Bruise symptoms and conditions

I recently had been prescribed macrobid for a uti I developed a cough after 4 doses that really hurt. After finishing the course of it I came down with the flu ( cough fever,body aches, etc.) and a rash all over my legs and arms of tiny bumps that itched. 2 weeks later I was given macrobid as a preventative measure by urologist to take for 30 days. I took the 1st dose before I went to bed at about 11:30 pm. the next day by 10am i couldn't finish my morning oatmeal due to sudden loss of appetite and nausea. Then I noticed I was starting to get body aches and my temp was elevating by noon. I took some aleve. By 2:30pm my I had a terrible cough that hurt my chest and my heart felt like it was beating out of my chest. Since I work for my PCP I told him about the symptoms and that I thought it was related to the macrobid and that this was listed as some of the side effects he checked my pulse and it was 133. I went home sick and he called to check on me around 6p.m. by then I was much worse my fever went up and I was coughing to the point that I was short of breath. I had headache dizziness, lightheaded and my whole body ached. and i was so hoarse I could barely talk and had what felt like a bruise on my left hip. He told me if I didn't start to feel better or got worse I should go to the E.R. I woke up at 10pm feeling worse and my heart rate was 120 after waking up from sleep. Went to the E.R. and my pulse was 142. they totally disregarded the fact that I told them this was side effects of the macrobid and they told me that could not be. That night I was diagnosed with bronchitis and uti. I was perfectly fine the day I took this med. I have never had bronchitis before. And my urologist had checked my urine 2 days before and said it was fine. i wasnt even having uti symptoms this was supposed to be preventative med. My PCP says he had his doubts but after looking at the side effects of this med in his MPR, I had almost every one that was listed. I will never take this med again. Antibiotics are supposed to help, not cause infections this should be taken off the market.

This is not a new side effect, but the same day I started taking Levaquin for sinusitis, I suspected something was wrong. Within hours, ears were roaring. First night, NO sleep, and that's WITH Ambien CR. Day 2.....depression! Immediate. This is in spite of having a severe depression under control for over a year. Sudden. I really started suspecting Levaquin then, but thought it was a coincidence. Took it this morning. Deep, dark depression. After reading these posts, I knew my suspicions were correct. The depression is getting better after 10-12 hours after the dose. This is really scary stuff. Really scary. Oh, yes, and I had the stomach pains, also. Told my husband it was just hurting like a bruise, not like indigestion or gas. I will report it to my doctor so they will no it's a "no-no" for me....in spite of all the websites that said how safe it was. Glad I found this website. Thank God.

I got the Mirena 1 year ago, at age 46, when my youngest child was 13. My doctor did not do anything to dilate my cervix and the insertion hurt very badly. I almost told them to forget it! I have a high threshold for pain and had both my children without any medical intervention, so it is saying a lot to say the Mirena insertion hurt. I decided to get it because of my heavy periods. My periods are much lighter, but last just as long (6+ days). Since May I've had a weird rash on my legs and tailbone. The one on my tailbone looks like a bruise. My shins are mottled and itchy. I've been to numerous doctors and tried many different medications. They have gotten better, but have not cleared up. It seems that my legs are not getting adequate circulation. Also, my belly and area below my navel are bright pink and itchy. I, too, feel bloated and pregnant all the time. Ugh! I experience heart flutters and once ended up in the emergency room because the school nurse, where I work, thought I was having a heart attack. Does anyone else have a rash like I describe? This darn think was so expensive, I hate to have it removed but, if it is causing this rash, I'll have it removed right away!

I've been on Yasmin for about a year and a half now... This is my first time really using birth control. I tried BC in my teens but hated the side effects so I got off them right away. Now that I am in a serious relationship and we're both in agreement we don't want to get pregnant until after we're married, I decided to start BC. I've had a few side effects but didn't really think much about them until I went for my annual pap last week. My doctor asked how the Yasmin was going. I told him that I've noticed I have little to no sex drive. He basically said that's not typical for Yasmin. I decided to get online and research side effects, that's when I came across this website. After reading several of the responses, something just clicked... I have many of the same symptoms!

