Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum. ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
Our Patient-to-Patient MS Forum is where you can communicate with other people who share your interest in Multiple Sclerosis. This forum is not monitored by medical professionals.
I have peripheral neuropathy (axonal). It is symptom and not a diagnosis. EMG result confirmed the neuropathy and type. They are trying to figure it out. I am currently being treated for lyme even thugh all my lymes test have been negative. My neuro said that people I don't have MS because people with MS do not get peripheral neuropathy...sigh.
I know that peripheral neuropathy is a symptom, not a disease. I am diagnosed with secondary progressive MS but I had some signs of peripheral neuropathy too. So I was tested for many many different things. My EMG was fine so were most of my tests as I have already written.
Things are getting worse and worse. My legs freeze increasing my spasticity. I cannot stand even minor enviropmental changes. As you understand I am not treated for anything, apart from MS, as we don't know what it is. Just some steroids hoping that they could help MS and the "X" peripheral neuropathy.
Rebeccah
Things are getting worse and worse. My legs freeze increasing my spasticity. I cannot stand even minor enviropmental changes. As you understand I am not treated for anything, apart from MS, as we don't know what it is. Just some steroids hoping that they could help MS and the "X" peripheral neuropathy.