Cheers symptoms and conditions

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I was prescribed Simva 30mg to replace Lipex which is no longer government funded 6 weeks ago. Since taking this medication I am waking up with tingling in my elbows and fingers blurry eyesight and what really worries me and no one seems to have mentioned is low body temp 34.2 and then a reading of 34.8 now averaging around 35.2

Please is anyone out there suffering from low body temp

I've been on it for just over one year and I have had great success with Topamax for my chronic migraines! I am at 200mg a day. I use to wake up with migraines in the morning and that has been greatly reduced. I use to never know when they would hit me and now I can figure out when which is usually hormonal - during my period. Before we (my neurologist and I) settled on the right dosage, we kept bumping up in 25 mg at a time and i would have side effects ... unpleasant (smelly gas, tingling fingers, other stuff i don't remember anymore), but after a few weeks, the side effects would go away. Now I don't have any side effects. I did loose weight, but only 5 lbs. I made a conscience effort to eat right and drink plenty of water because I read the forums about the bad health effects of the drug. I do loose words sometimes, but its a small trade-off for the migraines. Now, if I could just find something that would tame the hormones... Cheers!

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

Well it has been 10 days since I stopped taking Lipitor. I am now sleeping 7 to 9 hrs straight - headaches gone - not as moody as I used to be - better concentration at work and huge improvement in short term memory. I forgot to metion that my doctor put me on 40mg hence it didn't take long for the side effects to start. I saw my Doctor and explained that I was off the Lipitor and told him why. He is keeping an eye on me and I will keep you all updated.
cheers from Down Under.
Goose

My symptoms started with aches in my ankles and I thought I should stop wearing heals for a while. But then the tingling pain moved up into my lower legs and then my arms/wrists over a period of a few days. I felt like I was having constant shin-splints. I was heavy joint/muscle pains. Then the back of my head hurt really bad on the left side, just at the top of my neck/bottom of my head, and was also really sore to the touch. Then massive headaches. Probably migraines, although I have never had them before. My MD immediately put me on celebrex, which did nothing. I was eating Advil and Tylenol like candy and couldn’t sleep. So the doc put me on steroids (prednisone). That took the pain away. After a few days, while at work, the vision in my left eye went in and out (perfect vision to completely gone). I have never had any issue with my eyesight before - perfect vision. Then at one point (actually while I was in for my first MRI) my vision never came back. No one thought it was serious enough until I demanded to go to the hospital. I spent three days in the hospital, where they ran tests after tests (including MRI, Lumbar Puncture, blood work, neurological tests, echogardiogram, dobblers, etc). Upon leaving the hospital actually diagnosed me with Optic Neurosis, and gave me a 15% chance of getting MS later in life. We were all relieved it was not MS, like they originally suspected. After going to the Eye Dr, they told me that was not the case. This kind of eye stuff only happens to people in their 80’s! I will never regain my vision. If my diagnosis had been optic neurosis, it would not explain the joint pain. I have seen specialist after specialist over the last two months, and they still have no idea. Every test I have undergone has come back clear and I am perfectly healthy. My doc said we might have to go with the retinal specialists theory - which was a piece of cholesterol that clogged the artery in my eye. I just don’t get why a piece of cholesterol would have caused me so much pain over the rest of my body. After viewing this site and the Mirena pamphlet that I found online they give to the doctors, I really think it was the cause. The packet even notes, if you have symptoms like visual loss and headaches/migraines for the first time, to remove it immediately! I did not get mine removed until a month after my vision loss. Every doc I have seen I have asked if it was Mirena and not one of them thinks that could be the cause. But it is ironic, that when you see someone for the first time, the first question they ask is if you are on birth control or any other medications! I think I need to show them this site, so they can read other women’s symptoms. I did also have all the other symptoms as well - weight gain, irritable, oily skin, cramps, moodiness, vaginal odor, gross discharge, headaches, nausea, low sex drive, hot flashes, anxiety, restlessness at times, fatigue, and the list could really go on and on.

