Colonoscopy symptoms and conditions

I am looking for any information anyone has about the possibility that Singulair causes colitis or that it can lead to inflamed colon and bleeding colon. My daughter is 4 years old and has never been a sick child. In September, she started bleeding from her colon, and a month later, she was finally diagnosed with colitis after having a colonoscopy. The doctor prescribed Prednisone (steriod) and Phlagyll (antibiotic) (spelling?). I decided to stop giving her the Singulair that she had previously been taking because I didn;t want her to have so many drugs in her system as one time. After a few days of the steriods and antibiotics, she was well, with no signs of problems. Everything was going great for a few weeks, but last week I started giving her the Singulair again, and her colits symptoms have come back. Has anyone else experienced this in relation to Singulair?

I've had several bouts of Diverticulitis over the past 6 years, and this drug has worked like magic , after I was diagnosed visually during a colonoscopy. The first two rounds of 10-day therapy for two separate bouts which occurred months apart, produced no side-affects whatsoever, and the drug starting working quite soon, a perfect response. The third round however caused some stomach ache and mild dizziness for all 10 days. I realized later that I took the medicine after dinner for the first two rounds, but in the morning for the 3rd bout of diverticulitis, which occurred about a year later. Yet another year later for my 4th bout, I found that taking before bed was right for me, and even helped with my sleeping.

I have been on Yasmin for over 5 years, and just thought that I was a hypochondriac. After starting Yasmin I experienced severe nausea and unrelieved hunger pains. I saw a gastroenterologist who performed an EGD and Colonoscopy at the age of 20. It was normal and I was placed on Protonix to help with the GI issues. Also I have severe joint pains in my knees, hips, elbows and shoulders. I have been tested for everything from Lupus to Rheumatoid Arthritis, and it was all negative. I get headaches, have little sex drive if any, my skin is not clearer than usual and nor has it been since starting Yasmin. Thanks to all those people who have voiced their concerns and shared their stories, it makes us feel less crazy. I threw out all my birth control pills last night and I am going to try another form of contraceptive. I mean my headaches and chest pains have gotten so bad that they have forced me to go to the ER on several occasions. I DO NOT THINK THE BENEFITS OF YASMIN OUTWEIGH THE RISKS ASSOCIATED.

I have had a similar experience as many others who have written. I took Wellbutrin (with no side effects) for years, until my insurance company made me change to Budeprion in June 2007. Almost immediately I started feeling dizzy and had terrible nausea. My MD kept saying it was not the Budeprion, but that was the only new medication I was taking. Over the next year, I had a colonoscopy, endoscopy, CAT scans, MRI's, blood tests and breath tests to find out what was wrong. Everything came back negative, and my MD diagnosed me with Irritable bowel syndrome. On my own I decided to cut back the Budprion from 300 mg to 150mg, and I did feel a little better for awhile, but then the nausea came back worse than before, and I definitely noticed that it started about 4 hours after taking Budeprion. I decided to skip it entirely for a day or two, and each time I did, I had no dizziness or nausea. My MD can say whatever she wants, but I know the medication is what made me sick. I don't know if my insurance company will let me go back to Wellbutrin, but I do know I will never take Budeprion again.

