Misery symptoms and conditions

I just happened to do some research about lisinopril, and happened to stumble into this website. I am 43 years old, newly diagnosed with type 2 diabetics, i also have a history of hypertension and migraine which is under control. my physician just switch my medication from Norvasc to lisinopril, Im already on my 3rd week of taking it, 20mg a day, however, i noticed that i have more frequent headaches, more of a migraine headache that pulsate in one side of my head, i tried taking some over the counter medicine, but with no relief, i went back to see my doctor, and i was given some sumatriptan for the migraine, but at the back of my mind, i already suspected that the lisinopril might have triggered my migraine headaches, i have a relief when i take the sumatriptan, however the migraines keeps coming back. and its been seven days already, i was not able to work one day, because the migraine made me nauseated and vomit. i was doing well with my other medication, and never had migraine like this that last for 7 days up to now.after reading the comments. i have second thought of taking this medication.it seem like it might be the one that triggers my migraine headache. what do you think?

I took lisinopril for 2 months and throughout experienced dizziness and dray cough. Towards the end of the two months I noticed a small itchy rash on my neck. Then I had mirena IUD inserted, immediately my whole body including the head was covered by an itchy rash, have bumps all over my body. Doctor immediately removed the IUD, stopped lisinopril (I was telling her to stop lisinopril before - did not help), and i am still suffering. My fingers are swollen so difficult to type. I am 48 years old and my bp is back. i am taking HCL (water pill for BP) Monday going to see an allergist/immunologist. I am positive the lisinopril and mirena caused these symptoms. I was told it will take a while for this to go off. I had mirena for 7 days and see what a mess. both drugs have given this together. Until then absolute misery!

in 2006 i was attacked and bitten by a dog , the wounds became infected and was prescribed levaquin for the infection, about the 8th day of taking it i noticed bad joint pain, insomnia, anxiety, ringing of ears,and more symptoms, i was in good health before this, and have been in misery every day all day ever since!!!!
i have been told by my dr that i have fibromyalgia. if anyone has a doctor that will verify that the levaquin , and the trauma from the dog bite caused the fibromyalgia, please contact me , thanks

I recently began giving my 11 yo lactaid (store brand) because we noticed he had a problem with gas and diarrhea after eating dairy. Tonight he had 2 tablets with dinner and about 2 hours later complained of his stomach hurting. He sat in misery for about another hour and a half until he finally vomited. He also had diarrhea. He seems fine otherwise (no fever, doesn't feel "sick") and after reading all of these stories after doing a search I'm thinking that this must be what it is. I feel terrible as a mom giving it to my child and making him feel so horrible!

I began getting debilitating headaches 3 years ago. They were everyday and not the classic headache (no visual, nausea etc). It felt like a jackhammer to the back of my head every single day. My neurologist told me they were migraines. I was skeptical as every other migraine med had not worked. I began on Topamax at 25 mg twice daily. I started at this dose for a month. The body really needs to adjust SLOWLY to this med. My side effects were pins and needles in the hands and feet, strange taste in foods, flat tasting sodas, drastic cut in appetite. My doctor assured me these would go away. Headaches did not start to improve until the second month when I went up to 50mg twice daily. By the third month I was up to 100mg twice daily and I feel like I have my life back. I still will have occasional migraine breakthroughs, but nothing like the misery I had before. Within 5 months or so, food began to taste normal again and the pins and needles stopped. I dropped 30 pounds total on Topamax. It has been a life saver for me!! My advice for anyone thinking about this drug is to ease your way up slowly until your body adjusts. One week on a dose is not enough time.

I am a 46 y.o male who started taking Simvastatin almost 8 months. At first I had no problems. I am an avid swimmer who swims laps at least 3x a week and had a weight lifting program (light wghts./ numerous repetitions. About 2 months ago I got severe pains in my neck and shoulder. I thought maybe I was overdoing it so I ceased workouts and went to the chiropractor. After two months of misery and missing swimming I decided to look into the statins. I am going off it tomorrow and will see if that does the trick. If I cannot exercise and be fit the Statin is not going to be useful anyway. I have a feeling stopping will help because rest and treatment sure didn't. I will try and report back

I had Mirena inserted in Nov '08. I bled constantly for 6 weeks after and then nothing. I only have occasional spotting. At first I thought this was great - no period! (woohoo!!) but now I actually miss my period. It's not natural not to have a period! I've been experiencing a lot of side affects that I was attributing to turning 40 but after reading the symptoms others have been experiencing, maybe it's not due to my age. I've had problems with large ovarian cysts. I constantly have pain in my ovaries which I'm thinking it must be more cysts. I've gained weight and can't loose it no matter how hard I try. I have no energy and no interest in a lot of things I used to love to do. I have pain in my knees, pain in the joints of my fingers as well as mood swings, depression, anxiety, memory loss. I recently went to the doctors because I felt I had a constant lump in my throat - I went for an ultrasound and found I have multiple cysts on my thyroid. I'm not sure if this is all related to the Mirena, but I don't remember feeling this crappy before I had it. I'd like to have it removed immediately but I can't get an appt' with the GYN until September!

