Neck pain symptoms and conditions

I was in the hospital for a gall bladder surgery 2 weeks ago and found out while in there I had a UTI. The doctor's at the hospital put me on Clarithromycin the first day. Then my family Dr. came in and changed it to Levaquin via IV drip for another 6 days. I was then prescribed 2 pills for when I got home to take. The first 2 days in the hospital I had pain in my shoulder and I know that was from the air they blew into me for the surgery. BUT, after that, I have had continued shoulder, neck pain and now has spread into my wrists, my legs, virtually I feel like one big ache. Last night, I had to take my shirt off because it was hurting my skin for the shirt to touch it. My sense of taste is weird too. I have Ehlers Danlos Syndrome but I know that my pain right now is a direct result from Levaquin. I went in to fix one problem and came out with another one. Like I need that! I feel for all of you. I identify with most all of your complaints. I was on the drug for 10 days. I can barely grasp anything without pain in my left hand. I don't know what to do. Does this go away? Or is this permanent?

started taking lisinopri 5 weeks ago. feel headache, neck pain, bed leg cramps that wake me up from sleep. the worst is the anxiety, can't concentrate at work, shaking as if i am cold, can't sleep because anxiety, heart palpitations. I stop taking this 10mg yesterday because this is no life.

hair loss, neuropathy in my right leg, complete exhaustion, numbness and tingling, stabbing pain in my back that wraps around my chest, headaches, depression, paranoia, stomach pains, chest pains, tremors in my head, pain down my neck, pain in toes, blurred vision, tearing pains in feet, very weak, moody, pain in face, really bad symptoms week prior to period, cracking sound in joints, -- Have had symptoms for three years and just had a neurologist confirm today that all of these problems have been caused by my doctor prescribing avelox and prednisone!

I had the Mirena inserted when my daughter was 6 weeks old, August 2007. I had no problems (that I THOUGHT were related to it) until end of July this year. I had next to no period up until then and then bled for nearly 3 weeks straight. Went to the doctor who said I had a miscarriage...ok so let's take it out, it obviously doesn't work for me and go back to the pill which I had been on most of my life when I wasn't pregnant with any of my 5 children. After 3 weeks of being on the pill I had it removed on 9/10. No pain at all actually but haven't stopped bleeding since! Went back to the Dr on 9/23, felt my uterus and said seemed fine. No fibroids or polyps that he could feel. Changed my pill Rx and said it should straighten out within the next 2 cycles, if not come back...on 10/5 I went back without an appt and was told by the nurse to double up on my pills to try and stop the bleeding. I scheduled an appt to see the Dr the following am. Had an internal ultrasound done and a biopsy of the lining of my uterus. Results should be back on Tuesday... my Mom & Sister told me to look online about side effects with the Mirena and I found this page. I am comparing many of the things I have been experiencing and now realize perhaps they were ALL related to the IUD. I gained weight (am actually heavier then I was after my daughter was born and I lost all my pregnancy weight within the first month), I had terrible acne, headaches, back & neck pain, constant fatigue, emotional, decreased sex drive. It has been out 4 weeks today and although my acne has improved slightly, I feel like I have been on the brink of the flu since last Saturday, no motivation, pure exhaustion, and emotional roller coaster not to mention the cramping from my biopsy that probably wasn't necessary now I'm thinking and 4 days in a row home from work... I am hoping time will heal the way I feel once the hormones adjust themselves. The pill always helped me more then it ever hurt me. I'm glad I got the Mirena out as soon as I did. Just wish I would have known sooner what it was really doing to me!

For any person that got the Gardasil vaccinations and did NOT have any side effects or symptoms, PLEASE go and have a pap test done immediately! We are getting reports of these girls that had no side effects to the vaccine that are now getting cervical lesions and cervical cancer. So if you know of anyone that received Gardasil with NO side effects, PLEASE tell them to get a pap test done immediately!

