Waste of my time symptoms and conditions

I have been getting lupron depot injections since my laproscopy back in August and had no trouble the first month except for hot flashes. After the second injection I started to experience migraine type headaches and I would get the shakes really bad through the night almost as if I was coming down with the flu. I just had my third injection and the symptoms are worse. I feel tired, nauseated, body aches, chills through the night and hot flashes all day long. Will my symptoms continue to get worse as I go on? I have two more months of injections and I am contemplating not doing it. My husband and I have a beautiful little girl but really want another child. Is two more months really going to guarantee pregnancy or is it a waste of my time?

I really don't know what to do, I hurt so bad every single day I could cry. I was given Levaquin in March 2008 when I had pneumonia. I took it for 10 days and I hurt so bad still was very sick so I was put on it for another 10 days, so I took the Levaquin for a total of 20 days. I thought all this sickness was from the pneumonia. I had trouble getting out of bed, I could not even bend my knees, my feet, knees, elbows, and fingers were swelled up and I was getting all kinds of cracking in all my joints, headaches, stomach pains, all kinds of muscle pains. When I went back to work, I was telling a girl at work how I hurt and she asked me what kind of antibiotic I was taking, I told her and she said they had it on the world news . I said why is it still on the market. I seen 3 doctors about this and they think I'm nuts! They sent me for all kinds of xrays for all different parts of my body, what is that going to show! Its been a year and I still ache, I keep swelling up, joint and muscle pains, cracking, stomach troubles, problems sleeping, its terrible. I take pain medication for my back, I have 2 herniated discs, and I have to take more pain meds for all these other pains, this is not going to work. I even went to see a rheumatologists and he said I don't have arthritis. So Levaquin done a number on me. If anyone can help, or know what to do let me know!

I also have a child who has been on this drug for about a month and as I sit here and read these blogs the more I am remembering complaints made by my son. He has been getting into trouble at school lately, irritable, angry, sad, leg pains, stomach aches and also having trouble getting to sleep at night. I am an RN and it took me to glance at the pill bottle today to realize that I needed to do a little more research about this drug when I saw that it said "mood changes and depression". I feel horrible because after a great 2nd grade year I was disappointed that he was not behaving as well this year. I know know that the $60.00 wasted and tiring reprimanding was all a waste of my time! I owe my poor son an apology as I will be taking him off of this drug today! More information and advocacy needs to be available especially when core users are children who have little to no voice!!!

I have been taking lamictal for about two months now, slowly increasing about 25 mg a week to insure that I do not get the serious rash. I am not at about 150mgs a day now. I really do not like this drug. I waited patiently to feel different, better, for my moods to stabalize, and in place of feeling that way, i have been somewhat disoriented, more emotional, at a loss for words and I generally feel "stupider." It is a horrible feeling, i am usually very quick to my feet, and now i am lagging. In addition, I have been having very vivid, intense dreams, that I never had prior to taking lamictal. All I want to do is get off of this drug, however, i have to do so slowly because of this rash, and that too will just be another long waste of my time.