I know this is long, but I could really use your help, so I would appreciate you taking the time to read through to the end. (thanks :-) )

First, I want to thank everyone posting. I needed to read this stuff because I'm absolutely terrified of what's happening to me. I'm on the second week of my very first pack of Loestrin- my very first birth control pill EVER. I didn't want to start, but my OBGYN encouraged me to, once I told her I had 8 day long episodes of clots, cramping, vomiting and just sheer misery once a month. She said this would help if I'm sure to take it as recommended.

So I took the first one the Sunday after my period started, at 8:45am and have taken it religiously since. I have not changed my diet or routine. I exercise and eat fairly well. And there are no particularly stressful factors in my life. I am also quitting smoking- just down to 2-3 a day instead of 10 or 15.

Now that I've been doing this for 2 weeks, I think I would rather suffer what I had before. At least it was predictable! I have been bleeding for 5 days now. And this is NOT my time to be on my period. I'm sad and tired. I have back pain and on-and-off cramps. I have nearly no sex-drive. My boyfriend and I had sex at least 4 times a week and I masturbated on the nights we didn't. And although he is INCREDIBLY supportive, I can tell he feels lost and helpless around me. I don't want him to touch me, hold me, or even breathe on me! Normally, we are very affectionate and I am active and fun. Now, I just want to be left alone. I feel fat, unwanted, dirty, depressed...the list goes on.

I feel as though there is something seriously wrong with my body, because I shouldn't look or the feel the way I do or bleed like I am. I called the doctor and she said that I should give it till the end of the month. But 1 month is a long time to live with a depressed quality of life. 1 month is a long time to cry yourself to sleep with alcohol and Motrin.

I feel angry that the best the medical society can do is give us something that is trial and error, fully aware that it may hurt us, though temporarily, and make the lives of the people around us miserable. I am concerned the even my doc is in the pocket of some pharmaceutical company to give me a drug that she said would help and has only hurt.

Or maybe I'm just paranoid...

Anyone have any encouraging reasons why I should continue this? My sister, who was on Ortho for a while and DIDN'T like it, suggests that I stick out a little longer and I trust her opinion, but would like more. I'm open to suggestions or comments. (Especially if you know a way to stop my period so I spend less days of the month on it than I am on...)
Thanks :-)

We put our 3 year old son on Singulair 2 weeks ago for allergies. It seemed to be helping him. He is a very mild mannered kid that has never been an aggressive child and never bites or hits. In the last 4 days his mood has changed, and he has bitten 2 kids at school, hit one kid, bit and hit his grandpa, has been waking up with nightmares and has been very clingy to me (his mom). After reading the side effects of Singulair last night we contacted the pharmacist and told him what has happened and he told us to take him off the Singulair immediately and contact our Pediatrician. I am waiting for a phone call back now. I am saddened that a medication for Allergies can cause such a personality change.

OMG!!!! I've suffered all these side effects and just didn't realize it was this damned pill. I even visited by OBGYN about the lack of lubrication and pain during intercourse and we have not been able to come up with an explanation until now. Even my eyes were affected and my optometrists could not explain the vast changes. lets not even talk about the depression, i made some one else's life a total misery with my emotional swings . OMG!!!!!!! I
ve been off it for a few months and i actually started having feelings again and my emotions have been so much more stable.........I'm forwarding this site to all my gfs ................

Depression is not the word ....if this stuff was biblical, it would be the devil.
i have never felt like life didn't matter, i have never felt like i wanted to give up, but over the last few days i have, and i know it is a direct result of doxycycline. I stopped taking yesterday (had for lyme dis).
sever headaches, nausea, chest pain, panic attacks, etc....

NO WONDER THIS IS A FREE PRESCRIPT....they get you on your second visit after your doc prescribes zoloft or something for you.

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

I'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.