My 16 yr old daughter was also injured by Gardasil. She had 2 of the 3 injections (Jan 9th and March 9th, 2009). Before Gardasil, she was a happy, healthy and vibrant teenager. Since Gardasil she is sick every day of her life. She has dizziness, overall weakness, numbness and tingling in both legs and left arm, back pain, neck pain, pressure headaches, vision problems, breathing problems, chest pains, racing heartbeats, brain fog, stomach problems, nausea, diarrhea, weight loss, hair loss, jerking all over spells...the list goes on and on.

She was an A/B student but failed her 10th grade year because she was too sick to retain what she was trying to learn (brain fog). She no longer has the energy to go off with her friends. Most days she lays in bed, in pain.

This just doesn't happen to a healthy teenager!! And it just doesn't happen to THOUSANDS of other girls with no connection except they all had the Gardasil vaccine.

It doesn't take a rocket scientist to figure this one out.

Please educate yourself as much as you can before you allow anyone to push this unproven and unsafe vaccine on your daughter! The guilt is overwhelming from a mothers' standpoint! I thought I was doing something to protect my daughter. Instead, I allowed the doctor to inject poison into my child and take away her life!

These 'side effects' are NOT rare! They are happening every day to literally hundreds of thousands of young girls after receiving Gardasil. The numbers in VAERS is estimated to only be between 1-10% of the true numbers! Try asking some of us moms who have to deal with these horrible side effects every day if we consider it to be RARE!

Everyone should look at the other side of the fence and research this. There are thousands of girls that are coming down with strange illnesses, paralysis, gran mal seizures, etc. after receiving Gardasil.

We are now getting reports of girls as young as age 9 that are breaking out with genital warts and severe cases of cervical cancer AFTER receiving Gardasil. Some of these girls/women did not initially have any side effects from the vaccine.

There are perfectly healthy girls all of a sudden come down with all of these strange sicknesses (some that I cant even pronounce) after getting jabbed with Gardasil. All within hours/days/weeks?

Just like Merck's 'wonderful' Vioxx...what will it take? How many dead/injured before someone takes notice?

The doctor that literally pushed this vaccine on us at a routine doctor visit told us that there were no side effects except for soreness or redness at injection site.

She also told us that it would protect her from a whole LIST of things! I had seen the commercials but had not researched it.

As a matter of fact, I never really THOUGHT about vaccines until my daughter suddenly started having all of these strange health issues.

She was ALWAYS a healthy child, happy and outgoing, active and just a joy to be around.

Now, she is a totally different child. She is always sick..always in pain..and cries a LOT, so scared that she will die in her sleep from the breathing problems. She describes it as breathing through a blanket or that an elephant is sitting on her chest.

She has SO many of the exact same symptoms as all of the other girls that have been injured.

It is NOT a coincidence! All of these Gardasil girls have the same symptoms, some worse than others, but the bottom line is the one thing they all have in common is Gardasil.

These symptoms are NOT in their heads!

My daughter started having dizziness, overall weakness, pain and numbness in both legs and left arm BEFORE we found out about any of these other girls having the same issues.

When I called her doctor that gave her the vaccine (as soon as she started with these symptoms) she said it was NOT the Gardasil vaccine that is causing it. How could she be so sure? This is such a NEW vaccine...a DANGEROUS and UNNECESSARY vaccine!

HPV is not an STD (research this!).

Cervical cancers have gone down 70% since the PAP smear came along.

This is NOT an epidemic! Why are they mandating this vaccine for as young as 9 year old girls for a vaccine that doesnt even do what they claim it will do?

Girls are now coming down with cervical lesions and HPV AFTER receiving Gardasil! I'm talking about healthy young girls that did NOT have these things BEFORE getting Gardasil.

Young girls dropping dead within hours of getting the vaccine and they think we are all stupid enough to believe it was a huge tumor that was in her heart and had spread to her lungs? (I'm speaking of the 14 yr old that just recently died after receiving Cervarix).

If that young and healthy and active young girl really DID have this so called huge tumor, she would have had symptoms. A tumor like that doesnt just up and kill it's host without a 'wasting away and painful period'.

