Health food store symptoms and conditions

I would also just like to add that I have developed a ganglion cyst in my right wrist, and do experience frequent joint pain. I don't know if this can be attributed to the use of Yasmin.

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

Hi ! I posted on July 4th = serenity@42 ... I had mine inserted on June 18 during surgery as I posted, I was going to have it removed when I returned back to Canada. I called my doctor and he told me that to remove it, it take a second. He also told me that the side effects would diminish within 3 months, he also said "it is in your body, not mine", no problem to remove it. He told me to give it a week. This coming Tuesday will be a week to call him back. Now I went to a health food store to see if I can find something natural to assist in my side effects and I am taking Apply Cider Vinegar 600 tablets. They help reduce the bloating, along with my issue's from surgery *(lack of bowel / urine) = so this is helping me, you have to find the one that has "dandelions", which helps the urination of the excess water, I look 6 months pregnant at the time, now I look about 4 months, but this is helping me. As for the other side effects I had, the headaches have gone away, the moodiness is somewhat in control because I am aware of it and I make sure that I watch for it before I go off ! The swelling feet are still there, but I just had surgery 3 weeks ago, but still apart of the water retention ... I have not had sex with my finance yet because of surgery suggestions plus very minor spotting from surgery. The positive is that I have not had any period or bleeding from my period, but just spotting in the last day .. my doctor was surprised by that, and he said without bleeding, then this should outweigh the side effects, but totally up to me ... so I am going to give it a few more weeks to see if the weight comes off and the swelling in the feet go away, then I will decide what to do, I know it is a phone call away from removing it ... I want this to work so I am going to hang in there. Sleeping is getting better, I could not sleep plus having crazy dreams and waking up a few times a night, plus I forgot to add that I tend to be hot at night only, without sweating though, thank goodness. I have not had any hair loss during this whole time, and the acne has slowed down. I know that these are REAL symptoms because I know my body !!! I think that everyone had REAL feelings / symptoms as well and we must all honor what other women are going through and support each other not disregard others as EZRUST and NIAHSMOMMY have done ... This is a FORIEGN object in each of our bodies and some react differently but that is for everyone to decide if it is worth it or not pending their side effects. So to all that have had or are thinking of this for themselves, you read these postings and you have to make a decision for yourself on whether you either remove it and don't wait till it gets really bad or take the chance that you may only have minimal side effects. This is a great site to have support by most of us and to express your thoughts and feelings and know that you ARE NOT ALONE feeling these things ! Take care to all and I will update you as the days / week pass to see what come of this ... I will not let this Mirena Rule or Ruin my life that's for sure !!!!!!!!!
Take Care ... Serenity@42 !!!

I had my Mirena in for 20 months. I had it removed as i realized that it was causing many side effects including headaches, painful feet when i got up in the morning, bloated stomach and fat rolls! WEIGHT GAIN of 6kg or 13 pounds and i could not get it off (usually i can drop a kilo or two if i needed by eating smaller portions and no snacks), foggy brain, very tired and exhausted for no reason, lower back aches, tender breasts, no period whatsoever (not a bad thing), NO libido and possibly more - a doctor suggested he possibly suspected depression. After i had it removed, i bled for several days then nothing then a few days again. It has been 5 weeks since its removal and i have already lost 3kg or 6.5 pounds, and i have not felt tired unusually at all. All my other symptoms have pretty much disappeared overnight and i feel myself happy, exuberant self again. HIGHLY recommend removing your Mirena if you are feeling symptoms like mine. Condoms girls is all i can say, don't mess with your finely balanced hormone levels. Also i researched a natural product you might be interested in to regain natural hormone balance, Maca Root. Ask a naturopath at a health food store for more info. Stop searching for answers like i was doing, and do what you think is right for you and your body.

