Arms and legs symptoms and conditions

I take 200mg for partial seizures, added it to neurontin about 9 months ago.
At 300mg I lost the ability to type correctly and would forget what I was saying in the middle of a sentence. I forgot phone numbers and lost a ton of weight. My doctor said that meant I was on too much. I'm glad he put be back to 200 instead of upping the dose, which is what I see most people doing - adding more. I am taking as little as possible to keep the seizures away, and I feel pretty good on it.

My side effects currently are constant movement of my jaw and tongue, and my new side effect is a strange involuntary movement of my arms and legs. I especially notice it when I'm on the computer and I move the mouse, my arm jerks. (At least it jerks in the direction I want it to!!)

Overall, I am happy with it and feel lucky that I'm not having any terrible side effects. The jerking thing is a bit concerning since it is new and I hope it doesn't get worse.

I do think my skin has gotten messed up - not quite acne, but redness under the skin. No bumps though.

Oh - the tip of my tongue gets numb about 15 minutes after I take it. Weird.

Was put on 10mg lisinopril almost a year ago but the doctor has upped it until I am now taking 20 mg in the a.m. and 20 mg. in the p.m. I was okay when I was taking 10 in the a.m. and 20 at night but since he increased it to 20 and 20 I feel horrible. I assume it is the lisinopril because that is when I started this feeling of extreme fatigue in my arms and legs. The only way to explain it is that they feel very heavy. My blood pressure has gone down but sometimes it is too low. I am due to go back to the doctor in 2 weeks so I adjusted my medicine myself. I'm back to 10 mg in the a.m. and 20 in the p.m. I'll see if this helps the fatigue I feel in my arms and legs. I hope this clears it up. I was wondering if anyone else had this problem.

Hello I'm a 41 year old female, and I took Lipitor 20 mgs for 6 months about two years ago. When I called my doctor's office to complain about side effects they told me it couldn't be the Lipitor because I had been taking it for a month already, and would have had problems before that. I eventually took myself off of the drug 5 months later. Here are some of the side effects I experienced:
Itchy fingertips, increased blood pressure, 30lb weight gain, shaky hand writing, acne, poor driving skills, poor memory, hair loss, "frozen joints", IBS, incontinence, low grade fever, itchy feet, numb toes, numb hands, foggy brain, joint pain, muscle pain, foot pain, plantar pain, dizzy, jaw pain, back and neck pain, week ankles and wrists, nasal allergies, skin rashes, migraines, heartburn, Increase in Astham, heart palpitations, knee pain, difficulty standing up from sitting position, difficulty climbing stairs, water retention alternating in feet, hands, arms and legs, almost constant taste of bile in my mouth.
These are only the ones I can remember. Two years down the road everything but the muscle and joint pain and weakness is gone. even those have improved a lot. I stopped taking the Lipitor and lost all 30lbs I had gained on it, without dieting, in a months time. I still have two toes on each foot that are partially numb. I have trouble climbing stairs, and getting up from a sitting position. I can do both, but I move slowly while doing them. The pain in my muscles and joints drives me crazy, but I'm grateful that the rest of the symptoms have cleared up. My doctor never believed me about my symptoms, and neither does my new doctor really. Went to the emergency room for asthma that was not responding to my inhaler, and they were about to let me go home when I mentioned to the doctor that I had been on Lipitor. Suddenly a huge battery of tests were ordered including a CT scan and a stress test. When I asked the doctor why he said that they just wanted to be sure that it wasn't something other than asthma. Why did they do that after hearing about the Lipitor? Do they know something? Are there doctors who believe that statins are killing and seriously injuring people? I'm so angry. Even as I sit here typing I know when I stand up I will have massive amounts of pain that I will have to "walk off". My quadriceps have not recovered, and remain ridiculously weak.
If I can stop one other person from going through this I will be happy. Thanks everyone for taking the time to list your symptoms. It makes me feel better to know that someone believes me, and knows what I am going through.

