Pancreas symptoms and conditions

Horrible device in my opinion! I'm on day 17 with Mirena and the cramping, bloating, pancreas pain, sharp pain all over my body, diarrhea on and off, mood swings, headaches, flu like symptoms, major hair loss, extremely tired all the time, sleepy, can't sit in a certain position, can't walk without pain on my sides (stomach) or shooting pain through my legs and the list goes on!

I am going in ASAP this week to have it removed. I am aware of the possible side effects warnings, but many side effects I am experiencing are not in my brochure given to me by my doctor. I believe my body is rejecting the device and anyone experiencing similar or same symptoms as me should run to the doctor and have it removed. Unless of course you like torture and are willing to torture your family members along with you. :(

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time
~ Depression
~ Hungry all the time
~ leg cramps
~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS
~ oily skin and bad breakouts
~ Mood swings (huge...yelling fits at my husband and the kids)
~ fluttering in uterus
~Sore breasts..

I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the doctor, but nobody knows my body better than I do.. I am in it!! I have never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc.. ******e-mail me with Mirena in the subject line!!

I can not say that NuvaRing is the reason for my illnesses but I am a fitness competitor and athlete and have always been very healthy with the exception of IBS that was diagnosed 5 or 6 years ago.
I am 37 years old and started using NR in August of 2008. In late August I went to emergency for extreme pain in my back and stomach. They put me in surgery to remove what turned out to be healthy appendix. Since then I have been to the Dr constantly with fevers, sinus infections, ear infection, bronchitis and most recently am undergoing tests to find out why my kidneys and pancreas are infected. I have been on antibiotics 4 times since January.
I started putting time lines together and decided to research the NR further. After looking at many symptoms, I opted to take the NR out in April of this year and go back to the pill.
I go back for another set of tests on my kidneys and pancreas next week and hope to find all is well. I have been off antibiotics now for 3 weeks and no sinus, ear or upper respiratory infections for the first time in month.
This is all unfortunate because I did appreciate the convenience of the NR but I am not willing to risk my health.

I took 20 mgs a day for 5 days in September of 2006. I developed a terrible cough, but worse than that, severe chest pains & shortness of breath upon exertion. I still can't go up & down stairs; my pain is brutal and it's going on 3 years since it all began. Before I took the lisinopril, I hadn't been having any chest pains or trouble breathing.

Is there any hope of recovery? My doctors all say they've never heard of this kind of side effect; that lisinopril is a very common drug; it's clear that I have reduced lung function & definite pain & symptoms, but there is no way to isolate the exact thing causing it or to figure out how to make it go away; just to control the symptoms.

My theory: the lisinopril triggered an autoimmune response in which my body physically tries to reject my own lungs. Any thoughts on that one? I had been taking cozaar as an ACE inhibitor to slow the rate of my renal failure; I have type 1 diabetes and hypoparathyroidism, and while I needed meds before this episode, all I had to do then was manage my diabetes & I was able to live normally. Since this, it's been nearly impossible to do ANYthing. I am at the end of my rope & I want this to stop. But 3 years later, and while the shortness of breath is improved, the pain is actually worse now. I could sure use some advice & support. I'm on my way this week to get set up with a new dr. because we've moved, and I'm going to have to go through this whole thing again. Also - I'm trying to compile a list of other people who have had side effects with chest pain & shortness of breath. Also anxiety & panic attacks as collateral damage.

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 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...

I am taking Levaquin now, but after reading all of this I plan on not finishing the 3 pills I have left. My head is numb and feeling so weird. I have a constant headache which I hardly ever have and I feel dizzy and really out of it. My stomach is sick and nauseated. Feeling almost depressed which I don't know why. I just don't feel right. My shoulders feel heavy and tingly and I feel more sick now than when I started taking it 7-8 days ago.

Eyes sensitive to light, cloudy vision, tongue metallic taste, jaw pain, tooth pain, loss of circulation in lower extremities, joint, bone, tendon, muscle pain, high frequency buzzing in ears, pain from head to toe literally, chest pain, stomach pain, digestion problems, bloating, pain in liver and pancreas, kidney and lung areas, heart and right side chest pain...

