Fish symptoms and conditions

I am an active 60 year old.After being checked for diabetes I was told I was borderline and chose to try by changing my diet. Three months later at my next visit UI was told I was improved but my cholesterol was far too high and prescribed 40mg Simvastatin.Between then and the nest three monthly check I had numerous symptoms. My calfs throbbed, my shoulder ached and my sex drive decreased and I was always tired. The most frightening thing of all though was my concentration. I would be riding my motorbike or driving the car and suddenly snap to and realize my mind had been wondering and my concentration gone. (Ive had numerous near accidents.)
IU read on this site about "memory loss" and wondered if this was what was happening to me. My last three month visit was last week, my cholesterol is almost normal so I am stopping the pills and seeing what happens.
Steveb

I hate mirena. I had mirena for a year and a half. I had bleeding with intercourse, headaches, cramping, hair loss, depression, and swollen lymph nodes. I overall just didn't feel good. The strings migrated upward into my uterus. The doctor tried to "fish" the strings out, but had no luck and had to schedule a d&c to remove it. It ended up costing me about 4-5 grand for a small piece of plastic that has gave me nothing but trouble. I still have not had a period and can't get pregnant and it has been 5 months post mirena. My lymph nodes have gone back to normal now..just no period and no baby.

My husband was prescribed 40mg of this drug 2 years back,for his high cholesterol reading. He is an ex-services and has always been extremely fit, he was tired for almost a year, then he began having headaches to the point he had a brain scan, because he thought he had a tumor. He also has had knee and neck joint problems and now the joints of his fingers are giving him pain He now wakes up each morning feels really ill and feels as though hes being strangled, the sensation lasts sometime for hours and he has to lie down. His doctor said it was blood pressure but he keeps a monitor and his pressure has been normal. His doctor said he should continue to take it, but when you read all the symptoms that people are getting while taking this drug it makes you realize they are all just guinea pigs for a large scale trial of the drug

I have been on omeprazole for 2 months. I noticed I would get dizzy and hot flashes. I quit taking it and have been off for 7 days. I'm wondering how long it takes for these side effects to stop?? I feel light headed all the time sometimes I feel good and then I get dizzy again?? Please Respond??

Thanks

Update. The count down is on. Next week on Tues my 6yr old son will be having his tonsils removed. Only 5 months after the adenoids were removed. I am hoping once this is over the improvements I have seen will just get better! His sinus drained in April, 9 days after coming off Singulair after battling sinus infections for entire year or more actually. When his sinus drained the infection went right into the tonsils and he has had tonsillitis ever since. One thing I wanted to share is that around the same time he came off singulair we started omega 3 supplement. Both my son and I stopped Singulair the same day. We both started the Omega 3. Last week I had to stop his dose because of the upcoming surgery because it can thin the blood. I noticed this last week his nasal allergies kicked in. He did pretty good through this allergy season and wasn't on any meds a lot of the days. I hardly had to take allergy meds this time around also. Im allergic to trees/grass and this is usually my bad time. I really feel the omega 3 has helped a lot!!! I am also waiting to get the results of his blood tests to see if his cholesterol has gone down. Just wanted to share!

Does anyone who has been having negative side effects ever feel like they have a fishy taste in their mouth, fishy body odor, or fishy breath? This is not related to fish oil of any kind but would be because of pyridine.

You probably ask "how does CC come up with these question?" I am trying to look for clues as to what happens to montelukast if it ionizes.

Doctor prescribed 10 mg. Lisinopril four months ago for borderline HBP. Since then I have suffered from an itchy rash, chest and shoulder pain , extreme fatigue , low concentration and memory loss , a dry cough so annoying that I live on cough drops and a strange feeling in my throat like a lump is always there , and most recently I have developed pain and swelling in the lymph nodes under my armpits. I also have dizzy spells so bad that I have almost fainted a couple of times. Once it was so bad that I could not even get out of bed. I am convinced that it is the Lisinopril because I did not have these problems before I started taking it. I am going to stop taking this poison and see a Naturopathic Practitioner. I have recently read that fish peptides also called bonito peptides have been used successfully in treating HBP and is a safe and natural alternative to those Pharma drugs that cause so much misery. I will keep you posted.