About 2 months ago I started taking Lisinopril because they say it protects your kidney and I am diabetic. I just came back from an urgent care appt. where they said they don't know why my arms and legs have pain so severe that I can't think straight. As I read these posting, it occurred to me that this itchy throat that never goes away could also be a side effect. I am going to quit this medication to see if the pains go away, because I think pain makes the BP go up! I am going to get acupuncture for the pain now.

About 2 months ago I started taking Lisinopril because they say it protects your kidney and I am diabetic. I just came back from an urgent care appt. where they said they don't know why my arms and legs have pain so severe that I can't think straight. As I read these posting, it occurred to me that this itchy throat that never goes away could also be a side effect. I am going to quit this medication to see if the pains go away, because I think pain makes the BP go up! I am going to get acupuncture for the pain now/

Muscles spasms, sensitivity to light, burning sensations up and down my arms and legs, racing of heart, horrible sinuses, migraine headaches, chronic fatigue, hair loss, dry skin, Candida, acidity (low PH), low immune system, acne, joint pain, and the list goes on and on.....
My doctor told me I was fine and suggested I go on an anti-depressant. I am not depressed I told her. Since my doctor and other conventional doctors weren't helping me (all they wanted to do was prescribe more horrible drugs) I decided to seek an alternative MD. He said all these symptoms can most definitely be from my birth control. I went off Triphasil (Trivora) 3 weeks ago and am taking some herbs that are supposed to help correct the damage the medication has done. I now have a whole in my kidney, cysts in my ovaries, spots on my lungs, and an infection in my stomach (yeast also known as Candida). I have been sick for over 6 months now and am finally ready for this to be over. I can no longer go to the gym, work a full time job and enjoy social functions/outings. It is emotionally and physically damaging. Those of you who are on it...please stop! It is ruining your insides and making you weak. I am 30 years old and was on Trivora/Triphasil for 6-7 years. What a mistake. This is the ONLY drug I take and I used to be perfectly fine. As a matter of fact, I used to run 10 miles a day and now I can't even walk 30 minutes in the gym. Needless to say, I am very angry at the doctors for prescribing such medication to me, for the FDA for approving it and for our government for not doing their due diligence.

Im 35 have 2 children and had mirena fitted in Feb of 2008. It was the most painful thing i have ever experienced. There was a med student in the room when he did it and she said after it was over that was the most brutal thing shes ever seen. After it was inserted i bled for about two weeks but it did let up. In the months that followed I experienced the acne,(i have always had clear skin), the weight gain, the fatigue, the headaches, the fogginess, and the worst to me was a major personality change. I was miserable. Depressed and extremely on edge all the time. I blamed my constant crankiness on the fact that I could no longer fit into any of my clothes, and the 15lbs that i had gained. In August my mom asked me if i was pregnant cuz she said I looked like i was. The day after my mom said that I went to weight watchers and did manage to lose 10 of those lbs. Which isnt that great considering i lost 42 lbs in 4mths when i went on it after i had my 2nd daughter and it took me 3 1/2 mths to lose 10! Anyway, 2 weeks ago i started with this dizziness and the tingling feeling in my arms and legs. Went to the doc and she said I had an inner ear infection. Took the meds she gave me and still felt crappy. Then last Monday i had a total breakdown. I couldn't get out of bed, the left side of my face was feeling like it was numb. My cousin came to see me and asked me what was wrong and I simply said "I think im losing my mind!" She said well u haven't been yourself since you had "that thing put in". So her and i got on the computer and googled mirena side effects and WOW!! I could not believe what I was reading. I could relate to every woman's story. I called my doc and had to fight with the idiots at the front desk but I got an appointment tues the 25th to have it removed. The doc looked at me like I was crazy when I told her what was going on. She said theres no way mirena was causing that and i should go see a neurologist but shed take it out for me anyway just to ease my mind.
Well let me tell you how I feel today 5 days post mirena. I feel WONDERFUL!!! I actually felt better within an hour after she removed it. The tingling and numbness stopped and that foggy feeling was gone, and my insides no longer felt like they were being squeezed together. I started heavy bleeding on Friday (at walmart on black Friday, to give you a laugh). Im going through a tampon every two hours but i have to say it feels wonderful. I just feel great I don't care about the bleeding at all thats how good I feel. My stomach is flat again, and when i weighed myself this morning i was 7lbs down from Monday, and i haven't been dieting at all, ate like a cow on thanksgiving. I even look different in the mirror. I swear my skin had a grayish tint to it when i had the mirena and today im all pink and rosy again. When i think about how i felt and the mths of my life that i lost, i cant believe a form of birth control caused that. They really need to educated people more on this device. Yea the thought of not having a period is cool but at what expense? Ill take my period over feeling like that any day!

