Lifting weights symptoms and conditions

I have been on toprol for sometime now, and what I have found is, I have no sex drive at all which is causing problems in my marriage. I am always tired, can't remember anything short term that is and my shoulders are always hurting as if I have been lifting weights. I am also noticing bruises if any kind of pressure is applied to my skin which is weird. I also get swollen ankles and lots of hair loss. My vision is giving me lots of problems. I now wear glasses that are so thick you would think I borrowed them from the bottom of a Pepsi bottle. I just don't know what to do anymore. I have expressed most of my symptoms to my doctor, but my cries have gone unheard. I am afraid to stop taking the medication in fear of having a heat attack.. I have taken my daughter through a specialized school until she was able to manage herself but today I cannot remember how to do math or just simply write and essay which I think is weird. I am also having a hard time with spelling and reading long passages due to my lack of energy and concentration. Does anyone have advice that is helpful?

I got the Mirena put in in October 2007. I had just lost all my post baby weight and was feeling GREAT. then I immediately gained 20 lbs. I tried EVERYTHING to lose it. I went to extremes...power walking 5 miles a day, going to fitness classes, lifting weights, bicycling up hills, playing soccer with my kids. AND eating very healthy, small portions, minimal fats, no starches, or sugars, no eating out ever. NOT ONE POUND moved. What is so weird is the way the weight came on. It is all concentrated in this perfect little round bump on my belly making me look about 4 months preg. I can tell there is a lot of water there and I retain water terribly. I bloat all over so badly by the end of the day, I have to unzip my pants (even though I barely eat). I went to my doc thinking something is wrong and she assured me it wasn't my IUD but my age!!! After reading these and other posts, I was amazed to see SO many other symptoms I have been having since Oct. of 2007 that I Never attributed to the Mirena!!! My breasts hurt, my energy levels are up and down. I have had a terrible time emotionally, handfuls of hair falling out, NO SEX DRIVE, (don't have acne), irritable, depressed, impatient, headaches, complete space cadet, inability to make decisions, etc. All this since the Mirena was put in. I TOO want my body back and my SELF back!! I have an appointment in TWO Weeks from today to get it out and I cant wait!!! This can NOT be healthy!! I will report back to you and let you know what happens.
L.

Just had laprascopic surgery to remove a borderline ovarian tumor the size of a 6-7 month baby yesterday. I've been taking Lisinopril-HCTZ 10-12.5 for about 2 years now and have posted on this site before regarding my symptoms. Since this med works on the kidneys/adrenal glands and adrenal glands regulate some hormones I am wondering now about the possible connection between this med and my sudden cyst/tumor. The tumor was actually my left ovary enlarged to that size! Although benign, my very first symptom of this cyst started exactly when i began the med. It grew pretty rapid over a two year period. I have found no proof or mention anywhere and every doctor looks at me like I'm crazy, but my entire life I have NEVER had issues with my menstrual cycle or even much pain. After I began this med, I HAD to use ibuprofen every period. I began my cycle at 11 and not until 34 did I have issues - same time I began Lisinopril/HCTZ. Are their any women who are having female problems since taking this? Of course, the heart palpitations, arm and leg aches (like those of growing pains when you were a kid), dizziness, anxiety, depression, irregular sleep habits that I cannot break, increase appetite for mostly meats and proteins, some mild hair loss, abdominal cramping/tingling, hands and feet numbness, shoulder/neck pain, overall achyness, sudden/rash emotional extremes, even suicidal thoughts I know are side effects of this med.

I'm 40 year old male and I'v been taking ZOCOR for almost 2 years. I am very active ,working out 3-5 times a week both lifting weights and either running or eliptical training. MY cholesterol was a genetic issue and 20mg of ZOCOR at night has lowered it to normal some what normal ranges. I have noticed that my stools in the morning have been irregular. I have noticed more muscle pains in my legs when I lay down at night. I just recently had had my first ECG and now it appears there may be some sort of irregularly. After reading all the postings, it appears that alot I have a lot of the same side affects and just brushed them off. I now have a consult with a cardiologists. Has anyone else had abnormal ECG's after taking ZOCOR ?

richard

I got into a car accident several years ago. I now have severe arthritis in my legs and shoulders and arms. Lifting weights has helped with the pain in my arms and shoulders, but nothing helps with the pain in my legs. When I first got into the accident I was put on soma. I stayed on it for around fifteen years at eight pills a day. When ultram came out I quit taking soma with no problems. Additions not a problem I have. After a few years on ultram it wasn't cutting it so my doctor put me on lortab 700. This helps a great deal and I find that if I take at least two of my doses during the night and only one during the day,I'm much more alert. I don't know what I'll do when these drugs quit working because my husband is selfemployed and so no one will give me insurance so that I can try the new very expensives meds that are out on the market. As of right now, I'm thankful for Lortab.