That is a complete cover-up!

Just like the young girl that has been paralyzed and hospitalized for the last year, Ashleigh Cave. Because her mother was trying to speak out and find out what exactly happened to her daughter, they have now placed that child under protective orders! To shut the mother up?

This is all about $$$$$ at the expense of our young daughters (and now sons) health and lives!

It is an outrage!!!

Please see my posts at ******

And this website:

******

There, you can see other girls' stories and their pictures..there is also a memorial document with pictures and stories of young girls that have died after receiving Gardasil.

Educate Before You Vaccinate!!

Hi, I am a mother of 2, and not quite 23 years old and got the Mirena inserted at my 6 week check up after having my second. I read all the literature that the Dr. gave me and I was sure that Mirena was the right thing for me (no where in the brochures did I read anything about the symptoms Ive read about here or anywhere else on the internet). I started having incredibly horrible mood swings, bloating, fatigue, nausea (sooo bad, every day) back pain, neck pain, no sex drive (!!!), depressed, lazy, headaches (to the point where I thought my head was going to explode), constantly hungry, acne, smelled maple syrup constantly, complaining all the time about everything, weight gain (only 7 lbs but I just had a baby, I need to lose weight, and I'm nursing),chest pain, and some other symptoms but the most important one is the stomach pain i was having. The pain in my stomach felt like a knife, and I kept having pain in my right side. So after a few days of this pain I went to the dr. he ordered an ultrasound of my abdomen and I am scheduled to get that done Wednesday. My doctor thinks that I may have gallbladder disease or something else seriously wrong with me that we suspect is induced by the Mirena. Keep in mind that I've had this thing in me for about 4 months!!! So after my doctors appointment I typed into google "side effects from Mirena" and Omg, I wish that I had done that before I got the thing inserted, those brochures about the Mirena make it seem like a Godsend and I am all for a lawsuit due to the problems I am having and the depression Ive felt. My 3 year old has suffered from my mood swings, every time id feel it coming I had to make her go to her room :( that poor girl deserves to have a mother that is not so depressed and ill that she can actually play, and both of them deserve that really, and im doing the best I can.... anyways I removed it myself yesterday, i had a hard time finding it but I took it out and I feel as if a huge burden has been lifted, EXCEPT I have been cramping very bad, spotting and incredibly sick, i also read about this thing called "the mirena crash" no matter how long you've had it in, if the hormones were in your system then you are effected and can feel very ill from it (and it can happen to women who had no problems while on it at all, even after 5 yrs). Im hoping that I have nothing wrong at my doctors appt on Wednesday when I get the ultrasound, and it may just be a cyst, turns out that is a side effect of mirena as well, that and bleeding the first several months (oh yeah, I did for about 2 months maybe 10 weeks altogether) Im also hoping that my daughter whom I am nursing is not sick as well :/

oh and for anybody out there thinking that the only women gaining weight are fat to begin with, well I am usually 105 lbs, after my baby I weighed 145, lost some weight, went down to 130ish gained it all back then some, losing weight is easy for me because I diet and exercise like I should, now I am doing all that and nursing a child.... and hello weight, when it really should be goodbye... well goodbye mirena I WONT miss you!!!!

I took levaquin for 10 days and then cipro for 10 days after being misdiagnosed with bacterial pneumonia when I really had cocci mycidioidosus (valley fever) a creepy lung infection from a fungus that lives in the dirt here in Ca . Within a few days of stoping the antibiotics I experienced severe joint pain,dizziness,swollen neck ,hives,pain and tingling in my legs and feet,taste perversion,neck pain,hallucinations,nightmares,suicidal thoughts,dead skin,head ache,conjunctivitis. All of which I thought were valley fever related . A few weeks later I started noticing loss of vision and an inability to focus or concentrate on anything. I have ruptured 5 tendons and sometimes can't lift my right arm off the table.
I'ts been a year and 3 months and I still suffer from these side effects and about 3 months ago I started to notice some hearing loss and then ringing in my ears so load that it wakes me up!