OMG I am so glad I found this site!!! I have been taking YAZ for 4 months. I have been on/off several birth control pills, some with no side effects and some with. These are the worst!!! I felt like I was going crazy until I found this site. At first all I noticed was moodiness, instead of having PMS a couple days before my period I had it all month except for before and during my period. Then about 2 months into it I started feeling fuzzy headed, unable to focus, started having tingles in my arms and legs like when your foot is asleep. If I take the pill at night I have horrible night sweats and if I take it in the morning I am tired all day and have horrible dreams. The worst of it was I was having severe episodes of vertigo, the room starts spinning and I have to grab hold of stuff. It was really scary, I am a single mom and was scared that I might fall at home and my toddler would be unable to go for help. I thought maybe my iron or blood sugar was low so I went to the doctor and had a full work up on my blood - everything came back fine. The doctor wanted to send me for a CAT scan and I didn't want one as I had started wondering if it could be the pill. I am calling my gynecologist today to get it switched. Thank you so much for all your posts! Me, my family, and my job all were thinking I was going crazy or just a hypochondriac.
On a side note - I do have 3 teenage cousins who take this pill and have no side effects. However I have always been very sensitive to medication. This pill may work for some, but not for me.

my 95 yr. old mother was given 2 SMZ/TMP pills 12 hrs apart and within hours after the 2nd one, spiked a fever and became flush around her eyes and then her entire face. She ended up in the emergency room. Several days later she broke out with hives, red blotches, arm bruises, a skin infection, and blood vessel breaks on her arms and legs. She also itched terrible all over. Doctors thought it was her blood platelets causing this but they were wrong. She is allergic to sulfur drugs. Finally after 5 weeks now she seems to be improving. This is a very dangerous drug for some.

forget it! don't let it pass your lips! i am 38yrs old and going through a very stressful time in my life. my periods have always been regular and short. a couple of months ago i started experiencing 2 periods per month with the most recent one lasting 20 days. ugh! gross! my doc put me on this pill to regulate and stop the bleeding. started taking it right away and my period stopped almost immediately. a few days later i would start again with heavy bleeding that would last for about 6 hours and then be completely gone. a few days later, the same thing. this went on for 3 weeks. now i have started a full blown period and have another week and half until my brown pills. as mentioned i am going through a very stressful time in my life, but i am not a person to suffer from depression or be emotional. i always see the silver lining and can make the most of any situation. i eat healthy, i take care of myself. my sex drive has always been through the roof. i am in the prime of my life! now? i am tired. i am gloomy. i could care less about social engagements. i am negative. i have weird discomforts in my calves and abdominal area, i cry over spilt milk. sex? seriously? who cares about that?! if i could lay in bed all day, eat chips and dip, drink wine, cry and watch mindless tv ... life would be grand. this is not me! also, i get pimples in places i never thought possible -- my arms and legs! ew! my doctor wanted me to take this pill for 3 months. not a freaking chance. my other option is to get an ablation. i've known several people who have gotten this done and have never heard nor read anything negative about this procedure. bent over today with heavy (non due) bleeding and cramps, i just called my doc and said, "screw your pill, ablate me."

