Vengence symptoms and conditions

I was on doxycycline for three weeks because the doctor believed I had Lyme disease due to the slight headache, mild fever, and aching joints that I was experiencing. I was fine for the first few days, but then I began to develop some unusual symptoms. The symptoms fluctuated day to day, but I was never free from one or more of these symptoms: severe headache, chills, night sweats, tingling in my arms, weakness in my legs, ear ache, numbness in my face (especially my eyes and lips), anxiety, depression, insomnia, pain in my eyes, and neck, and stiffness in my jaw. At the end of three weeks, I seemed to have more Lyme symptoms than before I began the medication. My Lyme test was negative, but with my continuing symptoms my doctor recommended that I take the medicine for ten more days, and retest for Lyme. The first day back on the medicine I was sicker than ever. I waited it out because the doctor insisted that it was the best thing to do. I finished the medicine, and the effects were less intense. My second Lyme test was negative. I am being tested for Fifth's disease (my son was ill with it just as I began to experience my swelling joints - a condition that can not be treated, uggh). I seem to get worse if I don't drink all day and night - a lot of water is needed, all the time. The effects also increase when I go to bed, recline on the couch, allow myself to become nervous about my condition, or over work myself through the day. I was at the pediatrician with my son yesterday, and mentioned my problem, wondering how long it could take to get the medicine out of my system. She told me it could be as long as a few months. It's been two weeks since I took my last pill.

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

I started off taking Tenormin 50 mg 1 x a day and Lanoxin 25 mg 1 x a day about 21 years ago. I continued to have constant palps and skipped beats even though I was on these meds. I wound up developing vertigo after about 5 years that got so bad I had it daily. I ended up with severe sinus problems and was given a cortisone packet of pills (the kind that decrease each day you take them) to take. The vertigo left for 6 months, coming back again with a vengeance. I begged the docs to put me back on cortisone pills again, once more helping to stop the vertigo. However, at the same time I also stopped the Lanoxin. ??? I totally believe that Lanoxin was part of the problem causing the vertigo. I now only have it from time to time, maybe only a few times a year. I still blame the Toprol that I now take for the left-over vertigo. I was taken off of the Tenormin after about 10 years of taking it and put on the Toprol at that time and have been on the Toprol xl for the last 11 years. The docs said that I needed to be on Toprol XL, as it was an extended release and would help me much more around the clock. I did not notice much difference throughout the switch, but looking back I do believe that a lot of the things that I have been dealing with through the years are side-effects of the medicines. I have had irritable bowel syndrome, told I have fybromyalgia, then told I did not have fybromyalgia, hip and back pain, skin problems on one of my hands that started with the Toprol, headaches, tiredness, horrible weight-gain (without overeating!! Honestly.), I have averaged 5 lbs. a year and the docs never even listen to me when I voice my concerns, I have been diagnosed with anxiety, joints ache, ankels, feet, face and hands swell, stomach bloats something terrible, acid reflux, hiatial hernia, and I had a tumor removed that could have been a problem off my rectum (who knows what caused it), I have had CTs and MRIs of my head, twice, for the vertigo and what I was told was probably psuedo-tumor cerbri (because of months of severe headaches), told by my eye doctor that he wonders if I have beginning MS, everything came back fine and things seem to resolve and go into something else. I have been passed from my general physician, to a cardiologist, to a ENT, and a neurologist. No one can ever find anything physically wrong, but they did conclude that I definitely had benign positional vertigo. LOL, that means they could not tell me why I had it. I put a stop to testing when they wanted to do the spinal taps.

Now I am experiencing tightness around my lower rib-cage and feel as though I am sucking for breath, I have a terrible time falling asleep at night, I wake up gasping and swearing that I am dying. My rib-cage is numb around my right side, not so much the left side when I lay down to go to sleep at night. After a few bouts of this I finally fall asleep and sleep all night most times. My blood pressure is now on the rise 150/99 at the highest. I have been working out lately with a few positive effects, more energy, more endurance, less aches and pains, muscles are starting to tone up, however, no weight loss. I thought my bp was starting to lower, but found out it was actually up. I went to my family doc and she listened to me really good, realized at last that I was not shedding the weight despite the efforts I was making. She cut my toprol to 25 mg 1 x a day and put me on lisinopril, I did not tolerate the lisinopril so she switched me to dyazide, lowest dose 1 x a day. I have great positives ...no more swelling, weight loss, lower bp, HOWEVER, I am now having jitters, anxiety (somewhat), no appetite at all, a few muscle spasms in my arms and legs, nothing painful or severe, dizziness, slight headache that comes and goes especially through my eyes. I am also experiencing coughing, and raspiness...but I am also coming out of a bout of bronchitis, which got really bad with the lisinopril. I believe it is partly due to the meds.

