Believer symptoms and conditions

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!

I'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.

I was prescribed Avelox along with Prednisone by my allergy doctor for pneumonia. Even with a prescription insurance program, the Avelox costs $14 a pill. After 13 days on Avelox, my joints hurt so bad I can barely walk. My muscle tone is almost non-existent, and the muscles ache like I've been in training for a marathon. I daily became more depressed, and really thought I was dying. I went to see my internist this a.m. A chest x-ray revealed I still have a raging case of pneumonia, now in both lobes of my lungs. She wanted to put me in the hospital but agreed to put me on a Augmenting and another round of Prednisone to try at home a couple of days. Avelox should be taken off the market. I can not believe this medication which costs over $240 for one round of treatment was ever approved by the FDA. My doctor could not tell me when the side effects of the Avelox will diminish or disappear. DO NOT TAKE THIS DRUG IF ANOTHER WILL DO THE JOB.

I got the Mirenda IUD inserted about 3 1/2 months ago. Since having it I have had nothing but trouble. I have been bleeding almost everyday for the last 3 1/2 months. I probably have had 5 days of no bleeding. I also feel so bloated. I haven't weighed myself b/c I am scared to know but I am bigger now than 6 weeks after I had my baby. My doctor said that this device cannot cause weight gain but I am not a believer. My clothes are so tight and my tummy area is so swollen. I also have started cramping recently. I made an appointment to have it removed on Friday. Anyone have any other suggestions of birth control?

Hi, it's me Amanda. I posted a few days ago about my symptoms and my upcoming removal of my Mirena. I had it removed yesterday morning. It was no big deal at all. I barely felt it. I was just starting my monthly Mirena type spotting though which apparently makes your cervix soft and makes it easier to get out. So if you have any sort of cycle on Mirena schedule your removal during your cycle. I was very skeptical of some people's stories of feeling instantaneously better, but I'm a believer now! I started feeling so much better immediately. I started crying this morning when I work WITHOUT A HEADACHE for the first time since I can remember. No Advil Liquigels today, not one. I cannot begin to tell you how insanely happy I am about this. I feel like new person and my uterus just feels lighter and healthier already. I found the previous poster's information from her doctor very interesting about being small-framed and the Mirena being one size fits all. I only weigh 115 pounds and I violently react to many medications because they dose them for the average human. I usually take half doses of things, which I can't do with Mirena. I wonder if that had something to do with it? I will continue to update how my life is going without Mirena! Good luck everyone!
-Amanda

Our son was put on Singular almost 2 years ago to help with his "moderate" asthma. It has been the hardest 2 years for our family. My son who was already very senstive became very depressed. He showed no interest in anything. He was always sad and very down on himself. He had awful night terrors/nightmares. He didn't want to go to school or do anything. We continued to sign him up for sports/piano/scouts and it was a battle to get him to go. He always had headaches, which I thought were because of dehydration and made him drink water. We had him seeing a therapist trying to help him with the sleeping problems and the depression. We switched his room with his sister to physically make him closer to us at night. He was anxious and very irritable. If something went wrong, he couldn't handle it and had complete meltdowns. If he didn't eat anything for a while and his blood sugar got low, he was uncontrollable. To add to the problem was he was never hungry so I would have to force him to eat something about every 2-3 hours to prevent the meltdown.

The good news is that he has been off of Singular for over a month now and he is a new kid. He is excited to go to practice and will ask his dad to play catch with him in the yard. He is happier and we have not heard once "this is the worst day ever" which we had heard all the time before. He has not had one headache and seems to have a little bit of his appetite back. He is happy and holding his head high. Now, he still doesn't want to go to school (what 8 year old boy does), but he doesn't fight me when I tell him it is time to go. He does not have the meltdowns or the irritability. He even showed some empathy to my husband last week.

My husband and I are amazed at how different he is. We are also very upset that for almost 2 years we made his life miserable by forcing him to take this drug. I think for kids that are already sensitive to things it heightens everything! I am filing a complaint with the FDA and spreading the news to all my family and friends. I hope this information helps! I know I have learned a lot from reading these posts.

