Needles symptoms and conditions

I was given Bactrim for a Severe Bladder infection. I got hives all over me Just big itchy bumps, I felt like needles were going through my body especially my feet. Absolutley Couldn't sleep. Legs shook nonstop. Horrible experience for me!!!

I am starting to think I would like to be a part of a class action law suit, my daughter had to switch schools because of her mood swings, and vague hallucinations. and vague paranoia. She once ran into a parking lot she was so afraid of needles! Took her to a psychiatrist, sensed she was quick to put her on mood stabilizers and left before the eval. Recently her ped refused to up her dose of singulair and told me about depression. I subsequently upped her flovent and took her off her singulair. I did this after I heard her teacher saqy she kept on leaving the classroom to go to the nurse, and was exhibiting defiant behavior. and saying she was depressed, hearing music that wasn't there, etc. Now that shye has been off of it a week, she is a different child, and hasn't argued with me once. Hasn't cried for 5 days. has not argued w2ith her brother either! I feel I have the child back from 5 years ago when she started taking it! unfrigging believable! I would love to sue, because these episodes have almost ruined my marriage, and caused me to miss many days of work, and feel guilty when I didn't Thank-God I just took her off of it on a whim!

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

I started taking this medicine for a UTI I'm allergic to penicillin and I see that this is in this medicine, that's real great. Well the first night I took it, I was so tired all I wanted to do is sleep, I had the worst headache ever which made me moody and my neck and back just ached. On the second day I woke up and it felt like needles going through my feet they were swollen and itchy and red, i knew right then to quit taking the medicine and yet it spread to my hands and it was the same thing! Still have had a headache 24/7 since i started the medicine. It doesn't help! Look at all the other reviews! Don't take this medicine you take medicine to help you not make more problems!

I will never take this medicine again!

I have been on omprazole 20mg 2x per day for 1 1/2 years. I went off of omeprazole in December of last year because I was tired of taking drugs. In February of this year I went to the ER because I thought I was having a heart attack (severe chest pain, pain shooting up my left jaw and my left arm was numb). The doctor in the ER gave me Mylanta with lidocaine and told me to go back on the omeprazole. I did and haven't missed a dose since that hospital visit. Until September 9, 2009 I took my regular dose of omeprazole (one in the morning and one in the evening) I was having a lot of discomfort and was uneasy. That day I also took two aspirins. I had continued stomach and chest discomfort and took some Mylanta. My old doctor had advised my to up my dose in severe situations and I took a third 20 mg dosage and within 10 minutes my face and arm went numb. I was rushed back to the hospital , my blood pressure was 144/81 and I was having panic attacks. I felt like I was going crazy. The doctor ordered bloodwork and a cat scan (because of the numbness) all came back normal. No one addressed the chest pain. Maybe because the EKG I had in February was normal (I don''t know). They had no answers and told me to follow-up with my primary care physician. I went home and finally tried to go to bed, I couldn't sleep well, my mind was racing. The next day the numbness and pins/needles went all over my body. Like everything just went to sleep. I tried to relax and stay calm. I finally went to bed that night but had a hard time falling to sleep (my mind was racing and I was scared). I eventually went to sleep and woke up with less numbness but I had a stiff and painful neck with a killer headache. I don't get headaches that often and this was a major concern for me. I called my insurance and they advised me to go in for an immediate care/same day appointment. I did which was also inconclusive but the doctor asked about my omeprazole. I told her I haven't taken any medications since I was seen at the hospital because I was scared it was something I took that caused the numbness. She didn't say that my symptoms were related to the omeprazole but told me to not take it again and only use Mylanta for my stomach problems. She was not a fan of this medication and told me it is over-prescribed. I have not taken the omperazole since September 9, 2009 and the numbness is almost gone but I still have the tingling and pins/needles from time-to-time and neck and chest pain. No headaches. The doctor gave me a mild muscle relaxer (for my neck pain) but with everything that has happened I haven't taken that either.
I have fibromyalgia and I manage my pain without medications and I do have random symptoms from time to time because of the fibromyalgia but these were acute and terrible. I have never experienced anything like this and I am hoping since I have stopped the omperazole I will go back to normal soon..........

nuvaring was recommended to me because i am absolutely terrified of needles and my mom didn't trust me to remember to take the pill everyday.
i just started the nuvaring yesterday. and ever since then, i have felt simply AWFUL. i feel so weak that i can hardly stand up. i've had a headache all day. all i want to do is eat. i can't seem to sleep enough. i woke up this morning sweating. and i've cried twice today for absolutely no reason. i get irritated at EVERYTHING. and reading all these negative stories is freaking me out. should i just take it out now? i don't know what to do.

