Yahoo symptoms and conditions

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

I've been on Mirena for about 14 months now. For the past 3 months I've experienced this awful allergic reaction on my face. I'm not completely sure it's being caused by the Mirena but it's weird to me that every time I've gotten this rash it's been between the fist and last day of my period. the rash starts with hives on my nose, chin, under my lower lip, and cheeks, and by the next day is blisters that crust over. By the 4th-5th day or so it's just very dry looking skin. It itches and burns so badly though and I don't know if I go through this again. If anyone has any insight PLEASE email me at ******!!!!

memory loss, headaches, tias/mimi strokes, kidney stones, blood clot,vertigo, disorientation, muscle spasms, shaking, trembling could not control , dry eyes, stiffness in neck, back pain, twitching of all muscles , blackout when really sick, cant hold arms up, thought I had Parkinson, ms or Muscular dystrophy, motor skills are no longer great, arms and leg muscles bad, cannot write much at all, no strength in fingers or toes.
chronic fatigue and fibromyalga diagnosed not so sure after reading all these side effects.

My 19 yr. old son recently starting taking Levaquin for a tonsillitis (throat infection) and he has now had severe chest pains from the Levaquin. Has anyone else reacted this way from this medication and if so, what did you do to get the chest pains to stop. He has stopped taking the Levaquin, however the chest pains have not lessened. When he tries to eat something, the chest pains get worse. Please someone out there help me if you can! I hate to see my son in such pain.

i got mirena 2 weeks ago, since then i've experienced all the side effects..the worst is i've become so depressed that my fiance' is scared to death i'm going to hurt myself...my depression is broken up by periods of extreme anxiety..i'm afraid this is destroying my relationship..i am normally a happy person who likes to have fun and now all i do is cry and scream at people for no reason...and sometimes i have to fight hard to keep it from getting physical. I am now in the process of getting it removed because the mood swings are scaring me..not to count all the back pain, acne....and i work out and keep gaining weight..my fiance' and i are now looking into other forms of contraceptive....if anyone has any hints as to how to get over this or what else may work...please email me ****** any advice is welcome.

I have been on Cymbalta for close to 2 years for the last several months I have been forgetting more and more.. more frequently! My doctor increased my dosage from 90mg to 120mg. Now, I have had a nervous breakdown/anxiety attack was admitted to the hospital's outpatient treatment program and have lowered it back to 60mg. It is very hard to ween off of. The hospital doctor has prescribed Lamictal and Trazadone and my gastroenternogist has put me on Amitryptiline. Gee I feel like a Pharmacist now. This sucks! All for Clinical Depression and Fibromyalgia and IBS, Does anyone else have memory problems while on Cymbalta??? email me ******to talk.

I AM SO GLAD TO KNOW THAT MOST OF YOU HAVE THE SAME SYMPTOMS. I am 25 yrs old and I went from 117-162 in about 4 years. I have been miserable!!!!! I was diag. in Aug. and have been taking SYNTHRIOD ever since when I first started taking it I took the medicine in the morning like the bottle and the doctor recommends, but I felt just like all of you. So I tried taking it in the afternoon for kicks and giggles to see if it would help at all. After about a week taking it at about 2pm I started feeling like a champ so I continued and now a month later I have lost 10 pounds. Just a suggestion......... The one question I do have is that I recently noticed that I have actually been ovulating and I am convinced that I haven;t in years hince why I have no kids I guess... Could your thyroid levels mess you up that bad to where you spend years not ovulating or should I go through the expensive process to see a fertility specialists. This is a question that I asked my doctor and of course they want to do 1000 $$$$$$$ tests to find out. Which I have no problems with in the future if worse comes to worse but I would like some advise from my fellow hypo sufferers and see if anyone was in the same boat as mee before being diag.

