Cancer symptoms and conditions

I am 39 years old and work for an interventional cardiology medical device company in Tokyo, and so know the importance of controling one's cholesterol, keeping the LDL's low and the HDL's high. About two years ago, my doctor put me on 10 mg of Lipitor. Several months later I herniated a disc in my neck between C6&C7. From that point onward, I attributed all of my neck and back pain, and newly acquired total body muscle and joint pain, to the herniated disc, it made the most sense. Over the last seven months, I have really worked on my diet and began to exercise more (even though quite painful) and was able to lower my cholesterol. This resulted in my doctor lowering my Lipitor prescription from 10 mg to 5 mg. I noticed a slight alleviation of the pain I felt in my hip joints and calves. About two weeks ago I took myself off Lipitor completely and found further improvements in my total body muscle and joint pain. It's still there but greatly improved. In retrospect, I now believe the Lipitor may have been the culprit (or at least a contributing factor) to my herniated disc due to muscle degeneration in the neck, and all of the subsequent muscle pain, especially in my hips and calves. I fully understand I am not going to die from calf-pain, but may from heart disease. However, I have found my quality of life has improved tremendously over the last few weeks. Less irritability, better sleep, less pain, clearer head. I feel like I have lost two years of my life on Lipitor via personal suffering and lack of ability to do much of anything with my wife and two young daughters. We all need to take charge of our own health and therefore I encourage anyone who feels completely different after taking Lipitor to engage your physician, and make sure its the right option for you. If damage has been done to my musculature I hope I can reverse it. It is evident to me that some serious clinical studies should be done to investigate Lipitor's effect on muscle degradation and hope others will consider carefully whether or not do go on this drug. If you do, monitor yourself closely.

I'm a 70 year old woman, I have taken this drug for 3 1/2 yrs. I was prescribed Spironolactone 25mg for high blood pressure of 140/80. After researching the side effects I chose to stop taking this drug 2 days ago. First off, it's a potassium sparing diuretic and one isn't supposed to eat foods high in potassium, like fruits and vegetables a contradiction to what is needed for both high cholesterol and high blood pressure, does this makes sense no it doesn't. Also I was taking a potassium supplement, maybe I'm lucky to still be alive?
I don't think Dr.'s read about side effects or what one isn't supposed to eat or take along with the drugs they prescribe. They only look at what the drug is supposed to do, then prescribe it to thousands of patients their, victims. This is probably why they're considered, "Practicing Physicians!"
This drug is known to cancer. This drug is known to cause muscle pains. This drug has caused me to go Bald on the top of my head. This drug plays with ones hormonal balance, it can help make someone grow hair, or lose it. This drug should not be prescribed for simple high blood pressure, it is a very dangerous drug!
I have huge rashes on my ankle and now my hands, they say it's eczema or drug induced atopic dermatitis.
Please do yourself a favor and research the many side effects and cancer causing of this drug. If you're taking simply to lower your blood pressure find a safer drug and try to stop taking this one particular diuretic and use supplements and foods to lower it if you can.
I'm taking this and Lipitor which I stopped one week ago and this one two days ago thank God, I thought I was going to be a cripple for the rest of me life from the toxic side effects, all drug induced.

I took TraceLyte and unfortunately helped me to cure my cancer.
I was counting on that cancer to keep paying for somebody's Mercedes.

Hi, I am 51 years old and 10 days ago had a Mirena fitted as I have been having very heavy period bleeding for the 3 months. I was tossing up between an ablation (burning of the uterus lining) or having the Mirena. As my Aunt was thrilled with her Mirena I thought it would be a safe choice and it wouldn't be as traumatic on the body. I have had continual lower back and pelvic pain. I was quite scared last Friday that I rang the Specialist. I spoke to the nurse as the Doctor was away and she arranged a Pelvic Ultrasound. The technician told me that the Mirena was in the right place and everything seemed fine but every time they were scanning my left side I was in terrible pain. I haven't heard from the Specialist yet (will ring them shortly). The back/pelvic pain is so sharp at times that I can't move. I've just rang the Specialist and will see them tomorrow morning, fingers crossed this can be sorted out.

