Medical problems symptoms and conditions

Toprol XL I just started a week ago as the medicals cant get my blood pressure under control. I also take Lisinopril at 40mgs. Was told at 40mgs. of Lisinopril thats the highest dose there is (which I found is a lie from a lady I know when she told me her husband takes lisinopril XL or along those lines). Meantime..on Toprol..I cant figure how to describe it other than..when the medicals decided not to deal with my medical issues and gave me 1st Zoloft then Prozac. I had such bad reactions from them I told the medicals to deal with my medical problems dont blow me off with shrink pills! Meaning...I have the same reaction with Toprol as I did with Zoloft and Prozac...emotional, cant focus or concentrate..cant sit still..I look like crap because I cant sleep more than 5 hours or so...
Im already plump from middle aged (and I use to be bone thin at one time)..Im hungry..and yet I look and smell food and I about gag...Bits and pieces at times I can get down me though..Toast, yogurt, that kind of thing. IM tired and weak too...It takes everything I have in me just to peddle my bike 3 miles around the housing area I live. After that, I flop..
I have to pee every 2 mins too...Bad enough the pressure from fibroids on the bladder..Medicals say..Dah..they will shrink when you are finally post menopausal. ( I would love to tell that line of BS to the doctors with breast cancer or prostate cancer..see how they like it).
I am trying to give the benefit of the doubt here..give it time and see if these side effects wear off in time...But as it stands...
Between this crap and the migraine medications..IM sick and tired of not being heard/taken seriously by the medical community...Getting so Im all for alternative medicine and just let the medical doctors/FNP-C and specialists kiss my backside..

I was prescribed Cipro for a UTI infection 2x3days the first day I felt really bad! I was tired and had stomach pain along with nausea. The second day I also had stomach pain with headache and tiredness, my mind was foggy as well as my vision was blurred. I took it even though our clinic is against all medication for this exact reason bad reactions and death. I did some research this morning and have STOPPED the Cipro. I will start a 21 day detox to get this out of my system. I will help fight to get this product off the market! My niece is turning 10 years old and she has also been prescribed this medicine she has had many medical problems. It feels great knowing I may finally be able to help her. I know god has forced the infection upon me to help others. Please!! do the research before you take any medicine only you can make the decision. WE ONLY HAVE ONE BODY TAKE CARE OF IT!!! NO ONE ELSE CAN DO IT FOR US!!!

i had my mirena inserted 2 1/2 years ago after i had my 4th child. I just had surgery to have it removed it had moved and went through my uterus. Very painful, this is after having very horrible eczema and hives all over my hands and feet. I can't use my unless i have gloves on because of the blisters and they are permanently scarred from the eczema which we think was caused from the mirena because i didn't have it until about 2 months ago when i started other symptoms. Then i found out that it had went through my uterus which required laparoscopic surgery to remove and to top it off no health insurance so what i thought was going to be a less expensive birth control just cost me about 30,000.00 including doctor bills!!!!

Yasmin is great! I am 30 yrs old and have been on Yasmin for 4 years and my periods are reduced to a light 5 days (they used to be 8-12 days and heavy with clots). I have no more menstrual cramping as I did before. I have not had any pimples for 4 years. I have lost 15 lbs since being on Yasmin, but I also attribute that to being physically active and eating correctly. No change in moods, sex drive is better, boobs are bigger, energy is great. I am normal weight, healthy and active. I have no medical problems or risk factors. I just want to inform any of you that had problems with DVT, blood clots, or stroke..that all birth control pills (any brand) carry an increased risk of thrombosis. That is not a side effect unique to Yasmin. You are 2-3 X more likely to have a thrombotic event on OCPs when compared to women who are not on OCPs. Risk of thrombosis related to pregnancy is actually MUCH higher, 5-10 X compared to women who are not pregnant or on OCPs. So I'd stick with my OCPs to avoid the nastier side effects of pregnancy..

