Sentences symptoms and conditions

I am a 39 year old white female in the nursing profession (RN). I was placed on Topamax at the age of 31 for new onset atypical complex seizures that were later diagnosed as migraine induced drop attacks. I took Topamax for 3 years. I took 100mg a day. My family and I had moved to another state and I had to find another Neurologist. During this time I had many side effects from the medication that I blamed on my "condition." To make a very long story short, while taking Topamax, I developed a kidney stone, severe restless leg syndrome, weight loss, feet tingling, blurred vision, mood swings, slurred speech and mental confusion that went into amnesia. I had to relearn how to drive a car, spell, do 2nd grade math, use a computer, etc...
I now have permanent memory loss. I struggle every day with my memory issues. I have learned tricks of how to deal with it but have not been able to recoup any previously lost cognition. After nearly 6 years of being off the medication I doubt I ever will. I feel inadequate and embarrased with my inability to remember people and things or form normal sentences during a conversation! I know the information is in my head but I can't always pull it forward. Some days are worse than others.
I also have a harder time learning new things. The information just doesn't want to stay "stored" in my brain. (Not a problem patients or doctors want to see in a critical care nurse!)
I hope my experience will save others from suffering the same fate. Use extreme caution taking this medication. It can drastically alter your life.

I have been taking Wellbutrin 300 xl ( i believe - here comes the "Brain Farts" i attribute to Wellbutrin ) for seven years. I can tell you that i have noticed a small very very small amount of hair loss compared to most people but as i read thru these posts it appeared to me that MOST of them stated generic Wellbutrin. I will say i have had more hair than i am comfortable with appearing in my shower and bathroom floor and sink from drying my hair BUT i have NOT had the scary experiences that i have read here. I came to this site because i had to quit taking my Wellbutrin cold turkey because of some changes in the law in my state i have to drive 50 miles away to see my N.P. and because the office i was going to and the one she works in act like they have to send fire signals to each other instead of email and i am out of meds! so i was searching for side effects i could expect until i can get my meds back. i will tell you it is nice to see that i am not alone but i think it sucks that any of us have to decide if taking the medication and side effects are worth it! i also have problems with memory, spelling,speech, following thru with my thoughts much less getting them out of my head and making sense to someone else. did that make sense? ! ? i personally didn't notice any weight loss. my husband says i have the patience of a flea and really dislike " hate" a lot of things. i don't notice this but go back a couple of sentences and you will understand :)
After being here and reading all that i have i am afraid to continue taking this medication so i think i will just let it go and see what happens. i am also taking lamictal and seroquel and xanax and i am pretty sure i would be just as afraid of them if i went and looked them up but i have the choice as i am sure most of you do ...... do you take the meds and deal or go off the meds and well ... die?

Wellbutrin SR 200 mg. two times a day. Intensity. Nervous energy. Inability to focus sometimes. Memory loss. Speech can be disjointed and it's difficult to form complete sentences. I will often struggle to find the right word to complete a thought or trip up and not be able to finish a complete sentence smoothly. If I wait to take my second dose in the middle of the day my speech improves so I'm going to experiment with the time I take the drug whenever I have an important meeting.
From reading these posts I have now realized the hair loss that I have been experiencing is the result of Wellbutrin. I had no idea and have been experiencing this every since I've been on Wellbutrin. The texture of my hair is much courser and I shed hair at a much faster rate.

I began taking Adderall when I was about 16 yrs old.My doctor prescribed me 30 mg of Adderall RX. At first I would take it ALL the time (more than I was prescribed) and my grades improved tremendously..but then all the bad side effects began happening. I would get horrible back pains, had trouble swallowing (felt like I was swallowing a ball of dry food - usually happened late at night) Insomnia that kept me up all night. Another side effect that led me to stop taking the meds all together was that I felt like it was slowing my brain down. I couldn't construct sentences as easily as I once used to, and I felt like a ROBOT. I was numb to everything, my friends even started noticing my change. I was just a different person on this medication and not my usual bubbly self. So I stopped taking the medication daily and would only take it when I really needed it - for example, SAT'S, test, etc. When I got to college I began taking it as well for tests, long lectures, etc..but I started getting horrible migraines at night - not even Tylenol would work.. I used to have to lay in complete darkness and try to go to sleep. HORRIBLE. Anyway..has anyone found any remedies for the side effects you feel later on in the day when you start "coming down" from the medication? Tylenol doesn't seem to work..also, is it okay to be on sleeping pills and adderall? My doctor prescribed me both but I really felt like she was just handing out meds just cause she could so I didn't take them.

