Six years symptoms and conditions

ok, so I am 28yrs old just had my lap for endo on October 1 and my doctor has recommended lupron, and am going to be getting the med in a week to 2weeks,but after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do,and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? did any one have a baby after doing this. my bigs thing is being able to have a baby. Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

My doctor has upped me from 50 mg to 75 mg Toprol and i swear I am getting fatter by the day. Up until i was 55 i weighed 125 lbs now 5 years later i am 138 and cannot for the life of me shift it even 1 pound. Not only do i eat 6 to 9 fruits and vegetables a day, fish 4 times a week and chicken, no sugar in anything and do the 10,000 steps a day or treadmill. I probably eat and drink less and exercise more than i ever did and have never been so fat. Just out of interest I plugged in Toprol and found this site. I am going to go back to my doctor and ask her to change my medication.

My son was put onto 4mg Singulair when he was three years old. He is now six years old. For the past three years he has been a very quiet child, to the point that people commented on how shy and withdrawn he was. He never wanted to go anywhere or do anything. His favorite activity was lying on the couch watching tv. He was always thirsty, frequently went to the toilet,often complained of a sore stomach & had several bowel movements every day, did not sleep well at night, was often grumpy, could not concentrate for very long, was frequently ill with cold-like symptoms and did not really like you to touch/hug him. At the beginning of the year he was diagnosed by an occupational therapist as having low muscle tone. In March of this year, his pediatrician increased his singulair to 5mg. He began having terrible pains in his legs, to the point that he would cry and be unable to walk to the toilet at night. I took him to my GP who did every blood test under the sun and x rays of his pelvis and legs. He could find nothing wrong. The only thing that had changed was the increase in Singulair. I had a look on the internet and found this website. I immediately decreased his dose to 1/2 a tablet for a week and then 1/4 tablet for a week before taking him completely off it. Within a few days our whole family and his teacher and therapist noticed a huge change in his personality! He talks all the time now, he laughs a lot, he loves playing outside and has lots of energy. He teacher says he is much more receptive at school. His occupational therapist says his muscle tone has improved. He has not had one single leg pain since coming off the medication. He is sleeping well at night, his stomach is never sore and he has not been sick at all. Not even one little sniffle!! Best of all he is a normal, affectionate little boy. I feel very angry with the manufacturers of Singulair and with his pediatrician, it feels as though my son has lost three years of being a child. He felt terrible all the time and I had no idea! I have told everyone I know who has a child on singulair to look at the side effects.

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

im currently on my fourth month of treatment with lupron and would like to know if anyone that had fertility problems was able to conceive after a course of lupron...? im 32 and have 2 beautiful children, but would like one more before i undergo a hysterectomy...i have been diagnosed with endometriosis, adenomyosis and severe pelvic adhesion's. i was in so much pain that it was ruining my life...the lupron has been pretty great this time around...six years ago i did it without any add-back therapy, but this time im taking progesterone along with it and the side affects have been minimal...still have mood swings and a decreased sex drive, but no hot flashes or night sweats. its definitely worth the pain relief...for me anyways.

Hi everyone. So I got the Mirena two weeks ago. I did my research on the internet before getting this put in. I did see all the bad posts and I went in and talked to my doctor about it. She told me the hormone level that reaches your blood stream is so small that it cant have effects on you. She said she just wondered if the people posting on here just had other things going on or what not. She has also had the Mirena for six years and loves it.

On the other hand when I got it in I was on like day five of my period. It did pinch a little but wasn't overly painful. I did get cramps on the way home and I did take two ibuprofen before I went in. I would get sharp pains every once in a while too. Enough to where you stopped and said " ouch. " But I wasn't bleeding until like later on that day. I bled for a week and a half. I was bleeding to where I would soak two liners per day. It seemed like a lot of blood. Plus I felt like I was on my period the whole time.

My other side effect that I just cant handle at the moment are: my hair falling out. Im talking a ton of hair. I cant believe how much hair! ****** This is a picture right after I took a shower last night. That is from only one shower. Its falling out all the time. Its been doing it for about a week. But its every where!!

