This Is MS Multiple Sclerosis Community: Knowledge & Support

Hello!

I'm brand new, awaiting a MS dx, but likely won't happen until early next month.

Meanwhile, I'm taking control of what I can do myself. For now that's primarily with diet and supplementation.

My primary question right now is: What next steps should I take to boost my vitamin D level?

A couple of weeks ago, it came back as 9.9 ng/ml. That's obviously completely unacceptable. I took a 400,000 IU megadose almost two ...

HI FRIENDS A new reach indicates treadmills exercises can improve reaction time and cognitive improvements
please read more http://multiplesclerosisnewstoday.com/2 ... 4-71285713
regards
seeva

Hello, I recently read this interview

http://www.meandmydiabetes.com/2011/09/ ... -and-diet/

and found it very appealing. I have been following the Paleo diet for the last one and a half years and I find helpful to know some possible scientific fundamentals behind it (apart from the story of the inability to adapt of the human body to the big changes in diet in the last 10.000 years). The Rosedale diet seems ...

(Right off the bat, i havent been dx with ms) But im going through the motions.

I have been taking vitamin b-12 to see if it is a b-12 deficiency. And they say there is no unsafe amounts to take it and the excess will be flushed resulting in bright yellow pee. I have been taking 5000 mcg of methyl b-12 and 1000mcg of cyano b-12 (which i think equates to 90,000% over rda!)
Pee ...

I need to start vit D again. I've taken it in the past and felt much better and did not get the cold/flu going around at all.
1st question: what variant of D should I take for MS? D, D3 or something else?
2nd question: what brand? I've taken Nutri-West HI-D3 before and had good results but it is maddeningly difficult to get. Pureformulas is out of stock with no known ETA. The manufacturer wants ...

I am 32, male, I have had MS for 15 years - physically I am fortunately in a fairly good state without much disability. 5"10, 59kg (130lb) which isn't great. That's on the very low end of the healthy BMI range, which isn't exactly ideal.

http://www.neurology.org/content/82/10_ ... .155.short

I have just started prescribed Somatropin @ 2 IU per day and will report back on how I'm feeling.

There's been ...

Hi All,

I am new to any of the diets that exist to MS and am hoping that any of you can help me to explain eating of meat. If meat would be bad for MS, what is the underlying mechanism? Is it just the saturated fat, or are more mechanisms playing a role?

Thanks so much

Hello everybody,

I'm a 31-yo female and this is my first post after reading a lot.

I was taken into the hospital with numbness from my toes up to my neck plus 3 fingertips last March. First thoughts were directed to Guillain-Barre but testing did eventually point more towards MS. The MRI found an active lesion in my spine (C4-C5), an inactive lesion somewhere in the brain and LP showed oligl bands in the CSF. ...

I was just diagnosed yesterday and my MS specialist recommended tecfidera as first line therapy. Anyone with experience with this?

Dear All,

I am on Gylenia since September 2014 and I would like to start the Helminthic Therapy but I am worried that since I am already under an immuno supressant medication I may be exposing myself to too many risks as my body immune response to any other viruses/ cancer would be completly incapacitated.

I have asked 3 neurologysts and 1 is against, 2 are neutral regarding the use of helminths but none of ...