17 years symptoms and conditions

I am 17 years old and i got the three vaccinations of the Gardasil and ever since than i have experienced a lot of pain in my lower stomach area all the time like i have cramps. I have lower back pain all the time. Migraines run in the family and i usto to get them once in a while and now i get them at least four times a month. I dont know if this has anything to do with it... but im in pain all the time and, my mom wont talk to me because she thinks im lying and i dont know what to do.

I am 17 Years old. I began YAZ two months ago. I'm usually very athletic, outgoing, fun, and EXTREMELY energetic. Since I began YAZ my life has been turned upside down. I HAVE HAD MY PERIOD FOR THE LAST MONTH STRAIGHT! I felt like I was going insane, I'm so grateful to know that I'm not the only one. I wish I could have found all of this out BEFORE hand, my symptoms are just like everyone elses. Im depressed, cry over everything and anything, I'm angry ALL the time, have no energy, fight with my family and boyfriend over EVERYTHING. I feel like SHIT. Can I just get off of it? Or do I have to talk to my doctor or finish 3 months first? I don't know what to do :'(

I am so happy I stumbled apon this website. I thought I was losing my mind. I was on Yasmin for 3 long years and have been off for a month now. I am 37 and was on Triphasil 28 for 17 years (with no issues), my derm told me to switch my birth control to help my acne, worst decision of my life. I have lost all of my friends, my moods and me being paranoid all the time drove my friends away. I am so dry that I itch all the time. I have loss half of my hair, my scalp is sore and itches non stop. I have gained weight and my blood pressure is high. How do you go from a 34 year old normal woman to a 37 year old medical mess? YASMIN. every time I asked my doctors if it could be the pill I heard the same answer over and over NO! I was told that it was age and stress. Hello I am 37 not 97. Stress wouldn't you be stressed if all of a sudden you weren't the same person and no one had reasons why.Well I am no doctor but we cant all be making this up. I am hoping and praying that all of this isn't permanent and that I soon will grow my hair back and that my happy old self will come back. I wish doctors would stop prescribing this horrific drug!

I got my Mirena in October of 2005 when I was 37. Prior to that I'd had two surgeries to remove fibriods and had severe heavy bleeding (life threatening, actually). My new husband was scared to death that he'd married a truly defective woman! ;-) So when my doc suggested the Mirena, I was thrilled with the idea. Insertion was painful, but bearable even though I'd never had children. I had a rough couple of months with cramping and such after insertion, but I attributed it to going off a high-dose BCP after 17 years. My body had an adjustment period to get through. After insertion and a little spotting, I never had another period. To this day, 4 years later, I haven't had a period. After all the bleeding issues, I think I was willing to accept a few other side-effects to be flow free.

Fast forward 4 years - my symptoms? SEVERE lower back pain (I had no idea that Mirena could cause this until about a month ago), weight gain despite picking up a new sport and being much more active than previously (I've put on 40 lbs in 4 years despite trying to lose), and vanishing sex drive. I've not been abnormally moody, but I have seriously lost my ability to multi-task. I would never have connected that to the Mirena until reading this site. I've got an appointment with a new doc tomorrow (we recently moved) and my hope is that I'll be able to get the Mirena out at the same appointment. The back pain has gotten so bad that I'm actually occasionally missing work. If I bend over, I cannot stand up again without using my arms to push off something because my back is so weak. For the past 4 years, I've basically changed the way I function in the world in order to deal with it without even thinking about what I was doing. At this point, it's bordering on being debilitating and it has definitely gotten worse over time.

The weight gain has really been difficult. I've always had to fight my weight but in the past, I was able to maintain at the high end of 'normal'. Now, not so much despite eating a much better diet and getting significantly more (and more consistent) exercise than I ever have in my life.

Looking back, I'm trying to come to terms with why I've ignored these symptoms for so long. It's hard for me to truly remember, but I was so distraught with the blood loss and problems I had back then that I know I was willing to remain blind to other factors to be 'cured' of that. Honestly, as much as I can't wait to get this out now, I don't think I made the wrong choice at the time.

Let's see how I feel in a couple of months post Mirena.

