Fasciitis symptoms and conditions

I have had Type 1 Diabetes for many years (54) without any complications of the disease - until I had a mild stroke. Which didn't affect me. Now my doctor makes me take Lipitor. From the very start of taking 10mg Lipitor per day, I got muscle cramps and leg twitches whilst in bed; muscle weaknesses; I even got Plantar Fasciitis and now I limp slightly in that foot. Before I took Lipitor I used to sleep like a baby. Lipitor has made me from a relatively healthy person despite having Diabetes to what feels like an old lady at aged 55. I know it is Lipitor as when I stop taking the drug all unpleasant side effects mentioned above cease. The trouble is my doctor won't give my Insulin without Lipitor and I need Insulin to live, of course. So I am forced to take Lipitor. I find that exercise such as a good long walk during the daytime helps; without it (eg in bad weather when I cannot get outside) the effects of Lipitor are much worse. My cholesterol readings and blood pressure are always good (even before the stroke) so why should I have to be almost crippled by Lipitor?

My second trip to this forum. A couple years ago, I developed plantar's fasciitis in both heels and had to give up basketball (at 54), and it took about nine months to recover from that. I had been on Lipitor 10 mg, and, while I can't say there was a cause-effect relationship, I had no problems of this kind before then.

Well, I continued on the Lipitor, and this past fall got horrible impingement pain in one shoulder that evolved to a frozen shoulder (adhesive capsulitis). Tonight I did a quick google search on this and it led me back to this site. Again, I cannot PROVE anything, but I've NEVER had any trouble with joints and just have to wonder.

I read on one link that Frozen Shoulder is on the rise, and wonder if Statin use is possibly behind it. I'm at the point that I may go off these drugs and go hard core Atkins diet again, the only thing that got the excess 30 pounds I'm carrying off, and also gave me "textbook" numbers on my lipid profile.

I'm starting to think this drug is possibly the problem. It's not worth it to take a debilitating and crippling substance just to be able to eat whatever I want.

I was put on Levoxyl for 20 years. Hair kept falling out, muscles aches, acid reflux, plantar fasciitis, carpel tunel, tired, cranky, brain fog. I could barely walk and had developed a stutter. I was to be tested for Alzheimers at 45. I was told there was no other drug for hypothyroidism and it wasn't the Levoxyl doing these things to me.

Well I found another drug thanks to the internet and Yahoo Natural Thyroid Group. It was Armour. I have been on Armour for about 2 years now. All those problems I had on Levoxyl are gone. Completely GONE! Wasn't the Levoxyl huh?

Just checking in after nearly a year or so, during which I cut my 10 mg Lipitor dose in HALF! I knife the little white pills down the middle and take 5 mg per day. My doctor did not notice any difference and HDL/LDL etc, are still in the range he likes. So, let's see about symptoms. The Plantar's Fasciitis is still there, but much improved, probably because I gave up full court basketball (at age 55). I have a few other symptoms that I recognize from others posting about them, such as occasional muscle ticks, general malaise, and sleep disorders, but, in general, I seem to be tolerating the 5 mg dose better than the 10 mg dose, AND, most importantly, it IS at a therapeutic level. I have not mentioned this to my Dr., and will keep it that way. If he can't tell, then my plan is working, sort of.

I really think Lipitor is poison and will eventually kill anyone who uses it, but am hoping I can cheat the hangman with the 5mg doses. I don't want to go back to cholesterol readings in the 250-plus range, because heart disease is the big killer in my family.

We'll see how 5 mg goes. I'm not suggesting anyone else necessarily should try this, but I was amazed that the numbers on my labs were almost identical as the 10mg.

I was diagnosed bipolar a year ago and worked my way up to 200 mg of Lamictal a day but recently desided to wean myself off of it as I have found some chinese herbs that will stabilize my moods without the side effects. Since being on Lamictal, I have had horrible pain in my left foot when I walk and it just kept getting worse. The pain got so bad I could not stay at work. I am a welder and have to be on my feet all day but after two hours I would be in so much pain and have to take tylenol 3 with codeine just to make it through an 8 hour shift. I am now down to 25mg of lamictal and soon to be totally off. My foot is now healing and I feel great personally. I am not irritable or moody but am taking Chinese herbs . I noticed when I got myself down to the 100 mg level then went to 75 mg of Lamictal, I got really sick like I had pnuemonia and I had severe chills, bad headache, swollen lymphnodes and very nauseated with no appetite for three days. I lost 5 pounds during this time. I got through it but felt like I was haveing a illegal drug withdrawal big time.
Lamictal was poison to my system. I feel great now. I can now start to run and exercise again. For anyone who has interest, go to Ron Teegaurdens Dragon Herbs web site and find a natural way. you will be much happier.
Lamictal is bad stuff.

anonymous

Took leviquin 500 for 8 days before I realized what was happening to me. Side effects included: severe panic, altered mental state, constant sleep, loss of appetite, pounding heart rate. After 2 trips to the ER no help was provided. I stoped the Leviquin early (was supposed to take it for 3 wks) and immediately started feeling better. The anxiety is much less but still present and I still sleep all the time.

Has anyone had similar experiences and, more importantly, how long does this last?

Please help!

April 10, 2005- I was exposed to what is a suspected case of whooping cough and developed the symptoms quickly. I went in and was given something like tetracycline for 10 days. I was still coughing violently at the end and so went back in. A young doctor gave me Levaquin and I took 3 or 4 of the pills but developed a back ache and went in. That doctor x-rayed me to make sure I hadn't cracked ribs from coughing so hard. I hadn't. He put me on a different antibiotic. Within 3-4 days I went into the ER because I had one of my coughing attacks (they're violent and you can't inhale because a rubbery-like phlegm get stucks in your windpipe and your body tries everything to expell it!) As I coughed that time I suddenly felt a horrible pain, like something exploded deep inside my back, not a surface muscle. A separate pain started and that was a slow, burning, tearing feeling. I've never felt such intense pain. I couldn't raise my legs to sit in our car and so we called the ambulance. The ER md was more interested in my lungs and found that I did have some pneuonia as well, gave me morphine so that I could sleep for 24 hours, and told me to continue the antibiotics. He also told me to go ahead and finish out the Levaquin as well! And stupidly I did. I had pain from the tendon and whatever tear in my back for months. I couldn't sleep easily. I ended up having pneumonia again in Nov. 2005 and the coughing made that injury hurt again. This year I have Achilles tendonitis in both legs and fasciitis in one foot. I don't know how long it takes for Levaquin to clear out of the body and I also don't know if these symptoms are related to taking Levaquin last year. In looking back, I think it's odd that you'd prescribe a medicine that has the adverse effect of ruptured tendons and the like to a person that is having violent coughing for weeks on end. There were times during what we think was Pertussis, that I was coughing with that spasmodic type of cough 8 times a night and regular coughing every 5 minutes or more. If anyone was going to experience the adverse side effect, it would be a person using muscles repeatedly and violently! Don't you think???
I am so angry about all of this.