Eye doctor symptoms and conditions

Thankyou for posting all these indepth reviews. I spent more than an hour going through each one of them, they gave me a much better insight into the drug that I am taking - Loestrin 24 Fe.
I have been put on these to correct my heavy periods, I have been taking these since about a month and a half. I have never been on a birth control pill before. I noticed that I had difficulty in wearing my contacts the first month and attributed this to the pills since its a major side effect listed with using the pill. I spoke to my Ob/Gyn about this but she asked me check with my eye doctor first. But it just so happened that I never got a chance to visit an eye doctor.The problem ceased to exist when I changed my contacts, so I am assuming that it had nothing to do with the BC pills. Other than that during the first month I had headaches, which went away on their own, guess my body got used to the pills. The third side effect that I noticed in the second month (now) is the spotting (never saw that the first time around). Its not that bad but its definitely annoying. Other than that I haven't really experienced any other side effects. I have never been sexually active so cannot really comment on the libido part. My bleeding has decreased to almost one-half of what it used to be and I don't get the bad cramps that I used to get before, so this pill definitely seems to be doing what my doctor said it would do. Other than the spotting, I don't have any complaints with the pill. I haven't monitored my weight so thats one thing I will have to take a look at. Hopefully I wont have any other side effects, if I do I will make sure that I post them.

Good luck to all the ladies in finding the right pill............

I've used NuvaRing for over 4 years ~ LOVE IT! I always had a light period with no cramps or anything like that. The ring hasn't changed that. I think the only noticeable side effect I experienced recently is the inability to continue to wear contact lenses. My left eye has become extremely dry and no eye doctor could figure out why... I assume it's from the NR, though hard to imagine since I've been using it for over 4 years.

Well, seeing as that's my only complaint, I still think it's so worth it. I never used BC pills because I know I'd forget. The NR works great and I have never had any problems with it.

I have used Nasonex for about two years. Last spring, I developed vision problems which I didn't attribute to the Nasonex. In the fall, I was diagnosed with a cataract and glaucoma in my left eye.
I did not have any known risk factors and take very few medicines, so I believe the Nasonex caused the cataract and glaucoma. The first eye doctor never mentioned that the Nasonex could be causing my eye problems so I continued to take it until recently when I discovered it was probably to blame. I am now facing cataract surgery and the new eye doctor I went to told me I have the eye of someone 20 years older.

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

Has anyone had problems with their eyes on this medication, my have been going blurry and then I get a terrible headache.

This is the 3rd time I am taking levaquin in about 3 years. I had a MRSA type infection in my eye 2 years ago that I got in the hospital visiting my dying mother. She by the way died of a mysterious"infection" in her spine but frankly reading all of this I suppose it could have been caused by levaquin because they never found an infection but she complained of so much pain in her spinal collumn that they had to put her of morphine. No cause was ever determined but she was a dialysis patient and was given Levaquin on a regular basis for the infections that are common with having a stint in her arm. Her circulatory system collapsed and they could not do dialysis on her and she died after a week.
Getting back to my situation. I got the infection when rubbing the tears out of my eyes and woke up the morning of her funeral with a bad infection in the eye. Was going to eye doctor every week for 3 months thought I was going blind. Took 3 months of 750 mg dose. And multiple eye ointments. My eye sight took a hit and I now need to wear glasses for driving always. Used to have near perfect vision before this. This past year I took it again for Lyme's disease and after about a month after I developed and nerve or tendon pull in my neck that they could not explain how I got it. But I went to the emergency room and they gave me a neck support to wear.
Just was on Levaquin again for upper respiratory infection. Woke up in the middle of the night second day I was taking it. My head was pounding and it felt like it was going to explode (literally). At the same time my chest felt like it was collapsing. I thought I was really going to die and I was entirely coming undone in my mind. I called a friend at 2:30 AM and asked him (who is religious) if he knew any prayers for those who are about to die. I truly felt this was it - the end. No one told me about Levaquin's side effects until the other day when I was reading on the internet. I now have a pulsating sound in my ears that sounds like it is linked to my heartbeat. Never heard this sound before. Its been there for almost a week and it started a few days after I stopped taking the levaquin. I also have been noticing I have a shortness of breath and I am trying to move in a week. I keep getting very fatigued and have to lay down. Find myself falling asleep quite frequently.