I have been taking perocect 10's for the last 1yr or so and it is very bad when I don't have them I feel like crap. When taking just one it is like taking 3more 10 min later cause it does not work as well from when I first started taking them. When I run out I am looking for them everywhere and taking other pain meds to cover the withdrawals. Man it is so bad feeling like that the runny noise,sweating,being angry,shaking, throwing up,shiting my guts out etc. I have a chronic back problem and I'm only 24yrs old. I have a very supporting husband who is there for me when I'm withdrawing all the time and I love him for that cause if it was any other man they would of left me hanging. I advice anyone who starts this pain killer to only take it when needed cause the chemical in the pill will mess your who life up and you will have some serious problems for realist is true but how I'm going to stop I will take a week out of my life to go to the hospital for help. Also there is so many other medication that can make you sleep.(PEROCECT'S WILL MESS UP YOUR LIFE SO DON'T GO DOWN THAT ROAD, PLEASE TAKE THIS MESSAGE SERIOUS THEY ARE VERY BAD, DON'T COVER UP THE PAIN GET IT TAKING CARE OF AND IF THE DOCTOR GIVES THE PEROCECT'S TO YOU DON'T TAKE IT CAUSE THEY DON'T CARE IT IS NOT THEM PLEASE DON'T).

I am 17 years old, about to be 18, my fiance is my first and only sexual partner, and I am beginning to HATE loestrin. I have been on the pills for approximately a month and a week. When I first started them I would get extremely hungry and the more I ate, the hungrier I got. It was like a bad case of the munchies, not that I've ever smoked pot. But I was seriously eating anything and everything, even foods I didn't like. My stomach felt a little weird for the first couple days, but nothing too bad. Then I started taking the brown pills, and all hell broke loose. There were the cramps. Horrible, HORRIBLE, cramps, which I am still having 3 days after going back on the active pills. Cramps all through my lower abdomen and stomach, and the feeling that at any given moment my right ovary might drop out (which might actually provide some relief) I actually doubled over crying with the pain in the shower yesterday, and would have fallen and surely hurt myself if my fiance had not been in the shower with me and caught me before I hit the ground. Intense hunger. Followed by bought of nausea, that make me want to puke, but I can't. I am very, very, sensitive to smells. Perfumes, food, cologne, things that I formally found the smell appealing, now disgust me. My lower back, is KILLING me! I get dizzy spells, and lightheadedness frequently, and feel like I may black out. Most of the time I can get myself to a spot where I can sit down and let my body sort things out before I actually black out, but I'm waiting for the day I can't. I have been getting terrible, awful headaches that stay with me through most of the day. Sleeplessness. I had my "period" 3-4 days early, if you can call it a period. It was nothing more than a day and a half of light pink spotting and brown discharge that only showed up when I wiped, I didn't even need a pad. Now, we did start having unprotected sex (with the exception of the bc) at 5 or 6 days instead of 7, and I forgot to take my pills until 9-12 hours after I was supposed to a couple of times. Couple that with the lack of a normal period and all the side effects that could also be the side effects of early pregnancy, and I'm pretty worried. I would love to be a parent, as would my fiance, but I would have liked to have graduated high school first. If these symptoms turn out to be just the pill *** with my body, I would rather just take my chances either with a condom or no protection at all. Sometime in the next week or two I will probably be taking a pregnancy test as I am afraid to wait for my next period and continue the pills because if I am pregnant I know that it can cause damage to the fetus. If anyone has wound up pregnant while on loestrin fe please email me and let me know how you found out, and how things turned out. My email address is ****** Thank you so much for any help you can give a scared teen.

Not only have I been experiencing horrible depression and moodiness from this drug, but this week I found out I'm pregnant!! I took 5 pregnancy tests and their all positive. I'm on this birth control and we used a condom so how the hell did that happen?? I'm 17 years old, a student, a model.. this pregnancy has turned my whole world upside down. I'm seriously considering suing this company!!!

im 17 years old and i got my iud in 10/08 after having my first baby and it seemed to work until about 3 weeks ago when i figured out what the problem was. i gained major weight. had thyroid problems, got bad pimples ( more than the average teenager should get), lack of sex drive,brown milky discharge, bloody stool, depression, anxiety attacks, headaches, nausea, insomnia, and scariest of all, i had a seizure. GET IT OUT!!!! its not worth it.

