Embarrassed symptoms and conditions

Thank you, Yasmin takers and victims! I began taking Yasmin in 2004. I had no problems. In fact, all was well, I loved my life, started and finished a master's degree, and got engaged over the past few years, while taking the pill. About a month ago, however, everything changed. I began snapping at my fiancé, crying uncontrollably, thinking about ways to not be around people, and even thought about hurting myself to relieve the emotional pain I was experiencing. I thought I was all alone.

A week ago a friend of mine asked me if we could talk. She had been experiencing some of the same symptoms. I hadn't spoken to her about my problems, because I was embarrassed and felt I could deal with it all by myself. After she opened up, I was able to admit my own overwhelming anxiety. We promised each other that we would get through this together. And so, we began looking for similarities in our lives (diet, work, stress, etc.). Yasmin. We both take it.

Although I know that medication affects different people in different ways, it appears that the drug is affecting a lot of people in a negative way. Maybe we can bind together, and get something done, so that others don't have to experience what we have.

I had a Kenolog injection in Nov. 2006, for pneumonia. I got better and thought all was fine. After a 2 months i noticed a strange indention on my upper left buttcheek. at that time it was about the size of a quarter. Also at that time, never having heard of any side effects i was stressing Big Time about why I had this "hole" in my cheek. After going to a different doctor and having a sonogram and a bunch of people looking at my behind with No answers. I finally found a Kenolg complaint web site after google-ing indentation in buttcheek. I was shocked as i finally put 2 & 2 together! Now It's Sept. 2007 I still not only have a "hole" in my cheek, it has gotten much bigger, about the size of my fist!!! It's hideous! It also aches. I use to run now that hurts my glute.The doctor has been no help. I keep hoping it gets better, but so far only worse. Does it get better and heal up?? Is anyone currently involved in any lawsuits regarding this situation?
any info would be much appreciated.

I was a very healthy 23 yr old female. I cant believe that I finally found someone going thru almost what I am going thru. My name is Liane and My life changed on July 7th, 2007. I went to the hospital for frothy urine. They told me it was a UTI and gave me Levaquin for 7 days. I took it for only 5 days cuz ( I was allergic too) then were gonna start me on macrobid. Mean time my hands,face, and bottom half began to swell up. Me thinking it was from my period but this was different. I work in a jewelery store and once my rings that are a size 6 DID not fit at all I panicked. I had extremely bad back pain, high blood pressure. I did not feel same. On July 13th (Friday) I went to a hospital here in southern california and talked to a doctor and she said.."sweetie u don't have a UTI, I don't wanna scare u but I think that U have a Kidney Disease called Minimal Change Disease"!!!! WHAT!!!! Am I gonna die? She says no but come Monday u need to see a specialist and confirm. Now here is a Lasix pill to help take some of the water weight that u have gained away. Its already about 1:30am on Saturday the 14th. She says u will not sleep cuz u will be urinating all night. I said well anything to help me, i had went from a very healthy 5' 7" 155lbs woman, I worked out in the gym 5 days a week with my boyfriend who is a Police officer and bodybuilder for fun, so me swelling up and devastated me. I took the pill. and went to sleep. Nothing happened to me. That meant something was wrong. Later that day Saturday I felt BAD. My face kept swelling, blood pressure kept going up, heart racing. I went to E.R and told them I felt like I was gonna die, I think I have minimal change disease I need a specialist now. They admitted me for 5 days. My specialist came in and saved my life. I had a ultrasound and kidney biopsy and they confirmed what I already knew. I had Minimal change Disease. I ended up being allergic to Dilaudid, and compozine in the hospital. I was released on the 20th of july. and now began my treatments. 3 x's a day of Prednisone at 20mg each, simvastatin 20mg once a day for high cholesterol now, lasix 20mg once a day, and omeprazole 20mg once a day to prevent ulcers from the Prednisone., I hate the Prednisone. I broke out so much on my face. And its not pimples it bumps. I wake up every morning at 5a.m with nasty heart burn. then wake up every 2 hours after. Doctor told me to take all my meds at once and it helped a bit but still not completely. I too feel bloated in the mid section. I still suffer from edema in my legs down to my ankles. During the day gets worse but once I put my feet up and elevate them I'm OK. I have bad mood swings I don't know how my loved ones put up me. One minute I cry, 20 minutes I'm happy and wanna go out for a walk. This drug is gonna help me but then Do I really need to put myself thru this? But there is not other way. Just thought of sharing my story.

