Fibromyalgia symptoms and conditions

I have taken Avelox on and off for about a year now. Havent had any side effects until yesterday. My elbow and the back of my arm started to hurt. So I chalked it up as my fibromyalgia acting up. Then after I took my next dose my husband read the pamplet and was like I think its the meds. Well this morning I woke up and my face, hands and feet were swollen and I hurt all over. Went to the ER and they gave me benadryl and tylenol. They had to go look up the meds in order to see whats going on cause they were "familur" with it. Go figure I could of just stayed at home. I ask what about my tendons and he's like oh its just a reaction to the meds. So Im going to my regular doctor tommorow. Dont take this medicine.

Wow. This news gives me so much hope. I've been on the Nuvaring since it was still in the post-trial stages and nobody had even heard of it. My doctor recommended it because it was supposed to help with acne and weight gain, and I'd been having no luck with Yaz or Ortho Tricyclene. I've always had irregular periods, I've been depressive since high school, and I started having migraines when I was 13. Ten years ago, I was diagnosed with fibromyalgia. What this means is that all these symptoms that everyone was describing here, while they have been getting dramatically worse, were nothing I would even think of ascribing to my birth control. I've gained 40 pounds in the last 3 years, but I blamed that on my increased depression and general malaise. I'd stopped having migraines more than once a year, but now I get migraine-like (not usually as bad as the originals) headaches as often as 4-5 times a month. I've had insane mood swings ranging between white hot anger and debilitating depression (even having thoughts of suicide for the first time since high school), and sex burns and leaves me walking funny about 99.9 percent of the time. I thought it was just me, or the fibro (which leaves me feeling pretty sensitive all over); same with the nausea, especially in the morning and always during my period. Could this seriously be the Nuvaring? Oh my god, I hope so. An easy solution like that makes me want to cry from relief.

... but how do I do birth control now? Do we always have to use a condom? I've never been pregnant, so I've been told the IUD isn't nearly as safe if your cervix hasn't been violated by childbirth. Oh well, better than being crazy, I suppose.

I have been taking lyrica for about 6 months and have gained more then 50 pounds...it seems to help with my fibromyalgia symptoms but the weight gain is horrible!!! i don't know what i should do...i am currently looking for an herbal replacement for lyrica...if anyone has in suggestions please let me know thank you

After a year and a half of synthroid because of removal of my thyroid for cancer, I feel worse than I have ever felt in my life. Many tests have shown that there is no recurrence of the cancer. I would think I had fibromyalgia if it weren't that I read the blogs from other sufferers like me. I now take 150 mcg on most days. Some days I have to cut it down or skip it because I just cannot bear the body pain, weakness, brain fog, constant awakening in the night, severe cramping knee and leg pain, and muscle aches (there's no word strong enough to describe this pain -- 'aches' just doesn't do it). On the days I don't take synthroid I begin to feel like my old self. But my old self was 40 pounds thinner and losing. My old self walked three miles a day and hiked into the back country with my son. And my old self felt energetic and woke up every day with happy plans. Now I feel like an invalid. Some days I can barely walk. I cannot stand for longer than 5 minutes. I have tried cytomel, unithroid, and armour with varying problems. Synthroid is all that is left. Those of us who are dependent on this drug really need some good research on its effects. And we also need compassionate physicians who do not dismiss our pain and, it is not overdramatic to say, suffering.

To the best of my knowledge I never had any of the 'immediate' symptoms.
My problems are probably due to the fact that I was prescribed Cipro 3 possibly 4 times from Aug 06 - Dec 07 and then finished up Dec 07 with a round of Levaquin. My father is over 60 and was recently given Levaquin and had immediate and serious problems. He is seeing a doctor recommended by the CDC today. Yes, he is even working with the CDC on
this one. Due to all he is being told he is convinced that the medication is behind my medical decline as well. Since taking these medications (symptoms started slowly in 07), but after taking the Levaquin at Christmas time I never got up from the couch. My thyroid gland has quit working, my adrenals are shot, I have been diagnosed with fibromyalgia, chronic fatigue, blew out 3 disks in my back, vision is deteriorating rapidly, and really so many things I can't list them all. I had a complete physical
in Oct 05 and was given a perfect bill of health. Through Aug 06 I was riding my bicycle 33 miles per week. I'm still trying to figure out what hit me??
What my father has been told is that in some individuals Levaquin will attack the glands (like the thyroid) and will compromise the immune system. This damage appears to be permanent. All I know is that I went from being extremely healthy to terribly sick. If in a day's time I have enough energy to load and unload the dishwasher it is a banner day. I can
not work and seem to get worse instead of better as each day passes.