When I first started taking Januvia it was like a god send to me. My bs dropped and I started losing weight. Since sugars were not low enough, I started taking janumet. A1C results were consistently 6.3 even tho' I ate anything I liked. Have taken Janumet for almost a year now and weight is 135lbs (height is 5'3"). Nice, since I just couldn't lose weight earlier (also have an under active thyroid and a sweet tooth). I recently experienced my first hot flash in an air conditioned room no less (am 46 yrs old). Started having migraines around my period. Left shoulder hurt when I raised my arm or reached behind me. Digestive system was a mess. Never experienced high blood pressure but had my first high BP reading at my last check up. Stopped Janumet after reading posts here and started feeling better right away. Digestion is normal. Don't know what to do now.

MY APOLOGIES TO ALL FOR AN ERROR IN MY PRIOR POST. WHEN I CUT AND PASTED THE INFORMATION FROM MERCK'S WEBSITE NOT ALL OF IT APPEARED IN MY POST FOR SOME REASON. THE CORRECTED INFORMATION IS BELOW. CHECK THEIR WEBSITE FOR YOURSELVES TO VERIFY THIS.

THIS IS FROM THE PATIENT INFORMATION:

"What are the possible side effects of SINGULAIR?

The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side
effects in patients who were given a placebo (a pill containing no medicine).
The most common side effects with SINGULAIR include:
• stomach pain
• stomach or intestinal upset
• heartburn
• tiredness
• fever
• stuffy nose
• cough
• flu
• upper respiratory infection
• dizziness
• headache
• rash

Less common side effects that have happened with SINGULAIR include:
• increased bleeding tendency
• allergic reactions
• behavior and mood related changes
• drowsiness, pins and needles/numbness, seizures (convulsions or fits)
• palpitations
• nose bleed
• diarrhea, indigestion, inflammation of the pancreas, nausea, vomiting
• hepatitis
• bruising
• joint pain, muscle aches and muscle cramps
• swelling

Rarely, asthmatic patients taking SINGULAIR have experienced Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain symptoms that do not go away or that get worse. These occur usually, but not always, in patients who were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped.
Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right away if you get one or more of these symptoms:
• a feeling of pins and needles or numbness of arms or legs
• a flu-like illness
• rash
• severe inflammation (pain and swelling) of the sinuses (sinusitis)
These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist.
Talk to your doctor if you think you have side effects from taking SINGULAIR."

d27gayle POSTED INCORRECT INFORMATION ABOUT THE SIDE EFFECTS OF SINGULAIR. I JUST COPIED THIS FROM MERCK'S SINGULAIR WEBSITE. THIS IS THE CORRECT AND UPDATED INFORMATION. THIS INFORMATION DOES LIST DEPRESSION AND SUICIDAL BEHAVIOR AS SIDE EFFECTS.

IF PEOPLE ARE GOING TO SHARE INFORMATION ON THIS SITE, PLEASE MAKE SURE IT IS CORRECT BEFORE POSTING!!!!!!!!!

What are the possible side effects of SINGULAIR?
The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side effects in patients who were given a placebo (a pill containing no medicine).
The most common side effects with SINGULAIR include:
• stomach pain
• stomach or intestinal upset
• heartburn
• tiredness
• fever
• stuffy nose
• cough
• flu
• upper respiratory infection
dizziness
• headache
• rash

Less common side effects that have happened with SINGULAIR include:
• increased bleeding tendency
• allergic reactions
• behavior and mood related changes
• drowsiness, pins and needles/numbness, seizures (convulsions or fits)
• palpitations
• nose bleed
• diarrhea, indigestion, inflammation of the pancreas, nausea, vomiting
• hepatitis
• bruising
• joint pain, muscle aches and muscle cramps
• swelling

Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain
symptoms that do not go away or that get worse. These occur usually, but not always, in patients who
were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped.
Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right
away if you get one or more of these symptoms:
• a feeling of pins and needles or numbness of arms or legs
• a flu-like illness
• rash
• severe inflammation (pain and swelling) of the sinuses (sinusitis)

These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist. Talk to your doctor if you think you have side effects from taking SINGULAIR.

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'm on my sixth week of Levoxyl 50 mcg. I've been feeling great, and even losing some fat. I've been able to work my 14-hour Mondays without any caffeine at all as well. My pancreas must have been stimulated to work more efficiently, because I don't wake up hungry, I don't get the sugar crash and shakiness before meals, and I can go longer between eating without feeling homicidal.

The only weird thing: my lips are extremely dry. They're cracked, chapped and swollen so much it looks like I had a lip job. Even a tiny bit of salt hurts to eat it, as well as wine and spicy food. IDGI.