Hi there,

I had the Mirena IUD inserted on my 32nd birthday, 4 months after my son was born. The cramping was reminiscent of having my period but I felt better the next day.
I have been happy with the fact that I have had absolutely no trace of a period and maybe just a smidge of spotting here and there, until last week when I actually had to use pads for a week and then had old blood showing days later.
So far this is the first day that I haven't had to use a pad and I've noticed that I'd had migraines for the first time, I am exhausted but then I have a 9 month old who often gets up to feed during the night. I can't comment on my breast because I am breast feeding right now too.
I am extremely hot all the time. Just feel like there is an internal heater or as if I were pregnant again, I have noticed pimples around my face that I never used to have. They are big and painful. I am now cramping off and on and it can sometimes be quite painful.
My eyes are extremely dry and I often have to try to make myself cry to get tears to moisturize them while I am driving, My body does feel itchy often - until reading this site I often put it down to the fact that it was during winter and my skin just dried out.
My biggest concern is that my knees are extremely painful, and my lower thighs above the knee are often sore as though I have been lifting weights. I am out of breath when walking up our stairs and yet I have managed to lose 20 pounds of weight since having my baby, so the sensitivity and pain in my knee just does not make sense.
I've also experience light headedness and every once in a while out of the blue I'll get some tingling in my left hand. Weird.

I think I will print this out and show it to my OBGYN because he is very dot the i cross the t type.

Wow, thank you everyone for sharing your info, maybe all my symptoms are that from Mirena too. I certainly didn't have them prior to MIrena insertion.

Take care

Hi Ive been hypothyroid for about 12 years now. After i took radioactive iodine I was put on synthroid.125. Had blinding headaches constantly! Then after about 3 years I was put on levoxyl.125. Blood work sometimes comes back a little elevated but not much to say for the symptoms i am having still to this day.I am so tired i cant even go to the store. Symptoms are,
sever fatigued. headaches. muscle pain in chest and sternum. burning muscles, triggerpoints all over body. broken sleep .severe depression.Eye pain blurry vision lower back pain body feels like a punching bag.I could sleep for 12hrs and still be tired. These medicines have side effects that they are not telling us.I tried armour but it does not aggree with me. Im going to switch to either unithroid or leverthroid.If these do not work then i will try thyroler.Doctor wanted to give zoloft. Please I do not need bad medicine.
This all started when i had to take thyroid meds.Before diagnosis I was a fitness fanatic . I was doing aerobics heavy cardio, lifting weights etc. now i cant even ride my bike.The meds are no good doctors are a waste they think it is in your mind.Let them feel one day like this and see if they can function.I do not think they can.ill see what happens when i change my meds..fibromyalgia? no such thing Fibromyalgia is diagnosed when the doctors cant figure out what is wrong with you so they pawn off some atidepressives.

I was taking Levaquin for a sinus infection. After taking the first dose of 750 mg, I noticed that I started having tingling and numbness in my hands and arms. After the second dose, I started feeling the same tingling and numbness in my arms, hands, and legs. Because I had been having severe headaches anyway, I started wondering if I had some kind of neurological problem and my headaches were linked to the strange sensations. However, I noticed that I didn't have any problems with my arms and legs until after I started taking Levaquin. Some of my other symptoms were: tightness in my neck muscles and sore muscles. I also remember seeing a flashing light from the corner of my left eye and floaters. I stopped taking Levaquin after just 2 doses because it began scaring me and I feared what might happen after my third dose. I can't afford to take any chances with my health. That's why I appreciate this post, and I see that I wasn't just imagining these side effects. Since I've stopped taking this medication I still have problems with my arms. They feel heavy like I've been lifting weights and the ache. A couple of times, I've had to take pain medicine for the pain in my arms because they've hurt so bad, it feels kind of like when you hit your funny bone and you try to figure out why they call it a "funny bone" because it's definitely not funny! My arms hurt so bad I couldn't lift them, and I could type or write so I just took some medicine (tremadol) and laid down. It's been weeks since I've taken levaquin, but I still I have sensations and aching and heaviness in my arms. Has anybody been off of Levaquin for a considerable amount of time and found that the symptoms go away? Please give me some hope! :) Thanks.