I was given Bactrim after a laser procedure to my face. For the first seven days, my only symptom was a very red face which I unknowingly attributed to the laser procedure. On the eighth day, my face was very much improved in colour which I later realised was because I had accidently missed two doses of Bactrim. When I recommenced with the Bactrim the next morning, within a few hours my face was intensely itchy and red and I broke out in a rash all over my torso. At this point I became concerned and did some internet research, only to realise my symptoms were all Bactrim related. Apparently sulfite allergies are relatively common amongst the population, and I now know why I get a flushed face when I drink beer or wine.

had two sets of injections in my neck for neck spasms. First set in March 2nd in June. after the first injections I notice fatigue, I lost 33lbs. of muscle mass in three weeks. been lifting for 28 yrs. and it's all gone. Burning sensation in legs weakness in arms, legs. Adrennal and pituary glands have shut down testosterone level dropped from 675 to 75. chronic thrush (yeast infection) on fluconazole 150 mg. once a day. Drs. do not know when this will leave the body. Now have to see infectious disease Dr. because of the recurring thrush, possible liver damage from fluconazole. Also lost at least 3/4" in height.
Thsi stuff is vicious.

It all began with LISINOPRIL: Constant involuntary pulsating, twitching, spasming toungue, swollen tongue, difficulty speaking, extremely dry mouth...

As directed by my new internal med doctor, I had recently begun taking one 5 mg lisinopril one time per day for my hypertension. I also take one 5 mg Ziac daily. I am a 40 yo female. I took the lisinopril for 6 days before feeling too frightened and anxious to continue the medication. I have now been off of the lisinopril for a week, and my involuntary tongue movements are still present 24 hrs/day. This is a very disturbing sensation over which I am powerless to control or stop. I am preoccupied with it and full of worry. It is very obvious that my speech sounds thick and impaired, and I am embarrassed to speak around anyone now. I know that "other people's opinion of me is none of my business" because I know the real truth, but I hate for others to assume I am intoxicated or impaired in any way.

Anyone else have the twitching, pulsating, throbbing tongue movements? If so, how long did this last?

Thanks, MAC

I had the usual side effects: nausea, diarrhea, bad taste, etc. I wasn't able to finish the 10 day course (only 7 1/2). My biggest complaint is the bad taste and the furry yellow tongue. My doctor gave me an anti-fungal but it hasn't gone away. It has been 2 weeks since my last dose and my tongue is still yellow and furry! I am disgusted and embarrassed.