Hi, I am a mother of 2, and not quite 23 years old and got the Mirena inserted at my 6 week check up after having my second. I read all the literature that the Dr. gave me and I was sure that Mirena was the right thing for me (no where in the brochures did I read anything about the symptoms Ive read about here or anywhere else on the internet). I started having incredibly horrible mood swings, bloating, fatigue, nausea (sooo bad, every day) back pain, neck pain, no sex drive (!!!), depressed, lazy, headaches (to the point where I thought my head was going to explode), constantly hungry, acne, smelled maple syrup constantly, complaining all the time about everything, weight gain (only 7 lbs but I just had a baby, I need to lose weight, and I'm nursing),chest pain, and some other symptoms but the most important one is the stomach pain i was having. The pain in my stomach felt like a knife, and I kept having pain in my right side. So after a few days of this pain I went to the dr. he ordered an ultrasound of my abdomen and I am scheduled to get that done Wednesday. My doctor thinks that I may have gallbladder disease or something else seriously wrong with me that we suspect is induced by the Mirena. Keep in mind that I've had this thing in me for about 4 months!!! So after my doctors appointment I typed into google "side effects from Mirena" and Omg, I wish that I had done that before I got the thing inserted, those brochures about the Mirena make it seem like a Godsend and I am all for a lawsuit due to the problems I am having and the depression Ive felt. My 3 year old has suffered from my mood swings, every time id feel it coming I had to make her go to her room :( that poor girl deserves to have a mother that is not so depressed and ill that she can actually play, and both of them deserve that really, and im doing the best I can.... anyways I removed it myself yesterday, i had a hard time finding it but I took it out and I feel as if a huge burden has been lifted, EXCEPT I have been cramping very bad, spotting and incredibly sick, i also read about this thing called "the mirena crash" no matter how long you've had it in, if the hormones were in your system then you are effected and can feel very ill from it (and it can happen to women who had no problems while on it at all, even after 5 yrs). Im hoping that I have nothing wrong at my doctors appt on Wednesday when I get the ultrasound, and it may just be a cyst, turns out that is a side effect of mirena as well, that and bleeding the first several months (oh yeah, I did for about 2 months maybe 10 weeks altogether) Im also hoping that my daughter whom I am nursing is not sick as well :/

oh and for anybody out there thinking that the only women gaining weight are fat to begin with, well I am usually 105 lbs, after my baby I weighed 145, lost some weight, went down to 130ish gained it all back then some, losing weight is easy for me because I diet and exercise like I should, now I am doing all that and nursing a child.... and hello weight, when it really should be goodbye... well goodbye mirena I WONT miss you!!!!

was give coumadin in November, and by April my stomach hurt so bad I couldn't stand the pain. i hac a colonoscopy, and sigmoidoscopy. This doc couldn't find anything wrong. Made another appointment, ad just had the colonscopy, and sigmoid again. I have ulcers in my stomach, and the upper part of my intestines.

I know it has to be the coumadin.

I have been on Yasmin now since around 2004-2005.

I just recently started experiencing really severe mood swings, I would go so far as to say that I have become enraged over things that are so insignificant and that would normally would not bother me even on a bad day. This anger that usually starts right before my period made me start thinking that it might be from my birth control, even though it has only been an issue over the past six months. I have never in my life suffered from PMS, so this was very out of the ordinary for me, but I just assumed I was over stressed and ignored it.

I started looking up side effects of Yasmin, and came across this site which sent me into absolute shock.

Everything listed here by other people, I have experienced over the past four or five years. It all makes sense to me now after reading about other woman's experiences while taking this medication.

I started seeing a GI doctor in 2005 because of extreme diarrhea, nausea, fatigue, dizziness. They ran multiple tests and scans, I had an endoscopy and a colonoscopy which showed irritation. I've been on multiple medications for what they assume is IBS. I was also diagnosed that same year with asthma because of extreme shortness of breath. I am on asthma medication and inhalers because I get very short of breath with exercise which was never an issue in the past. I was 110 pounds, and healthy and active in 2005. I then started to gain weight, and at my heaviest I reached almost 180 lbs (and I am only 5ft 2in tall).

I have since lost weight, but can't seem to get below 140 lbs no matter how much I try. In March of this year I started having extreme pain in my right upper abdomen, and was told I had gallstones and needed to have my gallbladder removed.

It is just makes me so angry to know that no one is doing anything about this and this medication is still being prescribed to women. It angers me that my doctor's knew that I was on this medication and never once questioned that it may be the birth control making me sick. I don't even think the doctor's are aware themselves.

I have been on birth control since I was sixteen to help regulate my periods, and I am now twenty-eight. I have always had difficulty with the pill and have tried many different types of birth control medications. My doctor recommended Yasmin to me because they though I might have poly-cystic ovarian syndrome even though the tests never confirmed it. I will take my chances because I am not taking birth control ever again!

