Young women symptoms and conditions

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!!!!!!

after my second gardasil shot my hair started falling out i am looking to take action against gardasil please help yourself me and our young women that are being forced to take these shots and to us that are being told its perfectly safe please call 1800lawinfo and tell them your story with enough cases they will investigate

i too have went through losing my hair through gardasil a lawyers office is handing gradasil cases and if enough people come forward they will investigate this and that action please help yourself and our young women and children and call 1800lawinfo and let them know what your going through thanks

I think it is interesting the symptoms that you mention here. I have been on birth control pills since the age of 19. I am now 28. Over the past year I have had similar symptoms. I have been on so many different BCP's that is is hard to keep count. They don't seem to work the way they claim to. The last BCP I was on was orthotryciclen. While taking these I began to experience severe heart palpitations. So bad that they would wake me up at night. Because I wasn't sure if it was an anxiety attack or just being in my head I decided to ignore it. Four months passed by and it seemed to get increasingly worse. I had enough and decided to go to my PCP. She wasn't really much help either. Although I was tested for Mitral Valve Prolapse, which I was told affects younger women my age. There was nothing found. What I thought was interesting is I really felt that it was the birth control pills, but I couldn't find it as a side affect on the information that was provided in the box. The tech who was doing my echocardiogram began to tell me she also experienced the same feelings and found out it was her BCP. Once she confirmed what I thought was right, decided to stop taking them. After three months the symptoms began to disappear. I figured it was just the particular brand. I began to take loestrin 24. I started to feel the same symptoms again, just not as severe. I would feel my heart beat when I would like down in my back and my stomach. My heart rate would reach 90 to 100 sometimes. I know this is not normal. When I visited my gyno yesterday she told me it was impossible that it was a result of the BCP. Maybe it was just anxiety and or perhaps I should get checked out by a cardiologist. That is serious stuff when you are talking to a young person about getting there heart check out. I think if there are any other women out there who are experiencing any similar symptoms should speak up. So these doctors won't keep telling us it is all in our heads and help to take care of this problem.

NuvaRing was great for me for years and then I began experiencing most of the symptoms noted by others. However, when my LYMPH NODES become ENLARGED AND PAINFUL I realized it was time for me to take out the ring and give my body a rest from the foreign substance. Once I removed the ring completely, within two-weeks my HAIR BEGAN TO FALL OUT each time I washed it. After weeks, my JOINTS became so INFLAMED I could not walk even though I had been working out four-days per week for many years prior. I also experienced HAIR AND SKIN TEXTURE CHANGES, and ONGOING FLU-LIKE SYMPTOMS which included: BODY ACHES, SEVERE FATIGUE, NIGHT SWEATS (DRENCHING), HEADACHES AND WEIGHT LOSS. I saw numerous doctors to try to figure out what was happening to my body. After over a year, I was diagnosed with an AUTOIMMUNE condition (SLE). It has been two-years now, since permanently removing NuvaRing, and my condition has improved with time but my IMMUNE SYSTEM is still out of whack and my LYMPH NODES ARE STILL ENLARGED throughout my body. If anyone else has these systems and has been diagnosed with an AUTOIMMUNE DISORDER after using NuvaRing, please respond. CAUTION: please be careful young women as added hormones are not good for our bodies and really should not be pushed so readily by the health care profession. Also, keep in mind that your doctor will not back you when you are experiencing problems from medications that he/she prescribed. You will ultimately be told that the medication did not cause the problem in order for him/her to avoid becoming a party to a lawsuit.

Our beloved daughter has just been laid to rest....she was a gorgeous 22 year old Texan beauty......
She died suddenly of a pulmonary embolism just 3 weeks after starting this piece of **** drug called YAZ...
She was misdiagnosed with pleuracy,....
SPREAD THE WORD TO EVERY PERSON YOU KNOW WHO IS ON THIS DRUG THAT YAZ CAN BE A KILLER...OVER 4,000 SIDE EFFECT POSTINGS ON THIS SITE ALONE...SEE HOW MANY DIED OR ALMOST DIED FROM TAKING YAZ AND MAKE YOUR OWN DECISION...

Special thanks to the FDA and the Multi Billion dollar companyYAZ for their contributions to killing Americas young women...
God bless all who have suffered and perished from YAZ...