About eight years ago I felt heaviness in my chest along with some pain/discomfort when doing hard physical labor and occasionally in the hot-tub. Following my doctor’s advice and an angiogram, a stint was placed and medication administered – Lipitor and plavix I also went through a 6-month program for cardiac recovery including dietary changes and a proper exercise program. About six month following that I gradually just stopped taking my Lipitor and plavix and returned to my old eating routine and other life-style. I don’t smoke (never did) and don’t drink or otherwise indulge in any recreational drugs. I’ve never been hypertensive with blood pressures typically at 115/68. I maintain a trim and healthy appearing body just naturally or genetically. I eat lots of red meat, not a lot of vegetables, drink gallons of orange juice, and eat much more junk-food than I should. About six years after that (near heart attack) event I was given a “stress test” by my physician… I was then 61 and tested at the level of a 38 year old! Two years after that I had a significant heart attack out in the middle of nowhere! It took almost 6 hours to get me to an emergency room in Spokane, Washington (that’s a story of its own). That was on a Thursday – I was back to work full-time the following Monday (four days later). This time around with more drugs than I could swallow in one gulp! Lipitor, Plavix, Coumadin, aspirin, and carvedilol. The combination or amount was more than I could tolerate and I was weaned off all but the Lipitor and aspirin within a year. My heart has returned to nearly full-function and I have no physician imposed restrictions. All that said, I’ve been gradually developing muscle soreness (pain, actually) in my fore-arms and legs. I’ve been growing more lethargic and tired with each passing month. I’m now 65 and feel that the Lipitor is inhibiting my health… I want to get off it and be “normal” again. Or is it just being sixty five? Can I just quit taking the drug? Leaving only aspirin for blood thinning and the hope of a better diet for cholesterol control.

I have been on this medication for 3 months now. I am a 28 year old male, 6'2", weigh 211lbs, and in overall good health. My blood pressure average is 144/72 without the medication, but on the medication it seems to stay around 136/66. It took about one week for the blood pressure medicine to start working and when it did I felt very tired (which is normal). Now, in my third month I have started to notice new symptoms like severe headache in the right front lobe, severe tiredness, cold fingers and toes (in warm conditions), severe lower back pain, mood swings, blurred vision in the right eye (same location as headache), and a occasional twitch in my right thumb (probably not related to the medicine). When I first started this medication I did read all of these post and figured that everyone was crazy and/or nuts, but know I am thinking that I would rather stop the medication
and start seeking out for a better medication.. I know medicine has side effects but damn!!! Anyone else have cold fingers and toes while they have been on the medication..thanks

October 22, 1998 I had resp. failure (with intubation). My new pulmonary doctor put me on Singulair 10 mg once a day, a few weeks after. Within time, I started to have numbing and tingling in my face, arms, and legs. March of 1999 the symptoms worsened and started causing pressure in my face, arms, and legs, and anxiety started to kick in. I was told I had neuropathy and to take mobic. Symptoms getting worse, and went to a rheumatologist in June 1999, and he was suspect of singulair. The doctor thought that what I was experiencing was due to the singulair. He (the rheumatologist) discussed this with the pulmonary doctor and the pulmonary doctor did not believe this to be the case. Not forgetting, in March of 1999, I had a ct of the sinus area, and low and behold 1/3 of the cavity was and probably still is full of polyps.

As time went on, symptoms getting worse, and not one bloody doctor could figure out why I was feeling this way. In addition, at times, I was put on steroids for my asthma (not including my inhalers).

Two years ago, my body went into shock, leaving my left side very different than my right side. Affecting: my head, my face, my eye, my ear, my esophogus, my lungs, my arm, my leg.

I have been depressed and anxious not knowing what the heck was going on with me.