I have only been taking this drug for about 3 weeks and I could not explain at first but just knew things were off. I can not sleep, have terrible nightmares all night long, wake up at 4 if I do sleep. I am 53 and have long hair and my head itches all the time. I now fear hair loss as I have read in other complaints. My eyes are dry, I just feel off, majorly ! My back and legs ache all the time, especially when I first get up in the morning I can seriously barely move or bend down. I feel like I am 83 instead of 53. I have had no headaches but have had weight gain already, especially in my midsection. I feel off mentally all the time, not able to concentrate at all. I am calling my doctor on Monday and they have to give me something else. Has anyone else had these symptoms and what else can you take or do?

First of all, a big thanks to all of you who have shared your experiences. I am a biochemist, with a background in pharmaceutical research...I chose the Mirena IUD after careful consideration of it's active ingredient, Levonorgestrel. The side effect profile seemed pretty acceptable...until I started to experience nearly ALL of them...I am 33 years old and had the Mirena IUD placed in October of 2008 after the birth of my second child in June of 2008. The initial reaction was to be expected...cramping, a little spotting etc...nothing to be alarmed about. I still have yet to have a period (which I really don't miss so no problem there) I never gave a second thought to this until now...for the past month or so (coinciding with the weening process, since I have been nursing the entire time, I believe the side effects were not as noticeable) I have been experiencing the following (that may or may not be related to Mirena as my OBGYN has so adamantly pointed out, but after reviewing your posts I'm willing to bet they're connected) and are in order of occurrence: Major, but temporary, hair loss after 2 months or so; Major respiratory infection lingering over a month with difficulty breathing, tightness and pain in the chest at around 6 mos; And in the past month, several instances of motion-like sickness/ nausea, dizziness, blurred vision, major impatience/ mood swings, loss of appetite (pregnancy-like symptoms...yep, I was thinking man I'd be pretty pissed if I was that 0.01% pregnant statistic), and as of this past weekend, my first aurora migraine with tunnel vision and serious nausea and vomiting, to the point where I went to Urgent Care...who referred me to the ER...who wants to perform a battery of tests including a head CT. I have an appointment with a trusted GP tomorrow to discuss possible root causes...but it is to coincidental that so many women are experiencing these same symptoms! I am certainly leaning towards having this removed. CAN THOSE OF YOU WHO HAVE HAD THIS REMOVED PLEASE RESPOND IF YOUR SYMPTOMS SIGNIFICANTLY IMPROVED OR WERE RESOLVED!!! THANK YOU!
These side effects seem to go well beyond a 5% rate of incidence according to all of you who have reported. I will investigate further and keep everyone posted. As someone who is highly experienced in the pharmaceutical industry, you bet your a$$ I'm going to get to the bottom of this! Good luck ladies!

I have been on Loestrin 24 fe for the past 4 years. Everything was fine the first year to my knowledge. Now that I have gotten older and started noticing things more recently I have become worried about being on the pill. I haven't had a period in 3-4 years and when some might say its a blessing I am starting to get worried about it. In the last 4 years I have gained and lost weight dramatically but now it I haven't been able to lose any weight started working out and eating less but going no where. Gained 15 lbs in 3 months. My hair is starting to fall out more than usual. I have been getting really nausea lately feeling like I am going to throw up, my vision is becoming worse but went to the eye doctor and my prescription is the same. My anxiety is getting worse and had to be but on Zantax to calm me. I had to take a pregnancy test the other to make sure i wasn't pregnant because of the most recent symptoms. I going to go off the bill tomorrow to see if a difference is made of not being on it.

Hi Everyone, I took my Mirena out myself 3 days ago. I have made a couple comments on this site about it, but now I have my own questions. When I first took it out I was thrilled for it just to be gone. I still am, only I feel lousy. My head hurts, and I'm cramping, which is probably because I started bleeding yesterday... first period since insertion (unless you count the month of bleeding that followed that). Anyway, my head is killing me, I'm exhausted and today I woke up and all I want to do is cry! Maybe it's just what they call the "hormone crash" or maybe it's my period. I'm also experiencing stomach aches and lightheadedness. I don't feel like myself! I am so tired and my back is still killing me. How long does THAT take to go away?? When am I supposed to feel like myself again?? If anyone out there has answers, I'd appreciate hearing them!

