Single one symptoms and conditions

I haven't read through every single one of these but out of the couple of dozen I have, it seems like all of the issues are with the Lactase enzyme in concentrated pill form. I'm just curious if anyone has experienced these same violent side effects with the Lactaid milk. I've been using the milk for several weeks now and admittedly do experience some VERY mild nausea that I can almost certainly attribute to the Lactaid milk. Otherwise though, I have to say I have not had any of the violent pains and vomiting many others here have complained of.

I'm just wondering if it's not only the enzyme that's causing the problems but could it possibly be the actual process of the enzyme converting the Lactose sugar in the body that is causing the side effects. I'm just kind of thinking(typing) out loud here but........ I wonder if many of you who have complained about these violent symptoms would actually experience them with drinking the Lactaid milk vs. taking the pills. Only because with the milk, the process of the enzyme converting the Lactose has already occurred.

Would anybody be willing to give this a shot just to see if there would be a difference?

I took ambien about 5 years. I noticed I would wake up with food in my bed or candy wrappers all over the bed. I mentioned it to my doctor, and he shrugged his shoulders and laughed. Later, when my dad died I went crazy and would get up at night and talk delusional with outrage. They told me I had became bi-polar at 48. It freaked me out, and I have faithfully stayed on bi-polar meds because I never want to do that again. Now, I am wondering because I heard on the news a few years ago that this man drove his car to get something to eat in his sleep with ambien. I quit ambien immediately, and found I didn't eat in my sleep. Now, I am wondering if I am bi-polar? Several of my friends have never understood how I could be normal and then completely go crazy. They had never seen me angry or disturbed before that incidence. I am now wondering if it was an ambien side affect.

My daughter had her 2nd shot in August, 2008, she started having problems November 10, 2008.Since then, she passes out at least 5 to 6 times a month, she has Bradycardia, arythmias, vagal vasal syncope, and Heart Block. She has been in and out of hospitals. The only answer to fix this is a Pace Maker. Shes 18 years old, cannot drive, go onto college (at this time). She could not even go to her graduation ceremony because she was passed out in the bathroom and wouldn't wake up. I cannot find one doctor to connect this to Gardasil, I wonder why it cannot be traced back to the shot. I would love to voice my opinion to the public about her experience since this shot. Out of all the doctors that see her, not a single one can explain why this is happening to her heart, they say she is a difficult but interesting case.

This is in response to someone who suggested that if you just take the pill as ordered, you will be ok. T0 put it simply , you are wrong. There are more than a few people affected by this drug. The problem is most people assume that because they have high blood pressure their health is already compromised and they put the weird symptoms and problems they have on their overall health.
I started taking Lisinopril 5 years ago and not once did my doctor connect my sudden problems to Lisinopril.
I was told I needed my right shoulder cuff repaired cause I was overweight and I believed it. I was told I had GERD cause the abdominal fat was pushing the acid into my throat. I believed it. I started having menstrual problems I was told I was getting old ( I am on ly 42 years old). I believed it.
I started having memory and concentration issues I was told I was too stressed at work. I believed it. Started having heart attack and stroke symptoms. I was told I had high blood pressure and I needed to lose weight. I believed it. My knees and joints started giving out.. again I was told I was overweight. Lose weight and I will get better. I believed it. Started having rib cage pain like shingles and I was told it might be my gall bladder. I had a HIDA scan and nothing was found.
One day last summer I felt like I was dying a slow death and I went to the hospital and was found out I was in heart failure, heart rate was irregular and kidney function was impaired.
I was admitted to the ICU for 3 days. While in the ICU I had my blackberry and I started googling all of my meds and I came across this site and I suddenly felt like a thousand pounds was lifted off my shoulders. That was the last Lisinopril pill i took and guess what? EVERY single one of the above problems have magically disappeared.

I work in a healthcare setting where people are admitted that are critically ill. Whenever I see a particular diagnosis I immediately scan their meds and what do I see? Lisinopril. People are having joints replaced, stomach surgeries, shoulder surgeries, irregular heart beats, unexplained heart attacks, people are being diagnosed with Alzheimer and dementia on this drug. People are getting brain lesions and the list goes on and on.
There are over 30 million people worldwide on this drug. If drugs were so good why are people getting sicker and sicker.
Please don't take this drug. Do what you have to do to get your blood pressure under control.