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.

I've been taking Lipitor 40 mg. for over a year. A few months after, I started to notice my ankles were swelling a little bit. I attributed it to the warmer summer weather in Florida. It continued through the winter along with pins & needles on my soles and heels, and my doctor said it wasn't caused by Lipitor. After a 10 hr. flight to Europe in May, my ankles & feet were extremely swollen and painful. It hurt to just touch my ankles and feet. Even my toes were swollen. Bought compression stockings but it did not help. Walking on cobblestones was unbearable. I took my last Lipitor pill on May 30th.
Ankle pain is gone and the swelling has reduced a little but the pins & needles feeling is still here. Ankles look good in the a.m. but as the day progresses, the swelling increases. I don't know what to think! My only choice, I feel, is to wait it out and hope the swelling & tingling goes away. Anyone else with these side effects?

After 2 days of using Avelox for Chronic Sinusitis I felt like someone had stuck needles in my brain. Increased nausea and High Blood Pressure.
Once again Powdered Vita C to the rescue.

Ok, so here is a new one for you. I have had migraines for a very long time, since I was a teenager, and never really sought physician treatment because in our family a headache was "nothing to cry about". So, now that I am married with 4 kids and an advancing career, having migraines on a weekly basis isn't something I can live with anymore. So I went to my doctor. He said what about preventing them with Topamax. I know what Topamax is, I'm a nurse, I know what the potentials are, but I had not really heard of the side effects when using it in a perfectly healthy person. ANd I must say it has to be my own fault for saying "sure" and not investigating first. WARNING= Topamax is a drug for seizures, effecting the central nervous system, and will have effects on a healthy person's central nervous system. Now, not doing my research I will also not have known that you are supposed to be titrated very slowly up with increasing doses, starting at a suggested dose of 15-25 mg per day for the first week the 50 then to 100, etc. I was begun at 50 mg/day for a week then 100 mg a day thereon out. Please, if you experience the symptoms the pharmacy warns you about, but they are exaggerated, go back to your doctor!! Here are my symptoms by day
Days1-3- Normal effect- tingling hands/feet, taste loss of some drinks, foggy unable to think clearly
Day4-5- horrible head pain, back of my head, not like my migraine pain, stabbing and pins/needles in hands/feet, still can't taste, nausea, dizziness, confused (like I couldn't find my way to my doctor's office confused)
Day 6- And I am entirely embarrassed to say this one because I am a nurse, and I know what it implicates... Pseuedoseizure. I was in the doctors office, in the waiting room and I could not control my muscles. I knew it wasn't a seizure because I could hear some of what was going on around me, but something was not right. I couldn't move anything and I didn't remember everything. And all the above symptoms, along with. But, naturally normal CT...
Day 7- It happens again... And this time I have some right sided weakness and all the above, that's it, it has to be the Topamax, we are done. It's only been a week, so cold turkey.

That is my experience with Topamax, and unless I am actually seizing, it is a journey I will never take again, I have 4 little ones that depend on me too much. PLEASE research before you try whatever is handed to you!!

I have stopped taking Lipitor after 3 yrs. I was told I had a mini-stroke because of my slurred speech 6 mo. ago. Since then I have had a battery of tests and my neurologist told me "I don't think you had a stroke." I saw the words "Motor Neuron Disease" (I looked it on the web because I never heard of it before) on the script for my EMG. I blame it all on Lipitor and the wasting of the nerves and the muscles. I sound as if I am drunk. No one can understand me . I am taking speech therapy but it doesn't seem to help.

