Surgury symptoms and conditions

My experience with Lisinopril is brutal! I'm 37 years old and was prescribed this drug for high blood pressure. After 2 yrs. on a 10 mg. dose per day I started having numbness in both of my arms I also had sharp pain shooting down both arms at night to the point where I couldn't sleep.And when I did fall asleep I would just wake up an hour later in tremendous pain. Ive been to three doctors. They tested me for carpal tunnal and told me I had it. But didn't schedule any plan of action, so I thought with some rest it would go away but it didn't It got worse. Then I started to have severe back pain that went clear through to my So the doctor wanted me to get an ultrasound of my testicles to check for testicular cancer. The test was negative. Since the pain was on the right side in my lower ribcage area they then thought it may be my kidneys. They then sent me to a urologist who wanted to go up my penis to scope my bladder with a camera and check for bladder cancer. Which turned out to be a very very painful experience. There was nothing wrong he said. During this time the pain was as bad as ever. Then they wanted to do exploritory kidney surgery on my right kidney. I was thinking my god am I gonna die.....I went through the surgery and the doctor said there was nothing wrong.I could not believe I was in this much pain and they couldn't find anything wrong. I thought I was dying for real. Then I decided to go on web md and try to find out anything that it could possibly be. I couldn't find anything with all the symptoms that made any seance. A few months went by with no relief... I decided one day to google my medication (Lisinopril) and joint pain, w/ arm numbness well. This site popped up and I started reading and Im glad I did. I believe that for the past year that I thought I was dying and no one could tell me why is because of this toxic poisons pill Ive been taking for two years is the reason for all of it. Ive spent thousands of dollars, had two surgery's ,went through all this pain all because of a little poison pill for blood pressure. I have flushed my pills and I,m never taking the drug again. I warn anyone who has high blood pressure if your doctor mentions the word Lisinopril tell them no!!!!!!!!! It is poison for the body.I believe it would killed me if I hadn't stopped taking it and not one doctor mentioned it may be the pill I was taking everyday for my blood pressure.

I have been on Levaquin over 6 times in the past 2 years for upper respiratory infections. I just came off another levapak 750mg for 10 days and my biceps were feeling really tight. I mentioned this to my doctor but he said it was a common side effect. After researching this today I am shocked about the tendon damage. I have had distal bicep tendon surgery on each arm on separate occasions in the past two years. Now I am terrified this is going to happen again. None of the surgeons could figure out why someone my age (41) could do this twice in under 2 years. Has anyone found a way to reverse this? I am terrified to go back to the gym or even lift anything. My biceps are so sore and I have been off the Levapak for 3 days and my biceps seem to be getting more tight and sore each day. I can't face having another surgery. This drug should be taken off the market.

I have a herniated disc in lower back.Been dealing with it for about 7 yrs 3 of which have been chronic. I had a series of 3 shots in 3 weeks one year ago and had instant relief for about 2 months. My pain came back after this short pause with a vengeance. I just went back to the doctor for my second series of 3 shots but he really knocked the hell out of me this time. I have had a accelerated heart rate, puffy face, huge weight gain, anxiety, insomnia, incredible appetite, cotton mouth and some digestive problems as well. One good thing about it is that I do not have any pain(for now). I am scheduled for surgery in a month hopeful to get away from all drug treatments.

I was recently diagnosed with endometriosis. For the past 6 monthss i've been dealing with cramps so bad I had to be on percocet for weeks at a time just to be able to get through my days. After my laparoscopy two weeks ago my gyn suggested that I get on bc to help supress all fo the cramps and the cysts. As of right now i'm on day 7 and I'm miserable. I cry all the time and snap at my fiance constantly. I've been eating twice as much as i used to. I'm constantly exhausted and sex? What sex? No sex drive what so ever. It's completely gone. Not to mention I'm to tired to even bother anymore. And vaginal itching is very uncomfortable. No yeast infections, just itchiness. I'm calling my doc today to see if there's another bc that would make me a little less depressed. Last night I actually thought of suicide.
Ladies, you know your bodies the best. If something is not right, tell you doctors. Bug them until they listen and treat you properly. You do not need to deal with symtoms like this just because our docs got free samples from the drug companies. Tell your doctors what's going on with you. and good luck to all of you.