Hi, All! I went to the doctor on August 10th and had my Mirena taken out. My strings had retracted up into the uterus and I was VERY worried. It was a breeze.I didn't feel a thing, well maybe a little pressure was all. It didn't take long at all, to remove. I told my doctor that this thing was draining the life out of me. I was ready to hear This is not a side effect or this is not a side effect etc. He told me that Mirena has alot of side effects that are not even listed. My mouth dropped open. Wasn't prepared for that one. I started telling him just a few side effects I've had and the non stop bleeding since DEC 2008. He said he would definitely remove it. After my removal light bleeding the next day. On Sunday it started, I bleed HEAVY HEAVY blood clots and all, until the following Sunday and then it just stopped completely. I'm currently waiting my normal 28days to see if I get my normal period back. As for side effects My back where I could barely stand up. The pain is gone. I can get up and down fine without pain. My hair has stopped falling out by the had fulls. Memory loss is improving. Sex drive coming back. I've just noticed little things that I would complain about not even bring them up. I'm sure over time I'll notice more improvements. I'm so glad to have Mirena Out of my life. Also thankful to have understanding doctor.
Sorry for spelling and sentences.

Is anyone experiencing confusion, trouble thinking, trouble concentrating, decreased cognitive function, mental sluggishness, trouble solving problems or situations which require logical thinking, memory loss? Would love to hear from anyone experiencing any these symptoms and if so, how long were you on the drug.
Thanks!

I initially went to the doctor requesting my ADHD medication and within 10 minutes of talking to this guy he tells me I don't have ADHD and proceeds to tell me I'm bi-polar. I'm 30yrs old and was placed on 80mg/daily 40mg in the a.m. and another 40mg before bedtime. I was on this medication for 2 1/2 days and was taken off of it due to involuntary mouth movements followed by episodes of dystonia (neck, eyes, mouth and hands for hours at a time)...it was almost as if I was having a seizure without swallowing my tongue. I also experienced very blurred vision and now when I'm speaking to someone I feel like my brain went for a walk because sentences don't come out right and I find myself struggling to make rational decisions. I have now been off of it totally for 3 days and I'm still experiencing the blurred vision and I had 20/20 vision prior to taking this drug, The doctor wants me to try Abilify but the side effects of that drug are very similar to Geodon, I'm literally scared to even pick this up from the pharmacy and give it a try. My pupils are very dilated, I don't know how long this is going to last but it's affecting my job (meaning I haven't been to work in a week because I can't see straight. If anyone is experiencing the same issues after being off the medication for a while...can you tell me how long I am to expect this to go on.

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

I have been on Lamictal for Bipolar II for a little over two years now. The first side effect I really noticed was that I had zero desire to exercise anymore. I used to be pretty athletic, loved to go on hikes, now I could care less. Also, my brain is mush. I am a former honors/ Dean's list student; I had one professor in college tell me I was the only person in class who would ever be able to write professionally, and I have been trying to write the same novel for three years now. I forget how to spell words and how to formulate sentences. I can never find the right word. I forget what the plot is, what I wrote in the last chapter, so I am constantly re-reading what I wrote. I started to think that I had ADD because I couldn't focus on anything, and I couldn't remember if I had always been this way or not. Granted, I think I have always had a bit of a problem with executive functioning- organizing, prioritizing, completing tasks- but it has always been more of a problem with keeping my house clean, etc, NEVER with writing. Also, I have always been very good at remembering names, dates, events in history- the random sort of information that makes a person stellar at Trivial Pursuit- and all I can say now is, 'Uhhh... oh, man, I KNOW THIS.' Also, I am becoming incredibly antisocial, which I think probably has something to do with the fact that I no longer know how to talk. (A sidenote: I'd say chances are good that I have Asperger's; socializing has always been a challenge for me. My point here is that I'm wondering whether Lamictal is making the things I have problems with worse, ie, executive functioning, socialization..., etc. I used to be able to overcome these impairments intellectually; now that my brain doesn't function the way it used to, it's way harder to compensate.) I had a conversation with my husband the other day about all of it, whether he thought Lamictal was truly helping me. He told me that I no longer seem interested in doing anything anymore; that I am no longer sharp like I used to be; that I lack the vitality I used to have; that I no longer get excited about anything anymore. Now I know that Lamictal is a mood stabilizer, that I am on it to stabilize my moods, so obviously there are no longer going to be the highs that there once were. But now I feel so flat and dumb I just don't know. By the way, I have worked my way down to 75mg at night from 200mg. (Which is an improvement, I'll give you that- before I was scared to drive because I'd practically forget I was driving, that's how crappy my short term memory was.) Just so you know, I don't feel depressed, so it's not that my dose is too low and I'm experiencing depression. I just don't feel much of anything at all anymore.

