This Is MS Multiple Sclerosis Knowledge & Support Community

I am the person selling the electrodes. I turned in my L300 for the Bioness L300 GO. It may not solve all issues, but it certainly helps with the foot drop, and it allows me to use any type of shoe or go barefoot. It allows me to contra dance every Saturday evening, something I would hate to give up.

21 Quick Fit Electrode Left - A LCE-1100 (See photo) 6 Heel Pads (just the sticky pad) 1 Charge Cord $200 takes it all. Or B.O. Prefer Paypal you pay shipping I'll cover paypal fees. https://c2.staticflickr.com/8/7844/47203731711_92ac37b541_h_d.jpg https://c2.staticflickr.com/8/7828/32261489717_454e...

Hi Jimmylegs, Sorry I haven't responded, it's been a bit crazy here, took vacation time over the holidays, and it was back to work on Monday. Will ask my doctor for a zinc test, at my next appointment. Great idea about the sweet potatoes, will let you know how the experiment goes. Stay warm, this we...

Hi I have not heard about magnesium glycinate, will have to check it out, I'm almost out anyway. I know it is working because will wake with Charlie horses on occasion that are just horrible, if my level is too low, and used to have some spasticity but not much anymore. I never knew that D3 and magn...

Hi again! I take Magnesium Oxide, and take all vitamins at night, except B-100 and agal 900 DHA, which I take when I get up in the morning. I take so many other things, that it was getting a bit crazy, so I dropped the multivitamin, although I may add it back now that it is winter. I add pumpkin see...

Hi jimmylegs, I followed the MS Diet Book - Swank Low fat diet. I don't eat red meat, butter, cream, anything with palm oil shortening, most cheeses, or chocolate. :( Currently, I eat hearty oatmeal with fruit for breakfast, veggies and sometimes chicken for lunch, salad, piece of fruit and yogurt f...

Hi Everyone, I am new to the forum. My first episode was in 1975 with Optic Neuritis, but I was not diagnosed until 1993 with RRMS. Until about 5 years ago, I did not have any significant disability, but have progressed to SPMS, so no relapses, only progression. I have never taken any meds, and have...

Hi xpsychiatricmd, Thanks for the response. I was looking into having HSCT done in Russia, and was already approved when I heard about the trial and figured I would take a chance on the trial first. Some people really have wonderful results with the HSCT (Stem Cell Transplant), the earlier and more ...

Hi Everyone, I am new to the forum. My first episode was in 1975 with Optic Neuritis, but I was not diagnosed until 1993 with RRMS. Until about 5 years ago, I did not have any significant disability, but have progressed to SPMS, so no relapses, only progression. I have never taken any meds, and have...