What a rotten drug. The past seven months have been hell for me. I am 42 years of age and put on this crap last November. I have suffered from bad headaches, leg cramps, Insomnia, Plantar Fasciitis, mood swings and the list goes on. After seeing this site and all your responses I believe the best thing to do is get of the crap. I will write in 2 weeks to give an update.
cheers from Down Under

I to was put on Lipitor 20mg. took it about 1 month and had such pain in my leg muscles I couldn't hardly walk . I went to my doctor he said go off it and I should start Zocor in . A month the pain was worse I couldn't even walk around the mall . I couldn't sleep at night the pain was terrible. Once again I told the doctor he said stop it and we will wait 6 weeks and start Crestor. In six weeks the pain should be gone. It didn't go away I could hardly walk at my job teaching at a Pre School. The pain unreal.I have type 2 diabetes under control for years. Still is.I was told I had arthritis. But now they tell me I have spinal stenosis. I'm on paxil for the depression they said I had and. I feel as bad now as I did 4 years ago when I was on statins. I can hardly walk, my life is pain in my muscles that never leaves and now my back. I was active and watched my weight and walked 3 miles a day. Since taking these meds. I can no longer work, go shopping or go anyplace I have to walk . I have gained a lot of weight . I have something wrong with my knee .I have tried to explain this to 3 doctors and no one listens to me. My health turned for the worse when I started taking Lipitor in 2005. I don't think I'll ever get my life back I am only 58 years old and can't work to support myself.I can't even hold my 1 month old grandson and walk or lift him from his bed. Reading all your messages . I know my health going down like this is from the statin drugs I took . When I sit , I can't walk when I stand Then .I gotta sit in 5 to 10 minutes.And the pain in my knee has progressed. No doctor wants to hear my story and believe me. Thank God I found this web site and read this for my self now I know I'm not crazy. How can I get myself better ? Will I live the rest of my life in pain, and not able to function.Every time I see a doctor they give me another pill to take. I want to just throw them all away .There must to be an answer to this.

To monkeygril, i had to rush myself to the hospital on Sunday because the pain was that intense, they couldn't find the threads then they had a look and took swabs, i went for a scan on Tuesday and they said the coil had moved down my womb, i suppose all the contraction pains i have been having means my body is trying to push it out, im going to get it out on tues because i cant take anymore of this pain, and i have really heavy clotted bleeding as well which isn't very nice, ill keep you updated on how i get on,

Cheers for now x

I've been on nuvaring for 2 years and its the best birth control that I've used so far. The only side effects that I get are occasional hot flashes. I do experience some mood swings, which are "PMS" type mood swings, which have lasted only a few hours right before my period starts.

The hot flashes can be annoying but they are manageable, these happen to me when I have had the one week break from NuvaRing and then insert the new ring, the first day or two, i experience hot flashes.

Other than that, my sex drive has not changed, it is very normal and healthy.

I have been on various birth control pills, in the past, for 6 years. Ive tried "ortho-tri cyclen", which made me feel bloated, moody and depressed. I've also tried "ortho-tri-cylen lo"and it made me feel the same way. I have also tried Triphasil and it caused me to feel depressed, and i experienced bloating.
I do have to say that all of the Birth Control pills were more effective in controlling acne than with the NuvaRing.

I still get quite medium to heavy periods with NuvaRing with some menstrual cramps, however, the cramping does not last very long and it is a lot lighter than when I am not taking any birth control.

Overall, nuvaring is working for me so far. I recommend trying it out and giving it a minimum of 6 months trial before giving up.
Also, I found that taking a break from all birth control methods for about a year, and using other barrier methods (aka condom) have also helped me, as I felt like it gave me a break from synthetic chemicals and my body was able to be "natural" for awhile, I felt that was psychologically and emotionally a good idea for awhile. So if you feel like you are switching and just completely all over the place, I suggest that you might try taking a break for yourself, as a woman, to restore the biological settings and maybe try again with something new after a long period of time.

cheers : )

777
I've been noticing that you as well as bobby are continuously replying to many of the posting. I stopped taking lipitor in December after having chest pains for 10 months which included being hospitalized for 2 days of testing. I'm still having the chest pain although I believe it's getting better. There was a week in the beginning of this month that I had no pain at all but now it's back. My question to you and bobby is you keep saying you still have some side affects for months but fail to list them. What are they and with your experience, why does Lipitor cause chest pain? What have you found out in your research? Is this drug causing damage to the interior lining of the arteries? Is this why many people are getting the pains from?

Hi, I just posted a rather long story of my last year.. and have since read EVERY posting on Mirena.

I just want to say.. I have only heard positives about Mirena. I trust my OB he is excellent. I trust my friend who has been using the Mirena for the last 7 years.