I have contacted an attorney in Delaware who is willing to pursue a possible class action suit. I explained my side effects from this drug and told him of the countless others that are suffering as well. He said if I was willing to do the "legwork" and gather up names of others who would like to join this suit, perhaps we could get a class action started. If anyone is interested please reply by contacting me at ***** Please be sure to type "Kenalog" as the subject and include your name, email address, and a description of your experience with Kenalog. I will than gather your responses and forward them to the attorney. He will than contact you individually, so please include a contact number. This will take some time. So please be patient, as you know these cases take time. I have spent 15 months trying to get some kind of help from various doctors, to no avail. Someone needs to step up and take responsibility.
Hope to hear from many of you. Thank You

HORRIBLE SIDE EFFECTS FROM YASMIN!
I am 21 and I have been on birth control pills for 4 years. I used to be on a generic low dose hormone birth control until i developed an ovarian cyst which the doctors told me was because of the low hormone. So now im on Yasmin and i have been on it for 2 months. So far i have gained 6 lbs ( i have weighed the same since 9th grade until now), and i eat healthy , my eating habits have not changed. I am also super moody , i feel depressed, can't sleep, constantly crying, me and my fiance are constantly fighting because of my mood swings. I also get horrible cramps during my period and i bleed about 11 days after i have just had my period. The side effects are awful and Im thinking about switching to Mirena because I cant handle this anymore. Hope my experience is helpful.

I had the cortisone shot in my right knee and then got this terrible headache and couldn't sleep was like I didn't need to sleep
could this have some side effects from the shot?
by *******

i have been taking eltroxin 0.1mg. for more than a couple of years and i could not understand why i always feel dizziness,headache with vomiting,tired , legs cramps,easy cold & muscles joints pain please explain my e-mail add is ****** thank you and wait your reply

I am taking Wellbutrin and it has helped my depression and desire for drugs every day. I have bad ringing in my ears all the time but I can deal with that compared to the good it has done.. The problem is I'm a engineer which requires a lot of concentration that I have lost since I've been on Wellbutrin. I also have memory loss. I can't remember peoples names 2 minutes after they told me. I am a support engineer so I have to tallk to many people every day as well as typing cause and solution. I find myself having to read everything I type over again because I leave out words and sometimes what I type makes no sense at all. Wellbutrin has helped me so much but I think I will have to stop or lose my job. What a choice. Before I started taking Wellbutrin I never felt like I was in tune with the world. Smoking pot worked for me but we all know what the long term effect of that is. Codine also made me feel like I fit in. So Wellbutrin has fixed all those needs and feelings but I just hate the loss of memory, concentration, and ringing in my ears.

I have had the Mirena since October 2006. My Public Health Nurse suggested it...It was to help with my mood swings, such as crying all the time, and the feeling that something bad was going to happen. Once I got it,,,I noticed that I did not cry on a whim, in fact I could hardly cry! My nose and sinuses would actually hurt if I did have the need to cry...almost like my body was fighting the urge to cry. I did get neck pains and also I was not having my period for MONTHS! Until, I went to see a traditional healer and he told me that I was very sick...he gave me a special root to help me...and I bleed for 7 days straight..I felt so much better! and lost a little weight. But, the feeling of panic went away. But, now i notice that I am getting dizzy constantly, I cannot even bend to put my socks on. I walk with my hand on the wall to help me just in case I do fall....I have fallen 2 this week alone. I did have some neck pain recently, and I went to the doctor he basically told me I have fluid in my ear and it would take 6 weeks to go away...I told him about the neck pain in my neck on the right side...he never even bothered to check it. I am starting to wonder now If this birth control is even worth it...and I am seriously thinking of having it removed and then getting my tubes tied. I hope anyone out there who has the same symptoms like me would send me a message....******

Oh My God! Reading all of these is like reading about myself. In the last 8 weeks I have gone from being a somewhat normal person to a babbling idiot! I cannot concentrate on anything, cannot function in any normal manner, have become so depressed it is all I can do to get out of bed and get my kids to school in the morning and get myself to work,,,,,,,,we have never eaten out so much in our lives! I miss more work now then when I had migraines, and my doctor will not listen. I have tried to tell him that the Topamax is not working for me, but he insists that I keep taking it. I have tried cutting back, and the effects are worse then, I become edgy and irritable, and really cant function then. What do I do? I have developed a terrible wheezing and now have to use an inhaler and breathing machine, and have never had to use one of these before in my life! I have 8 year old twins, and am only 41 years old and am not ready to die. This is the worst stuff in the world and should be taken off the market! ****** (don't know if this is allowed here, but if so, somebody please contact me with any suggestions how to get off this terrible stuff)

I was put on Levoxyl for 20 years. Hair kept falling out, muscles aches, acid reflux, plantar fasciitis, carpel tunel, tired, cranky, brain fog. I could barely walk and had developed a stutter. I was to be tested for Alzheimers at 45. I was told there was no other drug for hypothyroidism and it wasn't the Levoxyl doing these things to me.

