Spelling symptoms and conditions

I know that for every woman, the side effects or various medications and hormones are different. I personally had the Mirena IUD inserted a little over 3 years ago on the recommendation of a friend who, at the time, had nothing but positive things to say about it. I went on that recommendation alone, and now wish that I had done more research into the side effects before having one inserted.

The initial insertion was not horrible, but not great either- a pinch at insertion, severe cramping and pain within a few hours, and a dull aching feeling in my abdomen for about a week. After that, though, I couldn't feel the IUD at all.

It was not long after that when I began to experience side effects. Like many of you, I attributed my symptoms to stress and life changes. I figured that my migraines, back pain, fatigue, dizziness, increasing urinary tract infections, and weight gain were a result of a changing metabolism and high-stress job.

When I went to my family physician to have blood work done (because I was declared anemic when trying to give blood), I was told that I wasn't getting enough iron and I went on iron supplements. (The supplements then made me constipated- sorry if that is TMI, but that was a very unwelcome result!) When I took trip after trip to my ob/gyn for antibiotics to treat UTIs, I was told that the UTIs were unrelated to the IUD. When I saw a urologist to have three separate tests done (one for hormone levels, another for uterine function, and yet another to test kidney function), all tests came back within normal range. Even when I went to the ER one Saturday morning, when my back was spasming so badly that I could barely walk or stand, I was told that my back pain was stress-related.

All the while, my friend (the one who recommended the IUD in the first place) was dealing with similar problems- weekly severe migraines, back pain, etc. She was being told the same things by her ob/gyn- none of her symptoms were related to the IUD. Since she and I trusted our doctors completely, we went on about our lives, upped our workout regimens, tried to de-stress as much as possible, took OTC pain meds when it was all too much to bear- and yet for both of us, our symptoms continued.

Then, in July, my husband and I decided to begin trying for a baby. I made my appointment to have the IUD removed (which was a painless process), and it was only then that I began to research the Mirena IUD online. My former ob/gyn had moved, and my new one seemed ill-informed about what to expect once the IUD was removed. I wanted to know how soon I could conceive, and she knew very little about the process- heck, she didn't even know what the hormone was called that she had given me to jump-start my period (it was progestin, by the way- a very common prescription that my paramedic husband knew quite a bit about, but the ob/gyn didn't even know the name of!).

Once I got online and found this site (among many others), I finally began to put two and two together. I am now firmly convinced that my symptoms were directly related to the Mirena IUD. Again, different women are affected in different ways, but I know that for me- nothing good came of messing with Mother Nature like that.

Now that I've had the IUD out for about four months, I feel like a different human being. I did experience the "Mirena Crash," but once that passed, I almost immediately began losing weight, my abdomen was no longer blown up like a balloon, my energy level and sex drive increased, my back pain is now gone, and I haven't had a migraine or UTI since.

I've since switched ob/gyns, but I now have a healthy distrust of anything medically new and experimental. I will never have the Mirena inserted again, and I will definitely research anything and everything regarding my body. Ladies, listen to your bodies- mine was screaming at me loud and clear for over three years, and even though I knew that something was very wrong, I didn't listen. I'm just happy that I "accidentally" figured it out. (Oh, and my friend will be having her IUD removed later this week. She and I now call ourselves the "sister skeptics!")

Follow up!!! (don't mind my spelling, it sucks!)
so i just left the ER. Come to find out, i am right! the mirena string is gone! it went up into my cervix and they said something like to the right side of my abdominal cavity going twords my right fallopian tube and has caused fluid build up which is also causing pain. they said my right overy is ovulating and that is some pain added to it. they also said they are worried bout infection and gave me a shot in my but and put me on antibiotics for 2 weeks and gave me 800 mg Motrin and told me they can not take it out but to call the OB in the morning and schedule to have it removed asap. she said they will have to put me out with anesthesia and dilate my cervix almost like I was being forced into labor... they said they will try and take it out that way.. and if that dont work, they have to do surgery to get it out. this sucks!!!! i will NEVERRR EVERRR recommend this thing to ANYONE!!! all my friends who have it are now also worried and want theirs out too! soooo many people complaining about it and it has some NASTYY side affects! now i know why i get so irritated... mad so easily... and can cry so easily too... it has caused a lot of problems in me and my bfs relationship.. once he sat here with me yesterday and read most of u, he was like wow... its not that im purposely ALWAYS being a B*TCH! lol!! thank you everyone for posting so i know im not crazy!!