I believe the Mirena was in direct relation to my developing anxiety, migraines and eventual miscarriage with complications after removal. The makers of this device states that the hormone stays within the uterus, but how can that be? Being one who doesn't tolerate artificial hormones well at all, my doc suggested this IUC stating the same. Ridiculous!!! I bled for 6 months after insertion...was told to wait it out. I developed anxiety which led to 911 calls thinking I was having a heart attack. I also had increasing amount of headaches and dizziness. After two years of increasing medical problems, I had the Mirena removed. Not surprising, my headaches and dizziness decreased, however, anxiety is still a problem, but not as bad as before when using the Mirena.
As for getting pregnant after removal...my best friend and I had almost identical experiences with our miscarriage. Both of us had the IUC removed, both of us became pregnant, both of us miscarried around 5-6 weeks and the development of this whole experience has many more similar details that are more than coincidence. Fortunately, my friend was ok, however, I ended up hemorrhaging and retained tissue/clot and have been dealing with this for nearly a month. I'm extremely anemic and stressed. I KNOW that the Mirena damaged my uterus and I now terribly fearful to try to get pregnant again because of the horrible experience I had.

I just came from my Dr. and he prescribed Singular for my allergies. He really convinced me to take it. So it's day 2 and I haven't taken it yet. I told my Dr. that the commercial on T.V. said a list of side effects that out weighed the symptoms of my allergies. This website has totally convinced me that I just threw away $135.00, cause I refuse to take a medication that has so many awful side effects. thanks for everyones input on this medication. and I hope for the best of luck with the people that are having such a difficult time with their medical problems.

Hi I have been taking Yaz since August of 2007. I never connected any of my symptoms with my bc until I recently saw an advertisement on TV for a lawyer who is filing a class action law suit. I then begin to research side effects of Yaz and everything made sense. For the past 1 and 1/2 years I have been to doctor after doctor trying to find out what is wrong with me. It started with fatigue, muscle aches, and a fever that wouldn't go away. I was tested for every disease and problem in the book and sent to doctor after doctor and they never could find out what was wrong with me. Shortly after that in September of 2007 I developed chronic hives that they also couldn't find a reason for. When I asked my dr. if the Yaz could be causing the hives and other problems I was told that it wasn't possible. So I continued to take the Yaz and suffer. I continued to have more and more medical problems. My hair began falling out, I became depressed and tired all the time. I have gained 20 pounds during the time I have been on Yaz. I am only 30 years old and I have always been very healthy and active and been able to maintain a healthy weight with diet and exercise but since being on Yaz it doesn't seem to matter how little I eat or how often I exercise I continue to gain weight. I have been very frustrated. I have had my thyroid tested numerous times because according to my doctors that is what the symptoms that I have been having seem to be but those tests were always negative. I even had doctors and people I know suggest that it's in my head. I just stopped taking the Yaz and I am hopeful that my life will go back to normal. I am now on medication to control the hives and I am hopeful that they will go away once I have been off the Yaz for awhile.

I am a 31 year old male, in decent shape (play basketball, volleyball, workout at least 3 times a week) but I have a family history of high blood pressure and have had it myself as long as I've been tested. Went to cardiologist as a check up on my slightly enlarged heart, long story short, ended up on Metoprolol (25mg) beginning of 2008 and have been fine but no real help with bp. Then was put Lisinopril (5mg) a few months ago and my blood pressure was great at last checkup. However during that time I had a couple of weeks where I was very dizzy, that sort of feeling your brain is taking a second to keep up with your head as you get up, along with a fogginess and what seemed like sinus issues but I chalked it up to weaning off of a small dosage of Zoloft I had taken for over a year. I also developed "the cough" everyone refers to, but since it is winter in New England I chalked it up to dry heat, even though it was a choking cough unlike any I've ever had before. Also during that time I seemed to completely lose my sex drive, again figuring it was just something to do with the Zoloft or general anxiety. Then in the past week I started getting a constant headache, having really interrupted sleep, very foggy and out of it, tired, dehydrated, constipation, nausea, all things that I would normally associate with allergies or some kind of sinus/flu, but yet I couldn't really pinpoint anything that would be causing it.

