Chronic fatigue symptoms and conditions

Reading these is both disturbing and a relief. I was put on YASMIN by my GYN after blood work confirmed my estrogen was low- I was 42 at the time and the GYN felt I needed the pill to boost my energy and she said it would "even out" mood swings. I stayed on the pill for 3 years.

I attributed my fatigue to being "perimenaupasal" meanwhile I stopped the pill 3 weeks ago and my fatigue has lifted, my aches and pains are gone. When I would try to research these symptoms I would come up with Lupus or some chronic fatigue issue, but I realize now it was this pill making me fatigued, moody, and thirsty!!

I have had blood work done to rule out any other type of illness or issue and realize so many other women are struggling with these symptoms, the pill that is supposed to make life better is making people sick.

Murdered by Levaquin.
This may be hard so bear with me. I need to give you a little background to show what an injustice (criminal you be the judge) happened to my soulmate. Her lifelong dream was a humble little spot in the wilderness and at 58 and on a disability we were able to make that happen; and she was happier than I'd seen her in years. Existing conditions included depression, anxiety, fibromyalga and chronic fatigue, and a thyroid condition that she got from over radiation for Graves disease many yrs. ago. Oct. 07 she came down with pnemonia and made a trip to ER. the Dr. saw something he didn't like so prescribed Levaquin. She left there sure she had lung cancer. Three days into a 10 day course her lower extremities became extremely painful and swollen, a call to her GP was never returned. We thought she was experiencing some effects of pneumonia or cancer. 2-3 wks. later a dr. appt. where she was in such bad shape she had to wear my shoes and be carried from car to wheelchair she could barely walk. An alternate dr. saw her. got xrays prescribed more levaquin and prescribed water pills for her swollen lower extremities. 2-3 weeks later side effects much worse has now traveled up to her midsection (peripheral neuropathy) she is now wheelchair bond going to dr. office and guess what lung hasn't cleared up yet so more levaquin with no solution or idea what is happening to her body ( she was terrified and in horrific pain. So she was prescribed 3 courses of levaquin and ignored the blatant side effects. The next several months at home were hell, the neuropathy continued up her body, she could no longer feed herself or hold anything in her hands. Every day the pain and frustration were unbearable and she cried for hours at a time. I couldn't get her to go to hospital as by now we knew what we were dealing with PN and it is irreversible and she knew she was dying and if she left she'd never see her dream home again. We finally got her to the hospital, they wouldn't accept my Achumes Razor and suggested numerous things conducted numerous tests including a Gallum scan and still no answers. She deteriated fast. She was within a week about 63 pounds and suffering severe sycosis with hallucinations. She experienced depersonalization. She had severe pain to the touch. I now know she is going to die and I'd promised her I'd never let her die in an institution but we could get no home care. They now wanted to kick her out of hospital after 3 months and suggested a hospice and although terminal she was undiagnosed so did not qualify. I have seen both parents a brother and numerous people die from a variety of ailments but this was truly a horror show esp. the psycosis and pain she was in. It scarred my heart and soul forever. No insurance so I am fighting to keep our dream home and keep her memory alive, made it a year but the future is uncertain. She died July 5 07, 2 days after she died the FDA put out a black box warning label so how come every time i insisted it was that poison they would not take me seriously. I now know what drives people over the edge to retaliate in some way. In Canada I don't think there is any class action happening, but in everybody that knew about it it would appear like gross negligence at least giving it to her 3 times after showing adverse reactions after first course. She was stolen away form me and her daughter just as she had reached peace and serenity. It breaks my heart continually and I don't know what to do with this rage I feel. It is now 13 months and no autopsy, apparently a hold up at pathology. Feel free to comment I really can't believe she's gone I haven't disposed of anything or even changed the house in any way.
M.