I have had my Mirena for 4 months now and I have also been miserable. I have been to my MD, tested for thyroid and diabetes. I went to my eye doctor because of weird vision problems. Weight gain even with exercise, bloated feeling, tired, hip and knee pain, back pain, hair loss...now I know it's all due to Mirena. I thought I was suffering from hypocondria since my doctor could not find anything wrong with me. I can't wait to have this removed, but at age 39 with 6 month old infant, I'm not sure what birth control method will be better.

My daughter had just about every reaction mentioned above. She was being treated for an acute flare of SLE (Lupus in the worst form.) Not only did she lose her kidneys (19 yrs old, second year in Pre-med at Baylor University. She began seeing strange "black ghosts" while in CCICU. The nurse talked to the Doc, he says oh, its only "ICU Psychosis". What??? She wasn't hallucinating, just strange vision. The came the pressure in her head. No one bothered to call in an Optho, so they did Lumbar Puncture after Lumber Puncture. They released us with the pressures still high. Suddenly, my baby sat up and said "Mother is my right eye open?" It was...I jumped into action, got her to a local doc who sent us running to Houston...my daughter lost all of her sight in her right eye and most of it iin her left, she has no peripheral vision or color in the tiny bit of vision she has. The depression is killing her. Her doctor says "yeah, it happend...200 out of 1000. Can you imagine..all he had to do was has a doc use his little light,look behind her eyes and my precious daughter would be simply waiting on a kidney and then back to medicine. Please don't let this happen to you or a loved one...insist that they call in an eye doctor. Our lives will never be the same.

I stumbled onto this website just today looking for information on another drug. Little did I know what I was going to find and so happy I did. I have been taking Zocor for nearly 5 yrs. now. My health has taken a spiral downhill. I too, have been experiencing almost every symptom that has been mentioned. Rt. shoulder pain, hand pain, pain and tingling in hands and feet, leg cramps, muscle weakness, numbness, memory loss, itching, fuzzy headed at time, can't concentrate, and trouble breathing. My doctor has told me my cholesterol is just fine the last two times I've had my checkup, but has never suggested I come off it. I guess I will be calling him tomorrow.

six months ago my dentist prescribed 500 mg and 500 mg of penn every eight hours for five days,, along with vicodin for a horribly painful gum infection in my root canal. To this day I wonder if I will fully get rid of all side effects of the Met. After 3 days I was soo dizzy and with extreme blurred vision, the pharmacist and dentist office stated it could not be the ant but the vicodin. I stopped the vicodine and just stayed with Motrin. I had the worst vertigo and blurred vision you can imagine, I felt like an infection was now in my brain, (yet was not) I felt like I had a toxic infection in my body. I would fight to concentrate mentally, I was very fatigued and sick feeling. This went on long after the tooth pain. It took about three months of strining for mental concentration, dizziness, toxic feelong to begin to go away. By the fifth month I could finally feel my personality had returned. Yet my vision has not and has only gotten worse. My dizziness is every so often. During the first months I kept running back and fourth to my doctor with no avail. It was the eye doctor MD that said he was very suspicious that I had an toxic allergic reaction to the Met. Between doctor visits, eye doctor visits, cat scan I have run my medical bills high. I am extremely worried about going blind.
It has now been six months - my health, my vision, my family, my job, my personality have all suffered from this.... Don't take this drug............