Was in the hospital receiving IV and inhaled steroids for breathing problems. Sent home with 10mg prednisone twice a day. It was even worse. ---puffy face, no sleep,and extreme weakness in my thighs--hard to even walk up stairs. Had a CAT scan of my lungs and my dr. was alarmed---said for a 112 pound woman,my stomach was the size of an obese person! now I'm going to have a stomach emptying test to see if that or the steroids is the problem.

I don't have any of the side-effects that are mentioned. The drug is designed to reduce blood pressure and heart rate. If you do not exercise or are over weight, your days are already numbered if you have had a heart attack. A persons has to exercise appropriately and get their heart back into shape or they will remain unhealthy. One person mentioned that their BP was 129/142. That is a very high BP. Yes it reduces you ability to do the same rigorous exercise. Reducing the drug (breaking it in half), taking it after your evening meal helped me. The pronounced effect is for about 8 hours after taking the drug. Taking it at about 5-7:00 PM or right before you go to bed works well, because it reduced your Heart rate and BP. Taking it in the morning after taking coffee is a mess-up. A number of drugs should not be taken when you want you most energy. The lingering effects are reduced. Certainly everyone is affected differently. I am 59, I have my heart attack at 56. The exercise, weight loss, and salt reduction are very important for anyone. Fluid retention increases blood pressure. If you are on Lisinopril and eat a lot of salty seasoned foods, your body will not react normally and you will feel terrible and have the combined effects of excess sodium on the systems in the body, especially nerve responses. I can not explain the coughing and gagging. I have GERD and keep it under control with Acidifex; however, after loosing about 10 pounds, (I weight 187 at 5'11'') I do not seem to need the drug.

Stop taking the drug and you may die, taking drugs off the market because a few people have problems is stupid. More people have died from tobacco and excess alcohol than all acidents, wars, murder, and the like, and we have done very little in comparison to deep pocket drug companies.
I understand how the drug works and how it doe3s not work. If you don't do what the doctors says....everything, especially dieting properly, exercising, and reducing stress,

Dear lovely people.

Thank you so much for all your postings. This site was literally my salvation. Nobody who knows me believed that I could be so ill for so very long. Family and friends say that I am a very strong person and not phased by anything, but believe me, even I could not overcome the side-effects of this deadly drug. It even resulted in me having hallucinations. It is interesting to note we are not alone in this are we?. You have to have been there to fully understand how truly horrific the side-effects are. It is interesting to note that compared to other drugs listed on this site as to positive side-effects of any drug (most drugs listed have either none or perhaps 1 -2 listings) all 353 of us!!! have been so desperate to know why we have been feeling so very very ill. We have therefore in desperation tapped into this website. We can't all be wrong. Some of you like me were or are in your darkest hour, but please, please hang in there. I took this poison for four weeks as an anti malarial medication for my holiday and it was only last Monday did I feel fully up to strength. I will do everything in my power to stop this medication ever being prescribed ever again. I have had every single one of the side-effects listed on this site. It may take some time, but you will get better and when stronger I hope like me you will try and do something positive about what has happened by actioning why this drug is never taken again by anyone by any one ever again/. Never would I want anyone to feel as ill as this. I promise it may take some time but YOU WILL come through this just like I have. I would welcome any feedback from fellow users as to what action they may also be taking as to stopping the prescribing of this drug.

Keep strong.

Kind regard to you all.

I was put on the NuvaRing by my OBGYN to fix endometriosis... that was 5 1/2 years ago... I'm now 26 and I have been having dizzy spells for a while... actually passed out twice while living in New York for the past 4 years... not fun when you're on the Subway! Recently - the back of my legs started hurting! Then my calves swelled up! All these new veins appeared and I rushed to my general physician! The first thing out of her mouth was are you on birth control... GET OFF! When i told her it was NuvaRing - she was 99% sure it was it! I had an ultrasound to make sure it wasn't blood clots and it's not... so I went to nuvaring website and one of their symptoms is pain in back of knees and swelling! RIDICULOUS!!!! I took it out immediately! Even the 32 year old who did my ultrasounds said she voluntarily got off all BC because of everyone she has come in there with liver, blood, heart problems!