I have been on prednisone for 11+ years due to having had a heart transplant. The prednisone keeps my heart from rejecting.
I have not taken it for 2 days and I am in the process of passive suicide.
I am driving out west into the desserts to sit and die. I can no longer
be around people for I am afraid I may kill someone or at least significantly hurt them. I have been homicidal and suicidal for 11 years due to this med. I would enjoy killing everyone and everything. I hate myself and I want to die.
Prednisone made me become "Evil"; Hell incarnated. I don't want to live
in a mental institution and my doctor will only give me Seroquel thinking this will help me. I tell him it doesn't help me but he thinks it does. Stupid fucking doctor. My transplant docotrs won't even listen to me when I talk about "mental" issues. Everything pisses me off. It is raining outside and this makes me so mad and stressed.
I have been in this psychotically angry and agitated state of mind for 11 years. I have punched myself many times in the head and banged my
head against walls trying to get homicidal and suicidal thoughts out of my mind to no avail.
I would like to try ECT (electro-convulsive-therapy) but I won't even
mention this to my doctor because he will literally laugh at me and make me so god dam mad that I would enjoy killing him right then and there. I'm sick and tired of living in hell everyday.
Do not take prednisone no matter what, unless your life depends on it. And then what type of life will you have? Maybe a life full of hate, rage, anger, homicidal and suicidal thougts even when you dream.
Fuck life!
Arthur X 1968-2009

My daughter is 6 and has been on singulair for 2 years. Anytime we miss a pill she ends up with a fever of about 100 and is exhausted. Within a couple of days of her medicine it's gone again. The doctors think it's a complete coincidence but I don't agree.

My daughter is 16 and was given Levaquin 500 for a sinus infection. While on the medication she was tired but not much else in the side effect category. Now here we are 4 weeks later and she has acute abdomen pain, extreme fatigue,nausea, a headache, and she has lost 21 lbs in 2 weeks. I took her to the doctor and they ran a cbc, chem 12, urinalysis, and an electrolyte panel. All came back negative. Basically my perfectly healthy little girl is suffering from this. I went back and looked at the Levaquin packet because I know it can sometimes take a few weeks AFTER medications are stopped for side effects to show themselves and of course, all her symptoms are listed.

I was just prescribed Lisinopril 10 mg about 3 weeks ago. I now have severe pain in my muscles in my butt....yeah my butt and really bad joint pain in my knuckles..I thought it might be arthritis, but now I guess it is all due to this med. which I will be stopping as well. Does anyone have a natural/homeopathic way to decrease blood pressure? I know the Chinese and jungle people have been using nature to cure themselves for thousands of years and I am going that route now once I find it.

You Can Now Boost Your Thyroid Function,

Eliminating Your Most Troubling Symptoms…

Without A Prescription and Without

Begging Your Doctor!

How? By adding a simple but vital supplement to your diet: Iodine.

Just how important is iodine? Consider this… about 25¢ worth is all that stands between an infant developing normally and one that’ll be severely mentally handicapped the rest of its life.

Iodine is essential to a proper functioning thyroid. But as we grow older, our thyroid starts slowing down. It just can’t metabolize the iodine it needs as efficiently, and that means the hormone produced (also known as thyroid) goes down as well.

There are 2 other reasons why most of us are iodine deficient:

Inadequate dietary intake, and
Exposure to toxic substances that displace iodine.

Iodine is a mineral, but one that is not abundant in the food we eat. Primarily found in very small quantities in seawater, soils are naturally deficient in iodine, especially the further away you get from the ocean.

Iodine is also fairly easily displaced from your body by toxins called toxic halides… fluoride, bromine and chloride.

Fluoride is by far the worst culprit. Found in toothpaste and in your water supply, every time you take a shower, brush your teeth or drink from the tap, your body gets a little exposure to fluoride, leeching out good iodine. And contrary to popular belief, fluoridated water is actually rather poor at preventing tooth decay.

Why is it in our water supply then? Poor science combined with corporate greed and political ignorance paved the way. Basically a toxic by-product of aluminum production, fluoridation was sold as a way to prevent cavities because some areas with natural fluoride in the water also had lower instances of tooth decay. Based upon that spurious observation, fluoridation began.

If You’re Human, You’re Most Certainly Iodine Deficient!

Because of these factors, 96% of all people tested are iodine deficient! This according to a study of 4000 patients conducted by Dr. David Brownstein, Medical Director for The Center of Holistic Medicine, and renowned author of several books on hormones, iodine and hypothyroidism.

The World Health Organization also concurs, estimating that 72% of the world’s population is being affected by iodine deficiency.

This trend is worsening. Over the last 30 years, the NHANES (National Health and Nutrition Examination Survey I) shows iodine levels have dropped 50% in the U.S.A. alone.

