Seeing spots symptoms and conditions

Thank You!!! I'm not the only one! I had the Mirena inserted in 2005,removed in Sept 2008. Painful cramping immediately that continued at odd times throughout time I had it. Bleeding for the first 4 months. Back Pain followed and landed me in the ER. At the ER I was told that I had blood in my urine. Antibiotics had no effect. Back pain continues today but is markedly less. Major mood swings leading to depression. Took Zolft at increasing doses with no effect. Never been prone to any of these before. Rages would come on over the littlest things. Extreme anxiety attacks leading into panic that left me completely irrational. Almost lost my husband and kids due to mood swings. Joint pain came then in my lower back and shoulders and wrists. Saw doctor, no reason ever found. Lumps showed up in my breasts that would swell and receed with my monthly cycle. Extreme sensitivity during sex with bleeding and cramping after. Cysts on my face and large acne bumps on my back that were so painful to the touch i could not even wear a bra. These spots took weeks to go away. Headaches that left me sick and weak on the couch seeing spots. Dr's insisted these symptoms were not related to my birth control.I had tons of fatigue but chalked that up to the depression. I also started having a lot of trouble with dryness in all of my mucus membranes. Even my eyes hurt. Over and over saw many dr's never could find what was wrong. This birth control nearly ruined my life and cost me three important years with my kids that i should have been at the top of my game. I have girlfriends who have received the mirena with almost exactly the same progression as me. I feel deceived by the listings in the information pamplets I received. I expected bleeding and slighter periods but never did they list these symptoms. I even looked at their website before I received it and they are not listed there either. I even had an argument with my gyno about having it removed because he knew of none of these side effects. I have seen a significant change since the removal. Mood swings down, energy back up. Kids say I'm like a whole new mom. To those ladies interested..contact K. in Texas to find out information about a class action law suit being filed.****** Don't let anyone else be hurt by this product. Who knows how long this is going to negatively affect our bodies?

I have waited long enough to tell my story. I am a 29 yr old single mother of 3. I started YAZ in Feb of 2008. I took it for 11 days. ELEVEN DAYS. It was about 4 days in that the headaches started. I couldn't stand light, I wore hoodies and sunglasses. I was nauseated. Saw double, black spots. Motion sickness.I could barely make it to work. I was out of control. I did not have control over my mind. I was crazy. My friend almost took me to the hospital to have me committed. There is no history of this in me or my family. The headaches would last from the time I woke up til the time I would go to sleep. Painkillers was the only thing that would keep me asleep through the pain. My dr immediately stop the the pills. I saw an eye doctor and they found nothing. They ordered an MRI. They found T2 Foci scattered throughout my brain. VERY unusual in someone my age. What that is, is my protective covering of my brain cells had been damaged there were gaps in its covering. I soon developed a stutter and a slur in my speech. The pain then moved throughout my whole body. They said fibromyalga and daily migraines. I'm now on topamax daily which gives me breaks in my headaches. I still get them daily. I still have pain in my body daily and I'm on painkillers daily. I have found a new dr who is wonderful. Who has recently taken blood. Who thinks that maybe it could be lupus. So I started researching Lupus...my symptoms and rashes match up. There is also a DRUG INDUCED LUPUS. and ORAL CONTRACEPTIVES is a KNOWN drug that can cause this!!! BUT IS THAT ON THE LABEL???? NOOOOOOOO!!! I was perfectly healthy before yaz, in kick boxing and now I walk and have the memory of a 60 yr old and my brain is permanently damaged. I have another MRI coming up to find out if there is more damage and I will find out the results of the blood work to find out what is wrong with me...but I blame all of this on YAZ and I hold them responsible. I SAY CLASS ACTION LAW SUIT....just have to find a firm with big enough BALLS to do it!!!

I have been on Warfarin since the end of Aug. 2007 when I had my mitral valve replaced with a mechanical valve. I will be on it for the rest of my life. My doctor.'s all assured me there were no side effects other than the bleeding risks. I now know this is not true. The side effects I am dealing with make me sometimes wish I had chosen a tissue (pig) valve, even though I would be guaranteed another heart surgery within ten years. I am 39 years old and a mother of two young kids. Since being on Warfarin I have experienced various body aches that come on suddenly but don't stay long; extreme hot and cold; itchy hands and feet; dry hair and hair loss; seeing "spots" usually followed by a headache; very thirsty; ongoing bowel troubles, possibly developed colitis; but the worst side effect for me is the fatigue and depression. I feel like I traded in my old self for my mechanical valve. Like I said, I'd have to have a tissue valve replaced eventually, and as bad as heart surgery is, I'd rather have 10 happy years w/out Warfarin than this struggle I deal with almost everyday. My brother is a surgeon and even he buys into the "no side effects" b.s. I work out as much as I can, which used to make me feel great, now I feel like it helps me get by but not the positive effect it used to have on me mentally.

I have been taking Yasmin for 2 months and suffer the following symptoms for the last 7 weeks, lack of balance and co ordination, problems walking which consist of shaking wobbly legs its like they are made from jelly , shortness of breath, palpitations, panic attacks, clumsiness, stomach cramp, constipation, diarrhea, clots whilst not menstruating, headache, blurred vision, dizziness, seeing spots, light headed, aching muscles, fluid retention, swollen hands and feet, abdominal pain, lack of period, mood swings, nausea, lack of appetite, sore breasts, bloatedness, tiredness, insomnia, pais in my chest, has any one else got these symptoms?

I was prescribed 5 days of 500 mg of Levaquin for a possible UTI. I had some vision disturbances - seeing spots and shapes that weren't really there on the 2nd day. On day 3 I had a night of complete sleeplessness. On day 4, I noticed a slight soreness in both calves. I thought it was just from gardening. On day 5 (after I had taken the final dose) the calve stiffness/pain got much worse - it was like the muscles had become extremely tight and was centered around the tendons. I realized it was from the Levaquin when the insert and way down at the bottom it said to call your doctor if you had leg or tendon pain. Since then, I have looked at several sites and it's very scary. I can only hope that the leg pain goes away in a few days - I can hardly walk and it hurts with every step. I have always been a very active person. If this is permanent, it will change my life completely, as I walk everywhere and right now can barely get down the street or up and down stairs. My doctor said that only prolonged use would cause tendon tears, but that is not what I am reading. It damages cartilage, muscles, tendons. That's one of the reasons they don't prescribe it for under 18-year olds.

It should not be prescribed for anyone. There are thousands of entries on the web about the sometimes permanent and very serious side effects of this toxic antibiotic. I feel very sorry for all of us.

Marianne
7/3/07

Girls,

just wanted to ask did any of you expereince the feeling like you were under water with your head???I have had severe blurred vision and seeing spots, is that another yasmin Legacy.....
Lisa