October 26th
2009
12:09 PM
Hello I am 40 yrs old and got a lung infection which cause swelling in my lungs so the put me on high doses of prednisone via IV for 21 days in the hospital. The drug saved my life and took it at the same time.
After I got out of hospital i was on 60 mg for 6 weeks the 30mg for 6 weeks then 20mg the 10mg. It has been a living HELL over the last 5 months or so.
I told my DR. i have very bad blurred vision and he said it because the med runs my sugar up but I check my sugar and limit my sugar and it around 100 all the time which is normal soits not sugar. Then he said well them you need to see an eye dr. cuz your eyes are going bad. I begged to differ with him and told him if there was something wrong w my eyes then why is is one day I see fine and the next day all blurred and then back to normal!? it this stupid steroid if you ask me plus on day my right eye is bad and next day my left uggh!
The WORST side effect it the brain fog as yall call it. OMG I feel like im loosing my mind and going crazy. The dr. says hes never heard of such with a wise remark and says you know where your at now right? I know where i am and what I say but I feel like its not really happening. Its like im dreaming it. I feel like Im trapped in my head and I lookout blurry eyes.
Before I was a very confident independent person but now I feel scared all the time i feel hopeless and ive went through 3 girl friends over the summer because of the extreme forward attitude the med gives me. I am not the same person I was. I some time just want to die. I'm extremely tire if i do any exercise at all.
Plus I have all the other typical side effect like the moon face and weight gain. I don't even look the same cuz my eyes have huge bags under them and a double chin I never had.
I feel for all of you because i know what your going through.
I saw one comforting post in here where someone said within 2 weeks of completely getting off the pred. he was his normal self.
I CAN TELL YOU HOW GLAD I WAS TO READ THAT!
Please if you have finished the med and have got back to normal don't forget about this post. Please let us know because we need any hope we can get to keep our chins up and not loose hope and go completely crazy or worse kill ourselves.
I have about 4 more months of this LIVING HELL and I will surely let you all know if it get better. If you have come off of it and are reading this PLEASE let us know if we get back normal at least w the brain fog. I can take all the side effect ok except for the crazy dream zone zombie feeling.
I WOULDN'T WISH THIS KINDA HELL ON THE DEVIL HIM SELF!!
Let's pray for each other that the Lord keep out minds strong until we get off the nightmare drug call Prednisone.
side effects:
brain fog, blurred vision, puffy eyes, depression, confusion, dizzy, moon face, buffalo neck hump neck, hopelessness
October 26th
2009
11:41 AM
I've had Mirena since Jan. 2006. This is what's going on with me.
EXTREMELY bloated all the time, diagnosed as IBS. I’ve tried everything: herbs, teas, diet changes, prescription meds (currently on anti-depressant (for the IBS, not depression) and an anti-spasmatic pill), and non-prescription meds (currently taking beano before every meal and gas-x after the beano has not worked!)
Irritability
Tired all the time
Not motivated to do anything
Forgetful
Loss of concentration, I have the attention span of a 3 year old it seems!
Heart fluttering and dizziness like a panic attack. The doctor actually said it was panic attacks but I honestly don’t feel “panicked” when they happen.
Fluttering in abdomen as if there were a baby in there
Sometimes feel a pulling or stinging sensation in my uterus
Hubby can feel the strings and we think they are irritating his manhood
A lot of these symptoms seem like depression but all praise be to God, I have a wonderful life. I have the greatest husband and kids I could ever ask for. I love our life. I’m not unhappy at all. I didn’t consider that it may be the Mirena until my husband mentioned that he thought the strings were causing the irritation on his penis. I started googling Mirena to see if anyone else had this problem and came up with so many “other” symptoms of Mirena. I thought “WOW!! Maybe THAT’S my problem!” Maybe it’s time to make that appointment to get it out.
