Wits symptoms and conditions

I received dilaudid after having shots in my back for pain due to degenerated discs. After the 6 shots I experienced serious back spasms, while still at the hospital. The doctor told me that could happen to some patients. Well the pain was so severe (from the spasms) and the invasion of by back from the radio frequency wave shots to deaden the nerves that I couldn't leave. He ordered the dilaudid and they put it in my I.V. and in about 10 minutes the pain was gone the spasms stopped. The only problem was that I didn't have my wits about me and some bad itching. A shot of benadryl fixed that, though.

I have a 4yr old boy who has been on singulair for 5 months. Before he began singulair he was the most happy, kind, gentle, loving boy. We had an awesome close relationship. I enjoyed just sitting there watching him play. I could not wait for him to learn something new, but EVERYTHING has changed now. I took him off of singulair on Sept 19, 2008 after accidentally running into this site while looking up children and OCD. Thank God I did. It has been 12 days since I found this and took him off. I couldn't type then because I was to upset. My son who never had ANY mental problems or anxiety is now completely riddled with it. Instead of playing all day care free like 4yr old are supposed to do, my son spends his days now clinging to me in fear that I may leave or go into a room without him and he will not be there to open the door. He obsessively has to open every door now. He spends his days getting upset at the smallest things. He now gets mad at everything I say, or I don't say it right. Our relationship is not the same now, and I am devastated. Before Singulair he slept through the night every night. Now he wakes up every couple of hours to go to the bathroom and say "are you still there mom?" ok "I love you" "Don't let the bed bugs bite" I have to answer "I love you to" and "you either" If anything different is said he will go nuts, and he will obsessively say this over and over and over again. This is not my son. He is a totally different person. I am so very scared that this poison has permanently ruined him. I mean he is so young and his brain is developing. It has been developing with this poison in it, that has ruined him. It has been 12 days and he is still doing the same ocd stuff. He still seems really agitated. His muscles hurt, his tummy hurts, his eyes hurt, his ankles hurt, and he has diarrhea. My beautiful boy is now mentally and physically SICK because of singulair. I feel really bad to, because I did not know at first that the singulair was causing this and I was always getting on to him for his behavior and putting him in his room. At pre-school a couple of days after first giving singulair to him he started crying ALL DAY at school, and I made him stay there because I thought it was just because he had gotten a new teacher and he needed to get used to her. I feel terrible!! Does anyone know if the ocd will go away or has he now learned the behavior?

My daughter had been on singulair from the time she was 8 yrs old until she was 14. This will sound as if I am a horrible mother but I just thought that she was a raging bitch. Without my knowledge, she stopped taking her Singulair for a few months and she became a different person. She was so sweet and loving. One night she came in my room having an asthma attack and I asked her if she was taking her meds, she admitted that she had stopped taking her singulair and I got on to her and immediately got her prescription refilled. Within a few days of taking the singulair she turned into a raging, screaming emotional wreck, a TOTALLY different person. I feel so bad that for 6 years of her life I put her on medicine that caused her to have screaming, uncontrollable tantrums, and severe mood swings that caused her to be miserable. It does seem to be the only thing that effectively controls her asthma symptoms but the emotional havoc that is causes her and the people around her is not worth the benefits. We have an appt. with her doctor to see what other options we have.

Our 4yo son was only on this drug for 6 days. By day 3 l was at my wits end trying to explain his behavior. He was kicking, punching, crying, back chatting, being uncontrollable and could not be reasoned with. His breathing had dramatically improved but OMG at what cost. He would cry at his own behavior, knowing he should not be kicking me, but kicking me anyway. He would sit on my lap and cry, saying l don't love him and everybody hates him, and that he is a naughty, ugly boy.
I sat down at the computer and googled singulair, look what l got. I am horrified that l was not warned that this could happen to my beautiful little boy. I am the one who feels ugly now, for every time l was cross at his behavior in the last week, behavior that l now believe he did not have full control over.