My husband also had pneumonia at Christmas and took Levaquin but does not seem to have had an problems. I suspect it was possibly the cumulative effect of having basically 4-5 rounds of the antibiotic in a years time. According to the people at the CDC that have spoken to my father the symptoms that I have can all be traced back to the medication. One never knows what effect a medication will have. Just please be careful when taking this medication, and limit how many times you take it.

Hi so glad to read this im calling my dr as i read!! i got my mirena in apr of 2005, i was one of the 1st pts my dr did one on. I have no children and am married, we wanted to wait to have kids and i have frequent migraines so the pill is a no-no. the day i had it put in i passed out while leaving the office. they said "oh wow that never happens"...hmmm wonder how many others passed out after i did!

i cant really report any bad side effects until about 1 yr after insertion. i started having terrible cramping where i couldn't even stand up. this would come and go every few months. then i noticed i couldn't urinate as well anymore...the stream was weak and it seemed like my muscles were tense or something. i now have constant pain and pressure of the pelvic floor, my abdomen is always bloated, i have gained 20lbs and i do weight watchers and cant lose a pound, i retain tons of water, i have fatigue and joint/muscle pain. I attributed the joint pain and fatigue to fibromyalgia which i have been dx'd w/ in 2007 but now i wonder if its this mirena!

i have been to different doctors and specialists because i don't feel well, i haven't for a few years now...now i wonder if its because of this mirena. im going to have mine removed and see how i feel. the urination problem is the worst! i always feel like i have to pee but nothing comes out...the urologist said all my tests were normal.

im so glad i read all these posts...i hope every woman reads this before deciding on the mirena.

I suffer from chronic fatigue syndrome and fibromyalgia. I have problems with painful joints and have fluid on my knees. I tried Aqua Ban to try to relieve the fluid on my knees. I started by taking 2 tablets x 2 times on the first day, I was fine. The next day I took same dosage. In the afternoon I started feeling unwell. I went to bed as I had terrible tummy pains, felt sick and went downhill quite quickly. The next day I felt worse and had cramping pains all day. I stayed in bed with a hot water bottle. I had no energy at all. This went on for 4 days and eventually I ended up with a pain in my pelvic region. I can only think that the Aqua Ban had such an affect because of the chronic fatigue/fibromyalgia? Has anyone else had an experience like this?

I am taking Levaquin one time a day, 500 mg. for diverticultis. I have fibromyalgia so attributed symptoms of EXTREME FATIGUE to that but this is fatigue like I've never known. I can't do much of anything. I don't work outside the home so will just deal with it if it cures my infection. I'm using sleep meds too...but that could be fibromyalgia kicking in too. But fatigue is much worse. I hope it kills those bad bacteria!

Severe breast pain, bladder infections, hot flashes.
More than a year after stopping Ambien I still have some pain, cannot wear a bra. As a sleep aid, though, Ambien was fine. I went to sleep when I wanted and woke up with a clear head in the morning. I can
see how some people who don't have
side effects like the drug.

I had some really odd-ball side effects from Lyrica. I was on 150mg twice a day for fibromyalgia, and it seemed to work initially. I was feeling pretty good, and thought I, too, had found an answer to my aches and pains. After about two months, I noticed that my hair was falling out and turning gray (I was 39 at the time). I hadn't had a menstral period that second month, either. I told every doctor I saw about these strange symptoms, but was prompty ignored.

The third month, I began to gain weight like crazy. I ended up gaining a little over 20lbs during the year-long treatment. My skin was dry and thickening around my thumbs and heels. My energy level began to really go down (it was never that high to begin with). My fingernails became brittle and broke with the slightest provocation. The grayer and falling out hair was coarser, too. I also was either sleeping all the time for days, or then couldn't sleep at all for days.

By the sixth month, I noticed that my wounds were also taking longer to heal. Being diabetic for the last 29 years, I thought that maybe neuropathy was starting to set in. Up to that point, I had never had any signs of neuropathy, and always was in good control of my blood sugar levels. Now, I was beginning to get worried.

The eighth month forward brought cracked heels, cracked toes, cracked fingers and thumbs. I began to have pitting edema, which I immediately informed my Rheumatologist about. I have chronic renal insufficiency, though not diabetic related. It was a gift from my OB/GYN during pregnancy when I became eclamptic. The edema was so bad that blisters appeared on my ankles and would not go away, no matter how high up I rested with my legs. My skin hurt all around my legs, and soon started to notice my face also swelling. Still, no comments from any of my numerous doctors.