35, male, athletic: i took 3x 500mg and immediately got sore joints and severe flu-like symptoms. i was completely bedridden, loss of balance, sore from head to toe, major bloating and cramping... MISERABLE. this was near the beginning of November. while most side effects have lessened, i have had tendon issues as recently as last week. basically, any "strenuous" exertion will injure the tendons, although i haven't ruptured anything yet. bottoms of feet were sore for a couple weeks for no apparent reason. having trouble remembering words, finishing sentences, etc... digestion seems to be "off", and there is a bitter taste in my mouth that has been there since the beginning. also, "phantom itch" deep in both ears that comes and goes, and earwax production seems to have ceased... weird. oh, and D-R-Y eyes, nose and mouth upon waking. very dry skin as well. it did kill the infection though. i guess i'll be back to normal again someday. i hope.

Reading over some of these posts and wanted to share my experience w/Lamictal. Been on it over 2 year, 400mg/day. Sever bipolar with mixed & rapid cycling episodes. Oh YEA...I have side effects too: blurred vision that comes and goes, super klutziness, confusion, hard to complete sentences sometimes (just can't find the words sometimes for the simplest sentence!), dizziness, prone to broken blood vessels under the skin when bump into something or carry loaded grocery bag over my arm, jittery, short term memory loss, feeling really stupid like my brain isn't working sometimes. BUT...I will stay on this med because it rally works for me and the above effects are and bad, just frustrating. It took me a good 5-6 months for the meds to work as they should. Be aware that it won't make things perfect, mood swings and even moderate episodes can be expected. I am pretty much in a constant state of mild/moderate mania (2 hr sleep/night, hi energy, talk to fast, mind racing,etc), which is fine for me, as it really curbed the depression (maybe only 1 day every 2 months now and its NOT a BAD downer) I have found the drug is a good "stabilizer" keeping me mostly in a normal to moderate swing...never any severe swing. If the side effects are not unbearable, stick with the med, just be patient. It sure works for me. Learn to laugh at the klutziness and stupid moments and understand its the med and you. GOOD LUCK TO YOU ALL!

I am a school teacher and got hit in the head by a student and suffered a severe concussion. I was having head swelling when I read, listen to any rhythms or use the computer. I get severe headaches after doing these activities which are most of my job. I am on worker's comp at this time and find that the doctors I had were horrible. The first two months I was on pain killers every six hours and they didn't work. Then I thought finally I thought I would get some relief when I got a neurologist. He put me on Topamax 25 mg the first week and then after 50 mg. He gave me Treximet even though I am allergic to Alleve he refused after that to give me anything for the onset of my migraines. I got really aggressive on Topamax. I was spacey. He then doubled my dose to 100 mg. The Dr. just said I didn't want to go to school even though I was getting worse and worse and could hardly take care of myself. . I was still having head swelling and headaches when I read etc. but my memory was gone and I was ready to throw thing and hurt others. My aggression was worse than when I had several courses of steroids years earlier. There were many times that I couldn't talk in sentences. I would forget what I was doing and also get lost. I was like an Alzheimer's patient. I couldn't get to my thoughts no matter how hard I tried. I have just got off Topamax and can now speak in sentences and the aggression is gone but my memory is still not completely back. I couldn't do simple subtraction or addition. I was better at it in the second grade than on Topamax. I couldn't remember 3 words after about ten minutes only one word. I couldn't draw a simple geometrical figure. I had all the same problems but on Topamax the addition of horrible side effects. The only side effect I could have used and didn't get was weight loss. My parents actually had to come and take care of me because I couldn't fill out the paperwork and also I couldn't even talk and was having fits and tantrums like a child. Thank goodness I had a regular Dr. that knew what was wrong and sent me to get weaned off Topamax. At that time I was told it would take 3 weeks to wean me off and there was no way I could go to school until it was out of my system. I kept telling the neurologist my side effects and even wrote him a letter explaining but he didn't pay any attention and acted like I was making it all up. I asked for a change of worker's comp doctors. He didn't like that at all and now I have to go for psychiatric testing before I go to my new worker's comp neurologist. All I want is to go back to school and to be able to do my job. I would have never had the memory, cognitive, reasoning, or speaking ability to get back to school taking Topamax.