-- By thatwhitemuslimgirl | Reply | (5) replies | Private Message me
October 13th
2009
10:47 PM
Was prescribed avelox for bronchitis. Took it for the full ten days. began having diarrhea. It has been 5 weeks since i stopped taking the medication and have continued to have diarrhea, cramping, abdominal pain. The diarrhea is a loose stool. Have had stool tests done and do not have a secondary infection from this.
-- By wvtazman | Reply | (1) replies | Private Message me
October 7th
2009
10:31 PM
My daughter just turned 19 years old yesterday. She is a Christian and has kept herself pure and plans to until marriage. She attends a Christian University. She had her last gardisil shot in May. Since this shot she has been complaining of severe fatigue, dizziness and has had no menstrual cycle. My first thoughts were concerns that this was caused by the gardisil shot.She just saw a doctor at her University last week. All the test run were negative and the doctor wants to further test for osteoporosis and place her on birth control pills to regulate her periods. She does not want this.The doctor did not perform a pap smere due to her being a virgin.I have contacted our local doctor and was informed that there was no way to tell if any of her symptoms could be side affects of the gardisil shots she received. My husband decided to investigate the side affects of gardisil and came upon this web-site. I am just wandering if this should be legally investigated and how could someone find out if there are legal ratifications for this problem. I am just praying that these are temporary symptoms and my daughter will recover and be able to have a children after marriage. Please pray with me and I will for each of you as well.
-- By mmrice | Reply | (1) replies | Private Message me
October 6th
2009
3:59 PM
I had the shot for a bad outbreak of eczema. This was a last resort thing. I'm not usually for taking any form of medicine other than natural stuff. The doctor warned that the possible side effects would be muscle spams and high blood sugar. She never mention anything about irregular periods or weaken immune system. I just had my period 15 days before I had the shot and a couple days after the shot I got my period. I few days later I got the stomach flu. While still having my period. Then a week later I had a ear infection. I still have my period. I emailed the dermatologist explaining the symptoms I was having, she informed me that its a side effect of the shot. She failed to mention it before taking the shot. I don't want to take another drug like birth control pills to cure something a drug caused in the first place. I'm now on day 17. My period has never been irregular. I'm a healthy 30yr old. Does anyone know if this goes away on its on? What are things you can do to naturally cure this? I appreciate any advice.
-- By eyecandymena | Reply | Private Message me
October 2th
2009
12:56 PM
I am 21, and I have been on NuvaRing for 4 years. I got on it to regulate my periods. I loved it because I did not have to take a pill everyday, and I would know exactly when I was going to start. After a couple months of being on the NuvaRing I was getting really really tired. I had no desire to do anything but nap. I had become anemic. After I got on iron pills, my energy level increased and I was back to normal. Also, during the first year my immune system went down tremendously. I was sick with more than I have ever been. Still I did not blame the NuvaRing. During the next year I started having bad stomach problems. I could not keep anything in without having to run to the restroom, and I was constantly nauseated. After losing 20 lbs, I decided to go to the Dr. After doing tests, his only response was that I had IBS. After a few months the stomach problems ceased. My appetite has decreased tremendously. My mother brought to my attention that ever since the NuvaRing I was constantly complaining about not feeling well. I was in denial. I loved knowing when I would start my period, and I could not take pills everyday. Life went on. The third year, I almost passed out at school. I have felt like this before, but only when I hadn't eaten. I went to the Dr. and I was found with a heart problem. I had a procedure, but I still feel out of breath occasionally. I have chest pains occasionally, as well. I still get really nauseated, but my immune system has gotten much better. Therefore, I tell my mother that I am better, no need to stop the NuvaRing. In the past year I have noticed that I am an emotional rollercoaster. I drive my friends, family, and boyfriend crazy. This past week it hit me that I could be having side effects from the NuvaRing because I have ALWAYS been very happy. After getting on here and reading everyone's side effects, I am amazed. Everything that I have been through the past 4 years is probably because of the NuvaRing. I am going to try to stop the NuvaRing and see how much better I can feel. I can't wait!