This drug has ruined my life.I have lost 2 profitable businesses,a house a car .a commercial building, my credit score is 309 from 760 a year ago.All from a stupid antibiotic that should not be sold in the first place unless you are going to die if you don't take it.....personally I would rather be dead I think.

I think that we (the 1000's of people effected by this drug) should protest,march at ORTHO McNEIL's doorstep and perhaps the FDA....write a letter ,call or write to OPRA...do something ...It's not right that they get away with selling this crap.

Please email me ...I see 1000's of you on these sites...lets get busy!

******

Thanks for reading

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.

Where do I start? Extreme lower back pain, no Menstrual cycle since March 3 2008 even after being removed (no I have been tested for menopause). Throat closing up, nasal congestion, body going numb, chest pain, neck pain,sever fatigue, uncontrollable twitching the list goes on. I have been in and out of the hospital for a year and four months now till we finally figured out it was Mirena this has cost me a fortune in wages lost and hospital visits.Run don't walk from Mirena it is not worth losing your life over. I believe it almost cost me my life several times now. I even told my mother I didn't think I would be around much longer if this continued. The Doctors did not figure this ou\t but wether your a believer or not I will tell you with no shame we prayed for God to show us what was wrong and he did! I immediately had Mirena removed and that night my nasal congestion went away. The other symptoms are a little slower and I am still having spells now and then. The Doctor said it might stay in my symptom for a while and to be patient. I have had enough already run as fast as you can from this IUD!

Started Taking Macrobid after for UTI after Bactrim did not help and Cipro made me break out in hives. I've only taken 3 pills and have started getting headaches and waking up with severe neck pain. It's horrible I can hardly turn my head because my neck is so knotted up and stiff. I'm not taking any more because after 3 different antibiotics that have made me feel horrible, I need a break.

I began taking Levaquin for a kidney infection. After the first pill (500mg) I had insomnia, joint pain and a little under the weather. I thought maybe it was a combination of the pill and still having the kidney infection. I figured the infection wasn't gone because the first med, Sulfameth/trimethoprim 800/160 I had a reaction too also. That was prescribed for 10day when I only was 4days into it with that pill. So I went from Friday to Monday without any medications. I felt that the kidney infection was still there because I was still hurting, not as bad as when I went to ER but knew it wasn't gone. So Monday night I started taking the Levaquin. Felt bad after the first pill but after taking the 2nd pill I became very weak, had ringing in my ears, eyes started to swell,had sweats nausea, stomach hurt and became very bloated, neck pain so bad I could hardly turn my neck. Pain running down into my shoulder blades, jaw pain, sore throat, nausea, felt like someone was squeezing muscle in left arm and squeezing muscle on left side of neck Started to have some muscle pain in right calf. Call Dr. on call and he said STOP taking the medicine, take some Benadryl and if gets worse go to the ER. Well, I took some Benadryl which made it seem a little better, but this is the day after and my muscles by my shoulder blades are so sore and have a burning sensation. I still feel somewhat weak but not as bad as last night. Seems I tired out real quick. This medicine made me feel like I was on the way out. I was prescribed it for 7 days and only took it for 2. Now I am very hesitant about taking anything as I have had reactions now to 2 different meds. Still don't know if kidney infection is gone or not. Does anyone know of any natural ways to rid yourself of kidney infection? I would appreciate any advice anyone has. All I know this has been 2weeks of @@@@ since I was diagnosed with this kidney infection.

I had taken Bactrim in the past without a problem. My daughter, however, has a history of rashes associated with Sulfa drug use. I didn't say anything to the doctor that gave it to me for a sinus infection. With in 5 days of taking it, I came down first with some pain in my neck. We were on vacation and sleeping in a new bed, so I dismissed it. By the end of the week, I had a fever going up to 103. The following day, my neck pain was so bad, that I had ice on my lymph nodes. The day after that I had broken out in a rash so bad that it looked like I had a terrible sunburn. My skin was even hot to the touch. By this time, I had realized it was from the medicine, and stopped taking it. The rash isn't as red, but it did spread out to my arms, legs, and torso. I called my doctor when I got home, and he just said to take an over the counter antihistamine, but I was not referred anywhere else. After doing research on the internet and carefully reviewing the warnings from CVS (where I picked up the medicine) I believe that I have Stephens-Johnson Syndrome caused by Bactrim. This is actually listed on the warnings, but not what the symptoms are of this illness. It has been more than a week, and I still have the rash, although not as bad as it was last week.