I have never in my life experienced migraines until I started Yasmin. Fortunately I've only had a few since I started but nevertheless, not fun. I do however get frequent headaches. While I'm on the subject of my head, my memory seems to have slightly diminished. I often have a hard time remembering the simplest of words, causing me to misspeak often. I even have a difficult time remembering what I did a few days before! I've always had a very good memory! Has anyone else experienced difficulty with your memory??

About 4 mos after being on Yasmin I had a really weird uncomfortable pain just above my inside ankle. A few days later that pain had traveled up to the inside middle portion of my calf. At this point the spot where the pain resided was now discolored, looked almost like a bruise. Within a few hours the pain had moved up my leg just below my knee, still on the inside of my leg, again discolored. To make a long story short I went to my doctors office and he said I had a blood clot in my leg. He told me to keep my leg elevated and apply heat that it should be okay. I haven't had any bad cases like this again but I do occasionally get a similar pain in my leg but the pain seems to subide after a day or so. Ladies, if you experience similar pains and/or discoloring on the back of your leg(s) make sure you see your Dr. This can be deep vein thrombosis which are dangerous blood clots, they can cause pulmonary embolism's- blood clots in the lungs.

In addition I've had many other side effects including: little to no sex drive, severe dryness down below (kind of causes problems in the bedroom...), slight vision problems (I usually have near perfect vision, now I often feel like my vision is blurry), odd colored periods (brownish colored), sticky mucusy periods, a very sharp yet dull and uncomfortable pain in my right breast (at least once a month), frequent Urinary Tract Infections, mood swings (had a bad one this morning, threw a fit because my hair took forever to dry- so trivial, right?), severe melasma (hyperpigmentation) on my upper forehead and the top of both cheekbones, and last but certainly not least very low energy.

I actually have a follow-up appt this afternoon with my Dr. I am going to ask him about other options for birth control. Thank you to all of you for writing about your symptoms! Your comments have really helped! Good luck to all of you!

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

My boyfriend was prescribed sulfameth (10 days/ 2x) for these bumps that appeared on his arms and legs and would appear anywhere that he would scratch. Within 5 minutes of taking the first dosage in the evening, his eyesight became blurry. He had a severe headache that night, chills and a high fever that lasted through the night. He took 2 ibuprofen pills but they didn't help. He couldn't get to sleep the entire night. He also became even more itchy than before he took the sulfameth. He couldn't move due to muscle pain and fatigue. His fever was still there by the time i got there at 7 in the morning and he was shaking uncontrollably. His heart rate was up. It looked to me that more bumps appeared on his body and some became a dark purple blotch, like a bruise. His fever broke around noon and stayed away for a couple of hours but it returned. His skin started to peel after his fever returned. At first i noticed it was on his nose and ear but i didn't think much of it since i didn't see it anywhere else. An hour later he texted me and said his whole body started peeling as if he had sun burn. His temperature is still slightly raised after over 24 hours.
I refused to give him the second dosage of sulfameth that morning and proceeded to call the doctor who had prescribed it. All she said was that he needed to come back in. No way in hell was i bringing him back there. She didn't even look at him for literally a minute and prescribed this crap. She said nothing of the side effects. There was no warning. Even though i looked it up before he took it, I didn't think it would be this bad.

I am a 40 year old female. I have had several sinus infections and had been placedo n Avelox before. The doc kept asking me if I had any plans on pregnancy and continued to stress the strength of the drug. However, I had NO idea what would become of this last time. I had been taking it for about 4 days and went to the ENT and was told to stop taking it because my sinuses looked good. That day I struggled to breath and had to literally gasps for air. I developed a bruise on my left arm that looked as if someone had pinched me. I didn't think much of it until I woke up the next morning with another bruise on the right arm. I continued to develop these bruises until there were 6 altogether. A few days later my body began involuntary jerking. I felt like I was having seizures. I became tearful and so afraid. This med needs to GO AWAY!!! I cannot imagine what would have happened if I continued to take it. BE CAREFUL if you're daring enough to continue it. Thank God I have a praying partner and family that would NOT let me go!