I have been on Lithium Carbonate (1800 mg/day) for over 4 years. Lived with diarrhea, acne, tremors, etc. throughout, but otherwise loved the drug. After filling toilet with blood several times last week, I went into the hospital. Colonoscopy & endoscoopy revealed severe diverticulosis and severe Barrett's esophagus, respectively. All involved are shaking their heads, as these tests were relatively normal 3 years ago. I suspect Lithium.

I have been on Diovan 80 mg for 3 years and have experience a lot of symptoms listed above. 8 weeks ago I got very sick and had constant diarrhea (my stool looked like it had oil floating on the water) and lost 40 lbs. After numerous blood work, ultra sounds, ct scans, colonoscopy and many stool samples I found out thay my pancrease was not working properly. The doctor told me that diovan had caused the problem with my pancrease. I now have to take a medication not to help me digest food and they have changed my bp pills. I am hoping this will work because I have missed a lot of work in the last 8 weeks and they tell me where I got so weak it will take me months to recover from this. Anyone having stomach problems please consult your doctor to see if you are having troubles with your pancrease.

Like many of the others who have posted to this site, I have been dealing with what I thought was IBS for the past 3 years or so. I'm healthy and mid-30s and couldn't figure out what was causing it. Colonoscopy and other tests showed that all was normal. I don't drink caffeine, coffee or alcohol. Healthy as can be. Finally discovered it was a dairy intolerance. Coming off dairy solved the diarrhea issue but really limited my diet. Shortly after I discovered Lactaid Fast Act supplements and started to take them at meals when I had dairy.

For the first three weeks, the pills worked great. I loved them. I could eat like normal again without diarrhea. But after that time, I started to feel a sharp pain in my stomach when I take them...like someone slugged me in the stomach. It always comes within 5 minutes of taking a pill. Since then, it has gotten worse. Gas, bloating, and a constant pain (gnawing feeling) in my stomach that nearly has me doubled up. I've never had an ulcer, but from what I've read, that's what it feels like. I decided to stop using the pills.

I just discovered this site and was amazed to see that others have had the same. I should have checked for side effects before I took it! I've not had the vomiting that many of the others have had, but I won't be taking it any longer and risking that!

Hoping there is some alternative solution out there. Hard to imagine the rest of my life without cheese or dairy in anything (bread, dressing, etc.).

There is a class action lawsuit for anyone that took Yaz/Yasmin birth control. I just saw the commercial the other day from an attorney in Denver and it's nationwide. Please call Nolan Law Group - Valerie Romo at 888-630-9340. They are handling it nationwide.

So let me tell you my experience...I started taking the generic form of Yasmin (Ocella), mind you I have been on four other birth control pills and had no problems. The first cycle I had with this pill I felt like I had the flu with no sinus symptoms, so I went to my doctor, it was flu season, did a flu test: negative. He told me it was just a virus and my body will kick it out in a few days...so I went back home and went back to bed...not six hours later I had a constipated feeling...go to the bathroom and I was having severe bloody diarrhea. I had to call my husband to come and get me to take me to the ER because my abdominal pain was so severe. The ER did a CT (yummy on the barium milkshake by the way, not!) they said I had colitis...went to a GI doctor and I went through 2 CT's, a colonoscopy, endoscopy, small bowel series, sonogram, and blood work to see if I was allergic to gluten and lactose...I was limited to jello and apple juice as my food supplements...I was STARVING for three months. I realized that when I would go to the ER they would give me antibiotics and I would feel better until about 24 hours after I ran out...I called my OBGYN and he told me flat out, stop taking the pill you are having ischemic colitis and it is a severe reaction to that pill you are taking...I also wound up having surgery because endometriosis runs in my family and he wanted to make sure mine didn't get any worse...which was wonderful...I quit taking the pill and I have to be on a pill due to hereditary gynecological issues...so I was put on Orth-Tri-Cyclin and Life is wonderful again!!! So for you ladies...some of you had it easy!! I almost had to get part of colon removed because they thought it was UC! Twelve weeks in a colostomy bag...NO THANK YOU!!

