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Wow...seems like a LONG time since I last had to face a Neurologist. Some here know the battle I have been dealing with since 2006 and here it is almost 2010!!! Can you believe it???!!! I have been keeping track of my symptoms since I last saw Dr. G. ...

Please Read!!! Diagnosed-type of MS that doesnt respond to the meds?

- Multiple Sclerosis Community

Ok, I have not been on here for a while. I guess I wanted to forget about being sick, since I was feeling well and had no answers. I had my first attack 2 years ago in March, lasted 6 months, extreme weakness in legs, to the point I couldn't walk for a few...

Has anyone tried the diet on http://direct-ms.org?

- Multiple Sclerosis Community

There is a very interesting web site with a diet for MS. The theories they present seem to be backed-up with scientific data and the testimonials are quite impressive The web site - http://direct-ms.org Do anyone have any experience with it? It is ...

NMO-IgG test

- Multiple Sclerosis Community

In reference to my previous post about neuromyelitis/NMO/Devic's disease, I have a question for all of you who have undergone labwork for MS and/or its mimics. If you happen to have your old lab reports, can you tell me if you've ever been tested for ...

What can I do to get my neurologist to try a less dangerous treatment?

- Multiple Sclerosis Community

I am happy to say I am in full remission from my recent exacerbation, after having chelation therapy and will be back to work next week. My new neurologist who is now the third to diagnose me with MS, now wants to put me on Avonex to prevent relapses ...

Has anyone else been diagnosed with Lyme Disease and Multiple Sclerosis?

- Lyme Disease Community

Hi all! I thought I would start by giving you a little of my health history. I had an attack of brain inflammation in June 2011, at a time of great stress in my life, with 10 of my 12 cranial nerves impacted. A subsequent 'sensory' relapse in Janua...

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