Nerve test symptoms and conditions

Hi Everyone! I am a 40 year old mother of 6 that has just had her second Mirena IUD put into place on April 10th, 2009. On Easter Sunday (April 12th) I woke with a lot of joint pain, back pain, breast pain, severe nausea, headache, dizziness, faintness and extremely low blood pressure (87/54). My first Mirena was placed in October of 2001, 6 months after the birth of my last child. All went pretty well with no real bad complaints the first time other than the normal cramping and bleeding. I didn't even have headaches or moodiness (my doctor thinks it was because I was breast feeding at the time and the body produces a lot of natural progesterone during this). Things took a turn for me in 2003 though and have progressively gotten worse since; I have had so many crazy ailments (everything from muscle spasms, thinning hair to stabbing pains behind the eye) , that even I was beginning to think it was all in my head! It all started with an ovarian cyst that had to be surgically removed in Dec. 2003, from there I was diagnosed with high blood pressure and an extremely high heart beat rate in Sept. 2004 (on meds to current date). I get sick very easily now and I had gotten strep 3 times in the winter of 2006, so I had to have my tonsils and adenoids removed in March 2007. I have now been diagnosed with Raynauds Phenomenon and Glaucoma and suffer from an array of symptoms. My most recent mammogram showed that I have a lot of breast cysts now as well. I have been tested for MS, Lupus, Lime Disease, RA and many other things; everything comes up negative. Due to the current symptoms and symptoms I have had during the first Mirena (never made the connection until now) it prompted me to do some research. What I found was just shocking to me! The Mirena is made with a synthetic progesterone (progestin) called levonorgestrel. If you research this, you will find a huge list of possible adverse side effects; many of which I have suffered from. I have read many different sites and posts from countless people that have been affected by the Mirena. Most of these stories have a huge similarity to each other. I am now 10 days into these symptoms; yesterday I went to my Dr. because the symptoms were not getting any better and I wanted to discuss the possibility that most of my problems since 2003 may have been caused by the Mirena. My doctor did not confirm my suspicions, but she did not deny that it could be a possibility either. What occurred to both her and I was that I had left the first Mirena in longer than suggested; it should have been replaced around late 2006 to early 2007, but I was sick and had other surgery, so I just kept putting it off. Due to this, the effectiveness of the hormone progestin was wearing off over the past year or so; in the past 6 months (until now) I have been pretty much symptom free (that was why I had the Mirena replaced). The fact that my symptoms are suddenly back and in full force only 2 days after the insertion of the new Mirena, strongly suggests that the Mirena is responsible for most if not all my ailments. Over the last 6 months, even my blood pressure had gotten better and I had to lower my dosage of meds to compensate for the change; now my blood pressure is jumping all over the place again. I am now considering having the Mirena removed before it causes any other symptoms and completely ruins my life! It horrifies me to think that the Mirena is still on the market considering the potential it has to cause havoc on other peoples lives as it has mine.

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'm on my first month of Topamax and going to work for the first time in two weeks! Someone mentioned feeling like a box of rocks on this stuff, its true, but in my case the dosage increase might have been too abrupt. I take it for epilepsy, 100 mg. I was completely non-functional during the transition! Not only was I so tired I couldn't move, so sick I couldn't eat (I've lost a lot of weight), but I was constantly dizzy. I would often get icy to touch and pass out, mores after eating.

Cognitively, I was severely depressed, and had a constant "noise" sensation in my head which I started yelling at during odd moments. I believe I even hallucinated at one point that the room was expanding. Mostly, people thought I was stoned because I would just stare at the wall and have difficulty talking to them without slurring my words.

It's been a truly terrifying couple weeks, however I've settled pretty quickly out of the major side effects. I think thats pretty much what happens for everyone. I'm happy to have my brain back.

60 YEAR OLD FEMALE: IN 01-05 I STARTED TAKING SINGULAIR 10MG AND ADVAIR 100/50 FOR ALLERGY ASTHMA SYMPTOMS. BY FEB. I WAS HAVING FOOT AND LEG CRAMPS. BY MARCH I STARTED COMPLAINING TO MY PULMOMARY DR.(WHO PERSCRIBED THESE), MY ENDO DR., MY ALLERGIST AND GYNO. MY ENDO REFERRED ME TO A NEUROGOLIST. I TOLD HIM ABOUT THE SINGULAIR AND ADVAIR SIDE EFFECTS WHICH MY PHARMACY CONFIRMED FOR ME. WELL I GET TO GO THROUGH A NERVE TEST AND AN EMG. NOW I AM TOLD THAT I HAVE A NEUROPATHY IN MY FOOT AND THAT I NEED A NERVE BIOSPY TO FIND OUT WHY. HE HAS NOT EVEN MENTIONED THE LEG CRAMPS THAT I CAME TO HIM FOR IN THE FIRST PLACE. THEN HE GIVES ME A PERSCRIPTION FOR NEUROTIN FOR PAIN. I TOLD HIM BEFORE THE EMG THAT WHEN I STOPPED USING ADVAIR THAT MY CRAMPS STOPPED. THEY DO NOT LISTEN. I STILL TAKE SINGULAIR BUT MY LEGS STILL FEEL FUNNY LIKE RESTLESS LEG SYNDROM. I DO INTEND TO STOP SINGULAIR. I AM NOW CONVINCED SINCE I TOO FOUND THIS WEB SITE THAT IMY PROBLEM IS DUE TO MEDICATION. I DO NOT INTEND TO GO GET CUT ON SO THEY CAN THEN TELL ME ITS MY MEDICATION. I TAKE UNITHROID, ZETIA, SINGULAIR, ADVAIR. THE LAST THREE ALL HAVE JOINT/ MUSCLE PAIN/CRAMPS AS SIDE EFFECTS. I REALLY THOUGHT THAT I HAD SOME SORT OF MUSCLE DISEASE.