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

I have been getting lupron depot injections since my laproscopy back in August and had no trouble the first month except for hot flashes. After the second injection I started to experience migraine type headaches and I would get the shakes really bad through the night almost as if I was coming down with the flu. I just had my third injection and the symptoms are worse. I feel tired, nauseated, body aches, chills through the night and hot flashes all day long. Will my symptoms continue to get worse as I go on? I have two more months of injections and I am contemplating not doing it. My husband and I have a beautiful little girl but really want another child. Is two more months really going to guarantee pregnancy or is it a waste of my time?

I've been taking Lamictal for almost 3 months. I've been struggling with mood problems for 14 years always being diagnosed with depression and being put on anti-depressants that did nothing to help. Finally a doctor dove a little deeper and diagnosed me with Bi-polor disorder. Lamictal and Trazodone. I stopped taking the trazodone because it made me feel like a zombie and made me gain weight. I have since lost that weight and am not having any weight gain problems on just the Lamictal. I am however having problems with headaches and actually eye aches if that makes sense. My eyes always feel dry or tired or something like that. I am also having trouble with memory loss. I often go to do something and forget what it was on the way there. At work i find myself stopping on my way to a task and wondering "where was i going, what was i going to do?" I'm also having trouble with spelling and like the others here it was never a problem before. But i will put up with these because Lamictal has made such a difference in my life. I feel more stable and stronger in the face of stress than i ever have before. Right now i'm just on 100mg maybe things will get worse when my dosage is raised but right now the side effects are bearable and in my opinion worth it.

I have been taking lexapro, lamictal, and wellbutrin for about 2 1/2 years for a lifetime of depression and anxiety/panic disorder. I had tried medication at age 15 and experienced all side effects and no benefits. But then at about age 21, I was so desperate that I gave it another shot...figuring there might be a difference in the past 6 years.

I started off with lexapro...and the first week I was soaring! I was jogging at 1AM and going out and enjoying life! I remember going to the movies with friends and laughing FOR REAL and having REAL fun!

At some point of course you level out and that was fine...but then it wasn't enough anymore so the lamictal and wellbutrin got added on.

Recently, my psych raised my (generic) wellbutrin to 300 XL from 200 SR.

I definitely noticed the difference between the XL and SR.

The real function of wellbutrin for me was getting me up out of bed in the morning. It gives me nervous energy, but that has been better than none at all.

But now I've recently realized some other fun side effects!

Memory loss and motor function impairment.

It's kind of funny because I think it has been going on for a good while, but I just didn't REMEMBER enough of it to piece it together. AHA good one right?

I am a hairdresser. A damn good one I'd say. Or...used to be?
I trained for and alongside of the best educators in the industry. I wrote the haircutting curriculum for one of the top education academies.

Now I feel like a f***ing idiot.

I've cut my fingers more in the past week than in the past 6 years. I find myself getting completely lost while doing someone's hair...like I've never been in that situation before.

Sometimes I have tremors that keep me for being able to hold my comb straight and still. My fingers seem to move more slowly and with less grace or control.
I type sooo much slower now.

I've also gone from having excellent spelling, grammar, and range of vocabulary...to forgetting common words...not being able to finish my sentences...and I find myself trying to sound out a word to figure out how to spell it. This doesn't work out too well.

I feel just plain dumb in general. I can't do relatively simple math in my head without getting confused. I can't process or answer a question under pressure.

Now I'm telling my DR. to stuff it, and try to wean myself off of this madness.

I really hope that these side effects aren't permanent. Then I'm just screwed.

I stopped a few times during this post at a loss for words.

Yeah so it stinks that I have lost my substitute for motivation.

Thanks for sharing everyone...you've made me feel like less of a failure.