I called my doc today to tell her about the twitching and buzzing feeling and to ask about the dyazide. My feelings are that I am experiencing a lot of different things, first the bronchitis, and all the meds I was taking for that...albuterol, musinex, tylenol w/codeine, and biaxin, then the decrease of my toprol xl, the bad effects of lisinopril (coughing and raspiness), and now starting the new drug dyazide (generic form). I really want this to all settle down and work out for the best, but it is getting to me now (after 2 weeks). Last Saturday I would up in the ER with shooting pains through my chest that left me very pale and lightheaded when it happened as well as very tight throug my chest and sucking for air. The ER did chest xray, chest CT w/contrast, bloodtests, urine test, bp's sitting, standing and lying down (it is highest while sitting), everything came back good. No heart attacks, no blood clots, no bronchitis anymore, nothing. Blood work was good, urine was good. I am beginning to think that perhaps my body is reacting to cutting the Toprol xl in half. Sort of a withdrawal. There is really nothing else it can be and I really don't think that the dyazide is that bad of a drug and probably not causing all of my problems now, maybe just a part. Which are the tingling, dizziness, anxiety, twitching, and coughing. I have only had 3 of the dyazide medication. But have read that withdrawal symptoms of Toprol can cause these problems for a while. I am also thinking that the shooting chest pains last week were also withdrawal of the Toprol as it had been 1 week at that point that it had been cut in half.

Any opinions, if anyone can make heads or tails of anything that I have wrote. Sorry for the length and if it is confusing.

I was taking Topamax for about 4 years for chronic/daily migraines. It helped tremendously after I had taken almost everything else with no success. Then I had an episode where I ended up with 5 kidney stones. They passed but my neurologist wanted me off the Topamax in case that was the cause of them. I went off and my headaches came back with a vengeance. I had them daily until I begged my primary care doctor to put me back on Topamax. I honestly would rather have stones than daily headaches. I am a mother to four and have a husband and a job. I can't live with daily migraines. After being back on it for about two weeks the headaches have disappeared. I take 200 mg twice a day. I do have memory loss and loss of words big time. It is VERY frustrating. I feel stupid. But I can live with that. I have tingling cheeks , lips and hands. I'm sensitive to sun and have to wear my sunglasses a lot more now. I now talk in my sleep- a little nervous about that :) I lost weight last time around but haven't yet this time. I am very happy, not sure if that is the RX or just me reacting to not having headaches. I guess you have to weight the side effects with the benefits. The choice is ultimately up to you. Good luck everyone!

I have been on 100 mg topamax for a few months now, and i was actually having people try my drinks bc i thought they was flat, and i would feel my fingers and my toes go numb and tingle. I honestly never thought for two seconds it was my medication. The only side effects i was warned about was weight loss (which hasn't occurred with me) and that i would be very thirsty, which i am. But i have NIGHTMARES about things im not even afraid of, and i have trouble spelling words i didn't before, and sometimes i can't even remember what i wore last week to school. Im starting to rethink this whole topamax thing, does anyone know any other prescriptions that will help headaches without the crazy effects?

