Rubber band symptoms and conditions

I was given Levaquin for a recurring sinus infection along with a staph infection that I got while visiting my mom in the hospital in March 2009. I took it for 8 days, then while clipping shrubs in my front yard, felt my tendon in my right ankle stretch out like a rubber band and then felt/heard a "pop". Then I had extreme pain and couldn't walk on it. Went to my orthopedic dr, he did an MRI and said that my posterior tibial tendon was torn. I was in put in a boot for 6 weeks. Another MRI showed that the tendon tear was healed, but the inflammation and tendon pain did not go away. Still have extreme pain and cannot walk without a limp, even with orthotics. Doctors don't know how to treat this, say that surgery will be required if the tendinitis continues and gets worse. The tendon is stretched out, deformed, and thickened, which is causing my foot to "fall over" and I already had flat feet. It has been over 2 months since the "injury". Does anyone know how to treat this? I don't want surgery.

My mom was given this drug for pneumonia in the hospital and had a severe allergic reaction to it. Her face and throat swelled up and she couldn't breathe and was immediately taken off of it, which is a good thing, because she has osteoartritis, and this drug would have debilitated her even more than she already is. She is 72 and should have never been given the drug. I am 47 but feel 72 after taking this drug. Has anyone gotten any relief from the tendon problems caused from taking this drug? I am now having depression from the continual pain and disruption of my life.

My girlfriend is 36 she had a kidney infection and got Levaquin IV in the hospital. Her legs were going numb and she could hardly get up to go to the bathroom in the hospital. She thought it was her infection. They sent her home two days later with 5 pill containers. One of them was Levaquin. She called me today and said she is having terrible pains in her hands, wrists, hips, and knees. She says she cant make a fist or hold a bag of groceries and her hands have swollen up so that she cant get her rings off. I told her I would do a search on the net to see if it might be one of the drugs she was taking. Slowly but surely I made it to the Levaquin. The drug maker fairly non chalantly refers to tendon rupture as a side effect effecting mostly people over 60 years old. I dug a little further and found this web site and was amazed at how many people are being poisoned by this drug. I am praying if she stops taking it the pain and debilitating effects will go away quickly. She has two disabled boys she has to take care of, including lifting them into wheel chairs and into beds. This is no joke! I am so angry at this drug maker and these doctors who often times do more harm than good.

I can relate to many of these experiences. Started out in my 20's with very irregular cycles, went to my first gyn after a miscarriage - the emergency room dr referred me to a dr that was at a fertility clinic. I had no idea why until I was actual a little more "awake" I was diagnosed with polycystic ovaries. I went through at least 6 or 7 different birth control pills, depo provera shot, nuvaring, then back on another birth control pill. finally we started doing the continuous suppression as I was bleeding at least a little bit every single day... for 2 years. I would still have my full blown period every 4 weeks or so, which also included a monster migraine on day one of the menstruation. Not only was my life being altered but I was starting to get anemic. Finally after a month of the continuous suppression my bleeding stopped. As did the menstrual migraines. I continued this way for 4 years. Didn't have a single period or migraine, life was wonderful.. or so it seemed. I have been over weight for most of my adult life. Finally decided to do something about it. I joined the gym with a friend and started losing weight. I dropped 55 pounds until... the dreaded bleeding, pain and hormones got out of control. I started bleeding every single day again. Finally made an appointment with my dr. She stated that when you lose weight it releases estrogen out of your fat cells. Gee, I thought losing weight was supposed to make you feel better!! I went on with it for a while thinking it would stop eventually and it just HAD to get better. In fact, things got worse. I started having horrible abdominal pain, eventually it got to be daily. To the point where I could not stretch or even hyper extend my right leg backwards. My abdomen felt like something had a rubber band tied to it from the inside. My dr said that she suspected endometriosis. However, due to my anemia... we had to wait. So back on the iron pills and wait wait wait. Finally, October 15th I went in for my lap. Sure enough, stage 4 endo, huge cysts on both ovaries. My endo had gone all over the place and attached itself to anything it could. Including folding my bladder in half! Good grief. I thought that I was just getting the weak bladder from getting older (I am 35 by the way). For the next couple of weeks after my surgery I felt pretty good. Finally pain free (still a little bleeding but not much). But, the end of December rolls around and here it is, back with all its fury. The pain is again horrible, my migraines are back, my energy is dwindling. The good life was short lived. My doctor suggested a series of Lupron shots. One shot a month for 6 months. My first shot in January (took me a little bit of time to decide if I wanted to do it) finally bit the bullet and got the shot. First few days, fine, no problem, no relief either but no life altering experience. Then one morning I woke up and realized I was not in pain. It was a strange feeling actually. But the time I got the second shot, no more bleeding, no more pain... However, the hot flashes, night sweats and the emotions came on. Holy cow. Drama drama drama. I could find any reason on the planet to argue, with anyone. Thank god I have a very understanding family and an even more wonderful partner. I think he has the patience of a saint. I still don't know how he puts up with me. If I am not trying to find some reason to pick a fight then I am crying like a baby... for hours and hours. These hormones are so out of control. I honestly don't know what is worse, the pain or feeling like the world is going to end in the next 2 minutes if I don't get this spill picked up.. I literally cried for 2 hours Saturday because my cat knocked a stupid bottle of car wax off a shelf in the back room. Good lord, I had the most horrible feelings coming over me and just could not stop crying. I bought a new bed 2 weeks ago and let me tell you. If I am not on one of my 13 hour sleep fests then I am laying in it crying and feeling sorry for myself. Or the even better part of indegestion or my favorite part.. gas. I honestly don't know if I can go on like this. I made an appointment to see my doctorr this Friday to determine what she thinks will happen if I don't complete the other 3 shots. just give me back the pain if you have to!

I started taking Advair 250/50 when I couldn't get any air in the upper part of my lungs. I was diagnosed with asthma as a child, but hadn't experienced it since I was 11. I am 21 now, and I have panic attacks, pain in legs (pain in my thighs, and it feels like a rubber band wrapped around my knees) and arms, splitting headaches, hyper-sensitivity, mood swings, back pain, heart racing for no reason(especially at night, it wakes me up), insomnia, pain in my chest (mostly on the left side near my arm pit that feels like muscle tightness), I sometimes get sharp pain in my chest if I take a deep breath, I've gained 40 lbs. in the past 8 months, and I am a nervous, emotional wreck. A year and a half ago, I was a completely different person. I've been to the doctor, and they can't find anything wrong with me. Although I am overweight now, my cholesterol and blood pressure are perfect, there is nothing wrong with my lungs (barring asthma). I am in great health, and yet I feel awful. All the time. I have no idea what to do, because my doctor's have told me that the only known side effects of Advair is potential damage to the teeth. I am outraged, but I am afraid to stop taking it because my lungs actually hurt when I don't. I'm also on an Intal Inhaler, but I haven't heard any side effects of this. Here's the kicker, the doctor that prescribed me the Advair wasn't even a respiratory specialist, and refused to reccomend me to one! I'm so glad I found this site because everything everyone has listed seems to be what has gone wrong for me since I started taking it. If anyone has any information on how they're doing now that they've stopped taking it, or the "withdrawal" effects of Advair, please post them. I'm hoping to wean myself off. Good luck to all of you, and thank you. Now I can stop being so worried that I have blod clots, lung cancer, or an aneurism. ;)

Thanks so much,
Jade
NY,NY