Recently ruled out thyroid, and lupus, and possibly ms.

Last weekend, I reviewed the letter from the rheumatologist (dated 1999) and the ct report from March 1999 (regarding the sinus/ polyps) and made copies to present to a pulmonary doctor that I have recently been seeing.

This past Monday the 10th, I had my appt with him. He knew of my situation from the last few visits (in addition, I had met him this past March for a pulmonary rehab program, and thought he seemed to be knowledgeable and compassionate). While waiting for him to enter the exam room, he had read those reports before entering.

The doctor looked at my hands (red as a beet and swollen) and said "You have Churg-Strauss Syndrome, and get off the singulair."

I had done my homework from a few weeks ago, where I looked up untreated polyps.
Untreated polyps, can turn into vasculitis. There are many types of vasculitis, to include Churg-Strauss Syndrome.

I then cross ref CSS and singulair, and low and behold, BINGO!

I have been suffering for ten years, physically and emotionally because of this drug!

There is also recent updates from the fda (fda.gov) regarding singulair, of which most recently includes anxiety and depression.

I suggest before taking singulair, be aware of the side effects. As soon as a side effect comes up, contact your doctor. Also, be aware of existing conditions (like me, sinus problems and asthma) for this could lead to churg-strauss syndrome.

This info is indicated on the actual disclosure (the paper insert that indicates studies, side effects, etc...) not the handout that is given with the drug.

By the way, I am now working with a new rheumatologist in Los Angeles (Cedar-Sinai affiliated) and a new neurologist.

mdklezmer

I was prescribed Avelox for a Sinus/ear infection. I was given 1 pill a day for 5 days. I took the first pill and within 30 minutes I was starting to feel very "out of it". I started to get very anxious and began pacing in my house. I couldn't sit still without becoming agitated and disorientated but I was feeling so spacey that I didn't really know what I was doing.

My arms and legs started to itch, then tense up and began to tremor. I even started arguing with myself OUT LOUD about whether or no I should go to the ER. Finally I just made myself lay down in bed and slept for about 14 hours.

The next morning I work up and felt like I had been in a fight. My muscles were sore and weak and I had flu like symptoms that kept me bed bound for 3 full days after taking only 1 pill.

I have been on 200mg of Topamax for almost a year, which helped my headaches immensely so I tried to ignore the itching. The itching got so bad (especially when I get hot and would sweat) that I had to go off of it. I have been off of it for about 4 weeks and I still itch, does anyone know how long this will last or if it will ever go away? If I am going to itch without the drug anyway, I might as well take it and have relief from my headaches.

Vertigo, weakness, fatigue, exhaustion, aching numbness in arms, numbness in face arms and legs, extreme pressure in head and neck, burning feeling radiating from the base of my neck through shoulder blades to arms, foggy brain, waking up feeling (for no reason) like I have a major hang over, chills, aching feet, weight gain, feeling very fearful of my symptoms because they feel like nothing I have ever experienced.
THESE LAST 4 WEEKS HAVE BEEN HELL!
I had my Mirena inserted on June 30 2008. I experienced mild discomfort for the first 4-6 weeks. The spotting was the worst of it and that was no more than an inconvenience. I was happy with my choice of birth control.
Then this hell began about three months after insertion.
During the last week of September the symptoms listed above started. They were mild at first but by within a week and a half I felt HORRIBLE. I suspected that it may be the Mirena, but at the same time I thought I was dying.
October 1 or 2nd (it is all a blur) I was home by myself when I started feeling the numbness and head pressure coming on again (my symptoms were coming and going, not constant) so I laid down on the couch to get off my feet. All of a sudden I felt like I was losing consciousness. I grabbed the phone and called my husband to get me to the ER. I thought I was dying. A blood clot or something. Once there, they did blood test after blood test, an EKG, urine tests, and basically I was told that there were no major system problems. I know this sounds a like classic anxiety, but I know it is not. I have to say they were very good there and encouraged me to see my family physician (whom I had already been to earlier that week) again.
I called to make an appointment to have the Mirena removed the very next day. My GYN kind of shrugged off what I was going through saying that it was anxiety and asked if I still wanted the thing removed!!! of course I did. Having that thing removed was very empowering. I was feeling so helpless and it was the one thing that I could do to possibly help my situation. The feeling of relief was amazing.
I did see my family physician again who agrees that what I am going though is related to the Mirena. She did ordered a CAT scan (came back negative) just in case.
Post removal (It has been 17 days) I have been slowly getting better. My "episodes" are getting more and more diminished and further apart. I have noticed that I am flooded with exhaustion after each of these "episodes". I also never know when there going to strike making it hard to make plans. My husband has been very supportive through out and was convinced before I was that it was the IUD. He has volunteered to get a vasectomy.
GOOD LUCK TO ALL YOU LADIES.
If you have stumbled across this because you are desperately searching for answers, all I can tell you is that I believe that the Mirena IUD has had devastating effects on many, many women, but hang in there you are not alone and you are not insane. What you are experiencing is very real. Have it removed ASAP!!!!!!!!!!