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

I am a male 45 years and used simivastin another statin for three and a half years. Over this time i had severe muscle pain at time then about 4 months ago the muscle pain in my legs came on with a vengeance. It started in both thighs then calfs got very tight sore ankles feet and eventually got in to my arms. A deep achey sort of a pain and an irritability that casesa feeling like a toxin in my inside elbows that makes me want to stretch all the time. I feel very weak compared to my former self. I tried many things to alleviate the pain but nothing really took the pain away or even decreased it much. sometimes i would lay and groan in agony. I especially noticed that draghts and weather changes made me feel worse????. I stopped taking the simivastin 6 weeks ago. I have not had a lot of improvement but must admit thet i have been trying to push my self over this and probably done more damage. My ck levels are normal but my liver enzyme is increased a little. I started also to take q10 and L- carnitine along with magnesium. I might be improving a little each day but nothing definite. I saw a rheumatologist who has no diagnosis and isn't to committal on whether the statin is to blame. He put me on celebrex which has finally given me some relief. Can anyone relate to the worsening of symptoms with cooler changes in weather? and is there anything else i could do to hasten recovery? Thank you to all contributors on this board although it is the first time i have contributed this board has been a scores of help to me.

I have been having difficulty with my legs from the knees down since taking Remeron for over a year. Normal walking is a chore, but let me get in a department or grocery store and I am in such agony with leg pain from the knee to my ankles. It is a heavy, throbbing ache. Pain pills, heat and sleep is the only cure. Never had this problem before this. If I ween myself off them, my migraines come back with a vengence.

I am a physician and a patient. I have been on singulair and advair for several years now and had weight gain, anxiety, depression, and mild improvement in asthma that I could tell. I had pneumonia 4 times last year and thought it was the environment. I left the Midwest and moved to the east coast where I stopped my meds for several months and all the above symptoms resolved. I recently restarted them several weeks ago do to increase in symptoms and anxiety/panic attacks came back with a vengeance I stopped them and switched to other meds and wow the side effects are improving again. I am not going to take them or prescribe them again.

I started taking YAZ about a year ago. The first three months especially I noticed that I could cry and wanted to cry about everything from the phone ringing to dropping a paperclip. I screamed at my then bf for hours about everything and nothing. I snapped at everything, I couldn't control anything. After three months when my body slightly adjusted other side effects took over. I had vision blurriness randomly, migraines almost every three days that overtook my life and barely went away with sever migraine meds, appetite off the charts, depression, face heaviness when sleeping which was incredibly painful, numbness in my extremities.. its been a nightmare. I got off for a few months because I wanted to be free of it, and i was. Unfortunately because of my medical condition I need to be on b/c for life. I started taking it again and have been on it for several weeks and ALL of the side effects are back with a vengeance including crazy acne and bloating. Someone shoot me. I hate this drug.

After reading these posts, I am glad I didn't change my mind about having the MIUD removed. I have had all sorts of problems since that evil piece of plastic was inserted. I didn't think much of it at first and thought maybe I am just tired because I have my period and cramps alllllll the time. The relationship I was in was bad and thought maybe I was tired and moody because of that. After a couple of months - boyfriend free - things didn't change. I had horrible mood swings, my concentration was shot. My work ethic went down the toliet, I felt like a 10 year old kid with ADD. No energy, back hurt on a regular basis, carpal tunnel came back with a vengence and TMJ (I don't know if that's related but I've never had it before), acne, weight gain, no sex drive, and a constant itching around my neck. I am sure the NP was ready to try to talk me out of it and wait the full 6 months for "side effects" to go away. Well, the last 5 sucked, I really didn't want to deal with this crap any longer, besides with the price of gas, I can't afford the money for the regular buying of feminine products. I am only 6 hours free of this and I am already feeling a little better. I don't have that "pressure" you feel in your belly and a have bit more energy. I am so looking forward to the next few weeks when things start to get back to normal!!! If you have any doubts about this thing....get rid of it. Its really not that bad to get it out, 99 times less painful than getting it inserted!!!

I cannot disagree with these negative postings more. I absolutely love the nuvaring. I have not gained any weight...of course I diet & exercise about 5 days a week....do those of you who have experienced weight gain exercise regularly? I have also had an INCREASE in my sex drive...I have been with my fiance for 5 years, and for the past 3 of those, I have had no sex drive whatsoever. I got on the ring & bam, it's there with a vengence...the only problem with that is that we're getting married in 2 weeks & I wanted to make it special & stop having sex a couple of months before the wedding...but I just can't get enough of it. I have dealt with depression & anxiety my entire 27 years of life, so if the nuvaring is causing that...it's not any worse than normal. The only side effects I've had is the discharge, (which yes, is very annoying) and tender breasts...but I can deal with that. Although I have noticed that I cry a bit easier...but I was always a crier as well. I cry when I'm mad, sad, happy...always have, so nope...guess that's not from the ring either. ALL birth control effects everyone differently. I'm not saying this for everyone, but sometimes a lot of people like to blame certain actions & physical changes on something & maybe this is the case...for some people. I've been on the pill before & I always got off it b/c of weight gain....well, it was b/c I wasn't eating properly or exercising. I liked to blame my mood swings on the pill as well, but once I thought about it, I still had those before & after taking the pill. The only reason I quit the pill was b/c it did give me acne. Anyway, just my thoughts....& I wanted to post something positive for the ring.