Then I finally started looking up things about the meds I was taking and came upon this site, and guess what? Everything and every way I was feeling was described in hundreds and hundreds of posts on this site. I don't think my side affects were quite as strong as some have experienced (for instance the cough is very infrequent, like twice a day) but I have only begun my journey with Lisinopril. So despite the warnings, I decided to stop taking it a few nights ago, and almost instantly I began feeling better the next day and since then.

I have since called my cardiologist and he has recommended I switch to Diovan, basically saying that based just on the cough symptom alone, he wants me off of Lisinopril as this is a known side affect. Now I am left debating whether or not I want to continue down this path of trying different combinations of pills to poison my body in order to lower my bp. It seems like others have noted marked differences between taking Diovan and Lisinopril, where the Diovan has been much more tolerable than Lisinopril (with a great decrease in any side-affects) but I'm 31 and although I know it will be very difficult to reduce my bp on my own (believe me, I've tried) maybe I'm too young to start with the "last resort" of these toxins. Just reading about the possibility that Lisinopril was robbing my body of zinc or other minerals, so that my immune system is greatly weakened, likely being the cause for most of the symptoms, is enough to ward me off of pills altogether. It's a sad statement on the state of health care in America when I am left to basically make such an important decision on my own, because I can't trust that my doctors aren't just working in the interest of the drug companies to boost their income. I don't want to have to choose between a silent killer and a horrible existence filled with "side-affects".

In the end, based on some of the reports on here, I think starting on 40mg of Diovan will be fine, but I will certainly be VERY wary of anything unusual and immediately find other options.

I'm glad I found this forum. I been taking zocor aka simvastatin for about 6 months. I started experiencing dizziness and lighhead about 6 weeks ago.
I am going to stop taking this drug immediately. I also feel like I am drunk but Im not. All my blood test came out fine. I went to the ENT Dr. and they told me
it does not look like a ear problem. All I know, I did not have any medical problems until I started taking this drug. I will let you know in 6 weeks if my symptoms improve or not.

chivazo.

Lisinopril has ruined my life! I used to feel great. I was diagnosed with high blood pressure, so my doctor put me on this poison. I've been on it for about five years, and each year have had different medical problems. My bp was high, but not terribly high before this poison (150 over 95). After going on the poison it went down to 130 over 80. I don't think it's been worth it! I've had a dry cough from hell, anxiety, insomnia, weakness, itchy skin, hives, pain in my abdomen, kidney stones, tired all the time, and worst of all it has affected my complexion, as my face is now red from it dilating the capillaries in my face. Luckily I found this site, and made a choice to get off this poison. I went from 20mg 2 weeks ago to 10 mg, and have been off it for 3 days. My blood pressure is slightly higher 138 over 88, but I don't care. I feel much better!! The last 2 nights I slept like a baby, and now feel like my old self. Before the last 2 nights I have NOT slept an entire night through for FIVE years. My skin is starting to go back to its normal color, and I don't fell so anxious. This medication is poison, but the MDs will tell you how great it is. This medication is the silent killer! Anyways, I'm going to go enjoy my day. Good luck.

