Pinched nerves symptoms and conditions

I got prescribed Levaquin for a Failed attempt with an IUD. It got stuck in my uterus and caused infection and lots of paid.So she put me on Levaquin and another strong antibiotic. I was really scared to take it because of all the side effects i read in the pamplet they give you at the pharmacy,so when i went back to the doctor i told her i was to scared to take it,she told me if i didn't take it that i could die and she would put me in the hospital with IV's if i didn't. So i felt like i had no choice. After the 2nd pill,i couldn't not sleep at all! it gave me insomnia soo bad..And im one of those people thats in bed by 9 and up at 6. Now im tossing and turning all night,and if i do actually fall asleep i wont get up until like 9 and that totally unusual for me. Now its day 8 and both my shoulders and my neck hurt so bad. Feels like pinched nerves and im so nauseous i cant stand it.Also, was driving to walmart with my kids 2 days ago and i had to call my mom to come get us because all the sudden i couldn't drive anymore. Got really dizzy lightheaded and felt like i was going to pass out at the wheel. i was very scared. i wish that on nobody! then when i got out of the car i felt like my legs hurt so bad they couldn't carry me. I never thought that any of that had to do with the pill until i read this..Im not taking it anymore and i have a week left..

I am generally classed as an active, happy and positive person, loving life.... but the last 4 months have been a blinking nightmare....
It seems we all pretty much have the same symptoms, horrid shoulder pain, muscle soreness, spasms, feet and generally feeling like "what the??" is where we are all at..horrid thoughts of MS? Motor Neurons, Parkinsons, etc. all sorts of possible sinister problems.
I too have stopped taking Lipitor only a week ago (and I only started back in October 2008 after "arguing with my doctor for many years not wanting to take it...and i didn't even know about the horror side effects, i just thought it was totally unnatural to strip the body of something almost totally,).. within 2 months I started showing signs of chronic neck C5/6/7 and left shoulder. Maybe I had injured myself once before and suffered pinched nerves, but the pain eventually went, but this is not normal or should I say usual...... I have constant buzzing of left thumb/forefinger and hand and my right leg. NEVER NEVER have I suffered from this type of symptom before in my entire 50 years... Even some days when the spasms are at their worst I get an itchy nose and tingling lips. The scariest symptom of a white flash in my left eye convinced me...So fed up with it and after stumbling on all the negative comments and side effects with this drug I made to decision to take control of my own life. It is too uncanny....As I said, it's only a week now free of Lipitor, I have increased my Vitamin C intake and making sure I take a Mega Multivitamin daily too. There is some interesting reading in various websites of Vitamin C vs Statins...

BUT it would really be nice to read any comments of people who have recovered from these rotten symptoms and what sort of time frame it took to get over them. Is there a light at the end of the tunnel for us all. Some indication of Recovery period is probably our greatest "want to know"... and also...when will i be able to enjoy cycling again. Thank you to everyone for the input and may our strength be returned, not only physically but spiritually as well. :-)

As I read through these posts, I had mixed feelings between thinking they were a little too whiny (please, no offense) to too many memories sweeping back in.
Here is my story... I was on Yasmin for a few years, a few years ago, from ages 18-21. I am now 26. I'd always been active and in shape, no major health problems. At 19, I started to get weird leg pains, tingling and numbness. It got much much worse. Long story short, I had two herniated discs in my lower back which was causing pinched nerves. I had steroid injections localized to my herniations. At this point my adrenal gland stopped working, my face swelled up like a balloon and I lost a ton of weight. Eventually, I had surgery on my back, but went to specialist after specialist to figure out what was going on with my non functioning adrenal gland. We figured that somehow the steroids had gotten into my bloodstream, which doctor after doctor told me was next to impossible. They were ready to do a write up in a medical research journal about my case. Eventually my 3rd Endocronologist (sp?) FINALLY told me to get off Yasmin. Somehow, this small bit of information was missed. My adrenal gland eventually kicked back into shape, my bloating went away and I finally and slow got healthy again.
So... coming back to Yasmin. After reading this site and continuing research on the effects of an influx of potassium, all of my symptoms lead straight to this source. The potassium increase caused the face swelling, muscle spasms, possibly even the nerve weakness (Only speculating, could have caused the herniation.) , from what multiple web sites state.
I must say that this is all speculation; however, light bulbs have just gone off in my head.
I was considering getting back on Yasmin because I now live in Thailand and they offer this pill. I have been on the NuvaRing and I love it, but I cannot find it here. If Yasmin was the cause of what happened to my body or not, I will not take my chances. Most of the symptoms listed by other women are effects of increased potassium. Please research this fact to become more informed about what is happening with your body. It helped me. I hope my story will in effect, help someone else.
And, I'd love to hear if anyone else had something similarly severe...

