Been waiting symptoms and conditions

I had the Mirena inserted in March of 2007. I was required to sign a release form before they would insert the device. That seemed very strange as no other birth control method I have ever used required a release form.
My former OBGYN Nurse Practitioner had no experience implanting the Mirena into a woman that had not yet had a baby. But she went ahead and did it anyway. It was immediately painful. I cried while it was being inserted. The Nurse gave me an NSAID and sent me home. I wallowed in pain for several days-to the point of screaming and crying at the same time. I called her to ask for something stronger. She told me just to take some Tylenol. For those of you who have had the Mirena, you KNOW it's not the type of pain that can be solved with Tylenol. She is a QUACK. Her name is Leda Riley at the Women's OBGYN center in Cookeville, TN. Yeah, for your sake, NEVER go to this woman. She does not listen nor does she care if you are suffering.
I actually had to call my general physician, who is much more understanding. She prescribed Tramadol (which makes me itch, as it is a narcotic drug) and also 600 mg tablets of Ibuprofen (which are hard on my GERD). But these worked a heck of a lot better than tylenol.
Before the Mirena, I had perfect skin-the type that looks airbrushed in a magazine. Now, I have redness, acne, blackheads and boils. My dermatologist has tried everything, including spot treatments of super strength benzoyl peroxide (10% and higher) to rid me of the acne. Nothing works.
The hair is another thing. There are these inch long hairs growing like mad on my neck and chin. I actually have to shave, cut or chemically remove these hairs. I had no such hair growth prior to the Mirena.
My moods swing wildly and have led to obsessional thoughts. My anxiety is so horrible that I have had to be put on Zoloft. This is really difficult for me, as I am a student Mental Health Counselor. In other words, I know what is going on-the contraindication between my body's hormones and natural chemicals to this Mirena.
Also, I have gained nearly 40 pounds from the Mirena. I don't eat much. We're talking 2 rice cakes for breakfast with water; no lunch and a kashi meal for dinner or a similar low carb dish. I don't drink sodas. I don't eat high carb foods. I don't consume mass amounts of sugar. Then, I look at the rotund version of what used to be my beautiful and curvy figure in the mirror. What I see makes me so upset that I just cry.
I know that what is going on with my body is wrong. You can feel it way deep down on a level that seems so basic, so subconscious almost. With the 3 week long periods, followed by spotting for another week, then back to the period---I am ready to have my old period back. In fact, I WANT it back. I don't care, just so long as I don't have to wear damned tampons any longer than 5 to 7 days per month! (Can I get an Amen?)
This was originally supposed to prevent pregnancy (although I have had one ectopic pregnancy with this thing already). I had good intentions, but this is horrible. If you look VERY closely at the patient info on the Mirena, you'll find out that the researchers and developers of this IUD have absolutely no idea how this thing really works (hence the release form?).
If you do decide you want to get the Mirena, please read the blog spots about the real deal behind this thing. There are other options with much less pain and change. Think very hard and remember that no matter your decision, there are hundreds of women supporting you everywhere.

Has anyone out there had an increase in urination? I started Yaz in Feb. and since then I've been peeing like a race horse. My OBY said it was probably an overactive bladder, typical for a peri-menopausal woman. I had tests for bladder infections and they read negative. I was in the middle of relocating my family across many miles and I just put up with the symptoms. Now I find out there is microscopic blood in my urine and I am scheduled for a slew of tests probing for tumors, cancers, polyps, etc. in my bladder and kidneys. My Dad had bladder cancer so I'm pretty scared. However, I am starting to wonder if there is a Yaz connection. I hate the thought of returning to periods where I couldn't leave the house because I was bleeding so much but all the risks here are scaring me. I don't have an OBY here yet but assuming I am not harboring cancer or an other disease (i.e., kidney stones) I think I'll go off Yaz. I already have horrible migraines and acne so I'm wondering if it will all get worse. My headaches are the same (2-3 times a month) with Yaz and my skin is better. It's been pretty good for water weight but as I said, I am in the bathroom way too much.

I have been taking Synthroid since Jan. 2006, am on 100mcg per day and all test results have been 'normal', I have been told to take this medication in the morning an hour before eating anything, if I do this...I have headache all day, I can't eat after an hour because I am so sick at my stomach there's no way. I feel hungry, but feel like if I eat it's coming right back up. Am having serious joint pain in hips, knees, elbows and wrists, my neck hurts really bad as well. I wake up to arms asleep anymore and just feel like I haven't slept in months...am very weak and very tired all of the time.

I have found that if I take my pill at night this gets a little better, but holy cow, don't tell your Dr. your taking it before bed...no, take it of a day. (don't know why this is a major thing?)

Anymore I feel like I am walking around with flu symptoms constantly, and the Synthroid hasn't done anything weight wise with me, because I was so HYPERthyroid before the RAI, I was very thin and looked like a bag of bones, have been waiting and excited about putting on weight...at one point I stopped taking the Synthroid and let myself go HYPO just so I could gain weight, it worked and I got up to about 130 pounds, was very HYPO so they told me critical that I get back on meds...I lost it again because it makes me so sick I can't eat.