I don't know how many of my problems are associated with NR, but after reading your posts, I am seriously wondering. Here's what I've got:

--tired all the time - no problem found with my thyroid, I've had it checked multiple times

--weight gain. I don't know how much of this is because I got married when I started NR and of course eat more complete meals rather than on-the-go kind of meals, or how much because I am so tired it is hard to make it to the gym. I will say, though, that for a couple of months I was really good (exercising for about an hour each day, four to six times a week, plus eating much better) and still gained weight. Disappointing. I don't try as hard now - what's the point if exercise and diet don't help?

--no sex drive or much enjoyment while having sex

--pain when having sex - not sure if that's cuz we only have it about once a week (I have to force myself for the sake of my husband). Now I take a bath after sex to alleviate some of the pain. Still annoying, though.

--nasal issues - I know someone mentioned having to take sudafed, I take it every day and also nasonex and mucinex... no apparent nasal problems to the doctors to explain this... I think it's overkill on the meds, but I take them because otherwise I am miserable with nasal problems

--headaches - I have never had headaches bad enough to take even tylenol or asprin before using NR, now I take ibuprofen about 5-6 times a week. I don't know if it is related to the stress of being married or not. I have graduated, so it is not related to stress at school, and stress has never given me bad headaches before. Basically unexplicable for me.

--problems with contacts

--pain in area right below breasts. Very tender. If I touch, it feels as though it will leave a bruise. It doesn't, but it hurts for about a minute before it goes away, just from pressing lightly.

--can't keep the nuvaring in. Not really a side effect, but very frustrating. I also have to keep pushing it in each time I use the restroom. I can't seem to get it in far enough, I guess.

--periods seem to be getting later and later. At first they came like clock-work, the day I took the nuvaring out. But after a year, the period seems to come about the day I put it back in, which leaves me freaked out that I'm pregnant. And they aren't even lighter. They still last about five to six days and are just as heavy, just late.

--muscle stiffness. It is a little hard to walk sometimes.Not sure this is related, but quite a few of you have listed it. Not many cramps though, which is nice.

I have been on NR since a couple months before I got married (about 17 months ago), and hadn't had sex before NR, so I don't know how much NR has affected some of these things since I don't know any different, but as I said before, these are some of the symptoms I have had while on NR, things with no apparent other cause. I am seriously considering another BC option, since I don't really like having no energy and no desire for sex (biggest problems for me).

I needed my copper coil changing and at my appointment I was recommended the Mirena due to increased blood flow. I did not have an opinion either way and took the advise of the family planning doctor. I had not until now read any reviews on this product. I was going to make an appointment to see my doctor due to my increasing depression. I am now going to have my Mirena removed this week.
These are my symptoms to date, (5 months).
No Periods (cool)
Very heavy and larger breasts, all new bras and have to wear sports bra to bed due to very painful breasts. I cannot run at the gym and have to walk on the treadmill.
I have put on weight and this is more of a problem I cannot lose any of it. 1-2lbs a month. I go to the gym, play squash and tennis.
People have noticed my weight gain.
I feel bloated and puffy.
Feel very tired and have to go to bed in the day at weekends.
I have been feeling very depressed and have got rather worried about it.
My partner says I have changed as a person.
I did have a very healthy sex life, mostly me leading and I am now not only not bothered either way, I actually do not want any sex at all.
I feel sick and have actually been sick.
I always have a bruise and I don't know how I got it.
I am moody and have become quite lonely.
I think that is plenty to be going on with.
I have read out what all you lot have said to my partner and he just said get that thing out and he is calling the doctor tomorrow to get the snip, something we have just left till now.
I am going to have mine taken out this week so hopefully I will get back to the 'normal' me very soon.

