Skins symptoms and conditions

I have been taking 20mg Lisinopril for six days for 140/100 BP reduction. Muscle cramps, muscle pain, dizziness, ringing in the ears (which I already had, but this medication has made it MUCH worse),some heart palpitations...generally scary and, on balance, I am going to find some other solution. Frankly, this is like taking a slow acting poison.

Has anyone had the itching? The horrible horrible itching like you want to peel your skin off in a not very pleasant area? My doctor started me on NuvaRing last Monday and ever since it's been like my skin is on fire. I took the ring out last Sunday, but am still itching sporadically. It's pretty unbearable. Any ideas on how to handle? Any help would be appreciated.

Hi everyone, like almost all of you I was so glad to stumble across this site. I had my mirena put in 4 months ago and when I was getting it put in my partner took the day off work and decided to tell his boss it was because he was coming with me to get the Mirena (I was horrified that he told him at the time!). But it turned out to be a blessing because my partner came home 3 days ago and told me that his boss asked him whether I had been getting deep pimples that never come 'to a head' and that his wife had them all over her face and couldn’t get rid of them and that she had put it down to the Mirena. I said to him, "Don’t be ridiculous, the Mirena does not give any side effects", and that was that. See I was told from my gyno that "The Mirena is perfect" and she said that the only people that go back to her to go off the Mirena "are people that are never satisfied with any contraception". And then over the past three days I realized that the bumps on my face that are deep under my skin have only appeared in the months after I got my Mirena and I have had worse pimples than ever before, and they have been untreatable with new ones appearing every day and I had never before had lumps that remain under my skins for months. It also wasn’t until I got onto this website that I realized the anxiety I have been feeling in the last couple months, weight gain and itchy skin have also all come about since the Mirena. I am tired all the time and never want to move or do anything and hate getting out of bed even with 14 hours sleep!!!!! Also - I have been pulling clumps of hair out of the shower drain and my comb over the past couple months - yet have had the same hairdresser and hair routine for the last 6 years.... I could not figure out why I was losing my hair and ended up having it cut from a mid-long length to above the shoulders 3 weeks ago, because there was just hardly any hair left. Also - about 2 weeks ago I told my partner (in an emotional uncontrollable episode which has become a frequent event since Mirena) that I had no reason to live anymore and just didn’t want to go on. First time I have ever felt like this, it was awful. I am normally the happy person at work who gets along with everyone and yet now I cant stand the look of any of them or even the sound of their voice makes me want to scream at them. WHOA, CRAZY!!!!!!! I have also lost any interest in self appearance and in the past few months have completely let myself go. I have also had sex twice since going on it. YES thats right - SEX TWICE IN FOUR MONTHS, aaaaaarrrrrgh. And to the most disgusting part of all - I have been getting an awful discharge that smells bad. I am a really clean person and was considering going to my gyno in the coming week to ask why it was happening….. I have been on many pills and the depot and whilst I experienced side affects with all of them, none of them were anything like this, I would get a side effect here and there on the others, nothing like this. Biggest waste of $800 ever. p.s. I wear panty liners every single day and night of the week.

Hi everyone, like almost all of you I was so glad to stumble across this site. I had my mirena put in 4 months ago and when I was getting it put in my partner took the day off work and decided to tell his boss it was because he was coming with me to get the Mirena (I was horrified that he told him at the time!). But it turned out to be a blessing because my partner came home 3 days ago and told me that his boss asked him whether I had been getting deep pimples that never come 'to a head' and that his wife had them all over her face and couldn’t get rid of them and that she had put it down to the Mirena. I said to him, "Don’t be ridiculous, the Mirena does not give any side effects", and that was that. See I was told from my gyno that "The Mirena is perfect" and she said that the only people that go back to her to go off the Mirena "are people that are never satisfied with any contraception". And then over the past three days I realized that the bumps on my face that are deep under my skin have only appeared in the months after I got my Mirena and I have had worse pimples than ever before, and they have been untreatable with new ones appearing every day and I had never before had lumps that remain under my skins for months. It also wasn’t until I got onto this website that I realized the anxiety I have been feeling in the last couple months, weight gain and itchy skin have also all come about since the Mirena. I am tired all the time and never want to move or do anything and hate getting out of bed even with 14 hours sleep!!!!! Also - I have been pulling clumps of hair out of the shower drain and my comb over the past couple months - yet have had the same hairdresser and hair routine for the last 6 years.... I could not figure out why I was losing my hair and ended up having it cut from a mid-long length to above the shoulders 3 weeks ago, because there was just hardly any hair left. Also - about 2 weeks ago I told my partner (in an emotional uncontrollable episode which has become a frequent event since Mirena) that I had no reason to live anymore and just didn’t want to go on. First time I have ever felt like this, it was awful. I am normally the happy person at work who gets along with everyone and yet now I cant stand the look of any of them or even the sound of their voice makes me want to scream at them. WHOA, CRAZY!!!!!!! I have also lost any interest in self appearance and in the past few months have completely let myself go. I have also had sex twice since going on it. YES thats right - SEX TWICE IN FOUR MONTHS, aaaaaarrrrrgh. And to the most disgusting part of all - I have been getting an awful discharge that smells bad. I am a really clean person and was considering going to my gyno in the coming week to ask why it was happening….. I have been on many pills and the depot and whilst I experienced side affects with all of them, none of them were anything like this, I would get a side effect here and there on the others, nothing like this. Biggest waste of $800 ever. Mirena = Evil.

I am writing on behalf of my elderly parent, Carmela, who has been diagnosed with Lupus since 1991. She has been on a small dose of prednisone since her diagnosis in 1991. In the last several months she has developed very many odd hazey type grey spots all over her body. Dermatologists and doctors are not giving her any answers. They took her off predisone because they THINK this may be the cause. She is on an inhaler and does not like it. She wants to go back on the prednisone as she is feeling chest congestion and lethargy. I read an article on the internet that describes prednisone may cause unusual bruising. I'm not sure if this is what her spots are. They are only the color grey and appear to be beneath the skins surface. They are soft or hazy looking. They are small, about the size of a dime. Has anyone heard of this before in Lupus (prednisone) patience. Any info you have is sure appreciated. S. ******

I had the Mirena put in September 07' and have had it for over a year now. I have gained 15lbs so far, and have had constant acne/skins issues. Also I have reoccurring bacterial and yeast infections. Apparently the Mirena is throwing off my ph. I too have no libido. I will be getting it removed asap.

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.

I am having severe all-over pain, electrical like jolts, headache and chills. I've had these symptoms before and they were gone in days when I stopped. Now it's not going away after 7 days. Last night I couldn't fall asleep because I was freezing and my skins hurt all over, just like the flu. Has anyone had symptoms this severe disappear when Advair was stopped?

I don't smoke, am thin, a healthy eater and have no other diseases and take no other medications except vitamins.