Stay away from Prednisone

My prayers to all of you who take these destructive "medications". here's my short story.

I had been diagnosed with Sarcoidosis back in 2003. My doctor gave me 60MG per day (three 20 MG tabs) for over six months, with the weening off period lasting another six. To make a long story shorter. I went through many of the same problems like, bloating in the face and body, rashes, a bump that looks like a wart--that still won't go away, and a continuing state of memory loss. I get baffled easy now. I also continue to go through mood swings.

But here's the kicker, I haven't taken Prednisone for over 3 years and I was trying to begin lifting weights. I thought I popped something in my arm, but the doctor says that I have "aseptic necrosis", that has developed in my left shoulder and soon to start in both sides of my hips. For those who don't want to "google" the term, basically parts of my shoulder and hip bones are not getting blood flow and are dying (necrosis).

With my memory loss, I am having difficulties performing at work and doing routine tasks at home. I did not think this "medication" would have affected me this much.

Prednisone needs to be on the banned list of medicines.

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.

In 10/2001 I was diagnosed with Prostate Cancer and my MD prescribed a Lupron 3 month Injection to reduce the size of my prostate prior to radiation seed therapy. l started having the following symptons immediatetly frequent hot flashes which disrupted my sleeping at night from 4 to 6 times per night and which lasted for 9 months, I was no longer able to achieve an erection, although immediately prior I was able to have sex with an orgasm. I loss muscle and gained weight. Seven years have past and during that time I developed a heart arthymia which I was hospitalised for all this despite forcing myself to stay physically active, by walking, lifting weights and doing manual labor. I have never been able to regain my strength despite my exercising. I am now suffering from an undiagnosed skin disease and low blood platelets which my doctor thinks is an auto immune problem. This drug has had a severe impact on my well being and I tell all my male friends that if they ever have prostate issues to avoid hormone therapy at all cost.

Right now, I'm in shock of all the reviews because I started the Nuvaring 08/17. By 08/19 when I checked the ring..a glump of white discharge came out. I thought then.. wow it's really starting to protect me. By 08/21 I had irritation down their and called the doctor...which was yeast infection. I ignored and took the medicine and thought maybe my body just trying to get used to it. By a week later... I was a walking nightmare. I would be mad at the world. I had all the systems of pregnancy. Breast tenderness, nausea 4 times a day, constant eating. I had lost 68 lbs in a year before I got on this thing and due to this ring in me I gained 8 lbs. and that's with me lifting weights 4 times a week and cardio 11/2 - 2hours a day everyday ...although I was eating for possible 4 people. I constantly slept my days away. You would've thought I should had been the most well rested person after all the sleep I did. When I came to this site... and read everything....I immediately ran to the bathroom and ripped it out. After 1 1/2 weeks.. was enough for me to see what it could've done. I want to say thank you to each and every one of you that typed a review because now... I don't have to walk around mad with the world. I'm sure when I walked out of stores and etc... people were calling me every name in the book due to my attitude and my co workers looking at me like...she's going to gain every bit of weight she lost if she keeps eating 3 separate meals just for breakfast not including lunch and dinner. GOOD LOOKING OUT... LADIES.. THANKS SO MUCH.

Hello All. I have been on Toprol 25mg for over 2 years. I had a mild heart attack & also have an irregular heartbeat. In the begining I did not really notice any changes. Since My heart attack

I have been jogging, Lifting weights, yoga etc. About 12 months ago I started gaining weight for no reason. I now have gained about 20 lbs in the last 8 months. I stopped taking it today on the advice of my Dr.

A few weird dreams but I for the last few weeks I have noticed feeling a little buzzed after I take the Toprol.

