Barley symptoms and conditions

Marini IUD side effects and marina crash side effects for my daughter….still going

February- pregnant 19 by 25 yr old first pregnancy...
Abortion first ever
IUD marina same day insertions as abortion
Yr later Sept bloated tummy, anxiety attacks, paranoid, tummy flutters, pushing sensation.. Odor, discharge something’s wrong
Next day….Marina removed, antibiotics, bacteria infection
Lab test all negative.
Next four weeks…. Barley any sleep, barley any food, depression, anxiety, out burst, rage anger, sadness, self verbal destruction, blaming self, tossing turning, moaning, soul hurts, very moody up and down, no patience, confusion, face breaking out…looking pale, skinny, unhealthy….It’s like a drug addict addicted to drugs but this is addicted to the guy who got her pregnant… no drugs ,no alcohol,
Call radio station, ask why are they not making sense…
TV.. fate/Destiny, symbolic meaning meant to be…..
Reality. .NOT an option….
25 yr old who got me pregnant was a fling off and on a yr..
Convinced self…… had to be with him ,loved him,
Drove over to his house daily,
Called daily, text daily,
Believe the earth was putting signs of fate and destiny to be together with him

Couldn’t be in public, took time off from work, saw counselor, who said needed anti- psychotic pills, depression pills, and sleep pills have hormones checked, thyroid level…. Alice in wonderland can’t separate reality from fantasy.
Saw another doctor, had test….white blood cells moderately high have to go do more testing. doctor said doesn’t need hormones checked…. said ADHD need meds again…
Feel crazy, feel like losing mind, drifting in and out of thought conversation, space out get into trance like sate, and feel as if I can’t control self,
Have to be with this guy, have to protect him. Pregnant because of him,
Convincing self destine to be together, family marriage future with guy..
Other times acceptance of rejection from him, never wanted to be together.
Lost three weeks of work., keys to car taken, keep texting him calling him…Girlfriends tell to stop….Ignore her..
What’s real and what’s not. Keep repeating questions seeing signs, from TV, radio, he wants me……he needs me…All in my head??? Everyone tells me…All in my head..
Can’t take ADHD pill, can’t sleep,….Confusion, blurry vision, see colors…..What’s real???
Snapping at family, angry, disbelief,he wants me….
Reality. Is he doesn’t can’t accept it….
Family thinks I’m loosing my mind…am I?
Over a guy? Who was just a fling? Who I thought was the One….
The reality shows, We are meant to be together…..But told It’sall in my head…
No family history of mental disorder, never have gone though this..
Always had confidence before marina IUD…..
Never chased guys, never had too…what’s wrong??? Why this behavior??
know’s better, he wants me,
Began Sept 26th..anxiety,flutters,pushing,bloating….swollen belly..
Still going Oct 28th..Removed Sept 28th 09…..after removal instantly feel better then BOOM!!! Downhill spiral of emotions began’s…..Still feel very clouded in her head, confusion expression......head tells her the opposite of what the family tell's her...
What can I do as a mother with great concern???? How do I get her back to the happy,outgoing,confident 19 yr old she was????

hello, guys.
after taking doxycycline ta hyclate i got a burning itch to my balls and penis
i stopped taken them and its taken about a week to be cleared from side effects what really helped me from the pain was barley green grass wheat grass and cucumber in a sliver bullet. if you guys are getting depressed brewers yeast,landmark education warnutoil help the brain, Tony Robinson is a motivational speaker and on one of his talk cds his got a great talk on acid alkaline concept of dieting called pure energy disk 4 get the edge. allot of quotes are from this book called Gods way ultimate health. and after reading that if you don't believe in YAHWAH GOD then read it again. peace

ive been taking prednisone for 2 doses..(2 days0 my legs were so sore when i woke up the first day i could barely stand i did do a little running around i am 28. but nothing that would have caused this.its painful to sit because it causes them to get stiff. it hurts to walk because it causes them to have to straighten out. its a catch 22. i cant call my doctor until Monday. so i don't know what else to do. no matter what i cant stop taking them im told.so i have no idea what to do. im in so much pain i cant barley do anything.