I'm a 47 male and took Crestor for a year. I experienced muscle tremors, constant fatigue and muscle soreness. Not just a little sore but as if someone had hit me so hard as to leave a muscle bruise in both arms. One night my left arm and leg began to tremor and it was as if they were too heavy to move.

What I noticed was that all of my little aches and pains became severe aches.

I experienced blistering on my hands, a common side-effect of your liver rejecting the medication but my doctor didn't pickup on the symptom. Instead, he gave me a steroid-based topical cream that actually eliminated the blisters but they would return within weeks.

I experienced lapses in my memory and I started to forget words. I would forget the names of things and I found myself substituting the word 'thingy' when I could remember what something was called (like a phone).

I visited the hospital 4 times and my doctor countless time. Each time my doctor treated the current symptom and not the person as a whole.

It became too much to bare when I started having chest pains that felt like something was crushing my chest. At this point I started to do some research and found forums like this one.

During my time of the worse pain, I felt like I was actually dying. I started to get my effects in order and finalized my estate.

I stopped my Crestor about a year ago, after about 3-6 months my muscles began to feel better. After a year, I am finally starting to feel like my old self again (not that I was all that well before).

Statin affect people differently, but there is NO DOUBT that these drugs can have adverse effects on people. Listen to the commercial for Lipitor, "contact your doctor if you have muscle fatigue or weakness"......

This has happened to me as well. I too have a dent in my right glut that appeared along with a bruise a few weeks following the Kenalog shot for poison Ivy. If anyone knows how to move forward with a class action lawsuit, PLEASE let me know.

I first had botox 3 weeks ago- I had one bruise from an injection site, but that didn't bother me. The worst was the anxiety- I felt constantly anxious and irritable, and I had horrible nightmares every night for about ten days. it got to the point where I dreaded going to sleep.
Ten days later the symptoms were gone and I had a smooth forehead but still a wrinkle between my eyes. After a consult with another doctor, I was talked into more botox - I wanted a filler instead. After the 8th injection I passed out. They put bed flat and gave me the rest. last night I felt really tired, and today I am extremely weak. Hope its very temporary-had to call in sick , and waiting for a call back from the doctor.

I was injected with Kenalog in Mid July 2008 to reduce the swelling in my tonsils (I had a bad case of tonsillitis). I was asked if I have allergic reactions to steroid injections, and to my knowledge, I don't. So I was given a shot in my upper right buttock on Thursday (mid July). On the following Friday I was no better (still mid July). I was still not able to swallow my own spit, let alone eat or drink, so I went back Friday morning. I got another shot in the same location of Kelanog. I was not told of side effects; I was told the swelling would go down in my tonsils/throat. Again, no results.

That Friday afternoon I was admitted into the hospital for care. A weekend of fluids and other drugs got the infection out. I stayed infection free for two weeks. It hurt for a week afterwards on my right buttock, but no bruising. I healed up, had my tonsillectomy (sp), and healed fine after that.

I noticed nothing wrong with my upper right buttock until about two weeks ago. I am in the process of getting a large rib/hip tattoo piece finished, and about two weeks ago I noticed a spot that looked like a small bruise a few inches from my tattoo in the spot where I was administered the Kenalog shots. I didn't put it together then. Two weeks later (This past Thursday, September 25, 2008), my tattoo artist was about to work on me and said, "You have a dent in your butt, what happened?" I had no idea it was even a dent. The "bruise" like mark now looked like a burn scar, red, and smooth and deep--dented.

The red mark is still dented and the same color. It's about the size of an inch from one side to the other. However, each day since it has been dented, the dented area has expanded fairly rapidly. The dent is now not only in that red area (the injection site), but also along my hip/upper thigh. It's getting deeper and traveling outside the red area, and the red area is the same color. This discoloration just started. I heard this is called Tissue Atrophy due to a misadministered Kenalog injection.

Does this dent go away or stop "spreading" by itself? How will I know if it will stop spreading; is it different for everyone? How can it be properly diagnosed as well? Can a biopsy be done to prove that this it what it is? Does anyone have any insight?