UPDATE!! I had my evil IUD removed today and the hardest/worst part was conveniencing the Dr. I wanted it taken out! She kept telling me that my symptoms (headaches, achey all over,panic attacks, quick temper, high blood pressure,sinus infection,cant sleep at night,no desire for sex ) were NOT related to the IUD and I just spent a lot of money to have it inserted.......she would be glad to write me a script for Wellbutrin (sp?) to help with my "issues". I was even more upset when I asked if she had ever googled "Mirena side effects" and she just laughed at me asking me if thats where I got the idea to have it removed. I was very disappointed as this has been my gyn for the past 12+ years and with my family history of breast and ovarion cancer we have always been on the same page. Well, I asked her if she was refusing to remove because I would be glad to get another Dr. to do it and thats when she agreed. It only took a breif 10 seconds and it was out(didnt feel a thing) I instantly felt better but feel that was just because I felt like a huge burden had been lifted and now I can focus on getting back to my old self. I wish others the best of luck for what ever they decide but would encourage you take some kind of action if you feel there may connection to your health issues.

Has anyone developed a thyroid cyst since having mirena placed?

I have been on both Diovan 160 mg and Diovan HCT 160 mg / 12.5 mg, started having trouble swallowing right away. After a couple years on this med suffered severe acid reflux so bad it burned through 2 prilosecs a day. I thought I was going to die of esophageal cancer. One day I forgot to take the Diovan and had no reflux. Doc switched me to a new different pill so now the acid reflux has vanished. Yes Diovan does cause acid reflux! Also joint pain, and I am wondering if it caused me to have an enlarged uterus as well, that I developed on the med. No fibroids or cancer, just hyper-uterine lining the tests revealed.

I have been on Percocet 10/325 for 2 weeks now but i feel like they do not help at all I have been on Lortab 10/500 for over 5years they stopped working so my doctor put me on these I have had 7 back surgery thyroid removed because of cancer also have to have surgery on toes in about a week the only thing this med does is I feel nausea all day almost to the point of throwing up but I do not feel any pain relief

wow...i must say i feel sooooo muh better now reading this website..this whole time i have been thinking i had fibroids or even ovarion cancer because what i have been going through...this is my 3rd month with nuvaring..i went bc free a month between those though only because my bf was out of state and the bc is expensive..anyway the first month was great i loved it and so was the second but my gosh..this month my period was normal at first..i had the usual 3 days then im done..then all of a sudden my period came back and it came back strong and for a long time i was on my "2nd" period for a total of 3 weeks and 3 days..and finally the bleeding has stopped but im still having the HORRIBLE cramps i have to have 800mg of ibprofn just to make them go away and even still ill still have a horrible headache..(usually in the back of my head) .my cramps are so bad they extend down into my legs..i finally took my ring out yesterday night to start my ring free week and i doubt that i will be paying for a new one...i have also been very moody and bitchy lol...sometimes crying for absolutely no reason...and as for sex drive...now that you talk about it..i haven't wanted to have sex...im just sooooo happy im done with this..and that i wasn't going insane lol..feeling so much better..well mentally lol...

I started this med yesterday for staph infection. My immune system is run down from 24 days of hemorrhaging with menopause and finding cancer in my bloodwork and catscan. My skin has thinned and I have large sores all over my body. This med was given to me yesterday and also my diabetes med was changed because my immune system is so weak it is kicking up my bloodsugars. Can you tell I am run down? I went to bed trying to throw up this pill today again and went to bed with chills while it is 105 degrees in Texas today. I even had to put on socks. I feel lightheaded and kind of out of it with blurry vision. Hard to tell what is from meds and illnesses but is no fun. At least I feel better not being alone with this. I am also burping a lot and I never do.

I am so grateful for this website. I found it in early of 2008. At the age of 11 my son went on Singular for mild asthma. He started taking it in November of 2007. Slowly we noticed different complaints he was having. The first was that he couldn't sleep. He was having nightmares. This had never been a problem. He started losing weight. He was complaining about leg pains and headaches every day. By February 2008 he had lost 15 pounds. This is drastic for an average weight 11 year old. They did blood work and everything came back normal. He started bruising very easily and all the other complaints were still there. His mood was very irritable and he is the most quiet gentle child you will ever meet. With new aches, bruising and the weight loss we were getting very frightened. They did a cat scan and more blood work in early April. Still, thankfully, they found nothing. No terrible disease or cancer was found.