I am so glad that a friend of mine found this site and told me to go on it and take a look for myself. I have been reading these stories for about an hour now and i am amazed at how almost all of you have the same story as I do. I never even thought about "the IUD" being the cause of my depression. I have two small children, my parents after 22 years got a divorce, my husband and I are having major problems (i have already scheduled to go see a lawyer. Thats how bad it is) and all along i now firmly believe that this stupid thing that at one point sounded so great may be the problem. I just thought it was everything that I was dealing with was just too much. I have horrible mood swings, don't have a sex drive, always tired no matter how much sleep I get, 6 out of 7 days i am crying, don't want to be around anyone and the list goes on and on and on. The only side effect that i don't have is the weight gain. But I always have the bloating and cramps and back aches. I called my Dr. about 10 minutes ago and asked to schedule an appointment and Thank God my doctor did not treat me the way the rest of your doctors are treating all of you. I am so sorry that they are doing that to all of you because it is our body and our decision to have this thing in or out. Just tell them that you are wanting to have another baby maybe that will help. I have to wait until my cycle comes back around and then call that day to have it removed and I hope that I will have the same instant relieve that all of you are having. Good luck to all of you.

I have had my Mirena for about 4 months. I have had the most uncomfortable breasts for about a month now, they have increased a full cup size (from D to DD). This wouldn't be so bad except for the fact that I can't even take my bra off because they are so sore. Has anyone else has this happen? I really don't want to have it removed it was bad enough getting it put in. Does anyone know if the symptoms will go away eventually? I do agree with you all that have said, if I didn't know better I would think I was about 3 months pregnant!! What's up with this stuff?

My throat started to tighten like someone with a fish or nut allergy.
My left eye leaks a sticky liquid and the lid is starting to droop. The lid also stick to the eye or feels like it, the eye feels like its fluttering. I have server Edma, I can hardly walk and cannot get rid of it even with water pills.

I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

Hi everyone,

I am a 25 year old female who was diagnosed with Crohn's disease one year ago. I stumbled on this website and wanted to share my experiences to let others know they are not alone and that their side effects due to Prednisone are completely normal.

In Nov of 2007, I was in the hospital for a Crohn's flare up and was put on prednisone through IV (240mg/day). After a three days I was released, but one week later, had another flare up and was back in the hospital in December of 2007. This time, I stayed for 6 days and was on 240mg/day again through IV, along with taking Flagyl and fluids for my flare up and infection.

At first, I lost about 10 lbs due to the flare up and all of the medication I was on. However, within 3 weeks time, I gained 28 lbs and was a complete mess. I looked different, felt different and was emotionally and mentally drained.

My side effects included: Severe moon face, buffalo hump, increased appetite, hair thinning and severe hair loss, night sweats where I would have to change pajamas 3-4x a night, OCD to the point where I would have to clean my entire apartment (even if it was already clean), restlessness, anxiety, no sleep and sometimes I would go days without sleeping, increased thirst and dehydration, swollen eyes and headaches, depression and mood swings, upper and lower abdomen swelling and weight gain (28 lbs in 3 weeks), suicidal thoughts, unbearable muscle and joint swelling and aching, forgetfulness and memory loss, blurred vision and dark hair growth on my face near my sideburns and underneath my chin and on the bottom portion of my face. Bottom line: it was unbearable and nobody warned me about the harsh side effects of the drug.

When I left the hospital, I was put on 60mg/day and eventually weaned off Prednisone over the course of 2 1/2 months and took my last 5mg dose in mid- February 2008.

It is now 2 months since I have been off Prednisone and as of now, I have only lost 7 lbs, but much of the moon face has gone away and I don't seem as swollen in my chest. My appetite returned to normal the day I stopped taking the drug and my mood swings subsided one week after stopping Prednisone. I still have the buffalo hump, but it stopped hurting and I am now able to sleep through the night. The fluid retention seems to have moved south towards my legs, arms, and lower abdomen. My doctors say that within about 6 months after stopping Prednisone, most of the fluid retention should go away and they recommend walking for 45-60 minutes/day to help with the fluid/weight gain.

