Inflammation symptoms and conditions

Where do I begin. I've been on prednisone for about 3 months now, and I feel like it has ruined my life. After having my son in February of this year I went for my 6 week check up and found out that I had high blood pressure and my kidney function was low. Before this I was pretty healthy. So, I was put on 30mg of prednisone in hopes that it would reduce or erase the inflammation. It reduced it for a while, then it went back up. While on the darn drug, Ive experienced moon face, weight gain, Im always hungry, acne, shortness of breath, and paining in my legs and back. The worse side effect has been the mood swings and anxiety, probably because it took something terrible happening to realize that they were really happening. My boyfriend told me that the drugs were making me act different, but I just thought he was picking on me as he did with my weight gain. Turns out, I have read everyone elses post and realized that many people experience what he says I've been going through. As a result of my mood swings and being so mean and demanding, my relationship may be over. I wish that he would understand that it's not me, it's the medication, but I can't convince him. Thats weird, especially since he pointed it out to me months ago. So now, I hate this drug. It's not making me better and it was a contributor in ruining my relationship. I want to just stop taking it, but Im scared I will get even sicker. There is no hope here.

Hi Everyone after reading all the posts and crazy medications everyone esp. kids and babies are taking I would suggest reading this book. It is called Healing the New Childlhood Epidemics and is quite interesting.
Written in 2007 by Kenneth Bock M.D. and Cameron Stauth it goes in depth the causes and healing of autism, ADHD, asthma and allergies. It is quite interesting as the causes of all four are similar and related. I am still reading it as my son just had ear tubes put in and always seems to be having sinus infections. Dr. Bock seems to have had amazing success by targeting detoxification, removing sources of inflammation, changing diet, etc. and transforming kids back into a healthier state. Hope it helps you.

I am 50, pretty healthy, but have had a new condition of inflamed and severely painful joints and muscles limiting activity. Doc put me on 60 mg prednisone for 3 days, then 40 mg 3 days and 20 mg 3 days. First day was ok. Since then I have been a raving lunatic! I read the post about the person chasing their cat around and had to laugh and relate. I flipped off the neighbors workers because they were backing up a truck and it was noisy! It is all I can do to keep myself in check. I have canceled/rescheduled all unnecessary appointments until next week when I am finished. I "sleep" about 3 hours a night. Last night I peed the bed. I eat constantly. I have to work and concentrate (teach college) and that is so hard. I imagine my students must think I am on meth. I can't take it any more. I have 1 day left and I am not going to take the last one. I hope that this regimen will have calmed down the inflammation and if it recurs I will seek alternatives. AM NEVER going back to prednisone unless it is life or death situation.
Good luck to all those out there who have to take it long-term. Bless your hearts.

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

I was on Yaz for two years before switching to Loestrin in July because of cost and because my Ob/Gyn gave me a discount card. I thought that Yaz was making me depressed. Well,I am still depressed and I have never had acne like I have now in my life. And its not premenstrual break out-its constant on my forehead and my back.
Worse, and most startling, is my inability to wear my contacts. It seems as though my blood vessels pop, my eyes get so inflamed and irritated. This concerns me most. I have been wearing glasses for weeks to allow the irritation to subside, and I fear that the inflammation was caused by the Loestrin, the only variable. What else is this pill doing to me, I wonder, after reading all of the other posts. I need to get off it, but switch to what???

Hello I am 40 yrs old and got a lung infection which cause swelling in my lungs so the put me on high doses of prednisone via IV for 21 days in the hospital. The drug saved my life and took it at the same time.

After I got out of hospital i was on 60 mg for 6 weeks the 30mg for 6 weeks then 20mg the 10mg. It has been a living HELL over the last 5 months or so.

I told my DR. i have very bad blurred vision and he said it because the med runs my sugar up but I check my sugar and limit my sugar and it around 100 all the time which is normal soits not sugar. Then he said well them you need to see an eye dr. cuz your eyes are going bad. I begged to differ with him and told him if there was something wrong w my eyes then why is is one day I see fine and the next day all blurred and then back to normal!? it this stupid steroid if you ask me plus on day my right eye is bad and next day my left uggh!