I was on birth control for 17 years because I suffered from severe cramps and bleeding when I was a teenager. Two years ago I was so sick - extreme fatigue, dizziness, nausea, severe constipation, severe depression, irritability, almost constant yeast infections and overall just felt very sick. I had gone to many doctors for many different testings and they all told me they couldn't figure out what was wrong. Some thought IBS, Chronic Fatigue Syndrome but nothing specific. I finally got to a point where I didn't want to live like this anymore and went to see a Holistic MD. He changed my life! The first thing he said was that I needed to come off the pill. Of course not wanting to ever have children - this was very scary to me. It took me about a year of talking to him about that that I finally decided to give it a try. OMG! I became a totally different person! Happy, full of energy, no fatigue at all, no more yeast infections, all my symptoms disappeared. It took about a year for the hormones to regulate because I had been on them for so long. I'm telling you all this because after being off of the pill for two years, I decided to try the ring which didn't work and then thought I'd try going back on the pill for my huge fear of pregnancy. Well, it's only been 3 weeks and all my symptoms are back in full force. I am miserable and will be taking myself back off. My quality of life is more important than anything else. The doctors don't tell you these things because they believe what that sales reps tell them who of course want to make a ton of money. As women we need to stand up and speak out so that is what I'm doing. My husband and I are researching other options but the pill is definitely not one of them.

tri-sprintec was awesome for me. I took it for 2 months and my boobs went from a 36b to a 36c. I stopped taking Sprintec because I didn't have the money at the time to get a refill and my parents would kill me if they knew I was sexually active *17 years old* and I am currently scheduling an appointment to start taking it again! (: My face also cleared up.

I am 17 years old and have been on NuvaRing for about 5 months. My doctor put me on birth control because i have polycystic ovarian syndrome (PCOS) and would not be able to get my periods on my own. I've noticed that ive been much more tired and can sleep longer but that isn't what bothers me. PCOS made me have severe cystic acne but after being on the NuvaRing for a few months my skin is completely clear. Also, I find it convenient not to have to take a pill every day. The side effect that really bothers me is the weight gain. I have gained 10 pounds over the past 5 months and being 5'2 I really can't handle it. None of my clothes fit, my face looks fatter, and I am completely insecure. My boobs went up a cup size which is always a plus, but I really can't deal with the weight gain. I've been on birth control before and it made me gain 10 pounds also, and I was wondering if anyone has seen the weight gain disappear after using the NuvaRing for longer periods of time. If not, I plan on switching to a low-dose birth control this week but if the side effects of weight gain start to go away I would like to stay on the NuvaRing.

I'm 17 years old and I started nuvaring in October 2008. It didn't occur to me that I wasn't myself until February 2009, and I honestly believed I was going crazy. I became so anxious and depressed about everything, especially my loved ones. My boyfriend is my best friend and my biggest support alongside my parents. I've been reevaluating every friendship/relationship i've been in. I've lost interest in my hobbies and passions. I've felt indifferent about everything, not to mention I have absolutely no sex drive. And I'm devastated that I did not enjoy my senior year of high school. I didn't think about the nuvaring until 2 weeks ago. I came on this website and read all of the stories of depression, mood swings, anxiety, etc. You have no idea how relieved I felt. I took out the ring on Saturday as usual and got my period today. However, I will not be continuing nuvaring. I still feel anxious, irritable, and I'm even second guessing that the ring is the cause, however I very much hope that it is and that I feel like my carefree outgoing self again soon. I'm angry that I didn't make the connection sooner because it made my senior year very upsetting and has slowly been hurting my friendship/relationship with my boyfriend.

I started taking prednisone when I was only 12 years old and I was on it for about a year and a half. At the age of 10, I was diagnosed with glaucoma, uveitis and cataracts and for about 10 years now I have had all these illnesses. My experience with prednisone had been HORRIBLE. Within two months alone, I gained 50 pounds, my skin started to get really really thin, I started to develop stretch marks ALL over my body with the only exception of my face and hands. I started to get the chipmuk cheeks to the point that my family was afraid that I was going to literally explode. My liver was damaged. My kidney was damaged. The vertebrates in my spine where being chipped away. There was a point in that year and a half where the doctors told me that there was a 70% chance of me going blind. The bottom line was that PREDNISONE WAS BRINGING NOTHING FOR ME EXCEPT RUIN. On top of that, I was constantly depressed. Kids at school would point at laugh hysterically at me. And if people weren't laughing, they were struck by fear and were trying to figure out what exactly I was. I remember this one instance in my school cafeteria where one girl stood up on the lunch table, pointed at me and screamed SHE'S AN ALIEN!!

I was and still am scarred physically and emotionally. My arms and stomach are really saggy because the skin is soo thin. As I said my entire body is scarred with stretch marks. I can't show the slightest bit of my body to anyone because I am so ashamed, embarrassed and afraid of peoples judgments. I am afraid that no one will ever want to be in a relationship with me.