I suffer from cluster headaches as well as several other ailments (Doctors say..."we know it's something we just can't figure it out"...sigh). With my latest bout of cluster headaches they decided to put me on prednisone..60 mg for 4 days...30 for 3 days..etc. until I tapered down. Worked great! Headaches went away and I was feeling wonderful (terribly agitated but physically wonderful) until I went off of it (headaches returned with a vengeance. They immediately started me on a second round of Prednisone at 60 per day. Third day, on this second round, I went to get out of bed and BAM!!! fell straight to the floor. I had absolutely no muscle control below my waist...NONE! Laid there on the floor for about a half hour (trying to get up as I flailed around). Managed to finally raise to a somewhat standing position. Walked (shuffled) down the hallway to the bathroom to try and use the toilet. Went to sit down on it and promptly fell wedging myself between the toilet and the wall...(a disturbing visual). A relative helped me (how humiliating) out from my predicament and we immediately called the doctor. I was told it was not the prednisone but a flaring of my underlying vascular/soft tissue disorder and to stop prednisone. Stopped prednisone, next morning went to get up and low and behold I could stand but I had excruciating pain shooting into my hips, knees and ankles which once again made me fall (from agonizing pain). Day three off of prednisone and the excruciating pain upon rising is better but far from over. Currently, extreme muscle fatigue...so weak my poor little muscles won't even quiver. Headaches are back. Red swollen face...ack!!!...what a nightmare.

I am a 56 year old woman and my doctor started me on 10 mg Lisinopril in March. Within 24 hours of starting it I developed a very annoying cough. At my next doctors visit she told me my bp was not down enough and wanted to increase the dosage. When I asked her if the cough could be from the Lisinopril she gave me some samples of Benecar HCT. The only problem I had with that was muscle weakness and some palpitations that went away after a few days. When I got the prescription filled I found that my insurance didn't cover it and it was quite expensive so I called my doctor back and she wanted me to try the Lisinopril again at 20mg and see what happened. That very same night the cough came back with a vengeance, along with dizziness. I decided to try to tough it out but after ten days now the cough is so bad it's unbearable. It keeps me up at night and I cough till I gag and cry. On several occasions I have coughed until I vomited. I couldn't take it any more and stopped taking it two days ago. I called my doctor today and she told me to stop taking it and now we're going to try Norvasc.

I took Chantix for about a month. It lessened my cravings to smoke, but I started getting heart palpitations really bad. I ended up in the ER one day and the Dr. told me that he had never seen that side effect. He looked up the side effects in his palm pilot, and found that it was the very last side effect in the list. I decided to get off Chantix to see if that would help. Well now I'm going to be on Toprol for the rest of my life. They won't say for certain whether it was the Chanitix that caused it or not. Coincidence? I'm not sure. All I know, is that my heart was completely fine before it, and now if I am an hour late taking the Toprol my heart goes insane. My cardiologist has no clue what happened (I've been to two). I'm only 33 years old, and taking this medication for the rest of my life.
Has anyone experienced heart palpitations after starting Chantix?

My Mother started taking Simvastatin 6 weeks ago after a stroke, she has stomach cramps and her lips are all swollen and sore. Does it do this. It's all most odd as these things were not there before starting this drug.