I cant believe I stayed on this torture device for so long! I was on the NR for about 3 years. I started getting migraines shortly after starting it, but liked the idea of being on a BC that was easy to maintain. The migraines kept getting more severe, more frequent, and lasting longer (4 days). I would vomit, have diarrhea, miss work, and social opportunities and waste my life away lying in bed in dire pain, sometimes to the point I wanted to shoot myself in the head to ease the pain.

Finally, last month, I took the NR out for good! I did have a very small migraine last month, but it was nothing compared to what I have had, and this month, I have not had a single one!

So long NuvaRing.

Hi everyone, I have just read all thirty pages of posts to try to find some answers to my crazy reaction to prednisone. My thoughts are with you all since I have had an usually severe reaction to prednisone. I was on prednisone for 1 week in October 2008 at 60 mg/day for a sinus surgery. I am still having the following side effects at full force:

Axiety to the point I can't socialize
mood swings
hot/sweating even in freezing weather
whole body shakes
severe migraines
tooth sensitivity
muscle pains
extreme thirst (I drink almost 2 gallons/day)
hungry all the time
moon face
water retention around waist
acne
hair loss
rapid heart rate
dizziness
nightmares
night sweats
high blood pressure
high hear rate

I'm not exaggerating, my parent's can contend to that. I do have a history of having sever reactions to medication and I've had all the gland and blood tests which all check out. I never had a single one of these before the prednisone - I was a healthy 22 year old.

I was wondering if any could tell me when this hell will end - my job and well-being depends on it!

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.

As most of you, my TSH always came back normal/border line as well. However, due to all of my symptoms - every single one for Hypothyroid - they went ahead and did an ultrasound. I had a nodule 15mm x 5mm on the left lobe and 5mm x 4mm on the right. Because I had the constant "turtleneck" feeling around my throat, it was getting hard to swallow and sounded like I was an 11 year old boy gowing through puberty again, because of the hoarseness, I had Total Thyroidectomy last week. My surgeon put me on 150mg of Synthroid. So far so good with the side effects, granted it's only been 6 days. I actually have more energy, and a decrease in appetite. I've already lost 5 lbs. Not real sure if my energy level has gone up because I no longer have a thyroid to bring it down or if it is from the medication. Either way I hope my side effects stay as they are, I could stand to lose another 50 lbs - haha

I am a 36 year old woman living in hell for 3 months now.

In early October of last year I was admitted to the Hospital with diagnosed bronchitis a possible pneumonia. I was given Avelox which is a member of the Fluoroquinolone drug family. At the time I was in sever distress, could not breath, and was extremely weak from the infection. I stayed in the hospital for 6 days while they gave me Avelox along with various other meds to treat my symptoms and was released after finally getting a clear chest x-ray. The drug had done its job. But it was a week later that hell started. I was re-admitted to the same hospital with sever abdominal pain. They told me that I had hepatitis due to a reaction from the Avelox. My Dr. Also suspected I could have Wilsons Disease so he prescribed a liver biopsy, to say the very least this was a painful procedure. The biopsy came back negative and the liver function began to return to normal just as the pain everywhere else began.

joint and muscle pain
headaches
insomnia
uncontrollable twitching
arm and leg numbness
neck pain/spasms
a mass on my left breast (further diagnosed after mammogram, CT and Biopsy as a side effect to the Avelox)

My internist, Rheumatologist and the liver specialist all suspect “Post infection pain syndrom”.

However, after hearing now 3 separate times from 3 seperate Dr's about the possible side effect of Avelox I did a little research and every single one of my “symptoms” are on the lists of dangerous side effects for this drug. Now none of my Dr.s can tell me if I will ever get rid of the pain I am in. None of them seem to be able to do ANYTHING but treat my symptoms. By treating the symptoms all they can do is pain management which means pain killers. I simply can not function day to day with most pain killers so I am forced to live with the pain.