I have AIHA and am doing better since getting off the Prednisone.
I posted back in Oct. 2008. I finally got off the Prednisone in Nov. and surely don't want to be on it again, ever, (hopefully). I'm still using Danazol but was at 400 mg a day, am down to 200 mg hopefully will go in remission, if not it's spleen surgery time. All the fat pockets do go away, it just takes time. I would advise anyone using Prednisone to take good daily vitamins and minerals ( got mine from the health food store), also Calcium with Vitamin D (Citracal caplets w/ D maximum dose). Prednisone depletes minerals, stay on a regime. I also have to take prescription folic acid. Eat and orange EVERY day for extra vitamin C, DR. advised me. I eat 3 good square meals a day and made sure breakfast was a main meal. Eat a small container of plain yogurt daily to ward off fungus, such as thrush, and to keep the intestinal track clean, plain is nasty, just wolf it down (Dannon makes a small container) A lot of people taking Prednisone have problems with acne. Wash your face daily then using cotton balls apply "Topical Hydrogen Peroxide" to the facial skin and let dry, then a moisturizer, face and body (Gold Bond is very rich for body). I use to turn on the fan and let the air blow in my face because it seemed to take for-ever for the peroxide to dry and the smell of it will gag you too! My skin stayed very clear while I was on the Prednisone for 9 months. My skin was the softest ever while I was on the high doses and I felt soooo good then also, but my mind was so foggy and feeling of being heavily medicated was hard, plus all the muscular shaking. I use to get mad getting behind people in traffic that drove like the little old lady wearing coke bottle glasses. Then I became that little old lady when I was on the high dose Prednisone. I told myself I would NEVER complain about any one going to slow in traffic again!!!! I still have joint problems after 4 months off but also heard it takes 2 months recovery for every 1 month on Prednisone. hopefully I will be better within the next year. I had a lot of nausea after getting down towards the lower doses, hated to get up in the morning, was like having morning sickness and bouts through out the day also. I would just go home after work and lay down and also on the weekends. I feel for anyone with small kids who have to keep up with work, daily family life and trying to cope with illness and drug life. I'm just glad my kids are grown while I'm going through this mess. My daughters have been very supportive and helpful. Lower doses for me were the worst though. My Dr. wouldn't give me anything lower than 2.5mg. I was having a hard time and cut those little suckers in 4 pieces and took them a week every day and then every other day till I could stop. It's hard at first going off but once off, didn't go back again. I haven't found anything yet to help the joint pain but they say time cures all. I still have racing thoughts at times and some concentration issues also. Sometimes I think I'm a little old lady with ADD!!!! ha ha Had some issues with anger, wanting to slap co workers into next week at times. A lot of problems with taking Prednisone is because the adrenals shut down and it affects what is called the HPA axis. The Hypothalamus in the brain controls numerous things in the body and I think that's why the body balance becomes disrupted, it effects hunger,taste, smell, weight, on and on and on. Everything at first tasted to salty or sugary. Some foods I didn't want to eat because they tasted awful. Maybe that helped me also with not gaining to much weight. The pituitary and hypoThalamus try to balance everything and with out the adrenals not working a person becomes screwy bodily and mentally. I did a lot of reading online while I was off work for 2 months, especially with trying to take care of my self physically. If you have problems with being hungry eat something protein, it will stick with you longer and eat small snacks between meals, like bananas or avocados, raw veggies too. I would make a pot of beans once a week, because of lower calorie intake and they are high in protein, any kind of legumes are good. For awhile I craved liver maybe needed the iron and B12. Try to take a short walk everyday, even if it's 2 blocks. Maybe this will help someone out there cause the Prednisone is crazy stuff. Take care of your selves and you will be better, it may not seem that way but you will get better in time, just don't GIVE UP!!! L. from Kansas

NO SIDE EFFECTS: POSSIBLE HELP WITH SUPPLEMENTS had very serious sinus infection. two weeks of anit-biotics with no result, symptoms got worse, before taking levaquin for an additional two weeks. within three days was back on my feet. i previously have taken the supplement MSM for continual joint pain in past years, and was pleased to find a wide array of other health benefits from taking it. Having two kids, building a home and busy work schedule led to neglect of my heath supplements. (not smart) Resulting in immune dysfunction, chronic sinus infections over the last two years. After realizing that my health was was in ruins, i decided to start taking my supplements again around the time of my course of levaquin. started taking my multi's again and more importantly my MSM ( similar to chondroitin or glucosamine) Note: I recently read that MSM has been proven to help the body fight infection, as it is required to be present for the body to fight infection. MSM is simply (organic sulfer) found in everyday food we eat. with processed foods and preservatives this element is removed. To make a long story short, after first taking levaquin, I did have some minor joint and back pain (among other things) started taking MSM and effects were diminished, and then gone. After reading what others went through, i made the correlation between the two, and with my previous history of joint pain i would think that i would be a prime candidate for these symptoms. It worked for me, it may work for you, and the worst case scenario is that is doesn't work but you become stronger and healthier from taking it. Brief History. I use to love to play basketball. after joint pain and swelling could only play once a week, and couldn't even walk up stairs the next day. after taking MSM continually for a couple of weeks i was able to play daily, for as long as I wanted. a true miracle. The good news: its at the health food store, it's really cheap, and its a completely natural supplement. take 1000 mg daily with meals or without. its worth a shot for no symptoms.