When I saw this website and the posts with similar side effects we took him off Singulair. The symptoms went away. He gained back the weight he had lost and each day the symptoms starting going away. Things have been great every since. I can't believe a medicine did all these terrible things to my child.

oh please your all a bunch of whiners. I don't understand that when people get something medically new that they seem to blame every little thing on it!!! seriously!!! if it were so bad it would not be on the market..... i have had it for two years.....a little cramping in the beginning which is NORMAL and as STATED on the side effects list. YOU MUST UNDERSTAND that these are listed because they DO AND HAVE happened to other people. That is why they are listed! NOW if you died, got cancer, pregnant or what have you then you can bitch. BUT PLEASE don't complain about the LISTED side effects. it is a wonderful product and it does just as it claims. yea the cramping sucks....the spotting is a pain.....men can feel it during intercourse and yes sometimes they can bump it and hurt you. also it causes cysts to grow on your ovaries which can sometimes require surgery. it can also grow outside your uterine wall at time. and it can fall out. all kinds of things can happen that are LISTED. what i would recommend people should do BEFORE they leap into bed with a new contraceptive is RESEARCH the SIDE EFFECTS BEFORE you decide you want it or not. its simple read the damn sheet and decide if you can live with the side effects. maybe one....or all...or none. THEN DECIDE.

My daughter had the Gardasil shots last year. The school nurse talked to these young girls and told them all the dangers of cancer. It is a scare tactic. Doctors tell you to get the shots as well...makes their offices LOTS of money...the insurance companies presently pay for the shots, and the are very expensive. My daughter passed out w/ the first shot. Never has passed out before. (Do not allow your daughter to drive herself to get this shot...for the adult women..have someone drive you if you choose to have this vaccination, although I would strongly recommend NOT.) My daughter, since she was vaccinated with Gardasil, has had multiple ear infections, warts, strep multiple times, flu-like symptoms multiple times...pretty much the immune system took a nose dive. She never missed school before...was exempt from school exams many times because she was never sick. However, after Gardasil, she has missed many days due to all the sicknesses she has experienced. It has been approx. a year and she hasn't been as sick lately. I am hoping the immune system will get back to what it was before the shots but I strongly recommend NOT getting this vaccination. If my daughter gets worse, I am tempted to contact a lawyer. We might should get a count on the women that have been negatively affected by this and go to D.C. This vaccine should have been researched more. Our daughters should NOT be guinea pigs!!

Had a steroid shot combo of Kenalog and something else for allergies about 3 years ago. Didn't make the association then about the deep indentations on my upper buttocks and the shot I had in that same area a few month earlier until I found this website. I just had another Kenalog shot (in my arm) for allergies about 5 weeks ago. Since then I've had two periods the second of which is dragging on and on. I was a bit panicked until I searched and found this website and another and found others who had the same symptoms. I called my primary doctor and they had no idea of this side effect. He said to come in for a follow up if my symptoms continue. Meanwhile, it is really stressing me out due to a family history of cancer. ******

Well I'm glad I found this site. I got the mirena 1 year ago this month and I think I'm going to get this thing out of me. Right now I have severe lower stomach pains that shot down into my girl area. I haven't had a period since Nov. 08'. I always always have headaches and here lately I think I have a problem with stress/anxiety and I can't stand it! I feel better now that maybe it is not me thinking all this crazy stuff in my head but its that mirena cause me to feel this way. Can anyone relate?

I am 40 and done having kids. I had the Mirena put in in Jan 2008 to help with heavy periods. Within 3 months I started to feel numbness in my left arm. It would come and go over the next couple of months. Then the numbness and burning spread to my left breast. I developed a breast lump in Nov.08 which was determined to be thickening of the breast tissue (through mammogram and ultrasound) The breast continued to be very sensitive and the arm pain became worse. In March Through a pelvic ultrasound 2 "tumors" were discovered on my left ovary. The doctor wanted to remove only the ovary. Once in the operating room he decided to do a complete hysterectomy. The tumor was a benign blood fill cyst witch burst and also endometriosis was bad enough to remove everything including the Mirena!! Its been two months now and the numbness and burning are still there! I am going to a neurologist to see what is going on. I always felt like the Mirena had something to do with all of this. Maybe I have irreversible nerve damage?