Since I got this in I have been tired. I notice a huge change with that. I just have been so sleepy. I was sleeping four hours at the most with my baby and I was doing so good not looking and being tired. Then he started sleeping 6 hours through the night.... and that made me have so much more sleep. I feel so much worse. I hate it!

Another effect: About 4 days after getting this in I just was mad. I told my husband I was just so mad that I couldn't stand it. Nothing happened to me.... but I was so pissed. I can tell I have changed. My moods have changed. Im being way more honest than I normally am. Little tiny things make me mad super fast and Im being mean. My husband even approached me last weekend and said that I have said a lot of mean things over the last two weeks. I can notice that Im different but didnt realize I was being mean. He can notice a huge change.

Just One More Effect: Sex drive is gone. I was talking to my husband the weekend before about my drive being very high... then BAM I got this thing in and its gone! The sex drive being gone, being mean, and careless is enough to ruin a marriage to me.

I just called to ask if I can get this thing out. I just cant do this anymore. I have to wait four more weeks before I can get it out. Plus I have to pay 150 bucks on top of the 385 to get it put in! I have read that some people tolerate this very well... and others just don't. I rarely have found someone that has been in the middle. Its one way or the other. Dont you notice that?!

Feel free to email me if you want to talk more. I honestly don't mind.
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Just shouting out... I LOVE the NuvaRing. Two years going and couldn't be happier. A good girl friend of mine has been using the ring for six years now and is still perfectly pleased. Endometriosis symptoms are lessened, hormonal balance is fine, cramps are lessened, and my once 7 day period has now gone to 3 days. To each their own, there is no perfect drug - but for me, this is about as close as it's going to get to perfection.

I have severe Fibromyalgia, as well as several spinal injuries. I have been taking Celebrex for six years now, and have experienced none of the problems described in the side-effects sheet provided with it from the pharmacy. It relieves my pain for several hours, and helps with the inflammation that keeps me from being a productive part of society. Without it I experience difficulty in doing even the simplest of tasks, because my pain level increases so drastically. My only complaint about this drug is that it is so expensive my welfare insurance constantly fights me on it; insisting I take generic forms of it which do not work as well, and DO cause me many side-effects that are not only unpleasant but are also unacceptable. While sympathetic to those who have experienced difficult side-effects, Celebrex has my vote; though I wish wholeheartedly someone would speak to them about the outrageous price tag they attach to it. I have worked in pharmacies, and know they more often than not charge $200 and upwards on many popular meds for which their cost is in the less than $20 range. Shame on them for this. And shame on the government for allowing them to do so. No wonder people are buying drugs outside the USA. But I digress. Celebrex is a very good and effective drug. I just wish I did not have so many problems keeping it in my medicine cabinet. Thank you for listening.

Reading this site shocks me I LOVE mirena! I've had it for about 6 years, on my 2nd one now, and absolutely NO side effects, lighter periods, no more acne, nothing.
I would even recommend it because you don't have to remember taking a pill everyday, and those bad heavy cramps and bleeding are GONE!

My son is 11 years old. He has been on Singulair for about six years. Ihave taken him to see a psychologist twice because of his terrible mood swings. He was diagnosed with depression last year. I am very concerned about this drug now. He has also suffered from migraines for two years. I also pulled him out of school and started homeschooling him because of the stress of school was causing three migraines a month. I also have a 19 year old boy who is not on singulair now. He took it for 8 years and was diagnosed with ADHD. He also went through depression as a child. I am making a appointment for my son to go back to his allergy doc tomorrow. Also I am not blaming my sons illness on singulair, but I am terrible concerned that it could have harmed my sons.

I had my mirena inserted in March of 2008, after talking to two different doctors and doing a lot of research about my options. I had been on the pill but was really irregular about taking it (which renders it almost worthless). Next I used Nuvaring--a GODSEND when I was in college! I never had to worry about timing and just sent for another three month supply through the mail. I decided to get Mirena when I knew my insurance would end when I graduated. I and 23, and have been in a monogamous relationship for six years which means my risk of contracting an STD which would lead to PID (which can be very very serious when you have an IUD, and the IUD makes it easier to develop PID) is low. My docs also told me the reason they usually only like to insert Mirena into women who have had children is these women's cervixes aren't as tight and closed as a woman, like myself, who has never had kids. This didn't effect insertion for me--it was a breeze after a few ibuprofen.