I have been on Lamictal now for almost 3 months for bipolar. I'm still not sure if it is helping or not. My husband says I seem better, but I feel almost the same as before if not worse. Has anyone noticed any major changes in their menstrual cycle? I'm on the pill and it would usually last 4-5 days with moderate bleeding. Now I get more annoying cramps than before but my period only lasted 2 days and it was more like spotting than a period. This makes me nervous, but my doctor said that it is more likely the risperdal that I had taken for a month when I also started taking the lamictal, but I don't agree. I recently went up to 200mg (1 morning, 1night). The morning one knocks me out but the night one has been keeping up!? I also feel less coordinated (hard to balance, knocking stuff down, klutzy). Also, it has been hard to put words together and recall correct information. Now I have to say" I think I heard or I think I remember". If I really need to remember something I have repeat it or really concentrate on the information. I used to not have to do that. Another thing I've noticed lately is hand and knee pain. Makes it difficult exercise to lose the 20 lbs I've gained. I don't know, personally I think I will give it one more month and if I still feel the same, I'm going off of it and looking into natural alternatives.

I am a 25 year old graduate student that began taking Topamax for migraines after I was involved in a bad car accident. I started taking Topamax in April of 2008 and by July I could barely formulate sentences, couldn't remember simple things like where I parked by car (in front of my apartment) and my family member's names, simple math was impossible, I was always tired but could never go to sleep, had numbness in hands and feet, and was very moody with suicidal ideations. I was then referred to a neuropsychologist to assess any possible brain damage from the accident since I was now having cognitive problems. They tested me for brain damage where I was diagnosed with Severe Brain Damage, I was reading on a 8th grade level, did math on a 4th grade level, needed to begin speech therapy immediately and my doctor felt I needed direct supervision at all times. I was initially told by my neurologist that the medicine would help with the migraines but would "make my thinking slow". That was a huge understatement. I was a 4.0 graduate student in the middle of my program and I suddenly couldn't perform basic daily activities. I have been doing much better since coming off the medication. I have the migraines less frequently but they are still pretty bad. I have regained most of memory, reading, and math skills back the rest is attributed to the car accident. I wouldn't recommend this medication to anyone and I think it should be taken off the market because it almost destroyed my life and had me and my family worried to death about a condition which symptoms were clearly being exacerbated by Topamax.

45 years old, female, diagnosed bipolar II in 2006. On Lamictal for 2 years. Initially, very positive effects of Lamictal - felt "normal" and stable for the first time in years. Didn't notice any side effects. Gradually increased from 200 to 400 mg per day 6 months ago as I still experienced mood swings with a tendency towards depression. I have been on 400 mg/day since August 2008. It is difficult to say what are the side effects of the medication, and what are "natural causes". Since doubling the dosage, I experience memory loss and increasing cognitive problems (slow thought process, difficulty putting together coherent sentences in discussions, fumbling for words. I have spent more than one hour on this posting!). I sometimes wake up during the night drenched in sweat. It could be that I'm menopausal, but I find it unlikely. Mood swings have perhaps become less pronounced, but I would like to regain my mental capacity. I plan to cut back to 200 mg of Lamictal - and perhaps some day learn to live with bilpolar II without medication and a lot of help from my friends and loved ones.

This is a follow-up to my posting on October 10th regarding my 57 year old husband who began taking Lisinopril in March of 2007. He was NEVER on any other medication prior to taking this drug. He suffered Depression, loss of memory, lack of concentration, can't focus and struggled with small task. We have recently had an MRI done and his brain has shrunk. Deadfred1 replied to my posting and he is a 36 year old male who has been on Lisinopril for 5 years. He has the same side effects as my husband. He had a recent MRI and his brain has shrunk!!! We visited a Neurologist with his MRI results for a second opinion and he is ordering more tests because "it appears to be indictive of Alzeheimers" with the area of the brain that has shrunk. How can this be??? This was a healthy, 57 year old NEVER on a drug in his life and within months of taking this, he is in Depression and having memory issues. Isn't anyone connecting any symptoms here??? Any Doctors out there with an "open mind"? This medication is was developed from the venom of a poisonous Brazilian snake!!! Hello...it's more like a slow death with Arsenic!!! My mother-in-law has been on this drug for years and years and years. She now sits with dementia in an Alzeheimers unit. Is anybody out there listening? Alzeheimers is becoming an epidemic in this country. Have we ever thought the medications we are taking is creating this devastating disease? Millions of people take Ace Inhibitors, millions of people have Alzeheimers. They are getting younger and younger according to the Neurologist. Why, because younger and younger people are being put on Blood pressure medications from poisonous snakes. Are there any open minded Dr.s out there that can "step outside the box"...don't just "think outside the box"...."step out for goodness sake" and start paying closer attention to the symptoms people are having. I am convinced there is a definite connection to my husbands side effects and this drug. Get off people. Get off.