After reading other people's experiences with Norvasc, I realized that my symptoms are almost identical. I thought it was rheumatoid arthritis and asked my doctor to give me some tests and all came back negative. I started 5mg of Norvasc about 10 months ago and about 6 months in I started to get muscle spasms in my feet, then spasms and muscle twitching in legs, arms and hands. Extreme flushing in feet, small freckle-like rash on feet, lower legs and ankles. Also have what I would call chronic fatigue and just cannot get myself up and down stairs well. I'm 57 and feel like 100. All over body pain is very debilitative. I've gone from an active, happy person to a cranky person in pain 24 hours a day. So, now I have taken myself off Norvasc and am waiting to see if there is an improvement in my health. I'm still on coversyl for my blood pressure and will talk to my doctor again. It is so true that you must be your own health advocate and try to stay on top of all your health issues.

They had me on a 600mg dose to begin with, which I cut way down to 200mg daily.I have high blood pressure and tachycardia and it does lower all that quite well. However, I am scared to go to bed at night, because I wake up shaking like I'm having seizures, I feel like my whole body is twitchy. Leg cramps, ringing in my ears, vomiting, nausea, dizziness, hot sweats, cold sweats, dark spots on the wall, (my blood pressure was normal), thirst, panic and anxiety, not caring about life or the house or bills, and horrible dreams, no appetite, then increased appetite, insomnia,and this all started about 3 days into the meds. Let your body adjust to it, yeah, it's getting worse so we'll see.

Hi everyone, I have just read all thirty pages of posts to try to find some answers to my crazy reaction to prednisone. My thoughts are with you all since I have had an usually severe reaction to prednisone. I was on prednisone for 1 week in October 2008 at 60 mg/day for a sinus surgery. I am still having the following side effects at full force:

Axiety to the point I can't socialize
mood swings
hot/sweating even in freezing weather
whole body shakes
severe migraines
tooth sensitivity
muscle pains
extreme thirst (I drink almost 2 gallons/day)
hungry all the time
moon face
water retention around waist
acne
hair loss
rapid heart rate
dizziness
nightmares
night sweats
high blood pressure
high hear rate

I'm not exaggerating, my parent's can contend to that. I do have a history of having sever reactions to medication and I've had all the gland and blood tests which all check out. I never had a single one of these before the prednisone - I was a healthy 22 year old.

I was wondering if any could tell me when this hell will end - my job and well-being depends on it!

Prescribed Avelox after previous antibiotic could not clear up sinusitis. Avelox cleared it up within three days, but I feel worse now. Extreme agitation/anxiety, tremors, twitches, no appetite, boughts of depression, dizzy, lack of coordination, accelerated heart rate, leg shake, cold extremities, very strange, vivid dreams. Doctor told me to stop taking and side effects should clear up in a few days ( I hope). This is nuts. I feel like I am going insane. I could not go to work for three days due to side effects.

The first two months I was on NuvaRing, I thought it was the best thing on earth. Unlike previous attempts with various HBC, my breasts didn't hurt and I didn't seem to gain weight. It also steadied my out-of-control PMS symptoms and made my period lighter and my cramps disappear. Those are definitely on the PRO side of things. Shortly after starting NR, I met a new boyfriend and after both being tested for STDs, we decided to ditch condoms. Woo-hoo! At first, we had great sex and I had no problem having orgasms. But as time progressed, I became extremely dry down there and developed constant yeast infections. Plus frequent low-grade headaches (sometimes escalating to migraine-like headaches), night sweats, itchiness, insomnia, and exhaustion. Now I find it extremely difficult to get physically aroused (before, a 30-second sex scene in a movie could get me off) and nearly impossible to orgasm. I have very little interest in sex, either, which sucks because I am finally in love with the most amazing man. I have told him time and again that its the NuvaRing, and he says he believe me, but I can tell he thinks it's him. So, we've decided to give condoms another try. I took out the NuvaRing. I guess I'd rather have nasty PMS and a painful period than lose intimacy and sexual pleasure. Just curious: Has anyone used the copper IUD (non-hormonal) or a diaphragm with any success? Thanks and good luck.