DJ

I've just started using Loestrin 24 Fe in mid December and I'm in the first week of my 2nd pack. I only looked it up to find out what it's cost is. My gyn's office gave me 3 sample packs. Most times new BCs are not covered by insurance and yeah, I don't want to pay $50+ for a new fancy pill! ;) In searching I found this site and read the post. I find them very interesting and enlightening! Yesterday and today I've felt 'blah'. I attributed it to not getting my paycheck on time (that would set anyone off!) and having to rearrange some things. Well there's a lot more important things going out there than my vanity! lol But yet I can't shake the 'blah' feeling. After reading the post of some who are experiencing mood swings and/or depression...I'm starting to think about this pill. I've always had heavy and long periods with cramps, major headaches,fatigue, you name it I get it! After my first pack of L24 for the first time EVER I had a light 3 -4 day period. I did get my normal craps/lower back pain the first day but my second wasn't spent in the bathroom every 20 minutes changing a Tampax as in the past. So that part is great! I was told that I have fibroids and in November I didn't get a period and freaked out. Took a test and it was negative. My period finally came on Dec 1 and with a vengeance! I spotted throughout Dec--probably fibroid related (as that is common I'm told) so when my gyn gave me three sample packs of L24 I started them. It's only my 2nd pack so I will finish it and if I'm still feeling 'blah' I will go back to Trivora and my longer periods. I've always been acne prone as well so I don't know if my breakout is due to L24 or not right now. I will monitor. Weight gain has never been an issue while on any pill but in Dec I was 138 and today (I weighed myself after reading these post! women! ha!) I'm 143. Still in my normal weight at 5'9. I tend to fluctuate with an 8lb range and my appetite is the same--so far. So again I will finish this pack. I don't know if I can switch in the middle of a pack since my period has passed now. I do have a prescription for Trivora and I'm ready to use it should this persist! I'm 42 and I've dealt with my periods all of this time..It's no big thing. I just don't want to bleed in between periods--if it's fibroid related. I'll see my herbalist about that! You know the doctors and pharmaceutical companies seem to be in bed with each other. We've got wonder what is being put into these drugs to alter what our body is supposed to do naturally. But what's a girl to do! :)
Nanette

Hi all! I just began taking YAZ two weeks ago and things were fine up until two days ago. I started experiencing itching on several parts of my boy an last night, realized I had hives on my waist at my back, near my underarms and have serious itching all over the rest of my body including the palms of my hands. Please, please, please if anyone reads this an has had similar side effects, please let me know. Furthermore, I did not take the pill last night as I knew this could be the only thing causing these issues. Does anyone know the reprecution of stopping the pill mid month? Please let me know and thanks for your help!

I have a herniated disc in lower back.Been dealing with it for about 7 yrs 3 of which have been chronic. I had a series of 3 shots in 3 weeks one year ago and had instant relief for about 2 months. My pain came back after this short pause with a vengeance. I just went back to the doctor for my second series of 3 shots but he really knocked the hell out of me this time. I have had a accelerated heart rate, puffy face, huge weight gain, anxiety, insomnia, incredible appetite, cotton mouth and some digestive problems as well. One good thing about it is that I do not have any pain(for now). I am scheduled for surgery in a month hopeful to get away from all drug treatments.

I have been on Doxy for about 6 months now to treat adult acne. It works brilliantly for my skin which is why I am hesitant about stopping it, if I do forget to take it for a day or two the oil and spots come back with a vengeance.
I discovered straight away to take it with food, taking it on an empty stomach caused nausea and dizziness, but I don't get this anymore.
The problem now is I find myself feeling more and more depressed, looking back Ive been flat for quite a while now. I seem to pick up every little bug going round and nothing makes me happy anymore.
I thought it was just me, but reading about it here, makes me wonder if its the Doxy??

I am 65 years old. Started Lisinopril HCTZ in November. Shortly thereafter began having a persistent tickle in my throat which caused me to to have a very dry hacking cough which then caused my sinus to drain and a lot of mucus to build up in my throat. The tickle and cough would pop up several times a day and night. After a couple of weeks I stopped the medication. The symptoms persisted for over a month. When they finally subsided I tried the Lisinopril one more time. Within one day the tickle & cough came back with a vengeance. I have now been off the medication for over 3 weeks and still have the tickle, cough and sinus drainage. It is now affecting my sleep and eating. I never know when the tickle is going to hit, but now every time I eat the food causes me to start coughing. My doctor took me off the medication and put me on Toprol which is a totally different class of medication. I am also trying Nasonex and Chloraseptic Spray and lozenges. I am considering going to an ENT doctor.