after about a week on my methadone my feet and ankles swell they diagnosed it as cellulitis but cellulitis doesnt go away w/out antibiotic treatment so the next 2x it happened i didnt get antibiotic treatment i just put my feet up and stayed off them and the methadone and the swelling went down! also after about a week i start to do random episodes of passing out once with my face in bowl of cereal and once doing dishes and this was at prescribed dosage!!! be very careful i am on blood thinners and i think the dosage builds up quicker in my system perhaps. i didn't tell doctor because they work for my pain better than anything else he has given me and its hard enough to get something that even takes the edge off my pain i have so many medical problems that three very reputable neurosurgeons refused to operate on me due to my risk of stroke and i am only 49! i have deg disk deg joint rheumatoid arthritis, bilateral neuroforaminal stenosis in lower back l4-5 and s-1 several disks that are dehydrated and dessicated , many bone spurs poking in spinal canal in cervical spine every disk in cervical spin either bulging herniated or previously operated on severe arthritis in feet toes and severe nerve damage in right foot where big toe and baby no longer can lift up neuropathy in right arm radiculopathy in left missing protein s in blood which is the protein that keeps your blood from overclotting so i have been on blood thinners since 29 yrs old and have had several pulmonary embolisms b4 age 29 and proper diagnosis and the list goes on! and yet even though i got my soc sec disability by myself w/out lawyer assistance due to list of medical problems which spoke for itself i still cannot find a doctor who will try to work with me realistically on a pain management program that even manages to take the edge off to enjoy the quality of life enough to be able to spend time with my 4 yr old granddaughter doing things like fishing and playing with her in ways that i would like such as camping amusement park rides (which they have forbidden!!!) can anybody out ther help me find a doctor who will not be afraid to prescribe something that will really work enough to put me back in the game off life ? did i mention that i need right hip replacement it is bone on bone and left isn't far behind and lower back was listed as severe bilateral neuroforaminal stenosis needing surgery also as of 2 yrs ago and also need several cervical surgeries and that i have a benign tumor in thoracic spine that cant be operated on but does still cause pain! so please if you can be of help to me/as winter is upon me now ,which as we all know multiplies most of our pain problems so speed of the essence!!!!xoxoxoxo please e-mail me if you know of any doctor who can be of real help managing pain no surgeon will touch me due to risk of stroke , i stayed awake for last major surgery it had to be done risk outweighed stroke risk if it didn't get done. i am currently on methadone 10mg 4x daily and it barely takes edge off and causes too many side effects which i wont tell dr. because it is the closest thing ive had to pain relief and have been on same dose for 4 yrs ,and my pain has no hope of improving but only the certain knowledge that it is going to get increasingly worse every day and my granddaughter only has me her grand papa and her uncle, my son, that she can depend on being ther in a good role model form as well as being her only consistent source of love ,affection and proper parenting! I love my daughter but her and her boyfriend ,my granddaughters father of course, are 2 of the most self centered people on earth and unfortunately they put their needs b4 thier own daughters on every level and in way to much detail for me to put here i need only say this combine 2 totally self centered individuals with a pretty big cocaine addiction and you will get enough with that to know my dilemma! they buy her many clothes n toys n moviiiies to keep her busy while they play but never enough food or mmeds or real needs such as affection, love ,food, drinks etc!! they both work in a hosp making great money but i have to provide my sweetie(grand baby) with food meds affection love and all the things they should be doing! this is why it is even more urgent i am able to function well w/out as much pain as possible she needs to be here with me and her pa pa in a healthy ,wholesome loving and affectionate home she loves to bake and read and learn with us she never wants to leave and it tears my heart out when i drop her home with her daddy and she cries hysterically because she doesn't want me to go and she wants to stay with me and i cant! so please help me find a good doctor who can help me function at highest level w/out pain but also as coherently and safely as possible!!??? i would be forever indebted to you for your kindness and help! e-mail is ******* please send referrals or recommendations of any and all sorts tysvm, i live in the area of erie county new york tysvm,xxxooo tysvm for all your time ,much love, pained and troubled grandma in n.y who needs your help to be able to help my sweet grandbabyxxxooo

IVE BEEN ON SYNTHROID FOR A LITTLE OVER A YEAR AND ITS BEEN HELL. I WAS STARTED OUT ON A 100MCG MY PERIOD STOPPED I HAD MOOD SWINGS HOT FLASHES AND MY IRREGULAR HEART BEAT IM 31 YEARS OLD I GAINED 42 POUNDS IN 1 YEAR MY FAMILY DOCTOR CHANGE MY SYNTHROID TO 125MCG WERE THEN I WAS RECEIVING TO MUCH NOW IM ON 112 WERE I HAVE BEEN IN REAL BAD LEG AND FEET PAIN AND AWAITING A CURE FOR THIS AWFUL ILLNESS IF ANYONE HAS ANY SUGGESTIONS PLEASE EMAIL ME B/C IM ALSO TRYING TO HAVE A BABY PLEASE REPLY ASAP