BUT I CANNOT deny the fact that since having the Mirena I have been I’ll. It has taken me over a year to work out the correlation between my condition and the Mirena, and have since searched for information to support what my body has been telling me. I am sorry but there are over 1,700 posts on this site alone about (mostly) the problems associated with this form of BC. I am shocked and horrified that what I have been going thru for so long is been experienced by other women too. Coincidence.. I THINK NOT..
Stay tuned I will be having it removed ASAP.. Hopefully I'll be back to normal.. I’ll let you know either way.
Cheers

I am 43 year old financial advisor at the second largest bank in the United States. I have always considered myself in very good athletic shape. Three star athlete in baseball, football and basketball in high school. I went on to letter for four years as captain of a division I baseball team. After college I continued to run, work out, and manage/play baseball up until this day. It was at my routine physical that my Dr diagnosed me with hypertension. No surprise I thought as being under plenty of pressure at work. My blood pressure was140/85.
Although I continue to work out three to four time's per week my weigh has spiked from 190lbs to 208 lbs in the year and a half that I have been taking Linsinopril. Until I found this web site I couldn't explain the cough, pain in the left side of my neck or the feelings of emptiness/depression that have followed me around like a cloud. That is when I can get out of bed and function that is. I used to be happy and fun loving. The person that you wanted to be around. I truly believe that this drug( that I have heard contains snake venom) is a big reason why I haven't been myself. I am not the type of person to spend time researching the internet and have always been skeptical of nuts writing or responding to any one or thing over the internet. I consider myself to be fairly rational and sane. However, this drug has made me dull and empty. My lowered sex drive almost ended my marriage. For a year in a a half I have been in a psychotic hell. I never thought about questioning my Dr. until recently when my marriage almost ended as a result of my feelings and anxiety attacks. Although my blood pressure is 115/70 my life has been a mess. I find it hard to believe from the posting here that only 1% of users of Lisinopril have suffered any type of serious psychological reaction to this drug. Perhaps the clinical trals focused on rats or elephants, but certainly not living humans.

I have since stopped taking Linsinopril (two weeks now) and the sun is beginning to come through the clouds again. If you have been taking this drug I plead with you to stop immediately as it seems enough clinical data was ever taken to fully understand the impact of this drug.

I hope that someone else does actually read this post and find it useful enough to impact their life. STOP TAKING THIS POISON

I am a 51 y/o white female that has been on Lipitor for 2 years. I am 5' 1" and when I had to go on it my cholesterol was 267 I weighed 112 lbs. I was shocked.... my doctor told me weight had nothing to do with cholesterol. She kept a close watch on me and my cholesterol came down...... and then my ex-husband of 17 years and I re-connected and got back together and I moved so I had to get another primary care physician. I took all my meds to her, she also kept a close watch on everything. At this time my cholesterol is down to 109 and I asked if I could stop taking it, as I take quite a lot of meds, due to different things and if I could stop anything it would be great, but she said it I stopped it, my cholesterol would go right back up. So since I am not experiencing any side effects I'm okay with continuing it.

I surely hate to hear what you all are experiencing with your Lipitor..... could your doc try another cholesterol medication?

The only one of my meds that is giving me any problem is TOPAMAX........ that we are using as a Migraine preventative! HORRORS!!! Today is pretty good day. But my cognitive abilities are in the trash... I say the wrong word when I mean something else...... I search my mind looking for a memory...... I am also on disability since 2002 because of the Migraines....... I have has them since 1978, but they got progressively worse over the years until I was sick more days per week, sometimes more than 7-10 days at the time, having to be in the hospital being rehydrated and on IV pain meds.......... and as awful as the TOPAMAX is.....it has been reduced the migraines to approx 2 per month and they do not last nearly as long.

So sorry, I got waaay off topic, but I know that it is not the Lipitor that is giving me the side effects as it the last med I had to go on and I had no new side effects....... but that TOPAMAX is kicking my behind.

I'am only 26 but I have been a insulin dependent diabetic since the age of three. Being a diabetic for so long has made it difficult for my body to maintain normal cholesterol and triglceride levels. (I'am not overweight and I am very active) At 19 I was put on lipitor but it gave me severe stomach pains when I called the doctor they told me "it was just a side effect" and should subside. I wasn't on it for very long when I found out I was expecting and had to stop taking it anyway (can't take statins while your pregnant it can cause severe birth defects) Anyways, after I had my daughter they said my cholesterol was fine and they weren't going to put me back on anything. Yes! Until just recently my doctor discovered that my triglceride and cholesterol levels were so high he had the lab re-draw my blood tests! Odd because I feel perfectly fine. Because of the stomach pains years ago with Lipitor he put me on Simvisatin and Antara. Every since I have been on the Simvastatin my cholesterol levels are perfect but I am soo tired all the time. When ever I tell my doctor he says it's because I am a young mother of three and work full time. But this is a different kind of tired. I seriously could drink a five shot extra strength espresso and fall asleep this isn't normal. All my blood work is fine. It has to be a side effect.