I have to comment on some of the Lamictal "new comers". I've taken Lamictal for 1 1/2 years. For the first 6 months, this was the miracle drug. As months went by, I began all of the same symptoms: fogginess, weight gain, short-term memory loss, NO libido, headaches, and nausea, to name a few. As of this moment, I am weaning off of the Lamictal. HARD to do. This is not a drug that can be "stopped" immediately. On my fifth day of weaning off, I am dizzy, tired, weak, irritable, and have vomitted. Only about 3 days left. I am starting Topomax after. I'm anxious to see if there is any difference. Especially the weight gain part. I went from 120 to 135 in one year. (I run and eat healthy meals.) I will continue to take Effexor, which, in 2 years, has had little or no side effects. My advice to anyone just starting to take Lamictal is to GO SLOWLY. My doctor had my doses increase so rapidly that I didn't really see if the lower doses would have worked. (I take 200mg.) The bottom line is to do what feels right for YOUR body, rather than a specified dosage. Best wishes to you fellow BP-ers!

Im only 16 years old and ive been on levaquin for about 3 days now. My doctor told me off the bat that the only thing wrong with the drug were some "theories" on cartilidge damage, how ever, now i see for myself, and for many other people that is not the only side effect. He told me that no one under 18 is supposed to have it but i caught a severe case of sinutitus, and a uti which ive had for 2 months and nothing was working, so he put me on levaquin, once a day for 7 days. Ive now been having the following symptoms and im extremely scared!!
1. Constant fatigue
2. Extreme Migraines
3. Nausea, vomiting
4. Rapid heart beat (and chest pain)
5. Stiffness in joints and horrible pain...
6. Constant anxiousness, to where i cant get to sleep
7. Dizziness

Is there anyone i can talk to who's had these same problems? please email me or something im scared and i don't know what to do my mother doesn't believe me and she says its just a head cold....

******

Please help me!!

I have been taking Yaz for a month and a half. The only medication I have been on in several years.
At work yesterday, my head started getting foggy. And my perception, was all messed up. After about 15 minutes of this not getting better, I started to lose my speech communication. I couldn't finish sentences or words. Stuff was jumbling together. In my right hand, two fingers went numb, then the whole hand. A client ended up driving me to the ER. I tried to call my receptionist, but I couldn't get the words out, my client took the phone and told her I was going to the ER. By the time I got to the ER, feeling started coming back, and I could communicate, in full sentences, if I paused between. By the time I was checked in and saw the doctor, I was able to tell him all that happened. With no problem, then a huge headache came on.
He wanted to rule out stroke, so did the CT scan and MRI. The nurse had some trouble getting blood from me. She kept mentioning that the blood kept clotting. The doctor sent me home saying my brain was perfectly healthy, and to go see my regular doctor.
A friend told me it was the birth control, because she could not take it, as she has lupus, and could have a stroke. She said it causes clotting. All of this was making sense to me. I looked up the side effects I had and found the "stroke symptoms", listed as rare, on Yaz.
My opinion of what happened, I had a blood clot that ended up passing through, and it could have become a stroke.
Another thing I read, besides the clotting. Was that oral contraceptives increase the potassium in your blood. I had been eating a banana for breakfast, 3 mornings in a row (the third on the day of this episode). The added potassium, could have been related to this episode.
How is anyone to know they can't eat something like "bananas" with birth control? I certainly didn't.
I am afraid to try any form of birth control at this point.