Thank God I found this website!!! I am completly at my wits ends and now I realize it's the damn pill!!! 3 months ago I came off using Nuvaring because I'd only used it for 2 months when I started bleeding and never stopped! Nuvaring was great for not having to take a pill every day, but it did something else to me that was worse. So the doctor suggested FEMCON FE. I continued to bleed for 2 months and was told to give it a full 4 months at least for my body to adjust. As I sit here crying and typing this to you all, it is an effect of Femconfe, I want to say "DON'T TAKE THIS MESS!" I will stop taking it today in my 2nd week of my 3rd pack of pills.
My symptoms are as follows:
My breast are killing me and I was already a DD!
I've gained 8 lbs after losing 20 previously!
I've have headaches constantly
I have cramping lightly, but daily
My anxiety is through the roof!
I am always depressed!
I've nausea to the point of vomiting a couple of times.
I have no sex drive.
and the worst of all, I have such severe dizziness, I can't function, much less focus!!! I'm a freaking' mess with this stuff!! I guess birth control isn't for me but this is by far the worst in my entire life and I'm 38 yrs of age!

To top all of this off, I read another ladies posting about having a touch of food poisoning and OMG!!!, I went through the same thing and wonder if it had to do with femcon as well. It was approx 3 weeks into taking my pills.
I had diarrhea for an entire week! I thought I'd die from dehydration! I'm actually hoping this was just a stomach virus. Who knows, but it just struck me odd that someone else experienced this as well.
Don't use Femcon ladies, and good luck with finding something that works well with your body.

Blessings.

My doctor just put me on this pill I haven't been on BC in 3 years but I have had my period since March and it's now June he thinks this will regulate my body so I will go back to normal. I have only been taking this since Tuesday it's now Sunday and last night I thought I was going to die. I couldn't sleep because I was soooo dizzy ever time I moved the whole room would spin. It's not as bad since I have been awake today but it's still there and I don't know if I should even take it today or not. Is anyone else dealing with this or is it just me?

Now a new side effect, I have posted other side effects that were enough to get off the remicade. I went in and had another surgery because the side effects of this drug was killing me.{see other effects I posted under Jbill} So now the Doctors are looking into Brain damage. I am going to have a MRI done to see if this is a reality, I feel as though I have lost my wits. this is not something that I came up with, it is starting to show up in others and is talked about among the doctors that treat us. I used remicade for approx 4 years and feel like it is a dangerous drug. It can work pretty good but would not take it on a regular basis. I will not take it again.

Two days ago I took out my third molars (wisdom teeth), afterwards I took a prescription strength 600mg Ibuprofen with no side effects. I took another pill 6 hours later, and I have been having the worst upper stomach pain, much worse than the tooth ache ever was since then. I have been waking up with agonizing pain every hour for the past two nights, and I can't even take Tylenol for my tooth pain now since my stomach is so messed up (I tried and it cause horrible stomach pain).

So on top of having to treat the stomach problem, I can't take any pain medication for my teeth and I'm just miserable. I'm 25 years old and have never had stomach problems before, the first night I thought I was poisoned or something and I was dieing. I think the small label on the bottle that says "if it causes upset stomach, take it with crackers or bread" needs to be replaced with "it doesn't matter what you take it with, it can cause much more pain that you have ever imagined." Because it actually doesn't matter if you take it with bread, or inject it to yourself, the function of ruining the stomach lining is because of it's anti-inflammatory chemicals, not direct contact with stomach.

I read about it now, and apparently the deaths from Ibuprofen and Aspirin (anti-inflammatory pain medications) caused by gastrointestinal problems is about as many as deaths by HIV-Aids in USA*. I don't see any Ibuprofen awareness rallies though. I wish I had time to sue someone because I really really want to.