Also, it's been 2 1/2 months before I saw any of these effects...why does it seem like my effects came later than others? Is that possible?

Thanks.

I HATE Kenalog! I had the flu back in March of 08' and my doctor gave me a shot of Kenalog. Soon after I had a horrible period that was totally out of the blue which made my husband I think that I may have miscarried. Come to find out through my own research (not anything my doctor warned me about) that kenalog causes irregular periods, but for months I went through the pain of thinking my body had miscarried. On top of that horrible feeling, I have a HUGE dent on my left butt cheek. It started out small and is now huge with a blue bruise in the middle of it. I feel very embarrassed being nude, and very paranoid about clothing. I feel like everyone can see it. I went to my doctor and asked him about it and he said "it is normal, and will go away with time." BUT the nurse who injected the shot in the first place, came in after he left and asked to see the dent and then apologized with a look on her face that made me realize I will probably be sportin' this dent for the rest of my life. It all smells fishy to me. My doctor didn't mention one single word about a possible side effect. I would NEVER have had the injection. We trust our doctors to tell us side effects that may cause us emotional stress, and possible disfigurement for the rest of our lives. Has anyone had any luck with getting a lawyer involved. I want compensation. I want to try the saline injections and don't want to pay for the treatment. AND I want to STOP this from happening to other women. I know it might be vain and I know my husband loves me for who I am, but I am a woman and don't want the freakin' Grand Canyon on my butt cheek!!!!

Like so many of you, I Googled "tissue atrophy" and have had the very same experience that you have had with Kenalog. I received a shot in late February of 08, shortly after I noticed severe bruising, which eventually turned into the atrophy I now have. I have taken pictures of it for the past several months...and now, 6 months later it is much worse...deeper and darker in color. Is anyone else having discoloration? Mine is a dark purple-red.
I AM PURSUING a lawsuit against the nurse that injected me because I was absolutely not warned of the side-effects...and now have had to suffer with this hole in my side.

It bothers me...and no one would understand unless this had happened to them I suppose. In addition, I received a second opinion and was told the atrophy was permanent...can anyone else confirm this?

I've also noticed other severe menstrual and emotional side-effects...this stuff can stay in your system for a long time.

I had a small lump in my arm after my first two shots which lasted about two weeks each. After my third shot, four weeks ago, I had a small lump again. It was just like the others until 3.5 weeks after the shot. Now it is increasing in size and marked with a bruise. It is very sore and painful to touch. Even if my shirt sleeve is resting on in, it hurts. Has anybody else experienced this side effect? My doctor said not to worry, but I am!

The nausea is tolerable, generally short-lived as long as I eat prior to taking the Chantix and drink plenty of water.

I have a sense of...fogginess....detachment, while at the same time, seem to sense clear hidden messages in the way people look at me, in what they're saying to each other, and to me. Yep, it's probably paranoia.

The nightmares are horrible. I dream specifics about deaths of loved ones, in horrible detail. I also awaken at least once a night gasping in terror, unable to get a breath.

The thoughts of suicide are strangely comforting and don't seem wrong at all. I'm depressed, but comforted knowing that I can end it if I really want to. Bizarre and I know it on some level at least.

I'm bruising easily this time. I mean REALLY easily. A small bump results in a hard, raised, dark bruise.

I developed a rash on my stomach that's been there for 3 days but seems to be clearing today.

This is my 2nd time taking Chantix and I'm 3 weeks in. I had the same symptoms last time and expected them this time. I'm smoke free but plan to continue with the Chantix as long as possible. The urge to give in and have one cigarette is too strong post Chantix. I tell myself everyday that the thoughts are NOT me, and that I can let them come and not act on them because it's the drug, not me.