Overall, prednisone helped to save my life and put my Crohn's into remission, but is one of the WORST drugs I have ever taken. My heart goes out to anyone who has had to take this drug and trust that you are not alone--and the side effects are real and they are harsh. I am slowly seeing that it takes time for the prednisone to leave your system and my doctors say that every day there is less and less in my body.

Stay positive, stay active & stay Healthy!!

I had been on Lisinopril for about 5 weeks, first on 40 mg. then I reduced it in half on my own, and have now decided to stop entirely and go back on Avapro. When I started it, I developed flu like symptoms and I thought I was just sick, but my body continued to fill "unwell". I had such terrible vertigo that I fell down 3 times and would get very dizzy when sitting up or bending over. Sometimes, the vertigo comes when I am sitting perfectly still! I became constipated and bloated with bouts of gas, headaches and sore throat in the evenings. My arms and legs were falling asleep during the night, so bad that I had to wake up and massage my hands and move my legs to get them circulating. Also, leg cramps have developed and cramps and shoulder pain that doesn't want to go away.I started to have to urinate all the time, as well! When I went to the doctor's office after being on it for 3 weeks, I complained that I was feeling awful (like I was going to die), depression had set in, I want to sleep all the time and have terrible vertigo, I was told that these were unusual symptoms and to try it for a few more weeks and see if these symptoms subside! Typical!!! It is thru researching blogs like these that I found that my symptoms are not at all unusual, but they are VERY ALARMING! I am a 46 year old woman and am healthy in every way. This medicine makes me feel as if I am being poisoned! I went off of it yesterday and am now doing an herbal cleanse to detox myself. I am also on fish peptides - which lowered my bp substantially in the past, but needed to find a reliable source that keeps it in stock all the time. It is safe and has no side effects.

I am a 55 year old male. I have been on 40mg of Lipitor for 2 years after having a stent put into my heart. About 6 years ago I was on 20mg ov Lescol for a year but I stopped taking it because my knees became very weak and I could not walk up stairs without holding on. I am now experiencing severe lower back pain down into my left buttock, leg muscle and knee weakness, and I also have mild depression or a lack of motivation may be a better term. I am going to stop taking the statins and see if I have any improvement. Several years ago, when I stopped taking Lescol, my knee weakness and pain did not improve. Through research on the internet I discovered that some symptoms do not improve by stopping the medication. My goal now is to ensure it does not get any worse.

I had a cholesterol of 237 and my doc wanted me take Lipitor. So i did for a month and a half. About a month into it, I started noticing that my mind was becoming foggy. So I started to take it at night. But then I noticed after a month that my right leg tingled for 2 days and I had muscle aches in in my shoulder and that my fingers started to feel weak, like I was losing my strength. I called my doctor and told him I cannot take this drug.

He pointed me to a Doctor Caldwell Esselstyn's website. It seems he reversed heart disease on a VEGAN diet. (Fruits, vegetables, grains and beans...NO MEAT, NO FISH, NO CHICKEN, NO DAIRY, NO EGGS... and so reluctantly I tried it. Even after 2 months, i noticed my body changing for the GOOD. I started losing 5 pounds every 3 weeks and my circulation was better, any aches and pains I had disappeared, my arthritis vanished. It is miraculous. Yes the diet is dull, but your taste buds adapt and all the food you used to love, suddenly tastes too salty, too sweet, too oily...I cant even tell you how much my body has improved in such a short time. I also previously had 2 blood pressure pills. Now I am down to one.

For anyone serious about improving their health. TRY A VEGAN DIET for just 3 months. I'm not kidding.

I just got an injection yesterday in my shoulder. The injection had the following in it: 1ml of 40mg per milliliter of kenalog solution along with 1ml of 1% lidocaine solution without epinephrine and 1ml of .5% marcaine solution.

Here is what happened after the injection... Within 30 minutes I was experiencing nausea and a headache on the left side of my head, behind my eye, and to the outer side of the eye. Within an hour I had pain radiating throughout my entire body! It has not been almost 24 hours and I am still in pain. My head is splitting, I'm still experiencing nausea, and the pain is all over in my bones and joints, and my hips hurt really bad. I'm also experiencing a terrible dizziness, and light headed feeling, and confussion.