I posted a short one, would like to add to it. My daughter was taken by ambulance twice last week to the ER, after having violent seizure like episodes. On second visit, she had several while we were waiting to be seen. She spent 5 days in the hospital, having these episodes as few as 10, as many as 30. lasting any where from 4 minutes to 40. She screams out in pain. It's like her entire back, including arms, legs, hands, feet are having a severe muscle spasm at that same time. If you look up dystonia, the definition fits. Dr. said it was too severe for that diagnosis. They ran EEG, EKG, Cat Scan, MRI, X-ray, extensive blood and urine work, video for 24 hours, with EEG. Everything was normal. DR decided it was stress and anxiety. Released from hospital still having episodes. I called a dystonia specialist in Maryland, she asked if she had the GARDASIL shots. Said it sounded like a side effect she had heard of. Well, after reading all these blogs, youtube, I believe it's the GARDASIL causing her problems. I knew it wasn't stress & anxiety. We are currently detoxing with ionizing foot baths, gluten free diet and meds from Health food store, called HMD-Heavy Metal Detox. I feel we are moving in the right direction. My daughter is a cheerleader, dancer and honor student. She just wants her life back. It has been on hold for 2 weeks now. I consider her one of the lucky girls, after reading many blogs. God Bless each and everyone of you. Sign the petition to stop hurting our girls.

I am SO sick at my stomach right now after reading all of these posts. My son is 2yrs old and was put on Singulair right after the new year. We have noticed a horrible change in his behavior....but we attributed it to his age and the fact that he is VERY strong-willed. However, thinking back, he has had some hallucinations. We had a babysitter tell us that when she tried to put him to bed that he cried and told her that there were monsters in the closet. When she picked him up and took him in the kitchen for a drink he kept reaching at the ceiling trying to grab something. Just last night he told me that he saw his Grammy dancing in the living room....my Mom wasn't even there. He has been throwing horrible fits to the point of gagging himself, hitting himself, kicking, hitting, screaming....you name it. At the end of them, I am usually in tears and we are both exhausted. I am not the only one who has experienced this with him....my Mom has too. He is also on Veramyst nose spray....both meds are for allergies. We have taken him off of both and decided to go a more natural route. We have bought local honey, an immune booster from teh health food store, and have him on a really good brand of liquid vitamins. It is hard as a parent to make decisions about your child. It is even worse when you realize that the decision you made has affected your child in a horrible way. I plan on giving him A LOT of attention tonight and giving him a big hug! I just want my fun, playful son back! Good luck to all of you and God Bless!

Besides having all over muscle aches with this medicine that 'doesn't get absorbed in the blood', I had so much hair fall out in 1 week. I called the doctor and she said it was not a side effect. Well, I had a huge hand full of hair to challenge that statement. I quit taking it and the hair is growing back in. I'm taking the red yeast rice capsules from the health food store and will see how that is working.

