Pulmonologist symptoms and conditions

Took Yaz years ago for some months. Do not remember many side effects. Starting taking it in July 2009 and within 2 weeks was hospitalized with pulmonary embolisms in both lung. Which means blood clots in both lungs. Doctor's could not find any other reason than Yaz. Please DO NOT TAKE THIS DRUG. I was a healthy 37 year old with not history of clotting disorders and now I have to have see a hematologist, pulmonologist and take Coumadin for the next 6-9 months. I never thought that a medicine could destroy me in as little of a time as 2 weeks. I thank God for getting me through it and am writing to warn any future users. Don't take this med.

I will be on prednisone for the rest of my life so my Pulmonologist says. I have an auto-immune disorder called allergic broncho pulmonary aspergillosis. I thought I was alone until I read all your messages when it comes to leg, and joint pain. My doctor acts as if I am crazy, and that it is not a side effect of the medication I am taking. It has gotten worse the longer I have been on the drug. I rarely sleep, and I have an appointment with him tomorrow. If anyone can suggest something that helped them I would love to hear it. I have tried everything, and the only relief is when I take pain medicine which I do not want to be on forever.

I was 54 at the time (2007) and in good physical health, however, after having my first round of chemotherapy as a result of breast cancer, I developed a severe throat yeast infection and my white blood count plummeted. I had ceased taking my many vitamins that have kept me in reasonably good health for the past 25 years because of nausea and generally just not feeling good. The doctors prescribed Levaquin.

Almost immediately, I developed heart palpitations and continued to have fever, nausea, and a rushing feeling throughout my body that was draining me of all energy. I could tell I was fading fast. Upon calling the doctors I said then that I thought it was the Levaquin but they insisted I stay on it otherwise they would put me in the hospital.

After the 4th day on it and with my blood pressure sinking (80/30) my husband called the doctor and they said to go to the ER. I again said to the ER doctor that I thought it was the Levaquin and he scoffed at that. After several hours and many tests, the ER doctor released me and said I could stop taking the Levaquin and he prescribed something to help me to sleep.

By the next day, I already started feeling better and within 3 days I was back taking my vitamins and feeling much better. I never took chemo again after this experience. Unfortunately since then, I have experienced severe ankle and leg cramps in the middle of the night, muscle spasms in my legs. I don't trust my ankles, they feel weak. I assumed it was linked to the chemo and never guessed it could be tied to Levaquin.

I went to my internist doctor who prescribed Flexeril which has helped with the cramps. My massage therapist has noted many times that my tendons and ligaments seem twisted and she has to really work on them which ultimately feels better. I never thought any of these symptoms were tied to Levaquin until last night when I saw the ad on TV regarding Levaquin and tendinitis. I will show this info to my Internist the next time I see him. How does one know if what I am experiencing is linked to Levaquin.

i posted on April 27th, on April 23rd, i stopped taking singulair, so i am here to UPDATE. after i stopped taking this death trap of a medicine, i already am seeing changes. i actually am breathing better then i have the whole time i was taking singulair, i can sleep through the night, and no HORRIBLE nightmares. jsut some normal ones, if any. but i feel like all the problems it has cause on my mental stability are still there, im guessing its going to get worse before it gets better with that. its really hard. now, me and my mom are starting to wonder if i ever had asthma in the first place, or if my dr. some how diagnosed me while i had a slight case of pneumonia. because the first time i was tested i was only breathing 60% of air, and even the nurses said i should be dead, or in an emergency room and she never not once, checked to see how my asthma was for 2 years. i honestly feel like i have been robbed of my life. its so hard to know something so little and simple, can have such a evil effect on you. because if i didn't have asthma i have been taking singulair for 2 years without needing it at all. imagine what that could have done. now im just so scared to sleep, because im scared i wont wake up. everything in my life is suffering and i don't feel like i have the strength to keep living the way ive been, im so scared every second, i am constantly checking my pulse, and now its even worse because i stopped the singulair. i already sent something to the FDA, and all that, but i doubt they'll listen. someone asked me a couple days ago "aren't you glad you at least found out your not alone" and i said "no, no one should ever have to go through what im going through, especially little kids". i feel like no one understands truly how hard this is, because its just an asthma medicine. this killed my mind, my spirit. and i don't know if ill ever be the same care-free person i once was. im constantly scared of everything, i always feel like no one wants to be around me, i just don't know. but not he positive side, im also not as weak, or tired during the day. i can actually bend down or reach up without feeling like a 98 year old women. my body is doing a lot better. its just my mind i really want back. i repost in a couple days, and hopefully everything will be a little better. PLEASE DO NOT TAKE SINGULAIR. i honestly think that, if it doesn't effect you at first it will in the long run. even if its 10 years later, you will start to slowly see something happening. just don't take it. i don't want anyone to feel, the way i do.

