Knees symptoms and conditions

I had my IUD removed November 12th after having it for two years. The removal was painless. Within twenty-four hours, the abdominal bloating was noticeably less and within a week, gone. I also noticed an increase in energy level and change in appetite. I am looking forward to getting rid of the gained weight over the past two years and getting back into the clothes I love. More importantly, I want to feel alive and attractive again. The only adverse effect of having the IUD removed was four days after removal, I had a very emotional, crying episode for the better part of the day. A minimal amount of vaginal discharge, similar to the start of a period, has been present for about six days. Otherwise, no problems. Also, my knees, hips and back are no longer hurting like they were. Don't hesitate to have it removed and don't let your doctor talk you out of it! It is your body and your right to make all decisions regarding your healthcare! Good luck to you all. Thank you for sharing your experiences. If you had not, I may have never put two and two together.

I got my Mirena o June 18th, 2009. It is now November 17th and I have an appointment to have it removed this Friday. It started with unexplained hives and rashes constantly. The bottom of my feet, my palms, my knees, upper arms, throat and stomach. I was on constant high doses of Prednisone and anytime I started lowering my doses, the hives returned. I went to the ER three times for swelling and hives so bad I could barely see and could barely breathe. seemingly caused by NSAIDS, which I had never had a problem with before.Next was severe lower abdominal pain accompanied by groin pain so bad I could barely walk. Friends said it sounded like cysts, but, when I had an internal ultrasound done, nothing was found. After that I had severe breast pain and swelling. The final straw was the constant all over muscle aches and joint pain in my knees. I feel like I am 100 years old! I am tired all the time no matter how much sleep I get. I went to a dermatologist and I mentioned the Mirena, as I had to my OB, his response was "middle age". I thought I at first has Lupus, but, the rash did not fit that description. I changed detergents, blamed it on a foster dog, anything I could think of. Finally after reading so many posts and finally finding a connection with the rashes and hives, it can be nothing other than the Mirena. I even noticed that this device had the second most posts on this site. I can not wait to have the Mirena removed.

500mg 3 times a day for 10 days, vomited once, have had a horrible headache that started day b4 yesterday, still kinda have it, comes in waves, sux real bad lol

i have Sinusitis, Bronchitis, and a severe respiratory infection.

i see some guy on here mad cuz the doctor didn't tell him he would have bad headaches, like the doctor was going to know in advance he would. this anti-biotic affects different ppl different ways, its really not his responsibility to go over every single side-effect this very common anti-biotic is going to have, thats why the pharmacy gives you a huge pamphlet informing you on the medication, if you would had read it then you would see that headache, diarrhea, and constipation are all common side-effects

i didn't read it however, until i came here and read what i read, which is comforting really cuz at least i know why i have the headache so bad, and why i lost my lunch yesterday, was actually worried maybe i had an infection in my brain and thats why i had it, i know, sounds dumb, but what can i say, im paranoid lol

One of the newest thing my daughter is experiencing is, her joints in her body hurt alot. Mostly in her knees and ankles. Anyone experiencing this?

it's been about 2 months since my Mirena REMOVAL and I am just now starting to see a clearing up of my skin on my face and back. My skin was so bad. I had cystic acne on my back and arms and oily skin on my face and back. It's so nice to scratch my back without feeling thousands of bumps lining my neck and back.
*I feel better emotionally too. I am not getting irritated or angry as easily as i was when i had mirena in place.
*No more odor or discharge
*i'm still losing my hair but I think it's starting to slow down
*My knees don't hurt as bad as they used to.
In General I feel better and i'm getting better every week. I am sooo glad that i had it removed and that my life can continue now without such horrible side effects. It seems like it's taking a long time but that's ok as long as i'm making progress. I had it for 20 months so it will probably take a little longer to be cleaned out of my system .
Good Luck ladies.

Burning sensation in joints ,specifically in knees started after 4 yrs of Arimidex use besides muscle pain,fatigue and weight gain inspite of exercise and diet control .Frequent fever lasting 2-4 days with lot of weakness.So far so good as long as I am protected of relapse.