More drugs than I have ever taken, Dr.s visits, time off work, stress and a standard of living that simply put is not living, not to mention the tremendous outlay of cash...to say the least I am frustrated.

My 9 1/2 yr old son started Singulair in July 2004 when he was 5 yrs old.Looking back now we realize that he started showing signs immediately. We only gave him Singulair in the fall when he had the most trouble with his asthma. His asthma was under control immediately but was not worth the damage that was done. He complained of pains in his legs that I just thought was growing pains. He would sometimes run a fever with no other symptoms of being sick and then the fever would go away. He would also feel like he always had to go to the bathroom, especially after he went to bed. I gave him Singulair at 7pm before he went to bed. The biggest change we noticed in him was the signs of attention deficit. We first noticed that he kept getting out of his seat at dinner time. No matter how many times we told him to sit down he would sit down and then a little while later he would get right back up. We realized after a while that he wasn't doing it to be defient he just couldn't help himself. I asked his Kindergarten teacher if he had trouble sitting in his seat or with attention but she didn't think he was any worse than any of the other Kindergarten kids. In 1st grade, at the beginning of the year, his teacher said he had trouble keeping his attention but then by January she said he was a different kid. We usually stopped giving him Singulair in December. The same thing happened with his 2nd grade teacher. I question his allergist in the fall of 2nd grade but his allergist said Singulair wasn't the cause for his ADHD symptoms. When his 3rd grade teacher contacted us in Oct 07 with the same complaints I realized that it must be the Singulair. I looked online for Singulair side effects and came across this website. I couldn't believe it. I was so disappointed in myself for not doing it sooner but we took him off Singulair immediately. I called his allergist the next morning and questioned him for a second time and he told me that sometimes parents of kids with ADHD just look for something to blame for their childs behavior. I couldn't believe he said it to me. We made an appointment at Children's Hospital Boston to have him evaluated for ADHD just in case but couldn't get an appointment until Feb 08. When we had him evaluated he had been off Singulair for over 3 months. The neurologist said he did not have ADHD. When I asked him if he thought Singulair could have been to blame for the symptoms he was showing and he said there was "compelling evidence" that showed Singulair does cause ADHD symptoms in some children. We were happy that he did not have ADHD but were so sad that we gave him this medicine for 3 years without realizing what damage it was doing. My biggest fear now is that there may be long term damage. All his symptoms have gone away but sometimes he still seems a little out of it and I don't know if it is just his age or his personality or if it might still be some long term effect from the Singulair. He is such a sweet, loving, caring boy and I hope that I didn't do any long term damage by giving his this horrible medicine. I hope that something will be done soon to get this medicine off the market. My prayers go out to all the families who lost children on this medicine. I can't even imagine the pain you are feeling but I thank you for getting your story out and saving other children! I am thankful that I was able to get informed by this website because God knows my allergist wasn't looking out for my son! His asthma has been under control since being off Singulair and just seems like a happier child over all!
Thank you!

I had my Mirena removed just this past Wednesday after suffering for 2 1/2 years with every single one of the symptoms all of you have complained of. Major weight gain and inability to lose any; acne; constant flu-like muscle aches; extreme irritablity; bloated; leg, face, hands & ankle edema; random nausea & dizziness; forgetfulness; cold intolerance; eczema on my hands; elevated blood pressure; hair loss ... I felt like a 90 year old 36 year old.

After endless complaining to a very dear friend (who is 42 and was researching BC because her doctor took her off of the pill) she had come across this forum as well as the few others like this and sent me the links. It never dawned on me that it could be the Mirena, so I made an appointment to have it removed.

So, I had it removed this past Wednesday ... just a slight twinge and it was out...nothing at all like having it inserted ... and feel better already. I started my period pretty much as soon as I got home from the doctor (hadn't had one in 1 1/2 years), although I've read some women take a few days/weeks to start up again ... and for the last couple of evenings I've had some pretty intense cramps (never had them before) ... but at least the bloat this time feels NORMAL for me for being on my period.