I'm 22 and started taking Loestrin 24 two weeks ago on the first day of my period. I only enjoyed a few days after my period before I started spotting again, and now it's non-stop. I have also developed acne after a couple of weeks, am experiencing cramping and back/neck pain, and am becoming slightly irritable.

I have taken Nordette before and experienced virtually no side-effects. After reading all of these reviews, I am strongly considering getting off this pill.

This is a sad yet enlightening day for me. I can't believe the things Nuvaring has caused for me. I am so glad that I questioned it earlier and found this site as a result. I originally tried NR in February 06 and continued for about six months. I don't really remember side effects from that time. We had a newborn and I was finishing my last semester in college, so I wasn't exactly sleeping a lot. I will say that my libido fell off the face of the earth. It has taken a while to get it back even a little bit. Ever since then I have asked my doctor what could be done and she just would tell me it's normal to lose my sex drive after having a baby. So in May my doctor put me back on NR to help shrink an ovarian cyst that she is worried about. She had me stay on the NR for 6 weeks straight through. I just took it out last Saturday and I will be done with it forever.

Here is what I experienced during my six weeks:
- Libido- zip. zilch. non. nuf said.
- 2 migraine headaches
- Severe neck pain to where I was about a day away from calling a chiropractor
- Couldn't wear my contacts for the past month- my eyes got really dry and itchy
- EXTREME burning during and especially after sex- and if I had to pee, my husband would have to give me a wet towel to ease the burning pain.
- Lack of appetite
- Really bad mood swings/ depression- I am a really optimistic happy person and for the last month I feel so negative and down about everything. I want to cry a lot and the anger has been awful. My boss and I got into multiple arguments and I wanted to walk out of my job. My son has been on my last nerve for no reason, and don't get me started on my poor husband.
- Waking up multiple times in the night and having trouble falling back to sleep.

Once I removed the ring, I have felt lighter and happier. I even sent my husband a racy text message because I was thinking about sex! And my neck pain has disappeared. Unfortunately, for the last week I have woken every night at 3am and stayed up til around 4:30am. My cramps have been awful. Usually they were really bad the first two days of my period. This time, they have lasted for 4 days so far and don't seem to be stopping. I have gotten extremely constipated and this is something that doesn't happen- I usually go the other way. So my stomach has been a wreck of gas pains and cramping. I have been exhausted.

I just wanted to share my experiences. My husband and I were talking the other night trying to figure out what was going on with me, so I feel a bit more reassured that I am not a psycho after reading so many others' problems. I took my computer in to him and read some symptoms to him and he was as shocked as I that this may all be from the NR.

