Many sleepless nights symptoms and conditions

I have been on Lantus & Humalog for about 3 years. I am a 75 yr old male T2 and the only other meds I currently take are Toprol XL and aspirin. After reading all these Lantus postings, I decided it was time to quit Lantus just to see what happened. Like one other person said, "all of a sudden the fog lifted"! I am a different person. I can now sing in church (after 3 days off of Lantus). Before this, I did not have enough breath to sing. When I was on Lantus I had many sleepless nights, suffering from RLS and leg pain. Now I am sleeping the entire night through. These benefits are the tip of the iceberg, I just feel better all over. Needless to say, I am injecting more Humalog now to make up for the absent Lantus but that will not be a problem. Please understand I am not advocating this for anyone else, I am simply reporting what happened to me. I see my doctor in a couple of weeks and can't wait to share the news with her.

I've been on 10 mg of Lipitor for approx 2yrs. A few months back I began experiencing severe constant right hip pain. A could walk through it, but had many sleepless nights due to the unrelenting deep pain. I had difficulty lifting my right leg without support from my arms. I'm 54 and otherwise in pretty good health. I stopped taking the Lipitor about 2 weeks ago and while I still have some pain it has decreased about 75%. I can sleep at night and am even pain free some of the time. If anyone has had a similar experience would appreciate knowing and if the pain eventually subsides and any suggestions to support the healing process.

Sorry for the long post! I started taking Levaquin in mid Feb and I'm still feeling the effects. I am a 37 year old female who has never had any kind of reaction to any drug. When I say never - I mean not even slight nausea. I was prescribed Levaquin for bronchitis - 500 mgs for 10 days. I took it for 5. My bronchitis cleared up but I experienced feelings of depression after 3 pills. No nausea, headaches or loss of appetite at all. After the 5th day, I experienced numbness and tingling in my hands and feet. I went back to the doctor that same day because I was terrified. I was prescribed prednisone. 5 days after that, I started experiencing full body pain. It hurt to even lay down. Went back to the doctor that same day was prescribed vicoprofen. It didn't really help. I was given a muscle relaxer to take w/vicoprofen and that helped me get through the day at work but the pain was always there and that caused many sleepless nights. I went back to the doctor because the pain had left my torso and pretty much my legs too but settled in my arms and hands and was even more intense than when it was all over my body and prescribed Cymbalta. The pain was so intense, I was crying the whole weekend. Since my doctor didn't believe the intensity of my pain, I was desperate for a moment of relief and felt very ashamed to have to call a friend who's an RN and she had her doctor prescribe vicoprofen for me. I was able to semi-function again. 1 week later went to a rheumatologist and was told I had swelling in my nerves in both wrists and it may be carpal tunnel, fibromyalgia, nerve damage or rheumatoid arthritis and given Lyrica. Had an EMG/NCV(Horrible) and the results were negative. I also had extensive blood work and was told on 4/21 that I tested positive for drug induced Lupus possibly caused my Ibuprofen. I stopped taking Motrin and my doctor prescribed Vicodin and I'm finally starting to feel better(the pain is not as intense) but I don't believe for one minute that Ibuprofen was the cause of the Lupus. I believe Levaquin broke my system down( I have Vitiligo - an auto immune disease) and made me even more susceptible to other auto immune diseases. Levaquin is finally starting to leave my body. My calves are stiff when I get up in the morning and my hands still hurt, but it's nothing compared to how I felt the previous 10 weeks. Sleep is still disrupted by pain.

I am going back for a blood test next week to see if the Lupus is still in my system. I'm happy for the people that have used this drug and have been fine, but for my body, it's toxic. Hopefully, there will be a blood test in the future that will show if you are prone to have severe side effects to this drug before it's prescribed.

For All of you suffering, you are not alone.I have found great comfort on this board knowing that I'm not alone.

Good evening all....I as well as you all have a story to share about my son. Kameron lived the terrible twos to the fullest and turned into the biggest sweetheart when he turned 3. But then his doc wanted to try something stronger for his allergies and thats when Singulair changed out lives. Kameron has been on that junk since about November/December and since then everyones lives around him has been pure hell. He turned into satan in the flesh. I have never seen as much anger as I do in my son. On a weekly basis we go through stomach pains, depression, anger issues, him not eating for days, many sleepless nights, and thats not even all of them. He has spit in my husbands face and called me very bad words (that nobody has ever used in front of him towards me), Ive walked around with black eyes from him (remember he is only 3), he has given me bloody noses and straight up told his dad and I both that he hates us, and doesnt love us anymore. We cant take him around our friends children cause he is very abusive and controlling with them. He shows no interest in the things that he once loved, like his toys and pets. We have taken him to the doc and have been told over and over again that he is just a typical 3 year old but a mama knows when something is wrong with her baby!!I havent seen my sons precious smile since this stuff has taken over him or even heard him laugh. Im taking him to a different doc tomorrow and takin all of your comments with me and I am not leaving his office till they do something for my son!! My thoughts n prayers are with all of you that are goin through this cause I myself now how hard its been..