The WORST side effect it the brain fog as yall call it. OMG I feel like im loosing my mind and going crazy. The dr. says hes never heard of such with a wise remark and says you know where your at now right? I know where i am and what I say but I feel like its not really happening. Its like im dreaming it. I feel like Im trapped in my head and I lookout blurry eyes.

Before I was a very confident independent person but now I feel scared all the time i feel hopeless and ive went through 3 girl friends over the summer because of the extreme forward attitude the med gives me. I am not the same person I was. I some time just want to die. I'm extremely tire if i do any exercise at all.

Plus I have all the other typical side effect like the moon face and weight gain. I don't even look the same cuz my eyes have huge bags under them and a double chin I never had.

I feel for all of you because i know what your going through.
I saw one comforting post in here where someone said within 2 weeks of completely getting off the pred. he was his normal self.
I CAN TELL YOU HOW GLAD I WAS TO READ THAT!

Please if you have finished the med and have got back to normal don't forget about this post. Please let us know because we need any hope we can get to keep our chins up and not loose hope and go completely crazy or worse kill ourselves.

I have about 4 more months of this LIVING HELL and I will surely let you all know if it get better. If you have come off of it and are reading this PLEASE let us know if we get back normal at least w the brain fog. I can take all the side effect ok except for the crazy dream zone zombie feeling.

I WOULDN'T WISH THIS KINDA HELL ON THE DEVIL HIM SELF!!
Let's pray for each other that the Lord keep out minds strong until we get off the nightmare drug call Prednisone.

side effects:
brain fog, blurred vision, puffy eyes, depression, confusion, dizzy, moon face, buffalo neck hump neck, hopelessness

I am 45 years old. I have had Mirena out for 3 weeks now (had it in for 9 months). At removal I went right back on the BC pill so there was no break in hormone levels. I have never had problems with the pill. I know some of you cannot use them. But for those who say "I just can't remember to take it every day..." consider the alternative of getting this IUD or keeping it inside you. The side effects alone are not worth it. In 3 weeks time that horrible facial/body acne has cleared up, the bloating is gone and my jeans fit much better although I'm not sure I've actually lost weight. A lot of it was just inflammation. The emotional issues just seem to have "vanished". I feel happy again. Imagine that (sarcasm intended). Libido much much better, with no pain or cramping. I started my period for the first time just this week. I thought it would be the period from "hell", getting revenge on my body for not having one for so long. But so far it is fine, and I'm glad it's back to tell the truth! Instead of spotting all the time or who knows when, I'll go back to light periods 3 days a month. Again, it beats the alternative. And a trick to try for taking the pill: put the pack somewhere around your bathroom sink area (away from kids of course) and just take it every morning after you brush your teeth. I mean you never "forget" to brush your teeth in the morning, so take the pill right after you rinse! It never fails. Also, you can tell yourself that if you did have a serious medical condition that required daily medication, insulin, for example, you would be good to your body and make it a priority. As long as the pill doesn't give you any problems, it's 99.9% effective and makes your periods very short and light, but predictable and right on time. No awful surprise breakthrough bleeding. The reliability of it is great. You just have to TAKE it. I'm only writing about the pill because it is the only other option I've tried and it worked well for me. If it's only a matter of inconvenience, try the toothbrush trick. It really works! Hope this helps some of you who are looking for other alternatives. Good luck!!

well i had the mirena inserted 8 weeks after i had my 2nd baby,which was was may 14th 2009,i felt fine tell about 6 weeks ago,i started having pain in the center of my chest rite below my breasts,went to the doctor he said it was inflammation,he gave me naproxen,which didn't help at all,went back to the doctor,still couldn't find anything wrong,the pain has spread to the left side rite below my breasts,now im having anxiety attacks every day,tired all the time,headaches,backaches,nausea,weight gain,hair loss,the doctor said i have bacteria vagionous,gave me flagyl ive been taking for 5 days now,i told my doctor at my last doctors visit i thought all this was from mirena and i wanted it removed,he told me to wait a few days to see if the flagyl worked,it hasn't so far,i have a doctors appt. tomorrow and im gona tell him to remove the mirena.i feel the mirena is causing all of this,i guess i will see.i just want to be myself again!