I had mirena inserted September of 2006 and for the first few months i was ok but then when i barley got my period and when i finally got it after 2 or 3 months it was BAD!! with cramps that hurt like crazy, i would discharge a lot..and i mean a lot throughout the day, then during intercourse i would feel soo much pain because of the mirena. I also noticed my mood was different from before and i had gained a lot of weight, im having moments where i have shortness of breath while im during normal things. Now that i haven't had insurance for 3 years and haven't been checked im scared to go...i want to get it out as soon as possible but i bet it cost a lot to get it removed.

I have been taking lisinopril for almost a year and it has decreased my sex drive. It has also decreased my blood pressure which is more important. My wife would prefer me to be healthy and doing it less often than dying on top of her. The only recent major problem I have had is dizziness and vomiting. I took it a few days ago and found myself sweating and dizzy. I tried to eat something and vomited it up in a mnute or so. I think changing my diet and exercising is more important than taking snake venom to open my veins. I am going to get off this stuff and try to eat right and exercise. I am a Black male 6'2" and about 265lbs. At 44 I should not be feeling dizzy all the time. Before this drug I took barley pills which made me dizzy as well. The nausea and dizziness are terrible and I think I will come off this stuff permanently after seeing my doctor. I do get nervous when I go to the doctor but I also know that I eat too much and at the wrong time and I need to exercise more. Worrying about the economy isn't helping either.

I've been on NuvaRing for a little over a year. I've read everyone else's side effects. Mine are similar, but I have also noticed that my skin has started getting dark pigments. It started about 6 months ago, mostly on my face, but in other areas of my body as well. I went to the dermatologist this week, apparently it is from the estrogen in birth control. I've been on all sorts of birth control over the past 10 years, I've never had this problem.

I also have low blood sugar but can be controlled by eating properly. However, about the past 8 months right at the beginning of my cycle my body is out of weak. A few times it has been in the middle of the night I'll wake up nausea, weak, in a cold sweat, I'll check my blood sugar and it'll be 42, 43. I know estrogen makes your cells more sensitive to insulin, which causes more sugars to leave the blood stream and your blood sugar to drop.

After my dermatologist appointment and barley being able to walk to my kitchen this morning with out passing out, I can't help but wonder if there is too much estrogen in the NuvaRing. I do know that I wont be using the ring again SPECIALLY after reading all the other similar side effects I share with other women.

Hello everyone..I have many great things to say about Neurontin. It has been a miracle medication for me. I was in a car accident in 2000 as a passenger my face and head hit the windshield at 80mph. my jaw was broke and the back of my teeth were broken.
Little did I know it was extremely traumatic! My MRI's came back fine and I moved on with my life. About 6 months later my life began to change a brown spot covered my eyesight in the left eye. I began falling all the time and having seizures.
I had another MRI's of by brain done it came back negative. Not one Doctor could seem to understand what was wrong with me. I was put on Topamax for bad headaches that seemed to help. I began loosing weight and continued having seizures(Granmal) where you lose ur vision and it began to effect my speech and i would become confused.
My life was like this for 5 long years. Life didn't get better, I began to be soo tired and felt exhausted all the time. One day out of no where , I couldn't raise my head to get out of bed for work, my whole right side was burning and i was in pure agony!!! i will never forget that day. I had to have my Daughter help me up and i could barley walk...I pushed myself to keep going thinking this is all in my mind!! theres nothing wrong with me.. The MRI's are negative. I proceeded with my day in so much pain and limping all day.
It finally went away and I was fine again fo a small amount of time, I started not being able to remember things ....and forgetting from one second to the next and getting lost when I would drive...i began to panic and have anxiety, I felt like my life was out of control. I called my Mom and she said she had noticed a change in me, things I guess I didn't even know. She said I couldn't hold a conversation as before and i would slur my words and I couldn't recall what she would tell me.
My attacks moved to 4-5 times a week sometimes having seizures 2-3 times a day. I ended up having to be taken care of and moving where my Mother was so she could watch over me. I didn't get better. I couldn't work and I couldn't do much of anything.
My Mother took me to a MS specialist and he was the one who noticed there was something wrong! My face and legs would jerk and I couldn't sit still ..I had so much going thru my mind what could be wrong? I had 2 Sets of MRI's this time and it wasn't fine this time...My Spinal Cord was barley attached to my Brain Stem and CV 5-6 in my neck.
I was at the stage of being in a wheelchair not that I hadn't been using one from time to time and needing a cane.
I was sent to ER Surgery and had a stay in the Hospital and really thought I was a lucky Person to have made it for 5yrs without dying. It has been 4years and I still have soo many problems, I'm held together with a steel plate in my neck that holds mt together.
I'm now 41 years old and I wonder what my future holds. I'm not the same girl I used to be and probably never will be. I have to have Neurontin 600mgx4 a day and 1000mg Keppra a day...Without it I would not want to live the pain is unbearable for me! The only negative side affect is my hair falls out and I have severe Insomnia. Neurontin is a Miracle for me!