I had my mirena inserted July 2006. Not noticing any real problems until recently, I have inquired just to be sure. Upon insertion I only had about 10 minutes of pain, and was fine for a while, like almost a year. First, I started getting migraines and had never had one before until 2007. Then fatigue set in. Chronic fatigue, foul smelling discharge, abdominal pain, back pain. Recently there were serious mood swings and they feel uncontrollable, and this is not fair to my husband or daughter. My daughter is three years old and i don't have the energy to play with her or the patience to deal with her. I feel like a failure of a mom because of the mood swings, fatigue, and depression. I have been married for almost 6 years and I have suddenly lost my sexual urges, they just fell off, and the way we were going I thought that that would never happen. But the thing that concerns me the most is the lack of period. I know they say that they will lessen but I haven't had a period since October 2008. Your period is a means of releasing waste, so I have pent up waste not going anywhere. Nausea set in between September and October 2008. I am constantly depressed and stressed for no reason my life is good. My husband has done some research because he said that all of a sudden I wasn't my normal self. I was put on medication for depression and none of the dosages worked, that is sad. We have agreed to have this "thing" removed. I would much rather try some condoms or even get pregnant again than to be a whole new person that I nor anyone else enjoys.

Ive been on meprozine or just plain demerol for 5 years now i do not take more then 1 pill in 24hr and then i try to put days in between doses i have OI a brittle bones and kidney stones and this is the only pain medication period that i can take with out having a bad reaction. as far as mood swings i don't have any if any thing it keeps me calm but it will only stop the pain if you take it on the first on set, if you wait and take it till the pain has gotten worse it simply wont work at all. there is one side effect it keeps me awake lol im the only person i know who can take this and stay a wake all night

I had the mirena inserted on Dec 5 2005, I had bleeding for about two weeks and nothing much, up until 3 weeks ago I "loved" my Mirena, I was happy not two to have a period not that I ever had any problems with mine's. I was not until I found this site that I started to realized that my "chronic fatigue" that started in April 06, the hair falling out, sudden anxiety and panic attacks, blood pressure going off the chart for no reason 175/96, after always having low blood pressure, being put on Lexapro and Valium, feeling sad, gaining 20 pounds, not able to lose them no matter what I did, the horrible headaches, migraines and tension headaches at the same time, the fidgeting, nausea and just a general feeling of not being well, that I decided to have that thing removed. Had it removed on 1-15-09, had to be put on a beta blocker 50 milligrams twice a day to lower my blood pressure. I "cried" when I read some of the entries, I almost got diagnosed with lupus, the doctors could not figure out what was wrong with me, I was given all kind of excuses, "well you are 40 now" maybe it is your family life, etc, etc, my mom whom is 74 has more energy than I do!!! Don't let anyone con you, this thing is evil, and Lord knows what kind of other damage it has done to my health. And like many of you I did have a period occasionally, I did not know when, but it was nasty smelling and brownish. Also as of late I started to feel a burning sensation on top of my vagina, I have not been intimate in over a year and had a full exam last year ;therefore, I know I done have any STDs. The headaches were the worst, I could not even comb my hair, I felt like if someone was cutting it in two. Post removal I have not had more bleeding, but I know it is quite early, either way, not having that thing, and even after taking beta blocker I have more energy than I ever had in three years. My son was born in Dec 2002 and I have never felt as tired as I felt while on Mirena. I had double vision, could not control my thoughts and everything was a major disaster, somehow I lost my ability to take control of my life, never again will I put my body through something like this

I am 34 years old. I am a pharmacy tech. I have asthma and allergies. I have taken singulair pretty much every day since it came out on the market. I've had asthma since i was about 10 years old. I took theophylline as a kid. Steriods on and off especially during times when my allergies are bad. I still use Advair during the fall and spring. Every drug has a side effect. However breathing is pretty good damn thing. Do I have days when I feel low? Yeah. Do I sometimes have nightmares? Yup. Are "natural" products the answer. Not always. The fish oil that some of the posters are touting can also cause GI problems. Some of the natural products contain herbs and other plant derivatives that can be harmful for a child that suffers from allergies. Not proactively treating asthma can be deadly. Some of the parents are suggesting steriods as the answer - those can cause weight gain, growth suppression and can lead to a worsening of asthma.