Here is the real kicker... I have severe drug and food allergies! There is virtually NOTHING I can take without having a reaction. I can only eat fish, fruits, and veggies, otherwise I get very sick, and have severe stomach cramps to a point I cannot even stand or walk! My doctor knows all of this, and he still told me this was perfectly safe, never been a reaction, and I would be okay. Only problem that may arise is infection, but that is extreamly rare!

Does anyone here have any idea what is happening to my body, and how long it might last?

One Jan. 2 of 2008 I had a stroke where the whole left side of my body was completely paralized. My speech was slurred and my son called the ambulance to take me to the hospital. I am 52 years old and am a Pastor. When the ambulance arrived and the paramedics began working on me to take me to the hospital I began to pray. I asked the Lord to heal my body. I asked him to take all my symptoms away and clear out my arteries if there was any blockage. By the time I arrived at the hospital I was completely back to normal. I give God all the glory. After the MRI the doctor acknowledged that I indeed did have a stroke and there shows damage on the right side of my brain but they just couldn't get over the fact that I had no residual disability. Now to the statin. Even though after all the tests they found out all my arteries were indeed clear with no blockages anywhere and all the tests on my heart were good I do have high cholesterol of about 260 of the bad stuff (this runs in my family). Before I left the hospital the doctor prescribed me to take 1 baby asprin a day and the generic version of Lipitor.

I know this sounds weird but that night I took only one capsule of that statin drug and by the next afternoon I began having pain in my legs and they got all wobbly and hard to walk. I had asked the doctor if there were any side effects of these statins and she told me that they were safer than asprin and that they should be sold over the counter without having to even obtain a prescription. She did mention that there were some very rare side effects (that only happen to 1 in 10,000 people) of it attacking peoples muscles but told me that if that happened I could just stop taking the medicine and the muscle pain would go away.

I never took another one of those pills but for about 3 or 4 weeks having muscle pains and cramps in different parts of my body. It was like something was moving around and attacking different muscle groups. I noticed one day that the muscle in my left arm was sore and very weak and it was like I didn't have as much muscle as before. Then the next day it was doing the same thing in my other arm.

Fortunately after those weeks all the symptoms have went away and I feel fine. The funny thing is I had felt great before taking that statin pill and only took that one. It was like poison.

Now since that happened to me I have been talking to many family and friends that are either currently taking or were taking statin drugs and every single one of them have had terrible muscle, memory, emotional problems since beginning the drug.

My uncle had surgery (not heart or artery related) about 8 months ago. I noticed that he was in very bad shape not being able to get around because of severe muscle pain and weakness. He was crippled. I was driving him one day and he was talking about all his pain and weakness in back and legs and shortness of breath then it hit me, statins? So I asked him if he was taking statins. He set and thought for a few seconds and said he had started taking them right after his surgery 8 months before and his muscle pains and weakness started right about that time.

I encouraged him to stop taking them for a few weeks and see what happens. Within 2 weeks he was much better and not about 8 weeks he is pretty much totally back to normal. He thanks me all the time. He said it must have been the Lord that prompted me to warn him about the statins.

I still have a cousin my age that has severe back pain and muscle spasms in his back that started about the same time he started taking statin drugs. He is no longer able to golf like he used to. I'm trying to get him to stop but the doctor has him convinced that the statins aren't causing the problems and that he must keep taking them.

I'm on a quest now to warn as many people as I can about these dangerous drugs. The truth is we are ultimately responsible for what we put in our mouth and if it hurts us we need to not swollow it whether it is the wrong kinds of food or bad drugs.

I've posted here before about my nightmare with Levaquin that began in December of '06. I had all of the usual nasty side effects including: anxiety, thoughts of dying, unable to eat, redness, chest pain, strange blood pressure and temp readings, and finally a ruptured bicep tendon. Still, one side effect that I have not seen mentioned is one I'm still curious about..... I had a tremendous change in my sense of smell. To the point where I literally could not stand the scent of the deodorant I have used my entire life. To this day I still cannot tolerate that smell (as well as changes in other smells). Has anyone else experienced anything like this? Just curious.