For the last year and a half I have taken Levothyroxine Sodium 50mg, now increased to 75 mg. I have gained a great deal of weight and developed arthritis in both knees. Some days my knees hurt so bad I can hardly get out of bed. Since my medication was increased to 75mg. I have been itching like crazy. It is not continually, but at times I just go into an itching fit. Please help! Is there any other thyroid medication that works without all the bad side effects?

I am 20 and had all 3 of the shots. I was going into my freshman year of college, and in September became very sick. I refused a blood test because I hate needles. By November I could barely walk on my own. The hospitals kept giving me medicine for bacterial infection, but it just kept getting worse. My fever stayed at 103 before I went back to the ER. A blood test concluded I had mono. Just figured I got this from being a freshman partier. During this time I also had an abnormal pap smear for the first time. My mom did research and found other girls who had cases of mono after the 3rd shot too. Very, very rare. Now I have to go to the gyno every 6 months because they found pre-cancerous cells. I also failed my first semester of college because I was so sick. This is all thanks to the Gardisal shot. I do NOT recommend. It should be taken off the market now!

I had the Mirena inserted July 2007. I thought the Mirena was the best invention ever! I have migraines so I could no longer continue taking the pill. My doctor and I discussed my options and we both thought the Mirena would be a good solution. I didn't want to have anymore kids but I was mentally ready to have my tubes tied. With the Mirena I would have lighter periods and no migraines and it lasted for 5 years. No remembering taking a pill every night. Sounded like a win-win situation to me. During the latter half of 2007 to early 2008, I gained 22 lbs. It appeared overnight (or that's how I felt). I blamed it on it being the holidays and eating too much. I increased my workouts, hired a personal trainer (not cheap) and dieted my butt off. I didn't lose a pound. Early this year my co-worker told me about this sight. She had the Mirena also. When I started reading the side affections that women were experiencing, everything started clicking into place. The weight gain. The hair loss. My hair grows like a weed. And I've been trying to grow my hair out for at least 8 months. It hasn't grown an inch even though I get my ends trimmed. The hair at the back of my head has broken off. It's shorter than the rest of my hair. I have ZERO sex drive. I'm moody (more than usual). I've made an appointment to have it removed Wednesday. I can't wait! I still don't know what I'm going to do about birth control.

This drug is lethal! I had a leg gash from falling over a fan in the gym which resulted in a MRSA infection. I ended up in the hospital with a violent reaction to SMZ-TMP DS which affected my central nervous system. I was out of control with severe pain in my whole body, nausea, headache, etc. Even after discharge, this drug was ordered to be continued!! Ended up in emergency again! What are these drug companies producing? And why are MD's not up on the side effects? I thought I was dying.

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much rennin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued well for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turning straight and my incredibly (can't do nothing with) thick hair started to thin and become style able. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kind of job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... In December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not going to have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA or I would have lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing blood work from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much rennin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much renin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued good for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turing straight and my incredibly (can't do nothing with) thick hair started to thin and become stylable. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kinda job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... in December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not gonna have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA, or I would of lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing bloodwork from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much renin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

I can hardly function on this stuff. I am a 28 year old mother of four. I tend kids, and am very involved in the PTA. I was put on prednisone 3 weeks ago after being put in the hospital for pneumonia and asthma. After 1 1/2 weeks I was 23 pounds heavier and my entire body is so sore it feels like needles stabing me all over. My face is soo fat I my chin touches my neck...UGH I want to scream... I was walking six miles a day just 2 days before my hospital stay..Now it hurts my knees just to walk down the hall...The ance covering my entire body is disgusting and I am soo agitated all the time, which is not good I have six kids to tend to. I am down to 2 pills right now and will be off within 4 days.. I sure hope the side effects will go away I can't live like this another week....