Our daughter spent her 21st birthday in ICU, Sunday the 13th. I took her to the ER with shortness of breath, chest pain and nausea on Saturday afternoon. She has been on Yaz since February with only the mild symptoms of: loss of apetite, mild nausea and some abdominal cramping. She was put on this BC to regulate her periods and relieve menstrual pain as well as excessive dark facial hair growth. All 3 of these were relieved by Yaz.
She has now spent 1 week in the hospital (2 days in ICU) and will be on coumadin for 3 to 6 months due to a very large pulmonary embolism (size of my knee cap) that was putting the right side of her heart in distress. She also has multiple clots in her right lung.
I am shocked to read through this website and see all that has happened to so many women. She can never take oral BC again in her life. There are no blood test results that indicate she was even predisposed to this type of reaction and is not family history.

didn't have Mirena, but another kind of IUC or IUD whatever you want to call it. I sure hope young women know they could die. Sorry to see these things back on the market. At age 21 I had complications, the device embedded in my uterus and became infected. No one wanted to admit it was the iud. The infection turned into acute peritonitis which is usually fatal. I did live, but had to have a complete hysterectomy. A bit extreme for a 21 year old. Spent 3 months in agony in the hospital. Took 2 years to recover. I had all the side effects associated with premature menopause - premature wrinkling, loss of interest in sex, not to mention no more kids for me.
I later did some research to find out that stones were inserted into camels to prevent pregnancy during long trips. The camels died screaming in agony in the desert from the stones. It works about the same on women.

it seems to be scents i have had the mirena i now have on going head aches in the right side of my temple and it stays for one to three days at a time i also have hot flashes through out the days and feel really light headed at times my coil is detached and i feel a lot of pain at times in side my virginia and abdominal area my back iis crazy with pain as well at time in the morning its hard for me to move my hands go numb sometimes and the sun hurts my eyes there is a class sign up and the girls on there have some what the same side effects as mine including weight gain im thinking what are the odds of young women all over the U.S. feeling the same symptoms and only thing linking all of us to geather is this mirena and not to mention the nussusness and major mood swings out of no where

Pulmonary Embolism - blood clots in my lungs which were caused by a presumed blood clot in my leg, which was caused by my Yaz. This is a very dangerous situation, and I was very lucky.

Please don't take Yaz if you have any alternative at all!
My 30-year-old, fit, non-smoking daughter is currently in the ICU after just the third pack of this KILLER drug, with a pulmonary embolism (major cause of sudden death in young women) and a clot in her leg. Thank God we got her to the ER in time--don't let it happen to you and your family. If you're taking it and get pains in your legs for no good reason, run, don't walk, to the nearest ER.

I have a 12 about to be 13 year old daughter who has been on Singulair now for quiet sometime, with a few breaks here and there. My question is considering she is 12 about to be 13 and is just starting to become a young women with PMS and all, how are we to determine whether or not the mood swings and insatiability is PMS or some weird side effect of Singulair? I don't necessarily want to stop her from taking Singulair considering the investigation is not over yet, but I don't want to continue putting her in harms way by keeping her on Singulair. Anyone have any suggestions?

My daughter was taking Yaz as a predecessor to going on Acutane for acne. After a couple months began having severe nausea and vomiting which we thought was due to the Acutane (it is known to have potentially powerful side effects) so we took her off of that treatment. The nausea and vomitting increased to the extent that she had MRI, sonogram, and ultimately colonoscopy and endoscopy to determine if there was cancer, etc. All tests were totally clean...so doctors said it must be in her head. She was also having significant mood swings and almost a paranoia. That is when I sat down and tracked back to as early as I could the initial slight nausea symptoms occurred. Determine it started at the same time as this BCP. Looked up the message boards and was horrified to see what young women were going through. I immediately told her to stop taking the drug. Within one week, my daughter could eat again and her spirits were lifted. Nice to have her back after thousands of dollars in medical tests. Very frustrating that the doctors, who knew her prescriptions, did not see the potential. Because of this and another prescription issue, I will severely consider whether I or anyone in my family will use the 'latest and greatest' drug. Will ask for what has been tried and true.