I am a male of 67 years old. I took Lipitor for a year, and after a few months of taking it, I felt muscle pains in my arms and shoulders, as well as my back. I felt weak and could hardly put my socks on by myself. I told my family doctor that I thought the problem was caused by LIpitor. He said it couldn't be possible, but he couldn't figure out what was wrong, so he sent me to a rheumatologist, who gave me an initial diagnosis of polymyalgia rheumatica. I went back for a checkup, and although the sed rate was normal, the C-reactive protein was elevated. He felt his diagnosis was an accurate one. He prescribed prednisone for me. I had some doubts about it, since I am diabetic, and was concerned about the elevated blood sugar it might cause. Well, it did elevate my blood sugar, and I weaned myself off it within three months. My blood sugar went back to normal, and while the prednisone helped the symptoms of muscle pain and aches, after I stopped it, the pain returned with a vengeance.

About a year passed after discontinuing the prednisone, and I felt worse and worse. Any time I engaged in physical activity, such as yard work, I was almost incapacitated for two or three days. I felt weaker and weaker, and by now, my activity is about ten per cent of what it was three or four years ago. I am unable to do anything physical without paying a heavy price.

I would tell the doctor that I felt the problem was caused by the Lipitor. He would dismiss my comments, saying that the pain should have gone away after discontinuing Lipitor. He sent me back to the rheumatologist with results of recent blood tests. Both the sed rate and C-reactive protein were normal. The rheumatologist touched my back and other areas, which caused me to jump. He said it might be fibromyalgia. I told him again that I thought it was caused by the Lipitor. He said the same thing my GP had said: if it had been the Lipitor, the pain would have gone away when I stopped taking it. I know the Lipitor caused the pain, because I tried red yeast rice for a couple months. The pain increased to almost unbearable, so I discontinued the red yeast rice. If I were not susceptible to the pain from the Lipitor, would the red yeast rice have increased the pain?

So here I am with a fuzzy diagnosis from the rheumatologist, and no clue from my family doctor (that he will verbalize, at any rate). My life has gone steadily downhill. I used to be a strong, active person, but now I can do very little, and my strength is a shadow of what it formerly was. What can I do?

I was diagnosed with graves disease last year, I had a really acute case that turned me into a total nut job.
In October after going through several thyroid storms and the doctors not being able to keep me stable with medications, I had a full thyroidectomy in October.
I started on .100 mcg of levothyroxine and then the dosage was gradually decreased, I started having a lot of random body aches, mood swings, lots of muscular pains and no energy.
They ended up raising my dosage and detected that I had a large vitamin D deficiency, after several treatments of taking 50,000 units of vitamin D, and also adding my levothyroxine dosage I started feeling better. I still have mood swings here and there, and feel sad periodically, but the last month or so I've been feeling more fine than I have in a long time. They have me on .170 mcg of levothyroxine for two months now. Last week I started getting headaches more frequently, and one of the times I got this nose bleed.
This past weekend I got a headache, and then later that night I had another nose bleed.
I don't usually get nose bleeds or this many headaches so I'm a little concerned.
Also the last time I was getting headaches and constant nosebleeds was when I was really hyperthyroid.
As far as the doctors go, I'm in between insurances and quite honestly I've been frustrated with both my pcp and endocrinologist...

Hello To All,

I too am on this med, I have been on it for 1 year as of July 2008-

35 pounds, brain fog, headaches, eye sight for reading, chest pain and fluttering heart beat. My doctor who is my friend has told me that he will up my dose... "Dear God" any more and I will go nuts. Does anyone know of any study done in a medical journal that theu could forward to me so I can show my doctor.

Please email me at ****** I would be so very thankful.

Thanks to all and be healthy.

I was prescribed 500 mg, twice a day for 5 days for a UTI. Immediate side effects were insomnia, restlessness and feeling sick to my stomach when taken without food - but I didn't really think twice about it. Approx 2 days after my first dose I woke up, was making coffee and got a sharp, VERY painful feeling in my abdomen. Ran into the bathroom and was shocked to see blood in the toilet, along with what appeared to be mucous. The pain went away and I just didn't feel "good" the rest of the day. Went to the bathroom twice with nothing until it happened once again. I went from thinking I had hemorrhoids, cysts, diverticulitis, etc. and almost went to the emergency room until we read the insert that came with my prescription. All of these were clearly listed in it. I stopped taking immediately and it has not happened since. I feel back to normal.

I am a healthy and active 26 year old who couldn't believe this happened. I am now taking Florastore (a probiotic you can buy behind the counter at any pharmacy) and eating Activia yogurt. Wish I had seen this message board before I began taking Cipro.

