July 21st symptoms and conditions

Hi. I just had my mirena placed on Sept. 5th, 2008 (5 days ago). I decided to go with this after just giving birth to my 2nd daughter on July 21st, 2008. All my girlfriends have it and recommended it as well as my ob/gyn. I read and watched a dvd about it and then after being told it's only going to cost me my copay of $27, I said oh yeah--for 5 years worth of bc, you bet! Anyhow, the insertion was quick and painless as I had just ended my period that morning, just had a baby 6 weeks prior, and my ob/gyn numbed my cervix. I only bled for about 5 hours after. After my doc placed the mirena he told me if I wanted to that night I could have sex with my husband and nit have to worry about a secondary form of bc. I was not able to that night due to my 2 children (one is 4 and the other is now 7 weeks), but we did get to the next day. I have actually had an increase in my sex drive since having this iud placed and maybe it is just the simple fact that it is a hassle free form of bc that is 99.9% effective. Lately however, in the last couple days I have been feeling irritable, increased anger, depression (which I already take meds for-but don't seem to help-they always had before for 10yrs), crying spells, a lot of anxiety, heart palpations, hard to get to sleep, severe headaches (not quite migraines), hot flashes, lethargic, and now nausea. If some of these symptoms don't go away, I may have to find another bc/iud that would better suit me (perhaps non-hormonal). I don't know that I would recommend mirena to anyone, but I also would not tell anyone it's horrible. Everyone's body reacts differently to medicines. So, if you have one good luck with it and if you're deciding on one, please read all the side effects and testimonials you can-on any that you choose and don't think it can't happen to you-you just never know! Hope this helps someone!

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

After reading so many of everyone’s stories, I feel I got off easy, but not without some agony. I developed a double whammy of acute bronchitis and pleurisy in my left lung. If you are not familiar with pleurisy, it feels like hit with a baseball bat in your ribs each time you attempt to take a normal breath. I was completely uninformed of the condition and it is now burned in my memory forever. I was prescribed azithromycin and Prednisone for a month. I started with two 20mg (40mgtotal) tabs for 7 days and then tapered off in the following manner. 1 ½ tabs for 7 days, 1 tab for 7days and then ½ a tab for the last 7 days. I have read many of the users who have been on Prednisone for years at a time and my heart goes out to each and every one of you. I experienced a large number of side effects for being on it for such a short period. My wife was ready to attach the ole cinder block to my ankles and drop me in the lake, but she stuck through it. The first side effects began within the first week. My appetite went through the stratosphere, my heart felt like it was going to erupt out of my chest on some nights and finally, my memory just went to (for lack of a better work) shit. After coming home from the grocery store on multiple occasions, I left the house key in the key hole on the outside, only to find it the next morning on my way out the door. My short term memory was just misfiring constantly. There are too many funny stories to tell. For some odd reason, I did not gain near as much weight as I should have given the mass quantity of food I ingested. The total weight gain was only around seven or eight pounds. The most prominent side effect was my mood swings. I am a laid back person my nature, but not for that 30 day period. I had to make a conscious effort to not put myself in a position to disagree with another individual. When it did occur, it was just not a pretty site. A few of the other side effects were lack of sleep and profuse sweating. I would wake up every morning and my pillow was drenched. I live in Austin, Texas, so the AC was pegged and 67 degrees and no one was allowed to touch the thermostat without grave consequences. I broke out the winter pajamas for the kids and my wife wrapped up in multiple layers of clothing, while I was spread eagle under the ceiling fan (Highest setting of course) in my birthday suit, and was still only the in the moderate comfort range. More side effects included swelling of my ankles and hands. I was not on it long enough to get the infamous moon face or the hump on the back of the neck. The side effects after stopping the dosage were no less entertaining. I took my last dose seven days ago. The three main effects have been rashes on my ankles and under my arms, severe energy loss and heartburn. The worst of it all has been my energy level, or the lack of. My energy level crashed so hard I have had to literally peel myself out of bed each morning. If I did not have a two year old daughter and a four year old son, I would probably still be asleep right now. It has been getting a little easier each day. I have started walking each morning now and hopefully this will end soon. I have also been drinking large amounts of water. That has seemed to help me out. The heartburn was easily treatable with some Pepcid AC. I hope my experience offers some solace to those in a similar situation and fair warning to those who are about to embark on this medication.

This may not be a very clear post. I am having difficulty remembering words and events. I had surgery on July 21st for a damaged nerve in my foot. The doctor put me on 500mg of Levaquin. I stayed on that dose for about 2 weeks. My foot and leg began to swell. I was also having trouble thinking. I was having muscle spasms in my legs and my right arm began to hurt. The doctors thought it was because my foot was infected and it had gone to my leg. To combat the infection they increased my dose to 1000mg of Levaquin a day which I have been taking for the last 4 weeks. I continued to get worse. They checked my leg for a blood clot last week and told me there was no way my arm pain was related. Of course there was not a blood clot. My last dose was yesterday, but when I woke up this morning I couldnt get out of bed because my leg and arm hurt so bad it felt like I had broken them. I have not even mentioned all of the crazy things I had started doing. I keep getting the year wrong and I say things that make no sense. Sometimes I would know a word but I could not say it out loud. The side of my head began pulsating today and my doctor was out of the office. I went to another doctor thinking I was having a stroke. He immediatly asked me if I was on Levaquin. He was shocked at how much I have been taking and told me to not renew the prescription. Now that I have gotten home I have a new symptom, bloody diarrhea. I have have diarrhea for the past 6 weeks also, but now there is blood. I am about to lay down and I hope now that I am off the Levaquin I will begin to feel better. After reading this site I am very worried. I own a mortgage company and I think everyone who works for me has begun to think I have lost my mind.