i'm glad that i found this site...thank you.
I have a seven year old boy and a four year old girl that have both been on singulair for a couple of years. The first year their allergies weren't that bad, so i didn't really make sure that they took it daily...the past year, allergies have been worse, so i was making sure that they took it daily and that they didn't miss a dose. My son was in 1st grade last year and by the end of fall, he was going to the nurses office daily for headaches and stomachs. Where his drawings used to be of flowers and all of us as a family, they started being of monsters. We also noticed that his pupils were dilated more than normal (you could barely see any of the colored part of his eyes) and took him to an eye doctor just to find out that his eyes were fine and there was no medical reason for the dilation. I also asked the doctor and the school to test for ADD/ADHD, with them saying that he didn't have it..At night, both my son and daughter started waking up for no apparent reason (they had both slept through the night since they were about 1) and being very scared for no reason. The mood changes have been more noticeable in my son, but like most, i chalked it up to "a phase" and just part of being a boy....my daughter got clingier and moodier, but i know how it is to be a girl, so i just took it with a grain of salt. My kids have not been on Singulair for approx. a week now, and my son is back to the boy i knew....skipping through the house and yard, catching bugs to just look at them and not pull them apart and kill them, sleeping through the night, no trips to the nurses, and eyes that seem to be normal again...my daughter is actually a pleasant little girl that can't wait til she see's her brother instead of pinching, hitting, and trying to hurt her brother........Long story short, since they've been off of singulair, i have my kids back. my son had circles under his eyes at times and a runny nose at times and we have to find something to help my daughters allergies (she gets eczema and is borderline asthmatic) but we will deal with that and find something that works without harming them.....
Thanks again.

i was given these eye drops after cataract surgery. blurred vision occurred along with severe pain on the whole side of my face into my jaw. twice back to eye doctor with no results. onto family doc. she diagnosed trigeminal neuralgia. had bad taste in month, down throat. reported these symptoms to eye doctor with no results. when i called and told them results from family doc. then was told to stop the use but i had already done so as it was usually the last drop i put in with the application of the other three types of drops i am using that had no bad affects.

I'm an adult female with severe sinus polyps, adult onset asthma and allergies. Initially Singular seemed to be helping my nasal polyps, when nothing else helped in any way. I made several attempts to use Singular, and proved repeatedly that this medication did, in fact, cause me severe side effects - even when I used a childs dosage. While using an adult rx for Singular, I immediately began experiencing horrific nightmares (which I have never had in my entire life). I also had extreme knife like pains in both ears, which made me feel like I had a severe ear infection, chest pains where it felt like a cinder block was lying on my chest, and migraine like headaches (which I've never had). I stopped the medication after about a week and the nightmares went completely away, but it took me a couple weeks to recover completely because I developed what felt like a respiratory infection and ear infection as soon as I stopped using it. Because Singular seemed to slightly reduce my nasal polyps on my first attempt, my allergist suggested I try using it again - almost a year later. When I first began, I completely forgot about the negative side effect and why I stopped using it in the first place, and just gave it another try. I again experienced the same horrific nightmares, ear pains, but this time got a strange rash/cluster of blisters under both eyelids which my eye doctor confirmed was an allergic reaction to something I was using. Singular was the only medication I had changed. My allergist thought I should give it longer to see if the symptoms went away (because they probably weren't caused by this medication - and were due to something else ???). Fearing going to sleep, I decided to try taking the medication in the morning instead of night, and had my physician reduce my rx to a childs dosage (5mg). The nightmares lessened, and the blisters under my eyelids went down, so I continued using Singular for about a years time. What I didn't realize, was that over this time I was becoming depressed, fatigued, and became easily agitated and short-tempered, which was very different since I was normally a very happy, energetic mom. My nasal breathing seemed to be slightly improved, so I just kept taking the medication - not realizing that it was causing all of the other problems I was experiencing. I became so fatigued and depressed feeling, that all I wanted to do after I got my kids off to school was to sleep until it was time to pick them up in the afternoon. I was also experiencing stomach pains for unknown reasons. I was certainly not myself. I didn't realize that while I was using Singular I had lost complete interest in everything that I normally loved in my life. And please note I'm 45 years old, and I was using a childs dosage. ( I can only imagine what this medication does to a child. )Fortunately for me, I accidentally forgot to refill my prescription for a few days and noticed that my depression started to improve. I decided not to refill my rx and stay off it to see if I continued to improve - and I have. Unfortunately, even though my depression has all but gone away, I'm experiencing symptoms which must be from withdrawal of the medication - and they are just as scary as the side effects were. Now that I'm not taking Singulair any more (and I've made no other medication changes), I have extreme fatigue beyond belief, and ache everywhere. My muscles are in such pain that I'm having difficulty doing things I would normally do. I have extreme weakness in both arms and legs, and my back aches almost constantly. And strangly enough, my asthma and allergies have slightly improved since stopping Singular - I thought for sure my allergies/asthma would worsen when I stopped completely - but they did not. All I can say is - please trust what your body is telling you - even if your physician tells you otherwise, and do not use this medication or any other if you experience adverse side effects to it. I would never give this medication to a child that wasn't old enough to tell me what he/she was experiencing, and would document the childs temperament, ailments if any, and what changed once the medication was started - and discontinue it immediately if even one adverse side effects occurred. One last note - I am still experiencing vision problems, which I feel are due to using this medication. Hopefully, no other permanent damage to my body will result from the Singular that I've already used - and I hope you Singular users will recover completely too from its dangerous side effects. Wishing you the best of health!