All I can tell you is that though I stopped using it about six and a half years ago, this dreaded drug has truly ruined my life from the very start of my childhood.

I was diagnosed with peti-mal epilepsy aprox 17 years ago. I tried many different anti epileptic drugs and had many negative side effects from teeth problems to depression and none of which controlled my seizures. 12 years ago I went on lamictal (600 mg a day) and I haven't looked back, I feel I have my miracle. So far I have no side effects, am completely seizure free and I have a life. BEFORE lamictal some side effects were poor concentration ( when reading a book I could not remember what was written on the top of the page by the time I got to the bottom), little co-ordination with sports (most times I could not catch a ball when thrown to me, this caused a lot of social problems), forgetfulness and I was quite clumsy. I hope you all can one day find a medication that works just as well for you or even better a cure. My heart goes out to you all.

Im 17 years old and I have have one daughter. I got the Mirena put in about ten months ago. At the beginning I bleed constantly, then had to put on estrogen pills for 10 days, after that I have never have a period or anything. I have...
-No sex drive (Im 17, I shouldn't have a problem)
-Breast tenderness
-Dizziness
-Migraines
-Depression
-Mood swings (I get to mad/sad so quick for no reason)

& I have no idea why. I want to know if all this is actually from the Mirena. I want to know if it would just be better to get it out. I don't want anymore kids right now {Thats why I got it in the first place} Please give me some advice on what you think.

I am 17 years old and am on my second week of Loestrin24. i am MISERABLY bloated. I have been bleeding since the day i took the first pill and the bleeding hasn't stopped, but it has lightened. The reason i started taking the pill was to help clear my minor acne but because of the severe bloating i am starting to think i can handle a few pimples. I haven't felt any symptoms of depression whatsoever but then again i am only on my second week. I am going to call my gyno tomorrow and stop taking this pill! So bloated!!!!!!

I do have bowel problems because of radiation enteritis (had abdominal radiation 17 years ago). On Fosamax I had stomach problems so bad that I had to be put on IV's to rehydrate. My problem now is last summer I had breast cancer, and my doctor is running me through aromatase inhibitors; two of which have already caused the same reaction (pain, vomiting, diarrhea, etc.) Both times ended with me back on IV's. Does anyone have any thoughts on this? I'd love to hear from you.

I had my thyroid removed because of cancer. I was 18 years old. At that time, I was put on Armour thyroid because that was the only thing available. I am now 56. Somewhere along the line they figured out how to make chemical thyroid and of course I was put on it - for the next 35 years. Blood checked so many times I can't remember, dosages changed. Always a runny nose, hot and cold always a problem. I drink something hot and I start sweating, I drink something with ice and I get the chills. Back on Armour now - not the absolute best - but certainly much better than synthroid! Still what do you do when you have no thyroid? Also to let you all know, after the thyroid was removed I was treated with Radioactive Iodine, and told that I probably could not have children. Well, I am stubborn - I have three boys - had them at ages 23, 25 and 37! Many, many problems through the years ( oh yeah, the radiation treatment that I had at 1 month old fried my thymus as well as starting the cancer - it took 17 years for the cancer to develop. It was only after all this that they began to find out the you really did need a thymus too. Oh well, I could go on and on. So find me a solution to my thyroid that is gone. Can we regrow it like they are regrowing ears, fingers, etc?? Something to look into for the medical profession...

I am 17 years old and I chose the NuvaRing as my form of birth control about 6 weeks ago. First 4 weeks I experienced no problems at all, despite one or two migraines the first week I had put it in, even my week-off turned out to be great. Recently, I have noticed that I have become extremely emotional all the time. Normally, small things never bothered me but now I jump at any thing that bothers me. I've become extremely clingy and have no desire to go out with friends anymore and just have fun. I even have trouble sleeping because of the constant racing thoughts. I have experienced no other side effects from the NuvaRing and I am really hoping that after my third month is complete, my body will be more adjusted and the depression will subside.
If not, in 6 more weeks from now, I am taking this thing out and tossing it for good!

I was prescribed this drug in hopes of keeping thyroid nodules and goiter from growing larger. My TSH levels have always been in the normal range throughout my life, so the theory that "normal TSH' means a working, normal thyroid is absolutely untrue. I am a prime example of a person who's numbers have always remained normal and yet their thyroid does not work properly. I have decided to discontinue this drug after 3 months of use. The weight is packing on faster than I can diet and exercise it off. My face is puffy, my stomach bloated and looking pregnant, and now retaining water. Anyone who does not believe that Synthroid causes weight gain, I welcome you to try this drug. It does the exact thing it claims it is combating. I am not hypo with levels of 1.07 and yet something odd is occurring within my body with this synthroid. I'm praying that if I stop the drug I might return to some form of normalcy soon.