As many of you have I started Fentanyl for chronic back pain and neck pain. My nurse case manager suggested it as she had been on it for 3 years and thought it was great. I started out with 50mcg for 3 days each patch. First patch I was a little drowsy feeling but by the 2nd I was used to it and it seemed to help a little. Enough that I had increased my walking and was hoping to help strengthen my back. Now to the horror, my calves continued to ache. At first I thought it was from the extra walking but it would not go away. Then I had the sweats and would just soak a T shirt while I was sitting in my recliner, then I would freeze to death. I thought something was wrong with my air conditioner. Then trouble sleeping and just 1 thing after another until the depression and anxiety started. I am disabled and my wife is a nurse so I'm home along a lot so I hid it. I would sweat like crazy and shiver and be so cold then get so anxious that I would lay down in be to try to rest and paw at my covers and even my clothes. I was either too hot or too cold. I would pace the floor so anxious I thought I was going to loose my sanity. The silly thing is that I was not putting together as being the Fentanyl. Our son had been diagnosed with a very bad brain cancer about 6 months before and I thought it my be partially from that. I fought it for a couple of weeks behind closed doors, although my daughter had call mom and said what is up with dad? He is having some type of problem. Well, to try to cut this to a manageable sized document I finally had to wake my wife up in the middle of the night shaking, crying and pulling at my clothes saying I'm *** and I don't cuss like that. She had warned me not to try this med but I was desperate to be pain free or at least able to manage it and be half way normal. She got me to the doctor and at first they were gonna cut my 50mcg down to 25 for 2 weeks and then go to 12.5 for 2 weeks. My depression and side effects were so bad that they wanted to stop putting Fentanyl into me asap. So I went 3 days with the 25 and 3 with the 12.5. I have been climbing the wall since Wednesday and have none in me except the residual and hopefully it will be out in a week or so. I just want to say that my depression is something that I cannot even explain. I ball and blubber like a baby at times for no reason. I cannot even see or talk to my kids on the phone because I just come apart. I'm constantly beating my self up over my mom dying from Alzheimers as if I could have done something. I think of times when the kids were small and literally want to go back there. It's not like saying hey remember when we used to do (whatever) I literally want to go back there. I know in my mind that it is impossible but I just cry to go back to the farm where my dad and mom lived. Mom has been dead for almost 10yrs. The doc gave me Ativan to take the edge off a little and Clonidine for chills and sweats. I've been off of it (Fentanyl Patch) for 3 full days now and the depression is still unbearable but the other side effects are a little better. My body aches were pretty bad last night though as I think about it.
I just wish some one could tell my how long it will take me to get back to my self, good sense of humor and loves to have fun with my family.
Thanks
*****

My husband stumbled across this website and first I would like to thank everyone who have posted their experiences on the NuvaRing. Because of you guys I now know I'm not losing my mind.

I started the NuvaRing March of 2008 and I started getting dizzy spells May 2009. I actually got my first dizzy spell when I was driving. Everything started to spin very fast!! My husband had to grab the wheel and tell me how to slow down and how fast to do it. That was the scariest thing ever!! My head felt a numbing sensation in my head. I had a pain above my left eye and it would shoot up my head and down my neck. The dizzy spells would come whenever, once every 8 days to twice in one day. I have had an MRI and an MRA done and nothing. The docs have had me on so many migraine meds to try to get a handle on this and nothing has helped. My longest migraine lasted for 14 days, that was in May. This month (July) I got a migraine on the 13th, took the ring out on the 21st, and had a dizzy spell this morning but this afternoon and especially this evening I feel amazing.

Since getting on the NuvaRing, like so many of you, my sex drive does not exist. It has caused so many fights between my husband and I. Its hard to tell him that he is still attractive but I can't explain why I'm not excited. So thank you for writing your experiences. He got to read that I'm not the only one and I wasn't making it up.

These last three months have been hell for my family and I. I have been like Dr. Jekyll and Mr. Hyde. So much tension has caused everyone to walk on pins and needles when they are around me.

So lets sum it up here, after being on the NuvaRing for 14 months I started getting dizzy spells, migraines, nausea, neck pain, twice I've puked because of the room spinning so damn fast, and very very VERY low sex drive.

I'M NOT CRAZY!!!! :)

I am 25 years old and have been on nuvaring since July of 2007 (so 2 full years now). I didn't really start to notice any symptoms until June of 2008. I didn't have any of the weight gain (I actually lost weight--probably due to a battery of other side effects I'm now noticing-- I was 125 in college and am 114 today).

In June 2008 my periods started to get REALLY BAD! I mean I would put a tampon in and an hour later be leaking like a river. I was at a movie one night and actually had to tie my sweatshirt around my waist and run to the bathroom because I had bleed through my jeans SOOOOOOO bad. For the last year I've had to change my tampon every 2-3 hours and always, always, always use super sized pads to make sure I don't bleed through any more clothes! I've noticed clotting the past few months as well. Before that I had NEVER passed clots during my period.