hi no one has described itchy skin mainly arms and back

My 2.5 year old son has been taking oral Singulair granules for 5 days. He has developed a vasculitic rash on his arms and legs. Is this a known side effect of the medication?

I was given Levaquin for a UTI about 2 years ago and ended up in the ER, the side effects were so bad. Thought I was having a allergic reaction,
heart poundings, felt like a just drank 3 cups of coffee, also muscles reacting slowly, like I couldn't move my arms and legs how I wanted to.
Unfortunately I have take Cipro a couple times in the last year, and the last dosage of that did it for me. On the 5th day I all of a sudden had extreme pain in my left knee, could hardly walk. I took a couple Advil and rubbed some icee stuff on it and it went away but that night my lower back and hips became also extremely painful. Severe pain. That was the last dose for me. (The pain was much less the next day and almost completely gone after about 4 days.) I called the Dr. and they told me to stop taking Cipro- which I had already done. What really bothers me though is I mentioned this to my orthopedic Dr. and he said he never heard of Cipro causing joint pain!
I am going to send him some literature, but wow!! couldn't believe that.

I was prescribed SMZ/TMP DS 800-160 for a UTI...one pill twice a day. I had been taking it for 2 days. On the 3rd day, I broke out in hives in areas on my chest, sides, back and stomach and the next day started noticing small bumps on my arms and legs, too, that weren't as small and irritating as the hives the day before. Needless to say, I stopped taking it that day, the 4th day. However, it's the 3rd day since I've stopped taking it and I am still itching and skin is still broken out. This medicine had also caused a loss of appetite and altered my taste buds, but the break out is the worst of all and is ongoing, unlike the other side effects which were back to normal shortly after I stopped taking the pills. If anyone else has experienced the skin irritations, how long did it take for it to stop after taking the pills?

WENDY.... IN UR POST ABOUT THE BLOOD CLOTS IN THE LUNGS.. WHAT WERE YOU FEELING THAT MADE YOU HAVE TO GO TO THE HOSPITAL? THIS PILL IS A LIFE RUNNER....I FEEL FOR EACH AND EVERYONE OF YOU... ANYONE THAT EXPERIENCED THE ANXIETY/PANIC ATTACKS ON THE PILL... AFTER STOPPING YASMIN DID THEY GO AWAY?....

I was on Yaz for a year, but had some side effects (tingling in the arms and legs, swelling) so my doctor put me on LoE24. I have been on it a month and my world has turned upside down. Just a few days after I started LoE24, I got Bell's Palsy, which is a condition where half your face goes paralyzed. I've had it before, so I thought nothing about it having to do with my bc. Well...2 and a half weeks later I broke out, like I was 14 again (im 21). Its all over my face and neck. I am going to the neurologist tomorrow, but I have been very irritable, TIRED, and anxious. I switch back to Yaz in a couple days....