ive been on prednisone and cortisone..2 doses i woke up and couldn't move my legs at all. the more i walked the more it hurt..the more i sat the worse it was to stand up and walk..idk what to do..i have to take this for the rest of my life..its just terrible to move.and my doctor wont be around for 3 days.

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

I used prednisone for sinus inflammation and it gave me bad side effects such as: irregular heartbeat and stomach upset and anxiety. It actually did help with the inflammation but I stopped using it because of the side effects. It made my lip puff out too, which i did not mind because i have small lips and i looked better with a bigger lip, lol! I am thin so if it made me swollen i did not care because i need to gain weight, i am only 105 lbs. I just started taking methylprednisolone tablets packet and they seem to work better and if it causes increased appetite that would be good for me because i lost so much weight because of my teeth and sinus pain i had everyday for four months. So far it is working but i just started it and will keep you posted. It does seem milder than plain prednisone I suggest you switch to this if the prednisone is not working for you. It sounds like most people are on too high of a dosage and take with food and a lot of water. Hope everyone feels better soon.

hair loss after prednisone?

i took 60 mg of prednisone for 1 month for a kidney inflammation. i tapered down for months and finally have been off it completely for a few weeks. i did lots of natural things and really had no side effects- my face did get puffy when i was tapering, at about 30 mg but that's gone now. and my lip hair came in fuller but it's pale blonde so it wasn't too much of a bother

however, suddenly my hair is falling out like crazy. i took advair for many years (only 1/2 dose) and didn't connect it with my hair thinning until i started reading this site. i weaned myself off advair and noticed soon after that my hair loss in the shower was minimal

then i went on the prednisone and i was still fine. has anyone noticed hair loss after stopping prednisone? will this stop after a while?

I have been reading all of your Simvastatin experiences with high interest and would like to share my adventures with all of you as well. My story began seven years ago when I was relatively healthy and enjoying life. My doctor prescribed Lipitor for my elevated cholesterol and two months later I found myself in the emergency room after having a severe bout with vertigo for the first time in my life. I have since spent the last seven years fighting this debilitating illness which continues to haunt me after having seen every top neurologist in my area and having taken every neurological test available. It would be as difficult to convince me that I was not somehow "poisoned" by Lipitor as it was for me to convince my doctor.

I was eventually prescribed Simvastatin 40MG and seemed to stabilize for a few years even though my dizziness problems persisted. Suddenly I began experiencing bouts of upset stomach and severe lower abdominal pain. I allowed my doctor to order basically every nasty test known to man in an effort to discover the cause of this new problem, but all have come up negative so far. Eventually I began to experience total exhaustion in the middle of my work day, not to mention the back, neck, and muscle pain that has been described so vividly in this forum. Basically, I have become a 53 year old man who feels much older, has absolutely no energy, and rarely has a day when I can honestly say I feel alive and well.

I am not a doctor and I can't honestly prove that Simvastatin is the cause of all of my problems. However, I do have common sense and after reading all of your thoughtful comments on the subject I would be foolish to at least not suspect that the drug may possibly be making me less healthy and not more healthy. Thank you all for opening my mind to this possibility and I certainly plan on discussing this with my doctor very soon, who may no longer by my doctor should he continue to insist that I take this nasty drug.

Hi All, we definitely need a lawsuit. I am finally my old self again after 2 years of hell. My nose shut down after moving into my new house 2 years ago. Went to a local clinic here. My Dr. gave me the Kenalog shot for "inflammation", she did not tell that it was a steroid. I am allergic to steroids. I was suicidal, depressed, had a breakdown, lost 10 lbs. in one week from not eating. Menstrual cycle went from 3 days for 35+# years to every other week for 7 days. OMG, I went thru 2 years of sheer hell. Finally had to have a partial hysterectomy this past May I AM SO ME AGAIN! WE NEED A LAWSUIT against Bristol Meyers. Thank God my husband was beside me, or we would have divorced. Poor Guy.