Well I posted a couple weeks ago and thought I would update. I intially thought I had no symptoms but lately it seems that in the morning getting out of bed that my muscles are extremly tight in my legs from my calf to my ancles. They seem to stretch out ok after a few minutes but i wondered if the damage has already maybe be not reversable. I just happen to have been seeing a physical therapyst for surgery I recently went thru for another problem altogether. I mentioned this drug to him and he had not heard of it. I told him of the tendon problems people have experienced. I asked him if he knew of any drug that can cause this effect and he stated cortizone can. He says its acks in destroying tissue, cells that act in supporting the tendon and allows them to stretch. . So knowing that a drug can actually cause the same symptoms some of you have experienced I am a believer now. I can see how this drug can possible reak havoc on any part of your body. So since i seem to have been feeling possible symptoms I was wondering if any- one has felt muscle aches and leg stiffness issues and how long after stopping the levaquin were the symptoms felt and what did they progress into if anything and did they subside and or go away all together. To me it seems that if this is about damage then its possible that just simple stretching can cause the tendon to snap. I can also see why some people may have recurring injurys. This would be a sign that one does not heal or the healing process is greatly lenghtened. I do plan on eating better and using some supplements to help.

To answer you concernedcitizen, what a great question,yes after singulair started, within 18mths we were prescribed,an antidepressant began with a c but cant rember, when that failed went on to lexapro,when that failed wellbutrin,when that failed and i was done with the bull chit we were trying bio feed back,cant say i was a big believer but we were giving it a try,of course nothing was going to work as long as we were taking singulair.These were all prescribed by psych docs

I'm a 22 year old who was diagnosed with dermatologists a couple months ago. I've been on different doses of steroids ranging from 5mg to 60mg for 5 months now. i was on 60mg the longest and just went down to 40mg. i go down to 30 mg next month. so far my side effects are moon face, swollen areas around my neck and collar bone, weight gain like 15 lbs, always have to wake up in the middle of the night and pee, my knees get shooting pains sometimes at night, light hair by my ears like sideburns, tired, helps with my muscle weakness a little, my eyesight seems blurry sometimes, chest always feels tight. I'm also on Methotrexate, Bactrim, folic acid, and Fosamax. it might be a reaction form all these but i think its mainly from the Prednisone. i cant wait to get down to the lower doses. i look like a different person and even tho all my family and friends know its still embarrassing. i fell like a whole different person. i cant wait to be normal again.

What a wonderful site.. thanks for all of you and your stories. I too was a Lipitor user ... 20mgs/day for at least 6 years. I didn't notice any problems until last summer. I couldn't grip a golf club so I didn't play all summer. My doc told me it was arthritis. Strange, no history and never had any problems til then. As the months went on, things got worse. Burning in my upper left arm muscle, so intense it would cause me to have to sit down. Heart racing, pain in back, shoulder and jaw, I thought I was having a heart attack. Started reading about Lipitor and told doctor I wanted off. Of course he said no way and he did an MRI thinking it was skeletal. He sent me to a neurologist, who immediately told me I have statin myopathy. Cause...Lipitor!!! Amazing he admits this, also told me his own doc prescribed it for him and he will not take it because he sees too many patients with these side effects. I am liking him and his honesty. I have been off Lipitor for 2 weeks now. Hands are much better but muscle weakness and burning and sometimes tremors persist but I am optimistic that this may take time but I will recover.