******

I had the Mirena put in six weeks after having our daughter, on June 30th, 2006. I never was able to loose weight, and felt very bloated, moody, with pains in my sides (ovary level), and then in the Fall of 2007, I noticed a significant loss of vision in my left eye. I went through $40,000 worth of hospital visits, and one 8-day stay, to figure out that the Mirena had caused a rather large blood clot to form on the outside of my brain in the main vein that crosses over the top outside brain. I have suffered from multiple ER visits with migraines lasting up to 72 hours, even after shots and meds. I have been going to the University of Colorado Hospital for treatment and it has taken over six months to get me on a medication regiment that will hopefully alleviate my debilitating headaches and now am living with the possibility that my vision may never get better in my left eye. The Dr.'s I have seen: an eye surgeon, a Neurologist, a Neuro-ophthalmologist, a Retinal Specialist, and the multiple local MD's. The tests run on my body and head have been very extensive, including blood tests, multiple MRI's and the final MRVenagram that tests the flow and drainage of and around my brain that found the blood clot and have ruled out everything from MS, to Pseudotumor Cerebri (which is a lifelong disease offering only pain management for the most part), as well as a macular deterioration related with people over fifty, not 24, they have also ruled out any pre-existing tendency for being prone to blood clots . This has been the scariest thing of my life and so consuming and debilitating, that I would never recommend the Mirena to anyone. I have missed so much work and the traveling to doctors have been a drain on our financial situation. This kind of information needs to get out there because Dr's are denying any relation to the Mirena. My Dr's have definitely diagnosed my problem as the Mirena. The swelling of spinal fluid was my body trying to protect itself and that swelling caused such great pressure on my optic nerve that my macula, where a person has central and fine detail and focusing, wrinkled in a layer of my eye that cannot be operated on. I can no longer read out of my left eye and the stress that created for my right eye is a contributor to the migraines. I also see double at night, when lights or signs are illuminated by the headlights of my car. I am seeing two images! This is very hard to accept and not being able to read for very long also upsets me. The likelihood of my vision repairing on its own is slim to none. Thanks Mirena. SO please, please help the word get out!!!! Also caution anyone you know who is planning on getting the Mirena, or who has one in to be aware of any changes. My experience has been very extreme but maybe women out there are going through the same things I have been and no one will recognize the relation to the Mirena. I am only glad my Dr. was willing to admit the Mirena was the cause.

I was weaned off 50 mg Toprol over an 8 day period (after having been on it for 4 years) and then had been off it completely for 10 days -- when my Dr. decided that what I was feeling could not POSSIBLY STILL be side effects from Toprol Withdrawal and so put me BACK on it at a lower dose (25 mg instead of 50 mg) - and 80 mg of Diovan (along with Prilosec OTC for acid reflux and a Hiatal hernia) - the Diovan made me so sick, I developed a bad cough and pains in my upper chest so I stopped that --- and low and behold after being back on the Toprol 25 mg for 2 days -- the severe chest tightness is BACK and worse than EVER -- it is horrible. I am a 33 year old woman with asthma (5'3 @ 135 pounds with no other health problems) -- my problem is without meds my B/P runs 140/110 (they say that it is genetic and that I do not work out and have a desk job - because I do not drink or smoke and I am not overweight, and I eat a very healthy diet) -- but the meds they want me take for it give me so many side effects I cannot STAND IT.. I don't know what to do -- I go back to my DR. Wed for a follow-up but cannot stand this chest tightness until then.......... Being 10 days off Toprol I was still have chest tightness and breathing difficulties -- but not as often and not as severe - so I thought maybe it just took a long time to get out of your system... My Dr. said I should have been feeling better after 3-5 days so that it could not possibly be the Toprol. I am at my WITS END and do not know where to turn or what to do.

I have been taking Lamictal for just over a year. Some of the side effects have been noticable for a few months, but others seem to just be appearing and getting worse. I have loss of balance and coordination, my vision is gettng worse, I have a hard time concentrating and finding the right words, I forget how to spell common words, I have short-term memory loss and feel spacey. I can always figure it out, but it takes longer. I began doing Pilates every day about 3 months ago and still cannot get the routine down and it is just as hard for my muscles as it was in the beginning. I can't seem to lose weight and have horrible acne on my face. I had 2 seizures before beginning Lamictal and am suppose to be on it for 2 years before trying to go off. Without insurance though, I am unable to do follow-ups w/ my neurologist and she seems unconcerned and unsypathetic to my situation, not giving me the time of day. She never even told me all of these side effects could develop, much less that they might begin long after I started taking Lamictal. Has anyone had these side effects after having taken the Lamictal for so long then stopped taking the Lamictal? Will these side effects go away after I stop taking it??

