bullied all through my school life and teenage years because i was very heavy at that time.Needless to say i ended up hating myself with a passion.When i left school i went on mission to lose the weight and i lost about 6 stone by eating healthy and fast walking.I can't tell you how proud i felt and iv never felt proud of myself in my life.Then the effects of my teenage years started to creep up on me.I needed to face them.That was a very,very painful time and to make a long story short i got severly depressed and BDD set in.And guess what?I was put on a drug that put the 6 stone back on again and even more.Even though the Doctor's have noticed this they have continued to keep me on this drug.Every time i bring up the issue with my doctor's there response is 'Oh you need to watch the diet'.Now I tell you, I DO NOT eat alot nor do i eat rubbish.And this drug is ment to make me feel better.Now how stupid is that.

weight gain, sweating, craving for sweets, loss of sex drive, no passion for life. Can't concentrate and have became a hermit. I never even want to go outside, let alone meet people or even visit old friends. Feel like I could be in a cave with a boulder over the entryway and I would be just fine. Was taking over 100 mg a day but am now down to 15 mg!! It has taken me a year to get here, that is how bad the withdrawal is. This drug has seeped into my very soul. I am afraid that I will not be able to get all the way off at this rate.

weight gain, hair loss, I feel tired all the time. I have lost interest in doing anything. Nothing excites me any longer. It is like I have lost my passion for life. When I first got on methadone it gave me energy and wieght loss but now it is the complete opposite. I want off this drug and was having the Doctor bring me down 5 mil a week and when I hit 20 mil, I got very sick and they had to raise me up to 40. They said going down 5 a week was way too fast. I don't know what is right. But since this drug no longer works for me, I can't see any reason to be on it. It is a waste of my money.