J.

Was prescribed Levaquin in November 2008 for suspected pneumonia, then 5 other times until last week. I've had really bad knee, thigh and arm and shoulder pain for the last 2 months. My legs get so weak and painful that getting out of a chair makes me want to cry, i've got to the stage that i need to hold on to something just to get on to my feet. My arms are rather weak, i can't even lift a small 10lb box without pains shooting down my arm. I've since stopped my last prescription of Levaquin 750mg daily for 7 days, the pain seems to have eased a little but not enough.

My pulmonologist keeps prescribing Levaquin each time i catch a cold or have shortness of breath. I was also taking 60mg of Prednisone from November 2008 until March for newly diagnosed Lung Disease. I've complained to him more than once about pain and weakness in my legs etc. He keeps telling me my muscles are deconditioned.

I've now started physical therapy and i'm doing aqua therapy, so we'll see if this works or not. Maybe it will also help my restless legs, which seems to have intensified this past few weeks.

Lumps under the skin all over my body and severe pain that feels like it is under my skin--like I've been skinned and the skin just laid back down raw and bruised feeling. I have to take time-released morphine for this pain and no doctor can explain the lumps other than to say it might be a side effect of the prednisone. I have never heard of anyone else having these lumps and skin pain, though. One post I read said their tongue was sore, which mine also gets when I take it.

One thing I want to emphasize is that the last time I read the printout that comes with an unopened new bottle of prednisone and that the pharmacists don't give you unless you ask, it said that the newest research suggests that you take the prednisone only EVERY OTHER DAY. Some symptoms may become a bit worse on the day off, but unless you are dealing with a potentially lethal disease, this keeps your body on its regular rhythm of making its own form of prednisone and thus prevents many of the side effects. I have been back on prednisone for 3 months now with the new one day on, one day off schedule, prescribed by my pulmonologist, and have much less of the side effects--no ravenous appetite and thus no weight gain, no swelling, no "moon face" and my lungs are still functioning much much better.
Please ask your doc about this or get the info sheet from the pharmacist (it is the very long one on tissue paper, not the one-page info sheet they are now giving us with each Rx.)

I started taking prednisone along with Cytoxan, a chemotherapy drug 15 years ago when I was diagnosed with an undifferentiated connective tissue disorder that led to symptoms like idiopathic pulmonary fibrosis. After a couple of years, the inflammation cooled off and I no longer had increasing scar tissue in my lungs (IPF is almost always terminal) so I was glad of that. However, sometime in that first year or so I developed hardish lumps under my skin and severe pain that felt like it was "under my skin" but not my muscles, as in fibromyalgia. The lumps are even more painful, and the skin feels as if someone tried to "skin" me and then just llay the skin back down.
I have had to be on timed-release morphine for years in order to function with this pain, as it is especially painful if I brush up against something or sitting or lying down pressure is intense. Also the skin on my tongue gets so tender I have to use kids' toothpaste or it burns terribly.
After 15 years some of the lumps have gone away, but I've recently had to go back on the prednisone for my lung inflammation.
The last time I got a new prescription for prednisone I read the tissue-paper printout (not the short one you get with every Rx, the one written for professionals which includes all the new data, tests, side effects, etc.) What I want to point out, as I've not read one person saying this, is that to avoid a lot of the side effects and the harm to the glands which produce our own natural steroids, is that they are now recommending that it is taken only EVERY OTHER DAY. They say there may be some slight increase in symptoms on the "off" day, but that this keeps the natural cycle in place in bodies subjected to this drug and therefore reduces symptoms.
This is what my last pulmonologist prescribed for me and so far I have had minimal side effects--no ravenous appetite and weight gain, no "moon face" and it has still helped my symptoms.
Please ask your pharmacist for the flyer that comes with the new package and read this for yourself and then take it to your doctor. It may not work for those in dire need of the prednisone but could perhaps be tapered to this once the first lethal symptoms die down. ASK YOUR DOC--I cannot believe I have not heard more about this as it's right on the flyer--but docs are so busy, it's understandable. I'm grateful my doctor is up on the new research because I don't mind taking the prednisone this time, and I used to HATE it!
Good living to all and I wish you all the healthiest life possible.