NO-ONE can tell me the Synthroid is not the cause of this problem, if I stop taking it I feel WONDERFUL, but my test reults are bad. After a while of course my feet become numb and I end up having some bad hypo symptoms, have tried breaking pills in half....oh Lord no, need it all...

Have been told they are thinking about raising my dosage again anyway, I can't do this, I will break down in the office if they try to raise it. Right now my TSH is fine but my T4 is 'a tad bit' off. I am already an emotional wreck, if they raise my dosage I am going to try and go a different route with this, am on my 3rd Dr. at this point anyway...

This website is wonderful! I finally have peace thanks to being off Advair and knowing that all those dreadful symptoms were side effects of Advair.
I have been on ASMANEX now for 29 days and haven't misssed my life before on Advair. When I was on Advair, my asthma was not in control. I used my inhaler at least 2X/day, I was panting when I exercised, my asthma woke me up at night and my leg cramps kept me from falling asleep for many hours every night.
I was on Advair 250/50 and felt awful. I now take ASMANEX 220mcg only once per day; before I go to bed and my asthma is in control. I am taking 280 mcg LESS of steriod than when I was on Advair and no Serevent and I feel better than I ever have!
It's amazing b/c I tried Advair 100/50 and it didn't work for me at all but ASMANEX(mometasone) is much more effective.
I have been waiting for this drug to come on the market for some time (it is the same drug as Nasonex just like Flovent is the same drug as Flonase) b/c I have horrible allergies which flares my asthma and I have found that Nasonex (mometasone) was far superior for clearing nasal congestion than Flonase so I assumed it (Asmanex) would work great for asthma too and I was right.
As a matter of fact Nasonex works so well compared to Flonase that at the moment it is pollen season and I don't even feel like I have allergies. Now that is amazing.

Dear Lisa,

a few posts ago I had already told about the blurred vision and thought you had found that.

Well, the blurry vision was so bad around January/February 2005, that I couldn't read anything, watch tv or work at my computer. It felt as if I looked through a milky window or such. Everything was like behind a "fog".

That has improved a lot, but it took time!! About 3 - 4 months AFTER Yasmin it slowly got better and I finally was able to work on my computer a few minutes a day, then a few hours and today I'm sitting here, working again the whole day long if I have to, read books and watch tv without big problems!!

But remember: IT DEFINITELY TAKES TIME!! And no one of us here can say, how long it will take for your symptoms to decrease cause every woman is different. I'd been taking this poison pill for 5 long years, so I think that I will have to be patient much longer than only one year... (Today I'm nearly 1 year off Yasmin and still not feeling 100% fit and healthy again!!).

The blurry vision comes back sometimes when I'm really nervous or under stress, but not as bad as it was last year at all. And remember: Every symptom brought on by Yasmin and the hormone chaos after getting off seems to get worse around ovulation and the time your period starts or SHOULD start (I still didn't have one since easter 2005 but in spite of that I realize more symptoms around 2 weeks a month.....).

And so it is with the libido thing. In my case my husband had to "ask" me, if we just could TRY it again, very slowly and careful (well, this time he had already been waiting for about 8 months, cause I wasn't fit enough at all to even just TRY...). I said yes (though I didn't really have the feeling, that I was ready for that thing again!!), and a few days ago I started this "thing" by myself, because I recognized, that my feelings came back and believe me, those were feelings I didn't have for many many years (you could say 5 years not really feeling alive under Yasmin......).

And I'm afraid, but 10 weeks off Yasmin is not really much... Sounds hard but that's a fact. At 10 weeks after Yasmin I still didn't feel, as if I would live any longer... But always remember: Every woman is different. No one can give you a time plan that is working 100% correctly in that case!!

So please give your body the time that it needs (and it can, I don't say MUST, but CAN last months!!) and everything will come back if you're just patient enough and believe in better times that are ahead!!

All the best to every Yasmin victim out there and stay strong and patient, there's light at the end of the tunnel!!!

Silke

PS: Sorry, that my posts always get that long...

I feel relieved to know that I am not going crazy, that many others are having unpleasant side effects to Singulair. I am 28 years old and started taking this medication about a month and a half ago for allergy induced asthma. Things were great for about a week, I was breathing great, never short winded, I could sleep at night breathing through my nose for once even.

Then came the second week on the drug. I realized I was getting restless at night, having horribly vivid dreams. I'm constantly nauseous and just starting to get more irritable, aggressive, depressed, tired. I bruise really easlily now, get terrible muscle spasms and cramps in my legs and feet. I've been waiting this out to see if it gets any better for I know these can be side effects, but I have just had enough. I'm thankful for this website, and the people who are telling their complaints. I will be stopping the medication tonight, and will have to consider other alternatives like allergy shots etc.