I had mine taken out today for all of the same reasons. I've also had horrible headaches daily for at least two months. My headaches, nausea and depression have started getting worse every week. Fortunately, I only had Mirena three months before now when I started putting things together. I've never had a problem with birth control pills and I've taken all of them. I used to get heavy and long periods- it took a while to find one to regulate my period. I love, love, love my OB. He told me the same thing today he told me when I got Mirena- that it has less side effects than any birth control pills because the amount of hormones released is lower. Nonetheless, he did agree that it should come out to see if it has been the cause of all of my misery.

I hate to think about the women out there with Mirena who are feeling tired, sick, and depressed and don't know why. Honestly, I don't know how I put it together for myself because I thought, IUD- NO SIDE-EFFECTS, it's just a device right, thrown in with a tiny bit of hormones, but at first I thought maybe I wasn't taking good enough care of myself and that was why I felt so bad all the time. Then the headaches . . . I thought that was sinuses . . . had a CT scan, came back okay . . . thought it was migraines . . . went to the neurologist, had an eeg, treated for migraines . . . still having headaches with nausea.

I almost didn't realize how depressed I was until my husband said something to me. He told me, "you've been depressed for three months now". Eureka!! I got Mirena three months ago. Plus, I am always under the treatment of a psychiatrist who monitors my medicine and am currently taking high dosages of prozac and wellbutrin. I've always had depression/anxiety problems and actually had to continue taking my meds while pregnant, just at half dosage. I had NO problems with post-partum depression (which was very much planned between my psychiatrist and medications). If I were to have problems arise with depression I certainly think it would have been closer to post-partum. I really don't think that my meds just quit working either. I realized that nothing gets me excited. I exert all of my energy into being a decent human being by going to work, taking care of my child, and trying to keep a somewhat-neat house. There is never time, energy, or desire for anything else.

I'm anxious to see how the next couple of weeks go . . . keep posting your progress and I will do the same. I certainly hope my symptoms start to subside . . . if not, I'm in trouble because I know that something is wrong with my body!!

Also, a Naturopathic Doctor told me to take Evening Primrose and it should aid in getting my hormones back to a natural level more quickly.

After 2 years and 7 months, I had my Mirena removed on 5/4. I had it inserted 3 months after the birth of my first child in 2006. At the time, it seemed like my best option due to problems I’d had with the Pill. I was on the Pill for 6 years, the first year or 2 weren’t too bad, but things gradually got worse. Because it was so gradual, it took me years to realize the cause of my problems. My blood pressure slowly got higher, my heart would often race, and I had anxiety and mini-panic attacks to the point where I never wanted to go anywhere. (My heart rate got up to 160 while waiting for the Dr during an appointment and my blood pressure was up to ~145/99) I also started getting migraines that got more and more frequent. I had an EKG and stress test and everything came back normal. I stopped taking the Pill and within a couple months felt a million times better and my BP went back to normal. I had no idea how much it had affected me and it still makes me sick to think of the years I lost because I felt so awful. I didn’t take anything for 6 months before we started trying to get pregnant and they were the best months in a very long time.

After I got Mirena, I thought it was great. I bled for about 2 months, then never really had periods after that (just some occasionally spotting). Three months after it was inserted, I lost the final 10 pounds of baby weight just by dieting. If I was emotional or moody during the first year, I just thought it was my hormones after having a baby. Slowly over time, I began to get more and more irritable. Everything and anything would enrage me. Rage is the best word for it. It would take a split second for me to fly off the handle. Everything irritated me, particularly anything my husband did. The more it happened, the worse it got and I began to worry if I would eventually lose control completely. Meanwhile, I slowly lost my desire to do anything. I’ve never been a big housekeeper, but our house has become a wreck and I have to force myself to get things down when people are coming over. If it weren’t for family coming to visit frequently, we’d really be living in a mess. I just never feel like doing anything and I’ve lost my passion for everything.

I’ve always had bad skin and have taken everything made for acne, including Accutane. My skin was the best it’s ever been the weeks after my son was born. Over the past 2.5 years, it gotten worse and now it’s as bad as it’s ever been. As my 30th birthday approached, I began to wonder if I’d have zits when I’m 70, then began wondering if the IUD might be causing it.

Also in the past year, I have begun to struggle with my weight. It had slowly started to creep up even though my diet hadn’t really changed. The past 6 months have been the worst. I constantly have a desire to eat and crave anything sugary which I’m sure has contributed to my weight gain. I’ve tried dieting and exercising more than ever before and couldn’t lose anything. Then I gained 10 pounds in 2 weeks. If I diet and workout, my weight stays the same – if I eat normally, I gain weight, just as many others here have mentioned. I’d say 80-90% of my excess weight is on my stomach and I’ve been asked twice in the last 6 months by strangers about being pregnant. I now weigh what I did when I was 7-8 months pregnant (25lbs over my pre-preg weight) and I look 6-7 months preg.

