Muslce symptoms and conditions

I had mirena inserted back in March of this year, and I hate it. The insertion wasn't too bad, just some mild pitching. For a few days after I had spotting and severe cramping. Since insertion I've had constant discharge and my doctor sent me for an ultrasound. It was placed correctly, no cysts, but still cramping and discharge. I have had no desire for sex, which I think is mainly due to constantly having shit come out of me.

I have had more headaches, back aches and hate the whole experience altogether. I am appreciative of this site and all the other posts, because I was really starting to think it was just me. Then after I had a second ultrasound, the tech asked me if my labor and deliveries of my two boys were quick. First one was 5 and 1/2 hours the second only 51 minutes. She says in her opinion, it sounds like my uterus is just rejecting having something foreign in me. So tomorrow I am going to my gyno and having this damn horrible thing removed.

I have definitely noticed a weight gain! I started really watching my diet and running and it doesn't seem to be helping. Also, I have had problems with severe muscle aches and swelling in my right leg. It got so bad that I started taking prescription Naproxen for the pain, so I can sleep. I had no idea others were experiencing the same thing.

I ran across this post as when I got really sick renovating a house I ended up a neurologist who recommended lamictal and that I was bipolar. My symptoms were bad neurological defect inability to concentrate intense burning headache, muscle aches, neurological pain in my arms and general stiffness and fatigue with twitching muscles, heart arrhythmia and anxiety. I couldn't understand how all of a sudden I had become bipolar however was under an extreme amount of stress (living in a half torn apart moldy house with no heat while serving as my own contractor under 300K of debt with no job as my arm pain interfered with my computer consulting practice ). I tried taking anti-depressants. My headaches got much worse and I turned a pale whitish yellow and developed fatty lumps under my skin called lypomas (wellbutrin) my friends (later) said I look like a cadaver. I felt like my symptoms did not match what was generally diagnosed as depression or bipolar but my regular doctor and neurologist insisted that I was depressed in some form or another. After another year or so of being really ill and trying different AD meds and finding no way out I was getting pretty desperate. I heard of a plce in Hawaii that a friend recommended cleans and unbllocks your interal organs using nothing but water. As a scientist and engineer and builder I was skeptical but felt like something like that might be the best path - it was a shot in the dark. I sold the house and dropped $5K on the treatment and trip to the big island It was like being let out of a cage my body turned from yellowish white to pink and healthy looking in less than 5 days. I dropped 20 lbs of the unrecognizable stuff out of my colon and liver. I believe I had a problem with cholestasis - stagnant liver bile that solidifies when you work too hard without drinking enough water causing bad digestion and absorption of nutrients leading to all sorts of problems incldung toxic liver and portal hypertension and jaundice. It's now two years later. The only thing that is wrong with me now is a small amount of fatigue and irritation in my frontal lobe when I work long hours at the computer. I continue the cleasing process and may go back. Contact me if you might be interested in the details. Drugs may be helpful to some and I may try an antidepressant to get me over the top but if you start medicating while your organs are not working well due to a lifetime of bad eating and lack of exercise ( or in my case working physically to exhaustion and then ordering out pizza and eating on the run for months on end) you might want to try another way. Oh and I'm not bipolar. Lamictal taken in the state of health I was in would probably have killed me. I'm now 41 and have a new life to look forward to and a whole lot wiser. There's a book called the amazing liver and gallbladder flush. It's the real deal.

i'm a fourteen year old girl, who has been completely healthy my entire life. about a week or two after i got the gardisil shot, i went on vacation in the outer banks. when i returned i started experiencing severe abdominal pain, feeling nauseated, fatigued, having muscle pains and confusion. i went to my family doctor, who diagnosed me with the flu and gave me antibiotics. days later, i wasn't getting any better so my mom took me to the emergency room where i was put on an iv for dehydration. i was sent home with medicine for the abdominal pain, which gave me no relief. i returned to the emergency room several days later due to the same issues, and was put on an iv for dehydration again. they took blood to test for a bunch of different things, but everything came back normal. i was sent home again, and over the next month i was referred to a gastroenterologist, where i had a CT scan of my stomach, an upper gi/barrium swallow, an upper endoscopy with biopsies, a MRI of my brain, and tests done on my liver and gall bladder, all of which came back normal. i was admitted to the hospital on august 20th, the day i was supposed to start high school. i was put on an iv again, and had liquids dripping in me for about 12 hours. my gastroenterologist seemed to think i was bringing everything on myself and might have a minor case of IBS. the doctor made me talk to a psych, who basically told me i must be stressed and had to be bringing it on myself. the doctor sent me home, telling my parents to force me to go to school. i cried the whole way home from the hospital, no one was even trying to make me feel better, and i hated the doctors for thinking i could bring something like this on myself. i started my first week of high school later than everyone else, i felt completely exhausted and threw up in the bathroom between classes. a day at school takes everything out of me, and i have to spend the next day in bed. my mom and i just saw all these side effects of the gardisil shot and are convinced that's what caused all this. i couldn't try out for the volleyball team, i've lost 14 pounds, i might have to re-do my freshman year because i'm missing so much, i can't hang out with my friends, i can't even go to homecoming and im honestly depressed because of all. this has ruined everything for me. don't let anyone tell you it's all in your head, its not, this is real and its effecting a lot of girls. please think twice before getting the gardisil shot