Hi
My husband has been prescribed 2 different blood pressure meds Lisionpril and metoprolol back in June. Come mid July he started to have trouble sleeping and slight tingling in hands and feet. Then it progressed to the arms and legs and then the face and chest. We have seen cardiologist, neurologist, sleep apnea doctors, Had EKG, MRI, Heart sonograms, Nerve test done due to the symptoms. Everything came back normal. He is miserable. The burning and pain is unbearable to wear he wants to cut his feet off and the only thing we keep hearing is well LETS DO ANOTHER TEST or TRY THIS MED. So now he is taking a a sleep med for insomnia and some seizure med for the nerve pain, thinking he may have neuropathy. This is going on 2 months now of trial and error and after reading 20 minutes of experiences, I THINK ITS THE MED!!!!!!!
What do we do then? He had high blood pressure so what meds are good with no side affects of burning or insomnia? Any suggestions or help would be of great appreciation. Thank you!!!

I just stumbled across this site and it has given me such renewed hope. I have GERD and have been on 40 MG of pantoprazole for about two months. My DR suggested taking two pills a day (one in the morning, one at night) for two weeks to see if that helped my lingering problems. It did. So much so I started eating like an animal again. Of course, this it me hard in the throat. In a panic (insurance wouldn't cover two pills a day) I added Prilosec OTC as my nightly solution. I had already noticed pins and needles in my arms and legs slowly developing. Exactly two days after including the Prilosec I was instantly hit with a panic attack and extreme anxiety literally out of no where. I had nothing on my mind and absolutely content moments before and then in a totally different mind set. I had paranoia and abnormal thoughts. I didn't sleep for almost 5 days (with a few hours here and there). I am 31 and have never had anything like this anxiety and like other readers here thought I was going crazy. I stopped the OTC when I thought it was the culprit and four days later I am doing a bit better. Reading the stories here I believe I am stopping the omeprazole starting tomorrow to see if I get even better. I feel like my entire body is shaking from this stuff and it is the only thing I have changed or added to my life. Thank you all for your stories as I was grasping at straws.

I am a 48 year old with 4 children. I am not showing signs of menopause at all. I have had increasingly heavy periods, sweats, headaches, mood swings, the whole nine yards so what the heck, I had mirena inserted today. My doc encouraged me to try it to see if my periods would get lighter or even stop. As far as side affects, I am already half psyco according to my daughters. I am still crampy off and on but I expected it. I just switched to this doctor because I was seeing satan who knowing I was very anemic from heavy periods let me almost bleed to death. I skipped two months due to low progestin but still built up the lining so when I was getting ready to have a period the third month, I went in for an ultrasound. The technician was wowed at how thick the lining was. She commented to me that I was going to have a really bad period when it started. My doctor did not advise me to do anything about it. He could have said to call if it went for longer than a week or to call if it was extra heavy but he didn't. My period was at almost three weeks and very heavy. I went to work on my birthday no less, and my potassium bottomed out as well as electrolytes. I felt so sick I went to lay down on the bathroom floor but felt nausea and cramps and thought I needed to use the toilet. When I sat down, I felt my arms and legs go numb. Out of vanity, I tried to stand and pull up my pants knowing I was passing out. I went down and ended up fracturing the fibula in my right leg. My friend knocked on the door and I came around and asked her to call the squad. After my 10 minute $750 ride in the squad, I was admitted to the hospital with a hemoglobin of 6. I stayed in for 5 days receiving 4 units of blood. Needless to say, I found the new doctor. My hemoglobin is now around 14 and I am starting to put weight on my leg. Hopefully, I am on the mend. I know there is a lot of negative response about the Mirena, but I don't have anywhere to go but up. I hope it works for me. If not, I will be on my way to the ER for an ablation.