My doctor said it'll take probably 2-3 months to get back to normal as far as everything else is concerned, but she wasn't surprised at all of all of the symptoms I had being Mirena-related, especially when I'd told her that my periods stopped completely. It's my own guess that the 20% who stop bleeding altogether are the ones most sensitive to the hormone and will more than likely have the most problems from it. I figured for me, anyway, if something is too good to be true, it's because it is. *lol*

I'm just thankful my darling husband has been so supportive and has had no problem weathering out my storm, so to speak.

Good luck to all of you that are having problems ... and listen to your bodies. This might be the perfect alternative for some women, but everyone's body is different.

My doctor prescribed lamictal after I reported hypomanic symptoms from prozac. The first couple of days on lamictal I thought it was the miracle drug; it really eliminated my mood swings. But as the days progressed, I began to have the following disturbing side effects:
- terrible insomnia (waking in the middle of the night and can't go back)
- horrifying violent dreams (of animals and people being hacked to death with machetes... interestingly, I reported this to my doctor and her response was, that just means your brain is adjusting to the chemicals...easy for her to say, she's not waking up with terrible memories of these disturbing dreams)
- weird pains and stiffness in my neck with swollen lymph nodes in the neck
- increase in anxiety and feelings of panic
- increase in feelings of anger and agitation
- feeling of detachment
- thoughts of suicide and the meaninglessness of life
- carbohydrate cravings and weight gain of nearly 4 pounds in 2 WEEKS!!
(weight had previously been stable for years)

These symptoms all appeared after taking the lamictal after only 2 weeks. Even though my doctor recommended actually INCREASING the dose of lamictal and/or adding prozac, I decided to wean off the lamictal (I was on the smallest dose of 25 mg) as an experiment to see if the symptoms would go away...
YES they did!! Every single one of them went away and were COMPLETELY gone after the second day of discontinuing the lamictal.

I know that this medication is being touted as the new miracle cure for bipolar II especially, but I think more clinical studies need to be done on lamictal. This experience was a very scary one and not unlike that reported by others on this site.

This medicine is horrible for me! I gave it a long while to give it a chance. Rapid weight gain, hair loss (ongoing), terrible aches and pains, hives, dead tired, terribly hot, irritable...the list goes on and on. After getting pro-active with my health care provider, I have now changed to Armour and now I'm remembering what 'normal' feels like again. I've lost all the weight I gained, my hair and skin feel much softer. I can't believe the amount of people that feel bad on this drug. It seems to be bad-mouthed all over the internet. I guess as long as the major drug companies retain it as the 2nd or 3rd best selling drug in the States and continue to fund, wine and dine and court physicians, we're never going to get rid of it. I chose to dispose of every single one of those evil pills. Armour stepped in to change my life for the better as Synthroid was slowly destroying me.

I have been on Synthroid for about 15 years for hypothyroidism. A few months after starting on it, I became sluggish with just no energy and my once thick hair was getting thinner and thinner. I told my doctor but she shrugged it off saying it was just my age (which at the time I was 45). She being the doctor, I assumed she was right. But awhile ago I started doing research and found in The New England Journal of Medicine that they were finding that Synthroid caused hair loss "in some people". It suggested using a thyroid hormone that used both T3 and T4 rather than the single one that Synthroid is. I went back to the doctor and she put me on Armour Thyroid. I have been on it now for 3 months, and my energy levels are way up, no longer sleeping my life away. My hair has not started growing back in yet, maybe it never will after all this time, but just feeling better is such a plus! (Of course I would feel a LOT better if my hair would thicken up again).

Are you aware about short and long term side effects of this Devil's drug??? Of course, everybody reacts differently while take or withdraw. But there are high number of people who react terribly bad!!! Doctors do not want to recognize and discuss this. They just keep silent... Do you know exactly how Prednisone works??? Nobody knows this for sure, even doctors!!! From my personal experience, and despite gradual withdrawal, I developed extremely high blood pressure, weakness, panic attacks, depression! Practically it ruined my normal life! Doctors have no clue how to deal with its devastating side effects. Steroids are not selective. When you take a steroid, the drug infiltrates the nucleus of every single one OF YOUR CELLS AND STARTS MONKEYING AROUND WITH GENES IT FINDS THERE!!! It probably plays with hundreds of genes. And just a small number of these genes control the pain and inflammation associated with inflammatory diseases, so steroids turn many of these genes off which is good thing. However, because steroids are not selective, they also regulate the genes that control kidney, liver, BRAIN, and HEART function - which is not good thing!!! It is likely that steroid treatment plays with other genes, too, including those we do not know about a lot right now...So, Prednisone pervades the entire body, which increases the likelihood of short-term side effects and long-term DAMAGE. My advice is: THINK TWICE BEFORE TAKING PREDNISONE!!!