Singulair has never made me feel like I've wanted to kill myself. I was more depressed and angry as kid when my asthma did not allow me to partipate in normal childhood things. I was sad and hated life when I couldn't keep up with friends at recces because I was having trouble breathing. You have to outweigh the costs with the benefits. I am more irritable when I have asthma flareup then I am on a normal day. For me, I choose to breathe. And singulair has been helping me for almost a decade.

I'm not saying the medication isn't causing these symptoms but maybe there is an underlying cause to your child's depression.

Any drug has a side effect. But without medical research and the medications that come with them - people would still be dying of simple diseases and we wouldn't have vaccinations. As a society, as a whole, we are a culture that looks to someone else to fix things and then blames the people who try to fix it. We need to stop being the "hot McDonald's coffee'" society.

Muscles spasms, sensitivity to light, burning sensations up and down my arms and legs, racing of heart, horrible sinuses, migraine headaches, chronic fatigue, hair loss, dry skin, Candida, acidity (low PH), low immune system, acne, joint pain, and the list goes on and on.....
My doctor told me I was fine and suggested I go on an anti-depressant. I am not depressed I told her. Since my doctor and other conventional doctors weren't helping me (all they wanted to do was prescribe more horrible drugs) I decided to seek an alternative MD. He said all these symptoms can most definitely be from my birth control. I went off Triphasil (Trivora) 3 weeks ago and am taking some herbs that are supposed to help correct the damage the medication has done. I now have a whole in my kidney, cysts in my ovaries, spots on my lungs, and an infection in my stomach (yeast also known as Candida). I have been sick for over 6 months now and am finally ready for this to be over. I can no longer go to the gym, work a full time job and enjoy social functions/outings. It is emotionally and physically damaging. Those of you who are on it...please stop! It is ruining your insides and making you weak. I am 30 years old and was on Trivora/Triphasil for 6-7 years. What a mistake. This is the ONLY drug I take and I used to be perfectly fine. As a matter of fact, I used to run 10 miles a day and now I can't even walk 30 minutes in the gym. Needless to say, I am very angry at the doctors for prescribing such medication to me, for the FDA for approving it and for our government for not doing their due diligence.

OH MY GOSH! I thought I was crazy until I found this site. Ok, I had my Mirena inserted January of 2007, and IMMEDIATELY experienced joint pain, pain in my hands and feet, and it's 22 months later.. the pain NEVER went away. I thought because I was a very hardcore athlete when I was younger, that this was par for the course, that I will be getting arthritis. I'm 34 years old. Crazy to say arthritis at 34? I think so. Well, I have been researching my symptoms for months and months online and gone to a few different doctors over this. My symptoms include chronic fatigue, headaches (on a good week 4 days out of the week), joint pain in my hands and feet, sensations in my hands and feet that feel like they are swollen (but they aren't), upper and lower back pain, heart palpitations, leg cramps, hair loss, ABSOLUTELY NO SEX DRIVE AT ALL, muscle fatigue, and I've gained 40 lbs since I had it put in... OUCH. NONE of this (except for headaches and some depression) was experienced before the Mirena. Funny, I never linked it to the Mirena. I've had my thyroid checked, been diagnosed with carpal tunnel (lol what about my feet? Good doc!) had blood sugar checked (nope, not diabetes!), well, now I'm on to getting checked for fibromyalgia. Kinda wondering though, if there is a link to fibromyalgia and Mirena, like it could induce it? Sounds like so many of you have the same symptoms, and many have thought the same things... fibro, diabetes, lupus, ms, hell, I even though lyme disease at one point. This is ridiculous... I'm having it out this week.

memory loss, headaches, tias/mimi strokes, kidney stones, blood clot,vertigo, disorientation, muscle spasms, shaking, trembling could not control , dry eyes, stiffness in neck, back pain, twitching of all muscles , blackout when really sick, cant hold arms up, thought I had Parkinson, ms or Muscular dystrophy, motor skills are no longer great, arms and leg muscles bad, cannot write much at all, no strength in fingers or toes.
chronic fatigue and fibromyalga diagnosed not so sure after reading all these side effects.

