18 years symptoms and conditions

I have been on topamax for about 7 months now for migraines && im about to get off of it. Im 18 years old and "trying" to do college but ive had so many side-effects its crazy. I cant go to the bathroom w/out taking laxatives cuz i just cant go ne more i literally have to take something everyday or i will be stopped up for a week or more. Ive been depressed and my anxiety has gotten worse.I take 150 and they want to put me up to 175 but i refuse because ive heard of people losing their hair taking it especially when they have a b12 deficiccency...which i have. I have horrible mood swings i can be happy one minute then sad or mad the next and i never used to be like this. Ive now started getting my migraines back so im stumped on what to do. I cant word things right....i was trying to say i didn't like something and instead it came up "im not to high"... yea so its deff a crazy drug but it can work for others and not. Not for me!

Wow. I am not even close to being done reading everyone's comments on Loestrin, and I am already EXTREMELY P.O'ed and at the same time relieved, at the fact that I found this page. I am 18 years old, and I started on Tri-Cyclin Lo when I was 15. I loved it, and never had any problems with it what-so-ever. It even helped with my acne problems. But a few months ago, my insurance decided to stop covering birth control, so my OBGYN decided to put me on Loestrin 24 Fe, because with the card you only have to pay 24 tops a month. But anyway, I now realize that all of the hell that has been happening in the past 3-4 months is due to Loestrin Fe. And after reading all of your comments I am POSITIVE! My Boyfriend and me have been fighting all of the time, and I have just been getting upset for no reason. I thought that it was because things between my boyfriend and me just aren't the same, and that maybe we are just growing apart.. but after reading all of your comments, and taking some time to think about it... IT HAS TO BE THE B.C! Before I started this pill we got along all the time... And also, my sex drive has plummeted so fast and drastically, to the point where my sex drive is NON EXISTENT. It has been hurting our relationship on top of my mood swings, because our sex life is also NONEXISTENT.. and we live together! I used to want to have sex all of the time.. and I haven't honestly wanted to have sex (not even once!) for the past few months...since I started Loestrin!!! Additionally, my face has been breaking out before periods excruciatingly bad. It has seriously hurt my self esteem. I have always had some issues with acne, but it has gotten ridiculous. I even bought an expensive acne kit that is supposed to be number one in the country, and it still keeps getting worse! .. And lastly I have been putting on a lot of weight, even though I have been eating the same.. also hurting my self esteem. Today, my bf and I finally came to the conclusion that "hmmm.. it most definitely might be the birth control." ..so I decided to come online and check out the side effects. AND BOOM! I see tons and tons and tons of comments from Women of all ages with the same, horrifying side effects. I am going to stop this birth control immediately. If my insurance won't cover anything else, and I can't afford any others, I will just deal with my cramps and longer periods. I never thought I would say this in a million years, but I would RATHER deal with the horrible cramps and long periods, than have to deal with the bull s*** that Loestrin has put me through. If anyone has anymore insight, message me or reply! Thanks.

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I am 18 years old and this is my first experience with BC. Loestrin FE 24 has ruined my entire view of BC. I have suffered many side effects of this pill, I am currently on my third pack of Loestrin. The side effect I have experienced are:
1. Moodiness/ Depression: I experienced this side effect during the first pack of Loestrin. Extreme depression was prominent at the beginning, I would randomly cry and I constantly down. Let alone my mood swings. My boyfriend would agree that I could be up and down within min.
2. Headaches: I have had horrible headaches daily with Loestrin. I started with my third pack of the pills. The headaches are terrible, it seems like I can only numb them with ibprofen but I can never fully get rid of it.
3. Spotting: How annoying is spotting? This side effect also started with my third pack of pills. I shouldn't even see any sort of menstruation for at least another 5-6 days. But yet here I am.
4. Massive acne before menstruation: I have always had really clear skin. Let it be before, during or after my period. But with Loestrin I am constantly breaking out. ESPECIALLY before my period.
5. Bloating/Constipation: I constantly feel bloated and feel like I am always constipated. I don't know what to do besides switch pills. I can't take it any longer.
P.S. This pill makes you feel that you are always pregnant. I see the signs but they are identical to the symptoms of the pill. So beware. I highly recommend NOT taking Loestrin FE 24

I have been dealing with Total neuropathy of my feet and legs for 18 years now and i was taking neurotin 300mg 3x's a day and that was not even putting a dent in my pain. 2 weeks ago I fell in the shower on Monday and fell down my stairs Tues. ( due to not being able to feel my feet) and I sprained my whole body and was in major pain. My Doctor prescribed 10mg flexeril and 50mg of tramadol. It has been a miracle for me!! the pain is gone from my nueropathy, I haven't slept this good in many years & I am hoping that after talking with my Doctor i can continue taking this ! What a difference this has made in my life. However the second and third day I was severely grumpy but I was aware of the fact so I was able to minimize it!