I CANT BELIEVE THAT I CAME ACROSS THIS WEBSITE.I AM SO SORRY TO HEAR WHAT YOU HAVE ALL BEEN THROUGH.I WOULD LIKE TO SHARE MY EXPERIENCE WITH YOU AS WELL......I HAVE BEEN ON YASMIN FOR ALMOST 4 YEARS NOW. JUST RECENTLY IN JUNE I NOTICED AN INCREASE IN MY BLOOD PRESSURE, I WAS EXPERIENCING CHEST PAIN, HEART PALPITATIONS, SHORTNESS OF BREATH, ANXIETY AND PANIC ATTACKS. I AM A HEALTHY 22 YEAR OLD ,WITH NO MEDICAL PROBLEMS. I NEVER HAD ANXIETY OR PANIC ATTACKS THIS HAS JUST BEEN BROUGHT ON ME OVER THE PAST FEW MONTHS.... I HAVE BEEN TO THE ER 4 TIMES SINCE JUNE... I FINALLY WENT TO MY OBGYN AND THEY TOLD ME TO GET OFF THE PILL... I HAVE BEEN OFF SINCE SUNDAY I DO HOWEVER KNOW THAT IT CAN TAKE A MONTH FOR A HORMONE TO COMPLETELY LEAVE YOUR BODY, SOI IM HOPING TO SEE SOME GOOD CHANGES... IM THANKFUL FOR FINDING THIS WEBSITE AND IM GLAD TO KNOW I AM NOT GOING CRAZY! FOR ANYONE THAT HAS STOPPED TAKING IT... ARE YOU NOTICING GOOD CHANGE?

MY STORY

My Mirena was removed on 29th May 2008.

I had the Mirena put in four years ago,I had terrible pain the day after, it was that bad I was going to go to the hospital Emergency to get the thing out but I put up(the worst thing I done in my life, Im paying for it now) with it and it and the pain got a bit better,had a lot of bleeding (spotting) for the first six months and then it finally went away. For the first year I thought Mirena was Great but then the problems started.I started to gain a lot of weight,facial hair,Very sore breasts, I also had a lump removed from my left breast a couple of years ago, but I didn't know until recently that it was most likely caused by Mirena. Some of the other problems I had, My stomach bloated, I look like I'm six months pregnant ,I have a cyst on my left ovary,dry skin,acne,strange depression,headaches,and the Worst of all I had to have my Thyroids REMOVED on 1st Nov 2006 and I'm pretty sure that was caused by Mirena as well, so now I have to take thyroid Medication for the rest of my life,I had the Mirena removed as soon as I done some searching on the internet for my unexplained medical problems, mainly my weight as I had weighed about the same my whole adult life and now I had put on a few stone and now I have to try and lose it,as for my thyroid I have trouble getting the Meds right its a real pain,blood tests all the time.I just don't feel I have much left in my life,depressed,sick all the time. I eat well as I have high cholesterol so its not that I over ate,I noticed you do feel a lot more like eating sweet things. I found a site called ****** and found out there are thousands of woman,girls with the same problems as myself and that there is a class action law suit going on to Sue. Its worth having a look at this site it helped me a lot.I feel so bad I don't go out anymore I don't see friends or family I'm to depressed about my weight now. I am in the process of trying to find out if there is a Class Action Law Suit in Australia.If anyone knows of a Class Action in Australia could they Please let me know. After having the Mirena removed about 6 weeks ago I thought I was doing ok only a bit of spotting,but about 3 weeks after having it removed I got my period and the pain was unbearable,I was in agony stomach cramps and I bleed so much I thought I was going to die from blood loss,also the scariest was the huge blood clots,very scary,must of been four years of period in 1 week I couldn't believe how bad it was, I felt really sick and weak,but thank goodness its eased off now after a week. I just hope now I might slowly start and feel like my old self. Im also on medication for heart palpitations,I get Heart palpitations (SVT) a few times a week,I had my heart palpitations just after my thyroid removal op and was put on ecg and my heart rate was 176 Beats per Minute I was rushed to Intensive Care and I had to have an injection called Impending Doom (It makes you feel you are going to die) to slow my heart rate,it worked and I was kept in intensive car for 3 days,very scary thing to go through I hope I never have to go through that again,my heart palpitations got worse while I was on Mirena and now I also take Magnesium to help control them as well as Metoprolol which I have been on for some years and I recently read that if you are on Mirena it increases the side effects of Metoprolol.

