Heavy metal poisoning symptoms and conditions

I have had my mirena since April of 2006. For the first two years it was the most wonderful thing in the world ( no cramping, spotting or periods). But lately I have been feeling very horrible. I have no desire to do anything. I am very tired, moody, gained weight (just around stomach area), depressed, joint pain and sik to my stomach. After reading a lot of the posting on this website. I realized that a lot of the women feel just like me. Now I know that I am not crazy. I also scheduled to have mine's removed on August 1, 2008 (yay!!!).

Why do I think I landed here, I have been having very bad mood swings mostly relating to anger and dissatisfaction in everything and everybody. Put the mirena in April 2008, braved it out for 4 months with the
1. spotting and all the time kept thinking that my
2. fatigue and no interest in everything was due the stress of having 2 kids, work and the pregnancy weight that I have to shed.
3. I am hungry always (maybe since I am breast feeding the baby)
I had a copper IUD between my first and second son,
4. I don't remember how that was ( am I in a mental fog?). must have been better than this one. I never wanted anything hormonal. I don't want pills. Dont even know why I went with this then. I know the doctor convinced me saying it has very little hormonal effects

Yesterday, I just lost myself over a silly issue, now I feel I am going to lose my wonderful relationships with people. My 3 yr old asks me If I am not angry any more uh!!!. Why cant I call the doctor to get it removed when I doubt it could be the IUD.
5.I am lazy( another symptom).

Do I have to wait a little longer or take it out and maybe get my self back.?
(What a question to an obvious answer)
Confused!!! lazy!!

I'm 19 and i've had mine since 2006...i've had most of these side effects but i never thought it was my IUD!!! I've always had an anxiety/depression/insomnia problem but it has gotten WAY worse over the past 2 years...i just never put it together.And i have had TERRIBLE cramps for 3 weeks now and i can't take it anymore.I've tried 3 or 4 times to get it removed but my doctors kept talking me out of it and telling me everything was fine,but obviously it's not so i'm getting it removed for real tomorrow @ 12:45!!!!YAY!!!!!!

i want to start off with IM SOOOOO GLAD I FOUND THIS SITE!!!

i though.. well i wasn't actually sure what to think.. i got my mirena at the end of January 2008.. at first things were going good... yes my periods got longer.. 3 times longer then normal actually.. i wasn't too worried because the OB said that might happen at first. then slowly i started loosing my sex drive ( im only 25 that really shouldn't happen) started getting achy, especially in my joints, so i started drinking more water. then my clothes started getting tighter.. i cut out soda all together and started watching what i eat more closely..i have also had some pretty bad anexity attacks lately.. which i never had before i got this thing.. i dint know what to do i though i was going crazy.. i talked to my doctors and basically got nothing out of that.. im now in my 6th month of having mirena and i have gained almost 30 pounds!!!! yes i have been hungry all the time but i either restrain myself fream eating altogether or eat healthy snacks.. i exercise daily and still am unable to lose any weight.. the numbers on the scale just keep creeping up and up.. im am moody and easily worn out.. i have no energy at all.. which isnt good with a 3 year old that has more energy then the sun.. i had no idea that mirena could cause any of these symptoms.. but the more i have been reading about it and the more site like these i find, the more i realize that the most likely culprut of losing myself is mirena.. i have decided that on Monday im calling my OB and demanding she remove it!! i want my old self back again.. i wasn't perfect but at least ill be me.. thank you all for sharing your experiences, you made a world of difference!!!!

I had surgery in August, 2006 for Endometriosis, and a Lupron injection 2 wks later. That one injection changed my life. Even though it was a year and a half ago, I'm still feeling the effects. Which is what brought me to this site -- I'm searching for an answer.

These were/are my symptoms:

-- I experienced immediate and increasing hot flashes that lasted for nearly 6 mos.

-- Extreme fatigue and the "activativation" of Epstein Barr Virus. I started sleeping 18-20 hrs/day and lost my career job because of it.

-- Cognitive dysfunction, memory loss, loss of concentration, etc.

-- Blurred vision (and I have otherwise perfect vision!)

-- To date, I have gained 40 lbs that will not budge no matter what my diet!

-- I have severe muscle weakness and burning (such as if I go up a
flight of stairs). Muscle atrophy and stiffness.

-- My joints (hips, knees, feet) hurt and I have a lot of back pain.

-- I have TMJ quite badly and it causes my arms to go numb.

Last year my doctor ordered a hair analysis for heavy metal poisoning -- and my levels were off the charts. I've read that Lupron is suspended in thimerosol, or mercury, and that raises a host of issues that I'd like to research, if anyone has info on that.

Today, I am doing much better in terms of being out of bed and active, but I am unable to lose the weight, despite an organic, all natural, gluten/dairy/sugar/corn/soy/caffeine/etc. free diet! My belly is always bloated and big.

I am really active, but I tire easily and still haven't been able to get over that "hump", as it were, and really exert myself. Before my surgery and the Lupron and the EBV, I was an avid dancer. It is my passion and I can hardly do it at all now. I cannot swim a full lap in a pool without my leg muscles burning.

I have read of some people having good experiences with Lupron, but I have read far more horrifying ones. Part of me doesn't want to accept that Lupron is the cause of what I'm experiencing...could it really be that simple? And part of me is happy to shed the burden of guilt that "I must just not be trying hard enough" in exchange for an outside cause. I guess research and knowledge is the best medicine in this case. =}

I was on Topamax for 10 days with a few minor side effects but nothing serious enough to quit it. My husband and I went to the library about 6pm. I am 46 and never wore corrective lenses but was noticing that the shelves farther away were blurry, I didn't worry too much since I had been having ongoing thyroid problems and figured my eyes were swelling (though that normally happened only in the mornings). By the time we got home and were sitting down to dinner I noticed that when standing in the kitchen the people in the other room were completely blurry. By 11 pm I could only see clearly within 18 inches of my face.

I awoke at 2 am with a severe headache and almost complete blurriness, I had to hold the pill bottle very close to my eye to be sure it was correct and even then could not be sure. My husband gave me the meds and I went back to sleep. I didn't wake up until 1pm!!! When I awoke all light was painfully bright and I could see NOTHING clearly! I was rushed to the hospital and was diagnosed with acute angle-closure glaucoma caused by TOPAMAX!!!

Thankfully the docs were able to reverse the symptoms but said one more day I would have been permanently blind. My eyesight has never returned fully, though I can function just fine and do not feel depressed about it.

Please, be very careful on Topamax. The stuff is dangerous to many people though a life-saver for so many others. Also, may I suggest to those with the tingling that you get your calcium levels checked as this is a classic symptom of low calcium. I just wonder how Topamax affects the other body systems, such as the adrenal and parathyroids.