Emotional stress symptoms and conditions

Hello all. I too am a new recipient of this "miracle" called Mirena! I just had my third son in late July, and I had weighed my options, and with some STRONG convincing from my OB/GYN, I had decided on the Mirena. I had it placed on September 20, 2008, and no more than two weeks later my hair began falling out! Now when I say "hair falling out", I mean every time I would brush off my shoulders, brush, comb or wash my hair I would get hand fulls! The hair loss got sooooo bad, that I couldn't sit down to a descent meal without finding MY hair in my food or strolled across the table. I'm always bloated. I bleed for weeks on end. My neck, arms, and arm pits, legs, and breasts are soo itchy it's ridiculous. I have had to treat a new yeast infection every five days since placement, and this, from a person who has only had a yeast infection maybe TWO times in my life. I am an emotional wreck. I mean, right now as i'm typing, I'm tearing up because I thought that I was going crazy. My marriage is on the rocks because I'm so temperamental, and heck, my husband and I have been waiting for love making for LONG ENOUGH! My newborn is only 3 1/2 months, and I can honestly say that I've had only about TWO weeks total to delicate to the intimacy of my marriage (now keep in mind ladies, that the last two to three months of pregnancy are not ideal for an emotional "stress ball" to be having sex either, so you do the math). But I am PROUD to say that I WILL BE CALLING MY DOCTOR 9 a.m. MONDAY MORNING TO SCHEDULE MY REMOVAL.!!!!!!!!!!!!!!!!!

Kenalog needs to be sued! I had the flu back in November of 07' and my internist had her nurse give me a shot of Kenalog. Come to find out through my own research (not anything my doctor warned me about) that kenalog causes all kinds of hormonal irregularities. On top of that horrible feeling, I have a HUGE dent on my left butt cheek. It started out small and is now huge with lighter colored skin tissue deep (1.5 ") in the middle of it. I feel very embarrassed being nude, and very paranoid about clothing. I know it is very visible in a bikini and under A-line fitting clothing. I went to my doctor and asked her about it and she said "it is normal, and that was one of the side effects." BUT the nurse who injected the shot did not say a word about any side effects when she saw the dent nor did she admit to any error of the injection. The Dr. said I will now have this crater/dent for the rest of my life. It all smells fishy to me. My doctor didn't mention one single word about a possible side effect. I would NEVER have had the injection. We trust our doctors to tell us side effects that may cause us emotional stress, and possible disfigurement for the rest of our lives. Has anyone had any luck with getting a lawyer involved. I want compensation. I want to try the saline injections and don't want to pay for the treatment. AND I want to STOP this from happening to other women. This is not a vain issue. It is an outright disfigurement/deformaty.

I HATE Kenalog! I had the flu back in March of 08' and my doctor gave me a shot of Kenalog. Soon after I had a horrible period that was totally out of the blue which made my husband I think that I may have miscarried. Come to find out through my own research (not anything my doctor warned me about) that kenalog causes irregular periods, but for months I went through the pain of thinking my body had miscarried. On top of that horrible feeling, I have a HUGE dent on my left butt cheek. It started out small and is now huge with a blue bruise in the middle of it. I feel very embarrassed being nude, and very paranoid about clothing. I feel like everyone can see it. I went to my doctor and asked him about it and he said "it is normal, and will go away with time." BUT the nurse who injected the shot in the first place, came in after he left and asked to see the dent and then apologized with a look on her face that made me realize I will probably be sportin' this dent for the rest of my life. It all smells fishy to me. My doctor didn't mention one single word about a possible side effect. I would NEVER have had the injection. We trust our doctors to tell us side effects that may cause us emotional stress, and possible disfigurement for the rest of our lives. Has anyone had any luck with getting a lawyer involved. I want compensation. I want to try the saline injections and don't want to pay for the treatment. AND I want to STOP this from happening to other women. I know it might be vain and I know my husband loves me for who I am, but I am a woman and don't want the freakin' Grand Canyon on my butt cheek!!!!

I took my 16 year old child off of singulair 6 weeks ago (3-28-2008). She started taking it 11-17-2003. She became dark, depressed, grades dropped, dropped out of dance and cheerleading, started cutting her legs with razors, stomachaches, headaches, anxiety attacks, trips to the emergency room. 6 months of fluoxetine given by her psychiatrist. Nothing helped her be happy again. Sad and Dark young woman. NOW: She smiles a lot, and is eating diner with the family. No headache or stomachache for a month now. She is sleeping better. Before she said that her mind would not stop thinking. She is taking pictures again and even asked me to order her book called "Understanding Exposure" and is talking about taking a class on digital photography at NMSU branch university to start on her college electives now. She is out more and even has a part time job at an ice cream parlor. Just lately I have stopped checking the trash for waded up tissues with blood (from cutting). Chris, I have had all her medical records sent to her primary Doctor and we are very willing to open them up. You have to have a child suffering to understand where we are coming from. The most dangerous place on earth is standing between a mother and her child. Singulair took our children from us and maybe changed them in some way forever.

My daughter has been off Singulair since March 29th. In my previous posting I explained that she had taken it for 2 years and last December started to experience stomach pain, and she became very anxious, agitated, and obsessive compulsive. We had every test possible and her anxiety only grew worse as the weeks went on. In February she was admitted for panic attacks and was given Paxil and Risperdal. When we stopped Singulair we noticed definite changes with her mood swings, personality, and affection. We saw a side of her that over time we forgot existed. She is so much better, but still on the medicines from her hospitalization. We have an appointment to discuss reducing these meds. But has SINGULAIR been out of her system long enough? She endured so much emotional stress that I know just stopping the Singulair will not be the cure all. Any input from anyone would be greatly appreciated.