They think that I have either crohns or ulcerative colitis. I have tried antibiotics, lialda, mesalamine enemas, with no improvement. After another colonoscopy they put me on prednisone at 40mgs, 30, 20, 10, then 5 decreasing weekly. Well the first week was okay. I had some of the side affects, insomnia, extreme hunger, and crazy. I could deal with that. But then when I decreased down to 30mg, my body flipped. I awoke from the middle of the night with burning pain in the knees. So bad I took 4 ibuprofen and threw myself in the tub with epsom salt. I thought okay that was weird because I have never had a joint pain in my life. I saw the gastroenterologist that day bc I was still having abdominal pain. He totally blew off the knee pain and said he had no idea what that was. I thought okay maybe it will go away. A few days went by and nothing. 3 days later and I awoke one morning crying in pain because of my legs. I called the on call doctor who also said he had no idea and go to the er. So I went crying hysterically for 4 hours. Even after 3 rounds of dilaudid I was still in pain. They suggested a Rheumatologist. So I went to one a week later who said I was going through steroid withdrawals. And there is nothing we can do but treat the symptoms of pain. I am now down to 10mgs have been out of work for 2 weeks and am absolutely miserable with severe leg pain, muscle weakness and fatigue. He also adjusted the drop down increments to 5 instead of 10. Anyway I will never take this drug again and I think they rushed to this one. Just wanted to share. I am glad I found this website because I went from a fully functioning physically fit 28 year old to a crippled crying crazy person. I think I was scaring my husband, honestly, until we both read some of your postings which were similar.

I started with Lisinopril and had severe isolated visceral angioedema. Thought I was going to die. The attacks felt worse than childbirth. Urine flow would totally stop and bladder would cramp. Bowels would not function. Over a 10 on the pain scale. Went off Lisinopril and 3 days later Dr. wanted me to start Benicar. Within 5 days I was in emergency room with visceral angioedema even worse than the Lisinopril. I have had CT scan, ultrasound, numerous blood and urine tests, PAP, colonoscopy and everything is negative. It has taken a full week for all symptoms to stop. I finally feel normal again after 2 months. I cannot take this family of drugs. And Dr.'s need to be more informed about this serious side effect. My Dr. never considered it could be the Lisinopril or the Benicar since I didn't exhibit any facial edema. More information about this rare, but serious side effect needs to be published.

Hi,

I have had my Mirena since March 2007 and until Nov 2008 have not had any real complications. I do still have a period, it's lighter but lasts just as long. In Nov 2008, I started having problems with dizziness, stomach pain, nausea and at the time I was diagnosed with an inner ear infection, I also had a CT scan done which was normal. But after taking the antibiotics as prescribed the symptoms persisted for 3 weeks then went away. It all started again in Feb 2009, waking with severe nausea every morning, loss of appetite, tired and stomach pain. I went to the ER and had bloodwork which was normal, and a urinalysis, which showed a UTI infection. I was given antibiotics for this, but yet the symptoms persisted for 3 weeks. Both of these episodes followed my menstrual cycle. After the last bout, in which I feel completely normal, it started again. My period was two weeks late this month (March 09) it started on March 18th and on March 19th I started experiencing all these symptoms all over again. I have, bloodwork, preg tests, a colonoscopy, a stool sample, and a pelvic ultrasound, all of which have been normal. I am scheduled in a week to have an ultrasound of my gallbladder, but I really don't think that's my issue. I have lost weight, have no appetite, and wake every morning at the same time with nausea. I am seeing my family Doctor again tomorrow, he has discussed sending me to an ENT, but he is also removing the IUD tomorrow. He is doubtful that it is causing these problems after two years, but said strange things happen so better remove it to be safe.

Has ANYONE noticed a change in bowel movements/bloating since being on the Mirena? Ive had it since August of 2008 and since then I have gained 20 lbs, ALWAYS bloated and my bowel movements have changed in consistency. My doctor has sent me to have blood work, CAT scan of abdomen and a colonoscopy and the results where all negative. At this point I have NO DESIRE to have sex, Im 42 and don't want anymore children and cant take regular birth control due to migraines. But at the end of each day my ankles are swollen and I feel huge?? Anyone with LIKE symptoms?