This drug although it works great on blood pressure truly, truly put me in pain. I experienced the most horrendous muslce cramps of my life. When I say this I am not just talking about a few. I had muscle spasms (charlie horse) in almost every single muscle of my body from my neck to my abdomen to my entire back to my feet and fingers. It was terrible.

I was on my second round of a 10 day courses of Levoquin for diverticulitis. 5 days into my second round, I started to have an allergic reaction every evening from 8:30 ish to midnight-ish. It would start with a tingly painful tongue, then tongue feeling slightly swollen ,then slighlty swollen and numb, itchy lips and gums, then to the back of my throat and up my ears. My salvatory gland production increased, was slighlty nauseated and had a headache. Then 2 hours into the reaction, I began to get short of breathe and had a racing heart and palpiations. I currently take prendisone for Lupus so I'm sure this masked the allergy to some extent. I continued on the drug for another 5 days of these nightly reactions, elimainating other meds and foods I was eating in an attempt to figrer out what I allergic to, until I finally saw my doctor who immediately discontinued my leviquin. Because of my Lupus, I am always in chronic pain but since taking the levoquin, every single muslce in my body is extremely sore and tender, even my scalp. I've been off it for 3 days and on high doses of prednisone and my lips are still a bit sore and puffy feeling and my muscles still hurt but seems to be improving a little bit but not as much as I would have expected being on such high prednisone.

Hi all, i live in NY and have been on synthroid. since i was 34 i am 50 now. Because of the huge normal range it is very easy to take too much synthroid. Doctors also do not know how to prescribe it...It is better to take a little bit less then move the dose up. Mohammed Ali( the prize fighter) thought that taking synthroid would make him a better fighter ,stronger etc... he took synthroid, though he didn't have thyroid issues, and became tired and sick.

So from my experience too synthroid much causes constipation, muscle cramps in the calves first , then everywhere, like your butt and then your pelvic floor which in turn can cause frequency. Your feet swell, you get much more tired and irritable then depressed. Your heart races then you have episodes of shortness of breath and horrible crushing anxiety. Also your hair falls out..

Also as you go into menopause with less estrogen you need less synthroid , (pregnant women need to take more)but NONE will tell you this so you just get sick all over and think that its just menopause!

I truly believe that there are millions of women out there with "fibromyalgia" who are just simply just taking too much synthroid... if 1.25 is the full replacement dose why would anyone be taking 1.65?

I am not a dr but i have come to see that they never suspect this medicine for the harm it can do.Part of this is that it is the most prescribed medicine in the country and the company who makes it is very powerful. And if you think that drug companies care if their meds make you sick than you should read about the Delcon shield and how the makers knew that the string wicked germs up into the uterus and they sold it and hid the results! I was not able to have children thanks to the good makers of this product.

so back to synthroid, I was taking .1 of synthroid with my numbers in the normal range and i had constipation frequency , muslce spasm in my calves,hair falling out , fatigue irritability , shortness of breath with anxiety... over a few weeks i moved my dose down( with email to dr) to a spilt dose of .025 in the am then 12 hours later .025 in the evening and ALL of the symptoms WENT AWAY! my advice to anyone who has the symptoms above is to tell their dr that they want to on a trail basis see if their symptoms are alleviated by less medication.If your dr says no ,FIND A NEW DR. , these are quilty of life issues and many drs are to busy to elp you titrate your dose , dont give up , you are only here once and you can get rid of the symptoms!!!

My mind was in a fog. I could not concentrate. Fortunately the fog lifted 2-3 weeks after stopping the drug. However now 3 months later I have extreme fatigue and modest muslce pain. I was a marathoner and triathlete, now I am exhusted after a trip to Home Depot.