I took Doxy for about 2 weeks as a remedy for a bump on my eyelid. This first exposure to Doxy seemed only to cause a little skin sensitivity and burning in my fingers, no big deal.

When my eye problem didn't go away, my eye doctor prescribed Doxy for a second time a month later. This time my side effects were much different. Within a couple hours of taking my first pill I felt a bit off, I felt anxious and unsettled. I Continued on the medication for a total of five days. During this time my side effects progressively worsened. The first few days I had very abstract thoughts, and began feeling strangely claustrophobic. By day three I was beginning to feel paranoid and fearful over just simple everyday things. Day five is when it all hit the fan. I started having difficulty breathing and feeling extreme tightness in my chest. My feelings of claustrophobia had also worsened to the point where I began having panic attacks, like I was trapped inside my own body. It was at this point I made a desperate attempt to search the internet for a possible cause, in hopes it might be the Doxy medication I was on. I was somewhat relieved to find this website and read that others had similar symptoms, maybe I wasn't losing my mind. I immediately quit taking the medication, but unfortunately the symptoms didn't go away for several more days. That night I was unable to sleep, I had mild nausea, and would wake up in the middle of the night in a panic and would shake uncontrollably. Lovely huh. It gets worse. I began to feel extreme fear and paranoia like I was going to die, or lose my kids and family. I began to feel if this didn't go away, I would not be able to go on. Thank God it did, and by day eight the extreme thoughts began to subside. I continued to have the breathing difficulty and mild depression for several days after, but the worst was over. Within a month I was back to normal.

I write this as a warning to those who are taking this med and feel anything close to this... stop taking it! I am a healthy, normal, 40 year old male, that has no history of mental issues, other than a "blue" day from time to time, and within six days I was entertaining thoughts of suicide. The psychological side effects of this drug NEED to be addressed. This is very serious stuff!!!!!!! Though it may be a small percentage of people that are susceptible, for those who are, it is a deep dark hole.

I started right out 3 years ago on 100 mgs. and within a couple weeks migraines were virtually gone! I thought it was a miracle! Only slight side affects for a couple years and only an occasional migraine but not a three day long one. So, I figure, small price to pay for all that relief, right? Now, for the last 6 months or so I'm falling apart! My memory is just gone! Sometimes I'm afraid to leave my house because I'm afraid I'll forget my way back home! I can hardly concentrate long enough to put a meal together and it just took me 4 tries to remember how to spell concentrate! Thank Goodness for spellcheck! I've lost 42 lbs. that I can ill afford to lose and I now I have started to have these anxiety things that I've never had before. I feel scared and nervous and no idea why. I was on a couple of drugs for allergies, a couple for arthritis and a vitamin. I dropped everything except the Topamax and the DR. put me on a 1/2 mg. Zanax twice daily for anxiety which seems to do nothing except make me sleepy. Now it seems all these side affects have just bloomed and I have this constant ache over my right eye which isn't a migraine but never goes away. I'm afraid to just stop the topamax because of what I've read about suddenly stopping. Doctors are no help, they won't even admit there is a problem. They just wanted to check my thyroid.It was fine.