I'm sitting here in tears reading all of your posts because I've also been on prednisone and have horrible side effects. I was diagnosed with metastatic breast cancer in my lungs in June of 2002 and, after starting at 60 mg/day then, I have been on 20 mg/day for years now. The very first posting that I read mentioned problems with the femur bone. Besides all of the other problems associated with this devastating drug, in December, 2007, I broke a bone in my left foot with no known cause for it. Then I started experiencing pain standing or walking in my left leg and was diagnosed with a fractured femur bone and after several months of trying to get it to heal (including an ultrasonic bone healing system), it just kept getting worse until an orthopedic surgeon recommended that I have a 16 inch rod put into my leg which I did and it ended up to be one of the worst decisions that I have ever made. After experiencing all of the prednisone side effects for almost seven years including depression, severe fatigue, weight gain, moon face, thin skin, cataract surgery on both eyes, hump on my back, mood swings, etc., the pain and suffering that were caused by that operation brought me to seriously consider suicide. I was also diagnosed with chemical neuropathy in both of my legs also which makes my legs so weak that I have to crawl up any steps and have trouble just standing. I actually have an appointment for this evening to have an x-ray done to see what is wrong with my knees and did not realize that this also is yet another side effect. I never make it through the night without waking up in pain and getting a pain pill and then getting up in the morning is almost unbearable with that "burning" pain. I am now on Cymbalta for depression, Xanax for anxiety, Percocet for pain, and of course 20 mg of Prednisone. I was told that I would have to remain on Prednisone for the rest of my life because of the lung scarring and COPD. After reading all of your comments, I have decided that I would rather put up with any breathing problems (and I don't even know how slight they may be at this point) than to remain on the Prednisone. I have tried weaning off several times but get so fatigued that I can't move and that's dropping one mg every week. I'm affected by the decrease but it gets out of hand when I get to 14 mg and I get so frustrated and depressed at not being able to do anything that I just go back up to the 20 mg/day. If you have been able to wean off of it, would you please let me know how you did it and what you had to go through? I'm 65 years old now but I have two wonderful granddaughters (ages 4 and 6) who I can't do any normal "Grammy" things with anymore at this point and I have to change this condition for them and for me. Obviously, the doctors don't recognize the severity of the drug because they just keep prescribing it and out of a regular doctor, an oncologist, an orthopedic surgeon and a neurologist, they can't seem to get together to come up with a solution. I have to say that I haven't considered suicide lately but I do wish that I would just die and be out of this pain. My family and definitely my granddaughters and wanting to see them grow up are the only things that keep me going. There are probably things that I'm forgetting but I'm sure that one of you have covered it in our posting. Although my family is so supportive, no one and I really mean not one of them, realizes knows what we all go through because of this drug. How could they know that something that is supposed to help you could cause these problems? My life is a living hell, all because a pulmonary doctor prescribed prednisone seven years ago and I trusted him to only do what was right without informing me of what was to come. I more than sympathasize with all of you. I sincerely appreciate the time that you took to post to this site and so thankful to know now that this knee pain is not something new that I have but another side effect of the prednisone. I wouldn't have known that if it wasn't for this site because I'd be willing to bet that after I would have had this x-ray done, one of my doctors would have just prescribed another medication to take. Please feel free to contact me directly with any comments or especially any help that you can give me. I know that all of you are going through the same thing so if I can do anything for you, even just listen and understand, please contact me also. Sometimes that's the only thing that people can do is to listen and someone who is in the same situation can always understand. I'm here for anyone who needs a hug for the day.

where do i start.... I'm 16 and my doctor is having me take this because i get ovarian cysts ALL the time. i started about 3 months ago and i hate it. before i started taking it i was a very very bubbly person who did really well in school. now that i am taking it i have changed. my math grade went from a 90 to a 50 and i got very frustrated when i was trying to make up my work and i would end up either walking out of study hall i had with her or i would cry. i had no ambition to go to school and while was there all i wanted to do was sleep. i started fighting with my boy friend a lot more and everything seemed to either make me mad or upset quite easily. it is very annoying. and with my family history of cancer i have to be careful of what i take. i would almost rather deal with the pain i got from my cysts then to deal with this.