Oh My God !
This is Madness.I just read all these comments and there is not single one of them that I do not have! I`ve been on Biaxin for 20 days now , and I went through every single step that you guys wrote. What the hell am i supposed to do with the Dizziness ? he gave me another one to use which is called Meclizine 25mg ? and IT DOES NOT WORK.
Luckily i finished 10 days of theraphy of Biaxin today.

Let me know if this dizziness will go away PLEASE !
Appreciate it.

I have just come across this site, while looking to find out why I have been experiencing heart palpitations for the past two months - out of the blue!!! and usually "exercise" induced. I had some tests and have been told they are Premature Atrial Contractions "PACs". I started taking Yasmin in April, after having tried others over the past year (tri-cyclen lo and alesse) which did not work for me as the progestin was not strong enough. I am in my 40s and never took the pill before. Yasmin was great, it significantly reduced my "physical" pms (severe inflamation, severe bloating, severe sore breasts) which I experience for 2-3 weeks a month. However, sometime in mid to late June, I started getting palpitations/tremors out of the blue. The first episode freaked me out and lasted for about two weeks. At first I thought it was allergy medication mixed with my thyroid med, which can happen - but I cut out the allergy meds and still got them. They seem to come about 6hrs to a day after I fexercise/figure skate and they last from 2 to 5 five days. It's very irritating and nerve wracking, and I feel very agitated. I am also out of breath more than usual when walking up stairs, a little light headed and have some tightness in the chest. My legs also are weak, which makes no sense given my exercise regimen. I then lowered my thyroid replacement from .125 synthroid to .100 - too much thyroid med can cause some palpitations. Anyone who has mistakenly taken a second thyroid pill having forgotten that they already took one will understand. Even with the lower dose I am still getting the palpilations. I am totally at a loss as to why all of a sudden this is happening to me (perhaps perimenopause??). I have had the odd flutter here and there in my live, but nothing like this. It just doesn't make any sense ag ll. Can one's health just change like this overnight?. I am otherwise healthy, slim, have "lower" blood pressure (apprx 100-90/70-60)I skate 3 to 5 times a week, I have a full time job and yes I do push myself, but this is getting ridiculous. The only thing I can attribute it to is the Yasmin, ... but my symptoms only started after a few months not instantly, whereas it would seem that most of the the women here noticed the side effects faster. I hate to stop the Yasmin because I will have to return to pms "hell", but I suppose I will give it a try to see if the palpitations subside. At this point, I have been offered a low dose "beta blocker" and have refused. I am stunned to think that all of a sudden I have heart issues, especially since my Dr has always kidded me my that I will never have heart problems with my blood pressure. I will stop the Yasmin tonight and post another message in a few weeks one it is out my system. Here's hoping it is the Yasmin.
KarenSkaterGirl

How BCP affect your blood pressure: I have NOT encountered a single one that does not warn about raising your blood pressure. That's why BCP's are not recommended to women with high bp to begin with.

Mircette (and Kariva) I have not tried personally, but a close friend has been taking it for a while. She hasn't had any problems besides heart palpitations, but not sure if the pill caused it or not. She's now switching to Nuvaring (less hassle, and I highly recommended it, as well as a gyno friend she has).

Nuvaring-I am on the second cycle. I never ever think about it, except when I have to insert and remove it, and they have a convenient computer program you can download to remind you, as well as a tiny timer you can carry around in your purse (can get it for free from their website). No headaches, no nightmares, no panic attacks. In fact, I don't even notice I'm on birth control, it's great.