Since April of 2008 I've been in a serious relationship with a loving man who recently became my fiance. We are deeply in love, but I have ABSOLUTELY NO DESIRE to have sex, none. This is worsened by the fact that sex causes me UNIMAGINABLE pain and burning to the point I try to avoid it at all costs (we've tried condoms, water based lubes, silicon lubes, gels, you name it, all to no avail!). I went to the OB/GYN in February of this year (2009) to tell her about my painful sex experience, because this was something completely new to me. She said I had vestibulitis (very similar to vaginitis) and gave me pills and creams to take everyday twice a day for the rest of like forever to try and help me. From reading some of these posts I'm thinking that getting rid of the nuvaring might just help more than those pills and creams (and the nuvaring probably gave me the damn vestibulitis to begin with!). I am also hoping to get any of my sex drive back at all. Please!!

The past two weeks is where the headaches, neck pain, dizziness, fatigue, nausea have really started to become noticeable. I almost couldn't finish making the bed yesterday and I've had a headache and neck pain for the past 8 days straight! I am constantly tired and have realized looking back that I've been constantly tired for pretty much the past two years. I've also realized that I've had some mild depression for the past two years as well. I pretty much haven't wanted to get out of bed or eat anything for the past few months and have no desire or energy to do pretty much anything.

I also think I have the mood swing issue. I cry, and I mean to the point I can't speak, over the stupidest things. And the crying comes on with no warning. I can be talking and fine one minute and a sobbing mess the next. I get really angry with my fiance for what seems like trivial things a lot lately. I get very irritable really easily and it seems. This is strange for me because in the past I have normally been able to stay pretty stable and even keel emotionally.

I took my ring out today, even though I really have like 10 days left for this month. Back when I was 19 and started on the Pill I did so because my cramps and periods were so bad I missed class or work. I am hoping that the next couple months aren't quite that bad, but I'm hoping to detox my system of this ring and start over. AND GET MY LIFE BACK!

I started the ring because of it's easy "put it in and forget about it for three weeks" convenience. When I was younger I was always forgetting to take the pill. I am not sure what kind of birth control I'll go back to when in a couple months, but I know it isn't going to be this EVIL RING!!!

I'm grateful to have found this site. My doctor put me on the ring because I was having such intense premenstrual headaches on Ortho Tri Cyclen Lo. The depression has been almost crippling since being on the ring. The first month was fine. The second month was bad. The third was so horrible I thought I was going to leave my husband because I felt so hopeless and alone. I took my ring out on Sunday. I don't think I'll be putting a new one in next Sunday. Doesn't seem worth it. The depression isn't even premenstrual anymore; I have it during my period too. Oh, and the periods are SO heavy. The first three days, I'm changing my tampon every couple of hours and have to wear back-up panty liners. And, I got a migraine this month right before my period.

Question to the others: Does anyone have neck pain? I had it on Mother's Day so bad and couldn't figure out what I'd done to injure it. Looking back at my calendar, I was premenstrual then. Now, I have the exact same neck pain, and I'm menstruating. I'm wondering if this has anything to do with the ring.

It seems that everyone is having similar symptoms. I have been on Doxy for about 14 days now and I'm feeling worse every day. I am on it because i had been bitten by a tick and contracted Lyme disease. I don't know much about the disease but it has me freaked out. I started taking the antibiotic 2 weeks after being bitten; losing my balance and almost falling to the ground. I also had a couple of dizzy spells after eating. I seemed to feel a little bit better the first week of taking it but started feeling the side effects. It started out with the occasional dizzy spell then came the exhaustion, anxiety, depression, lower back aches, soreness in the back of my eyes, stiff neck, headache in the back of my head, flu like shivers, racing heart, and complete body aches. I also found out the hard way not to go out into the sun while on Doxy. Felt like the tops of my hands were being pricked with a million needles and burning. I wish I could stop taking the drug and be done, but I am already scared about the outcome of the Lyme disease. I hope I can feel normal again soon.