Hello, I have been on synthroid since 1999. I am hypothyroid with hashimotos. Endr. docs couldn't seem to get any levels right so I went to my Intergretted doctor . and he put me on 1/4 grain armour so I took anywhere from 50mcg to 100mcg of synthroid in the AM and 1 armour at night. It worked but after a short while I felt terrible. Then I had to start taking high blood pressure presc., it was about 170/116 after I had some shots in my back for pain, never had hp. before these shots. In Sept. of this year I stopped the Topralxl because I felt my heart was pounding out of my chest which I was in hospital for they said I was having a heart attack, had anigram, but I didn't have a heart attack and and angigram came out good. Then this summer they put me on 2 Topralxl. My heart was pounding with 4 extra beats so with a ultra sound{echo]of my heart and 24 hour halter it was all good, so I figured it had to be something I am taking. So that lead up to the stop of Topralxl which I researched and took a few things from Health Food store and got my pressure down to 140/80. My heart quit racing and beating so hard, but still felt depressed, puffed up, confused, teeth felt loose, urinated a lot, gained weight, rashy on my neck, tired all day, did not sleep good, eyes were always red and watery, skin and hair dry, blemishes on my face{ I am'56 yrs. old] just didn't feel good and the list goes on. Came across this site and read them all. Realized so much from you all. Sythroid only has T4 which your cells should be able to covert T3 out of that. T4 stores in your body and T3 is used up as the day goes on. But some peoples bodies don't convert the T3. Several people have talked about TSH which is your thyroid stimulating hormone which comes from your Pituitary Gland. When you thyroid or your meds. don't give you enough thyroid of what you need the Pituitary kicks in there to tell your thyroid gland to to produce more. It's not good for your TSH to be high so Docs. put you on a higher dose of Sythroid or whatever you take for the pituitary to stop producing TSH. So I want to say I am not a doc. but have felt so terrible and researching what I could I quit my Synthroid on the 29 of Dec. and started taking my armour thyroid 1 AM, 1 late afternoon and 1 PM on my own cause I figured I am still getting my T4 and T3. I went to my Endr. Doc. yesterday and told him I went off my Synthroid and just taking Armour. and told him I felt so terrible, after stopping the Topral heart felt great but the rest of me felt drugged, I just felt desperate and horrible. So again it had to be something I was taking. Well I have to say that I feel 100% better than I was. I am much more alert with my surroundings and whatever i am doing, sleep so good, teeth feel good, no rash, urinate normal, not confused, face cleared up, eyes not red or watery, pretty much I already feel normal again. Working at my job is not exhausting, my neck, which I didn't mention before quit hurting. In a whole it was the right thing for me but maybe not for everyone. I just felt that it was slowing taking me out. Blood Pressure, Thyroid issues are to be concerned about but seems like a person should feel better not worse with the meds. So this is the information I have learned and I'm sure there is much more. So good luck to you all and listen to your body and talk to your doc.about how you feel. It can be very scary when you are diagnosed with something but we are all different in what our body needs and our side effects.

I have been on lipitor 10mg for about 6 mths (after reacting to lipex with severe hip pain and going off that). Am now experiencing abdominal pain, severe headaches, excruciating neck pain and to top it off a droopy eyelid and loss of extreme peripheral vision after a bout of flashing auras and fluid like waves in the outer edge of my eye. After tests my retina is not detaching so what is the cause then. My cholesterol is high when not on lipitor and am wanting to lower it without drugs. I could do with losing 10kg weight but will that bring down the cholesterol. I walk every morning for 30-40 mins. Diet is healthy, a few junk things each week but not overly so.

I have been on Advair since Feb. of this year, I have had a lot of these side effects but didn't really realize it was from this med. At first I was told to take it 2x a day, reading the directions it says it has to be 12 hours exactly apart. My work schedule didn't allow that so I just took it 1x....Working 2 jobs I just thought when I couldn't sleep and was always tired, it was from working a lot. When I told the Dr. about not being able to sleep more than 4 hours, I was told since I was taking the meds 1x a day that wasn't it. After a bad cold and bronchitis I was told I had to take the Advair 2x a day, now i'm more tired than ever, still can't sleep and have a headache that won't go away even with migraine medicine. I'm even jittery and forgetful--kinda ditsy now and itchy off and on all day...After reading this blog site I see its not in my mind and i'm going to stop taking this med. I think i'm going to the health food store and find something natural.

Advair made me tired, so tired, I felt like the simplest chore was exhausting. I was told by the pulmonologist that of course the fatigue was unrelated to the medication. Personally, I think the doctors push the meds that they get perks from the pharmacy companies. They may get good results from 75% of their patients but be darned the 25% that may be sensitive to the meds, Modern medicine?

I am 39 years old and have been on Omeprazole for 6 years. I have had the worst year ever. I was always a healthy and fit guy until 2008. I had chronic headaches and extreme fogginess which led to me having an MRI and seeing a chiro(all negative). I had chronic chest pain which led to EKG's, stress tests, ER visits, and tons of blood work ranging from cardiac, glucose, liver, renal, thyroid, etc...(all negative). Did gastroscopy and found esophagitis and gastritis. Upped the dosage of Omeprazole. Then I started getting tremors, muscle cramping, muscle pain, fatigue, blotchy red skin, and continued fogginess and lightheaded.