I have been on Levoxyl 0.112MG for about 18 years. I do have some of the symptoms described by others, hair loss, hot flashes, etc. , but I think the alternative to this is a lot worse. If I do not take it for long periods of time, it gets to the point where I am freezing cold and the bags that develop under my eyes are embarrassing. I think the problem with most of you that are having very bad side effects is the dosage. If the amount is off just a little bit you can feel like you were just run over by a truck. I went through this many years ago. I would suggest continuing to change the dosage until you get it right. I wish I did not have to take it but it is absolutely necessary in my case.

I am 18 years old and ive been on the nuvaring for about 2 months.. Ive been depressed, angry for no reason, snappy at my boyfriend and on top of that- my once amazing sex drive has dropped off the face of the planet. Ive been on edge and anxious, ive had constant headaches all day, plus calf/foot cramping. Ive woken up in the middle of the night almost every night since i put the ring in.

I just took it out this morning after researching and looking on multiple websites, and im so so SO happy i found this website.. Already im noticing a difference in myself this afternoon and its awesome.

I find it sickening that when i brought this up to my gyno she had no idea about the symptoms i had been having and i type in "nuvaring" in google and it brings up thousands of pages of symptoms, side effects and even deaths.. Its scary.

Ladies, do your research, no more nuvaring for me.

My daughter had her 2nd shot in August, 2008, she started having problems November 10, 2008.Since then, she passes out at least 5 to 6 times a month, she has Bradycardia, arythmias, vagal vasal syncope, and Heart Block. She has been in and out of hospitals. The only answer to fix this is a Pace Maker. Shes 18 years old, cannot drive, go onto college (at this time). She could not even go to her graduation ceremony because she was passed out in the bathroom and wouldn't wake up. I cannot find one doctor to connect this to Gardasil, I wonder why it cannot be traced back to the shot. I would love to voice my opinion to the public about her experience since this shot. Out of all the doctors that see her, not a single one can explain why this is happening to her heart, they say she is a difficult but interesting case.

I came to the conclusion myself, luckily, that Yaz was causing my weight gain. After having back surgery in April and gaining not a pound while not working out, I have been on Yaz for four months and I literally have gained 10 pounds in the past three weeks, my boobs hurt like when I was pregnant and I have even been lactating a little! Ugh! Sex drive...gone. Headaches, lack of motivation, could sleep ALL day. I took Yasmin for years and years with no problem at all. I recommend against this method of BC if you aren't taking it for a specific condition. It's just not worth the hassle OR a new wardrobe! I'm almost 40 years old, have been working out since I was in my teens and have not weighed this much since I was pregnant. I know that the trainers in my gym think i'm some kind of closet eater or something! I'm working and working and getting fatter!
The symptoms all are things I experienced while pregnant with my son - 18 years ago! If I wanted to feel preggers, I'd get preggers! My new husband probably thinks I'm letting myself go now that I'm married. Luckily he's very sweet and understanding. It was his idea to change my BC back. Call you doctor. Now!

So wow, i didn't expect to find everyone else having the same problems as me. Im 18 years old and was prescribed doxycycline for a testicular infection i got from a nasty river i swam in, i digress. this drug does seem to be helping, ive been on it for almost two weeks now. HOWEVER, im sure i have insomnia, and like other posts here, i feel very paranoid lately.
i hope there aren't any severe mental lasting side effects
Contrary to other posts this medication has subsequently helped with my acne. However my clear face is not worth the hell ive been going through with this nausea and insomnia. luckily my prescription is almost up and i HOPE i can go back to sleeping normally.

I just turned 18 years old and was prescribed Doxycycline Hyclate 100mg, BenzaClin (Benzoyl peroxide), and Differin 0.3%. I've been on benzaclin and differin for about 3 years now. About 2 months ago I was prescribed doxycycline for my acne. I specifically told my dermatologist that I wanted a higher dosage of acne medication since the minocycline 5mg wasn't strong enough for me; I had taken it 2 years prior to my visit. But when I would take doxycycline I'd feel a litte bit of nausea coming my way so I decided to drink some water with it. Shortly after I'd get something to eat. I'd feel better soon after. I've been on this medication for almost a month now and I'm not feeling any adverse side effects. My acne has somewhat cleared up but then i breakout again, around the same area. I'm hoping my acne will clear by the time I go for my check up in feb but if it doesn't, i want to be prescribed accutane instead. Also, stop the medication if you're having horrible side effects, obviously there's something wrong. It could also be an allergic reaction, I'm just fine but then again, I'm not allergic to anything and I also avoid a lot of sun exposure.

