Time bomb symptoms and conditions

To all the women still taking this drug: I beg you to stop taking this medication and read all of the posts on this site!!!! Here is my story... I was on Yasmin for 6 years. About 4 years into taking the drug, I noticed a mass on my right side. It was a painful mass that I could easily feel, and it eventually because so uncomfortable that I could no longer sleep on my right side, and it affected basic movement. At the same time, I was beginning to show some side effects of Cron's disease (which runs in my family), so my gastro doctor told me to get a CT scan and an MRI. The tests revealed a gigantic mass on my liver and I was told to see a liver specialist right away. I went to KU Med and was told that I had to have emergency surgery right away, and that I was basically a walking time bomb.... If I tripped and fell, it could cause this mass to rupture and I could bleed to death. He also told me that if I had gotten pregnant while I had the mass, it would almost certainly lead to death for me and the baby. Nonetheless, they cut me open from the middle of my chest clear down to my belly button. They did a liver resection and removed my gall bladder and several lymph nodes. The mass on the scan turned out to be 2 grapefruit-sized benign masses, called Focal Nodular Hyperplasia - most commonly caused from the hormones in birth control pills!!!! Ladies, this was major surgery.... I was in the hospital for 9 days and out of work recovering for nearly 2 months.... and this all took place 2 months before my wedding!!!!!! The MASSIVE stress I endured caused me to have panic attacks and I thought I was going to literally die. Keep in mind that my CT and MRI were purely coincidental. If my GI doctor had not ordered the tests, I would have never known about the masses, and God only knows what would have happened to me.... Anyway, this whole ordeal has DRASTICALLY changed my life and affected all of the people I love, my husband included, who has to endure all of my pain and anxiety. BOTTOM LINE - IT'S JUST NOT WORTH IT! TELL EVERY WOMAN YOU KNOW!

To make a long story short (I think). Taking Celexa (20 mg) for more than 4 years definitely caused decreased sexual sensations (numbed nerves), though it did change my life. In October Switched to Wellbutrin XL. Withdrawal from Celexa was not easy but Libido is definitely back. Problem is I am angry ALL the time at my husband. In fact, I've been angry almost from the get go from switching to Wellbutrin. I have also been puzzled by slight hair loss in the back of my head at the hairline. I have of late experienced abrupt halts in thought processes and my periods, though I am 45, have suddenly become irregularly. Frankly I didn't realize that Wellbutrin could likely be the cause of these symptoms until I read some of these posts. I really would like to wean off of this drug (was prescribed 300 mg but have taken 150 mg due to feelings of being 'wigged' out on higher dosage - did up the ante for just over a week to see if that would help but didn't seem to matter)...Nevertheless, I really think Wellbutrin is causing me to feel deep resentment toward my husband. This is not a usual emotion for me and it pretty well started immediately after I began taking Wellbutrin. I really could use your opinions(s). IS THE WELLBUTRIN causing the anger??? Did the Celexa simply MASK existing problems??? Is it a combination of both. Is this depression again or am I in the process of slipping back in??? (anger was not a previous symptom of my depression though black clouds, low esteem, doom and gloom and sadness were) Also, aside from anger and sheer resentment, I feel as if I'm spinning my wheels, that I'm in rut and that no matter how I try to move forward, I can't - I really feel lost and am so angry at my husband and see him in such a different way that it is almost to the point of being ridiculous). THANK-YOU so much for your replies.

please can u tell me does anybody on this site suffer from memory loss cause they are taking simvastatin

You can read the tragic story of my sister and the use of Paxil at her website. It is very tragic. Some people claim Paxil has helped them. BUT for others it is like a time bomb waiting to go off.

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I started taking 60mg of Prednisone two months ago and one week ago it was lowered to 40mg a day. I have gained 10lbs in that time, have the moon face, acne on face and chest. My face has grown black fur on it. My mood swings are terrible. I feel like a time bomb waiting to go off. I feel like I am always angry. My anxiety level feels like I am about to jump out of my skin. My doctor has agreed to start tapering me off of the Prednisone as now I am also on Imuran, Cytoxan and Methotrexate. Does anyone know how long does it take for these side effects to go away after you are off the Prednisone??? Do any of them lessen with a lower dose???

After 1 week. I experienced moods that I had never encountered before. I had extreme irritability and dark thoughts. I wanted to get rid of my pets. Hated my kids, and hated everything. People at work or on TV, I felt like killing them. I felt like a walking time bomb serial killer. I immediately stopped taking the Lamictal after 1 week. I could tell a difference by the next day. I was still depressed but not suicidal or full of hate that I experienced on the Lamictal. This type of side effect can happen with any mood stabilizers or anti depressant type drugs. I'm glad I knew this, or I would have killed my pets, family and myself.

I'm a 37 year old female and have severe asthma and allergies and have used pregnisone on and off for 30 years. I believe I am the poster child for the long term side effects. My immune system is shot to the point that my normal medicines for asthma (ventolin, advair) and allergies (tylenol sinus, claritan, visine A) and ezcema (elidel, hydrocortisone, etc. - - NOTHING works!

In the past 6 months, I have developed various infections that the doctors have not been able to identify. My eyes are swollen and red with large amount of white/yellow secretions. Vaginal secretions. Face swollen. Skilled covered in a rash with ezcema out of control. Sharp pains in my back and stomach. Constant asthma. Abnormal hair growth. It is to the point that it is impossible to function and each doctor just wants to prescribe more pregnisone. I feel as if my body is a walking time bomb and it is so full of all the cortisone from over the years and has just decided no more.

I admit that I too readily believed in the doctors when they would rapidly prescribe the pregnisone. Only now am I paying attention to the long term side effects.

Has anyone had tests done to test their immune system and other organs for damage? Thanks and best to our pregnisone club.

This site is God sent. I can not believe what I am reading on this site concerning Singular and all of the behavior, tantrums that people like myself are experiencing with their children. I have a 5 yr old that has been on Singular since the age of 2. The tantrums, crying if he does not get his way, etc was always based on the fact that he is an only child and spoiled. I once was told that my child was "like a time bomb waiting to explode." I met a mother who was having the same problem with her son and told me it was the Singular. I immediately got on line and found this site. I am taking my son off of Singular today. I feel guilty that I had my child on a medication that would cause such terrible side effects. To all of you who have posted on this site, I would like to Thank You for educating others on Singular.

A good friend of mine (82) was recently rushed to the hospital because he woke up and could not get out of bed. After a week,he is now in rehab using a walker and going through leg exercises to build back his leg strength. The doctors are suspecting the Lipitor he has been taking (10 mg 2 times a week for about 3 years.) to be the cause of the muscle "atrophy". After reading these stories on this web site I am shocked to hear about all the problems Lipitor has seemingly caused people. I tried Lipitor for about 6 months, and had leg cramps in the tops of my legs (where they meet the body) and the Dr. promptly took me off of it and now I'm on Zocor, with no apparent side effects-but I'm reading up more on that.

Now in reading about Rhabdomyolysis (a severe side effect with muscle breakdown and kidney failure), I'm asking the doctors to check for that as my friend has had some symptoms-weight gain, weakness and now not being able to walk. You know, these men don't complain about aches and pains and many may be walking around with a time bomb going off inside them with these symptoms.

If anyone has experienced something similar, I'd love to hear from you, especially how long the recovery of muscle use can be.
Thank you.