OH YEAH!

The original story I was going to post was that today I went to the deli to get lunch and I got everything I was going to get for my coworkers...and forgot to get my sandwich. The check out lady is mean to me so I didn't go back. :\

I've been on Doryx for a few weeks now. My mood has changed a lot. I am a creative writer and I have not written anything new since I started the medication. I am taking it for acne and it works but it is affecting me mentally. I have no desire or new ideas to write. I've even gotten bad with my spelling and I used to be an Ace at that. I may just get off of it because my writing is my livelihood (fyi, i just second guessed the spelling of livelihood as I am typing this).

I took Yasmin for about 2 years, and didn't seem to have any side effects at all. I never gained weight, lost hair, felt nauseous, or anything. Then on Halloween 2004, I suffered a moderate brain hemorrhage. I was 21 years old, and very healthy with no prior health conditions. The doctor said he didn't know the cause, I had several tests done, there were no signs of aneurysms (I am not sure of the spelling there) or any AV malformations. He said it could possibly be the birth control, but he can't be sure. I was immediately taken off of the pill and all other birth control pills because of it, and have had no problems since.

Hi, All! I went to the doctor on August 10th and had my Mirena taken out. My strings had retracted up into the uterus and I was VERY worried. It was a breeze.I didn't feel a thing, well maybe a little pressure was all. It didn't take long at all, to remove. I told my doctor that this thing was draining the life out of me. I was ready to hear This is not a side effect or this is not a side effect etc. He told me that Mirena has alot of side effects that are not even listed. My mouth dropped open. Wasn't prepared for that one. I started telling him just a few side effects I've had and the non stop bleeding since DEC 2008. He said he would definitely remove it. After my removal light bleeding the next day. On Sunday it started, I bleed HEAVY HEAVY blood clots and all, until the following Sunday and then it just stopped completely. I'm currently waiting my normal 28days to see if I get my normal period back. As for side effects My back where I could barely stand up. The pain is gone. I can get up and down fine without pain. My hair has stopped falling out by the had fulls. Memory loss is improving. Sex drive coming back. I've just noticed little things that I would complain about not even bring them up. I'm sure over time I'll notice more improvements. I'm so glad to have Mirena Out of my life. Also thankful to have understanding doctor.
Sorry for spelling and sentences.

let me just say i have never been the same since taking this drug almost 5 years ago! don't take it!

I can't believe what im reading here... I too have been taking doxycycline for bronchitis(spelling) i thought i was dying... the first day i took one i puked within a half hour of taking it, after that i continued taking it with food, then on day 3 i woke up in the middle of the night sweating so bad my sheets were soaked and not to mention the headaches are unbearable. i quit taking the pills right after and have a doc app/ this drug is ridiculous and obviously there are a lot of people who seem to have the same side effects.. i think it should be pulled

My husband was taking coumadin and then developed an infection. He was ordered Bactrim D.S twice a day and by the third day he was bleeding in his brain. He had to have bilateral subdural crainiotimies twice to flush out all the blood in his head. He almost died. He now has severe headaches and some short term memory loss.

Got married about a couple years ago and went on Yasmin. First BC and as I've never had any BC did not know what to expect. I felt fine but now reading all these makes me realize that the weight gain, NO SEX DRIVE, NO VAGINAL MUCUS (have to use tons of lubrication), re-occurring thrush could be attributed to Yasmin.
I stopped Yasmin last year December as now ready for a baby, its been six months and still haven't conceived, still dry and use lubrication....and also have milky discharge from breast but not pregnant. Had an MRI scan and showed pituitary anenoma (not sure of the spelling) basically a small tumor of the pituitary glad that secretes too much prolactin in system caused by imbalance of hormones.
I'm only praying to God for healing and hoping that my body would go back to normal rather than start other medical treatment.
My advise.............. come off Yasmin, DO NOT TAKE ANY BC

I've been on Topamax (100 mg 2x per day) for 5 years as mono therapy for epilepsy. I switched over from Depakote which was a *nightmare* and it has been great, no seizures. I've had the pins and needles, diminished vocabulary and memory, and intermittent eye twitching but this week my right eye (why is it always the right eye?) has started twitching almost constantly. It is frightening and embarrassing and I am not sure what I should do.. I guess it's back to the neurological drawing for me because I am not sure why it's happening now. Has anyone else had the eye twitching occur after long term use?