Hi everyone,
I have not posted in awhile because I have been going through a really tough time. I have gotten worse. I been off about 7 weeks now. I am sorry and also embarrassed to say that I had to start an A/D called Lexapro. I was always into everything natural and never would do this before but the Yaz has just totally messed my brain up. I became so suiscidal and depressed where I could not even leave my house. I have 2 children who I could not even take care of. I tried everything natural for a couple of weeks with no success. It was basically death or try this medication. I had no choice. I have only been on it for a week a very low dose and still feel horrible. The sleep jerking is the only thing that got a little better. But now I read all your post and feel helpless that I could not do this on my own like all of you. I also was healthy and happy before this pill. Never had thoughts of anxiety or killing myself. I wake up in pure panick since taking the Yaz. Now the muscle weakness makes sence. I have been suffering with muscle aches and shakiness since the pill too. i just thought it was me. Nothing about me is the same anymore. I lost alot of weight but now my fingers are puffy and feet are puffy since going off the pill. Yasmin and yaz are such dangerous pills. I really feel it scrambled my brain. My doctor does believe the pill caused a chemical in balance in my brain with the serotonin and 2 other hormones, I can't remember the name. They control our stress levels, sleep levels and pain feelings. He really believe the pill altered these chemicals. My body forgot how to sleep. I feel like my brain is so scrambled. My thyroid became alittle hyperactive too from the pill. The body aches are sometimes so unbearable, my legs and feet are the worst. It makes you feel like there is something else wrong with you. I have pain in my head always, my vision is not the same. I just get so sad because I feel i will never get better and now I had to take this stupid A/D. I am so scared but what choice did I have? I really feel that we need to do something. Something needs to be done about this medicine. I am so angry that we are all suffering like this. IT's like they put somekind of chemical warfare in it or something. I am in touch with other woman from other websites that were on this pill and they are so sick too. We all want answers of what really happend to us after this pill. Sometimes its hard for me to get out of bed. Did other people feel like this? I feel like I have the flu. I have all these brain fogs all the time. The sleeping is the worst, it;s like my body really forgot how to sleep. I still get the muscle twithcing alot at night. Does anyone get muscle twitching? Please let me know.

I went to the doctor Friday night worried that I had pink eye. He says "No, your eyes are fine, nothing wrong there, but your cough sounds awful." so he listens to my lungs and says I have bronchitis. Yeah, I had a sinus infection a couple of weeks ago and the cough never went away. So I say, ok, what can you do? I have no insurance, the place I currently work at is cheap. He brings me 5 sample packets of Levaquin, 750 mg. Says to me "These are really good. Take one a day for the next five days. They should do the job, they are $25 a pill." I think, wow, that's some expensive medicine.
ANyway, I come home and take a pill around 8. I have a second job that I work on evenings and weekends, so I have to get up in the morning to go. I can't sleep like usual. I wake up every hour or two. First I am sweating, I get up and turn the heat down. Second time I wake up with tears running down my face, I'd been having a nightmare about one of the kids I watch dying od SIDS (How twisted is that?) Then I just keep waking up.... I go to work yesterday morning and after about 2 hours I start to get real light-headed and nauseous and my ears were burning like someone had embarrassed me to the extreme. I came home after being at work 4 hours. I felt sick to my stomach all day but thought it was because I hadn't eaten. WHen I finally ate, I couldn't stop eating. Then I did, and 2 hours later I was feeling sick again.
Not thinking anything about it being the drug, I took another one last night at 6:30. When I finally went to bed at midnight, the nightmares started all over again. I wake up crying, my body wracked with sobs, tears rolling down my face.
I don't want to keep taking this medicine if it is causing all of this but I don't have the money to go back to the doctor for something else, and I can't afford to still have bronchitis. What am I to do?

I feel really embarrassed to have to comment on this but I really need an answer because I am really bothered in the bedroom. I love the weightloss and I am losing hair which I was unaware it was related to the topamax to thanks for that info. I get extremely lubrigated/wet in the vagina (even when I am not aroused). That is not even the worst part I found that when I came there was a strange odor. I changed my diet and everything and it didn't change. I know I don't have an infection because I went to the gyno not long before. Am I alone???

I have been taking Lipitor for 3 years; I started having problems with my finger and thumb on my left hand. I passed it off as arthritis. Not being aware of the side effects of Lipitor. Then I started having numbness in my finger tips. My Dr said it could be a pinched nerve in my neck. However, tests are expensive with no insurance, so I bypassed the MRI. In the last 6 months I have been getting weaker in my legs, I can hardly walk a block without my legs starting to shake. Yesterday I was at work and went to walk down a flight of stairs and almost fell. I had to do a lot of walking and my knees started giving out on me. I was so embarrassed. I had to stop and rest, and let the rest go on. My husband saw a Lipitor commercial and heard the side effects one being Muscle weakness. I have stopped Lipitor affective today. I will be sending my Dr an e-mail immediately after this to let her know I am discontinuing Lipitor. I am afraid of what I have done to meself. I just hope I can get my health back.