I have had life-threatening spasmodic breathing episodes for the last year. My GP attributed it to asthma, because that's what it looked like, and they have given me prednisone shots and later on, antibiotic shots, to control it (for about 6 weeks at a time). I have well-controlled type II diabetes, so predisone can cause it to go out of control fairly quickly. Prednisone also caused some occasional pain in my feet, probably because of the elevated blood sugar. All the asthma drugs they gave me actually made me sicker, like Advair, etc. Lo and behold, I was able to talk my doctor into a referral to an allergist, and my allergy numbers are off the charts! All grasses, most trees, and many animals were high enough to cause anaphylaxis, especially when surrounded by more than one. Anaphylaxis can cause the labored breathing I suffered. Meanwhile, I have the lung capacity of an Olympic swimmer. I have an elderly friend who has gone to the hospital several times this year with the same problem. After I found out my results, I talked to his wife, and they discussed the allergy and infection aspect with the doctor. Turns out he had fairly severe allergies and infections that made his life-long asthma go way out of control. With a medicine for infection, he is 10 times better - the asthma is under control because it is not being jump-started by the low-level infections he suffered. I don't even have asthma, it just looks like asthma. I will begin years of allergy shots, just like in my 20's. (I am 55). The upshoot? Some people are suffering severe asthma symptoms. Others have a combo of problems which are exacerbating the asthma-like problems. Doctors who think you only have asthma tend to only treat asthma. Prednisone greatly reduces inflammation, which is a common factor in all the above diseases. So, calming the symptom doesn't mean treating the source. You long-term asthmatics should also look inot taking allergy tests if it is considered safe (they DO inject a small amount of allergens in your skin), and not spend 100% of your time with the pulmonary specialist who is only looking at your lungs. Also, you really need to do some cause and effect testing with antibiotics or similar to see if you have some type of infection. My friend and I are both on our way to better health because we went beyond treating the symptoms.

I was given this shot by an idiot of a Dr who told me that it was "for inflammation". He never told me it was a steroid and even though I asked repeatedly about side effects, I was brushed off with "if you don't have a reaction within 15 minutes, I would not have any". I wish I had trusted my gut instinct and never let him do it. I have only been on it a week so it hasn't dented YET, but I have mood swings, irritability, insomnia, jitteriness, dry mouth, racing heartbeat, and though I am eating only 1200 calories a day, I am already gaining weight. Does anybody know if there is a way to get this out of your system faster? I had a hysterectomy so I do not have the bleeding issues.

I am 29 years old and started taking Yasmin in January 2009....by month 2 I had severe pain in the nail bed of both hands....I kept hoping it would just go away...then 2 weeks later both hands hurt not just the nails...I started having to take advil just to get through the day...I figured it was the side effects of Yasmin b/c it was the only change in my lifestyle...I kept taking it thinking perhaps it was just my body trying to adjust....a couple weeks later my arms started to hurt....long story short, I stopped taking the pill in June 2009 and had to fly to my mother's house for help b/c I had gotten to the point that I was barely mobile and everything hurt...I felt like I was in an 80 year old's body....I had severe joint and muscle pains everywhere and I starting looking like Professor Klump, my hands and feet where so swollen I couldn't do anything (even picking up a pillow to make the bed hurt)...I asked my doctor if it could be the Yaz and he insisted no....I was told that it looks like I have arthritis...but I stuck to my guns and said that it was way too much of a coincidence that my health started deteriorating around the start of Yasmin.....my doctor decided that he could help me detox my body to get rid of any Yaz left in there and to see how I felt after....he did put me on celebrex (arthritis med) to relieve the inflammation and pain...I am also taking a diuretic to flush out my system...I am on day 2 and already feel better...I'm not sure if it's b/c of the celebrex or the detox, but I will know in 2 weeks when I finish all the meds.....after reading all these stories I feel a bit of relief...I'm not crazy, these symptoms really could be b/c of the Yaz!!