So if you have had any bad experiences with Mirena please let us know,it will help others with their problems, hopefully. I just wish I never got Mirena and my advice is DON'T its not Worth the risk,if the Doctors had of told me about the BAD side effects I would NEVER of had it put in. Sorry about going on so long, Good Luck to you all,

Thanks Net.

google mirena-side-effects.****** (a mirena help,info site)

UPDATE

I have had it out nearly 3 months now my painful breasts feel normal again,I haven't lost any weight yet, but will soon hopefully,I do feel a lot better but still get some of the symptoms back just before my period.

I get sooo mad when i think of what Mirena done to me and all the other women and how bad some of their side effects have been. I get mad when i read some of the other ladies stories and the terrible things they have gone through ,

Perforations,Miscarriages,IUD's lost in their body,

Hystorectomy,and the rest. I want to wish them all the best, and we WILL get Better and Bayer ,Mirena will PAY some day for what they have done to US..

I've been taking Doxycycline for two days now. I have a severs case of insomnia. I have not slept in over 36 hours, which is very unusual for me. I am experiencing shortness of breath, extremely exhausted (but can't sleep), nausea, dizziness, feeling of something in my throat, and weird weird moods (getting mad for no reason, which isn't usually me and people are noticing that something is different).
I'm supposed to be taking it for another 5 days for an infection. Any advice on what I should do? This whole no sleeping thing just isn't working for me.

I think Fosamax KILLED MY MOTHER. My mon was previously healthy with no known medical problems. No hypertension, no high cholesterol, no diabetes...nothing. She was taking Fosamax for osteoporosis prevention. She developed an acute liver failure. There was no viral, bacterial, or cancer linked to this sudden onset of liver failure. She received a liver biopsy and within one week was dead from bleeding from the biopsy site. I have recently found some journal articles linking Fosamax to acute liver failure. MY HEART IS BROKEN. Do not take this drug without doing in depth research on its side effects and discontinue it immediately if any side effects occur. God Bless.