I had Mirena put in on Monday at noon and had it removed on Wednesday at 4:30. The time in between was awful. First, the IMPLANTATION (and don't let anyone tell you it's an INSERTION - it's IMPLANTED) was honestly the worst pain I've ever had. It compares to slamming your finger in a door. My eyes immediately teared and I kind of screamed and jumped. The dr. said "It'll only hurt like that one more time." WHAT???? Sure enough, it hurt like that again, then it was in. Then the cramping started. It continued through that day, eased up, hurt a bit the next day. Then my stomach started hurting, and I began developing a bruise on my skin on top of where the Mirena was. It felt as if it were trying to push its way out through my skin. The next day I woke up feeling almost normal, but that afternoon thought I was in labor. Was crying, couldn't take deep breaths or it would REALLY hurt, severe cramps worse than any menstrual cramps I've ever had (and I've had BAD ones). My husband called the doctor and I went right over and had it removed. Within 1-2 minutes I felt normal again.

What upsets me the most is not the promotional piece of literature that only told me the benefits, but the fact that my gyno presented it as The Device That Would End All of my Problems. I would expect a more fair assessment from a doctor.

It ended up being her partner who removed it, and he said, "Mirena's not for everybody." I really wish it had been presented in a more unbiased way upfront.

Anyway, the pain is over now and I'm taking Loestrin. My advice would be to just REALLY SERIOUSLY consider what you are doing before you get this device, and be ready to have it removed if it doesn't work out for you.

HI, i too have to say i am kind of relieved after reading this website that i am not alone with my experiences of the kenalog injection. I was given kenalog injections to treat hayfever, although i wasn't told the name of the injection. They did help and i probably would of continued this year if it wasn't for the side effects.
I was told that to have one a yr was safe, then just before xmas i noticed a dent on my hip, this started getting larger and looked almost like scare tissue, I too was worried i had some sort of flesh eating disorder. The dent is still there and i will never have that injection again. I also have been experience problems with my hips and pain around my coxis,i am not sure if this too is related to the injection. I was told by my doctor who is very good that the kenalog had eaten my fat tissue causing a dent and that it will get better in time.

Was given iv levaquin in hospital for pneumonia (sat night). Oral the next day. The following day (monday) all the joints in my body started to ache. Hard to move. Especially ankle. Dr said stop antibiotic. Ankle and joints sore all week. Friday I had a huge pop in my ankle. Large bruise and swelling. Turned out to be a second degree sprain with ruptured blood vessel. Caused by levoguin. It has been 13 days since the pop, ankle still popping, swelling will not go down. Does anyone know how long this drug lasts in your body?

I am freaking out!! I just found this site and can't believe what I'm reading. I have a huge crater in my right buttock as well. This is the second time it has happened to me. After the first incident, I went to the doctor and she said she didn't know what it was, that it must have been due to trauma. This is the same doctor who prescribed the Kenalog shot for my allergies. It started out as a large bruise, so I assumed I must have hit something really hard and damaged the tissue. Now, a couple of yrs later, I have another, larger crater. I thought something really bad was wrong with me, so I decided to google and see what I could find. I am truly blown away by this and VERY upset that they did not warn me of this. I called the doctor, but they haven't returned my call yet. I'm concerned is this going to continue to get deeper? I also believe it affected my period as well. I have always been very regular, but for several months after the shot I would start my period every couple of weeks.

I took Levaquin the first time (that I know of and remember) in Dec 2006..probably for bronchitis or pneumonia. I started having strange symptoms, headaches, achy body, etc but chalked it all up to being sick. I have since taken in 4 more times - even after talking to my Dr about the strange things that were happening to me. I just realized by reading everything online that all of these things are more than just me being out of shape...I have had about 75% of the problems associated with this drug, but simply thought I was getting older, out of shape and ill. The headaches are the worst, the sharp pains that radiate through my skull at any given time for no apparent reason and the constant radiating pain coming from my shoulders, the funny vision issues that happen off and on, the incredible pain in my jaw that leads to what I call a 'pulled muscle' in the right side of my jaw, the severe pain in my muscles, mostly in my feet and shoulders but has now started in my wrists, taste of metal, night sweats are ridiculous! and I have started missing my period with this dose of Levaquin, however the new lower back pain that I am feeling is about 10 times worse than that of meses cramps, the sharp shooting pains in muscles sometimes happen in my arms, legs and knees. The very odd feeling of having a bruise when I touch any part of my body to scratch or rub it....the pain is extreme. I have made about 100 excuses for each of these things that I have experienced over the last year and a half and now I feel that I can probably blame it all on Levaquin, I have a doctor's appointment with a new doctor Thursday and am hoping she/he can provide some relief of some of these issues. Please make sure all your loved ones know not to take this drug!