Having the Mirena IUD put in was the worst thing I have ever done to my body! I am 33yrs old, have 3 kids - 9, 2 1/2, 1 1/2. They told me to come in when I started my period because it would be easier to insert, so that's what I did in early November 2007. (Since then, I have had non-stop bleeding or spotting every day.) I didn't have as much pain as some people have described, but it was more uncomfortable than I expected. The next day I developed a bad, bumpy, itchy rash on both of my legs from my ankles to just above the knee. I thought it was just a fluke, and it starting going away after two days. It was gone within a week. I started having very bad mood swings - angry, short-tempered, irritated, irrational, paranoid, and I wanted to cry over everything. (I normally don't cry over anything - I am not an emotional person.) I got a few deep, itchy pimples on my face, which normally I don't get either, but I figured I just needed to get used to the hormone. Then, my upper back and chest started itching really badly the second week, and I got pimples all over those areas - I have only ever had them at about age 13-14 and not as bad as I do now! I became fatigued, and I have gained 5 pounds. Don't get me wrong - I have been eating everything in sight, but I feel terribly hungry half an hour after I am done eating. So that part is my fault, but I'm not used to be being hungry all the time for no reason. I have religiously gone to the gym 4-5 times a week for an hour and a half a day for the past year and a half. For the past two months I have gone twice a week, and struggle to make it an hour. My endurance is terrible. My muscles - particularly my legs - burn like I've had long strenuous workouts, which I just mentioned is not the case. My sex drive - NONEXISTENT. Luckily for my husband, I know it's a side effect and haven't told him - he would probably take it personally - so I just go along with sex when he wants it. I finally had to get over the fact that I had non-stop spotting, but sex is not enjoyable when you feel self-conscious, and no foreplay because of the spotting if you know what I mean. (Sorry if that's too much information but I'm sure some of you can relate.) My husband was also not thrilled about the strings - I wouldn't be either if I was him. I had a non-stop migraine for 9 days straight - I maybe get two of them a year before Mirena, and they last about 3-4 hours. I normally have 20/15 vision - better than most people - and I found I was struggling to see things I normally could. I have been occasionally nauseous, but that has been minimal. My breasts have been sore. I am sure I am forgetting other effects, but as you can see the picture here is pretty grim. I went back to the doctor three weeks after insertion, and he told me that he couldn't tell me what to do, but that it is not rational to expect to feel perfect after 3 weeks, and that most people adjust just fine after about three months. He further explained that he has personally put in several hundred, and only one person has ever wanted it removed. He said my "side effects" probably had other causes and this was coincidental, and that the few that could come from the Mirena would settle down. Well, for the next month it got worse. Yesterday, after working a 12 hour graveyard shift, I forced myself to stay awake three more hours until the doctor's office opened. I went in with no appointment, and told them I would sit there all day if I had to, until it was removed. They managed to fit me in with the nurse practitioner, and she also asked if I was sure I didn't want to give it one more month to settle down. After reading everyone's stories on this site, I was pretty sure that was pointless. So she removed it as I asked, and at least treated me with respect and didn't try to tell me it was in my head ( like the doctor did.) She said it could take up to 20 days to get the hormone out of my system. (Which is funny, because when you get it inserted they tell you the hormone acts only locally within the uterine area and doesn't get into your "system" - LIES!!!) Well, I went home, went to sleep for 4 1/2 hours before I had to be back to work for another 12 hr shift. But guess what - even after getting little sleep, I felt much better than I had in two months. My headache was gone. While sitting at work, I noticed I could see things at a distance again. I had a pretty stressful night, and not once did I feel emotional. Just a little tired from lack of sleep - but it was worth it!!! I am almost 24 hours from when I had it removed, and see a light at the end of the tunnel. I hate to sound pessimistic, because I wanted really badly for this to work out. If anyone tells you what you are feeling is in your head - or has another cause when you know the symptoms started at the same time you got the Mirena - DON'T BE BULLIED. They will try to make you feel like you are the only one complaining, but you're not. There are many of us. Trust me on this one - you will feel better if you get it removed. If you are reading this and haven't gotten it yet - keep this info in the back of your mind. If you want to try it and it works out for you, great! But if it doesn't, don't stick it out any longer than you have to. I also extend my sympathy to those of you that had it in longer than I did and are taking longer to recover, especially those who have experienced traumatic pregnancies and miscarriages since. I hope you take some comfort in knowing your stories have helped me make a great decision - having it removed. I also had a friend read all of your postings because she was considering this as well - she has since changed her mind.