You girls have no idea how thankful I am that I found this site. Short history - I'm 33 with four children and was diagnosed with a dermoid cyst on my right ovary and a fluid filled cyst on my left 04 November 2004. My gyn put me on Yasmin because she said that my symptoms were typical of high estrogen levels and that by boosting my progestin the cysts would dissolve. She said that without a blood draw so I insisted on one and she ordered it but also told me to start the Yasmin anyway. I wouldn't be taking the white pills, however, she wanted me to continue the next pack to keep the progestin level high. I started that assuming I was doing the right thing. Three weeks later I heard nothing about my blood draw so I called. My estrogen level was fine which meant I had no idea what caused my cysts or what would make them go away. SO, I called the doctor who said I'd have to make a consultation appointment and that ended up being 30 Jan. 2006. Yes, I have to wait three more weeks to see her. I'm NOT happy, but I am also very sick.

For four years I've been HEAVILY involved in kickboxing and weight lifting and now I can barely get out of bed. I've been throwing up like I'm pregnant, nauseous like I'm pregnant, getting migraines like I have a tumor, and appetite? HA! I can't stand the sight or smell of food. Girls, you talk about an eater ~ I can get down! Sadly, I haven't worked out since October because of the cysts making it painful so I decided to hit the gym last night and I even went light on my weights. Nope. Left early...had to puke. In addition to having PTSD and OCD, I now have depression because I'm so SICK all the time.

Someone, please tell me that this will go away or that I'm doing the right (or even wrong) thing. I read that someone's back looked like a warzone. OMG, my FACE does. I'm VERY picky about my face and hair ~ my hair has fallen out in bird nest clumps and my face is a map of the US. It's SO depressing. WHY? I'm 33 and I've NEVER had a health problem and now with two STUPID little cysts, my world has crumbled.

So, is this Yasmin side effects? The vomiting, migraines, my eyes not being able to move without losing equilibrium, my face becoming a connect the dots trick, food becoming the enemy...it really feels like I'm pregnant but TRUST that I've not had sex. It's too painful from the cysts.

HHEELLPP...

Love in advance -
KiDS

hmm.

ok.

not good.

I have been taking microgynon for 2 months - during which time i have put on weight and a week before each period would have eaten a pint of worms to not feel as depressed as i did.

coupling this i put on stacks - (hey it may stop you getting pregnant but it just make you look and feel 6 months pregnant!)

i had heard that Jasmin would help prevent this due to it's lower doses, so would help not only the side effects like the screaming banshee rearing her head, but would also help reduce weight and help with clearing the skin.....

so you guys - have just ruined my big exciting venture into taking this 'miracle' pill...

soooooo....... whats the deal huh?
we all want the same thing, the same results, what IS the best bloody pill to take???
damn things - i hate the whole package of it all... it's not like our bodies are REALLY going to accept anything is it - it's un-natural, and it does'nt seem fair we have to go through so much s**t either.

if anyone knows of a good one - speak - and quick!

peace & love to every single one of you x

Hi!

Wow. I cannot echo enough praises for this website! If it was not for this website, and all of your informative posts, I would have never known that the solution to my problems would be as simple as switching birth control! I was on Yasmin for about 3 1/2 months (I have been off for a week now), and although I didn't notice any side effects right away, about a month ago I started having (1) back pain (2) leg pain (3) tingling/numbness in my limbs (4) heart palpitations and shortness of breath to the point I almost passed out several different times (5)trouble sleeping (6)emotionally fragile, and then about three weeks ago, my feet and ankles started swelling and were incredibly painful.

I was searching the internet, desperate to know what was wrong with me and typed in "swelling feet" and one website mentioned that birth control could be a cause. From there I typed in "Yasmin and swelling feet" and it brought me to this website, where I found EVERY SINGLE one of my symptoms had been experienced by at least one other person on Yasmin. I immediately called my obgyn and mentioned my side effects and teh website, and he took me off the pill and I'm now in a "detox" stage. Already I feel A TON better. My feet stopped swelling almost immediately, and although they aren't completely back to normal, they are very close to being there, and are getting better every day. All of my other symptoms have since subsided as well.

The only problem I'm encountering now are symptoms from "withdrawal" of being off the pill -- bad headaches and I'm exhausted all the time.

Can't wait to have this drug out of my system!!