All of these issues have gradually gotten worse over time, but significantly so in the past 6 months. My fits of rage began to scare me and I would feel like my head and/or chest were going to explode when I would yell. I started to realize from my previous experience with the Pill that my blood pressure was going up again. I had also begun to get migraines again which I hadn’t had since the Pill. Then I began to feel like I was living in a depression medicine commercial. I’ve never dealt with depression before even when my husband was gone for months at a time in the Navy. Yet all the sudden I felt like I could check off all the symptoms for depression. I started having irrational and scary thoughts that I had no control over and they would go as quickly as they came. I began to get frightened because I felt like I had no control over myself, my thoughts, or my emotions. For whatever reason, I decided to look up Mirena and depression and couldn’t believe what I found - pages and pages of people describing exactly how I felt with all the same symptoms. I had been contemplating it anyway, but I decided then that I was going to get it removed. I went to the doctor and my blood pressure was higher than I expected. She gave me BP meds and offered me meds for everything else. I got the impression that she probably thought I was blaming too much on the Mirena. I would have agreed if not for my experiences on the Pill. She had never removed one, so she referred me to an OB/GYN. They couldn’t see me for over a month and there was no way I could wait that long because I knew it would take a while for my body to get back to normal. Amazingly, I found someone who got me in 4 days later. I was so excited! As everyone says, it’s a lot easier coming out than going in – just a pinch that lasts a second. So far, I haven’t noticed a huge difference (it’s been about 3 days). I felt less bloated the second day, but it seems to have come back a little yesterday. I have been very thirsty since the evening after I got it removed and have been peeing as much as I did when I was pregnant. I slowly feel like my desire to constantly eat is going away and I am not craving sugar as much.

I also wanted to mention, I started the blood pressure meds the day after I got them. I will say that it has helped my irritability a little and I no longer feel like I’m going to explode when I get angry. Now that the IUD is gone, I’m sure it will go back to normal on its own in month or 2. It’s frustrating because I got Mirena because of my BP problems on the pill. I was under the impression that there wouldn’t be any side effects and now I’m back to where I was when I stopped the Pill. I lost several good years with my husband because of the Pill and now I’ve lost almost 3 more and the first 3 years of my son’s life because of this stupid IUD. If it weren’t for our son, I don’t know that our marriage would have survived the last 3 years. I just pray that I will get back to being me and will be able to be the mother that my son deserves.

A few other side effects I’ve noticed after reading all these posts that may also be related are greasy hair and skin, hair loss, facial hair, memory loss/lack of concentration, and the strange odors and various infections that others have mentioned. I used to not be able to wrap my fingers around my ponytail. Now I can almost wrap them around twice. Like most of the other side effects, I blamed it on aging, stress, etc. I’m interested to see if it starts coming back now.

I know this is a really long post, but I wanted to include as much info as possible in case it might help someone else. I probably would have gotten it out sooner, but I didn’t think there were any side effects. For now, I am not going to take anything. I want to know whether the side effects go away and not have to worry if something is caused by a new birth control. I may try something else in 6 months or so, but we’ll see. My husband doesn’t want me to take anything ever again, but I really don’t want to get pregnant. I don’t think I want any more kids, but I’m only 30 and not ready to do anything permanent yet. My new OB/GYN mentioned Implantation, which uses a different hormone, but I don’t have much faith that it won’t have the same effects. I will probably just try different pills and keep an eye on my blood pressure. I plan to post updates when I can to let you know if things get better. I hope that my story helps someone else.

I was on prednisone in 2005 first time ever. It completely ruined my life. I was before the prednisone (for just 10 days) a very calm happy person. After seven days I started having terrible mood swings, blurred and darkened vision, savage anxiety all the time, and the deepest depression i have ever known. I lost a business, a marriage, half my family, my sanity, composure, and ability to work. The doctor better hope to hell I never catch her out and about. Anyway after four years of pure hell I am finally able to work again and feel pretty normal most of the time. This drug does much more harm than good. I had a simple yet severe allergic reaction and was prescribed this terrible drug. Words cannot describe the personal hell I have been through. I think that most if not all doctors should be put out of their misery. I for one have started a movement to take out the doctors before they take us out. This is war and Im not going away that easy. If your life has been destroyed by prednisone do not do anything drastic. Just remember that just because your doctor poisoned you that it does not last forever. You will eventually feel better. It might be after your sanity has been tested to the limits and you lose everything you ever worked for but eventually you will come around. As for me I am starting my plan very soon. I absolutely believe that their is a movement in this country to take out or cripple as many trusting people as they can. The fda, cdc, ama, and others are evil.