-- By mm2188 | Reply | Private Message me
August 29th
2009
7:35 PM
I used prednisone for sinus inflammation and it gave me bad side effects such as: irregular heartbeat and stomach upset and anxiety. It actually did help with the inflammation but I stopped using it because of the side effects. It made my lip puff out too, which i did not mind because i have small lips and i looked better with a bigger lip, lol! I am thin so if it made me swollen i did not care because i need to gain weight, i am only 105 lbs. I just started taking methylprednisolone tablets packet and they seem to work better and if it causes increased appetite that would be good for me because i lost so much weight because of my teeth and sinus pain i had everyday for four months. So far it is working but i just started it and will keep you posted. It does seem milder than plain prednisone I suggest you switch to this if the prednisone is not working for you. It sounds like most people are on too high of a dosage and take with food and a lot of water. Hope everyone feels better soon.
-- By jaynee02 | Reply | (2) replies | Private Message me
August 14th
2009
2:44 PM
42 and taking Lipitor 40mg for 6 months. No other issues. 20 lbs overweight but also work out 4 times per week and feel to be in good shape. Lower back pain in middle of night that last until I get up out of bed and it started about a month after taking the Lipitor. If I get up, it goes away. Was so bad that I went and bought a sleep number bed thinking it was my old spring bed. Did not get better. Tried not taking the Lipitor for one night and the pain stopped. Took it again the next and it was back. Going to doctor to ask what is up?
-- By joer | Reply | (2) replies | Private Message me
August 8th
2009
5:30 AM
Warning: I do not know if this is related at all (or if there is anyway to know for sure). I accidentally saw a connection looking up conspiracy theories, and I can't seem to find any "real" information about it at all.
My daughter at 14 years of age had this shot. She didn't feel good after, but I thought "normal" vaccination reaction and haven't thought about it since. Feeling a bit faint, a fever, and such.
However, last September (a few months later) she was diagnosed with autoimmune hemolytic anemia. It started with her heart racing, she looked pale (and sometimes even yellowish), tired all the time, her urine turned a dark color, and fainting. Not knowing anything about this I assumed that she was dehydrated, and had her drink lots of water. Until she started fainting, at which time I took her straight to our family doctor. (Another reason that I wasn't to worried is she actually had been to many doctors who didn't seem to think this was abnormal.)
She started on high doses of prednisone to keep her immune system depressed, and has now moved on to mercaptopurine (as the steroids made her suicidal.)
I plan on bringing this "possible" connection up to her hematologist and I will report back (she has an appointment on the 11th.). However, I think it is better to do a little scare here, and possibly help someone rather than take for granted that I am not sure... (So take this information with a grain of salt.)
Also note that this was sudden onset, they can find no cause, and we have no family history nor any of the other typical reasons (sometimes can be "medicine" induced.) 10 months later she is still testing positive on her combs test though.
-- By terrasears | Reply | Private Message me
July 19th
2009
7:50 AM
I've been on a 7 day regime of Levaquin 500mg for an a infection that wasn't cured by other antibiotics and I can say it's worked. Yea I had a some muscle craps in the legs and some leg pain and a first day bout of nausea but overall, it's worked great for me.
I'd suggest that anyone on it do as my doctor said and either eat at least 1 cup of yogurt a day and/or take a Probiotics pill. The antibiotic/any antibiotic kills the "good germs" that help raise your bodies immune system and helps with digestion and the Yogurt/Probitic pills help grow the "good bacteria" back and ease the side effects while on it. Good luck to all
-- By sjoseph2000 | Reply | Private Message me
July 16th
2009
11:56 PM
I started this med yesterday for staph infection. My immune system is run down from 24 days of hemorrhaging with menopause and finding cancer in my bloodwork and catscan. My skin has thinned and I have large sores all over my body. This med was given to me yesterday and also my diabetes med was changed because my immune system is so weak it is kicking up my bloodsugars. Can you tell I am run down? I went to bed trying to throw up this pill today again and went to bed with chills while it is 105 degrees in Texas today. I even had to put on socks. I feel lightheaded and kind of out of it with blurry vision. Hard to tell what is from meds and illnesses but is no fun. At least I feel better not being alone with this. I am also burping a lot and I never do.