I was on Nuvaring for 3 years. During those 3 years I developed the following symptoms that at the time I just blamed on old age, being in my upper 30's.

Asthma like symptoms--After my breathing problems got progressively worse over the last year on Nuvaring, I went to a pulmonologist. I'm a non-smoker that couldn't even walk up one flight of stairs without loosing my breath. I had tests, MRIs and CT Scans. They couldn't find anything that would cause my breathing problems. I tried Advair and inhalers. No medications helped. The Dr. decided to take me off Nuvaring just to see what would happen with my breathing. After quitting Nuvaring, my breathing is back to normal. I can exercise and walk up steps again without feeling like I'm fighting for air.

Arthitis like symptoms--pains in my hands, knees, waist. I never did go to the Dr. for these symptoms, simply because the symptoms went away after quitting Nuvaring. Some days I couldn't even sit still because of the hip/pelvis joint pain. I thought I had carpal tunnel because I couldn't even grasp a cup or throw a dart.

Hair loss--I had some thick hair before Nuvaring. The only thing I can blame my hair loss on is Nuvaring.

I've been off of Nuvaring for 15 months now. Yes, it's convenient and affordable. But you can't put a price on a healthy life!

I wrote a post few days ago about Singulair and how great my daughter is doing since she started to take this medication three months ago.
Then I started reading about all the side effects that other children had because of Singulair. I GOT SO SCARED!
So scared that last night I stopped giving Singulair to my daughter.

From January to September my daughter had asthma every other week. She was put on steroids (prednisolone) every time she couldn't breath. Then in September the pulmonologist said we have to take control of the situation because so much steroids can damage a little body.
She made me feel I had been a terrible mothers since I always refused to give her singulair.
She convinced me and then I started Singulair, but now I feel worst because I have the feeling I am giving poison to my daughter even if her asthma is under control.

My 7 years old stopped Singulair 12 hours ago, I do not know what is going to happen now. Of course I cannot call the pulmonologist anymore in case my ds gets bad.
Somebody here said that she is giving her son Nordic Naturals Fish Oil, Culturelle probiotics, vitamin c, and changing his diet - increased magnesium and decreased dairy.I will love to have more information about this alternative way of controlling asthma. I do not remember who wrote this post. If there is a web site of a doctor I can contact i will do right away. I live in New York.

I need help. Thank you so much.

Oh my gosh. I am on this website because I googled "behavior issues with Singulair" Both of my children are on Singulair. One from as young as 5 months old. Both Pulmonologist, allergist and Internal med Ped. insisted that it was a safe drug. They aren't living with it. My 7 year old has taken it consistently for 5 years and recently upped is having behavior, aggression, insomnia and constant reports back from the teacher on his behavior. We had him psychologically evaluated and they found nothing uncommon to his age. All his issues are described in almost everyone of these side effect threads. I am just afraid to take him off and feel the blame if something serious happens. I am calling tomorrow for possible alternatives.

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities.

Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

Started with a Pred pak for a sinus infection. Made my heart race and had tach and early heartbeat, which kept me from sleeping. Went to Cardiologist. Several doctors denied that the Pred would cause the rapid heartbeat. Then the Cardiologist did an echo and found a pericardial effusion and some weird spots on my lungs. They suspected lung cancer which may cause the effusion, so I had surgery to do a pericardial window and a lung biopsy. Then a pulmonologist decided to put me on Pred again...steady dosage...because she didn't know what else to do. (Didn't have lung cancer) I didn't have any more funny heartbeats, so maybe the pred didn't cause it after all. But I've gained 40 pounds. My hair has grown faster, and I've gotten some facial hair (not supposed to have that, being a female)...which I call fur. Moon face with cheeks that are hard, muscle cramps, can't sleep, but once I do go to sleep, I can't wake up. Tired all the time, headaches, joint pain-sometimes severe, dry skin, generally bad attitude, with very little patience, low potassium levels which add to my muscle cramping problems, difficulty swallowing, indigestion which I've never had, with painful and burning reflux. And occasionally when I eat, I have the rapid heartbeat again. I go in search of food like I'm going to store it in my thighs for winter. Anything you eat will turn to fat, including protein. Can't wait to get off this stuff which will take until June of next year. Then my doctor says it will be 3 months before all these effects wear off. No one told me I would get fur.