I wish all of you the BEST! Prayers for all of you.....

Avelox! :-(
I don't no where to start.. I initially went in to the doctor and was diagnosed with bronchitis and was prescribed Avelox. I had been on antibiotics before but never this one. Well I took my 1st dose and with in 30 minutes my mouth was consumed with a very bitter acrid taste. As I continued on taking 1 pill once a day, by pill 2 and 3; I was waking up in the middle of the night in a pool of sweat shaking the glads under my neck aching. It seemed that the floor and room was spinning. Pill 4 and 5, I experienced burning head ache, it felt like acid was slowly being poured over my brain and the diarrhea that I initially had in the beginning got worse not just watery but now slimy and mucusy along with the burning head ache that I'm having trouble even typing this comment, I have extreme heart burn even spiting up bial in my sleep. I have all of this going on while trying to make it to the bathroom room, room spinning and my heart is pounding and my legs are shaking so bad I can barley let my self down on the toilette. Pill 6 and 7, I have slurred speech and I can barely complete a sentence much less write this comment so please for give my typos. I've been lying in my bed thinking that I'm dieing trying to figure out witch one on my family members I should contact because something bad can happen and I don't know how bad it will get. As of right now 6:30pm central standard time May 7th I'm considering going to the emergency room! I just hope there is no permanent damage. I will have since discontinued my prescription and will let you know how it goes.

I started Lupron in April of 2008. The year before this I worked HARD to lose 80 lbs. I finally got down to my goal weight because I was tld my endometriosis symptoms could be relieved if I wasn't overweight. I had a laparoscopy in March of 2008 confirming my diagnosis- Lupron was a last minute decision because of my age and status the doctor didn't want to do the hysterectomy right away. My endometriosis is spread throughout the body- including the lungs. While Lupron helped with the pain I was experiencing, it caused other pain. Pain that I can no longer even deal with. I became lethargic, depressed, and angry. My hair was falling out in large clumps. I didn't gain weight right away.. except a pound the first shot and three pounds hte second shot but I figured that was alright if it was only like 15 lbs total. I oculd deal with that. Here I am almost a year later. my last injection was in August. I gained a total of 47 pounds. I am a fat slob. I couldn't work out because my bones hurt so bad while taking the medication. No one around me knows what I went through physically. They al think that it was just some excuse to be a lazy fat cow but it truly HURT to move. Just simply walking from my bedroom door to my bed killed me. It hurt my ribs, my knees, my shins, my back. There were times when I couldn't even get out of my bed ebcause I just didn't have the energy. Then the depression started shortly after losing a large amount of hair. By now I am thinking about how ugly i've become on top of how fat I am. Nothing went right but my doctor pushed the shot. I figured hes the one with years of experience he couldn't possibly be this wrong. I trusted him. When I would go to him with complaints of my weight gain he would tell me to stop eating. The problem was... I wasn't eating. I was too sick to my stomach to bother. Then when I would get hungry i'd over eat. I bled a lot through the shots and I still had pain here and there but I was too afraid of what he'd put me on next if I complained. I started to forget simple things. My career was going down hill because they were sick of me not being 100% commited to my job any more. I cried all the time. I finally got sick of the weight gain while I was on my shots and I decided to work out regardless of how I felt and three times I passed out in the gym and was transported to the hospital where I had to listen to their advice on being overweight WHICH WASNT THE REASON I WAS PASSING OUT TO BEGIN WITH but no one wnats to hear what I have to say. Every one just assumed that I was this pig who never worked out in her life and over did it this time. What no one understood was that three months before the incident i was my average weight. I was tachycardic all the time- my normal resting heart rate while i was on my shots was 162. During a work out it would get up to 220!