I had a mild heart attack 14 months ago (aged 56). A stent was inserted in an artery. I was put on four medications (Lipitor was at 40mg) so what caused what is up for grabs.
Friends told me I was slurring my words - which I experienced as an inability to find words and hence I could not talk at talking speed. The Metoprolol was reduced and I also started taking Co Q 10 as I had read that Lipitor reduces both cholesterol and Co Q10. The slurring reduced. I also had sudden pains as if a sharp object was being pressed hard on the ends of my fingers and toes at random. The doctor shrugged.
Since my heart attack my memory has been poor and I have been noticeably clumsy.
About 6 months ago I started to get left knee discomfort - I can relate this to water on the knee from an impact at age 11. It hardly ever caused a problem since. I went to Physical therapy and had ultra sound and it seemed to take ridiculously long to improve. And at that time I was becoming increasingly aware of a "bruise" to my left elbow (I am left handed). I felt like a complainer! I had bruised my left elbow but could it hurt 3 months later. I had an X-Ray and the elbow was fine. I was getting similar sensations on the other side of my body (knee and elbow) but at like 10% of the intensity so I dismissed it as nonsensical.
Then I awoke at 3.00 a.m. one night with incredible pain in my lower left arm.
The orthopedic surgeon I saw said I had tennis elbow and I got a cortisone injection. I was beginning to feel as if my body was decaying and getting torn internally.
I then read a blog and a disability insurance assessor said she always asks if people who have been diagnosed with tennis elbow are taking Lipitor. Ping!
I quit Lipitor. Two nights later I had unbelievable cramps in my lower left leg. I have had the pins in the end of the fingers and toes again and the inability to find words appears momentarily.
But I have far more energy. My biggest surprise is that I am breathing more deeply. Spontaneously I am taking really deep breaths. I started at the gym within a week of quitting. However I am being careful. I will take a cholesterol test in a month, and have gone almost dairy free, and am vegetarian every other day and will continue with CoQ10

Hi everyone!! I have contacted a attorney who is a nationwide medical malpractice. I gave him this web site info so you all may be hearing from them. Hope that helps you all!!

I have been taking Levoxyl for 1 1/2 yrs, I had my thyroid removed due to severe hyperthyroid. In the past year, I have been getting pains and weakness in my hands. It is so bad now, I can't open a jar or lift a frying pan. It hurts sooo bad. My legs hurt and my knees have real bad joint pain.
The funny thing is, it's not every day and not always both knees. It is however all the time in my hands. Last week I went to an Arthritis specialist in San Antonio. He ran every blood test avail. Tested for Rhum. arthritis, Lyme disease, AA, and all kinds of stuff. He x-rayed my knees and injected cortisone in my knees and hands. - that hurt -
He found nothing wrong!
I searched on line tonight for "Levoxyl and joint pain" and this site came up. Boy am I glad I am not the only one who is questioning this horribly possible side effect. Oh, I also have memory loss. I feel like I am 80 yrs old. Just to make sure you know what type of person I am, here goes: I am fit, active, 37 yrs old and 115 lbs, I eat well and take vitamins, non smoker, non drinker.
On Monday, I am calling my doctor. I am printing this web site and all of the postings like mine. There must be something I can be put on that will fix this. Can anyone tell me if they have no Thyroid and have gotten off this stuff; does the hand pain stop? Does it get better or is this permanent damage?

Kerrville TX