I am 20 years old and my sister is 17 years old. My sister received her first shot about a month and a half before I received mine. Her arm was sore for a few weeks. After a few weeks have passed she began to itch all over her body, and began to have blotches all over (the worst spot was her ankles and feet-they looked swollen). She went to the doctor and he said that he did not think it was from the gardasil shot, but could be irritated and dry skin. So, not thinking it would happen to me as well, I received my shot. Everything seemed fine, no pain at all. But then About a month later ( a week ago ) I woke up to itching ALL over(extremely bad on my stomach & arms). I tried using an anti-itch lotion and took medicine to attempt the itching and redness to go away and keep washing myself , but it did not really do anything. When I woke up the next day, it was mostly gone and the doctor said he did not think it was from the shot either. I just found it to be quite a coincidence that my sister AND i both received itchy-blotchiness around the same time period after the shot. But, after my sister received her second shot she was perfectly fine, with the exception of a soar arm where the shot was taken place. I did not go for my second one yet, but I hope everything turns out okay! If anyone else received any type of blotches or itchiness please let me know, we are very curious to see if its happened to anyone else too.

On Dec 21 2008 my 17 years old was prescribed SMZ/TMP DS 800-160 Tab for possible staph infection. She is/was to take 2 tablets every 12 hours for 10 days. By day 5 of this dosage, she had severe flu symptoms. Took her back to the same Doctors office but saw a different Doctor and was informed that she was only supposed to take 1 tablet every 12 hours for 10 days. She has been taking the the correct dosage for 3 days and the flu symptons are not as severe, as of today her skin is a little red (like too much sun) but not bumps or hives. We will continue to watch closely. Hopefully she will make it to day 10 without anymore problems. She does not want to go back to the same Doctor's office again.

Im 17 years old and started getting sick a lot after getting my period at the age of 13. after numerous tests, and 2 years later i was diagnosed with both hashimotoes and graves disease. the doctors put me on synthroid and for a week i felt great. then after that i no longer wanted to take it. i didn't like the way it made me feel. i've been on the medication now for 2 years and my hair is so thin. it keeps falling out, and its very noticeable. i get a lot of headaches and severe cramps. i'm almost always tired. i get my levels checked every two months like the doctor wants. they are regular. anyone else feel the same? my mom is considering switching doctors.

i am 17 years old and i have been on birth control for over 2 years,,
for the first 6 months i was on Yasmin && then my doctor wanted me to have a less hormonal birth control and switched me to yaz the only side affect was little weight gain...
i have depression but i never considered that it would be a cause of my birth control.
sometimes it gets bad... but my doctor said it was just an imbalance of serotonin in my body
my mom is extremely scared b.c she doesn't want me to have the dangerous side affects that she has recently been hearing about Yasmin... but are yaz and Yasmin the same?
i have been becoming increasingly worried about the birth control im on now.. i want to have children when i grow up. but after hearing that death could be a result of the birth control im on... im only 17 im just a kid...
im extremely scared now... although i haven't had any of the side affect i have read here.. im still extremely nervous especially since i have been on the drug for so long...

just found out
that the birth control im on could cause

* Deep vein thrombosis (DVT)
* Pulmonary embolism (PE)
* Stroke
* Heart attack
* Death
* High blood pressure
* Heart disease
* High cholesterol
* Overweight
* Liver cancer
* Gallbladder problems
* Diabetes

is this true? could i really die?... im terrified right now

I take Klonopin and Celexa and my mood and feeling are better than I remember before I started them. There are many other positive outcomes we have notices. I used to have many addictive behaviors and many of them have ceased. Now for the issues: I fall asleep every time I sit down. I have had arthritis since I was a young teen, so I do need to sit down for breaks anyway. I used to fall asleep from time to time, but now it is everyday. If I am in a meeting I nod off and start snoring. I was not able to work while depressed and anxious with panic attacks. I feel better, but I still am unable to work. I plan to stay on Klonopin as any other of the drugs would probably only be worse. When I was on Ativan about 17 years ago while I was in the hospital it only took me 5 - 15 minutes to fall asleep for at least 8 hours. I have friends that can drive long distances on these drugs, so it is not like this for everyone thank God!