I have been taking Zoloft for over 7 years, Zoloft it might help you when you have \Depression because it seems that it works for a short period of time, or course everybody is different, after seven years taking Zoloft for Anxiety I got to the conclusion that the Science don't really know how the brain works, in my personal experience I notice that Zoloft it keep you thinking constantly so the antidepressants are good only if you take them for a short period of time after that like in my case it just make my life miserable, go down on the medication little by little, do exercise at least 3 times a week, drink water eat properly and pray to God almighty it will go away, change things in you life that affects the way you think, be positive talk to yourself all the time, stay away for the medication at least if your problem is anxiety don't take Zoloft I regret the time when I start taking it, it doesn't over for a long time, the brain doesn't know what to do when are giving serotonin everyday, this year I set a personal goal of get rid of Zoloft for good, if were not born with Anxiety that means for me that you can and you will be like before, our body has the ability of heal itself I believe our recovery from anxiety is life change but basically if you have seen that your medication it's not working don't try another one they just don't work for long treatment, try it's hard but the longer you take it the harder it's to get away, pray to God if you are a believer you will be better, I hope this helps for you.

I have been on Wellbutrin XL 150mg for 5 days now and have noticed that I am very short with people and experiencing anger. I tend to lash out. Will this go away?

Ive been on Zoloft for 2 days and the first day I took it I had bad Diarrhea and my teeth hurt they feel like I had them clenched all night long and I can barley eat. Ive been getting gas,nausea, and I feel faint and like I'm going to throw up. I'm on the Zoloft for Anxiety, is this normal or could it not be related to the Zoloft and I have something other than the anxiety????

Are there any people who can report good things about this pill? I haven't started it yet, but now I am really nervous because there aren't very many positive side effects. I know everyone responds differently to BC but a little encouragement would be nice. I recently was on Ortho Tri Cyclen- Lo and didn't have a very good expierence I just hope this one will be better :)

I was prescribed Levaquin 750 for 5 days for resolving pneumonia. I didn't finish the last pill due to increased heart rate and severe anxiety. These symptoms did stop for me. However, about a good 2-3 wks later my wrist started hurting. I thought I may have slept on it funny or something. Then a day or two later, my jaw started hurting so bad I couldn't chew at times. Another 2-3 days which leads me to today, I am having tingling/shock sort of feelings running thru my legs and arms and still having the jaw and wrist pain. I have an appt next week with my doc. I'm sure she'll send me thru all the tests everyone here has mentioned to no avail. This is very frustrating and scarey. I wish folks would repost and let the rest of us know how they are progressing. I will post back after my visit. I am going to try the magnesium and 5-htp the gentleman said worked for his wife. I am becoming a firm believer in a more holistic and natural approach to healing. I know sometimes chemical medicines save lives but this one has caused my life a lot of pain that I feel was not necessary for a very light case of walking pneumonia. Good luck to everyone. Please keep your progress updated to help the rest of us out.

Hello all, after reading all of your messages I am convinced now that the Lipitor is to blame on my symptoms as well. I began 10mg of Lipitor about 3 years ago and this past February was increased to 20mg, my cholestral readings was at 98 and now at 90. I also quit smoking in February. In April started to experience extreme pains in my arms and back, thought it was the mattress or pillows have replaced every pillow in the house, and have begun pricing mattresses. Have extreme bloating, gas and constipation. Went to the Drs. and was told its a reaction to quitting smoking as nicotine is a natural laxative. Sounds beleivable, never though of the Lipitor increase. Breast extremely tender and sore, went to the OB, had a mamograpghy everything fine, OB suggested researching Lipitor and bingo I'm a believer. Called cardiologist today and she has immeditaly lowered it to 10mg, and wants to see me in 3 weeks as a follow and possible wean off all together. I need to research the cholestral numbers and see how good or bad mine are at the moment. Again thanks everyone for taking the time and writing about your experiences and reading everyone elses. Good luck to all

I am a 30 year old woman who has been on Toprol (25 mg) for a week now. My doc prescribed it for mild hypertension and rapid heart rate. So far, I have had terrible indigestion and other "digestive issues", as well as difficulty sleeping. Fatigue and frequent urination (especially at night) have also plagued me for the past week. I have been taking my BP and heart rate readings every day and have yet to see a noticeable improvement. After reading all of the posts on this page, I am extremely nervous and wondering if I really need to be on this medication

My daughter is 5 years old and has been on singulair for 1 week. i have already noticed a dramatic change in her behavior. she has become irritable, mean, nasty, and emotional. she has had me in tears on a daily basis. she has turned into a monster. we will be calling the doctor in the morning!