Hi, I just put the NuvaRing in about 2 weeks ago and so far I'm not exactly impressed. It's nothing real BAD but it has completely changed the dynamics of my vagina. It is dry, with a stinging feeling inside all the time - after sex is way worse, and my vagina gets so sensitive that it throbs and aches on the outside, and stings on the inside.

I thought "ok, give it a chance to adapt" but really, there is a foreign object in my body which is

A) unhygienic - it will catch all sorts that will sit in there and fester - lots of semen. The self cleansing action of the vagina (it sheds its walls very quickly, and is full of mucous membranes) is hindered. And
B) I can feel it inside, but not like you would feel a 'foreign object'. I can feel it as it an almost painful uncomfortable achy feeling that is like almost a cramp. Hormones leaching into my flesh - very unnatural I have to say.

What The Man Thinks
Last night whilst having sex, my partner came, and I moved slightly and he gasped with pain and said "I thought that felt a bit strange" - the NuvaRing had hurt his penis but he didn't realize until afterwards as it had directly and intensely stimulated him, it was only afterwards that he realized it was verging on very painful. Not good.

He can also feel it when we have sex and finds it a bit off putting - he is also having sex with the NuvaRing, not just me.

In my opinion, I'm really glad that people are thinking of new ways to administer birth control, but I don't think this one is a winner. I hate condoms with a vengeance but you know what? They get more and more appealing every stinging day.

Don't forget ladies that the greatest experiment ever performed on women was the big fat bullshit regarding oestrogen. We have been experimented on for 50 years, yet right at the beginning scientists knew that oestrogen caused cancer in rats and mice, AND WOMEN. Don't ever forget that pharmaceuticals are out to get your dollars, and will fudge results, fire people, ruin lives and make you sick. Next time you have something wrong with you, try going to naturopath for a proper solution - they actually know what is going on with your body and don't prescribe a ''one size fits all' drug answer.

That's it for me and the NuvaRing!
I tried. I failed.
: )

I used to take Lamictal 150mg at night, no problems, but started feeling anxious in the afternoon/evening. My Dr. Rx'd 300mg lithium at night to see if it would help the anxiety, but I had very fitfil, unrestful sleep to the point where I was not sleeping much and very tired all day. So, the Dr. took me off lithium and substituted Tripletal 300mg in the evening. That worked, but I was still a little depressed & she increased my Lamictal to 200 mg at night. I started waking up after about 4 hours with horrible nightmares. I thought the nightmares were from Trileptal because that was a new med, but even after I discontinued it, I still get the nightmares/panic feeling that wakes me at night. I took 2mg Lunesta for a while to help me sleep, but then I slept too much 10-12 hrs. I take the Lamictal now in the morning & don't get those nightmares & I sleep fine now, but I feel anxious & dizzy and have trouble concentrating, again about 2-4 hours after I take it in the morning. Dr. says I can take ativan to help the anxiety, but I feel like I need to get off Lamictal and try something else. Maybe lithium will help if try to take it now witout the Lamictal.

I am having tingling burning sensation in my feet, legs and hands and arms. My blood pressure was not improving on 5 mg so I upped it to 10 and those symptoms are much worse. The tingling sensation goes all the way up my left arm and up above my knees on my legs.

I have tried to take the Lisinipril before and stopped for these same reasons. My doctor does not seem to think that it is due to the Lisinipril. so I tried it again and the burning, burning sensation is driving me crazy and keeping me awake. I have to get up and stand in cold water for a while to get some relief.

I have not read about anyone with the same symptoms. Does anyone out there have these symptoms??

I have taking Omep,Losec, or Domparion??? for the last 3 yrs. The major side effect for all 3 have been knee and calf cramps after going to bed. The morning starts with the cramps, and they are getting more frequent. I place a ice pack on the area, and it subsides for awhile. Hot baths seem to inflame the area. Any suggestions??? The acid refux is gone. I have taken myself off the medication, and the AR returns with a vengence. Interesting about the comment re: generic drugs, I hope you are wrong, as the insurance company that we have will only pay for the generic. When on group plan, I didn't care - but now...... Anyone else experience this? I am also on Lipitor, which have the leg cramp side effects??????