Did I mention i still have constant heartburn despite all the Omeprazole. I have done everything...tilt up head of bed, bland diet, no coffee or alcohol, no eating late evening etc....

Doctor put me on Fluoxetine (Prozac) for all my stress and anxiety from these crazy symptoms. After seeing this site and reading all your testimonies I am now thinking it is from the Omeprazole!!! Scary thought to stop since my chest pain and heartburn can be pretty severe and constant. What do I do? Feel like I'm caught between a rock and a hard place here.

Changed the texture of my hair, now it's stiff and breaks constantly. Also falling out- FAST! Most hair is gone. Unable to digest food and pain in right side of head. Doctor won't believe that any of it is from the Lisinopril HCTZ and won't try something else. Have limited ability to pay for medical treatment due to disability and can't seek other medical advice so am stuck with this due to high blood pressure. Any suggestions?

Pain in right side lower back (around waist area). Like you have gas in your back. Constipation...dizziness.
lizzy

I was on Lipitor for less than a week 2 years ago and the muscle pains were so bad that moving my head was painful. I called the doctor's office and was instructed to stop taking the medication; which I did and felt 'back to normal' within a few days. I haven't had my cholesterol checked since that time, or if I did before surgery, no one mentioned anything negative about it. However 6 weeks ago I had a heart attack. Apparently my cholesterol was twice what it should it have been, and my potassium was incredibly low. So I'm now on Lipitor (standard procedure after having a heart attack and high cholesterol seen as the cause of it) to ensure that another blockage does not occur.

The only problem is I'm now bloated even though I've changed my diet drastically (no more junk food or soft drinks, no 'white' flour products, no dairy products with more than 5% M.F and lots of veggies and fruits). I've lost 3 or 4 pounds but my pants are too tight around my waist, and now I have a my upper abdomen bulges over the waistline. Besides that, I get muscle 'kinks' in very places and after sitting for more than 10 minutes I limp when I take the first few steps.

People have told me to 'keep taking Lipitor and Plavix' but exercise more. The only problem with that is that I have a brain aneurysm and the neurosurgeons don't think it can be operated on 'without it being a very high risk procedure'. The first one ruptured 10 years ago and since then I've managed to control my blood pressure. However the meds I took for that was what lead to my potassium being so low that my electrolytes were imbalanced. That combination of low potassium and high cholesterol is what lead to the heart attack.

I'm 54 and feel as though I'm losing control of 'how' I feel. Between Lipitor, Plavix and diuretics and medication for hypertension I'm not sure if it's one drug in particular that's making me 'ache, limp and look like a blimp' or if it's because of the interaction of all of them. How do I decide 'what' to stop? What's more important to look after first - my heart or my brain?

EVERYONE PLEASE READ!!!! GARDASIL HAS DESTROYED MY LIFE! I am 24 years old and a year and a half ago I was graduating college and planning to be a professional dancer and go to law school...I was perfectly healthy and energetic! In February of 2007 I received my first Gardasil shot. After a few days I started to feel as though I had a Urinary Tract Infection and was also feeling more tired than usual. The doctor gave me an antibiotic and sent me on my way.

In May of 2007 I received my second Gardasil shot and yet again, a few days later I started to feel like I was getting another Urinary Tract Infection. I went to the doctor numerous times between the second and third shot...all for bladder and urinary tract pain. For months I was on different antibiotics and they were not making the pain go away. After visiting a number of urologists, I found out that the urine cultures had all been coming back negative - showing no sign of an infection, so the antibiotics were pointless. All tests that I had run, both blood and urine came back normal. It is not standard procedure for a doctor to call you if your test results come back normal, but there was clearly something wrong, so I searched for a urologist who would believe me that I wasn't making up the pain I was in.

In August 2007, I had a cystoscopy done (they took a scope and went into the bladder to look in the bladder wall) and they concluded that I have an incurable bladder disease called Interstitial Cystitis. This is a condition where there becomes a defect in the bladder wall causing it not to have the protective mucus layer inside of it. The pictures of inside my bladder show red, raw skin, obviously showing the severity of my case of it.

There is no evidence as to what causes Interstitial Cystitis, and there is no proven successful way of treating it. The initial signs are exactly the same as a Urinary Tract Infection (painful bladder spasms, painful urination, body aches and back pain). The main difference is the fact that it is not an infection. There are thousands of people with Interstitial Cystitis who are misdiagnosed as having chronic Urinary Tract Infections.