Guest 33599 and 33598 and others.
I have been reading your postings.

In Dec. 2005 I was given a weeks worth of Levaquin. Withing first hour of first two pills I passed out on ride home from our local ER. This may or may not have been a reaction to the Levaquin, it may have been what the ER doc says was a "vagal" response.
But first night home after another dose of this Levaquin next day my shoulders and arms burned so bad and hands went numb and cold and insides went haywire with shooting pains and bladder feeling haywire and twitching all over, itching, complete insomnia with extreme anxiety and a few quick little nightmares. Scared out of my 54 year old male wits.

Next morning crawled to couch, ate half a piece of toast. Within minutes abdominal insides started to get sore and this intensified to point of holding stomach . Then body started getting weak from already weak feeling of flu before this. I felt like I was going into shock. I WAS going into shock.

Couldn't even hold hands up from laying down position. Started to see spots, freaking out, called ambulance agian. Went to local ER agin. Told them I felt like I was going to die. They did blood, urine, heart tests. Found nothing. Gave me atavan and when this calmed me down ssent me home.
Starting right then and there I was physically devastated. Went back to ER one or more times again that week.

Each time I would tell them I couldn't walk, eat, sleep, nerves fried...pains in shoulders arms. Soon they were calling in Psyche ward. How humiliating.
EACT TIME I TOLD THEM...the only medicine I was taking was this Levaquin. They NEVER ONCE said to stop taking this. Not knowing anything I kept taking it for next 4 days. 7 days total.

I didn't put the two together. I didn't know. Trusted them completely. Trusted them to know if I should stop taking this poison. And they were told each time I went there that thiswas the only drug I was taking.
Looking back, I think they were completely uneducated about this drug. Maybe the actual Docs in ER knew only about the "immediate" reactions to this drug and not the systemic ones that showed up in different ways within forst day or two such as burning shoulder and arm pain, nerve system problems etc. Gastrointestinal as well.

To this day every doctor I mention this too angrily denies Levaquin could have done this to me.

On top of so many tearful truths about the suffering I have been through...is this wall of denial with these doctors.

Here on the internet ( right there for these not wanting to know doctors to see ) are "thousands" of testimonials about the "same" symptoms by all of us soon after ingesting this poison.

The FDA would not have issued that warning in 2004 to pharmacies etc. if they didn't know something like what we are all screaming to the world we know. Tragically.

I could print up a 6 inch thick binder full of reports ( including the FDA one ) and studies and testimony from thousands like you..throw it on the desk of a denying doctor in any field and they will not even look at it.

It's like this information about Levaquin doesn't exist and they do not want to look at it when it's placed right in front of their face! What kind of a tragically sick injustice is that?

I wish we could prosecute every doctor who keeps saying Levaquin doesn't do the things you and I know it does. You and I have done more research on this drug than they have!

Of course a certain percentage of these reports may not be totally accurate...even the most stringent scientific studies have flaws. But the sheer number of these Levaquin reports and the basic similarities in them are staggering in their obvious implications.

You don't dismiss tens of thousands of complaints by sufferers. And I guarantee you that for every person that has a computer and has reported the same scary symptoms suffered after taking Levaquin, that there are 10 other people out there at least who don't ever go on a computer and don't know where to go to report this..and many like me for months...who didn't even know that Levaquin may have been the cause of all my medical maladies.

What you are seeing here on the computer is the tip of the iceberg!

This could turn into a national scandal if it were properly reported and the true numbers of victims could be traced.

Vioxx killed 50,000. They know this. And it should have been a crime that the makers of that drug and the professionals who kept prescribing and selling this drug even after they were hearing that thousands of patients were complaining about it...kept pushing and using this killer drug.

Exactly like all of you, I had the burning pain, my shoulders, arms, even hands...my muscles, knees, ankles all hurt and still hurt and are weak. I get colder than I ever have..then kind of weird sweats. fell like I am going to faint so muc even one YEAR later. So so so sick feeling all of the time. Can't even remember all the horrible feelings I have. Financially ruined. Doctors treat me like you know what. Most doctors do not have patience as they are so booked and always seemed rushed and tired at same time. They have ways of getting you out of their care. Scheduling your visits farther and farther apart. Chastizing you hoping you will leave them. Constantly recommending psych care and anti-depressants and being short during your visit. Their tone and body language and these other things are so clear.