I haven't been on this site since about 7/08...and I am sorry to hear of all really crazy, uncomfortable side effects that many women have experienced. I had the mirena put in 3/15/08. It was recommended by my doctor because I have stage 2 endometrosis.
Overall, I would say that I have adjusted pretty well. My symptoms were and still are: occasional dizzy spells (less than a minute), some occasional tingling in my hands when I wake up (as if I was laying on them when I was asleep but wasn't), and I have had 2 REALLY heavy periods, the first was about 3-4 months after it was inserted. I bled for 3 days straight and was using super tampons and pads and was soaking through them in less than 30 minutes. I called the doctor on the 3rd day to see if this was "normal". I was told it usually takes at least 6 months for your body to adjust. At this point, I still have breakthrough bleeding for about 3 weeks a month and need to use pantiliners about every day as a "just in case". I still get my period but it is definitely shorter and lighter than before and most noticeably, less painful cramps overall.

Hi Girls,

well, it has been almost a year now for me without the Mirena and I am so happy. I have to say, I love having my period again...weird, i know. I feel so much more in tune with my body and have learned to appreciate it and all of its womanly things. My depression is much, much improved, i'm sure partially because of having the Mirena removed but I know it is mostly because of EFT (emotional freedom technique). it is a form of acupuncture that you can do on yourself without needles. you just tap on the same median end points on your body and say certain statements. Girls, it has completely transformed my life! I am genuinely happier on a daily basis and have cleared up all kinds of issues for myself. I had the most severe eczema all over my hands and body, it was simply debilitating and made me hate and life, as well as horrible depression issues. It's gone now because of the help of EFT. Please check out the website, it is a free download to learn how to do it. ****** it is said to help "when nothing else does"...it's the truth! Please check it out!

I wish you all abundant happiness and health! I am grateful for all of your posts and kind words! It was so nice not feeling alone with this whole IUD thing. Thank you! Please feel free to contact me if you have any questions about EFT or want some help with it. I love it so much and want everyone to know about it and use it!

I am currently going through what you have described. I am on my sixth day of using Niaspan er 500mg. It is around midnight and my entire body is on FIRE, I itch, red blotches and my hair feels like needles pinching my skin when I move. My face, neck, chest, back, shoulders and legs was literally RED hot to touch, not to mention my heart started to race and felt like I needed some fresh air or cold shower to calm down. From what I read on (******) it sounds like I was flushing and had a reaction to the medicine. I am 33 years old and in good health. It seems like you should take Niaspan at bedtime and take with ibuprofen to reduce side effect. The funny thing is I have been taking ibuprofen all week since my low back is aching…Go figure. Not sure if I will continue. Plan to check with doctor tomorrow.

November 14 I was given Avelox for a sinius and ear infection. My husband had taken the sam medication 4 weeks earlier and had absolutely no side effects what-so-ever. When my infection reaccured my doctor decided to give me Avelox since it was a stronger antibiotic. I took my first pill prior to going to bed. I woke up Saturday with a headache and a general feeling of being agitated and moody. I took the second pill and as the day went on I began to feel some tingling in my arms but contributed to a neuro test that I had had 2 weeks prior where they shock your nerves. The tingling got worse by that evening (Saturday). Sunday I took my third pill still relating the the tingling to possible nerve damage from the EEG. I had to keep shaking both arms from time to time because I was also experiencing some numbness. I took my 4 pill on Monday early am. By 9:00 the tingling was extensive and the numbness was also becoming more regular. During all this time I was having intermittent severe headaches as well. By Monday night I was going crazy with both my arms tingling constantly and then my left hand got really heavy, I reach up to rub my arm and realized I could not feel my shoulder. I got a needle and pricked it and could feel nothing. This brought back a severe allergic reaction I had back in the 80's to Vistaril. It clicked in my brain at that point that it was not nerve damage from the EEG but possibly an allergic reaction. I immediately went to the web and keyed in allergic reaction to Avelox and found this site. I was stunned. Needles to say I did not take the pill Tuesday and went straight to my physician. He was hard pressed to believe that my symptoms were being caused by the Avelox. I even brough copies of some of the entries on this site. He did not want to accept that but changed my antibiotic and said that if it was the medication then the symptoms would start to subside by Wednesday. Wednesday afternoon both arms were considerably better and by Thursday mid-day I was back to normal. I did tell my physician that although he might not be convinced I was 100% positive that it was an allergic reaction. I will be calling him today to let him know that I was right.