After reading all the side effects from Advair. I am glad I decided to wean myself off this horrible drug. My pulmonologist gave me a sample after I was diagnosed with asthma in March. Before I was diagnosed with asthma I had a severe bout of bronchitis followed by pneumonia. At first I felt much better using Advair, but then the horror kicked in. I experienced hoarseness and felt like I had an obstruction in my throat. I am not going into all of the side effects I experienced with this drug because it is a repeat of what people are saying on this website.

I stopped taking it two weeks ago. I am already noticing how much better I feel. The withdrawal has been difficult. I have no intention of taking this drug again. I plan on using alternative medicine in the future.

This drug must be taken off the market!!!!

I was started on Topamax late 2007 after a week long migraine that did not respond to my usual migraine medication, Relpax 40mg and Xanax 1mg and I needed the second dose 2 hours later. I was given samples of Topamax 25 mg with a schedule to slowly increase the dose. The first 3 days I noticed an improvement in my migraine. By the 4th day, I started coughing. As I increased the dosage of Topamax, my coughing got worse and more frequently. I had to return to the doctor a week later for the cough. I thought I had been exposed to bronchitis because I had worked in the church nursery.
However, the doctor heard a wheeze with my cough and stated I had asthma. This came as quite a surprise because I have never had any lung problems or asthma problems and I am 52 years old. I was referred to a pulmonologist who put me on 2 inhalers (one steroid, one rescue inhaler, nebulizer treatments, chest x-ray, Oxygen to be used a night.
I was still having severe coughing spells every time I moved or tried to talk. I would have to run to the bathroom every time I started to cough because the coughing was so violent that I experienced severe urinary incontinence every time I coughed. I checked the internet and with my pharmacist, both stated that developing a cough was very common with Topamax. After learning this, I slowly reduced the Topamax until I could stop using it. As I was reducing the Topamax, my cough started to decrease. When I mentioned to my doctor about my problems with Topamax, he stated that Topamax did not have any respiratory side effects. I had a brochure from his office for Topamax that stated Topamax should be used with caution with people with lung or asthma problems.
I am now taking 800mg of Magnesium, CoEnzyme 100mg, and Vitamin B 2 100mg twice a day as a preventative. These supplements were prescribed by my neurologist. Since starting these supplements, my number of migraines has decreased.
Kay/redpoppies

I was diagnosed with adult allergic asthma one year ago at 38 years old. I started having problems breathing ONLY AT NIGHT on occasion and palpitations. Had a physical and ekg, totally normal. Went to allergist and they said I have alot of allergies and diagnosed me with the asthma. Funny thing, weeks before I niked 20 miles, hiked 12 miles, canoed 3 miles, played golf in a 3 day span and no problems. Since they told me this and started me on advair I haven't been able to jog more than 2 miles or bike more than 8 to 10.

Its very strange indeed, I have gotten more paranoid feelings when just get a little out of breath, and sometimes cant keep still in a car or sitting down.

I cut back on sugar, sodium and started exercising a little every day, only 15 minutes. But came down with a cold recently and back to square one. I am trying to take the advair only ONCE a day instead of twice and almost feel withdrawal symptoms like shakiness, paranoia, irritability. Does anyone have any idea about this? I am really confused! Thanks... J

I have adult onset asthma that has gotten progressively worse since I moved from a small Midwestern town to a larger city in the Sonoran desert. On account of this progression in asthmatic symptoms and flair-ups, I switched from Flovent 220mcg to Advair 500/50 about a year ago. For a long time, Advair really seemed to be helping my asthma. Outside of gaining 10-15 pounds in this year (which I asked my pulmonologist about and was assured that inhaled steroids cannot be responsible for), I have fortunately not had many of the aforementioned side effects. However, in the past month after experiencing a bad flair up while studying abroad, I have developed severe heartburn, nausea, acid reflux, a sore throat, and mouth sores. I take the medicine as prescribed and am always sure to properly rinse out my mouth, having been warned about this. After reading everyone else's entries on this site, I am now curious if Advair is doing more harm that good.