I just got done reading a lot of this page, I was in tears. I'm a 23 year old female; I started taking Advair 250/50 (two times a day) about 3 1/2 years ago for COPD. Before my problems started I was working overtime every week, just financed a car a year previous, moved out of my parents and felt like I was on top of the world. Minus my general anxiety and clinical depression, I was only on 2 medications plus an albuterol inhahler.
I kept getting sick, was having trouble breathing, so I was put on Advair; at first It's like I read in almost all these forums...It's a miracle drug! I was able to breathe, but I noticed I was starting to feel pretty lazy, in 2 months I gained 30lbs. I kept taking it along with a lot of other medications for more problems that seemed to keep coming along. In late summer of 2005 I had a seizure while I was at work in a restaurant kitchen. I was opening and had passed out between 4 fryers and a flat-top grill; an ambulance picked me up. I kept getting dizzy spells and vertigo, I started having seizures a few times a week; I was released from my job on a long-term medical leave because of the hazard it was for me to work there. Things kept getting worse, It got to the point of averaging 17 pills a day because of medical problems. Before I got sick I weighed 131lbs, I currently weigh 170lbs. I was having seizures everyday, then every other day, and it slowly decreased over time. I went through so many tests, I'm still going through them. I started having really bad bowel problems which I'm still dealing with; It's sort of like IBS. I also deal with chronic daily stomach/abdominal pain; in a laproscopy, the doctor said that my small intestine looked like "a bag of snakes". Another daily pain that I'm still dealing with mouth/teeth/jaw pain. Although I rinsed my mouth out after each use, I believe Advair royally screwed my mouth up for life. My gums bled everyday, I had to use a kids toothbrush, my gums were peeling off; It was told to me that It's like a mouth yeast infection. The gums over my canines started receding and didn't stop until I quit taking advair. The nerves on my canines are exposed and partially rotted, other teeth have chips and are rotten around them. The gums above my canines are still raised and will still flare up from time to time. I haven't been able to work since August 2005. I've been denied disability twice. I have panic attacks when I'm around people. I'm scared to drive because I've had a seizure behind the wheel. I'm in so much pain everyday that I normally don't move unless It's to use the bathroom. I used to cook 80 hours a week, hang out with friends, and work out. Now, I can't work, can't be around people, and take enough medications to start a pharmacy. It's odd how it all seemed to start when I began Advair. One other thing, I'm constantly coughing up these weird mucas spheres. My advice if you're thinking about taking advair...well, I'll just say if I would have known that this is what it'd do to me, I would have chose bronchitis 4 times a year.

thyroid .I had to have mine removed.
MIRENA is the worst thing i ever tried.
Dont risk it,its not worth the medical problems you will get.

I can't believe I've stumbled on this website. Until now my symptoms did not make sense to me.
I had my Mirena in 2005 after the birth of my son. My life has changed dramatically since then & I didn't put it together until now. I was plagued by nasty vaginal discharge from the start. Though my period stopped completely what replaced it was a terrible vaginal odor that no amount of washing, deodorant spray, etc will cure. It's a bacterial infection that will not leave me alone. I almost always have it. Before the Mirena I never heard of it. My sex drive & sensation is virtually none. I even went as far as having a female piercing as I read it increases sensitivity. This is upsetting as I've never had problems with odor, loss of sensitivity or inability to achieve orgasm. Along with this I've experienced a large weight gain, abdominal bloating, migraines, aching joints, decrease in vision, back pain, dizziness, exhaustion, increase in body hair growth yet limp thinning hair, & fibroids.

I have an appointment in July to get this thing out & wish I had been more informed of the side effects.

Just an update about the class action suit discussed previously, and Aamaya had provided us with the Florida attorney, Justin Wikin: I got a letter in the mail yesterday stating that they would not be pursuing suit against them. They said that they deal mainly with wrongful death cases and it does not mean that the case does not have merit, just that it is not their specialty. I will be doing some research here locally in Ohio to see if I can locate a practice to pursue this. If anyone comes up with something, please let us all know.