My girlfriend has been taking Quasense for 6 weeks now. She went on it because her period was all whacked out. The first couple of days I noticed the Extreme Mood swings, and Severe Nausea in the morning. The Nausea went away after a week or so. She complained of being dizzy is uncomfortable with the acne she is getting and weight she has gained. She is getting depressed and feeling tired all the time. We are busy people always doing something, But she just doesn't have the energy anymore. As the weeks went by her moods are getting worse and she is having extreme stomach cramps and began spotting. Which shouldn't be happening for another two months. This Pill sucks. I'm tired of seeing her in so much discomfort.

I have been getting Kenalog injections on and off since I was a teenager. I am now 38 years old. I get these injections about once a year and depending on how bad my allergies get, sometimes twice a year. It is the ONLY MEDICATION that I have ever been able to take that has completely relieved my allergy symptoms. I to have got the "dents" into my skin at the injection sites, which over time have resolved on their own. My hips ache as well but fortunately only just sometimes. Exercise relieves the pain. I am a nurse and know full well the "adverse" side effects from this medication and am reminded by my physician every time I go for the injection. The misery of dealing with my seasonal allergies when nothing either prescription or over the counter helps makes me incredibly grateful for this medication. Everyone will react differently to every medication. People need to realize that it will not work for everyone and there are serious side effects. That is when YOU need to decide if the risks are worth the potential benefits. For me they are, every year I dread spring and summer and will dread it even more if the FDA pulls this drug.

Hi everyone, I have just read all thirty pages of posts to try to find some answers to my crazy reaction to prednisone. My thoughts are with you all since I have had an usually severe reaction to prednisone. I was on prednisone for 1 week in October 2008 at 60 mg/day for a sinus surgery. I am still having the following side effects at full force:

Axiety to the point I can't socialize
mood swings
hot/sweating even in freezing weather
whole body shakes
severe migraines
tooth sensitivity
muscle pains
extreme thirst (I drink almost 2 gallons/day)
hungry all the time
moon face
water retention around waist
acne
hair loss
rapid heart rate
dizziness
nightmares
night sweats
high blood pressure
high hear rate

I'm not exaggerating, my parent's can contend to that. I do have a history of having sever reactions to medication and I've had all the gland and blood tests which all check out. I never had a single one of these before the prednisone - I was a healthy 22 year old.

I was wondering if any could tell me when this hell will end - my job and well-being depends on it!

I have only been taking this pill for 6 weeks. I am 44 and was put on it to help with severe cramping (I would pray for death every month). I have not been on any type of birth control since I was 23. I also have never been pregnant (not by choice). I have read hundreds of reviews from users on different sites and do not see anyone having leg cramps (calves). They are so bad at times that they hurt the next day from cramping so bad the night before. I have called the nurse and am waiting for a call back. I also have noticed that I am way too emotional and it has only been 6 weeks. I'm just not sure I can wait out 6 more weeks. Every night just about now I seem to be sick to my stomach or have diarrhea. I have always had headaches so I can't contribute Loestrin 24 to that. I have gained about 5 pounds...which I certainly don't need. Like I said in the beginning, my most severe side effect is the leg cramping. I wish they would just do the hysterectomy and put me out of my misery!

I received my first shot on Kenalog three weeks ago, for a bulging disc in L5, and it took me from a 8 out of 10 pain scale, to a 2. After two weeks , I received my second shot, and now I feel about 98% better. As an added bonus, my Psoriasis of 15 years, that no Doctor could seem to control, has all but disappeared! Also a severe pain in my r/foot under 2nd tow area, has completely gone away, after 10 years of misery! I also am seeing my two toenails, and one fingernail restoring themselves to normal again(the nails had fallen off years ago, like a fungus, but it was not fungus). My dermatologist told me it had no cure and that I would have to deal with it! Kenalog benefits have FAR outweighed the negative effects so far... I have lost about 5lbs in 3 weeks, and anxiety is a mild issue, as is mild night sweats, but for me, this is a small price to pay for pain relief that was making my life miserable!

28 year old 6 ft 4 in 200 pound male. cholesterol approaching 300 on 80mgs a day of simvastatin. Legs and arms immediately sore after a round of horseshoes. How ridiculous. trouble concentrating, can't sleep, have sour stomach. have the trots daily. Great way to live. This sucks!