I've had my Mirena for over 8 months now, and after the first 3 months or so my cramps (which were in my lower back and were very sharp) and my bleeding (which lasted about a month) were gone. I had periods for a few more months..but I have been COMPLETELY period/cramps/bloating/mood swing free for the past 4 months. I'm very happy about Mirena! A little acne, but NOT a big deal. Please remember these posts are almost all by women who have had bad experiences...What about those of us who have had good experiences? Mirena, like any hormonal contraceptive, effects different women in different ways.

Hi, Ive had the Mirena for 2 weeks now and it has been TERRIBLE, I have had terrible sharp pains off and on... I have never had kids but is a contraction like the pain that I am feeling? My doctor suggested that I have it put it since I felt sick with the pill and specially if I am not ready to have a baby yet. I've been married six months now.... I don't know if this will go away and I don't know what to do, the only thing good about this is that my sex drive is much better, lol... but this is terrible what should I do? Should I have it taken out and will it hurt?

I have a pretty severe form of cystic acne which I had a 9-month treatment for when i was 16. It went away completely after a course of accutane up until about 5 months ago when i started smoking cigarettes for the first time. within a few days, i had full blown acne again around my mouth. i'm 23 and its been literally six years of perfect skin i didn't even have to think about. i didn't realize it was the smoking until a month and a half ago. so i stopped, and the acne cut down drastically but not completely, so i went to the dermatologist for medication.

i was given doxycycline, 100mg twice a day. ive been taking it for a month and my skin is back to perfect however I feel like i'm forever feverish, i get extremely nauseated if i don't even enough to eat when i take it, and i get insane hot flashes within 30 mins of taking it. i'm basically sweating nonstop all day long everyday. i want to stop taking it but i don't want the acne to return. i cut down to one pill a day and already see some acne returning. i'm so glad i found this site -- none of the side effects ive seen listed include hot flashes or constant sweating. i also have pretty intense lower back pains

I thought I was crazy until I found this site... I've been toying with the idea of taking the nuvaring out because I've been so ridiculously depressed lately, exhausted for no reason, and my sex drive is basically at zero. I had almost convinced myself that I'm just depressed but started thinking about the nuvaring. I've been on it for almost 2 years now, and had minor problems at first but then after I got used to it, it seemed fine. Lately, it's been getting worse. Before I lived with my boyfriend (and in the same city), I worked at a horrible job that made me miserable and depressed and gave me horrible headaches... I thought it was just that, my job. But it's not any better, except the headaches are somewhat better... but I'm more depressed than ever, my sex drive is worsening, I'm crabbier than ever, all I want to do is sleep but when I do sleep it's not good sleep, I have zero energy, I can't bring myself to do the smallest tasks, and I'm so insecure and scared that my bf doesn't love me anymore. I even think I've developed anxiety. Sex hurts almost worse every time, I get that burning thing other people have been discussing, and it burns after sex when I urinate. I asked my gyno about the pain during sex and she almost acted like I was crazy. I think I'm ready to take this thing out. Condoms, here I come again. There were positives to the ring, like a way lighter period, I only have one sort of heavy day, and the rest are super light, and my cramps are nothing compared to what I used to experience. But those positive things do not outweigh my other experiences. The point of going on BC is so you can have sex without getting pregnant... well having sex once a month because I feel bad that my boyfriend isn't getting any is so NOT worth the money I spend on this thing and so not worth the side effects. It's so weird that for almost a year though I was fine on it, it almost makes me think that they changed something about it. And it's weird that the doctors seem almost brainwashed. I'm not the only one who had the gyno acting like they were crazy. I'm hesitant to take it out now, I still have 2 1/2 weeks until I'm supposed to take it out, but I don't want to wait another 2 1/2 weeks if I could start feeling better by then if I took it out now.