My 4 year old Son has had diarrhea from about the last 4 weeks... we have started some tests for Celiac disease but today it only occurred to me today that he has been on Singulair for about that time frame... after all the worry and reading these other storied Im even more convinced that it maybe the Singulair..
Im just hoping that someone might read this sometime today or the next couple of days to tell me if when they come off the singulair how long did it take for the diarrhea to pass. My son had is last tablet 2 nights ago ( so he has only been off it so far for one night. But he still has the diarrhea.. should it have started to come out of his system already.

after taking cipro for a few year for prostrate infection I have developed a
reacurring cyst on my wrist. Has anyone experienced this sort of problem?

Ok so...I started taking Loestrin 24 almost a year ago and I can't really complain too much. I've had a few pregnancy scares because of missed periods but they were just that- missed periods. And there's nothing wrong missing a period or two imo :D
About two weeks ago I ran out and couldn't refill so I neglected to take any pills for a week, figuring I would just pick back up when I could. I've since started taking them regularly again but in those two weeks my personality changed sooo much. In an attempt to describe myself I'd say I was...confused and depressed, for no real reason. My stomach was so messed up I don't even want to share the details. And the strangest thing... I've noticed two VERY SMALL spots (one on my upper thigh and one on my butt) that are slightly red and drier than the skin around it. I'm positive it's not an STD but I'm concerned nonetheless.
In conclusion, I'm gonna take my pills regularly from now on.

But seriously if anyone else has gotten weird small spots of dry skin, plz respond cause it's definitely worrying me a little.

I have been on 100 mg topamax for a few months now, and i was actually having people try my drinks bc i thought they was flat, and i would feel my fingers and my toes go numb and tingle. I honestly never thought for two seconds it was my medication. The only side effects i was warned about was weight loss (which hasn't occurred with me) and that i would be very thirsty, which i am. But i have NIGHTMARES about things im not even afraid of, and i have trouble spelling words i didn't before, and sometimes i can't even remember what i wore last week to school. Im starting to rethink this whole topamax thing, does anyone know any other prescriptions that will help headaches without the crazy effects?

As with others on this forum, memory loss is a side effect I'm experiencing with Lamictal. In fact, it's THE only side effect. I began taking Lamictal three years ago, and have maintained a dose of 300 mg a day. My short-term memory is practically non-existent. I have to write EVERYTHING down, and sometimes that isn't even enough. I've been known to forget what I've read only minutes before. I used to pride myself on my impeccable spelling, and now I'd say I'm at a fifth-grade level. In fact, I feel like I'm about ten years old. I've been taken to task over and over by employers who are frustrated with my poor performance. I've lost one job and due to lose another any day. Sure, my mood is stabilized, but for what good if I can't even support myself? I would definitely go off this medication if there was a good chance I would get my memory back, but I haven't come across anything in my internet travels that indicate this is a possibility!

I am on this medication for seizures. Besides all the other side effects being posted (typing, speech, spelling, forgetfulness, etc), I have EXTREME daytime sleepiness. To the point that I will not/cannot drive and have to stay where I'm at until I "wake up". I have been off work for 5 months, but had to go back for financial reasons. I work partial days and go home and take a nap, which the neurologist prefers I don't. Anyone experiencing daytime sleepiness (disorders)??? Thanks

I am a 25 year old woman with 3 kids. I was prescribed TOPAMAX 3 months ago. I am on 150mg a day. My DR. told me to take them at night before bed and I have to take a TYLENOL PM with it so I can sleep at night and drink 64 oz of water a day and 8 oz of citus a day to help flush out my kidney's, cause TOPAMAX does cause kidney stones. I was having about 17-20 migraines a month before getting on this medicine. They have cut down to about 5 but I take RELPAX and in about 30min my migraine is gone. People who don't know I am taking the TOPAMAX don't notice my side effects. I do have some side effects, memory loss, loss of concentration, I have lost about 15lbs with the help of dieting I was 134 now at 118, spelling, sometimes my words come out abit slured, my eyes are sensitive to light I need sunglasses to go outside,.I feel tired sometimes no matter how much sleep I get. Well I hope this helps...