Ive been off them since August and I haven't lost a single pound. I get up at 4am every day and work out. I park as far away as possible. I use the stairs instead of elevators. I eat healthy. I cut out extra sugars and stopped rewarding myself when I deserve it. I started these shots at 155lbs and today I am 215. Ive been on a strict monitored diet, diet pills and work out regimens and I am still 215. My knees kill me nad sound like velcro when I walk- ive even fallen a couple of times because they hurt that bad. My back still hurts and my neck still wont turn to the right completely because of a nerve that pinches or what have you in there that sends the sharp pain through my face when I move. I still have the depression but i think thats more because of my weight now than it is anything else.. and I finally ended up losing my job.

I recently saw my OB for a follow-up where he stuck me on yet another birth control. This one makes me vomit and gives me stomach cramps so Ive decided im done. I won't take another pill because its making me worse. Id rather have my uterus fall on the floor than pop another drug.

I was on Femcon FE for 6 months just for hormone replacement I have been on BC for 10 years never had the problems like I have with this drug. Severe arm muscle aches but worst of all lower back muscle cramping at night so bad I could barley get out of bed in the morning. I was starting to think I had arthritis, numbness in fingers and arms at night as well as stiffness in my fingers joint pain in my knees very bad. All this was a constant and the back cramping was getting worse with every night. I have stopped taking this drug 1 week ago and already see big improvement in mood, numbness is gone and the back stiffening and cramping has greatly improved, the muscle aches are almost gone Thank god I figured out it was this horrible drug.

Hi I started taking Lipitor when I was about 41 and gradually noticed a big toe becoming numb. Then later another toe became numb. I had just started swimming about this time with fins and thought at first it may have been caused by them. But then I stopped swimming and the numbness continued. I visited a Neurologist a couple of years ago who tested for everything and found some peripheral nerve damage to the feet. I said the only thing I could think of was Lipitor. He said here was no conclusive evidence it causes this but explained how nerves are made of Lipids and lipitor limits the production of lipids. I stopped taking it but later my GP said I need to go on something for my cholesterol. He put me on Crestor. I took a Lipitor the other week and my toes tingled that night. So I am convinced it is Lipitor. I am not sure how to reverse the damage though.

I cant believe i have just found this page!!

After feeling more sore inflamed 'hormonal' spots on my poor cheeks i decided to look up 'mirena related acne'.. i knew that it had some side effects, like possible skin breakouts, but i really didn't think that i would have ended up with skin like a pubescent teenager.

i was diagnosed with severe endometriosis after years of complaining to my gyne at 19. i tried all the usual route of contraceptive pills, oestrogen and the mini pill, but non seemed to suit me, so i was recommend the 'mirena'.

i first had one implanted 4-5 yrs ago, this had to be removed after barley 5 months. i was doubled over in agony on the bathroom floor and often had my breath taken away with excruciating stabbing pains.

i had my current one inserted in May 2007 at 23, under general anaesthetic whilst having a laparoscopy to try and remove some of the endometriosis. Granted i felt rough after being in surgery for 5 hours, but once all the stitches were gone i thought i would begin to feel human again.

i have put on quite a bit of weight, i went from 7 1/2 stone to just over 9 stone in just over a year (i don't know what it is in lbs sorry!) believe me at 5ft in height it's noticeable!!!!

i have never previously had migraines until the mirena, i now have them every 2-3 months or so.

my poor long suffering boyfriend thinks i no longer 'fancy' him as my libido has gone!
my breasts have become so painful and swollen it hurts to sleep on my side, its painful if i even try to run up stairs, and the boyfriend is no longer allowed to touch them!!

and at certain time in my cycle, my tummy becomes so swollen, i look 5 months pregnant, in fact i was asked the other day when was my baby due...i was really not impressed!! during the swollen tummy time sometimes when i am sitting down it feels like the mirena may burst out of my back passage.. (not a nice image i know) there is a sharp stabbing pain and then a wave of nausea comes over me, this stabbing pain can last on and off for a full day.. i have told this to my gyne.. he had said it must be irritable bowel syndrome!! i have never had IBS before!!