I am 43 yr old woman and have been on simvastatin on and off for the past 3yrs, it's only since coming across this website that I have actually managed to find a connection between this awful drug and a whole heap of medical problems. The most recent course made me so ill that I thought I had an incurable illness that no one could diagnose, at times I have been in so much pain I thought I was going to die. It started with severe knee pain, I have a little arthritis in the knee but doctors were baffled at why it would hurt so much as x-rays on knees and hips were ok. I ended up having an operation to cut a ligament, that was over a year ago and had been in crippling pain ever-since. Also; foggy head, headaches everyday lasting all day, pain in jaw, shoulders, neck, swollen throat, incredible limb swelling, numbness all down right side, kidney problems, weakness in muscles, aching hips and legs, itching, insomnia, to name a few. I complained to my doctor when I was prescribed 50mg of this poison because as soon as I took it, I immediately felt ill and collapsed from terrible weakness, couldn't even lift a feather. They reduced it to 20mg, and I blindly kept taking it, in the meantime, my leg function was worsening, my back was killing me, I couldn't sleep because of the unbelievable burning in my shoulders, hip, neck and legs, everything hurt so much. I have been in tears from the pain and frustration of not knowing what was happening to me, painkillers, even high potency prescriptions just didn't work. I was a healthy gym-going person with a slightly high cholesterol reading, and suddenly, I was almost crippled, unable to function or look after my family, couldn't even handle simple chores that I had done a thousand times before, couldn't think, speak well, do crosswords, it was unbelievable. I have had ECG's, heart stress tests, been to and fro to doctors, hospitals, specialists, even seen an osteopath with these pains, they must have thought I was a hypochondriac! Finally, I insisted on an MRI on my thigh as it had changed shape as there was a lot of muscle wasting in both my right arm and thigh, and so much pain. A lump had also appeared and was really worrying me. The doctor tried to fob me off and said it was a fat lump, I argued that if it was fat it wouldn't hurt so damn much, so the result of the MRI is that I have a tumor which is getting bigger. If I find out that this is a result of the medication, the gates of hell will open.
I took myself off this lethal stuff immediately as soon as I realized there was a connection between it and my debilitating condition, though it's too late to save my 12 yr relationship, that went down the tubes because I just couldn't function well, oh, and my job. and any chance of working after being ill for so long.
I have been off it just a few days but already I feel almost human again. I know it'll be a while before I can see a marked difference and do some of the things I used to be able to do like walk the dog!! but I am furious with my doctor's and have written a letter of complaint, and have told them that I would rather take my chances with god and be a happy person than ever trust them again. I am in no doubt whatsoever that this drug has ruined the last 3 years of my life and probably caused irreversible damage to my leg muscles. Why take a pill because the doctor said so??NEVER AGAIN from now on everything will be checked via websites like this, I am so disgusted that instead of helping me, my own doctor just prescribed other medications I need not have had because of this pill when all he had to do was take me off it. I find it hard to believe that they don't know of these side effects, or pretend not to, how can they not make the connection?? Absolutely furious. I am in worse health now than I ever was, there should be a serious health warning before this is given to anyone, and the first port of call for any complaints should be the doctors who prescribe them instead of offering alternative solutions. This is a time bomb waiting to explode.

I am here because I am an allergic person. Food allergies are a significant part of my medical problems. New Zealand is planning a comprehensive study of food allergies and children. See video.

http://www.tv3.co.nz/News/HealthNews/Kiwiswithfoodallergiesatriskduetolackofinfo/tabid/420/articleID/51880/cat/59/Default.aspx

I have had my Mirena IUD in for 5 years now, and am having it removed tomorrow - yay!!! The only thing I'm NOT looking forward to is the contraction to have it removed (my Doctor reminded me to take a pain killer 1 hour before removal!). Whilst I have had a relatively good time on the Mirenda IUD and didn't have a single period once it was inserted - compared to a friend who also had hers in for 5 years and still had monthly light periods - I am beginning to put 2 + 2 together and have seen the reason for some of my "medical" problems as being linked to the Mirena!

I have had a decreasing sex drive for the past 5 years - which my husband says is "psychological" and I should be able to "think" myself into wanting sex!!! (I've told him that us women don't think about sex every minute like men do and it is impossible for me to feel like making love in the build up to actually doing it!!) I have also experienced weight gain - I am the heaviest I have ever been and my diet hasn't changed much from before I had the Mirena put in!

I think it may work for some people, and I am glad I have tried it; but I certainly don't intend to get another Mirena after I have this one removed!

I was prescribed Singulair last winter after a severe allergic reaction. I have taken it throughout the winter with no noticeable side effects. For the past several days, however, as the pollen count has risen, I have been experiencing strange symptoms. I feel a bizarre pressure in my head, and a ringing of sorts in my ears. Also, I can't sleep - I feel exhausted, and try to go to sleep, but I wind up feeling agitated and have to get up out of bed.