After a year of all this strange stuff, I took myself off of the Lyrica. It was a hard choice, as the meds helped to silence the strangling pain in my muscles. Within a month after discontinuing the drug, my period came back. Three months later I noticed that both my hair and nails were stronger, and my hair wasn't falling out as much.

Six months later, and I notice now that my wounds heal like they used to. My hair isn't as coarse, and my nails are much stronger. My sleep schedule is still not right, and I still have the deep cracks and crevices to my thumbs and heels, but it is much better than it had been. I have also since tried Lamictal, but am having tachycardia and shortness of breath, along with a marked rise in my blood pressure. This, too, I discontinued and am feeling somewhat better. The muscle aches and pains and fatigue are back with a vengeance, but I will put up with them as long as I can. I am on so many meds anyway, that my body is probably kissing my toes in thanks!

Luck to all who are on this drug, and hope it works for you without all the weird side effects I put up with!

Honestly thank you for this website! I mentally feel better if not physically yet. I was prescribed 3 day/2 dose Bactrim for a UTI. I have NEVER had a reaction to antibiotics or any type of medicine. I can no longer say that.

That said...thought I was dying. My temperature was 102 for days, every muscle in my body felt so sore I felt like a car had hit me and then hit me again, ridiculous size headache, massive stomach pain, insomnia, thought I would faint every time I stood up, could barely walk, no appetite, etc. It was ridiculous and I thought I was going crazy because how can one medicine do all that?? I now have a whole new respect for antibiotics.

Since I was feeling so horrible by the 2nd day on it I went ahead and finished the last day. (hindsight probably stupid)

This is my first day off and all my muscles are still killing me, especially my neck, chest, stomach, back. Still feel weak and my temp. this morning was 101 and went down to 100 now.

And I don't know if it was the medicine or just being sick but I've been so 'out of it' today and just depressed. I can not WAIT for this medicine to be out of my system! And I will never use it again.

To add insult to injury I'm not sure if it cured the UTI all the way. Not running to the restroom but still have slight (non-painful) tingle down there.

I'm a 45 yr old female, I've been on Singular for many years (originally for allergies and then asthma too) and have quit three times due to "possible" side effects and tried other asthma medicines. Inhalers make my GERD worse and I'm anxious all the time. I have to say Singular is the only thing that really works for my asthma and I keep going back to it because it does work. Also, I found that when I quit and expected my depression, headaches or fibromyalgia to go away they didn't... so I own these symptoms now regardless of Singular. I've always had mild depression and anxiety and all the prescription drugs for this I find are really too strong and are made worse then by Singular. For mild depression I find taking SAMe and St. John's Wort to really help me. Can't say if it would help others but you might look into it. I think it's important that doctors understand a link with depression and Singular but for some of us there's not another choice.

I've taken Ultracet for about 4 years almost every day, morning and night time and sometimes in the afternoon depending how severe my pain is. I take 2 pills each time. It does help take the edge off my pain. My doctor said my Fibromyalgia is as bad as it can get, plus I have severe arthritis through my whole body. I can hardly stand up straight and trouble walking. Ultracet seems to help better then Ultram for me. I'm concerned about how long I've taken Ultracet and damaging my liver or other organs. Does anyone know how long you can continue using Ultracet before it does damage. I'm very concerned about that issue because it does somewhat help with pain. I haven't noticed any side effects using Ultracet. If anyone knows how long you can stay on Ultracet without any harm, please post your knowledge or experience. Should I also have my blood monitored periodically?

Wow. I started taking this when it first came out, a couple of years ago. I had DM w/uncontrollable BS's. BS's came down significantly. But now, a couple of years later, I've been experiencing a few night terrors, when first put on insulin and Januvia, I gained 20# and can't! get them off. I also have fibromyalgia,...so I didn't even think about the Januvia possibly accelerating, increasing, or changing what was going on with the fibro.

I get violently sick anything with Metformin, and swell up like an air balloon (gained 50! lbs. on the Avandia & Actos (MD screwed up and gave me both in maximum dose--I've had leg swelling ever since.) Anyone have any leg swelling/edema? They keep trying to put me on anti-depressants..I've had "real" depression before, and I don't have that kind of feeling, just exhausted, like I can't get going...fibro...or Januvia?