My symptoms are

Massive hair loss by the roots, which started about 2 years after going OFF the pill and hasn't stopped. Some hair still hasn't grown back yet.
Bloating with water retention (this is where the bigger boobs come into it).
Leg Cramps
Pins & Needles in legs and toes
Cold/numb spots on one leg
Can go without sex for long periods

However, the benefits are:
clear skin, no mood swings. No depression.

I came home from work and opened my new bottle of Niaspan er 500mg. It was late and my wife was asleep. I read the bottle and it said take 2 tablets before bed with food. I did and about 4 hours later, my entire body was on FIRE and my hair felt like needles pinching my skin when I moved. I can deal with a hot flash or flushing but I was literally RED hot to touch, forget the feeling that I was having a heart attack or stroke.
I am only 41 years old in good health and a little low good cholesterol. I tried again few days later with one pill(after my wife had a good laughed) and experience the same nightmare. No hot flash, I was BURNING RED and my hairs were needles pinching my skin as I put ice packs around my neck.
I understand this is just a form of vitamin B-3??? Has anyone tried some form of herbal version of a B-vitamin?? Has anyone tried to take during the daytime????

IT IS GOOD TO KNOW I'M NOT ALONE, LIKE ALL OF YOU I THOUGHT I WAS GOING CRAZY AND SO DID EVERYONE AROUND ME. I'VE HAD MY IUC SINCE JUNE 3, 2008 AND I'M GETTING IT REMOVED IN 2 DAYS, AFTER SEEING THIS SITE. I GOT ON THIS SITE LAST NIGHT BECAUSE OF THE SEVERE MOODS SWINGS AND DISCOVERED ALL MY OTHER PROBLEMS THAT I WOULD HAVE NEVER THOUGHT WERE EVEN LINKED TO ONE THING LET ALONE MIRENA WERE THE SAME PROBLEMS I READ OVER AND OVER ON THIS SITE PLUS A FEW THAT WEREN'T ON HERE. I'VE BEEN HAVING PAINS IN MY FINGERS, TOES, AND BREASTS LIKE I'M BEING JABBED WITH NEEDLES, JOINT PAIN SO BAD I WOULD FREEZE UP, NAUSEA, FELT LIKE I WAS PREG. TOOK 3 TESTS ALL NEG., HEADACHES, SINUS TROUBLE, NERVOUSNESS SO BAD I FELT LIKE I WAS SHAKING ON THE INSIDE OUT, PELVIC PAIN, BACK PAIN, ITCHY SKIN AND MY SCALP ITCHES SO BAD I'VE HAD MY HUSBAND CHECK ME FOR LICE SEVERAL TIMES, IT'S HARD TO BREATH AT TIMES, HAIR LOSS, PAIN DURING SEX, AND NO DESIRE FOR SEX AT ALL. THE MOOD SWINGS ARE THE WORSE, I WAKE UP P-ED OFF BEFORE I EVEN OPEN MY EYES, I HAVE NO PATIENCE AT ALL, I DON'T CARE TO TALK TO ANYONE, I TREAT MY HUSBAND LIKE I HATE HIM. I HAVE A 17 MONTH OLD AND A 4 MONTH OLD THAT I HAVE BEEN TRYING TO HAVE FOR 15 YRS., 10 YRS. OF NOTHING AND 7 MISCARRIAGES AND EVER SINCE I GOT MARENA I HAVE FOUND IT HARDER AND HARDER TO DEAL WITH THEM. BEFORE I GOT THE IUC MY YOUNGEST ONE CRIED ALMOST 24/7 AND I HAD NO PROBLEM DEALING WITH IT NOW SHE HARDLY EVER CRIES AND I GET FRUSTRATED THE MOMENT SHE STARTS. I HATE FEELING THIS WAY, I FEEL LIKE A TERRIBLE MOTHER, WIFE, DAUGHTER, AND FRIEND. I CAN'T WAITE TO HAVE IT REMOVED.