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

My Mom was prescribed Levofloxacin ( AKA Levaquin) by her retarded doc for a mild cold and a sore throat.
After taking 2 tablets of 500mg each my mom is down is severe pain all over her body! she has joint pains, neck pain, arms, palms shes got severe pain all over her body!
She also has severe itching on the palms and her arms as well..
Headaches,
Things aren't looking good.

She in real pain! She tells me she just wants the pain to stop and that she was better off with the cold and sore throat.

She has stopped taking Levaquin.

Anyone got anyway to help her? something?? She is asleep now but tmr Im going to ask her to drink some kefir..

Thanks

I was prescribed topiramate (it finally went generic- I've been trying to get this med pre-authorized by Medicare for years) a couple of weeks ago for off-label use related to bulimia, more specifically, for weight loss. I also take lamotrigine, an anti-convulsant, for bipolar disorder.

I began at 50mg/day for 2 weeks then titrated to 100 a few days ago. The side effects I've noticed so far are opposite to most of the ones noted here. I am not lethargic or sleepy at all. It's 3:10AM and I am wide awake, as I was last night. I had an excess of energy today and plenty of words to express my ample thoughts. However, my brain working in a sort of backwards fashion, these are the exact sorts of symptoms that signal mania and are extremely dangerous to somebody who has my condition, so I am on strict notice with the doctors and will most likely be either taken off the topa if this continues for another day or two, or put on an anti-psychotic as a preventative, which of course would be counter-intuitive to the weight loss idea as atypical cause gain. You can see from my writing style of run-on sentences that my thoughts are a bit jumbled.

Also- numbness in the heels, irritability, neck pain, itching.

I shall try to post back if I don't wind up in locked ward :-P

Was on Lipitor 2 years ago and had to come off because of side effects - sever muscle pain.. Prescribed Niaspan instead .. 2 months ago my cholesterol rose to 7.1 and my doc put me straight back on Lipitor - 10mg.. Feeling lousy - neck pain, leg pain, dizziness, fatigue ... head feels fuzzy all the time and get sudden twinges in my chest.. Had stress test done last week and all ok.. Also have severe digestive problems. Going to wait until 2 full months done and going to get bloods done again

January of this year I was diagnosed with Alopecia Areata (spots of hair loss). My Dermatologist has been injecting Kenalog-10 every 4 weeks on my scalp. The hair is slowly growing back but the injected area feels bruised "always", and "yes" I have an indent on my head :(
I have noticed that I've lost about 20 lbs since my 1st visit, irritable & have head & neck pain on a daily. However, since mid April I've been having an abnormal period. (VERY ABNORMAL-Like every other week)
Does this have anything to do with the shot? Has it happened to anyone else? I've been reading everyone's side effects and it seams like it's targets at the bladder.

I was prescribed Doxy 100mg twice daily for 14d for a Mycoplasma pneumonia. Day 6 I started to get a bit dizzy and some changes in my vision, sort of having a hard time to focus but I just though it was symptoms of fatigue or just being hypochonric. From day 8 I started to get really depressed and felt that I was going to die and that everyone was leaving me. On day 10 I also started to get anxiety attacks and had extreme difficulties to concentrate on anything. By this time I also got tremor, weakness and tingling in my arms and severe neck pain. Throughout this time I was aware of the risk for benign intracranial hypertension, but I didn't get any headache or nausea until d 16, i.e. 2 days after I stopped the medication. I never had fever. I then dropped 6 pounds in a week and had a hard time eating. It is now 6 weeks since I stopped taking the medication. My pneumonia is totally gone. The depression/anxiety is almost gone although some social withdrawal and lack of initiative still remains. It's still a bit up and down but much better. My neck pain is still there but is also getting better and I only have minor tremor in my arms. The visual changes still persist but every now and then I feel like my old self again for a few hours/day. The whole episode have been, and still are, the worst experience of my life. I keep my fingers crossed that it will all go away over the next few weeks.