I have been on Arimidex since 2005 ,will be completing 5 yrs in 2010 .After 4 yrs ,I have started having burning sensation in my joints ,more so in my knees .I have been doing exercises prescribed very regularly ,I have added at least 7 kg in 4yrs .I have a controlled veg diet.Fatigue and body ache are the other side effects since the beginning of the drug.

I took Zocor for 25 days when I suddenly had such pain at night in my upper arms that I couldn't raise my arms up at all. It's been 2 full weeks since I stopped taking Zocor, and every single night around 7 I develop severe pain somewhere in my body, usually in my hands, knees or feet. It's in a different place almost every night. Tonight it's in my left hand across the whole top of my hand, below the wrist. Can Zocor cause this kind of pain so long after stopping taking it? And I only took it for 25 days! Please help - this really hurts and I hope it will improve.

I just want to say how happy I found this site. I'm not alone! I thought I was going crazy or that my body was shutting down completely. I had my mirena put in Sept. 2006 and my body has become something I don't even recognize. I am extremely bloated all the time and it hurts every time I eat and use the bathroom. I keep on thinking maybe I have Irritable Bowel Syndrome, but it doesn't make any sense because the symptoms showed up after I had the Mirena put in. I thought it might be food sensitivities so I got tested and have been trying to cut those foods out but it doesn't seem to be helping. I have tried all sorts of natural remedies but it never seems to go away.

I have gained 40 pounds since I the Mirena put in even though I have never have had weight gain problems before, I eat healthy and I am active. I also have a difficult time concentrating and focusing on anything. I also get dizziness, depression, irritability and mood swings. I also have been experiencing a sharp pulling or stinging in my uterus at times as well as joint pain (especially in my hips, knees) and painful intercourse with bleeding afterwards. My hair is also falling out and I have lost my desire for sex.

I've also noticed a drastic decline in my immune system. I have never been as sick as I have been in the last three years of my life. I seem to always be getting sick. For the first three months after the Mirena was inserted I had frequent bouts of yeast infections, bladder infections and still three years later I have these types of infections frequently. Not only this but I seem to catch everything that is going around when before the Mirena I hardly ever got sick.

Finally after reading the posts on this site I can trace all the changes in my body to when I had my Mirena put in. I am so upset that I have been suffering for 3 yrs with these side effects and it has taken until now for me to figure out that the Mirena doesn't just effect your uterus it effects your WHOLE body. I cant believe I trusted the doctor I went to when I had it put in that said that the hormones would only affect my uterus. NEVER, NEVER USE THIS PRODUCT!! It is coming out as soon as I can have it done! Please ladies if you know what it is like to have it removed let me know.

i have had excruciating pain in my right knee and upper part of my right leg while only being on Advair diskus 250/50 for about 3 weeks now. It did help with my wheezing however i cant sleep at night because of the muscle pain i have been having. I NEVER have had issues with either of my knees and am seriously considering stopping the Advair!!!

I was prescribed Avelox for a sinus infection that would not go away. After 4 days of taking it I have had severe cramping in my joints around my ankles, knees, shins and calf muscles. I have pain in my fingers too. I feel totally out of it, and dizzy. I have little to no appetite. This is a terrible drug, and should be pulled off the market. I was desperate to get rid of my sinus infection, and now I find myself having bigger problems from the side effects of this drug.
I have had pain now for 4 days. Does anyone know when this pain goes away?

I am a 52 year old female and my bad cholesterol is fine but my good cholesterol is low. I have been taking Lipitor now for a few years and have numb hands and feet to the elbows and knees. My feet are extremely sensitive, worse at night and now I'm getting sharp pains that feel like a bug just bit me. My tongue is also always numb and I do get migraines.I have insane stomach issues and food intolerance. I also take medication for high blood pressure, acid reflux, & thyroid. I have now been diagnosed with type 2 Diabetes but control that with diet so far. Until four years ago I had nothing wrong with me. I am slim and healthy. I had a lump in my thyroid which was removed and there was a trace of cancer. Then like dominos all the other conditions lined up. I have had MRIs and all the tests and doctors insist that I am not a severe enough diabetic to have neuropathy. I can hardly wear shoes now and it hurts when I wear runners while I walk and exercise. Does any of this sound familiar to anyone? I hate that my health has become so much a part of my daily life. Does anyone have neuropathy as a result of Lipitor and am I even taking the the right medication since I don't have high cholesterol?