Hello everyone. My name is Michael, and my experiences with Advair were so horrific, I thought I would post here as a both a cautionary to those who would use this product, and to validate those who thought "they were crazy" while using it.

I was diagnosed with "World Trade cough" as a result of my four month exposure from that disaster. It finally culminated in frequent walking pneumonias and a sinus-drip initiated cough, which is really part of a complicated process from GERD, also World Trade related. Finally, the pulmonologist diagnosed the obvious "RADS", Reactive Airway Disease.

I was prescribed Aidvair Diskus inhaler 500/250 twice a day, along with Nasonex and Nexium. The first two months seemed uneventful. As my cough cleared, I saw no reason to take the medication anymore and slowly titrated its discontinuation.

Then everything went awfully wrong and my nightmare started. First, panic and anxiety attacks, which I hadn't suffered since World Trade overtook me at different times of the day. Only the Toprol for my high blood pressure kept me under control and out of the E/R with uncontrollable tachycardia. Next, the Depression which also was overwhelming, and the compounded fears from physical symptoms. Then the "TRUSH" came in my mouth and a concomitant fungal infection in my groin. Swollen glands in my neck. Fever, fatigue, listlessness joined the symptoms.

Though a committed heterosexual, a bachelor party a month ago raised spectre's too awful to contemplate and I insisted on the most ultra-sensitive diagnostic blood tests to rule out dreaded disease ( I did responsibly use a condom ). The 24 hours from yesterday to today were like sitting on death row, awaiting an answer. ALL NEGATIVE, including Diabetes.

Then I saw this site and had to enroll to tell this story. All of it was here from the THRUSH, which scared me the most, to the Depression and anxiety attacks, which made my fears really get out of control. The Advair had nearly destroyed my immune system.

I am taking "CLORIMAZOLE" for the fungus, which is no bargain...liver toxicity and nausea. Still, far preferable to the feared diseases.

I learned that so-called "modern medicine" is little advanced from the witch doctor. If you read the Pharmacology inserts, half the time they don't even know why something works, and they can't isolate the good effect from the bad. Then, they assault your body with another extreme ( anti-fungal ) to combat what they caused from the first medicine.

My new girlfriend is Chinese. Next time I am sick, I am trying alternative medicine. In the meantime, for anyone prescribed or handed a sample by their doctor, AVOID THIS MEDICATION IF YOU CAN!

I'm 18 years old and I've been taking Advair (500) for about 4 years. I've had very persistant asthma my whole life and my Advair seems to save me from having to use my albuterol around 6 times a day. About 9 months ago i lost my voice for over 2 months. After that went away I had a break for about one month then around 6 months ago I developed what seems like a smokers cough yet I don't smoke. I just got a chest x-ray done and they said it was normal. They put me on steroids and antibiotics but it doesn't seem to be helping.

Could it be the Advair? I don't know that I can go without it even if it is. I want to get rid of this congestion in my lungs. I'm sick of coughing up mucus daily. Does anyone have any advice?

I am diagnosed with COPD. On March14, 2008, I visited my pulmonologist due to having a bacterial infection in the lungs and nose. I was given a script for Levaguin 750 mg for 7 days. After my first dose, my feet felt like they were on fire. I spoke with the pharmacist and he said it could be a side effect. I finished the meds with a lot of trepidation, feeling uneasy and anxious. However my large toes began to have a tingling sensation, which I reported to my PCP and he said to keep a check on it. I just came from my PCP today, July 8,2008 and now, in addition to my lung problem, I have peripheral neurophathy, involving all my toes and also my hands. This medicine is dangerous, as looking back at the time after I took this medicine, I was seriously considering ending it all! I will never take any medication in the future until I research it thoroughly. I trust my PCP and I trusted my pulmonologist, but I feel the pulmonologist should have informed me of the possible bad sich effects. Be careful out there!!!

You people are freaking me out. I just started today with my first dose of prednisone for my first bronchitis diagnosis. I've been sick for 3 months and thought this would be a good med for me to rid the coughing. I'm starting to reconsider taking any more if all I can expect is long term adverse effects. I took this once before years ago for a severe skin allergy. I got the psychosis initially but then adjusted the dose. Then, I would get euphoric and full of energy, like being on a stimulant. I had no idea the round face thing was due to this, I thought I just ate too much while I was home sick for 2 months. I think I'll try the herbal alternative route. If it works, I'll write again and let y'all know. Thanks for all the comments.