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

I believe that my friable cervix is from the hormones so close to my cervix that are constantly being released from my NuvaRing. All tests for STDs and abnormalities came back clear. Other than that, I do not have any noticeable side effects.

I've been searching for answers on LONG TERM side effects of Lupron hoping that it could give me answers as to what's going on in my body now!
23 yrs ago my fertility dr. gave me Lupron to inject MYSELF EVERY DAY (experimental back then). I had SEVERE endo since the age of 16 and was fighting that as well as trying to get pregnant thru invetro. I was 26. At 29 I had an emergency hysto. Now at 48plus I have chronic tendonitis where the tendons will shred off of the joints. I have been diagnosed with C spine and T spine disease, osteoarthritis and a mystery that I'm going to have to go to the Mayo to figure out (hopefully). I have tumors that are growing in my lower back...growing around nerves, tendons and bone, They aren't sure why they are there, why they are growing, or even what they are. Surgery removed 2 of them...but pathology shows foreign matter other than tissue/bone. All they DO know is that it is not cancer. One year ago I started losing weight (25 pds) for no reason. I'm now holding my own at 112 and hoping to figure all of this out. I can't help but wonder if Lupron or any other experimental drugs I was on has something to do with this. Is there anyone out there that used this drug so long ago??

I took Ambien for 2 years. I had all of the common side effects: hallucinations, memory problems, loopiness, nightmares, etc. However, I eventually started smelling smoke all of the time. Since Ambien was the only drug I was on, I stopped taking it. After a couple of weeks, the smoke smell faded. Life went on as usual, and I became pregnant and gave birth to a beautiful boy. That night I couldn't fall asleep even though I was exhausted. I tossed and turned all night, and the nurse started showing concern for me. She asked if I wanted to try a sleeping pill, and contacted my doctor. They ended up giving me an Ambien that night, and that night, the smoke smell returned for a few days. Fast forward several months after giving up Ambien completely. I developed a nasty head cold that gave my sinuses a pounding. That was when the smell returned. I began to piece things together, and went to the doctor. I asked him if he thought the Ambien damaged my sense of smell and if sinus conditions like congestion, allergies, and sickness exacerbated the problem. He did first check me for a brain tumor, but agreed with my assessment. He has seen thing like this happen to people, although not specifically with Ambien since it was a newer drug. He thinks a combination of the drug and sinus problems permanently damaged my olfactory nerves. He told me to try Flonase, and within a week of smelling smoke, it goes away. seven years later, the smoke smell still comes and goes, but actually cues me to what is going on in my sinuses at the time. I know when my sinuses are congested or irritated, and I take Flonase for relief within a few days to a week. Not saying everyone will have this problem, but it is something to be aware of...

I was a healthy 23 year old. I have had a pretty rollercoaster 3 yrs. I had a baby young, lost my mother to cancer, moved to FL. came back to NC, moved in a stressful house(knowing it would be) had issues with the father of my child(now resolved) and lost my brother. I started getting the attacks maybe a month after I lost my brother. I was put on Zoloft(50mg), it seemed to be working, but only being on it for about 2 weeks I started to have fluttering around my heart. I saw my doc and she took me off of it. I'm also on birth control. Now I have insane thoughts that something is going to happen or something bad is going on in my body. I have these weird headaches. Sometimes I get them and sometimes I don't. It feels like my head has this fullness most of the time. Or I'll get this quick zapping feeling on one side or both. I have an app coming up and I will be bringing this up. I haven't had any of these symptoms since being on/off the meds and my birth control.

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

day # 3 ive got the worst yeast infection i was fine b4 i put it in now im uncomfortable ........bloating,fatigue, nausea,headache,.. all after 3 days called the doctor he said to give a month just use some monistat but it is now midnight and i just took it out, and you know what...... instant relief im not putting that thing back in ( from my fiance.....fellas don't let her do it you will be sorry)......well back to the pill : ) keep posting this was very helpful