I took levaquin, cipro and avalox in a 4 month period due to a severe sinus infection, back in Jan to april of 2006. I had tolerated it most of my life, but at that time, I had had 'neck surgery due to 2 pinched nerves, left shoulder operated on, major tears, due to extreme 'flat roof roofing repair' for 6 months trying to save our 'dream home from satan'. (we lost it, foreclosure)
I complained to my dr the next day, (and most every week) he ignored my halluciations, (actually "snickered" in my face), mood altered, ignored my complaints of feeling like a hot rake tearing my muscle and tendons apart. pain, told me to continue taking it:(, blame me for listening and NOT doing research soon enough, I learned later the dr is supposed to STOP the drugs immediately to rule out tendonitist to prevent pernanent irreverable damage AND it's not to be given to 'muscle challanged people'). after that 3rd round in a 4 month period, I told him I'd rather die than to take them again. mom always told me I was allergic to pennicilin, I wasnt, it helped clear my infection.

I now have hodgkins lyphoma, (affects men mostly, i'm female, 51 yrs of age), I shouldnt have 'this cancer'. My face started breaking out w/2 types of skin cancer, basal cell, and precancer A. keratosis eveywhere. I was 120 lbs, cut muscles, always had been physical. Now, flab, lost mucle strength everywhere. Every day now is filled w/severe pain and NO dr will listen, I've been called crazy so many times, I could puke. The dr's dont WANT TO KNOW because of the extensive lawsuits that will exist due to them NOT knowing side effects and stopping meds, it's their 'brotherhood', protect each other no matter what the patients 'cost' is, as in mine, complete mind and body destruction:(
To MOST people, this drug is okay. To many of us, it's a life destroying slow death. Cant work, cant get disability. Have reached for 'help to heaven' so many times, but never followed through:(. I still HOPE for some dr to listen and do necessary tests so I can sue the crap out of my previous g.p. He should have known . HOPE is a forbidden 4 letter word, yet I cuss like a sailor.
Peace my fellow quin sufferers, Sandie in S.C.

Hi. I am in remission from Multiple Myloma and have had compression fractures so I am on a lot of other drugs also. It is hard to separate them all. But since taking Zocor and have been experiencing light headedness and just a general wooziness like I am off balance. It is worse when I have been sitting down a great deal of the day. Today has been awful. I am always hurting, and am frustrated I am not getting better faster. After reading this I am wondering if some of my pain isn't from the Zocor, not the after effects of my other problems. They have done tests and can't find pinched nerves or anything. Is anyone having problems like this? Thanks Linda

I have diagnosed osteoarthritis, two joint replacements, looking at a third, and my knee hurt at time. Bad fall over a year ago led eventually to spine surgery with fushion of several vertebrae. Before fall I had some back pain and have had the shoulder pain for years(and now requires partical reaplacement). I was very active and relatively athletic doing agility with my dog. After fall and sugery for pinched nerves, I have never felt normal. Too much pain all over, fingers still numb, don't feel safe running with my dog. I suffered muscle degeneration due to the pinched nerves. Finally after numerous expensive test etc, rheumatologist suggested kenalog shot if I didn't feel better soon. Also tentative diagnosis of gout but my stomache could not handle pills for gout. So I got a shot of kenelog. - Super! I felt "normal" for the first time in over a year, didn't feel weak in knees, felt I could walk faster and further. Positive side effect was clearing my sinuus' and clearing up cough from phlem from sinus area. Got shot about 5 weeks ago and it has gradualy faded. I do not feel as painedl, but my activity level has decreased. I want another shot.