Please let me know if a class-action lawsuit is ever filed against this Pharm Co because I will file a suit to get this dangerous drug off the market. Yasmin/Yaz almost took my life in January 08. My OB/GYN put me on Yaz in Oct 07 for bad periods and cysts on my overies. Within a month my entire personality changed and I started losing my hair. I experienced a complete loss of sex drive, became depressed and was either constanting crying or raging at someone. However, my adult acne did clear up. On 1/27/08 I experienced extreme pain in my calf that moved up to my thigh within 48 hrs. I went to the ER and was told that no only did I a condition called DVT (Deep Vein Thrombisis-blood clot) in my leg but that the clot had broken off and moved into both of my lungs and I had bi-lateral pulmonary embolism. I can't even describe how incredibly painful this was. I was admitted into the hospital for 1 week and was put on powerful blood thinners, which I will be on for about a year. It's now been nearly 6 months since I was diagnosed and the DVT and it is still in my uppper thigh. But am grateful to be alive. If you would like to contact me I would be glad to answer any questions regarding this situation and my email addy is ****** PLEASE DO NOT TAKE YAZ OR YASMIN OR LET ANYONE IN YOUR FAMILY TAKE THIS MED, IT COULD KILL YOU.

I had used NR for six weeks when I woke up at 3 am with SEVERE chest pains. Went to the ER and was diagnosed with *substantial* pulmonary emboli (blood clots in the lungs). I was hospitalized for five days and am now under the direction of a pulmonologist and hematologist for the next six months while I'm on blood thinner therapy. I had to do injections into my abdomen twice a day to prevent further clotting until my blood reached a theraputic level with the Coumadin (blood thinning drug).

Usually, pulmonary embolism afflicts sedentary people or those who have recently had surgery or those who have cancer . .. etc etc etc. I am a 33 year old personal trainer. I have ZERO risk factors for this to have happened to me . .. other than the nuvaring. It was determined that it was the cause and I was told to remove it immediately and to never never never use it again.

Please be careful in your decisions to use this product. I used it for the convenience of not popping a pill daily as I would usually forget. Wish I would have just looked a bit further into the possible side effects before choosing to go ahead with it.

My son is almost 9, he has been on Singulair for 3 years. Last Friday the pulmonologist took him off of it. My son has been sleep walking since about the time he started singulair, have noticed major behavior changes. He gets very angry over nothing, he is extremely sensitive, he is not the happy little boy he once was. He has horrible dreams. Over time this has gotten progressively worse. I have to say that since last Friday when he was taken off the singulair, I have noticed a huge difference. My happy little boy is coming back! I told the Pulmonologist my concerns ans could this be side effects and he replied "YES", Also, he feels that my son has outgrown his asthma which is wonderful. I feel so horrible for all these children and families going through this. Parents, remember you are your child's best advocate. don't let the children suffer.

I have been on Effexor for at least 4 years and am now taking 225mg per day. I was not aware that it is addictive until checking on line. My doctor never told me and I wonder if he was aware. What should I expect when I begin to go off Effexor.
It seems that now when I don't have to go to work all I want to do is sleep. Yesterday I got up at 5 PM and had gone to bed at 10 PM. Although usually not for so long, I have been wanting to sleep my weekends away since he uped my dosage but didn't realize what was causing it.

Follow up to my post earlier today...

I took the my son to the doctor this morning and he was somewhat dismissive of the recent reports on Singulair...says he's had a lot of kids on the drug and never heard a peep about side effects until last week when the report on suicidal tendencies showed up. He did advise that when these kinds of behavior changes happen after a new drug is started he would recommend that we stop taking the drug no matter what it was, but I still felt uncomfortable with his response to us.

I felt like he was accusing me of making it up or only coming up with it because of recent news and message board posts. In fact, I made the appointment BEFORE I saw the posts. I was worried about his behavior BEFORE I saw the posts. It's just that seeing the stories from everyone else basically confirmed my suspicions that it might be the drug causing the problems.

I feel like I definitely wasted OVER AN HOUR waiting for a doctor to spend five minutes making me feel small.

Last night was the last time my son will take the drug, and I don't care what the doctors think of me.