Well I found another drug thanks to the internet and Yahoo Natural Thyroid Group. It was Armour. I have been on Armour for about 2 years now. All those problems I had on Levoxyl are gone. Completely GONE! Wasn't the Levoxyl huh?

I was prescribed 7 days 750mg of Levaquin on 9/10 and finished 9/16. I was originally diagnosed with bronchitis but went back to the Dr. yesterday cause I was not doing any better and he now says it's viral. I've gone to the hospital because I passed out on 9/13 and continue to faint at least once a day. I have tingling/numbness in my hands, ankles, toes, my knees hurt, my lower back is in a lot of pain, almost to where it is not tolerable, I'm dehydrated (I'm drinking and eating, just not as much) it is extremely painful to eat, my tongue and my gums hurt terribly. Last night I had a horrible dream (I don't dream usually, not nightmares) and today I started to hallucinate (mildly) A week ago I was functioning normally, a mother of 3, playing with my kids and now I can hardly walk without assistance, I can't go to work, I'm in constant pain. Someone please give me some kind of guidance. Will these feelings ever go away? What should I do? Thank you!!!!

In 2006 at the age of 38 after 4 years on Yasmin I had a mini-stroke. I am writing a non-fiction memoir about my experience and am very interested in hearing from anyone who has had a bad experience with Yasmin (or indeed, any other hormonal contraceptive.) I invite you to have your story included in my book. I am particularly interested in incidences of blood clot and of course, stroke, plus any withdrawal symptoms experienced from the drug. Please email me at ****** including your full name, age, location, a brief gynecological history, and the main facts of your experience. Thanks!!

I'm 18 and i received the 1st injection wen i was 17 in November 2007 and the only side effect i had since, was that my period didn't come...i had my last shot in June n it still hasn't come and i just started college so its been about 3-4 months...my little sister, on the other hand, passed out on 2 occasions after her 1st injection (she just turned 15 by the way n had the injection on her birthday in July). After reading all about recent side effects gardasil has, i wonder why they didn't mention any of the side effects before.

I HAVE BEEN ON TOPROL-XL FOR 2 YEARS. 25 MG. IN AM AND BLOOD PRESSURE WOULD FLUCTUATE UP TO 170/116 AND GO BACK DOWN TO 140/85. THEN WAS ALSO PUT ON NORVASC 25MG. IN PM. I ALSO AM HYPOTHYROID WITH HASHIMOTOS. MY SIDE AFFECTS HAVE BEEN EXTREME. SWEATING, HAVE TO CARRY A PAPER TOWEL OR SCARF TO WIPE SWEAT OFF, SPACED OUT, TIRED, FORGETFULNESS, RACING HEART, LEGS ANKLES SWOLLEN, THEY FEEL SO HEAVY, WEIGHT GAIN, EYES WATER, NOSE WILL HAVE NASAL DRIP, CONSTIPATED, SORE NECK, HEADACHES, THE LIST GOES ON. THIS SUMMER I WENT TO THERAPY FOR MY NECK, HAD ECHO AND WORE 24 HR. HEART HALTER, WHICH I HAVE FOUR EXTRA BEATS, WENT TO ENDRICONE DOCTOR WHO RAN TESTS FOR EVERYTHING, 24 HR. URINE, TESTS CAME BACK WITH TSH HIGH, EVERYTHING ELSE WAS NORMAL BUT FOR MY HEART EXTRA BEATS ENDR. AND FAMILY DOCTOR TOOK ME OFF NORVASC AND PUT ME ON TOPROL-XL 25MG IN PM ALSO AM. WELL FEELING LIKE I WAS READY TO GIVE IT ALL UP, LIKE I WAS DYING, I QUIT TAKING IT LAST NIGHT AND HAVE THOUGHT ABOUT THIS ALL YEAR, TRYING PEPTACE AND CELERY SEED EXTRACT. I FELT SO BAD THAT I KNOW IT COULD BE DANGEROUS TO QUIT THE TOPROL-XL LIKE THAT BUT I FELT LIKE MY HEART WAS GONNA BURST AND IT WAS GANNA TAKE ME OUT ANYWAY, AND DOCS. WOULDN'T LISTEN AND I HAVE BEEN IN TO THEM A LOT WITH ALL MY ISSUES. I AM 56 AND HAVE ALWAYS BEEN ACTIVE, OUTDOORS TYPE PERSON. I WALK 2 MILES ON TREADMILL EVERYDAY AND 30 MIN. OF TAE-BO EXERCISE. I WORK 5 DAYS A WEEK AND HAVE LOTS TO DO AT HOME. THEY TRIED TO PUT ME ON CYMBALTA, LEXAPRO, ELIVOIR FOR THEY SAID WHEN YOU FEEL THAT BAD YOU CAN GET DEPRESSED, I TOLD THEM NO, I AM NOT ADDING ANY MEDS. KNOWING I WOULD GET WORSE. PEOPLE AT WORK, MY FAMILY WILL SAY YOU DON'T LOOK LIKE YOU FEEL GOOD OR IS SOMETHING WRONG, HOW COMPLICATED IT WOULD BE TO EXPLAIN. SO I AM LISTENING TO MY BODY CAUSE FEELING THAT BAD ISN'T RIGHT SO I HOPE THIS WORKS. I COULN'T FEEL ANY WORSE ANYWAY. SO GOOD LUCK TO YOU ALL AND ALL OF US ARE UNIQUE TO FIND WHAT MIGHT WORK FOR US, AND MOST THOSE PRESCRIPTIONS ARE FOR ONE THING AND THEN TRIGGER OFF OTHER THINGS THEN YOU GOTTA TAKE ANOTHER MED. FOR THAT. I AM GLAD TO FIND THIS SITE.