I began taking omeprazole in early june for burning in my stomach for gerd. I started with 20mg twice a day. I felt extremely bloated. I couldn't eat, or lay down. I had to sleep sitting up, and even that didn't work. I was regurgitating the little food I ate. I told my doctor, and he told me to go down to just one pill a day. The bloating went down for about four days, and then came back. I am not on this drug anymore... it has been two weeks. I had an endoscopy yesterday, and I was told that there was a bit of inflammation in my lower esophogus, and stomach (no bleeding). Well the burning pain is gone, but now I am dealing with indigestion. I get a full stomach after only a few bites of food. I am only able to eat one meal a day. I can't drink much water because of the full feeling I have all day. I am very frustrated since I can barely eat (I feel dizzy as a result). I think this drug has thrown my digestive system off balance as I did not have these symptoms before the drug. I understand that this drug changes the ph of the stomach acid as well as lessening the production of it. Because of this, it can potentially bring a bacterial infection, and digestive enzymes cannot help digest food under these conditions. Gastritis can come about from the bacteria, and if I am lucky and do not have this, well I may have indigestion due to lack of certain enzymes. I am trying to get to the bottom of this. I bought digestive enzymes to take, but I want to get a blood test first to check to see if I am lacking this. Is anyone having the same symptoms as me? I will update.

I have 21 years of age and my experience with the drug Kaopectate was appalling, I had a strong Diarrhea for two days and usually fix the problem with Pepto-Bismol but this time it does not work without result so I decided to try for first time Kaopectate and with a single dose caused me a problem of constipation strong after three days without going to the bath or a night awoke feeling that my stomach would explode, difficulty breathing, nausea and pain three months I have this problem I have spent thousands dollars and all this time has been a nightmare I could not eat or even drink water, I could stomach inflammation causing pain and nausea my normal weight was 140 pounds and lost 15 pounds in three weeks, now slowly improving and I am Kaopectate opinion is a very strong medicine and I think that is a danger that is available without prescription.

I had the Mirena inserted almost 2 years ago. Over the past 6 months, I have had horrible joint pain and swelling in my ankles, knees and hands. I have not been able to wear a wedding ring in 4 months. I hurt so bad that I can't sleep and recently I have felt that my fingers, toes and palms of my hands are cramping. My calves get so swollen, they shine and no one knows why. I have had MRI's, X-rays, innumerable blood tests, nerve conductions and a bone scan. Other than the bone scan showing inflammation, EVERY test is normal.
Because of these increasingly debilitating symptoms, I started wondering if they were related to the Mirena. That is how I found this website.
I had the Mirena removed yesterday and I think I may see some decrease in swelling today. Even though I still hurt, I am not cramped.
I see that many people experience swollen joints, has any one had their fingers swell. My swelling never goes down, I have it 24/7. If so, can anyone share there experience after having the Mirena removed. Did your joint pain and swelling go away?

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

Hi everyone,

I decided to go online to look for Mirena side effects because I have been having a lot of problems every since I got mine. I felt so relieved when I found this website because I realized I wasn't alone. I've had my Mirena for 3 and half years, and I have experienced almost every single side effect that the other girls on here have. I didn't have any of these symptoms before getting Mirena. After my first child I didn't have any side effects but after my second child I got mirena and this is what happened.

My hair up front on top has gotten very thin and I have always had very thick hair. I have always been a very laid back, friendly, happy person but since I've had the Mirena I've been moody, irritable, depressed, and I have had anxiety attacks. It also seems like I have a harder time feeling satisfied or happy about anything. I've had migraine headaches and joint pain which I never had before.