I'm taking Wellbutrin and Lamictal (150 mg for both) for at least 5 months now, as a mood stabilizer. Like many people have said on here don't let these bad reviews scare you away from trying it, at the very worst you will take it and not like it so you can stop. But for me it was amazing how it stabilized my moods. I didn't expect it to be so noticeable. I had tried Topamax right before but it was terrible for me- it made me sooo out of it and I had a very hard time talking (finding the right words, pausing in sentences frequently) Lamictal didn't do that to me. I have started to get acne on my jawline like many others have posted, I didn't think it would be related but I've NEVER had acne on my jaw and cheeks they are really tiny bumps of acne, but a lot of them. The reason I started to look at this site for people's side effects was now I have terrible neck soreness and stiffness. I mean BAD. It's slowly working it's way to the middle of my neck as the day goes on and feels like it's going down the middle of my back as well. Very weird, I haven't exercised or done anything in the past 4 or 5 days that would have pulled a muscle, so make what you will out of it but I'm going to stop taking this drug. It's unfortunate because I really did like it and am worried how my moods will be after stopping it. But TRY IT, it has been at least 5 months of me being more stable so that alone is worth the clarity. Also, I'm a woman with usually heavy periods but didn't have that side effect with this drug and I lost weight didn't gain any with this one either, but I'm sure that had a lot to do with the Wellbutrin which is notorious for weight loss rather than weight gain. Also, if you start to feel good at a low dose as I did DON'T INCREASE IT! I hate hearing people say their doctor's wanted to get them to the "therapeutic dose" even when they felt good, your more likely to have neg. side effects if you go higher than you need. Everyone is different in how their body metabolizes the medicines. Do your research and hold your ground, make sure you have a doctor that will listen to you, that's key.

My doctor put me on topamax for daily chronic headaches. I worked my way up to 200mg and had all the symptoms, tingling in my hands and toes, short term memory loss, hard time putting sentences together, etc. I backed myself down to 100mg. and the side effects lessoned up significantly. I stayed on 100mg for almost a year (lost 10 lbs.) One day I decided that I was going to ween myself off and started going down 25mg every week until I stopped altogether. Since I have stopped, I do get headaches, usually 1 or 2 per week, nothing like when I started out on the topamax. I have gained 20lbs since stopping the topamax but no longer have a memory problem or putting together a complete sentence. In my opinion, you should try to take the lowest dose possible that gives you the greatest relieve from your pain.

i heard something on the television about a lawsuit involving advair and came across this site looking for information. i have been on advair for aprox 8 years. when i read some of these comments i began to cry. it so said exately what i have been feeling right down to being diagnosed with rhumetoid arthritis and fibro. i spent 6 hours in the er last week with a heart rate of 112. i went to my doctor as recommended after my visit and he blew me off because he was mad i went to the er and told me to go see a surgeon to cut into my collar bone, go down to my lungs and biopsy them. i see a different doctor next Thursday for a second opinion. i am so tired of being sick and to think, it could all be from this one thing. i am going to talk to the doctor about this on Thursday.

Previously posted 8 year old son w/ suicidal ideation and depression...I'm seeing comments about "inattentive." I've been saying my son is ADD for years....How many of you saw this possible side effect? Off of Singulair for 14 days now....behavior unbelievably improved.

My son is off singulair for two weeks now and is showing improvements. He was on it for 7 years and at the beginning we blamed it on steriods, even though his dose was low. When he went off the steroids, the behavior didn't stop. I questioned the allerist if the singulair could be doing it, but was told no, it doesn't have those side effects. I don't blame the doctors because they weren't given the info. He was extremely emotional, cried for no reason, had no confidence, didn't like himself. We on more than one occasion have told his older sister that when he hits his teenage years we would have to watch him for suicide, as his reaction to problems was sooo out of whack! He was on motrin for headaches 4-5 days a week(blamed it on sinusses). Unexplained stomachaches. These symptoms came on over years, not right away. I have always thought that the steroids had done damage because he took them when he was so young. Until the news reports hit, and I started reading other people's stories and doing the "OMG, that's my kid!", I never put the problems on singulair. I was still skeptical, but took him off. His symptoms immediately got 100x's worse for a week. But funny thing is, his headaches are gone, his stomachaches are gone and he seems much less emotional. The strangest thing is, EVERY night, he comes in to kiss us good night 7 or 8 times, and sometimes by the 7th time he is crying and can't explain why. This has been going on for YEARS, EVERYNIGHT, never a break. It stopped! Just stopped cold 7 days ago. Comes in once, says goodnight, leaves and falls asleep. I know this isn't a coincidence. After years of wondering what's wrong with my kid, now I feel like I've been poisoning my him for 7 years. I'm not skeptical anymore.

Ive only taken the pill 2 times so far. Already looking for the reason why my Dr. Pepper tastes bad, and I haven't slept since I took the very first one. I studder and can not complete sentences after I take it. I have a call in to the Dr. He said it will go away. Im not so sure I believe him. Insomnia I am a single mom, and work in a nursing home how unsafe....