THANK YOU SO MUCH FOR THIS SITE! I was beginning to feel that I was getting old too quick. I have been on Lisinopril for about a week and for the past two days I have had such severe muscle and joint pain that it even hurts to type this, it is in my hands, elbows, knees, and feet, and I look like a little old lady going to the store all hunched over and barely able to walk and I'm only 29!!! I don't care what my doctor says I'm quitting this medication today and going back on my old meds. Hopefully this excruciating pain will go away.

My dad had taken Avelox 400 for 5 days prescribed by a doctor for Bronchitis. He is a cardiac patient as well. After 1 week he developed the following symptoms in the order: high fever, Swelling in the ankles and knees, mild jaundice, thick sputum, rashes all over the body, difficulty swallowing food, conjunctivitis affected like discharge from the eyes, poor mental co-ordination, skin tearing in the lips, diarrhea, difficulty passing stool, anxiety, confusion, low blood pressure, insomnia, slightly impaired vision. I only hope and pray he recovers soon. I really do not know why this drug is administered to people when there are other alternatives which are milder. This drug has not done any good to anyone.

sorry forget to mention. any recovery from Lyme disease?

Within 5 hours of first dose, I had "severe body aches" like those with the flu. My joints and muscles hurt so much that night that I had to call my parents to help me take care of my kids the next morning. I told the doctor who prescribed it, and he said to try to stick it out for the week...what horrible advice! Thinking it was crazy advice, I reluctantly took doses 2, 3, and 4 and experienced the joint/muscle pain each time, but I guess I just somehow tolerated it as if I had the flu. My hands became rather puffy as well. After the 5th pill, I woke up in the middle of the night with HORRIBLE joint and muscle pain, which was so awful that I could barely move; I was able to move a little bit, with extreme pain all over my body--particularly my knees, wrists/hands/thumbs, feet, and shoulders. I felt and heard unnusual snapping, cracking, and popping all over my body when I would move around at all. I stopped the med immediately, and noticed some improvement over the next several days. It has since been 9 days since the last dose, and I still have considerable pain in my knee, my thumbs/wrists, and arms. Unable to do my regular exercise, I tried gentle swimming and light water aerobics several days ago, but found even that to be too painful to do. I'm still unable to pick up my young children, drive without pain (mostly in right knee and muscles connecting to it, when pushing the brake) and am still somewhat limited in typical daily activities. Also, for the last 5 days or so, I've had a strange nodule present on a tendon in my thumb which has been hurting since taking the antibiotic. This has been a very frightening experience, to say the least.

hi i came across this site through sheer desperation to find out if all the terrible symptoms my 13 yr old daughter was experiencing was through any of her asthma/allergy meds She has been on singulair since she was 5yrsold . But gradually over the past year her symptoms are that bad that she has weeks off school with dreadful headaches, stomach pains, mood swings which have been going on for last few years but put most of these down to puberty kicking in (but how i think i was so wrong). she has an allergy to peanuts which has been confirmed through tests but i was finding that lots of different foods were causing allergic reations which i could not understand(put it down to e numbers etc) she has been off this last week through yet again more headaches,chest infection, nausea but now the most terrible symptom is that of very painful ankles. knees, which are that sore she has been in tears.Since reading these post i am going to take her off the singulair but will do it at a gradual rate 1/2 tablet then 1/4 etc as she has been on this for a very long time and sudden withdrawal seems to be very risky. oh i also forget her rhinitis is also a major problem which causes her to be terribly bullied at school due to how noisy her breathing is and her snuffling being so often and seems to be getting worse. I am very grateful that i have come across this website.

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

I've now taken 12 days of 21 day course of treatment. After struggling with acid reflux, nausea, etc., I thought I'd share some things that I found that helped me tolerate it better in hopes it may help others.

I take a pill as soon as I get up and then another as soon as I get home from work - 5:30 a.m. and 5:30 p.m. I drink a good 4-6 oz. before I take the pill and another 8-10 after swallowing the pill. I try not to eat any later than 2 hours before going to bed, which has dramatically reduced and mostly eliminated the acid reflux.