-- By judith53 | Reply | (2) replies | Private Message me
July 3th
2009
2:05 AM
My precious daughter, Trinity, aged 5, had UTI symptoms, and I took her to urgent care on 7/1/09...she took her first dose at 3pm on 7/1, and about 4.5 hrs. later said her head hurt on the top of her head (almost has NEVER complained of her head hurting her whole life!). Then, today, 7/2, she has been having lots of eye discomfort and pain and has red eyes (poss. from fever?), and the most striking symptom after taking sulfamethoxazole-Trimethoprim DS is that she says she feels VERY sick and has been about to cry and just looks at me pleadingly and says her stomach hurts. Also, she cannot eat much. She says she wants to eat, but she can't. She has felt like she wants to throw up, but hasn't yet. ATTENTION: Go to http://www.remedy-bladder-infection.com/children.html and you can use a NATURAL URIBIOTIC derived from fruit that the e.coli is attracted to, binds to it, and then is detached from your urinary tract walls, and can be washed out by your urine. I will NOT be giving her anymore of this, as I know it wipes out the beneficial AND the bad bacteria from her intestines, and 80% of the immune system is in the intestines! I was just afraid cause she was so sick, and I thought these antibiotics were the best thing to use...I just tonight found the sight about the URIBIOTICS! Try those! I will protect my daughter from this!
-- By bel4jesus | Reply | Private Message me
June 27th
2009
11:29 PM
My daughter had the Gardasil shots last year. The school nurse talked to these young girls and told them all the dangers of cancer. It is a scare tactic. Doctors tell you to get the shots as well...makes their offices LOTS of money...the insurance companies presently pay for the shots, and the are very expensive. My daughter passed out w/ the first shot. Never has passed out before. (Do not allow your daughter to drive herself to get this shot...for the adult women..have someone drive you if you choose to have this vaccination, although I would strongly recommend NOT.) My daughter, since she was vaccinated with Gardasil, has had multiple ear infections, warts, strep multiple times, flu-like symptoms multiple times...pretty much the immune system took a nose dive. She never missed school before...was exempt from school exams many times because she was never sick. However, after Gardasil, she has missed many days due to all the sicknesses she has experienced. It has been approx. a year and she hasn't been as sick lately. I am hoping the immune system will get back to what it was before the shots but I strongly recommend NOT getting this vaccination. If my daughter gets worse, I am tempted to contact a lawyer. We might should get a count on the women that have been negatively affected by this and go to D.C. This vaccine should have been researched more. Our daughters should NOT be guinea pigs!!
-- By janstew | Reply | Private Message me
June 11th
2009
2:46 PM
OMG...I want to thank everyone for their comments, as I thought I was just crazy, I have not been able to walk more than 25 steps in three years because of this stupid Lisinopril. I could honestly just cry. Three years have been just taken. My daughter was 8 and now she is 11. We have not been able to go to the mall one time because mommy's muscle pain and weakness is so bad and it is just embarrassing to try to walk around a mall or the airport. I am only 39 there is no reason my primary Dr. should not have caught this. I have been referred for and had multiple MRI's, cortisone injections, nerve testing and nerve blocks, taken Tramadol until I can not take it anymore. Thank you all of you. Thank you. God Bless you, in Jesus name, Amen.
-- By moorepain7645 | Reply | (1) replies | Private Message me
May 27th
2009
5:12 PM
I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.
-- By xxanonymousxx | Reply | (13) replies | Private Message me
May 25th
2009
10:45 PM
My 14 year old daughter who had the gardasil shot approximately 2 weeks ago, just came down with a urinary tract infection, yeast infection and sore throat. I took her to the doctor for this on Friday. She was sick all weekend with fever, throwing up. Today, (5/25/09), I looked down her throat, and her throat looked like the top of a snow mountain. I was certain she now had strep throat. I look her to urgent care. The doctor took a throat culture, and it came out negative for strep but positive for MONO. What the heck!~ Is this related to the Gardasil shot! If so, do I want to put my daughter threw the next shots. I have never seen my daughter so sick in 14 years. Please advise to your opinion.