Since my Mirena I have experienced extreme dry eyes. It is so bad that sometimes at night it feels like my eye lid is going to stick to my eye ball. I thought it was because I had lasik surgery, but that was six years before having the Mirena placed. I have been seeing an eye specialist and other doctors and no one can figure out the problem. My first guess was the Mirena because this problem didn't start until after the Mirena was placed. Now after reading other stories I'm really convinced.

I've been using the Nuvaring off and on for almost six years. I started using it after I had my son in 2002, and I never had any problems with it. I used it for a couple years, had to stop b/c of my insurance. I went back to it after the birth of my daughter, in early 2006. I started having a lot of problems around December, 2007, but I didn't even think that it could be because of the nuvaring, since I had been on it for so long already. I was having stomach problems, awful headaches, horrible anxiety, depression, mood swings, had no energy at all, horrible burning pain after sex. I started having spotting and periods that lasted for up to a month, and would pass huge blood clots. I talked to my obgyn in February and she told me to just switch my rings right away instead of keeping it out for a week for my period. That stopped the bleeding for about two months, then my period came back with a vengeance. I bled for over a month, stopped for a week, bled for a few more weeks. It was ridiculous. I've finally given up on the ring after yet another month-long period. I took it out a week ago and I have finally stopped bleeding. I've noticed a difference with other symptoms as well and I really hope my body gets back to normal soon. I found this site last week when I was trying to decide if I should stop using the ring or not and I couldn't believe how many women had the same symptoms that I've been having. I never realized that all of the problems that I've had were all due to my birth control. Now I'm stumped as to what birth control to try next. I've been reading up on them and they all seem to have horrible side effects like the ring. If anyone has any suggestions, please let me know!

I took Singulair for a little over a year. In that time I have quit my job of six years, dropped college classes that I was previously excited about, and generally didn't give a damn any more about anything. My dreams became dark and horribly violent nightmares leaving me shaken throughout the day. I couldn't concentrate and was thinking I should seek professional help. My wife was worried that it was her and I couldn't figure out what my problem was.

About 6 or 7 weeks ago I heard there had been links to mood swings and depression from taking Singulair and immediately stopped taking it. It sounds cloche but it was as if the clouds parted and the sun began to shine again. I have become much more like my old happy and motivated self. My wife has noticed a huge difference as well as my friends and former coworkers. I am still having a little bit of a hard time staying on task but each day gets better and better. I sleep much better and the nightmares have stopped.

I think I'd rather deal with the allergy symptoms rather than take the FDA sanctioned poisons put out by firms like Merck. Their practices are criminally negligent but nothing will probably come of it because the regulatory agencies are in their pockets. It's all about the bottom line profits--public health be damned.

I'm just heartbroken over this. My 6-year old identical twin boys have been on Singulair for 4 years to help control severe asthma. Looking back...I now realize there was a definite "personality" change in both of them after going on it. I've been living with it for 4 years now and have just "gotten used to it." Since October, one of my sons has experienced severe back pain, abdominal pain, fatigue, swollen lymph nodes (though I don't know if this is related), and sadness. I have put him through tests because I just knew something was wrong - he has had an MRI spine, CT chest, abdominal ultrasound, and lymph node biopsy (all negative). I am just crushed because I wonder if I have put him through these tests for absolutely NO reason. That all along, it has been the Singulair. My other son has had insane mood swings for the past 4 years and I had just chalked it up to his personality. He can be extremely mean to his brother and has indicated to me that sometimes he just doesn't "want to be."

The only positive thing out of this is that I learned how insightful my pediatrician is. He took both boys off the Singulair about 6-8 weeks ago. I have noticed a slight improvement in his symptoms, but they have not yet all gone away. I'm hoping there's not lasting damage...

I am a 35 yo male who has had asthma since I was about six years old. I have always used Albuterol/Proventil to deal with any immediate concerns. Additionally, I have used the combination of Pulmicort/Serevent as a long term medication. I felt like the initial effects of that combo were spectacular. At some point, though, the doctor moved me off of that combo to Advair, explaining to me that the latter was just a combination of Pulmicort and Serevent. To this day I don't know the validity of that.