I love it. I've had it for a week now. Very little spotting, minimal cramps, and no discharge. I was told of the side effects, and knew all of this before I got it. Hormones act differently to some people. I did not react well with the patch or pill. So far, so good with Mirena. I don't think a lawsuit or complaint is exactly the way to go. You should start with talking to your doctor more and seeing if they give out pamphlets or just did not tell you everything you were supposed to know. I also believe not everyone's symptoms should be blamed on Mirean. People usually "feel" things they don't really have, esp. after coming on here and reading things. You can make your body feel that stuff. The insertion was not comfortable by any means, but it also wasn't a pain that I would ever cry or scream over. I'm 21, relatively healthy, and never had children. I work in healthcare and see people react like this all the time-no tolerance to pain, and just wanting an excuse as to where some of their "pains" come from.

Even more information regarding subcutaneous atrophy and the class of drugs which Kenalog fall in to:

"Subcutaneous atrophy developed in a 36-year-old woman at the site of a triamcinolone acetonide (Kenalog) injection for subdeltoid bursitis. Occurrence of local atrophy after corticosteroid injection is relatively frequent yet unappreciated. It is more common in young women and girls who are given preparations with a lesser degree of water solubility. Although the condition is often reversible, instances of long-term disfigurement are well documented. This complication of a useful treatment method can be avoided by following a set of precautions for local injection of corticosteroids."

The above excerpt from a 1986 article in the U.S National Library of Medicine. There is also an article as far back as 1967 in the British Medical Journal (10/14/1967) that puts forward the same theory (though it is argued about in the editorial of the Journal).

Anyone who has experienced this problem should print this out and show it to their doctors. Presumably and hopefully your doctor is aware of medical journals and respects the DATA!

Thank God for the internet or I would have thought I was as crazy everyone else. I too have experienced the horrid hair loss and no one can tell me it is due to pregnancies as I have had thick hair following both my children's births and now 4 years after my last child was born I have had major hair loss (have had iud for 2 years), and all this time I have been having nightmares of waking up completely bald, and it's the Mirena. Have had terrible headaches and depression, mood swings too. I would rather be pregnant til I croak than keep this thing in one more day.

I agree with goodyearchic I too have had my Mirena out for 3 weeks now and I would like to say to anyone doubting whether they should get theirs removed- go for it. I feel much much better, my spots have gone, my mood swings and craziness have disappeared and I feel fantastic. Whether it is psychological or not I don't know all I do know is that having the Mirena was one of the worst decisions of my life.

I'm 22 years old... I'd been off of birth control for 2 years when I started NuvaRing in October. My gyno said it was great with very few side effects. I have always had really clear, pretty skin, but since I have started NuvaRing, I have had awful breakouts. I am constantly nauseated, have terrible headaches and the mood swings are unbearable. My fiance thought I was losing it - I'd be high as a kite one minute, then rock bottom the next.
Luckily I found this site... does anyone have any recommendations as far as other options? Is OrthoEvra (patch) worth it? Please reply... thanks, ladies!

I began with the NuvaRing as my first birth control a few years ago.. I switched off of it because the ring had irritated my inside and it made it hurt to have sex. Then I developed some complications in my ovaries. I was never told if that was due to the NuvaRing or not, but my periods have not been the same since. I quit taking birth control for a few months and I didn't have a menstrual cycle for 7 months. Then I went back on the pill and It started up again. I recently just went back on the NuvaRing and I am experiencing the same thing that I did the first time. However, I haven't experienced the nausea or headaches that other women have reported. I am horrible taking the pill and I refuse to take the shot or use the patch, that's why I went back on the ring, I WOULD NOT RECOMMEND THE NUVARING TO ANY YOUNG WOMEN THINKING ABOUT BIRTH CONTROL! Thanks.

Guest #40983:

OMG if you are having leg cramps take the Nuva Ring out IMMEDIATELY and either visit the ER or call your doctor. I can't believe whoever gave you the prescription did not warn you that leg cramps are THE serious indicator of birth control-induced blood clots, which can and have killed young women on the Nuva Ring. The clots travel from your legs into your lungs and brain, causing a stroke. If one leg is swollen or red, or cramping severely, take the ring out!!!

Husband put in hospital on day 4 of taking this drug for SEVERE vomiting and diarrhea, lost 13 lbs in 3 days!, will be in hospital for AT LEAST 4 days! Have found out a young women (late 20's - early 30's) was put in hospital for SEVERE abdominal pain on day 3 of this drug treatment. BEWARE THIS DRUG!