I have been on loestrin for 2 months now. For the past month I have been an emotional wreck, and for the passed week I have had anxiety, heartburn and stomach cramps just below my ribcage. My lower back is killing me and my stomach is spasming. I just took my last birth control pill this morning and start the reminder pills tomorrow. I totally don't feel myself. I haven't got my period since i've been on it. My doctor put me on it because I was bleeding abnormally heavy for me two weeks after my period. I really want to not start a new pack, but i'm nervous that i will bleed heavily again. the anxiety is causing me no to sleep.................I hate this pill

I was diagnosed with cancer of the Kidney and subsequently had it removed; this was after I had been taking Byetta. During the course of injecting the Byetta for my Type 2 Diabetes I suffered from severe vomiting, fatigue, dizziness and just over all feeling ill. I would appreciate knowing if anyone else has had this problem (Cancer in particular) after injecting Byetta.

I have been on 20 mgs Lisinpril for about a year. The most notable side effect I had was ACUTE PANCREATITIS, for which I spent several days in ICU in extreme pain. I only hope nothing permanent was done to my pancreas. Now I only take Atenolnol for my hypertension which seems to do the trick by itself.
Nicole

Has anyone experienced uncontrollable diarrhea? My mom recently went off of Enbrel and has had terrible diarrhea. It started about 10 days after stopping the Enbrel injections. The doctors have taken multiple blood tests, EUS scope from her throat down into the stomach, pancreas etc. She has had a CAT SCAN, colonoscopy, antibiotic and antidiaherral medications. NOTHing has helped! She is 5ft. 1" and weighs about 77lbs. NO matter what she eats, or even if she doesn't eat she has diarrhea. No pain, no gas, just a lot of gurgling in the stomach especially when she lays down. Any help would be appreciated as the doctors are baffled!

Strange happening. I have pancreatitis with having a Whipple procedure done 4 years ago tying off a large tumor on my pancreas. Because of this I am now a type 2 diabetic with high blood pressure. both stemming from the surgery. Recently, within the past year, I was put on lisinpril. Because of financial reason's I stopped taking the Lisinipril but just recently seeing a new doctor I started taking the lisinipril again and after two days have experienced severe pancreatic pain. Finding out by way of my son in law going into emergency and finding that he too has the same conditions and is taking lisinpril. Doctor's told him Lisinipril should not be taken by anyone with severe pancreatitis.

Has anyone experienced excessive weight gain using Januvia? About 13 months ago I started taking J. and I've not lost any weight since that time. I had Lap-band surgery 19 months ago lost 58 lbs the first 7 months, started the Januvia, had what I thought was Lap-band problems, gained a few pounds and the few pounds are now a plus 40. I've spoken to a pharmacist and he says there cannot be any connection to Januvia, however I've begun to question Januvia as the advertisements on TV state that Januvia has not been tested with insulin and I'm taking Lantus at night and Januvia in AM. Januvia can be used with insulin at the description of the Doctor???? I'm very concerned about myself and Januvia. Any comments 2bears

I have been on Levoxyl for about 9 years and have felt awful. I have had weight loss, dry hair, thinning hair,dry skin, muscle aches, migraines and the list goes on. I just got out of the hospital Monday after 4 days of testing of my heart and lungs. I was admitted for racing heart. The doctor's conclusion was anxiety! They said that Levoxyl has nothing to do with my rapid heart rate. The endocrinologist prescribed taking levoxyl .050 on day and .075 the next also a beta blocker, Xanax and Zoloft. I can not take any of these meds b/c they make it almost worse. I KNOW it is not Anxiety and it from the Levoxyl but what do I do?? I am a mess right now can not be in this condition with four young kids and a husband. None of the doctors would say it was the Levoxyl and instead prescribed more and told me to check up with blood work in 6 weeks. I took the .050 yesterday around noon and by 7:30pm my heart rate picked up again and continued until 4:30 this morning. I can not sleep more then 2 hours at a time and wakeup feeling like I am crawling out of my skin. PLEASE let me know of any solutions.