all this at 24 nearly 25, i'm supposed to be enjoying these years, but with my skin the way it is and my body confidence shot, it is really really depressing.
i just thought for so long i was being silly and over reacting to everything, but obviously i'm not the only one..i would not recommend the Mirena to anyone, i fact i would not wish it on my worst enemy. ther are far too many side effects!

hi no one has described itchy skin mainly arms and back

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 was prescribe SMZ-TMP 800-160 DS 3 days ago on July 2nd for an infected hair follicle in my right armpit. I took the first does that evening and not long after felt really nauseated, almost like I had the flu. I consulted the page they always give you with prescriptions and it said that nausea was a side effect and that should go away after a couple of days. Well the next morning when I woke up I had no appetite and still felt a little nauseated but not as bad as the night before. I did take the 2nd dose and by mid morning the nausea was getting worse and by early afternoon I was developing a fever. Took a couple of Tylenol and toughed it out through the rest of the day at the office. When I got home I took my temp and found it to 101.3, took some Tylenol and called my pharmacists and he indicated that temp and nausea were really nothing to worry about. Felling a little reassured but still like I had the flu I took the 3rd does and about an hour after I took I started to feel the worse yet. I checked my temp again and found it had climbed to above 102 and for some strange reason my tongue would go numb for short intervals, almost like it had been shot full of novocain. I got absolutely no sleep that night, and given that the info sheet said to notify your doctor right away of you develop a persistent fever that next morning, July 4th, I called the office number and got the answering service and they had the doctor paged and when he finally called me back he was quite concerned over my reaction to this medicine and said I had to be seen by someone today because of the persistent fever. Being that it was the 4th of July the only option was the ER so off I went. They ran a few tests and found that yes I was having an adverse reaction to this evil medicine but I should be fine in a couple days. It is now July 5th, more then 36 hours since I took the last does, and the nausea is finally gone and my appetite is slowly coming back, but I still have a fever but it is slowly coming down as well or maybe the Tylenol is finally working, either way I hope by the end of the weekend to be feeling better.

Oh boy! Side effects to coming off this med! UGH! I am going through them as I type! It is the most horrible way to feel! I have tried in the past on several occasions to get off this med...but never had accomplished the feat as it is nearly impossible to get through the day! At my highest dose I was taking 300 mg daily... the Dr. weaned me down slowly and now am trying just to get off of 75mg daily! I am on day 4 without Effexor xr... needless to say the side effects are getting worse instead of better!
I am experiencing: dizziness, tingly feeling in my whole body, night sweats, almost hard to do anything because I feel as if I have the flu!!!!
To anyone who is given the choice to take this med...DON"T!! Getting off of it is the hardest thing to do! In hindsight... when I am on it fully it is a great med. It helped me regain my life without panic, anxiety, depression etc... Idk... people don't understand the hell we go through with all these meds. My poor husband can't take my complaining anymore! Although either can I! I feel like going and getting a pill right now just to feel better!

Hi All,
I am very concerned about the effects of Geodon. My 12 year old daughter is on it has been on it for some time and now is having speech problems. When she talks its as if she has what I call a"Mush Mouth" you can barley understand her and it's almost like a whisper talk. Has anyone else experienced this? Please I am in need of any input. Thanks,Annette from Michigan

I suggest to anyone that has Hashimoto's Thyroiditis (type of Hypothyroidism) to have a blood test done for Celiac Disease. There has been research done linking Celiac Disease and Hashimoto's Thyroiditis. Celiac Disease can be controlled by a gluten-free diet (wheat, rye, and barley free). In the US, not many doctors recognize/know of this link. I have been hypothyroid for 20 years (had Hodgkin's Disease (cancer) - radiation/chemo at age 16) I have 2 sisters with Hashimoto's Thyroiditis and were iron and B12 deficient. I was diagnosed with Hashimoto's Thyroiditis 3 months ago with iron and B12 deficiency. I have been on a gluten-free diet for 2 months now. My dosage of synthroid (levothyroxine) was 175 mcg and now is down to 137 mcg. I hope that I am one of the lucky ones that will have their antibodies to their thyroid normalized (no more synthroid!) I have a couple of days left before my next blood test and I hope that it goes down more. I am feeling better now than I have in a very long time. I have attached a link for those of you interested. It is an endocrine article from Finland outling the link between Celiac Disease and Hashimoto's Thyroiditis (among other things). I hope that this helps some of you. http://edrv.endojournals.org/cgi/content/full/23/4/464