49 post surgery, chemo, radiation. Took it for only 2 and a half month,
Initially had buzzing sensation in body, panic at night, increased hot flashes....and then it got worse, sever abdominal cramps...Doctor tokd me to take pain meds. I wen another two weeks, pain unbeatable, got a sonogram....It had grwon me huge ovarian cysts!!!
This is not commonly mentioned, but alloiver the web.
I may have to have more SURGURY. Ansd possibel removal of my ovaries.
I am furious. After all I went through. It is a miserable drug.
I am angry when they make light of women not able to take the side effects.

I was dianosed with an immune disorder of the inner eye. It was advanced enough that regular treatments were not effective. So the dr. started me at 60 mg of prednisone and started to taper it off at 20 mg. every 2 weeks. At 6 weeks, it was observed that my symptoms had reappeared and so he started back at 60 and the tapering was much, much slower (50 mg, 40 mg 30 mg 25 mg 20 mg 15 mg 10 mg 7.5 mg 5 mg 2.5mg) the first week I had panic attacks and wanted to physically attack people. I couldn't sleep. After that I had mood swings, fuzziness, forgetfulness and confusion, all I wanted to do was lay on the couch. I had heart palpitations, moon face (people thought that I'd had dental surgury) went from a size 6 to a size 12. I had terrible yeast infections, and wanted lots of fluid and had frequent urination. It was horrible. By the time I was done (and I had withdrawel symptoms long after I stopped taking it) I'd lost 2 years to the side effects. I do get to keep my eyesight. Fair trade, I suppose. In the next year and a half I lost weight down to a size 2, not as good as it sounds, all my muscle tone had gone and I'm having to rebuild from being nearly skeletal. The worst part of it is.. at any time I can be put back on prednisone and will probably choose to over losing my sight. At what point does one have to worry about osteoporosis? How much prednisone for how long effects the bones? There are things I'd like to do, but I'm not sure if I should.

5 years ago my left vocal cord was paralyzed. Doctor felt this was caused by virus. I had surgury to fix then. In November 2006 my allergy doctor changed my allergy medicine to Advair. Soon after my voice starting giving way and I started choking, coughing and had severe phlegm. I passed this off as a bad cold and did not catch the connection. My wife noticed my voice was getting worse through the holidays. By January this year I starting gagging and choking for no reason. My center of my chest felt as if it was severly bruised. I had the gurgling, trouble sleeping at night and I could not breath. It felt like my throat was blocking after coughing and I could not get air in. Constant nasal drip. I made an appointment with my specialist thinking something with my vocal cords was going on. They did not see any major issue with my vocal cords but could tell my voice was in bad shape. I go for more testing end of February 2007. I have a constant metalic taste in my mouth. We saw the post made here after I could not breath. My wife was almost ready to call the ambulance. This stuff is REALLY SCARY. I went off Advair immediately. We called the specialist to tell him. I feel better now but know that something is wrong here. I'm still choking some but not like I was.

Had surgury to remove ovary from endrometerosis then in about 5 yrs. had a laparascopy to remove endro again. I am 31 and the Insurance would not pay for complete removal of female organs to get rid of it once and for all. So doctor said Lupron Shots. I was on them for 3 months. It started out after 1st month with cravings leading to weight gain, severe headaches, being dizzy, breathing problems, THEN by the 3 1/2 month mark things changed drastically pain in foot couldn't walk traveled to my shoulder and arm thought I was having a heart attack so was ambulanced to hospital all test showed nothing. I could not walk was in a wheelchair and pain plus all the other effect above. Sent to a neurologist who told me some truthfull answers finally. SIDE EFFECTS LISTED FOR THE PHYSICIANS TO KNOW BUT NOT TOLD TO ME WERE ( PARALLISES AND COMPRESSION OF THE SPINAL CORD) I did not have my 4 th shot of Lupron and after a 2 more months and a lot of prayer from my church family God came thru and healed me I am up out of the wheelchair and walking as if none of this nightmare happened. I have to deal now with the excessive weight yet hopefully it will go too.