-- By sherryj1 | Reply | (1) replies | Private Message me
May 11th
2009
5:06 PM
I started taking Lisinopril for high blood pressure and 3 weeks after developed urinary tract symptoms (frequency, pressure, some discomfort, itching). The first time I went to the gynecologist to leave a urine sample, they prescribed me antibiotics, which I took for 7 days and still the symptoms continued (my urine had tested negative), so I went back and gave them another urine sample, it tested negative again, but had blood in it. They gave me a higher dose antibiotic for 3 days, the symptoms were still there. After that, there was nothing they could do, so they sent me to a Urologist.
By the time I got in to see the Urologist, a month and a half had gone by and I decide to quit taking the Lisinopril to clear my body of anything. I ended up getting a kidney scan, which was normal... and then a urinary tract scope procedure, which was normal.
After these procedures, I noticed that I started getting better and thought I might have just had "Acute urethral syndrome (also called noninfectious cystitis) causes symptoms that are similar to those of a bladder infection but that continue for longer periods. It is not an infection. No bacteria or other microorganisms are in the urine. The cause of acute urethral syndrome is difficult to determine. Possible causes include injury or irritation, allergies, stress, a disorder of the nerves, or problems with the immune system. You may be able to relieve symptoms of acute urethral syndrome by avoiding bubble baths and other irritants and not drinking citrus juices and caffeinated fluids."
So, I went back on Lisinopril, which was a few weeks after I quit taking it. After only 3 days, I started getting the frequency, discomfort and some itching... I could only figure out that Lisinopril had everything to do with my symptoms. This is still to be determined, but I feel like my urinary tract is feeling better every day now.
May 10th
2009
7:46 PM
I took 20 mgs a day for 5 days in September of 2006. I developed a terrible cough, but worse than that, severe chest pains & shortness of breath upon exertion. I still can't go up & down stairs; my pain is brutal and it's going on 3 years since it all began. Before I took the lisinopril, I hadn't been having any chest pains or trouble breathing.
Is there any hope of recovery? My doctors all say they've never heard of this kind of side effect; that lisinopril is a very common drug; it's clear that I have reduced lung function & definite pain & symptoms, but there is no way to isolate the exact thing causing it or to figure out how to make it go away; just to control the symptoms.
My theory: the lisinopril triggered an autoimmune response in which my body physically tries to reject my own lungs. Any thoughts on that one? I had been taking cozaar as an ACE inhibitor to slow the rate of my renal failure; I have type 1 diabetes and hypoparathyroidism, and while I needed meds before this episode, all I had to do then was manage my diabetes & I was able to live normally. Since this, it's been nearly impossible to do ANYthing. I am at the end of my rope & I want this to stop. But 3 years later, and while the shortness of breath is improved, the pain is actually worse now. I could sure use some advice & support. I'm on my way this week to get set up with a new dr. because we've moved, and I'm going to have to go through this whole thing again. Also - I'm trying to compile a list of other people who have had side effects with chest pain & shortness of breath. Also anxiety & panic attacks as collateral damage.
-- By melbish | Reply | (1) replies | Private Message me
May 8th
2009
3:02 AM
I have been on prednisone for 11+ years due to having had a heart transplant. The prednisone keeps my heart from rejecting.
I have not taken it for 2 days and I am in the process of passive suicide.
I am driving out west into the desserts to sit and die. I can no longer
be around people for I am afraid I may kill someone or at least significantly hurt them. I have been homicidal and suicidal for 11 years due to this med. I would enjoy killing everyone and everything. I hate myself and I want to die.
Prednisone made me become "Evil"; Hell incarnated. I don't want to live
in a mental institution and my doctor will only give me Seroquel thinking this will help me. I tell him it doesn't help me but he thinks it does. Stupid fucking doctor. My transplant docotrs won't even listen to me when I talk about "mental" issues. Everything pisses me off. It is raining outside and this makes me so mad and stressed.