I, too, have atrophy from the Kenalog, which is unsightly and causes me great emotional pain. Can anyone recommend a good attorney for this?

Thank you.

I have been on mirena now for 10 months. I was on the depo for 10 years prior. I loved my depo adn only went off of it after Kaiser said I could not do it any longer. I was told that mirena was a god send and a lot like my depo. I can say that the combination of depo and mirena I have not had any period at all. but that is where the happiness ends. I have experienced moths of breast pain. it hurt to touch them let alone put anything on them. after about 6 months and numerous trips to the vet it disappeared. then I got a small rash on my neck and by my arms. went to dermatology and since then I have been there, or to my primary or an allergist every week since then. the rough severley itchy skin is constant. remarkably every 29 - 32 days it fades for 2 days or so and just when I am sure it is going away wham back it comes and each time it is getting worse and worse. having never had any skin problems before I believed the doctors tha tit was folliculitus, then they said dermatitus, then they said uticaria and then hives or the last straw i was causing it that it was in my head. i just got a new allergist and while she doesn't knwo if it is my mirena she can tell me I have histamine levels that are off the chart. my husband is allergic to a lot so we already use free & clear everything and my housse is spotless but I am still being told it is soemthing I am doing to myself. I have also been reevaluating my things and I relaize I have been experiencing a lot of numbness and joint pain. so much so that my primary sent me to a rhuematlogist and he ran every test for lupus, and many other diseaeses adn even cancer. I was going crazy. Iwas beginning to think maybe I was mental. I have since been researching mirena and I am finding it so much more than what the pamphlet says. I finally got the nerve to call my ob, adn she ahs since been researching things with me and we know for sure that no matter what next week I get my mirena removed. I am just feeling so alone and depressed. I am 33 years old and instead of enjoying my new marriage I am contemplating a divorce becasue I do not want him to be stuck with soemone who might be crazy. seeking support and anyone else who feels this way.

Complete Nightmare. Please read...I was on Minocin for a week. I developed major CNS (central nervous system) side effects including major light sensitivity, back pain, runny nose. The worst of the lot were the mental side effects which included extreme paranoia, the inability to concentrate, depression, suicidal thoughts. I couldn't go to work, I was up all night crying, couldn't socialize properly or look people in the eye. i felt completely out of my mind and didn't know why..until i stopped taking the drug the next day.

My mother who is a registered nurse accompanied me to my dermatologist the following week to describe my experience. Let's just say he denied my claims and that there could be any connection between my side effects and Minocin, rushed me out of his office without treatment or refunding the fee that I already paid to see him, and continued to cancel my future appointments with him. I never heard from him again.

Over the following months, my mother did her own research at her hospital. Turns out,she witnessed and heard of many young women come in with the same side effects..and they were in a mentally unstable state. They were admitted to the psych ward and most were suicidal.

I know this sounds extreme and everyone's body reacts differently to drugs, but this is a true recount of my experience with Minocin and I wanted to share it.

Background: I've never taken regular prescription drugs other than anitibitocs for infections, and am otherwise a healthy person. I have no history of depression and was not going through any emotional stress at the time. I was not on the pill at the time, so my body was not bombarded with high levels of tetracyclin (which Minocin is of) although I was on the pill for a year, 3 years prior.

Slight throat irritation and nausea, but mostly EXTREME FATIGUE accompanied by slight irritability. Whether the emotional stress is a result of the medication or the fatigue, who knows, but what's the difference? This was on 150mg per day just before bed. 75mg seemed to get rid of most of the side effects but it naturally wasn't as effective. But still, give a lower dose a shot if you don't like the side effects, it may work for you.

I am so relieved that I came across this website. I am on my second month of Yasmin and am experiencing most of the symptoms that the other testimonials posted. I have been at my lowest point in my life for no reason. I have been crying, having the most bizarre mood swings, and extremely meloncoly. This is not like me. I am usually a very enthusiastic and uplifting person. Along with the emotional stress this pill has caused, I have been having intense stomach pains and diarrhea on a regular basis. My mother and boyfriend have been so worried about me because of my abnormal behavior. I just called my mom and BF as well as my doctor and therapist. I am not crazy and feel terrible that I had so many people worried about me. I am not sure if quitting the pill in the middle of the cycle will be the best bet. I am now terribly worried about birth control and how it will effect my emotional, physical and mental health. Thank you all for sharing and hope everything works out.

This is the first time I have ever taken levaquin. Never heard of it before this. I have always suffered with joint pain, back aches, and swollen joints. I have athritis. I am not even sure what the infection is, in my body. I had a swollen lymph gland in my groin area. Have been taking tests, and may have had a mild kidney infection. I have just found out I have diabetes too. The dr. put me on bextra for the joint pain, and levaquin for the infection. 500 mg for 10 days. I have had NO side affects that stand out. Actually, I feel much better. no joint pain, no nausea, no headaches and no tired feelings. I had all this before I started the levaquin. I did expreience one or two nights of not being able to sleep and feeling anxiety, but with everything else I am going thru.. I just took it as emotional stress. I have taken other antibiotics in the past that have given me a yeast infection.. but the levaquin has done well for me. I only have one left to take. I think allot of the side affects I have been reading are actually allergic reactions.. I was on prozac for 2 wks once, years ago and it put me in the hospital with all the stuff I am reading here. I hope you all get well and recover from whatever is making you sick.. Peace!