After reading a

I am a male of 67 years old. I took Lipitor for a year, and after a few months of taking it, I felt muscle pains in my arms and shoulders, as well as my back. I felt weak and could hardly put my socks on by myself. I told my family doctor that I thought the problem was caused by LIpitor. He said it couldn't be possible, but he couldn't figure out what was wrong, so he sent me to a rheumatologist, who gave me an initial diagnosis of polymyalgia rheumatica. I went back for a checkup, and although the sed rate was normal, the C-reactive protein was elevated. He felt his diagnosis was an accurate one. He prescribed prednisone for me. I had some doubts about it, since I am diabetic, and was concerned about the elevated blood sugar it might cause. Well, it did elevate my blood sugar, and I weaned myself off it within three months. My blood sugar went back to normal, and while the prednisone helped the symptoms of muscle pain and aches, after I stopped it, the pain returned with a vengeance.

About a year passed after discontinuing the prednisone, and I felt worse and worse. Any time I engaged in physical activity, such as yard work, I was almost incapacitated for two or three days. I felt weaker and weaker, and by now, my activity is about ten per cent of what it was three or four years ago. I am unable to do anything physical without paying a heavy price.

I would tell the doctor that I felt the problem was caused by the Lipitor. He would dismiss my comments, saying that the pain should have gone away after discontinuing Lipitor. He sent me back to the rheumatologist with results of recent blood tests. Both the sed rate and C-reactive protein were normal. The rheumatologist touched my back and other areas, which caused me to jump. He said it might be fibromyalgia. I told him again that I thought it was caused by the Lipitor. He said the same thing my GP had said: if it had been the Lipitor, the pain would have gone away when I stopped taking it. I know the Lipitor caused the pain, because I tried red yeast rice for a couple months. The pain increased to almost unbearable, so I discontinued the red yeast rice. If I were not susceptible to the pain from the Lipitor, would the red yeast rice have increased the pain?

So here I am with a fuzzy diagnosis from the rheumatologist, and no clue from my family doctor (that he will verbalize, at any rate). My life has gone steadily downhill. I used to be a strong, active person, but now I can do very little, and my strength is a shadow of what it formerly was. What can I do?

I have been on Lipitor for over a year know after having a heart attack at 43 and having two stents put in. I was diagnosed with Fibromyalgia by in 2002. Recently, I have been having more arm, leg, back, pelvic, hip and hand pain then ever before. I am going to talk to my doctors now about the side effects. I have just know decided to start halving my Lipitor and may ween off of it completely. I'm on Niacin and Zieta in addition to the Lipitor. Have also been having a lot more digestive problems lately...am to be scheduled for a upper GI. I came here looking for info on the fact that although since being on Plavix (didn't realize Lipitor could be culprit) I have had bruising...today I found knots under two bruises on my upper arm. Not only are there knots but they (the bruises) are a different shade of blue (if that makes sense). Thanks to all who have shared their stories.

Nine months after given CIPRO via IV at the Hospital, I am still crippled.

I was a healthy 58 years old working full time. Now my tendons, muscles, ligaments hurt all over my body. I have very limited flexibility.

I am sooooooo aggravated that doctors don't believe you and they want to treat you with prozac.

I am sooooo mad that nothing I can do but suffer.

Lawyers said unless doctor diagnosis Tendinitis nothing they can do and doctors insist it is Fibromyalgia.

I am a 39 year old man with peripheral neuropathy and migraines. When I was diagnosed 3 years ago, the pain in my right leg was horrible and headaches daily. My Dr. put me on Topamax and I was so happy, it seemed to help but one night( about three weeks into it) I went to bed and awoke in the morning legally blind. Topamax was stopped that day but it took 4 months ( and changing the prescription in my glasses 3 times) for my vision to return to 20/20. The doctors tell me I was lucky as some people have perminate lens damage from the optical pressure change.
My doctor said I could not take any thing in that class of medications as it would probably have the same effect on me. So he decided to put me on Cymbalta for the neuropathy. He said it was being tested as a possible use for neuropathy but had not been proven. It works great for the pain and oddly my migraines have gone down to about two a month.

i have acne. bad leg cramps and yes i have noticed my skin staying tanned longer than normal. my mouth is very dry and i am depressed often. not normal for me. i am a very outgoing person and i have been withdrawn from my friends since taking mobic. i thought it was just the fibromyalgia. have headaches very often. some weight gain.