I've been following the instructions to the letter - not eating 2 hours before or 1 hour after taking the pill and no dairy for 2 hours in hopes it would give maximum absorption to get rid of the Lyme Disease. However, I've found that by keeping something on my stomach during the times I can eat, my nausea has also been lessened. I was really struggling with nausea about 45 minutes after taking the pill, but have found increasing the water to the levels indicated above helped reduce the nausea.

All that said, I'm feeling some fatigue, am a bit lightheaded and my stomach is bloated and a bit tender. Still, it's not nearly as bad as some of you are reporting and while I wondered at Day 4 if I could complete all 21, I'm now hopeful I'll be able to make it. I will, however, be doing a happy dance when I take the last of the pills next Friday. Good luck to all - hope maybe something I've suggested may help someone!

I had back surgery in July and caught two infections from the hospital, Staph and pseudonymous. I had a picc-line put in and was put on Cipro oraly and Ancef. I got Steven Johnson syndrome from the Cipro and almost died. I looked like a burn victim and swelled from head to toe that was three weeks ago. They pulled me off the Ancef and Cipro. It took a week of me running 103 + temps and the dr. kept telling me its a virous until the rash showed up and my tongue swelled and private parts and throat started to swell shut before they decided to admit me. Then once all that was done and they figured it out they put me on impernem to kill both infections. They pulled my picc-last week and put me on Doxycycline. I have done my research and know that the two are related I asked my dr. what the chances were of a reaction again he told me less then 1%. Ha! I am seeing an infectious disease dr. by the way. Since I started the Doxycycline last Thursday I have developed hives I called the dr. and was told they are not worried about it because I am not running a 101 temp and I am not swelling, plus they don't even know if the Pseudonymous is cured. What do I do? If I go off the antibiotics I will die and if I stay on them I am probably going to die. My joints hurt all the time now and I am only 31. Do I look for a new dr.? Can someone please help me? This is the only website I have found so far where people have had the same reactions as me. These antibiotics are dangerous they need to be taken off the shelf. Thank you and good luck to everyone who is struggling with this.

I took doxy for 5 days then stopped because of side effects. It is 12 months later and I still have a very uncomfortable burning feeling on arms, chest, and back.

Has anyone had this prolonged side effect? Has anyone been able to get rid of it?

Thanks

I am a 34 yr old registered nurse and I was given Levaquin for a kidney infection. I was very pleased that by the next day my symptoms from the infection were gone. Unfortunately, after 5 out of 7 days of taking Levaquin I developed pain in my knees, wrists,shoulders,ankles and hands. My hands are swollen and difficult to use even to type this. I am very familiar with Levaquin and give it to patients all the time without even considering these symptoms because they are dismissed as "very rare"! Obviously they are under reported because doctors don't attribute these complaints to the drug side effects. I pray that this pain goes away soon for myself and everyone else. I have learned in my career and in my own experience that though doctors are the ones with the ability to diagnose and treat, WE are the ones that must be our own advocates! I will definitely never give Levaquin without warning patients of potential side effects.

Wow, what an eye opening experience it is to read all these posts! I was just about at the end of my rope thinking something was horribly wrong with me. Now I firmly believe it's the Levoxyl that is wrong.