I'm 18 years old and I have sex quit often with my boyfriend.
everyday. and the first two months on loestrin 24 i had CRAZY periods! Like 15 days long.
the first week of the month would be nothing,
then BAM! I got my period 9 days straight , stop two days, and then on the brown pills for 5.

But what's weird now, is that i'm on my third month and nothing.
i've got four more days on my white pill until i get to the brown pill and i've been so constantly worried that i'm pregnant because the first two months were so strange and then NOTHING on the third month?
I'm just hoping i'm not pregnant and that the pill is just acting differently.
whatever it is it's scaring the shit out of me.

I am 18 years old and have been on Loestrin 24 Fe since July 1st. This is my first time on birth control. For the first week of taking it I was on my period and it lasted almost 7 days with 3 more days of spotting after. I have not noticed any of the horrible side effects that i have read here. But recently for the past 3 days I have been extremely irritable. I have crazy mood swings in a matter of seconds. I could be having a great happy day and suddenly I'm on a rampage or I feel like crying. I sometimes have weird vivid dreams but thats normal for me. I am normally a carefree happy person. My boyfriend has experienced most of my mood swings. He's just as concerned as I am. I feel really bad for f***ing out on him and everyone else. I hope this doesn't last long.

My experience with yaz was terrible. i have been anxious and tired unable to sleep, moody, loss of appetite, loss of interest in anything, i feel depressed. i don't get excited or happy or sad or angry i don't really feel any emotions. i did stop taking yaz but it is still in my system and therefore still effecting me, my boyfriends brothers girlfriend also took yaz and in her very own words "this is the devil pill". i must agree. i would not recommend yaz to anyone. i am 18 years old.

I just started my second pack of pill yesterday and I don't know if I like these pills. I am taking zoloft also for anxiety and my side effects are horrilble. I have had a hard time falling asleep (I literally have to lay in bed with my eyes closed for hours before falling asleep), I have terrible nigh sweats and wake up drenched in sweat, I sleep all day long, I have horrific nightmares which I never had before, and massive headaches.
I am not sure if I want to stay on the pill, I know it is only my second month and it takes a couple months to regulate but the side effects are ruining my social life. I feel like a zombie.
About the third week in my first pack i started spotting (or what I thought was spotting). It lasted 8 days, and my normal period was only 6 days. I bled just as much as on my normal period and has severe cramps as well. The only reason I got my 'period' was because I was about an hour off on taking my pill the previous day. It is pathetic.
Has anyone else had these symptoms? Or have any suggestions on better birth control pills.?
Oh and I am 18 years old.

I have been on zoloft for 18 years, mostly at 50 mg. This time period includes when I was pregnant and breastfed my son, now age 9, who is a special needs child. I regret taking zoloft during my son's babyhood but was hooked, told it would be OK by my doctors and was afraid to go off. I have never gone above a size 14 before going on zoloft, usually hovering around size 10 or 12 and wishing I was an 8. Well, I am now a size 24 and weigh over 200 pounds. My stomach is so huge people often think I'm pregnant which is a source of huge embarrassment for me. I find it impossible to control my desire for sugar which I crave to boost my energy. I am often sleepy in the afternoon yet can't get myself to bed early enough. I am apathetic about everything except my son. I have gone months without sex and didn't miss it at all -- thank god for a saint of a husband. Recently I started up sex with my husband even though my drive was still very low, as I saw it really helped my marital relationship. How nice it would be to actually feel a sexual desire before we start up. I crave wine at night to calm me down despite being on this drug. I feel like my brain is sluggish and I've lost some major IQ points. I hope that's only temporary. I have no desire to leave the house and would be happy to stay home all day which is I'm sure due to the drug. I can't get myself to exercise. I feel this drug has put me into a sort of walking coma. I want to go off and will begin soon -- I have set myself up for a tapering schedule that will extend to over a year using liquid zoloft and going down over 10% a month to minimize the brain zaps and depression backlash. I hope I can do it -- my husband wants so badly to get back the size 10 sexy woman he once knew. I want her back too. I hate this drug with a vengeance and am furious I was ever put on it. Absolutely furious.