Hello,
I am a 37 yr old male and have been on Lisinopril 20/25 for about 6 months now. I was asked to switch because the medication I was on before was not approved by my insurance carrier and this medicine is one tenth the cost.
I have never really put all of this together until I found this site. I have become increasingly confused and find normal tasks more difficult. I have always struggled with slight depression and anxiety but it has become much worse. (One of the side effects I knew nothing about before this site.) I constantly have the feeling I am going to dye or that something terrible is going to happen to me or my family.
My wife asked me yesterday if I felt that I was more confused lately and she said I was not acting myself for the last few months. Now I may know the validity of that question.
My other bothersome side affects are the feeling of a lump in my throat that I can not cough out; irregular heart beat and occasional high BP with pounding heart beat; Numbness in one or both hands; Mood swings and loss of patience.
I have just attributed these symptoms to getting older but now I know I am not going crazy!!!! Thank God for this site.
Good luck to everyone else...

OKay, I don't know if this has anything to do with Mirena or not, but I have had my implant since August 2006. Typically I am a very happy, healthy person. I eat extremely heathy (almost all organic, tons of vegetables & fish & almost no processed foods). Anyhow, for the last 6-8 months have have become VERY moody. I am often grumpy, I cry everyday, I have pain in my joints (I believe it to feel like arthritic pain). My finger joints are always sore. I am a fit person & am uncapable of opening a jar anymore. And, I have this nagging pain in my lower back to the left of my spine. Like I said, I'm not sure if this is because of my mirena implant, but I take no other medication, I don't even take OTC pain meds. I'm only 27 and consider myself to be very healthy. I'm not sure what else it could be. I suppose I will have it removed & see if I can become a normal human being again. I appreciate anyone else who can share their experience...I just want to know if I'm crazy or not???

I took Levaquin 750 mg for 2 days. The first night it made me sleepy and drowsy. The second night I took it, I was high. I felt like I was a zombie. I sat in front of my computer rocking back and forward. And al I wanted to do while I sat there was take more and more and more levaquin. I wanted sit there and eat them like they were candy. That urge was so overwhelming. So, I hurried up and I flushed them down the toilet except for 3. Knowing that they were there, I wanted to eat those 3, so I flushed them.
That was the worst night of my life. I said to myself if this is how high suppose to feel. I don't ever be high.
This drug need to be taken off the market.

I had a heart attack a little over 15months ago & am now on several different meds. For the past 10 months I have been coughing& I mean coughing, can hardly breathe. The cough wakes me up at night, I feel as though I am short of oxygen & have to tell myself to be calm, take a slow deep breath .I am starting to resemble a fish that is out of water. I have told my doctor on many occasions but to no avail. I have also put on 15 lbs on weight . I am too afraid to come off the Lisinopril as I don't want another heart attack. I can't afford another med as i am self pay & can't afford another expense.....I am trying to tell myself that i can live like this, but now the coughing is annoying my work collegues...Also having vivid dreams, am out of breath with any exertion, blah, blah, blah...Anybody got any ideas??? Or should I just stop the meds & die??? Sorry, that was a little dramatic, I am just very tired. Thanks for taking time to read this. Good luck to those of you in the same boat.

Hi Everyone it's Hill, here is my weekly update. It's has been officially one month post Yasmin He*l. I have had 2 or 3 pretty good days in a row. Very very slight numbing and tingling, but I mean slight. I felt really good today, however, I'm starting to feel bit week and groggy. I'm assuming this is b/c when on Yasmin I would normally be starting my period tomorrow like clock work. I'm not sure if it is actually going to come or not. So I'm just writing it off as that time of the month. Did most of you experience a timely menstral cycle, or was it delayed?

I was also wondering if anyone has felt completely starving after stopping Yasmin. I am trying to lose the weight I gained while on Yasmin, however I am always hungry. I can eat a full dinner, not like huge pasta dish, but fish, vegetable and piece of breat and not be satisfied. I'll want something else. It's like this constant empty stomach feeling. Has anyone else experience this.
Thanks,
Hill

I just started taking this, but my concern is the increased appetite. If anyone has had this side effect let me know.