I still currently have Mirena in. I have had it for 2 years 2 months. I am 27 years old. I have had no children. I was on the Depo shot for 8 years. Then switched over to Mirena. I was happy and it worked well for me for about 6 months. Then I began to get the dreaded side effects starting with horrible scaring acne. I got many treatments from my dermatologist including trying to take Yaz birth control (he knew I already had Mirena in) to try to stop the acne. The only thing that did help with the acne was blue light treatment combined with Levulan but I have to go often to get it or else the ance comes back full force and the acne treatment is expensive. For the past year I have had a sharp shooting pain in what feels like my right ovary shooting down my right leg. I went to OB/GYN after multiple pap smears/ultra sounds and blood tests, she couldn't find anything wrong. She sent me to see GI doctor. I went to see him in July 2008. He thought I might have appendicitis so referred me to get abdominal CT scan. Insurance refused to pay. He said I should get a colonoscopy. I refused. I have been ignoring the pain near my right side and down my leg ever since. If I really did have appendicitis my appendix would have burst by now. For the past couple of nights I have begun to have night sweats. I do believe all of the above is related to Mirena. I have begun to discuss with my husband alternate birth control and removal of this thing. If we get a law suit going I want to be involved.

I cannot tell you how glad I am to have found this website!!! My husband I got married in October 2007, and I began using the ring since condoms didn't make sense to us as a monogamous couple and the risk of missing a pill was too high. Up until yesterday, I was extremely excited about the pill. My sister and some friends of mine had experienced frequent vaginal infections with the pill, but I found that mine actually lessened! My periods were shorter, my cramps nearly disappeared, my face was the clearest it had ever been and (I thought) there were no side effects!...

In November of 2007 (a month after I began using the NuvaRing) I started to experience intestinal bloating, cramps and diarrhea. We chalked it up to the difference in food and climate (I had moved from small town Illinois to Mexico City) and stress levels--although my stress levels were MUCH higher in college and high school. My mood started to deteriorate, I was constantly exhausted, and in December 2007, I developed severe digestive problems, a swollen pancreas and chronic (15 - 28 times per day) diarrhea. I was already a fit size 6 when all of this started and in just one month I dropped 13 pounds and size 4 clothes fit me loosely. Once again...we chalked it up to me being in Mexico and subjected my body to several rounds of fierce antibiotics (given to me by three different specialists). When that did nothing to help, my husband took me to get a colonoscopy. They found nothing. I spent hundreds of dollars on allergy tests and treatments. No improvement. I went to a general practice doctor to take blood, urine and stool samples. They found nothing--no amoebas, no bacteria and no other rareties. Chiropractors, acupuncturists, herbs, enzymes and probiotics did nothing to help me.

Then between February and March 2008, I gained 35 pounds (that I could not lose even with anorexic-like diet and exercise)--but maintained the digestive problems. Since that time any food with fat, carbonation, alcohol, artificial coloring, or spice has caused me so much bloating and gas that I no longer go out to eat and party with my friends. Miraculously, NO ONE--not one single doctor or specialist--suggested along the way that it could be my birth control. I was told that my depression, weight gain, loss of libido, digestive problems, chest pains, night sweats, mood swings, numbness/tingling in my fingers was all in my head! Thank you all so much for your posts! It's like seeing a light at the end of the tunnel...

My mother, 70 years old, been on Coumadin for 3 years (doctor said best to take since she suspected heart palpitations). Mother developed gradual memory loss, over the 3 year period, we didn't think anything wrong!! just a part of aging process!! Then one night she fell on the floor, stroke, we took her to hospital - done MRI and CTscan - result: severe brain bleeding. From that time - 4 months ago - she is now diagnosed with Dementia. I cant even describe how I feel about god damn Coumadin. Wish they never given it to her in the first place.