I have been on NuvaRing for about 3 years now and never really noticed any side effects. Normally, I have bad cramping and a heavy period, but NuvaRing relieved me of that. But for the past couple months, right before and during my period, I will get the most intense 3-4 day migraine/headaches. I have to constantly take Excedrin or something, the pain doesn't stop. So now that a couple months have gone by, I spoke with a girlfriend of mine she said that her old b/c used to give her headaches. I googled Nuvaring and headaches, and here I am at this site. I am so happy I found this site because I have had NO sex drive at all and I really thought there was something wrong with me. I am young, happy, in a beautiful relationship and my fiance thinks Im not attracted to him anymore. It makes perfect sense though, this has happened ever since the NuvaRing, i really just have no want or need to have sex at all-like its a task or something. Its horrible. And I saw several mention the discharge and the yeast infections and the UTI's. Wow. I have unlimited prescriptions that my gyn had to write me because I get UTIs. I keep asking my gyn what causes them and he tells me sex and not urinating after sex and blah, blah. I''ve heard every single reason and believe me, I avoid all of them and still get them. I am the most careful person ever because my UTIs are horrible. I wont have one, then BAM, it burns to urinate, i urinate blood, i go to the bathroom every 5 seconds, horrible cramps, paint in my back. Horrible.
Seriously though, I am in shock that it took so long for the headaches to start and for me to look into this medication more. I was 118 pounds when I started this pill (around 17 or 18 years old)...at 21 years old...I am 150 pounds. All of which, I definitely wouldn't blame on the ring, but never in my life have I gained so much weight for no reason. I was even working out at the gym and couldn't loose a pound. I feel like giving up, because by the time I get out of work all I want to do is sleep. I have zero energy, I am always tired and never want to do anything. And it seems like so many other people on this site have had these issues to. I hope my story helps someone else in their decision to stop NuvaRing. Thankfully, I just took out my last one on Sunday and didn't spend the $150 for a 3 ring refill. Crazy prices, especially when you pay good money for insurance.

Well these are crazy. I got the Mirena inserted Just May 2009. I have no children, I am only 18 years old. I just got married, and the OB/GYN said the Mirena was the best thing for me. Well, I am going through so much, i have had a cyst on my ovary. I go off on my husband about every little thing in the world! i just crying out of no where!, i spot all the time, i discharge a lot, i am always hungry, i constantly pee, i really thought i was pregnant, which i still think i am, which i need to go get a pregnancy test. This is just scary, i want it out now!!

I have taken Lamictal for about three years since I was 19. I feel like I'm experiencing the memory loss of a 60- or 70-year-old. I've always been quick and witty with impeccable grammar and spelling. These days, I struggle to remember words and their meanings, spellings and pronunciations.

I can't remember conversations I had with people half an hour before or items on my to-do list. I MUST write everything down. Sometimes, if it's in my planner, I still don't remember to do it.

It has affected me in my college classes, on the job and in my relationships. I hate the feeling that I'm less intelligent and quick as I used to be when I'm just 22. My short-term memory is shot.

Along with memory loss, I struggle to focus (always have been a straight-A student), follow conversations and often feel confused and need people to restate their thoughts so I can understand.

It's just so embarrassing to be so spacey. I didn't put it together until my sister (also on lamictal) told me about the memory loss and it clicked. At least there's a reason for my new-found stupidity.

Thanks for telling me doctor. Oh wait, she didn't.

****Are you having severe headaches, vision problems, dizziness, ear pain, nausea?? If so, you may be experiencing what my daughter did. Please, please seek immediate treatment from your physician and request a CT or MRI. This is the only way to detect blood clots. Unfortunately, my daughter did not have that chance. She was 18 years old. I do NOT want to scare anyone! I want to raise awareness of the side effects and prevent any of you going through what my daughter did. Listen to your body and go with your gut. If something doesn't feel right, you need to get it checked out. You may need to be very persistent with your doctors too. Don't give up & give in to them. If you are having any of the side effects I listed above daily, you need to follow-up with your physician immediately!!****

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

I'm so happy to have found this forum because I've been very confused about how I've been feeling lately. I've had the mirena in for 3 months and in the past week I feel as if I have become a completely different person. I haven't felt like myself since I got the mirena but didn't know if it was for other reasons (not concerning the mirena) but now that I read all of these posts I really think that all of my problems are stemming from this. Please comment if these things seem familiar! Lately I've felt completely worthless and depressed, constantly crying and irritable, and EXTREMELY sensitive to everything (looks, comments, tone of voice). Even though in my head I know its not what I want I continue trying to break up with my boyfriend of 9 months and constant arguing. I feel horrible for him to deal with these mood swings but I absolutely am not myself. I'm 18 years old and I feel like there's nothing left for me. I always think of how I'd rather sleep all day because then I couldn't feel like everyone hated me and didn't want me around. ALSO- I've almost completely lost my sex drive which is abnormal for me. At first I thought I was depressed or bipolar, but I think mirena may be the problem!!

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.

Im 23 years old. One of the youngest people that is on coumadin I got sick when I was 22. I developed blood clots on my liver and stomach. Due to blood deficiency. I was told by the doctor it was inherited by one of my parents. My side affects are very fatigue, tired for no reason, skin blotches, slow memory, I get tired after 10 minutes of running like Im ready to collapse. Im always dizzy. =( I feel very fragile. I do get depressed sometimes because I feel like im very young at my age for this to happen. I found out I have to be on coumadin for the rest of my life. But we all move on....

E-mail me ******

Hopefully someone can share there idea's or another source of help.

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.