To the best of my knowledge I never had any of the 'immediate' symptoms.
My problems are probably due to the fact that I was prescribed Cipro 3 possibly 4 times from Aug 06 - Dec 07 and then finished up Dec 07 with a round of Levaquin. My father is over 60 and was recently given Levaquin and had immediate and serious problems. He is seeing a doctor recommended by the CDC today. Yes, he is even working with the CDC on
this one. Due to all he is being told he is convinced that the medication is behind my medical decline as well. Since taking these medications (symptoms started slowly in 07), but after taking the Levaquin at Christmas time I never got up from the couch. My thyroid gland has quit working, my adrenals are shot, I have been diagnosed with fibromyalgia, chronic fatigue, blew out 3 disks in my back, vision is deteriorating rapidly, and really so many things I can't list them all. I had a complete physical
in Oct 05 and was given a perfect bill of health. Through Aug 06 I was riding my bicycle 33 miles per week. I'm still trying to figure out what hit me??
What my father has been told is that in some individuals Levaquin will attack the glands (like the thyroid) and will compromise the immune system. This damage appears to be permanent. All I know is that I went from being extremely healthy to terribly sick. If in a day's time I have enough energy to load and unload the dishwasher it is a banner day. I can
not work and seem to get worse instead of better as each day passes.

My husband also had pneumonia at Christmas and took Levaquin but does not seem to have had an problems. I suspect it was possibly the cumulative effect of having basically 4-5 rounds of the antibiotic in a years time. According to the people at the CDC that have spoken to my father the symptoms that I have can all be traced back to the medication. One never knows what effect a medication will have. Just please be careful when taking this medication, and limit how many times you take it.

Severe joint problems, unable to hold even a kettle. vicious mood swings, constantly tired, lots of weight gain, sore eyes, always tired, nightmares, sweating, chronic fatigue, been in hospital and treated for pelvic inflammation.

I have used the NuvaRing for about 3.5 years, starting after my 6 week check up when my daughter was born in 2004. In the beginning I felt like it decreased my sex drive but also that maybe post baby body that caused that too. For three years I had no problems. I had noticed breast tenderness throughout but other than that no side effects. About 8 months ago it began with a missed period, then two periods in one month. My OBGYN recommended 'resetting' my body by taking out the ring until my next cycle and starting it up again. I followed his directions but the next cycle came along with a bladder infection followed by a yeast infection. Over the next 4 months I either had one or the other, continually visiting my doctor I didn't make any connection to the two. Stomach pain, chronic fatigue and kidney pain also added to the list. My doctor prescribed a series of medications followed by blood tests and a referral to a specialist. Over the summer my husband asked that I stop using the ring because my sex drive had hit rock bottom. After a few weeks of taking out the ring, the burning sensation during urination has gone away. Stomach cramps and back pain has ceased and no infection to date. I am in my early thirties and after a week off the ring I realized what they mean by 30's sex drive. My husband and I are both happy with the changes. I visit my OBGYN again in a few weeks to revisit non-hormone options for BC

I was diagnosed with PTSD, Major depression and social phobia back in 1996, when i was 17. I was being treated by a quack psychiatrist who prescribed me Zyprexa in 1998. I never heard or seen things that others couldn't hear or see until i took this drug. Let me tell you i've probably been on a third of the pills in a PDR but NEVER have i been on a drug that destroyed my life like Zyprexa. It caused me to have angry outburst. Zyprexa caused me to have SVT (Supraventricular Tachycardia) in which my heart would nearly race out of my chest. It also caused me to have Sleep Paralysis in which i was seeing demons. Zyprexa put my athletic body into a chronic fatigue and hypersomnia and i gained 150lbs in 15 months of taking this drug. The quack psychiatrist no longer has a license to practice...it seems he had many patients die on his meds. I filed a class action lawsuit against the drug maker of Zyprexa that is still in effect. 10 years after taking this drug the weight will not come off and it's caused me to develop health problems such as diabetes, hypertension and high cholesterol.