But they are very clever ways get rid of you as a patient without officially doing this in a way that could be catagorized as unethical...so you can't sue them.

It's like a landlord wanting you out and doing everything within the law to make you feel so miserable you will leave on your own.

Cynical? Oh, absolutely. But its' the truth in my case.

I am still so sick that even as I write this I feel like I am going to faint. I have so many other symptoms now that you wouldn't believe it. Red, itchy rashes on my legs and back of elbows that come and go. A wheeze in my right lung that I have to see a pulmonary guy about. Feeling my pulse so strong it shakes my body on left side. Constant shaking. Nerves seem actually damaged in their heightened sensitivity.
I don't even sweat right. I feel so anxiety ridden I can't tell you. Sick to my stomach constantly ( lost 35 pounds in first 3 months ) couldn't eat. Metallic taste in mouth. Swollen throat feeling...doctors dismissed this as the didn't feel lymph swelling, but GI doc looked in my mouth the other day and said "your tonsils are inflammed."

I keep telling doctors I feel like I am being poisoned. They look at me as if I am completely crazy and paranoid. Especially when their tests don't show anything.

I feel like breaking down and crying so much which I have done. And I'm a 55 year old male that never ever ever acted like this in my first 54 years. Raised a family, worked, married to same first wife for 25 years.
Never saw a psychiatrist in my life. Never a drinking, drug or smoking problem.

I have been told to lie to hospitals ( by one doctors nurse and another med professional I don't want to mention here because I am still seeing her/him) ) and say I am homicidal or suicidal to get in to the hospital because based on my tests not showing anything and a pcp who will quit believing their is anything more wrong with me besides my sanity...I cannot get any more specialized/all at once, more technical studies.

The getting in through the psych back door does not work for me because it isn't true. I am not going to lie to get in a hospital. I would think that the truth that I feel like I am dying would be enough. Once I lie and I get caught at it I would never be taken seriously again.

But I would like toxixcology tests, especially for the chemical florine, which I have read is the culprit in the Flouroquinolones family of antibiotics poison.
I would like an endocrinologist to test me in every way they can.
I would like someone who specialises in nerve damge take a look at my entire central nervous system.

I know money is the biggest obstacle as I have none. But I pray constantly that somehow, somwhere, someday, someone will find something that explains why I feel like I am dying one year after I took a weeks worth of Levaquin.
And that I can finally prove that I am not just crazy. I will tell you a truth here. I fear I will be committed as my symptoms seem to be getting worse not better. And when they don't find anything in the basic medical exams...they really go after you in labeling you mentally ill.

More and more, my complaints are met with silence...and then within minutes a person from the psych ward comes in.

Dear God. This is truly anightmare. If I was a screen wrioter it would be a great movie that would truly scare viewers.

Just imagine getting an illness and having your body go haywire and feel like you are going to die..yet no one can find anything to explain it...and so they all start the process of committing you. To feel this way physically and to also fear this shoving into the mentally ill realm happening at the same time is a real life nightmare. One that unfortunately I am living. And if you want to read about thousands of others feeling like this ... just type in Fibromyalgia and go to that big board sometime. That board is a living nightmare also. Thousands of people all looking for cures and sympathy to very similar hard or impossible to diagnose illness's that are ravaging their bodies like me.

Sorry for presenting such a bleak pictre here....but it's the truth. It is happening all over the country. Just look at how many Fibromyalgia boards and groups and meetings there are.

God help you and I.

Girls,

would love feedback if anyone had high bpressure after the pill and if so for how long, im really worried mine wont go back to normal (onky raised the month before i stopped). SILKE i read that your bp was high in your earlier posts , did that lower and if so how long after as you know this month is my third month mark and its still 150/100 and its scaring the wits out of me that its gonna be like that forever.ALOS LEFT BREAST PAIN today on day 10 after my period, never had this before and im scared....

Lisa