I am in total shock. I cannot believe I found this site.
My son is 18 years old, and has cold induced asthma. He has been on singulair for many many years. Since taking the drug, his outbreaks have been only once a year, and just this year he has not had any flare ups! I was a huge believer in singulair, until now....something has happened to my son...I watched a video of him last night when he was about 10...he was happy and patient and loving. He was always a straight A or A-B student. Within the past 4 years, he is so mean that I am at my wit's end. He can hardly stand his dad, and despises his younger brother. I'm not too high in his book on some days either. Of course, you would think it is just teenage hormones, but I've never seen anyone that is so hateful of everyone as a teen. He is a star baseball player, and doesn't like his coach, and doesn't like most people! I have sat her and just cried my eyes out reading about everyone else....I don't know if I can stop him cold turkey, but I'm going to call the Dr. and then not tell anyone and wean him off his singulair, and see what happens. To think my boy will be going to college in the fall and he has had to suffer all these years! Why in the world has someone not told us about this? (I guess I shouldn't have watched Erin Brockovich last night! I'm ready for a fight! LOL). My brother is a nurse and laughed me to scorn when I asked him if singulair might have some side effects that would make my son so irritable. I am SO excited, and pray that this is the cause of his anger.

I would strongly suggest that anyone taking Maxide or the generic medication supplement it with potassium. I know that it is not supposed to deplete the potassium and other electrolytes, but it can. Since potassium is water soluble, the body flushes out what it doesnt need so it wont hurt you and will probably help eliviate a lot of the side effects, namely cramps, dizziness, light-headedness, anxiety, aggitation, fatigue, and so on. Start off with the recomended dosage and increase after a day or so if you dont see results. As soon as I feel any of these side effects, I take potassium until they go away. It takes about an hour for it to get into your system so give it time to work. Most people dont realize the importance of potassium and that most of us are at a deficient of it. Also, magnesium helps the body retain and absorb potassium, so you may need that too. I'm not a dr. I just want to share with others what has helped me. My husband is now a believer since he finally gave in and started taking potassium and hasnt had a migraine since. Until then, he had them almost daily for years and the drs couldnt find a cause and nothing else helped.

I am sorry sorry that so amny of you here have experienced all these horrible side effects. I guess I am lucky that after seven days of levaquin, Three weeks after stopping it, my biggest complaint is the rash hasn't quite left and I am itchy and dry, still have some muscle tightening and cramping in calf muscles.
The people who say " I have taken this drug with little or no side effect" Thats all fine and well and i am truly happy for you.....But people who are saying " It's people like you who don't finish thier medication and then wonder why drugs aren't working anymore," and " You all need to not blame everything on the drug and maybe some of these so called side effects are just caused by your pre-existing diseases and condition" I truly hope you sceptics and scoffers and critics never suffer or have anyone you love suffer from one of these drug reactions, because you WILL become a believer real fast. And furthermore I was perfectly healthy before I took this drug.

My father who is 82 was given Levaquin after a Urinary Tract Procedure. After 3 doses became very sick. He was taken to the E.R. in an ambulance with heart palpitations, trouble breathing, sweating, loose stools and confusion. At the hospital the doctor put him on an I.V. drip of Levaquin and wrote out a prescription for my mother to fill for more Levaquin which she administered to him herself.
When I arrived at the hospital he was able to relate to me that his symptoms began while taking the Levaquin. I checked the internet and found hundreds of testimonials against this drug. Needless to say I had the drug discontinued immediately and got him out of that doctor's care and out of the hospital. His health has improved greatly, but he is depressed, tired, and is not himself at all.
This man was an intellegent and vibrant person who danced the fox trot at his grand daughter's wedding just a month ago.
Today he admitted to me that his abilty to reason and remember things has been coming and going. He insists that it all began with his taking the Levaquin. I, for one, believe him one hundred percent.
My question is how can we get this poison out of his system?
I am a great believer in natural medicines and therapies. Has anyone tried anything that has helped.