Pain at front of left shoulder, so Doctor wrote prescription for Voltaren, which I then read up on at this site. Too many side efects so I told Doctor no. He then said a steroid shot would be quicker and easier with 'no side effects' as it would be injected deep into the shoulder, not near the surface. I read your side effects long list, called the Doctor's office back, and canceled my shot appointment tomorrow. The Doctor said I may only have to have 1 or 2 shots. There is no way I would take the "chance" of getting any of these side effects to lessen my shoulder pain, especially now understanding this is not a cure but apparently just a temporary relief which means I may have to keep taking these shots to keep the pain down. I'll put up with the pain until it either heals or I get surgury. My Doctor applied for permission from my insurance company to get an MRI but they declined saying that it wasn't the 'proper procedure', that drugs or steroids must be used first. Seems like the MRI would be least invasive and provide the more exacting diagnosis. I shouldn't have to subject my entire body to drugs and inject steroids wih known bad side effects just to get an MRI from an Insurance company. I intend to write the insurance company a letter contesting their decision. There must be a better way!

Well, I found this site just AFTER I started a new med for my BP. Finally figured out the lisinopril was the cause of my horrible cough. I started taking the drug in Nov of 2003. And had a surgury in Dec ....thought the cough was from the tube down my throat. Then it was flu/cold season. The cough steadily got worse, more frequent. My wife overheard someone say their doc was changing their BP meds because of a cough. Well I have been off lisinopril for two weeks and the cough is mild now. However this site brought to light ALL the other symptoms I never realized were from the drug.
Eye twitches,head sweats,vivid dreams.
The lisinopril did control my BP.
Hopefully this new med will work as well.
Lisinopril is just not the right one for me.
Good luck to Everyone!

9 months after marriage, prostate cancer was discovered. The choice was surgury or Lupron with radiation. I chose the latter because radiation is pervasive and could pick up micro cancerous cells as well in the vicinity of the prostate. I experienced the usual symptoms from Lupron, but the prolong effect, 2 years after ceasing injections is lethargy and laziness. In addition to insomnia and weight gain, some 15 Lbs and a breasts simiar to Cushings syndrom. But I am alive, because the actuaries for cancer are 4 years to death and it is a miserable death. So I am grateful. There is no sex drive, neither with Viagra and I no longer have the desire, but I owe a responsibility to my new wife, who has told me it does not matter, but I am sure that she would be much happier if I could perform that ritual. The most important ailment which affects me is my inability to generate income due to tiredness, sleeplessness and memory loss which leads to poor decision making and certainly less aggression. These are the symptoms that have remained after the hot flashes and the noctornal presperation has past. Prior to cancer inception, I had the discipline to make the 6 AM swim at the YMCA for a mile. Now I am trying to get into the pool twice a week for 1/4 mile after which I have to repair to bed for an hour to recover. Medicine has pushed us too far past the normal limit of existance and we should not be ungrateful for that if uncomfortable side effects accompany our efforts for preservation on this earth. I am grateful for Lupron for its curative effect regardless of the side effects

when i got my first shot of lupron was in march of 2003.it was a one month dose to help cure my endometerosis. I wa the worst thing that i could of done. I got a sever headache right after the shot was givin with in the next four hours i experianced a headach like no other and was throwing up uncontrollabley, as for the rest of the month i had to bear through i couldnt sleep due to the nite sweats. i would awake in puddles litteraly, and then freeze to death trying to go back to sleep in phoenix arizona. i got hot flashes so bad i would feel like i was going to pass out and i seemed to walk around in a daze. Anyway i getting so ill from the medication i lost my job and now i am still here fighting the excruciating pian because even though i cant have kids i am only 23 and i might want one one day. this disease is so hard and for those who cant have kids they wont give you the cure wich is a hystorectomy, so us , all of us unfortunate soles are left to either become addtict to pain killers, because of the severity of the pain, or just try to deal with it, and for those that do i commend you. there has to be some humanity for our kind some kind of treatment that can help us if the doctors wont due surgury and birth control jus wont work besides making us twice as ill from the lupron. SOMEONE PLEASE HELP US!

I would not try to start a day without taking my Pletal. I have a vascular problem that causes my right foot (two toes--big and the one next to the little toe) to feel as if they are frost bitten. The pain is so severe, it is unbearable.

I had surgury and the blood clot was removed from my stomach. The blood clotcaused the blood not to flow freely to my right foot.

Since the surgery, at times my toes get tender, but nothing like they did before taking Pletal. I take 100 mg in the morning, and 200 mg in the afternoon.

I do have a headace and dizziness sometimes, but I can bear it. After all it is better than all the pain I had in the past.