I was on Zoloft, and I was diagnosed with sensorimotor polyneuropathy also..I was having terrible spasms in my legs..Charlie horses every night...the calves of both legs were so sore....when I read about serotonin syndrome, from taking serotonin uplifting drugs..which Zoloft is...I weaned myself off..my spasms stopped promptly....now I'm going to go back to my neuro dr. And have them to do another test...it's been 3 yrs. Since the last test...the more I have been researching theses drugs, the madder I am about all the things I have been dealing with...Hope you find some answers too...
I was reading your post and found it interesting. I have the same symptoms you have and my dad and grandma had polyneuropathy. I started all the test you have mentioned and when I got to the printout that read. Impression :
Nerve conduction studies showed evidence of sensorimotor polyneuropathy of axonaldegenerating type. EMG showed denervation in the leg muscles. They suggested a muscle biopsy, I checked out of the race and said I'll just have to live with it. I am 69 years old, not a lot of time to spend on tests that won't change anything I read on and what perked my interest was the drugs. I have taken Levaquin for years. Makes me wonder. Thanks for your posts.
Hello Happymom081,
No I have not taken any of those kinds of dugs
I also have sensorimotor peripheral neuropathy. I got this because I took the antibiotic Cipro. Everything started while I was taking this drug. I only took it for 3 1/2 days and I could not even do a calf raise after 2 or 3 weeks. Cipro belongs to a class of antibiotics called fluoruquinolones. They also include Levaquin, Avelox and many others. They usually have a 'flox' in the chemical name (ex. Ciprofloxacin). Have you taken any of these antibiotics. If so, that may be the cause. It can happen months after taking them. They are associated with many many different adverse drug reactions.
Hi. No I don't have an absolute answer as yet. I've worried about MS as well especially since I always get worse in the summer. I have had a diagnosis of a hereditary peripheral neuropathy but my Neuro says these particular symptoms are caused by that. It has been suggested that migraines can be the cause as well as TN trigeminial neuralgia but still no absolute answer. I have not had an MRI with contrast nor has one been ordered so for now I guess MS is not a huge one to worry about.
Sorry you are experiencing these symptoms as well they are not nice and can be scary
Wondered if you ever found out what was wrong? I am having the EXACT symptoms and test results as you did, and worried about MS
reposting this question please.