I have used Advair off and on for several years and I've never felt like I've gotten the same results as the previously mentioned combo. In the last two or three years I feel like it's done nothing. Additionally, in the last two to two and a half years, I've developed a low-level wheeze that is with me all the time 24/7. My albuterol does nothing for it. And -- it feels like I have a lump or something in the back of my throat. Some kind of constant obstruction.

The current theory of my ENT (my asthma doctor is worthless on this matter) is that I may have acid reflux. So now I am taking Prilosec OTC to see if, after a month or so, the low-level wheeze disappears.

Has anyone else with a history of asthma developed a constant, low-level wheeze that is unaffected by short term inhalers?

I think all of you folks with side affects are are blaming your ills on Lipitor rather than putting the blame where it belongs: on your own mental health. I am a 65 YO male and I have been on Lipitor for more than six years now. I have no side affects, I work out four days per week with cardio and weights and feel that Lipitor should be added to the public water supply. My total cholesterol has gone from the high two hundreds to under one-forty on a single daily dose of 10mg. All of you hypochondriacs get a grip.

Recently took a twenty day run of 500 mg Levaquin for a cellulitis infection that popped up after a knee surgery. It seems that unlike most people I tolerate the drug pretty well. The only side effect I have noticed is a little muscle stiffness when I wake up which is quickly remedied through light stretching and a warm shower. After being put on this medication I looked up it's side effects and was frightened by how many people have had terrible and debilitating side effects. Next time I'll trust my doctor and not look them up. I think any lost sleep and nervousness can be attributed to worrying about side effects that never came up.

The more I use Alka-Seltzer it seems to have an addictive effect. I crave it.

If you want to see the story about the SINGULAIR AND SUICIDE click on on this page and the news affiliates have the video and the story.

I had been taking Lipitor for well over six years to help lower my Cholesterol count with no know side affects. A problem developed about two and a half years ago with nerve damage that gave me excruciating pain in my shoulder and arm. After an MRI and three cortisone shots I was referred to a neurologist for help. He had no idea what was causing the problem.

About six months after many doctors could do nothing for me, and referring me to a physical therapist, my wife showed me a story in a magazine, which I can no longer find, that talked about problems with Lipitor that had not been properly documented. The article talked about exactly the side effects I was having. The article said there was a problem with nerve damage. It had been well documented that some people had muscle problems, but it was not know there could also be a problem with nerve pain.

I contacted my doctor and stopped taking Lipitor. Two months later, the pain just disappeared. The very day the pain ceased, I had a visit from a good friend of mine who is a Radiologist and who had studied Lipitor because of a problem he was having.

He explained that Lipitor was doing the job it was supposed to do, namely keeping the liver from producing all fats. The problem I was having was that I had injured a nerve and Lipitor was keeping the liver from producing a particular fat needed to help heal that nerve. It seems that the myelin sheath around the nerve needs that fat to help the nerve heal itself, and Lipitor was preventing the production of that particular fat.

Once I quit taking Lipitor it took about two months for the healing fat production to do it's thing. Recovery of the nerves in that arm has been very slow, but they do seem to be healing now.

I thought this was such an important finding that I notified all the doctors I had seen about this problem. To my great surprise I heard from no one. Not even a thank you. I guess that since they didn't find the solution, they just were not interested.

I hope this discussion helps someone else. Thanks for listening.

February 18, 2008 9:46pm
Hi, I too just ran across your website. I had a doctor's appointment today to find out why I have numbness in the right leg, achiness in the joints, lower back pain, problems walking where sometimes I have to walk with a cane, restless leg syndrome, and terrible leg cramps. I am a 56 yr old female. I quit using Advair about one year ago after using it every fall, winter and early spring for about six years. While using it I too had heart palpitations that woke me up in the middle of the night. They disappeared after I stopped using it. But the joint pain and walking problems still persist. Does anyone know if they will disappear in time? The doctor is sending me for tests for Arthritis and Neuropathy.
-- By leegc