Oh my god. I can't believe I have just stumbled upon all these women talking about the same problems. Feeling chronic fatigue, depression, listlessness, anxiety and insomnia, bloating and loss of a sex drive! (THATS birth control for ya! Ha!) I also experience aching muscles, headaches, and a brain fog that makes me feel like a fraction of my former self. All of these symptoms, among others, can describe Candida overgrowth.

I have had my Mirena for 2 1/2 years, and I never put together these symptoms and the IUD! Even though they started shortly after my insertion, I also had some serious life circumstances happen to me and assumed I felt crummy from that. Also, I loved not thinking about birth control and was convinced that the small progestin-only tips had to be the most gentle form of hormonal birth control out there. And no period! Sweet. I also worked in the field of sexual health and trusted my doctor completely. I recall in hindsight getting really sick right after it was inserted, and asking my doctor if I could be having bloating and intestinal problems from it, and she said it was unrelated.

I called to make an appointment to have the Mirena removed shortly before finding this site, because since I have discovered I have candida overgrowth, I have learned it can be onset by hormonal birth control. Candidiasis Albicons is the same yeast that causes yeast infections, and when the healthy flora of the digestive tract are compromised, it can spread out of control, becoming systematic. That's what happened to me. If this sounds all to familiar, please check it out and see if you have it too.

I am getting better already, after committing for the last two weeks to the candida diet, where my body is detoxifying and I am coming back to life. (Many western doctors know very little about this, so don't be surprised if they laugh you out of the room and prescribe prosac. Trust your gut, literally ;)

I don't believe the Mirena caused my candida overgrowth, only that its a factor in it, like taking antibiotics or heavy metal poisoning. I felt compelled to share my story, because I am starting to recover, and I can't tell you how good it feels to feel better after 2 1/2 foggy years. Don't give up on your health.

Also, I am writing because removing the IUD won't fix your problem completely, just like it didn't completely cause it, so if you have think you may have systemic candida, find out. You will need to continue treating it after you get the IUD removed, so you get the full recovery you deserve. Hoping for more healthy ladies!

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 am a 60 year old female and have been on Lisinopril (40 mg.) for at least10 years. Before that I was prescribed Zestril, but a generic was often substituted (Lisinopril). So it's hard to say just how long I've taken the Lisinopril. I'm amazed to read the side effects listed here. I've experienced almost all of them at one time or another. It's scary. I've tried to quit the Lisinpril a couple of times, sometimes just because I ran out of the prescription. But now I am substituting a natural supplement for the Lisinopril. I'm trying Holistrol (HiQi). I've been on it for about a week. I checked my bp when I started the natural and will check it again after a week. It was high when I first checked, but I had been off the Lisinopril for a few days by then. I'll continue to monitor and take the natural supplement and then will report back.

These side effects are very similar to those experienced by people diagnosed with Fibromyalgia and Chronic Fatigue Syndrom ( both of which I've been told I "might have"). My diagnoses came from several doctors in my hometown and even from the Mayo Clinic. I'm wondering how many people with these diagnoses are taking Lisinopril?

My side effects are starting to leave my body, but after so many years, there are many layers of toxins to release. But I am confident that I am doing just that ~ releasing toxins!

Thank you for listening and especially for sharing your side effects. This is bad stuff in my opinion and I'm glad to have started the process of clearing this poison out of my body.

Ann

Thank you so much for this information. After a year of endless blood tests, specialists and other diagnostics with no answers I have been diagnosed with chronic fatigue to label a concoction of symptoms that include dizziness, extreme fatigue (I have been a runner daily for 8 years but can no longer run), regular 'infections' akin to my vagina being on fire, irregular pap smear, difficulty orgasming (previously never a concern) and so many of the other symptoms listed above that it feels like a checklist reading this amazing site. As I work in a hospital I have undertaken extensive review of medical journals to see if any clinical studies have identified concerns with the mirena - I couldn't find any and so have dismissed my symptoms as unrelated but have always had a gut feeling about it. From being extremely active and passionate about my work, I have had to scale back and back until I now work only three days and rest for the remainder. I can't thank you enough for validating my suspicion that the mirena might be the culprit - it's the only variable my husband and I can think of since the symptoms emerged. I'm going to get this stupid thing out of me as soon as possible.