I have been in this psychotically angry and agitated state of mind for 11 years. I have punched myself many times in the head and banged my
head against walls trying to get homicidal and suicidal thoughts out of my mind to no avail.
I would like to try ECT (electro-convulsive-therapy) but I won't even
mention this to my doctor because he will literally laugh at me and make me so god dam mad that I would enjoy killing him right then and there. I'm sick and tired of living in hell everyday.
Do not take prednisone no matter what, unless your life depends on it. And then what type of life will you have? Maybe a life full of hate, rage, anger, homicidal and suicidal thougts even when you dream.
Fuck life!
Arthur X 1968-2009
May 7th
2009
10:43 AM
I just completed a 10 day cycle of one tab at 400mg a day with minimal side effects. I experienced some dizziness in the evenings and some tightness in the chest. That was it, no weird dreams, no nausea or vomiting. I was prescribed avelox to lessen the possibility of pneumonia, (sp) as part of a bad cold. I have weaker immune system after being diagnosed with multiple myeloma 5 years ago. I guess I was just one of the lucky ones. I took my last pill yesterday so am waiting to see whether the side effects I experienced are gone.
-- By barryd | Reply | Private Message me
April 26th
2009
5:41 PM
I have been taking lisinopril for about 2 1/2 years now. About 4 weeks ago I was having trouble sleeping, my legs hurt real bad and when I would wake up I would have a numbing tingling sensation in my legs and feet. Went to the doctor asked her if it could be the meds and she said she didn't think so and to continue to take it. I still continue to have problems, tired, weak muscles, hurt and a raw lump in the throat feeling. She sent me for a brain mri that showed white lesions on the brain. She said it could be from high blood pressure but said my has never really been that high or it could be MS. I am right now waiting to see a neuro dr to see if I have ms but after reading all these post I am wondering if it is the lisinopril. Has any one else had these types of symptoms?
-- By cheri21157 | Reply | (2) replies | Private Message me
April 16th
2009
11:56 AM
I am a perfectly healthy, 24-year old young lady in excellent mental and physical health. I eat right, exercise regularly and I have no history of any health problems. In August of 2007 I started taking Yaz, it was prescribed by my gynecologist and I always got free samples, so I began taking it. In November of 2007 (almost 4-months after starting Yaz) I began having severely painful and scary gallbladder attacks. After multiple tests, I found out that at 22 years of age, my gallbladder was functioning at 0% and had to be removed immediately. I always thought that it was odd and my family did too because there is no history of gallbladder disease in my family at all and I was way too young and healthy to have my gallbladder fail. During the first few months of taking Yaz, I noticed that I was moody and tired beyond belief. I lost a few pounds though. For the first couple of months, my acne got worse, but then around the same time that I had my gallbladder removed, my acne started to improve pretty rapidly. A couple of months later I was diagnosed with IBS and have suffered digestive problems since.
I was in a relationship when I started taking Yaz and for no reason at all I lost all interest in sex and developed anxiety and an aversion to touch and in January of 2008 I broke things off with my boyfriend for no reason at all. In March of 2008 I started having severe anxiety and panic attacks. At times I even had thoughts of dying and thought that "at least I won't feel this way anymore."
To soothe those feelings I began drinking and partying and found that I felt better with the calming effects of alcohol. I drank at least 4 nights a week for about two months until I started gaining weight from the drinking. I don't have an addictive personality at all and so I just quit drinking cold turkey. It tasted horrible anyways.
In May 2008 I met the most wonderful man in the world, and yet, I was unable to ever really "feel" anything for him and I always felt emotionless and empty. My anxiety and panic attacks continued and I absolutely had no sex drive. We would have sex, but eventually my aversion to it took over and we began fighting for no reason at all and I became panicky and depressed again. In July 2008 I developed a severe allergic reaction to peanuts and had to be taken to the emergency room. I have never had any allergies and have enjoyed peanuts all throughout my life. In August of 2008 I developed an allergy to penicillin and broke out in hives. I had never been allergic to anything in my life, and all of a sudden, I had two allergies!!!