Please bear with me as this is a bit of a long story. I was put on lisinopril 5 years ago for hbp (not bad - 140/85). 5mg of the drug quickly controlled it. But at a check-up a year later my doctor heard irregular heartbeats and added a beta-blocker to control heart rate. For the next few years I had terrible depression, throwing my whole life into a mess. Eventually I couldn't even work. I also had terrible joint pain all over my body, the cough, poor sleep, nightmares, red face, and skin so dry I was embarrassed to meet people. The depression clouded my thinking to the point where I just thought I was aging really rapidly and really badly. I never thought of the meds. Stupid, I know. Finally someone told me that beta-blockers can cause depression. That was all. I went to a new doctor and asked to go off the beta blocker. Miraculously, despite horrible withdrawl symptoms, mainly rapid heart rate (I too, went to the ER a couple of times), I immediately felt like a new person. Most of my side effects were gone but my heartrate has never been normal or regular. I have been off the beta blocker for 6 months and my bp is ok. Recently I went to a cardiologist because of the irregular heart beats and rapid heart rate. He renewed my prescription for lisinopril and scheduled me for a bunch of tests but now I'm wondering if the whole disaster has been from taking lisinopril all this time. Neither of my doctors have ever even thought of it but I've been doing some research, including finding this site. I know you don't just stop taking bp meds. Any input out there on getting my doctor to consider this as a possibility and also any other family of drug that would control bp without all these side effects?

I'm red. I mean my body has a redish tint to it. My face looks flushed, like I am extreming embarrassed and blushing!

I have taken prednisone a few times before and never noticed any side effects. However I am on a larger dose than I was on last time. I am currently on 40 MG a day for 3 days then 20MG a day for 3 days.

I asked the pharmacist specifically if there was any side effect with Prednisone and sunlight (direct and indirect) and she stated there was not!

I asked becuase I have been using a tannig bed in preperation for a trip to Hawaii next weekend. I am not sunburnt, there is no pain or heat involved with the skin. Has anyone else experienced redness? I am typing this Sunday night Jan 22. I am calling my doctor in the morning , just found this site and thought I would give it a shot

Thanks

In response to suetim1031, #13070, my 9 year old had been on singulair for 4 1/2 years. He was also on multiple medications for acid reflux. For the past two years, I have been talking to his doctors about his EXPLOSIVE behavior and the possibility of it being caused by any medications or combinations of medications that he was taking. Both his PCP and his Allergist assured me that none of his asthma medication would cause such issues. My son has, on way too many occasions, said he wished he was dead, he hated himself, has kicked walls, and put his hand through the first pane of a glass window!!! That was the end. I am embarrassed to say that I never checked online for side effects to his medications, because I checked with his doctors....which I thought was the right thing. I could not believed what I read on this website. So many people were describing my son and I finally felt there was an end to the terror that was happening to our family!! He has been of of singulair for 2 1/2 months now, and though he still has explosive moments, they are much shorter in duration and much less often. I hope this behavior continues to improve over time, but I do have concerns that his prolonged use of this drug have caused permanent damage. Needless to say, his asthma and allergies are beginning to appear again (they were completely under control for the past two years) but I can handle some treatments and inhalers over the jekyll and hyde child my son had become. I am told there are some holistic alternatives for asthma and allergies, I am going to look into them. Best of Luck to you and anyone else who has experienced the extremely scarey side effects of this drug!!

hi, I've been on celexa for 5 years. I gained 47lbs. I was very thin before, never past 99lbs. Now, i'm 147lbs and sad because of my weight. My doctor put on lexapro. I decided to cut my daily dosage of celexa from40mg to 20mg. I never took the lexapro, because I'm tired of taking all this medication. This is my third day on 20mg. I feel ok, so far.
Does anyone know if after I get off if my weight also will decrease. I am desperate.The summer is coming and I'm embarrassed even to wear a bathingsuit.