I have been taking Omeprazole for 2 months! I did experience relief from my acid reflux. Here are my side effects: Extremely dry mouth, blurred vision, itchy eyes that feel like sandpaper. My eyes are extremely sensitive to light. Just two days ago I woke up with spider like webs that appear in the front of my eyes. My eye doctor told me that the fat-like jelly substance in my eyes has torn to cause this effect in my eyes. I also see quick flashes of light. My eye doctor says this is a side effect of this medication. My whole body feels like all the acid in my whole body has dried up!

I will no longer take this medication. I will find alternative help for my acid reflux! I do not want to lose my eyesight!

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan

PS Does anyone know how long these severe body aches last after completely stopping. Its been 6 weeks and its just a little better. My doctor told me to fight it out or get back on pred. NO WAY!!

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan V

I'm experiencing some VERY concerning symptoms and have a feeling it might be from the Mirena. And my doctors think it's just stress! SOMEBODY HELP!

I had a baby 4 months ago and at my postpardom appointment I was talked into getting the Mirena. After I had it inserted it all started with severe cramping and light bleeding that still has not subsided. I have been suffering with chronic headaches, dizziness, and facial numbness. I've also had bouts of anxiety and leg cramping and recently starting to have pain in my neck and one of my lymph nodes on my left side has become present and tender to the touch.

I mentioned all the these symptoms to my OB/GYN and he said "it's NOT related to the Mirena, go to your Primary Care Dr. and get some tests done" Well, I did that, got a full CBC and had my thyroid checked and all of my blood work came back normal. My Dr. said I am stressed after having the baby and to get some rest. I really wanted to have a CT done but after reading this I am beginning to think it's the Mirena as I had not had any of these symptoms prior to the IUD. I think i'll make an appointment to have it removed.

Anyone ot there have any of my exact same symptoms???

I gotta tell ya this is scary. I am a 30 yr old guy my wife is 27 we have four children.Our last one was born Mar. 2007 She has been on Yasmin 6months or so.She has never been regular on periods. Well a few weeks ago she started having massive headaches.As of June 31st her doctor said she has migraines. Well by July first her left eye went blurry by the 2nd she has lost vision in both eyes.She only sees light and is very cloudy and can see shadows. We made 3 trips to ER. They did Cat scan and it was neg. the doctor said she might have even had a mild stroke because her left cheek went numb. By the 2nd we were in ER again because of total vision loss. They did a lumbar punture and no Meningitus. cat scan again neg. blood work neg. except UTI sound familiar ladies??? By the 3rd we visited her doctor and she passed out and was rushed by EMT to Hosp. They did and MRI,MRA,had a eye Doctor called an ophthalmologist clear her of vision problems.She has talked to a neurologist. So here is a 27 yr old female with all the test's coming back normal but she can't see.They even had a psychiatrist talk to her because she is on Prozac because she has PCOS and had half her ovaries removed and almost died.They even suggested that she had conversion disorder(google it).Finally I decided to check side effects for all her meds. When I checked this one I almost jumped outta the chair.She has about 10 symptoms. But before I get too excited has anyone had vision loss for a period of time and did it come back once off of it?? I'm throwing these away

Here are some more side effects that I encountered during my ordeal with Lipitor. A week after I started the medication, I started experiencing blurry and decreased vision, this used to go away and come back sometimes, I could swear I always had 20/20 although I never went to eye doctor, but I never needed glasses all my life, if fact any type of glasses will blurry my vision and make me dizzy. I had my first eyes exam a couple days after I discontinued Lipitor, guess what? I have 20/20 vision.
More details about the back and right arm pain, not only the pain was unbearable, I felt my muscles sagging and they did not have any strength, this thing sucked the life out of my muscles, it made me very tired and easily irritable. My fist victim was my little baby ( my beautiful 4 year old), her daddy couldn’t hold her anymore, I even avoided staying close to her, because anyone who touches that right arm will make it feel like another deep stab to the arm deep into the bone. I have never experienced pain like this. I knew about toothache when I had a cavity at 23, but it was fixed and went away, I even experienced the pain of a broken arm at 16, but this thing was something else. The other victim is my wife, I stopped doing stuff, I used to be a very active dude, I do stuff on weekends with family and even every day after work ( you name it, park, boating, swimming pool, malls etc..). It felt like I was dying one piece at a time, going down the tubes fast with no clue of what was wrong with me.