In September of 2008 my immune system went down the drain and I developed a severe and life-threatening MRSA infection. I was in and out of the emergency room for a week straight and didn't get better from it for over 3 weeks. The doctors thought I had to have some sort of AIDS or Cancer to be getting MRSA at such a young age....but all tests came back negative multiple times and they just shrugged me off as an exception to the rule.
In October of 2008 I got a severe intestinal infection called c. diff.
This took two weeks for me to get over and was absolutely horrible!!
What was happening to my body??
What was happening to my immune system??
In November I started having problems with my blood sugar and I always felt like I was on the verge of passing out unless I ate on a constant basis.
It was horrible!!!
By this time, my acne was gone, my periods were shorter...thanks Yaz.
But, I had
Migraines/Severe Headaches
Fluctuating Appetite with weird cravings for salty and sweet foods
Low Blood Sugar with light-headedness and weakness
Blurry Vision (even though my eye doctor has told me repeatedly that I have perfect vision)
Brain Fog
Severe Anxiety
Panic Attacks
Nervousness and Restlessness
Inability to pay attention
Moodiness/Snappiness
Depression
Long episodes of ataraxia where I just couldn't feel any kind of emotion
NO SEX DRIVE
An aversion to touch
Hot flashes
Body aches
Thinning hair
My gallbladder quit functioning
I had a very weak immune system
and I had developed allergies to things I had been in contact with all my life...
I had back aches and neck pains
And I had severe Insomnia in spite of the fact that I was exhausted all the time! And when I did sleep it was worth nothing....
In January of 2009 I quit my job and dumped my 'perfect' boyfriend.
In February I was unable to get a hold of any Yaz bc and therefore since I wasn't having sex, I skipped February. I felt better in February and never made any connection and so I got back on in March and since then I have never felt worse in my life!!!! I've been doing research on the effects that Yaz and other bc hormones have on our bodies and it is astonishing how much it can psychologically and physically damage our bodies. I have felt like I am going crazy and slowly dying for NO REASON AT ALL>
Yaz is a nightmare!!!
I have been off of it now for 2 days and even though I still have some of the same symptoms, I can slowly feel myself getting back to normal. I've been told that it can take up to 2-3 months to get bc completely out of your system and for your body to adjust so I'm coping and being hopeful.
During the last month or so, I have even considered taking anti-depressants and anti-anxiety medications because my life is a nightmare, luckily I looked deeper into my situation and discovered the culprit b4 I put something else in my body...
Yaz is not worth it.
I will never recommend it to anyone.
The pharmaceutical companies don't give a crap about us!!!
They just want our money and don't give a shit what their chemicals do to our bodies!!!
When I have little girls of my own someday, I will never let them take b.c.
I have been letting all of my friends and family know.
I would love to participate in a class action suite or an anti-Yaz campaign....
Anything. If you know let me know because I don't ever want anyone to have to go through what I have gone through with Yaz.
Ladies....Please do significant research before you ever put anything into your bodies.
April 13th
2009
2:00 AM
I'm in my 5th month of taking Yasmin, and in my 4th month I developed rashes on my face and all over my body. They look like inflamed skin with heads of pus, and very itchy. I first thought it was some severe skin reaction unrelated to the pill because I've taken bc before (ortho-tricyclen) for many years and that never happened. But after reading this forum, I think the cause is Yasmin. I've never had any skin issues like this before, and what's worse is that my immune system has been weakened and I got a bad flu-like illness with high fever in my 4th month of taking this pill. In fact, I'm experiencing my second rash reaction right now, and I'm in my 5th month. This time I'm heaving as well. I think I will stop this drug tonight. I'm so glad you are sharing your experiences on this forum because reading this helped me figure out why I've been so sick. From what I'm hearing, this drug is awful! Nobody should risk taking it because it is even worse than high dose pills, in my experience.