I had to take Doxycycline for 3 weeks last August when a tick bite I had developed the classic "bulls eye"... a sign of Lyme disease. Everything went well for the first 10 days then I started getting kind of nervous and couldn't sleep well at night. I was constantly starving, really ravenous and had to eat constantly otherwise the nausea got worse. I was glad when I was finally able to stop taking the meds, BUT then after 24 hours I became depressed and really fuzzy in my head and disoriented. This lasted for another 2-4 days. I'm feeling much better now, but I have noticed that I'm just a lot more sensitive to other stimulants...coffee, sugar, alcohol, chocolate. I know I have a few other allergies, hay fever, food allergies etc. I was just wondering, does anyone else out there who has had a negative reaction to doxy have any other allergies or intolerances, or asthma? How much sugar, either in the form of sweets or alcohol do you usually consume? Daily, weekly, monthly...none at all? Feedback would be greatly appreciated. I would like to get to the root of this problem.

I just came back home from the dr. We made some tests and my 5 years old daughter is allergic to house dust mites and has beeing diagnosticated with athopic asthma. The dr. prescribed Singulair. Now, after reading all the posts, I freaked out and I have not idea what to do. I am really sorry I did't ask about side effect, but I considered, her beeing a dr, knows better than me. My thought now is: I'm not going to give my daughter Singulair.

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

Ladies!
When my mum pointed out this website, and blogs bout Yasmin,
and after reading just a few,
i bursted out crying.

after just 3 months on Yasmin
i was completely, utterly depressed.
being a 15 year old then, it was the worst thing
in the world.
i am a highly trained athlete,
and this pill made me gain over 7 kgs.

training 8 times a week, and 3 dryland,
and STILL packing on the kgs was
unimaginable.
i became completely self conscious,
and stopped eating for days on end.
training suffered, but my muscles and body
suffered more.
all my muscles got completely fatigued and
i lost most of my fast-twitch muscle fibers.

apart from this i obtained a COMPLETE
Fluid retention in every part of my body.
thighs and face the worst.
i couldnt move my joints very freely,
and nothing would let this go.

the absolute worst part was the depression
and anxiety that came from this all.
i remember having 2 weeks off school,
and all i did, was stay home, in bed and cry.
i broke up with my boyfriend, and didn't want
a n y o n e to care about me, i even made a list,
of everyones names and crossed them
off as they hated me.
i cut myself, and hurt myself, especially on my legs
where my mind just hated seeing them,
and feeling this way.
could NOT stand being in my swim-wear during training,
i would run out, and cry if i saw someone look at me.
paranoia.

to feel this out of control with your own body,
is the worst feeling in the world.

i would cry.
everyday. every night.
and i couldnt stop.
i would be moody, and angry, and hopeless,
and start verbal fights everywhere i went.

and i didn't even know why.

after reading this all,
suddenly, everything made sense.
my doctor, told me, in specific words

"they call this the 'luxury pill' its the most expensive,
and has least side effects than any of the others."

i showed her this website.

after i went off it, i had the three day blues,
mum said, just like after pregnancy.
i cried, and cried and cried.
would be sitting in class, and bursted out in tears.
things were horrible.

its now about 6 months later, of not being on anything,
my periods just began back after not having them
for 4 months, and my body, is no where
near how it was before i went on pill,
but its getting there :)

one day I'm going to be an amazing swimmer.
and on the Australian team.

i guess, if i had not had this experience
i would never be this determined now.

I Would NEVER Recommend This Pill
To Any Girl Or Woman.

EVER.

Its Amazing What One
TINY Little Pill Can Actually Do To You.

stay strong girls,
x x x

contact:***
for any other questions. :)

Its crazy how the nurses tell you its all in your head. I dont understand this at all. I had a coil for about ayear and a half and have just had it out. I wanted it out before but was talked out of it by the nurse at the family planning clinic. What I really dont get is that on the information booklet that comes with the coil it says that there are side effects, much the same as individuals on here have experienced, but the nurses/doctors deny it?!?
Something needs to be done!!!

After hving had this thing out for 10days now, my skin is still awful-but I tink it may get worse before it gets better, pain is gone, mood swings improving and sex drive almost immediately returned to normal. I am soooooo happy to have that bloody thing outta me! and condoms are not as bad as i thought they would be.

Will keep those of you who asked me to updated!
Cheers :D

*Information being overlooked?*
I don't know how many people have noticed this, but when you look below a post where the number of 'replies' is listed, it seems the only way you can read the replied information is to click on 'post reply'. I have noticed a lot of good information may not be read simply because of not being accessed.
I'm pointing this out only because I am trying to help draw as much attention to problems with this medication I feel people should be aware of. I also feel very strongly (due to my own personal research) that Toprol can be dangerous...good luck to those who are dealing with it.