No serious side effects. I want to add my experience as I see everyone
here has a side effect. I am always wary about medication, and I have taken
statins mainly Zocor and Lipitor off and on for 10 years or so. I have familial
hypercholesterolemia, so diet hasn't helped much, and I have tried all kinds
of food supplements etc. I do take CoQ10 based on reports I have read, not from any side effect. If there are any side effects its not significant that I can
notice it. Sometimes I am forgetful, hard to say if its caused by the drug, as
the times I have been off it, has been much different.

I wonder if high cholesterol is a real problem, I wonder if high triglycerides are worse? Lately I found what seems like an improvement by eliminating high glycemic foods like rice and replacing with barley and oats. Barley also has some fiber and other things that are apparently helpful. Grapefruit is also helpful, but there is a warning not to take it, if you are already taking statins. Based on all this side effects reported here, I feel I might need to try once again, to try an alternative. I am maintaining my 10mg Lipitor, though I had been planning to move back to Zocor as its cheaper for me. I will take a test
in 2 months to test my current barley diet, and recent exercise routine to see
what improvements can happen. Then if successful, I might get off statins,
maintain the non-glycemic diet, exercise and in addition take a lot of grapefruit and a reasonable dose of niacin.

In the past I have tried ginger, garlic, Chinese herbs, and more then I can list here without much help. Occasionally I had been surprised by low readings,
once when I had come back from a 10 day meditation retreat. I have read that cholesterol can change due to stress, and this is a very variable thing. I have
taken lab tests within 2 days from the same lab and seen almost 20% difference (with fasting). I think each body is different and one needs to take a very long term, positive attitude of experimenting and not feeling discouraged too much, but always reading and trying different things and being careful of how you interpret the results.

I would rather ignore the high cholesterol, except my brother died at 65 from cardiac issues, but he also had diabetes. I am now 51.

openlotus

I am finally off Loestrin and I do not have to take Yaz either yayyyyy!!!! The nurse called me and put me back on ortho tri cyclen that I start tonight! Loestrin was making me have sharp pains in my head, I was moody, and nervous, my heart would beat fast at times and my chest would hurt, I gained about a pound, my legs hurt and I just did not feel good and I barley had a period which made me feel worse bye bye Loestrin!!! Thank God I am starting back on ortho tri cyclen that I am used to and now I know my periods will be back on track and I will feel normal again!!!! Good luck to anyone else just wanted to update you all!!
Jennifer

Hi. My eight year old daughter has been on singular for 6 months. She has had chronic stomach pains that she says feel like pressure. Her appetite is terrible. She always says she isn't hungry. I have to search for anything I think she will eat. She is very tall and very thin for her age. She grew an inch in the last year but gained no weight. First time her growth just stopped. No surprise as she doesn't want to eat. I took her to the doc several times and they think she has acid reflux and have given her 2 different acid eliminators ( which freak me out as well) Said she should see a gastroenterologist. We have appointment in March . I started reading this site and thought well maybe it's the singular. So I called her allergist and told them I was taking her off to see if that's why she has the stomach problems. They said I could since it wasn't a big trigger time(seasonal) and she wasn't sick with any cold or flu) She gets mild asthma when sick. Her allergist asthma doc thinks her stomach aches are related to the mucus dripping into her stomach. I have taken her off all meds to try to see if it could be the Singular. She also has been very tired and can't keep up in her dance classes. Her school teacher had to put her in the front of the class because she said she wasn't paying attention. She seems to lose it over anything that requires focus or attention.She also seems kind of depressed. She is worried that something is really wrong with her. This child used to eat normally and is gifted academically .Her tests results(taken while on the Singulair) went way down from last year. She was put in gifted pull out program from last year results but would have barley made it in this year based on her much lower scores. That does not make sense to me. Never has had attention or focus problems before. I will keep everyone posted. Does anyone know how long it might take to get this drug out of her system? Has anyone else had this kind of reaction to this drug? I also wonder whether she had reflux before but this made it worse? I had her blood tested for Celiac and general stuff and nothing showed up.I wanted to get the Singular out of her system before we see the G.I. doctor. anyway thanks, Elizabeth