-- By awefulyasmin | Reply | (3) replies | Private Message me
April 9th
2009
1:23 AM
I had Mirena placed when my husband got back from Iraq. That was 5 years ago this month. All those years, I loved that I didn't have to worry about periods or birth control. Unfortunately, I had to worry about everything else. I blamed everything on stress. Learning to be a family again when my husband got home was hard. Then, we had no income for a year after he left the Army. Then, he got a new job and we moved and I went back to school. Stress, stress, stress. I blamed my weight gain on stress. I blamed my constant heartburn and acid indigestion on the weight gain. I had joint issues that I also blamed the weight for. I had chest pains and actually was afraid I was having a heart attack--I'm only 36 now. I thought being fat was the reason for that too.
I figured I just needed to lose 50 pounds. I'd go to the gym and get on track. I was hardly eating anything, since everything made me sick. I'd plan to go to the gym, but the next day, (I don't work, just go to school online), I'd have no energy. I would stay in bed for hours. I stopped cleaning my house, didn't care what my kids ate for dinner. I stopped doing my hobbies. I was so depressed. I saw one other lady here had said that she HATED her husband and he hadn't done anything! Ditto!!! I was ready to file for divorce and the poor guy wasn't even in town!!! He was on a business trip!
I had the Mirena taken out April 1. Yesterday, I went to the doc to confirm (though I already knew it) that my blood pressure was dangerously low. (84/52) I'm not allowed to drive, shower, stand for any length of time... This happens to me when I get sick or my immune system takes a hit. Since I'm having bleeding similar to what others are, I assume that's the problem and my BP will hopefully go up in the next couple of days.
However, I'm happy. That is something I never was before. I'm still tired, but I'm not sleeping on a regular schedule yet.
The biggest thing that no one has mentioned yet is HUNGER!! I'm SOoooo hungry. The day after removal, I woke with my stomach growling. I don't remember the last time my stomach growled! I can't seem to eat enough, though I'm scared to gain more weight! I'm thinking maybe my metabolism is going back to normal??!! Anyway, anyone else had this?
K.
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October 30th
2009
1:19 PM
I just want to say how happy I found this site. I'm not alone! I thought I was going crazy or that my body was shutting down completely. I had my mirena put in Sept. 2006 and my body has become something I don't even recognize. I am extremely bloated all the time and it hurts every time I eat and use the bathroom. I keep on thinking maybe I have Irritable Bowel Syndrome, but it doesn't make any sense because the symptoms showed up after I had the Mirena put in. I thought it might be food sensitivities so I got tested and have been trying to cut those foods out but it doesn't seem to be helping. I have tried all sorts of natural remedies but it never seems to go away.
I have gained 40 pounds since I the Mirena put in even though I have never have had weight gain problems before, I eat healthy and I am active. I also have a difficult time concentrating and focusing on anything. I also get dizziness, depression, irritability and mood swings. I also have been experiencing a sharp pulling or stinging in my uterus at times as well as joint pain (especially in my hips, knees) and painful intercourse with bleeding afterwards. My hair is also falling out and I have lost my desire for sex.
I've also noticed a drastic decline in my immune system. I have never been as sick as I have been in the last three years of my life. I seem to always be getting sick. For the first three months after the Mirena was inserted I had frequent bouts of yeast infections, bladder infections and still three years later I have these types of infections frequently. Not only this but I seem to catch everything that is going around when before the Mirena I hardly ever got sick.
Finally after reading the posts on this site I can trace all the changes in my body to when I had my Mirena put in. I am so upset that I have been suffering for 3 yrs with these side effects and it has taken until now for me to figure out that the Mirena doesn't just effect your uterus it effects your WHOLE body. I cant believe I trusted the doctor I went to when I had it put in that said that the hormones would only affect my uterus. NEVER, NEVER USE THIS PRODUCT!! It is coming out as soon as I can have it done! Please ladies if you know what it is like to have it removed let me know.
-- By danealfrancisco | Reply | (1) replies | Private Message me