I went on thyroid meds about a year and half ago for just slightly under active thyroid. I was actually lulled into it because the Doctor assured me it was a completely safe medicine and taking it would help me lose weight. Always a welcome thing. So I started on 50 mcg. I noticed some degree of improvement. I was sleeping better and having more energy during the day. Next checkup, the levels are in the normal range but just barely. So he doubled the dose. Two weeks later I broke out in a horrible itchy rash. I actually thought about the meds but then I didn't change meds, I was just taking more. I called the doctor and he said, "No this medication won't do that." So I change detergent, soap, everything I could think of and nothing worked. Finally I said, enough and I skipped a dose. During the day the rash got a lot better. Next morning I took another one and within and hour I was itching like crazy again. I stopped taking them, waited a week and called the doctor again and told them. His reaction was "You have to take this." I said, No, I don't and I won't. He actually argued with me that the rash could not be caused by the meds. Now I realize at that point I should have called another doctor but he's in my town, convenient, yada, yada, yada. Anyway he called me in another med which he said was the same active ingredient but different brand. Enter Levoxyl. I've been on 100 mcg for 3 months during which time I have felt progressively worse. Most of these things I didn't attribute to Levoxyl until later. Initially I noticed I was having the hot/cold flash thing. I have no comfort zone. I'm either flushed and sweating or chilled so my nights are spent constantly either searching for cover or kicking it off. Next thing I noticed is that my breasts would swell. Naturally that was a concern but about the time I would decide I needed to see about it, they would be normal for a few days. Sleep? What's that? Tired all the time. Started having confusion and forgetfulness. I even told my co-worker I thought I was losing my edge. I was all of a sudden forgetting things I had done automatically for over 15 years. Then the really scary stuff started. I would wake up in the middle of the night with my heart racing and feeling like I was in a fight for my life. I was afraid to go back to sleep. Joint aches and pains across my upper back, my knee. Tingling in my feet. It just keep getting worse and worse. Still didn't think of Levoxyl. Then Monday of this week I didn't have a pill to take. I forgot to get it refilled. Monday at lunch I told my husband I felt better than I'd felt in months. Tuesday took the regular dose. By noon the mental fog was back, back was hurting and I just felt like crap. Tuesday night went to bed early because I was so tired. 11:40 woke up with the worse anxiety attack I've ever had. Heart was pounding and I was breathless. Wednesday morning I got up and the light came on. I did not take the pill. Entered Levoxyl in google and found this site. I am so angry at my doctor I can hardly stand it. I even went to the official Levoxyl website and all these side effects are listed except for the swelling breasts and confusion but I've noticed several posts here that list those. During those two days I didn't take the freakin' pill both problems improved greatly. This morning, I reluctantly took half a pill. I plan to to that every other day for a few days then skip two days, then three, until I'm off of it. I don't know at this point what I'll do about my thyroid but I won't take this stuff and I won't ignore feeling like crap again. This is crazy. Where is the FDA? Oh yeah, being entertained by the drug companies. What a shame.

Thanks to everyone who has taken the time to post here. It is a sad commentary when we can't rely on our doctors to take care of us but we sure can't. If he had just told me about the bone loss, I would never have started this drug in the first place. My Mother suffered with that and that is something I would not trade for a few lost pounds and a little more energy. No thanks.

I have been on Welchol to help lower my cholesterol along with the lipitor and I have such muscle aches and pain especially in my feet, knees, arms are sore along with my right shoulder, headache everyday and very tired. Not sure if I am going to fill my prescription today..I ache all over.

I was about 1 month in to my 3 month cycle of taking doxycycline for blepharitis issues when I started having symptoms. It started on a friday night with extreme indigestion. There was a lot of pain in my chest and also into my arm. I was belching and very uncomfortable. Next day I woke up and only had the pain in my arm, belching and pain in my left abdomen under my rib cage.

I thought it was just really bad indigestion from something I ate so I continued with the medicine. Within a few days time I deteriorated more and more. The pain in my abdomen had spread from just being on the left to being left, center and right. I also got random pains all over my body it seemed. This seemed to come and go throughout the day. My vision would blur, I had extreme anxiety and also depression, my arm remained weak and then my legs got weak as well. The fatigue was overwhelming. I'm usually an insomniac who struggles to fall asleep by 1:30. I began to struggle to stay awake until 11. The lymph node in my neck also enlarged, and I began to experience a loss of appetite. I have currently lost 5 pounds in one week. I also always feel dehydrated and in a fog. I went to an urgent care clinic and the doctor really just thought I was crazy from what I could tell.

I stopped taking doxycycline about 5 days ago and the fatigue is slowly letting go(very slowly). The blurred vision has cleared up a bit but still comes and goes. My mood is still very down and I can't help to still feel anxious and can't stop wondering if I have some deadly disease process going on. The heartburn and abdomen pains are also subsiding slowly(I feel a little better each day).

I'm glad I found this website. It's helped me not freak out as much about my symptoms(although I still have my moments). Since I started feeling bad I've convinced myself that I have heart attack symptoms, pulmonary embolism symptoms, symptoms of AIDS and symptoms of lymphoma. It's still hard to not feel like doomsday is upon me but reading that many of you have had similar feelings and side effects makes me feel a little better.

I just hope this clears up soon because I think as long as I feel pain, tired or anything off I will be anxious about it. I have fear of ending up on Mystery Diagnosis lol.