I am a 60 year old female and have been on Lisinopril (40 mg.) for at least10 years. Before that I was prescribed Zestril, but a generic was often substituted (Lisinopril). So it's hard to say just how long I've taken the Lisinopril. I'm amazed to read the side effects listed here. I've experienced almost all of them at one time or another. It's scary. I've tried to quit the Lisinpril a couple of times, sometimes just because I ran out of the prescription. But now I am substituting a natural supplement for the Lisinopril. I'm trying Holistrol (HiQi). I've been on it for about a week. I checked my bp when I started the natural and will check it again after a week. It was high when I first checked, but I had been off the Lisinopril for a few days by then. I'll continue to monitor and take the natural supplement and then will report back.

These side effects are very similar to those experienced by people diagnosed with Fibromyalgia and Chronic Fatigue Syndrom ( both of which I've been told I "might have"). My diagnoses came from several doctors in my hometown and even from the Mayo Clinic. I'm wondering how many people with these diagnoses are taking Lisinopril?

My side effects are starting to leave my body, but after so many years, there are many layers of toxins to release. But I am confident that I am doing just that ~ releasing toxins!

Thank you for listening and especially for sharing your side effects. This is bad stuff in my opinion and I'm glad to have started the process of clearing this poison out of my body.

Ann

I took Cipro and had a persitant leg twitch, and did not think anything at the time. many symptoms came around a month later. all over body twitching, burning skin, muscle pain, tendon pain. maily on left side of body. Also, insomnia, dark circles under eyes, horizontal depressions in fingernails...just to name a few. It has been almost 2 years and I have sense been diagnosed with fibromyalgia by PC, I need to go to a ruemy. I have never had these pains until cipro and I still have all of them most of the time.
I told my mother not to take Cipro or any in the same class. She was prescribed Levaquin and called the nurse and said she did not want anything in the same class as Cepro, and thew nurse said "Oh no it is not, I did hear Cepro was bad". So she took them unaware. She was so sick after first pill. she thought it was severe flu. She could not even move her arms because of terrible shoulder pains.

My mother and I have both been diagnosed with Hashimoto's Thyroiditis and we both take levothyroxine. We both experience extreme pain and she has been diagnosed with fibromyalgia. I have not been diagnosed with fibromyalgia but I experience the pain body also. Another thing. I have been losing my hair. No reason, it's falling out from the root and I have some serious thinning. Memory...what memory. I can't remember anything. Has anyone received advise from a MD? Thanks

i started taking yaz a couple months ago and developed a blood clot in my lung, a pulmonary embolism. i was hospitalized for a week in may of this year. i have visited many websites to see if other women have developed blood clots due to yaz and i have found a startling number of women that have developed blood clots, and a couple girls who even lost their lives. the side effects of birth control are explained to us before we start taking them, and it is expected that some women will experience the side effects, and this is normal. however, when a disproportionately large number of women start having serious health problems due to yaz, then something is not wrong with us, something is wrong with yaz. i have seen many women express an interest in starting a class action lawsuit and i am trying to do so. i have worked in a personal injury law office for the past 2 years and know an excellent lawyer looking to take on a case of this nature and magnitude. if you or your loved one has developed a blood clot, lost their life, or have developed another serious health problem due to yaz than please email me at ****** with your name and an email address i can reach you at. A class action lawsuit requires a large number of plaintiffs. I have already gotten a few emails but need many more before we can make this happen. please email me... help me and yourself.

i feel no emotions while taking effexor. no anxiety, mind you, (which is what i was using it for---GAD.) so no anxiety is good, but is it good to not feel any sorrow, empathy, joy or happiness??? I feel like i am just going through the motions of life, not really living it. but if i don't take even 1 dose, the anxirty comes back. (but the other emotions come back too) i cry more if i miss a dose, and that used to worry me into thinking i am depressed....BUT it is normal to cry when you feel sorrow or empathy. and maybe the tears have to come flowing out as a form of release, because they were withheld for so long by the effexor. other possible side effects could be: insomnia; headaches, clenching teeth, biting cheek and tongue a lot, constipation and weight gain. (hard to know if these are side effects of effexor, or symptoms of fibromyalgia).

I've been taking Trazodone for 4 yrs, it helps my neck muscles relax during the night, and also helps me sleep. I have FM (fibromyalgia). My chief side effect is E.D. I thought it was the Traz but in looking thru all your reports of side effects I don't see one mention. I used to enjoy sex w/ my wife (she LOVES to make love!) but now, not only can't 'get it up' but don't even think about sex, EVER. I'm a 50-yr-old male, and this is kind of scary. Michael Douglass' wife could walk by in a bikini, and my remark would be, "How 'bout them Cubs?" Anybody have a similar experience?