I am a 27 year old female and have suffered from migraines for 10 years. My neurologist prescribed 12.5 mg for the 1st week, 25 mg the 2nd week, 37.5 mg the 3rd week and 50 mg by the 4th week and then we will re-evaluate on the 6th week. I am on my 2nd day and have experienced a few side effects.....tingling in my arm and lips, frequent diarrhea, carbonated drinks taste flat, trouble typing/spelling and a burning sensation in my eyes. My arm also feels heavy and dead. I am willing to give topamax a try--I can't stand living with my migraines! I think the most bothersome side effect is the inability to type/spell correctly. Hopefully with time, these effects will subside. Wish me luck! (hope I spelled everything correctly!)

I went on Loestrin 24 about 3 weeks ago and have kept telling myself to wait it out. From the first day I started to feel depressed but I stayed with it. Ive started to fight with my boyfriend of 2 yrs now and questioning our relationship more than ever. I have NO sex drive what so ever, Im constantly depressed, I have anxiety and my mind is constantly all over the place with weird thoughts that I have NEVER had before. Ive already started to gain an uncomfortable weight. I am 5'4 and 115 pounds, very active, and I eat very well so the weight gain does not make sense to me. The only plus is that my boobs are getting bigger...but feeling like total crap and hating everyday of my life isn't worth it. Im debating going off of this pill but keep telling myself to ride it out. I was on the shot for about 5 yrs and went off of that about 2 yrs ago. I started back on this pill because I get really bad PMS...the shot made me gain about 20 pounds. So I dont want to go back on that. After reading all of these horror stories - Im beginning to think that my 3-5 days of serious PMS are totally worth it vs. 3 weeks of serious depression

I have stopped taking Lipitor after 3 yrs. I was told I had a mini-stroke because of my slurred speech 6 mo. ago. Since then I have had a battery of tests and my neurologist told me "I don't think you had a stroke." I saw the words "Motor Neuron Disease" (I looked it on the web because I never heard of it before) on the script for my EMG. I blame it all on Lipitor and the wasting of the nerves and the muscles. I sound as if I am drunk. No one can understand me . I am taking speech therapy but it doesn't seem to help.

I have been taking 200 mg. of Lamictal (now Lamotrigine) for 5 years. I have had cognitive issues for probably about three years at least. Memory loss, sudden loss of flow in conversation, completely forgetting words and the spelling issue which was previously impeccable. It's embarrassing and frightening. I can't get through ANY given day without losing my belongings over and over again. I feel disabled (seriously) and I jokingly tell people I need an "aide". The scariest thing was last week I was going to return an item to the store and COMPLETELY forgot my PIN # for my debit card. I have been using the card nearly daily for a year and a half!!! It panicked me but I thought of course I would remember it later. NOT!!! Never again, it's gone!!! That's when I decided to search the internet for "severe memory loss" and came upon this blog. I didn't even think of the Lamictal. And I pride myself on my thorough research!!! Certainly the doctor never mentioned this side effect and I just gave it up to being 49!!! A little early for Alzheimer's!!!

The funny thing is I have also had skin problems (acne) for the first time in my life the past couple of years with it really getting bad last summer. I weaned myself off the Lamictal b/c I had read it could cause acne (another thing the doctor never told me). Well, I was completely weaned and omg, the mood issues were severe!!! So reluctantly I titrated back up to the 200 mg dose and immediately my mood was stabilized.

I don't know what the h--- to do, but something needs to change. The memory thing is terrifying!!! No wonder I am having so many problems with my job!!!

Maybe a new med, maybe not . . . My main issue was severe depression (both situational and chronic) which Lamictal seemed to stabilize. Do the benefits outweigh the side effects??? I think NOT . . .

FRUSTRATED IN MICHIGAN :(