49 year old male started 4 years ago at 20mg and 10mg HCTZ. some results in lowering BP. 2 years ago MD upped it to 40mg because BP inching up. quit smoking 3 years ago, not one puff since. After MD upped mg the side affects have really kicked in. I experience all the side effects listed on this site with the exception of the cough which I started with but went away after a couple months. I have had stress tests, Holter monitor for heart arrhythmias, mri, blood work, stool samples, colonoscopy, and all sorts of other tests all coming saying I'm ok, yet I don't feel ok, I get progressively worse. After 4 weeks of 5 day a week exercising with weights and aerobics to get in shape to return to racquetball I have had it. I couldn't last 45 minutes my second day out. I felt like I was hit by a truck and it took a couple days to recover.
My MD attributes the issues to aging. I going for a second opinion and third if necessary. I am told by my MD that there are no studies showing these side affects for this medications. However I look at this web site and find it hard to believe that these doctors just haven't seen any evidence of what we are all suffering from. Why don't doctors really listen to patients. We are asked to listen to our own bodies and told we know our bodies better than anyone, yet when we bring up these issues we are treated like children.
No real answers, just questions

My now 17 year old daughter was prescribed Yaz back on 7/12/07. Since then she has had an extreme problem with constipation. She has been to the doctors several times, and is now seeing a gastrointestinal specialist because she can only have a bowel movement if she takes a laxative. The pediatric doctor had her on miralax from April to October trying to get this problem under control. It has not worked. We are seeing the specialist and they are running her through a battery of tests, which will now possible include a colonoscopy (at 17 !!!!). She has been extremely moody and aggravated - which I attributed to her age of course. She is no longer extremely athletic, she doesn't really do a lot. She is not the same person, definitely is a homebody now - never going out hardly with friends,etc. She has also had a 20 pound weight gain and for a tiny girl, this has had a huge effect on her. I have watched all of this, and never really thought about the yaz connection until today when a friend sent me this email with a link to this site:
******

that is when I got scared thinking maybe her problems were all caused by yaz. of course her acne cleared up, but her periods are still irregular and spotty. has anyone else experienced the bowel problems???

My daughter has been experiencing extreme stomach cramping since the beginning of September. She had her last Gardasil injection (3rd) along with a tetanus booster late July. She has gone through an upper GI ultrasound, colonoscopy, endoscopy, capsule endoscopy, etc. Her gastroentologist thinks she has a pulled muscle. She has lost over 10 lbs. (didn't have 10 extra to lose). After reading these entries, I believe the common denominator here is the Gardasil.

If that is the case, we need to get the word out.

I was put on birth control when I was 21 years old and I started with Estrostep FE for irregular and very painful periods. 9 years later, after complaining of unusually light periods and horrible hot flashes I was switched to Yasmin to see if that would make a difference. I was fine with the Yasmin for about 6 months but then I came down with what I thought might have been a stomach virus. I was fine until June of that year when I came down with what seemed to be another stomach virus. I found this odd as I had not had a stomach virus since I was eight years old, but I seemed to have contracted two within six months of each other 22 years later. By the time July hit, I was experiencing these "stomach viruses" just about every other day. I would have horrible acid indigestion and the sensation of needing to vomit (but I never would) which would send me running for the bathroom for hours at a time just in case I did. For over a year I sought the advice of doctors and had been theoretically diagnosed with the following: stress (always the first one), acid reflux disease, IBS, and gastroparesis. I have gone through an endoscopy, gastric emptying scan, colonoscopy, two ultrasounds, two CT scans and an MRI. Drug wise I have been put on Prevacid, Compazine, Zofran, Zegerid, Imipramine, Reglan, Levsid, and Erythromycin. I now am buried in medical bills and the whole thing has caused me to miss a month of work without pay. I also was struggling to eat and, at one point, had dropped 25 pounds which is very frightening for someone with my tiny frame. The mental anguish was unbearable and I was actually at the point of welcoming a diagnosis of cancer just because it would have been answer. The idea to stop taking the Yasmin actually came from a fifteen minute conversation during a birthday party with an obstetrician. Within two weeks of stopping I was absolutely fine. I gained all of the weight back in record time and am once again a person who rarely ever needs stomach aids (in three months I've only taken two tums). Stopping the Yasmin made absolute sense because the nausea episodes would only occur between 9am and 2pm (weird, just like morning sickness) and my thyroid levels were all over the place. One blood test would show them as normal and another would show them as sky-high. I questioned my ob-gyn why she said my blood tests were normal when my thyroid levels were actually twice the normal level. She merely shrugged it off as being "normal because of the Yasmin". No wonder I never felt well! I've been off Yasmin for three months now. I've only gotten one light period that lasted for three days. It was over a month ago and it took almost two months to happen after stopping the Yasmin. I don't know if I'm sterile because I have heard cases of girls becoming infertile after long-term use of the pill (any kind). I am definitely interested in joining a class action lawsuit because I don't feel I should be the one stuck with all of these bills. Has anything been officially started yet?