Wow, I'm so glad I found this site and now realize it's not "just me" as one doctor put it. I have had my Mirena in for 18 months. The first year was great, no side affects at all. 6 months ago I started getting bad allergies, the worst PMT symptoms ever starting three weeks before my cycle which I barley get anyhow. I continue to struggle for breath on a daily basis and I have never been this tired in my entire life. I have been in and out of doctors surgeries wondering what's wrong with me, even seeing a naturopathic. Nothing helped until I found this site, I have never had children and I don't plan to have any. I thought this would be a great 5 year at a time solution for contraception as doctors claim I am too young to be "fixed".
Now I truly believe I need to have this removed for my own health. When I do I will repost the outcome.

First and for most...I AM SOOO HAPPY I FOUND THIS!
I was starting to think I was pregnant with my side effects of this drug.
I just started taking Yasmin 2 month ago. I haven't weighed myself but I am so bloated I look like I've gain maybe 7-10 pounds.
I've gotten so depressed and just angry for no reason. I recently went with my husband to his company x-mas party, then the after party and had THE WORST TIME! I'm usually a pretty out going person but I was just sitting there being a bitter and angry b_tch for no reason what so ever.
I've been feeling nauseated, and constipated, super tender breasts. The list goes on!

One thing though I'm wondering if anyone els has had....I'm not totally sure if this caused it but since taking it, while my husband and I have sex, I get to moist we barley feel each other. Then when I stand up it just drips. Sorry for being so crass but I really want to know if anyone els had this happen to them.

Want to know of a better pill to try??? TRI-LEVLEN!! I was using this for years, with literally NO side effects. I had to switch though my provider no long carries it. It's a shame!

I am male 37 years old. In June 2007, my blood test shows 249 total cholesterol. After that, I was taking super B-complex, fish and flax seeds pills. It went down to 213 total cholesterol (40 HDL, 136 LDL and TRI 176). And I asked my family doctor to give prescription for Zocor(I asked particular drug because I will get good discount rate at my employer's place). he gave me Zocor 20 mg. After taking 1-month medication I felt some inconvenience during sex . You don’t feel it normal. I can’t do much exercise and some times feel depressed. I usually do 1-hour exercise or any form of exercise (Yoga). After Two months I tested my blood cholesterol level. It shows now total cholesterol 181(LDL 93, HDL 42 and TRI 223). And also showed ALT and urine protein little elevated. Now I stopped medication for past two days, feeling better at day time but night I am having weird dreams and indigestion problem. I guess these are withdrawal symptoms. I would go for natural medication like regular exercise, diet (oat meal, high fiber content, less sugar, less white rice). No more Statin drugs. Any one have same problem?

I have always been extremely active. I surfed every day, was swimming, I worked out at the gym several times per week. I am now 34 years old. In my 20’s I used an inhaler maybe one every few months if I got really sick but never ever needed it as a crutch to live. When I was 30 after going into a doctor for bronchitis I asked for an inhaler but they prescribed Advair in addition to an inhaler. They said this would help me to heal faster and stop the symptoms. Well I started taking Advair twice as prescribed. It did relive my shortness of breath but now I felt shaky, couldn’t sleep well and 3 weeks into it I started feeling dizzy all the time. I never had a asthma attack before. If I was sick I might use an inhaler but never did I feel my life threatened until now. After feeling dizzy I stopped the Advair. Well one day later I had such a bad attack I ended up in the hospital. Advair undeniably has made my problem much much worse. I noticed ever since I started Advair if I stop taking it my breathing gets so bad I can barley walk across the room. I never ever had this problem before taking this garbage. Its now 4 years later and I still take it but it took me 4 years to wean off this crap. I only take it when I feel really bad but then discontinue as soon as I can. I should also add I take my inhaler every day now. Never used to take it at all. I feel Advair put my system over the edge where there was a small breathing challenge burst into a full fledge illness after I started on Advair. I must ad in the 4 years I have been eating about 80% raw organic foods, taking lots of vitamins and supplements. I feel this is all I can do to start to live a normal life and hopefully be off Advair all together.