I'm 5'11 and I had always been extremely thin. I didn't have any problems losing weight after my first child, but since I have gotten Mirena I have gained a lot of weight in my stomach area but nowhere else. It's almost like a swelling or inflammation that won't go down. I've also had the strange feelings in my abdomen of movement that the others had, but I know I'm not pregnant. I've had these feelings for almost 2 years now.

It hurts really bad sometimes when my husband and I have sex, especially if he hits the spot where the Mirena is. My sex drive is completely gone, which seems like a common problem among the others here. I also noticed that fishy smell that the others have talked about that won't go away no matter what products you use or how much you wash. I also have gotten acne on my body which I had never had before in my life. I have some on my arms, face, chest, and back. It's terrible. I also have had the lack of energy so many of you said you had.

Even though there are all these terrible side effects, I think the worst one is that I don't feel like myself anymore. My husband says I don't seem to get excited about anything, and I seem more withdrawn. I have much more social anxiety than I did before, and sometimes I feel like my heart is racing and I can't get it to stop. I would have it taken out right now if i had the money to get my tubes tied. Unfortunately I don't have health insurance so I'm trapped for now.

Three and a half years ago i suffered a heart attack, i had three stents put in and was put on Aspirin 75mg, Cardicor, 1.25mg, Tritace 5mg and Lipitor 80mg. I was fairly fit at the time, didn't drink or smoke and ate properly.

But now i'm suffering, i've been to the hospital and my GP, but are told there is nothing wrong, my hear tis good. So why am i suffering with light headedness, pains through my body, back, neck, chest, stomach. So much so i thought i had gall stones or kidney stones. My right knee can't be touched, it is so sore. Chest heaviness, eyesight getting worse, slurred speech, depression i could go on.

I've said this to my doctor, he just brushes it off and says i'm on them for life, ....apparently standard treatment for anyone who's had a heart attack. I walk 5 miles a day, eat 5 or more fruit and veg, don't smoke or drink, do all what i'm meant to. My cholesterol is really low, but so is the HDL too. I was never recommended CoQ10 or a vitamin B complex.

It was my mother who told me to research the side effects of all the meds i'm on. I agree, we all want to live a long and healthy life, but at what cost. I am now of the opinion that doctor's are so use to thinking they are near god like, they have forgotten that we are individuals, that we know our own bodies. I'm sick of the fact that the large pharmaceutical companies send out there sales reps to doctor's surgeries and that is what is deciding what the patients end up taking and not the patient's problem.

DOCTOR'S WAKE UP TREAT THE CAUSE NOT THE SYMPTOMS!!!!!!!

May 25th, 2009
11:20 A.M.

Started Singulair 5/14/09. Within last week or so started having extreme pain in shoulders, hands (especially thumbs), wrists and hips. Put ti down to arthritis. Pain has been getting worse every day. Thought it was a food allergy so stopped eating fruit and have cut out all sugar. Yesterday realized that pain has increased so it wasn't the food. It suddenly dawned on me that it could be the Singulair. Stopped taking it last night and am already much better. Still some pain but not so excruciating.

About a month before my Dr. gave me Advair. After a few days on it, I went to bed and thought I was having a heart attack. Pain across my back and down my arms, up my neck and across my chest. This happened 2 nights in a row and decided to stop taking it. Called my MD and he said to stop it immediately. However, he thought it really might be my heart so I had an echo cardiogram and stress test. They said my heart was perfect. After 2 days off the med had no more trouble..

My take is that these "air" drugs are not for me. My MD is on vacation and won't be back until Wed. I will speak with him then. Hopefully by then all paij will be gone. Will post again to report results of stopping Singulair. Reading all these posts also made me realize my depression, irritability and crying has probably been a result of this drug.

By: Fed Up

my boyfriend has been on prednisone for 4 years and he is terribly snappy and aggravated all the time and short tempered and does not think that he is... i love him so i deal with it but its getting harder because he dosnt feel this is correct every time i ask him something he bites my head off and almost everything i do irritates him gets on his nerves the mood swings are out of this world sometimes and he totally thinks im being a lala in his words...will someone respond to this so i can show him and he will know im not just saying these things
all this