Oh My Gosh - as I sit here with abdominal cramps typing my experience - I can see the light at the end of the tunnel. I started taking Lisinopril in late April 2008. On May 2 I had severe abdominal cramps and massive vomiting for 8 hours. Finally got myself to ER after I sent my family on to our vacation (I joined 2 days later). The ER attributed it to food poisoning. Lo and behold, I had another "attack" on May 9th. Back to ER I went (my husband witnessed my attack and insisted I go). They took X-rays and MRI - found intestinal inflammation but didn't know why. My internest send me to gastro dr. Third attack hit on June 5th and gastro doctor sent me to major hospital ER. They, too, did MRI & blood work. Looked at gall bladder, pancreas, stomach, intestines, etc. They found intestinal inflammation. Gastro Dr. took more blood and did more test (CT, MRI, Colonoscopy, Endoscopy). He couldn't find anything so he sent me to rheumatologist. She did add'l blood work and genetic testing. She though I had an auto-immune disorder - like Mediterranean Familial Fever! Please...! But all her tests came back negative. She too had no answers, only treatment for symptoms - Colchicine and Prednisone. Yuk. After having my 8th debilitating attack yesterday (since May), I've had enough. I went to the Web and found this wonderful site - along with some others with helpful info. I don't have confirmation that the lisinopril is causing this - but it sure sounds like it. I am a 49 yr old female and I've had no "life changing" events in my life (except for this nastiness) and have been on no other meds. I find it interesting that out of all the doctors I've seen - and all knew of the lisinopril - that none suspected this as a side effect.

I am a mother of a beautiful 11 year old girl, who was a healthy 10 year old little girl until she got her second Gardasil shot! She received her shot on 1-28-08, and started having nausea shortly after (within a few days). She didn't mention it. Within a few months she started having abdominal pain. She was hospitalized on 4-20-08 with pancreatitis. She got out of the hospital four days later. She was on Morphine while in the hospital and went home with Vicodine. She still had residual abdominal pain for the next few weeks, but the doctor said it was normal. She went to school 2 weeks later and started having severe abdominal pain again. We went to the doctor's office where they found out that her enzymes were elevated again. We then were referred to a gastroenterologist. She has had countless blood test..... negative. She has had an endoscopy, a colonoscopy, many CT scans, fecal tests, and now she will be going in for another endoscopy, but this time she has to take the capsule cam. She was so normal before the shots she was boring, but now she has to miss school on a regular basis ( before she was an honor roll student) and has to miss out on some of the most fun school activities. All the doctors act like she is making it up and they think I'm just some crazy mom that wants to drug my kid. They keep wanting to label her with IBS, but she has no signs of IBS other then the abdominal pain. She now has been on several meds. with no help. She now has joint pain headaches, blurred vision, and she says that she feels weird, with no other way to describe it. I feel like everyone wants to turn the other way rather then to accept that this drug is hurting these girls and focus on treating them.

I know this is tough, tough on the girls and young women that are effected, tough on the parents, and tough on everyone who loves them. Please, just remember that you are not alone! I will fight till I die to try and find out what is wrong with these girls. Just remember that you have options, if you do not want to get your child vaccinated, you can visit ****** and there you can find out what legal rights you have to not vaccinate your children if you don't want to. They have the forms that you need and you can download them there.

I am so sorry for all of you that have been effected by this drug! You will all be in my thoughts and prayers, as always. Just please, spread the word, the more we talk, the more that don't have to be hurt like this. Thank you all so much for sharing your stories! They help more then you know!!!!!!