Peace

im 25y/o pretty athletic guy (always exercising and lifting weights) but turned out to have slightly high blood pressure (doc said prolly from drinking energy drinks every day for 7 years) anyways i was prescribed 12.5mg tablets of lisinopril and my first side effects were deep beating heart.. like I can feel it at times just out of no where.. light headedness at times, stomach cramping and most importantly I got retograde ejactulation (which means sperm goes into bladder instead of out through penis). Im also not interested in sexual activity anymore... Its horrible to think I might have to take this medicine for ever.. I dont know im thinking maybee not takin it would give me a better way of life than living with these side effects.. Im not even myself anymore, im all calm, slowed reflexes.. People are joking around and im like drugged up just listening not really joining into conversations... this is stupid that this medicine aimed to help us seems to actually hurt us as well.. I cut my pills in half with a pill cutter in hopes maybee the lower dosage will net me less side effects and still healthy BP.. we will see..

Hello Gang,

I have never felt so sick in my entire life. I started taking Yasmin two months ago (I only went through two packs of pills). I have felt like I am going to die every day of this last month. I have had severe migraine headaches, body aches, chest tightness, dizziness, SEVERE anxiety and EXTREME fatigue. My sex drive has packed up and gone, I have terrible vaginal dryness and I am never hungry. I used to work out every day but now find that the very thought of lifting weights puts me to sleep. The strangest part is how the "illness" kind of comes in waves, I'll be fine all morning and then I'm freaking out/sick all night. I have panic attacks and I'll start crying for no reason. Sometimes I lay in bed and worry that I have cancer or a tumor or all types of various diseases. My boyfriend has been extremely patient throughout the whole thing but I feel terrible because we hardly have a chance to get romantic because I'm constantly sick or simply worrying that I might get sick later on. I actually just had four vials of blood taken yesterday to make sure that I'm doing okay. They also gave me chest xrays due to the chest tightness. The thing that really bugs me is that aside from being frustrating, confusing and scary, it is proving to be quite costly since I now have to pay for my doctor's visits and doctor's expenses. I just switched over to Loestrin two days ago so I'm hoping that will help get me back on track. Until then, I'm just gonna have to hope that this stuff gets out of my body and that the feeling of looming death vanishes. I'm all for going to the news or Oprah or maybe dateline nbc. Women should know what they're getting themselves into because it seems obvious that if doctor's are prescribing this to us, they must have no idea what they're doing. And that thought is equally as terrifying as the constant sickness.

My husband takes prednisone for bronchiolitis obliterans residual from two bone marrow transplants for leukemia. On and off this steroid for nearly a decade now. The emotional roller coaster; the poor management by some of his previous doctors; the easy bruising; the effect on his sleep and his mood stability. This is a horrible medication that saved his life. Damned if he does and damned if he doesn't. Before his last crisis where he had to go back on it, he actually told me that he'd rather die than start it all over again. He changed his mind, but what a toll it takes! Weight gain and the devastating effect on his body, his self image and his self esteem is the absolute worst. Before the leukemia hit, my husband lived in the gym lifting weights and staying trim effortlessly. He missed the exercise as a coping mechanism during his treatments. When he was physically able to exercise again after two hip replacements, two shoulder replacements and leukemia in remission - he developed the lung problems and started thsi prednisone cycle of submission. He is still trim but lives with this globe of abdominal fluid and weight that seems to have migrated from the rest of his body to his navel. Years ago all of this abdominal girth seemed to resorb back into his body leaving just stretch marks when his steroid use decreased. Now despite a decrease, it remains stubbornly in place and seems to be growing. It profoundly affects his breathing as well. If he eats too much at all, he can't breathe well. He has tried calorie reduction, Atkins, glycemic index diets and nothing seems to work. He can't get aerobic enough to tackle the weight. I have searched for a personal trainer or a nutritionist or anyone who might help my husband with an indvidiualized plan. Any ideas how best to xupport him?

I am a 46 old black male, I have been on Zocor for three years now, after taking Zocor I have suffer a tremendous hair loss. I had a full head of hair before I started taking the medicine and now my hair has thinned out very badly in the top and the back of my head. I still have hair folicles in those areas but it look bald. I have been lifting weights, eating good meals and exercising to overcome my cholesterol problem. I hope I will not loose any more hair.