i have been on advair for a year and a half and in this time i went from having perfect teeth to having my teeth rotting out.one of my doctors told me that she dosent think that advair did it but then another doctor told me yes it did and the dentist say he thinks it might be caused by the advair.has anyone one out there had this happen to them.please if so let me know.you can email me at ******i could really use the help.

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 was recently in the hospital they gave me toradol and now two days later my arms and legs are in very bad pain i have on and off headaches and i am so tired but cannot sleep. i took some ibuprofen and that did not help i have lost my appetite and i have yellow color to my skin now i have tried on the internet to get help right now and have found no relief i do not have the money to go back to the hospital so if any one has any help my name is Nicole my e mail address is ****** please help if you have any information.

After being on Lipitor for over 5 years, I was told to stop cold turkey by my doctor after my routine blood test. Within 10 days I got blood clots and a pulmonary embolism. I had been on an aspirin a day for over 10 years, I drank cranberry juice often and always ate green leafy veggies. I never had any blood clots before coming off the Lipitor and I am convinced that it caused them. It has been a struggle with the pains in my legs ever since. Has anyone had the same or have heard of someone with the same side effect? ******

I am a 54 year old male who started taking Lipitor about 4 years ago. It seemed OK at first, but over the next several years I began to have increasing amounts of joint pain after exercise. Nor muscle pain, joint pain. And it seemed to be a result of exercise. By the time I stopped it, I was hurting after everything, not just exercise. I felt better within the first two weeks, but it took about 4 months for me to be able to exercise vigorously again. Over the years I seemed to have forgotten how much vitality I used to have. I am a physician, and because of the long lag time until I felt better, I wondered whether improvement might have related to other factors, so after about 5 months I decided to restart Lipitor. It surprised me that after just one dose, I got back all of the joint pain and fatigue when I was at my worst on Lipitor. I was really hurting. Needless to say, I didn't take any more.

Coincidentally, a physician friend of mine who had statin induced polyneuropathy had a similar experience. After his symptoms went away he found that after only one dose the entire polyneuropathy came back.

Stopping and restarting the drug is a way to test the correlation between the drug and the side effect. For such a large spectrum of side effects to recur after only a single dose, it argues that the problems that my friend and I had was due to some sort of immune memory response. I have not seen this in the medical literature.

I am off it now for about 8 months and am able to comfortably play singles tennis and jog - much more energy (and I took 200 mg of CoQ10 a day with the Lipitor).

I have had Mirena for about nine months now and I absolutely hate it. I have mood swings all the time, when I get a period it's very light but lasts 10-14 days! Not to mention I have had no sex drive (if anyone else has had this problem please email me at ******) since it was placed and I have noticed a dry itchy scalp and dizziness. When the doctor put it in I sat up and a pool of blood spilled out on to the floor, I also got extremely dizzy and got really warm like I was having a heat flash. I cramped the whole day! I'm so glad I found this website I am making an appt to have this removed ASAP!