I was first diagnosed with hypertension in the late 80's and have been on several different medications to treat it. I think that Lisinopril is the worst that I have been on. I have extreme fatigue and severe dry and burning mouth, sore tongue and difficulty breathing and flu like symptoms. I have anxiety and PTSD so my symptoms have been blamed on that. With all these symptoms,
I sometimes wonder if it would be better off to have the hypertension.
Sometimes my mouth and throat is so dry and sore, I can't eat and I have difficulty breathing which is not addressed with asthma medication. Daytime symptoms are bad at night but when night time comes, it is almost impossible to sleep.
I would be interested if anyone has these symptoms and would like to hear from you.
Jenny

I'm a 37 year old female and have severe asthma and allergies and have used pregnisone on and off for 30 years. I believe I am the poster child for the long term side effects. My immune system is shot to the point that my normal medicines for asthma (ventolin, advair) and allergies (tylenol sinus, claritan, visine A) and ezcema (elidel, hydrocortisone, etc. - - NOTHING works!

In the past 6 months, I have developed various infections that the doctors have not been able to identify. My eyes are swollen and red with large amount of white/yellow secretions. Vaginal secretions. Face swollen. Skilled covered in a rash with ezcema out of control. Sharp pains in my back and stomach. Constant asthma. Abnormal hair growth. It is to the point that it is impossible to function and each doctor just wants to prescribe more pregnisone. I feel as if my body is a walking time bomb and it is so full of all the cortisone from over the years and has just decided no more.

I admit that I too readily believed in the doctors when they would rapidly prescribe the pregnisone. Only now am I paying attention to the long term side effects.

Has anyone had tests done to test their immune system and other organs for damage? Thanks and best to our pregnisone club.

I started getting very exhausted with lower back pain and had felt like I had to urinate constantly. I went to my doctor and found out my gall bladder and pancreas was inflammed. I am now waiting on more lab results and 5 days after stopping my sypmtoms are still the same. I am at the point were I have missed 2 days of work because I have been so miserable. My boss is pissed at me, like its my fault. Thanks vytorin and your unsafe ways. Just say No to statins!

My daughter has been on prednisone since October, 2006 -today is July 25, 2007. She is a 35 years old with asthma and allergies. Originally the pulmonologist thought she had ABPA (Allergic Bronchio Pulmonary Aspergelosis) and put her on 60 mg daily. This year has been a nightmare for her. That original diagnosis apparently was erronous, but she was kept on the high dose for breathing issues, with instructions to lower it as she could. As of today she is on 30 mg. daily. Side effects? So you know she is no "loser", she is a PhD in Biomechanical Engineering, has two patents to her credit, has spoken at numerous medical conferences (for vascular surgeons and cardiologists), and has had countless articles published in medical journals. Now she can't concentrate much less sit still, has not read a book in months (she used to read at least one book every week), she has two research publications that need to be finished but she can't focus on the work, is totally exhausted and needs to rest after only a couple of hours of mild activity, has a face she has described as looking like a mongoloid. Her beautiful, big, blue eyes are slits in her face. Clothes that fit yesterday wouldn't fit today - and those that fit today won't fit tomorrow. She craves food in the middle of the night and said she usually eats 2 bowls of cereal. She has terrible pain in her torso. Her esophagus has become so eroded she is on 6 different meds for that, and as a result cannot eat salads or raw fruits or anything that might irritate the lining of the esophagus. Her body is covered with huge dark bruises. The latest side effect made evident happened this past Saturday night. She fell striking her shins on a carpeted step. Her skin has become so thin that it actually burst open. She said it reminded her of when we'd blanch tomatoes in boiling water to peel them, and how the tomato skin would just burst open. That's how her leg was. That little fall cost a trip to the ER for stitches, tetanus shot, and antibiotics. Her husband is a career military, so since they married 1 1/2 years ago she's lived in 4 states, there's not much history among doctors. She lives now in Kansas and has started seeing specialists through the university there. We just wish she could go to Mayo Clinic for complete evaluation, but unfortunately military insurance doesn't seem to cover the best.

I had a shot of kenalog in my knee for a problem I have when I run long distances. I was told that it would have a 50% chance of helping but it could prevent surgeries. He never mentioned side effects. After the injection- my period came a week late and lasted three days longer than normal. Four days after it ended I got another period. This one was accompanied by severe headaches(I never get headaches) This period lasted another nine days. I went for my follow up and questioned the doctor about it and he said he must have forgotten to mention it but that it can cause some hormone irregularities but that it should go away within a month. I have been so exhuasted and barely able to function. It was five days since my last period and now I got another one today! I am furiouse because I was trying to get pregnant! Now I am freaking out because I am seeing on this sight how long this can really last!

After all of us have had these same problems you think we would be able to sue the company. What can we do becuase I'm on board if you all want to have a class action law suit. How do we start it?