I received my third Gardasil shot in October of 2007 and that is when EVERYTHING fell apart. The bladder pain became constant and there has not been one minute in a day since that shot I have not been in unbearable pain. This is when everything else in my body began to crash down as well. The other health problems and side effects from the Gardasil that I am having are constant sore throat, vicious migraines, vision changes, back pain, body aches, joint pain, sinus problems, vomiting, constipation, dizziness...I could keep going on forever!

I have tried all of the conventional treatment for Interstitial Cystitis and have gotten NO relief from the pain and other side effects. The doctors didn't know what to do, so they put me on OxyContin and a diet consisting of no acidic foods. That has now posed its own set of problems seeing as now my body is addicted to the narcotic, and I have gone from 5'6'' 125lbs to 100lbs over the course of a year due to the diet. I am extremely malnourished and have to take B12 vitamin shots once a week due to the severe anemia. I am 24 years old, and feel like I am 100. I can not live a normal life, I am going to lose my job from numerous absences, I lost my fiancé and am not able to have an intimate relationship anymore, I am extremely depressed, I have to have my family clean my apartment because I am too sick to do it, I can not do social activities because I am too tired and in pain. This vaccine has DESTROYED my life! I am desperately seeking out someone else who is having bladder problems due to the Gardasil so that I can contact an attorney. This needs to be OFF the market a soon as possible so that it does not run any other lives! Gardasil has caused some deaths, but in my mind, I'd rather die than live with the pain I am having. I did notice there are some posts regarding girls getting urinary tract infections... PLEASE PLEASE PLEASE have your urine cultured because there is a good chance it may be Interstitial Cystitis!

I am desperately looking for someone who is having some of these symptoms so that I can go to a lawyer and get something going before things like this happen: Numerous states are pushing to make it mandatory that girls receive the vaccine before they enter the 6th grade. We can not let this happen! We all need to stick together and somehow fight this and get out lives back!

Let me know if you are IN - and also what you thought about my post!

You can email me at ******

Bless All of You!

*~Amber~*

Hello all,
I'm a 45-yr old Air Force Major (Male) recently diagnosed with asymptomatic chronic Atrial Fibrillation (As in I have it and was walking around not knowing it). When I went to see the cardiologist, my B.P. was only 120 / 74 (Which, until they changed the rules, used to be normal)and he puts me on Diovan 80mg once a day plus Coumadin 5mg. Well the Diovan almost made me faint and I had numbness in both arms, plus a funky rash, kind of like chicken pox showing up on my arms and thighs.
I went online and read horror stories of Diovan so I stopped taking it immediately (I had only taken four doses and never had any horrible symptoms until after I took the meds!). Then the Dr. put me on an Event Monitor and it showed I was indeed in A-fib all the time, plus at night, my heart was racing briefly to 200 a minute while I was sound asleep. So he puts me on Toprol XL 100mg once a day.
Immediately I had trouble sleeping (Which I never had before, ever!) with crazy dreams and tossing/turning. My B.P. dropped to 88/65 and my fibrillating heart rate was 64!!! I was so mad because I actually felt better before the meds. I found this site and saw what everyone was posting and immediately took myself off the Toprol XL.
The day after stopping the Toprol I had slight chest pains (Like angina or gas bubble) but they went away on their own. I slept fine the next night.
I'm having an Electro-Cardiversion done on the 21st July to see if I can stop the A-fib and get in normal rhythm. I know the Dr. is going to be mad at me for stopping the Diovan and Toprol, but I'm sorry, I'm convinced there is a better way to beat all this (Namely exercise and eating right). Being in the service means you have to be Mr. Physical and Mental "perfect" all the time. I cannot afford to be diagnosed with depression in my line of work! Thanks to all on this website and I wish you the best.
PS. for those who think I'm being ignorant of my medication, I have a nice fat insurance policy and Power of attorney for my wife and kid in the event I keel over!!! I may be medication intolerant but at least I took care of my family.

I'm not sure what I should be feeling with this yet...I'm just wondering who's experiencing what side-effects. I've had bad experience with Advair...pain all over the body. Qvar is not helping...so I was given this. I'm afraid to try it, considering the side effects listed are similar to that of Advair. Would anyone recommend this drug at all?...or is it the same deal as the rest?